Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 79618 |
| ensemblid | ENSG00000147421.18 |
| hgncid | 26137 |
| symbol | HMBOX1 |
| name | homeobox containing 1 |
| refseq_nuc | NM_001135726.3 |
| refseq_prot | NP_001129198.1 |
| ensembl_nuc | ENST00000287701.15 |
| ensembl_prot | ENSP00000287701.10 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 28890395 |
| end | 29053262 |
| strand | + |
| ver | v1.2 |
| region | chr8:28890395-29053262 |
| region5000 | chr8:28885395-29058262 |
| regionname0 | HMBOX1_chr8_28890395_29053262 |
| regionname5000 | HMBOX1_chr8_28885395_29058262 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1260 | 343 | 90 | 49 | 158 | 12 | 32 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | ATGCT others(1255): Show |
chr8 | 28885395 | 29058262 | ||
| a0001c0002 | 0/0 | 1260 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | ATGCT others(1255): Show |
chr8 | 28885395 | 29058262 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 3710 | 77 | 18 | 14 | 32 | 5 | 7 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | GTTGA others(3705): Show |
chr8 | 28885395 | 29058262 |
| a0001c0001t0002 | 1/0 | 3711 | 75 | 2 | 8 | 55 | 0 | 9 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | GTTGA others(3706): Show |
chr8 | 28885395 | 29058262 |
| a0001c0001t0003 | 0/0 | 3716 | 60 | 17 | 4 | 32 | 0 | 7 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | GTTGA others(3711): Show |
chr8 | 28885395 | 29058262 |
| a0001c0001t0004 | 0/0 | 3707 | 50 | 16 | 16 | 7 | 4 | 7 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | GTTGA others(3702): Show |
chr8 | 28885395 | 29058262 |
| a0001c0001t0005 | 0/0 | 3711 | 16 | 11 | 1 | 0 | 3 | 1 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | GTTGA others(3706): Show |
chr8 | 28885395 | 29058262 |
| a0001c0001t0006 | 0/0 | 3717 | 14 | 2 | 0 | 12 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | GTTGA others(3712): Show |
chr8 | 28885395 | 29058262 |
| a0001c0001t0007 | 0/0 | 3707 | 12 | 11 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | GTTGA others(3702): Show |
chr8 | 28885395 | 29058262 |
| a0001c0001t0008 | 0/0 | 3715 | 10 | 5 | 1 | 3 | 0 | 1 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | GTTGA others(3710): Show |
chr8 | 28885395 | 29058262 |
| a0001c0001t0009 | 0/0 | 3716 | 5 | 0 | 0 | 5 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | GTTGA others(3711): Show |
chr8 | 28885395 | 29058262 |
| a0001c0001t0010 | 0/0 | 3711 | 4 | 2 | 2 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | GTTGA others(3706): Show |
chr8 | 28885395 | 29058262 |
| a0001c0001t0011 | 0/0 | 3712 | 3 | 0 | 0 | 3 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | GTTGA others(3707): Show |
chr8 | 28885395 | 29058262 |
| a0001c0001t0012 | 0/0 | 3711 | 2 | 2 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | GTTGA others(3706): Show |
chr8 | 28885395 | 29058262 |
| a0001c0001t0013 | 0/0 | 3707 | 2 | 0 | 0 | 2 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | GTTGA others(3702): Show |
chr8 | 28885395 | 29058262 |
| a0001c0001t0014 | 0/0 | 3716 | 2 | 2 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | GTTGA others(3711): Show |
chr8 | 28885395 | 29058262 |
| a0001c0001t0015 | 0/0 | 3714 | 2 | 0 | 2 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | GTTGA others(3709): Show |
chr8 | 28885395 | 29058262 |
| a0001c0001t0016 | 0/0 | 3717 | 2 | 0 | 0 | 2 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | GTTGA others(3712): Show |
chr8 | 28885395 | 29058262 |
| a0001c0001t0017 | 0/0 | 3711 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | GTTGA others(3706): Show |
chr8 | 28885395 | 29058262 |
| a0001c0001t0018 | 0/0 | 3712 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | GTTGA others(3707): Show |
chr8 | 28885395 | 29058262 |
| a0001c0001t0019 | 0/0 | 3710 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | GTTGA others(3705): Show |
chr8 | 28885395 | 29058262 |
| a0001c0001t0020 | 0/0 | 3680 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | GTTGA others(3675): Show |
chr8 | 28885395 | 29058262 |
| a0001c0001t0021 | 0/0 | 3716 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | GTTGA others(3711): Show |
chr8 | 28885395 | 29058262 |
| a0001c0001t0022 | 0/0 | 3739 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | GTTGA others(3734): Show |
chr8 | 28885395 | 29058262 |
| a0001c0001t0023 | 0/0 | 3716 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | GTTGA others(3711): Show |
chr8 | 28885395 | 29058262 |
| a0001c0002t0002 | 0/0 | 3711 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | GTTGA others(3706): Show |
chr8 | 28885395 | 29058262 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0293 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0050 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0004g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0004g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0004g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0004g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0004g0022 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0004g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0004g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0004g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0004g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0004g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0004g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0004g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0004g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0004g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0004g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0004g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0004g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0004g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0004g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0004g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0004g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0004g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0004g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0004g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0004g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0004g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0004g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0004g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0004g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0004g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0004g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0004g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0004g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0004g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0004g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0004g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0004g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0004g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0004g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0004g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0004g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0004g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0004g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0004g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0004g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0004g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0004g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0004g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0004g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0004g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0005g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0005g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0005g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0005g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0005g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0005g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0005g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0005g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0005g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0005g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0005g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0005g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0005g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0005g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0005g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0005g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0006g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0006g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0006g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0006g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0006g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0006g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0006g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0006g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0006g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0006g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0006g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0006g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0006g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0006g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0007g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0007g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0007g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0007g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0007g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0007g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0007g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0007g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0007g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0007g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0007g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0007g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0008g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0008g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0008g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0008g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0008g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0008g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0008g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0008g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0008g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0008g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0009g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0009g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0009g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0009g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0009g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0010g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0010g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0010g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0010g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0011g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0011g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0011g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0012g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0012g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0013g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0013g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0014g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0014g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0015g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0015g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0016g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0016g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0017g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0018g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0019g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0020g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0021g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0022g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0023g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0002t0002g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0225 | EUR | GBR | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG00140 | hp2 | a0001 | c0001 | t0004 | g0022 | EUR | GBR | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG00280 | hp1 | a0001 | c0001 | t0004 | g0044 | EUR | FIN | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG00280 | hp2 | a0001 | c0001 | t0005 | g0172 | EUR | FIN | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0279 | EUR | FIN | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG00323 | hp2 | a0001 | c0001 | t0004 | g0028 | EUR | FIN | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG00408 | hp1 | a0001 | c0001 | t0017 | g0213 | EAS | CHS | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG00408 | hp2 | a0001 | c0001 | t0003 | g0085 | EAS | CHS | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | CHS | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0135 | EAS | CHS | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0195 | EAS | CHS | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0133 | EAS | CHS | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG00544 | hp1 | a0001 | c0001 | t0006 | g0328 | EAS | CHS | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG00544 | hp2 | a0001 | c0001 | t0004 | g0047 | EAS | CHS | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0136 | EAS | CHS | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG00558 | hp2 | a0001 | c0001 | t0003 | g0078 | EAS | CHS | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG00597 | hp1 | a0001 | c0001 | t0004 | g0051 | EAS | CHS | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0203 | EAS | CHS | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG00609 | hp1 | a0001 | c0001 | t0003 | g0080 | EAS | CHS | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0264 | EAS | CHS | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0207 | EAS | CHS | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG00621 | hp2 | a0001 | c0001 | t0008 | g0067 | EAS | CHS | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG00639 | hp1 | a0001 | c0001 | t0004 | g0042 | AMR | PUR | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0214 | AMR | PUR | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG00642 | hp2 | a0001 | c0001 | t0004 | g0342 | AMR | PUR | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG00735 | hp1 | a0001 | c0001 | t0008 | g0074 | AMR | PUR | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG00735 | hp2 | a0001 | c0001 | t0015 | g0242 | AMR | PUR | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG00738 | hp1 | a0001 | c0001 | t0004 | g0034 | AMR | PUR | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG00738 | hp2 | a0001 | c0001 | t0004 | g0064 | AMR | PUR | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG00741 | hp1 | a0001 | c0001 | t0004 | g0038 | AMR | PUR | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG00741 | hp2 | a0001 | c0001 | t0004 | g0004 | AMR | PUR | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG01069 | hp1 | a0001 | c0001 | t0015 | g0233 | AMR | PUR | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG01069 | hp2 | a0001 | c0001 | t0004 | g0027 | AMR | PUR | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG01070 | hp1 | a0001 | c0001 | t0004 | g0037 | AMR | PUR | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0290 | AMR | PUR | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG01081 | hp1 | a0001 | c0001 | t0004 | g0049 | AMR | PUR | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG01081 | hp2 | a0001 | c0001 | t0004 | g0020 | AMR | PUR | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0114 | AMR | PUR | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG01167 | hp1 | a0001 | c0001 | t0004 | g0023 | AMR | PUR | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG01167 | hp2 | a0001 | c0001 | t0010 | g0311 | AMR | PUR | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0252 | AMR | PUR | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0155 | AMR | PUR | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG01243 | hp1 | a0001 | c0001 | t0004 | g0063 | AMR | PUR | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0256 | AMR | PUR | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0202 | AMR | CLM | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0280 | AMR | CLM | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG01256 | hp1 | a0001 | c0001 | t0004 | g0043 | AMR | CLM | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0248 | AMR | CLM | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG01261 | hp1 | a0001 | c0001 | t0007 | g0012 | AMR | CLM | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0198 | AMR | CLM | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0309 | AMR | CLM | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0285 | AMR | CLM | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0243 | AMR | CLM | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG01496 | hp2 | a0001 | c0002 | t0002 | g0283 | AMR | CLM | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG01516 | hp1 | a0001 | c0001 | t0005 | g0291 | EUR | IBS | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0289 | EUR | IBS | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG01884 | hp1 | a0001 | c0001 | t0004 | g0056 | AFR | ACB | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0234 | AFR | ACB | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG01928 | hp1 | a0001 | c0001 | t0010 | g0230 | AMR | PEL | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG01928 | hp2 | a0001 | c0001 | t0003 | g0075 | AMR | PEL | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0205 | AMR | PEL | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0308 | AMR | PEL | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG01975 | hp1 | a0001 | c0001 | t0004 | g0030 | AMR | PEL | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG01975 | hp2 | a0001 | c0001 | t0003 | g0112 | AMR | PEL | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02004 | hp1 | a0001 | c0001 | t0004 | g0025 | AMR | PEL | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0226 | AMR | PEL | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02027 | hp1 | a0001 | c0001 | t0013 | g0033 | EAS | KHV | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | KHV | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02040 | hp1 | a0001 | c0001 | t0003 | g0087 | EAS | KHV | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | KHV | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02055 | hp1 | a0001 | c0001 | t0018 | g0303 | AFR | ACB | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02055 | hp2 | a0001 | c0001 | t0010 | g0300 | AFR | ACB | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02056 | hp1 | a0001 | c0001 | t0006 | g0329 | EAS | KHV | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0170 | EAS | KHV | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | KHV | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0219 | EAS | KHV | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02074 | hp1 | a0001 | c0001 | t0004 | g0048 | EAS | KHV | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0270 | EAS | KHV | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0209 | EAS | KHV | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02080 | hp2 | a0001 | c0001 | t0009 | g0082 | EAS | KHV | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02145 | hp1 | a0001 | c0001 | t0004 | g0055 | AFR | ACB | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02145 | hp2 | a0001 | c0001 | t0005 | g0302 | AFR | ACB | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02155 | hp1 | a0001 | c0001 | t0008 | g0094 | EAS | CDX | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0314 | EAS | CDX | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0321 | EAS | CDX | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0152 | EAS | CDX | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02257 | hp1 | a0001 | c0001 | t0003 | g0181 | AFR | ACB | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02257 | hp2 | a0001 | c0001 | t0007 | g0218 | AFR | ACB | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02258 | hp1 | a0001 | c0001 | t0005 | g0282 | AFR | ACB | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02258 | hp2 | a0001 | c0001 | t0004 | g0058 | AFR | ACB | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0119 | AFR | ACB | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0158 | AFR | ACB | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02293 | hp1 | a0001 | c0001 | t0004 | g0021 | AMR | PEL | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0284 | AMR | PEL | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02300 | hp1 | a0001 | c0001 | t0003 | g0107 | AMR | PEL | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0310 | AMR | PEL | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0316 | AFR | ACB | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02451 | hp2 | a0001 | c0001 | t0004 | g0128 | AFR | ACB | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02572 | hp1 | a0001 | c0001 | t0014 | g0117 | AFR | GWD | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02572 | hp2 | a0001 | c0001 | t0004 | g0061 | AFR | GWD | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0304 | AFR | GWD | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02615 | hp2 | a0001 | c0001 | t0003 | g0210 | AFR | GWD | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0134 | AFR | GWD | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02622 | hp2 | a0001 | c0001 | t0007 | g0013 | AFR | GWD | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02630 | hp1 | a0001 | c0001 | t0007 | g0018 | AFR | GWD | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02630 | hp2 | a0001 | c0001 | t0010 | g0312 | AFR | GWD | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02647 | hp1 | a0001 | c0001 | t0005 | g0301 | AFR | GWD | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02647 | hp2 | a0001 | c0001 | t0004 | g0060 | AFR | GWD | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02698 | hp1 | a0001 | c0001 | t0003 | g0106 | SAS | PJL | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0212 | SAS | PJL | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02717 | hp1 | a0001 | c0001 | t0021 | g0343 | AFR | GWD | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0237 | AFR | GWD | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | GWD | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02723 | hp2 | a0001 | c0001 | t0003 | g0211 | AFR | GWD | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02735 | hp1 | a0001 | c0001 | t0003 | g0076 | SAS | PJL | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02735 | hp2 | a0001 | c0001 | t0005 | g0151 | SAS | PJL | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0258 | SAS | PJL | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02738 | hp2 | a0001 | c0001 | t0004 | g0019 | SAS | PJL | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02809 | hp1 | a0001 | c0001 | t0005 | g0178 | AFR | GWD | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02809 | hp2 | a0001 | c0001 | t0006 | g0326 | AFR | GWD | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02818 | hp1 | a0001 | c0001 | t0003 | g0179 | AFR | GWD | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02818 | hp2 | a0001 | c0001 | t0004 | g0054 | AFR | GWD | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02886 | hp1 | a0001 | c0001 | t0012 | g0297 | AFR | GWD | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02886 | hp2 | a0001 | c0001 | t0014 | g0118 | AFR | GWD | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0164 | AFR | GWD | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02896 | hp2 | a0001 | c0001 | t0004 | g0126 | AFR | GWD | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0253 | AFR | GWD | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02897 | hp2 | a0001 | c0001 | t0003 | g0165 | AFR | GWD | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02922 | hp1 | a0001 | c0001 | t0004 | g0065 | AFR | ESN | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02922 | hp2 | a0001 | c0001 | t0005 | g0175 | AFR | ESN | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02965 | hp1 | a0001 | c0001 | t0005 | g0173 | AFR | ESN | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02965 | hp2 | a0001 | c0001 | t0008 | g0123 | AFR | ESN | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02970 | hp1 | a0001 | c0001 | t0003 | g0153 | AFR | ESN | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02970 | hp2 | a0001 | c0001 | t0004 | g0057 | AFR | ESN | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02976 | hp1 | a0001 | c0001 | t0007 | g0015 | AFR | ESN | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02976 | hp2 | a0001 | c0001 | t0005 | g0176 | AFR | ESN | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0241 | SAS | PJL | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0163 | SAS | PJL | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0306 | AFR | GWD | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0325 | AFR | GWD | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0324 | AFR | MSL | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0223 | AFR | MSL | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG03130 | hp1 | a0001 | c0001 | t0005 | g0177 | AFR | ESN | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG03130 | hp2 | a0001 | c0001 | t0007 | g0010 | AFR | ESN | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG03139 | hp1 | a0001 | c0001 | t0004 | g0110 | AFR | ESN | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG03139 | hp2 | a0001 | c0001 | t0004 | g0125 | AFR | ESN | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG03195 | hp1 | a0001 | c0001 | t0007 | g0014 | AFR | ESN | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG03195 | hp2 | a0001 | c0001 | t0008 | g0121 | AFR | ESN | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0236 | AFR | MSL | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG03209 | hp2 | a0001 | c0001 | t0008 | g0339 | AFR | MSL | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0182 | AFR | MSL | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG03225 | hp2 | a0001 | c0001 | t0008 | g0002 | AFR | MSL | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0341 | SAS | PJL | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0224 | SAS | PJL | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG03486 | hp1 | a0001 | c0001 | t0007 | g0016 | AFR | MSL | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0247 | AFR | MSL | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0194 | SAS | PJL | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG03490 | hp2 | a0001 | c0001 | t0008 | g0068 | SAS | PJL | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG03492 | hp1 | a0001 | c0001 | t0004 | g0031 | SAS | PJL | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0200 | SAS | PJL | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG03516 | hp1 | a0001 | c0001 | t0007 | g0062 | AFR | ESN | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG03516 | hp2 | a0001 | c0001 | t0005 | g0217 | AFR | ESN | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG03540 | hp1 | a0001 | c0001 | t0004 | g0124 | AFR | GWD | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0305 | AFR | GWD | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG03579 | hp1 | a0001 | c0001 | t0006 | g0116 | AFR | MSL | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG03579 | hp2 | a0001 | c0001 | t0007 | g0011 | AFR | MSL | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0229 | SAS | PJL | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG03654 | hp2 | a0001 | c0001 | t0004 | g0040 | SAS | PJL | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0257 | SAS | PJL | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG03669 | hp2 | a0001 | c0001 | t0004 | g0024 | SAS | PJL | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0156 | SAS | STU | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG03688 | hp2 | a0001 | c0001 | t0003 | g0071 | SAS | STU | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0294 | SAS | PJL | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0184 | SAS | PJL | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG03710 | hp1 | a0001 | c0001 | t0004 | g0039 | SAS | PJL | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG03710 | hp2 | a0001 | c0001 | t0003 | g0070 | SAS | PJL | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG03834 | hp1 | a0001 | c0001 | t0004 | g0036 | SAS | BEB | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0143 | SAS | BEB | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG04115 | hp1 | a0001 | c0001 | t0003 | g0086 | SAS | STU | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0160 | SAS | STU | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0168 | SAS | STU | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG04199 | hp2 | a0001 | c0001 | t0003 | g0009 | SAS | STU | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG04204 | hp1 | a0001 | c0001 | t0003 | g0008 | SAS | STU | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG04204 | hp2 | a0001 | c0001 | t0004 | g0035 | SAS | STU | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18522 | hp1 | a0001 | c0001 | t0003 | g0122 | AFR | YRI | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18522 | hp2 | a0001 | c0001 | t0005 | g0216 | AFR | YRI | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0277 | EAS | CHB | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18612 | hp2 | a0001 | c0001 | t0003 | g0088 | EAS | CHB | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0271 | EAS | CHB | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18747 | hp2 | a0001 | c0001 | t0003 | g0090 | EAS | CHB | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0180 | AFR | YRI | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18906 | hp2 | a0001 | c0001 | t0008 | g0003 | AFR | YRI | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0261 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18941 | hp2 | a0001 | c0001 | t0003 | g0089 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18943 | hp2 | a0001 | c0001 | t0006 | g0336 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0263 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18945 | hp2 | a0001 | c0001 | t0003 | g0115 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18947 | hp1 | a0001 | c0001 | t0016 | g0330 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0259 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18949 | hp2 | a0001 | c0001 | t0006 | g0108 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0161 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18950 | hp2 | a0001 | c0001 | t0003 | g0069 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18951 | hp1 | a0001 | c0001 | t0004 | g0041 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18952 | hp1 | a0001 | c0001 | t0003 | g0081 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0265 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18953 | hp1 | a0001 | c0001 | t0011 | g0278 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18953 | hp2 | a0001 | c0001 | t0003 | g0079 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18956 | hp1 | a0001 | c0001 | t0006 | g0333 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18956 | hp2 | a0001 | c0001 | t0011 | g0201 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0317 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18959 | hp1 | a0001 | c0001 | t0006 | g0340 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18959 | hp2 | a0001 | c0001 | t0008 | g0073 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0275 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18960 | hp2 | a0001 | c0001 | t0003 | g0096 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18961 | hp2 | a0001 | c0001 | t0003 | g0083 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18962 | hp2 | a0001 | c0001 | t0003 | g0084 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0262 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18965 | hp1 | a0001 | c0001 | t0004 | g0045 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18965 | hp2 | a0001 | c0001 | t0011 | g0313 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0296 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18968 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18969 | hp2 | a0001 | c0001 | t0003 | g0091 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18972 | hp2 | a0001 | c0001 | t0022 | g0334 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0266 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18974 | hp2 | a0001 | c0001 | t0009 | g0129 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18980 | hp2 | a0001 | c0001 | t0003 | g0098 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18981 | hp2 | a0001 | c0001 | t0006 | g0335 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18982 | hp1 | a0001 | c0001 | t0003 | g0113 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18982 | hp2 | a0001 | c0001 | t0023 | g0331 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18985 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0269 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18986 | hp1 | a0001 | c0001 | t0003 | g0104 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18988 | hp1 | a0001 | c0001 | t0009 | g0130 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18988 | hp2 | a0001 | c0001 | t0004 | g0046 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18992 | hp1 | a0001 | c0001 | t0003 | g0281 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18998 | hp2 | a0001 | c0001 | t0003 | g0105 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18999 | hp2 | a0001 | c0001 | t0013 | g0032 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA19000 | hp2 | a0001 | c0001 | t0006 | g0066 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA19002 | hp1 | a0001 | c0001 | t0009 | g0131 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0267 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA19004 | hp1 | a0001 | c0001 | t0003 | g0099 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA19006 | hp1 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA19007 | hp2 | a0001 | c0001 | t0003 | g0095 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA19009 | hp2 | a0001 | c0001 | t0003 | g0109 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0274 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA19010 | hp2 | a0001 | c0001 | t0020 | g0053 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA19011 | hp2 | a0001 | c0001 | t0019 | g0162 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA19012 | hp2 | a0001 | c0001 | t0016 | g0327 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0298 | AFR | LWK | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA19030 | hp2 | a0001 | c0001 | t0007 | g0017 | AFR | LWK | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0315 | AFR | LWK | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | LWK | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA19057 | hp1 | a0001 | c0001 | t0006 | g0337 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0318 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA19062 | hp1 | a0001 | c0001 | t0006 | g0332 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA19062 | hp2 | a0001 | c0001 | t0009 | g0132 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA19064 | hp1 | a0001 | c0001 | t0004 | g0052 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0276 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA19065 | hp1 | a0001 | c0001 | t0003 | g0077 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA19072 | hp2 | a0001 | c0001 | t0002 | g0273 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA19076 | hp1 | a0001 | c0001 | t0003 | g0102 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA19077 | hp1 | a0001 | c0001 | t0003 | g0100 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0272 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA19079 | hp1 | a0001 | c0001 | t0006 | g0338 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA19079 | hp2 | a0001 | c0001 | t0003 | g0101 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA19083 | hp1 | a0001 | c0001 | t0006 | g0111 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA19084 | hp1 | a0001 | c0001 | t0003 | g0093 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0295 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA19085 | hp2 | a0001 | c0001 | t0003 | g0103 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA19090 | hp2 | a0001 | c0001 | t0003 | g0097 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | YRI | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA19240 | hp2 | a0001 | c0001 | t0012 | g0174 | AFR | YRI | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA20129 | hp1 | a0001 | c0001 | t0004 | g0059 | AFR | ASW | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0292 | AFR | ASW | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0255 | EUR | TSI | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA20752 | hp2 | a0001 | c0001 | t0004 | g0026 | EUR | TSI | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0235 | EUR | TSI | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA20805 | hp2 | a0001 | c0001 | t0005 | g0171 | EUR | TSI | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG01123 | hp1 | a0001 | c0001 | t0005 | g0286 | AMR | CLM | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0288 | AMR | CLM | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | ACB | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02109 | hp2 | a0001 | c0001 | t0004 | g0127 | AFR | ACB | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | ACB | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | ACB | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02559 | hp1 | a0001 | c0001 | t0005 | g0215 | AFR | ACB | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0307 | AFR | ACB | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG03471 | hp1 | a0001 | c0001 | t0004 | g0029 | AFR | MSL | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0120 | AFR | MSL | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0299 | AFR | USA | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG06807 | hp2 | a0001 | c0001 | t0007 | g0005 | AFR | USA | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0293 | REF | REF | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0050 | REF | REF | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:28970316 | G | A | 1 | a0001c0002 | 1 | HG01496.hp2 | synonymous_variant | LOW | c.297G>A | p.Pro99Pro | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/10 | 638/3711 | 297/1263 | 99/420 | chr8 | 28970316 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:28890402 | T | C | 1 | a0001c0001t0012 | 2 | HG02886.hp1 NA19240.hp2 |
5_prime_UTR_variant | MODIFIER | c.-334T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/10 | 73466 | chr8 | 28890402 | ||||||
| chr8:28963863 | A | G | 2 | a0001c0001t0016 a0001c0001t0023 |
3 | NA18947.hp1 NA18982.hp2 NA19012.hp2 |
5_prime_UTR_variant | MODIFIER | c.-5A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 2/10 | 5 | chr8 | 28963863 | ||||||
| chr8:29051357 | T | TAACC | 14 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0006 others(11): Show |
163 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(160): Show |
3_prime_UTR_variant | MODIFIER | c.*217_*220dupCCAA | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 10/10 | 221 | INFO_REALIGN_3_PRIME | chr8 | 29051357 | |||||
| chr8:29051484 | T | C | 2 | a0001c0001t0013 a0001c0001t0020 |
3 | HG02027.hp1 NA18999.hp2 NA19010.hp2 |
3_prime_UTR_variant | MODIFIER | c.*329T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 10/10 | 329 | chr8 | 29051484 | ||||||
| chr8:29051898 | T | TA | 7 | a0001c0001t0003 a0001c0001t0009 a0001c0001t0011 others(4): Show |
73 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(70): Show |
3_prime_UTR_variant | MODIFIER | c.*763dupA | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 10/10 | 764 | INFO_REALIGN_3_PRIME | chr8 | 29051898 | |||||
| chr8:29051898 | T | TAA | 2 | a0001c0001t0006 a0001c0001t0016 |
16 | HG00544.hp1 HG02056.hp1 HG02809.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*762_*763dupAA | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 10/10 | 764 | INFO_REALIGN_3_PRIME | chr8 | 29051898 | |||||
| chr8:29051898 | TA | T | 3 | a0001c0001t0001 a0001c0001t0015 a0001c0001t0019 |
79 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*763delA | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 10/10 | 763 | INFO_REALIGN_3_PRIME | chr8 | 29051898 | |||||
| chr8:29051898 | TAAAAAAA others(1): Show |
T | 4 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0013 others(1): Show |
65 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*756_*763delAAAAAA others(2): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 10/10 | 756 | INFO_REALIGN_3_PRIME | chr8 | 29051898 | |||||
| chr8:29051919 | C | A | 1 | a0001c0001t0017 | 1 | HG00408.hp1 | 3_prime_UTR_variant | MODIFIER | c.*764C>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 10/10 | 764 | chr8 | 29051919 | ||||||
| chr8:29052006 | C | T | 4 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0013 others(1): Show |
65 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*851C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 10/10 | 851 | chr8 | 29052006 | ||||||
| chr8:29052200 | A | G | 1 | a0001c0001t0020 | 1 | NA19010.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1045A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 10/10 | 1045 | chr8 | 29052200 | ||||||
| chr8:29052210 | A | G | 1 | a0001c0001t0020 | 1 | NA19010.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1055A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 10/10 | 1055 | chr8 | 29052210 | ||||||
| chr8:29052212 | T | G | 1 | a0001c0001t0020 | 1 | NA19010.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1057T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 10/10 | 1057 | chr8 | 29052212 | ||||||
| chr8:29052217 | T | G | 1 | a0001c0001t0020 | 1 | NA19010.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1062T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 10/10 | 1062 | chr8 | 29052217 | ||||||
| chr8:29052224 | GCTTATCA others(20): Show |
G | 1 | a0001c0001t0020 | 1 | NA19010.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1070_*1096delCTTA others(23): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 10/10 | 1070 | chr8 | 29052224 | ||||||
| chr8:29052254 | T | G | 1 | a0001c0001t0020 | 1 | NA19010.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1099T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 10/10 | 1099 | chr8 | 29052254 | ||||||
| chr8:29052442 | T | A | 1 | a0001c0001t0020 | 1 | NA19010.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1287T>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 10/10 | 1287 | chr8 | 29052442 | ||||||
| chr8:29052526 | T | G | 1 | a0001c0001t0020 | 1 | NA19010.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1371T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 10/10 | 1371 | chr8 | 29052526 | ||||||
| chr8:29052560 | A | ATCTATTT others(17): Show |
1 | a0001c0001t0022 | 1 | NA18972.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1405_*1406insTCTA others(20): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 10/10 | 1406 | chr8 | 29052560 | ||||||
| chr8:29052561 | A | G | 1 | a0001c0001t0022 | 1 | NA18972.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1406A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 10/10 | 1406 | chr8 | 29052561 | ||||||
| chr8:29052569 | C | T | 1 | a0001c0001t0022 | 1 | NA18972.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1414C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 10/10 | 1414 | chr8 | 29052569 | ||||||
| chr8:29052571 | G | C | 1 | a0001c0001t0022 | 1 | NA18972.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1416G>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 10/10 | 1416 | chr8 | 29052571 | ||||||
| chr8:29052798 | C | T | 2 | a0001c0001t0005 a0001c0001t0012 |
18 | HG00280.hp2 HG01123.hp1 HG01516.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1643C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 10/10 | 1643 | chr8 | 29052798 | ||||||
| chr8:29052799 | G | A | 1 | a0001c0001t0014 | 2 | HG02572.hp1 HG02886.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1644G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 10/10 | 1644 | chr8 | 29052799 | ||||||
| chr8:29052863 | A | T | 1 | a0001c0001t0020 | 1 | NA19010.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1708A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 10/10 | 1708 | chr8 | 29052863 | ||||||
| chr8:29052880 | G | A | 16 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(13): Show |
239 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(236): Show |
3_prime_UTR_variant | MODIFIER | c.*1725G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 10/10 | 1725 | chr8 | 29052880 | ||||||
| chr8:29052976 | A | T | 1 | a0001c0001t0021 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1821A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 10/10 | 1821 | chr8 | 29052976 | ||||||
| chr8:29053055 | G | T | 1 | a0001c0001t0020 | 1 | NA19010.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1900G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 10/10 | 1900 | chr8 | 29053055 | ||||||
| chr8:29053056 | T | G | 1 | a0001c0001t0020 | 1 | NA19010.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1901T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 10/10 | 1901 | chr8 | 29053056 | ||||||
| chr8:29053184 | A | T | 1 | a0001c0001t0020 | 1 | NA19010.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2029A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 10/10 | 2029 | chr8 | 29053184 | ||||||
| chr8:29053230 | G | T | 1 | a0001c0001t0007 | 12 | HG01261.hp1 HG02257.hp2 HG02622.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2075G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 10/10 | 2075 | chr8 | 29053230 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:28891597 | A | G | 1 | a0001c0001t0021g0343 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-58+919A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28891597 | |||||||
| chr8:28891687 | G | C | 2 | a0001c0001t0008g0002 a0001c0001t0008g0003 |
2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-58+1009G>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28891687 | |||||||
| chr8:28891978 | C | G | 1 | a0001c0001t0004g0342 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-58+1300C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28891978 | |||||||
| chr8:28892419 | C | T | 1 | a0001c0001t0002g0341 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-58+1741C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28892419 | |||||||
| chr8:28892436 | A | G | 15 | a0001c0001t0006g0326 a0001c0001t0006g0328 a0001c0001t0006g0329 others(12): Show |
15 | HG00544.hp1 HG02056.hp1 HG02809.hp2 others(12): Show |
intron_variant | MODIFIER | c.-58+1758A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28892436 | |||||||
| chr8:28892468 | C | T | 2 | a0001c0001t0003g0324 a0001c0001t0003g0325 |
2 | HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-58+1790C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28892468 | |||||||
| chr8:28892564 | A | G | 5 | a0001c0001t0001g0319 a0001c0001t0001g0320 a0001c0001t0001g0321 others(2): Show |
5 | HG02165.hp1 NA18954.hp1 NA18973.hp1 others(2): Show |
intron_variant | MODIFIER | c.-58+1886A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28892564 | |||||||
| chr8:28892901 | G | A | 1 | a0001c0001t0004g0004 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-58+2223G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28892901 | |||||||
| chr8:28892912 | A | C | 196 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 others(193): Show |
197 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.-58+2234A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28892912 | |||||||
| chr8:28892967 | T | A | 2 | a0001c0001t0003g0324 a0001c0001t0003g0325 |
2 | HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-58+2289T>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28892967 | |||||||
| chr8:28893347 | C | G | 1 | a0001c0001t0002g0341 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-58+2669C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28893347 | |||||||
| chr8:28893609 | T | G | 1 | a0001c0001t0006g0326 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-58+2931T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28893609 | |||||||
| chr8:28893747 | A | T | 1 | a0001c0001t0002g0318 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.-58+3069A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28893747 | |||||||
| chr8:28893789 | G | A | 1 | a0001c0001t0007g0005 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-58+3111G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28893789 | |||||||
| chr8:28893864 | C | T | 199 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 others(196): Show |
200 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.-58+3186C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28893864 | |||||||
| chr8:28893905 | C | T | 1 | a0001c0001t0008g0123 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-58+3227C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28893905 | |||||||
| chr8:28894031 | A | G | 1 | a0001c0001t0002g0317 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.-58+3353A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28894031 | |||||||
| chr8:28894040 | G | A | 1 | a0001c0001t0003g0134 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-58+3362G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28894040 | |||||||
| chr8:28894045 | G | A | 2 | a0001c0001t0003g0006 a0001c0001t0003g0007 |
2 | NA18968.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.-58+3367G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28894045 | |||||||
| chr8:28894268 | A | G | 10 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0122 others(7): Show |
10 | HG02280.hp1 HG02572.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.-58+3590A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28894268 | |||||||
| chr8:28894428 | T | G | 2 | a0001c0001t0003g0008 a0001c0001t0003g0009 |
2 | HG04199.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.-58+3750T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28894428 | |||||||
| chr8:28894476 | T | C | 2 | a0001c0001t0003g0324 a0001c0001t0003g0325 |
2 | HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-58+3798T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28894476 | |||||||
| chr8:28894522 | C | T | 1 | a0001c0001t0001g0316 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-58+3844C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28894522 | |||||||
| chr8:28894588 | C | T | 58 | a0001c0001t0001g0072 a0001c0001t0002g0092 a0001c0001t0003g0006 others(55): Show |
58 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.-58+3910C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28894588 | |||||||
| chr8:28894717 | A | T | 1 | a0001c0001t0007g0062 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-58+4039A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28894717 | |||||||
| chr8:28894897 | C | A | 15 | a0001c0001t0006g0326 a0001c0001t0006g0328 a0001c0001t0006g0329 others(12): Show |
15 | HG00544.hp1 HG02056.hp1 HG02809.hp2 others(12): Show |
intron_variant | MODIFIER | c.-58+4219C>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28894897 | |||||||
| chr8:28894942 | C | CA | 8 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0002g0001 others(5): Show |
9 | HG00423.hp2 HG00558.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.-58+4276dupA | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28894942 | ||||||
| chr8:28894942 | CA | C | 20 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0122 others(17): Show |
20 | HG01884.hp1 HG02145.hp1 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.-58+4276delA | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28894942 | ||||||
| chr8:28894954 | A | C | 5 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0122 others(2): Show |
5 | HG02280.hp1 HG02965.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.-58+4276A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28894954 | |||||||
| chr8:28894959 | A | G | 2 | a0001c0001t0003g0122 a0001c0001t0008g0121 |
2 | HG03195.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-58+4281A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28894959 | |||||||
| chr8:28894990 | C | G | 1 | a0001c0001t0001g0315 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-58+4312C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28894990 | |||||||
| chr8:28895445 | T | C | 229 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 others(226): Show |
230 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(227): Show |
intron_variant | MODIFIER | c.-58+4767T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28895445 | |||||||
| chr8:28895495 | C | T | 5 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0122 others(2): Show |
5 | HG02280.hp1 HG02965.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.-58+4817C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28895495 | |||||||
| chr8:28895631 | C | T | 1 | a0001c0001t0003g0115 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.-58+4953C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28895631 | |||||||
| chr8:28895635 | G | A | 4 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(1): Show |
4 | HG03834.hp2 NA18975.hp2 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.-58+4957G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28895635 | |||||||
| chr8:28895669 | A | G | 3 | a0001c0001t0006g0116 a0001c0001t0014g0117 a0001c0001t0014g0118 |
3 | HG02572.hp1 HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-58+4991A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28895669 | |||||||
| chr8:28895674 | C | CAAAAAAA others(4): Show |
5 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0122 others(2): Show |
5 | HG02280.hp1 HG02965.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.-58+4999_-58+5009d others(13): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28895674 | ||||||
| chr8:28895674 | C | CAAAAAAA others(5): Show |
2 | a0001c0001t0014g0117 a0001c0001t0014g0118 |
2 | HG02572.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-58+4998_-58+5009d others(14): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28895674 | ||||||
| chr8:28895674 | C | CAAAAAAA others(6): Show |
1 | a0001c0001t0006g0116 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-58+4997_-58+5009d others(15): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28895674 | ||||||
| chr8:28895674 | CA | C | 5 | a0001c0001t0001g0139 a0001c0001t0002g0001 a0001c0001t0003g0112 others(2): Show |
6 | HG01975.hp2 HG02486.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-58+5009delA | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28895674 | ||||||
| chr8:28895687 | A | T | 1 | a0001c0001t0003g0114 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-58+5009A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28895687 | |||||||
| chr8:28895688 | T | A | 15 | a0001c0001t0006g0326 a0001c0001t0006g0328 a0001c0001t0006g0329 others(12): Show |
15 | HG00544.hp1 HG02056.hp1 HG02809.hp2 others(12): Show |
intron_variant | MODIFIER | c.-58+5010T>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28895688 | |||||||
| chr8:28895714 | A | C | 1 | a0001c0001t0001g0314 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-58+5036A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28895714 | |||||||
| chr8:28895765 | A | G | 1 | a0001c0001t0011g0313 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-58+5087A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28895765 | |||||||
| chr8:28895808 | A | G | 1 | a0001c0001t0004g0110 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-58+5130A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28895808 | |||||||
| chr8:28895851 | T | C | 310 | a0001c0001t0001g0072 a0001c0001t0001g0138 a0001c0001t0001g0139 others(307): Show |
311 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(308): Show |
intron_variant | MODIFIER | c.-58+5173T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28895851 | |||||||
| chr8:28895891 | A | G | 1 | a0001c0001t0004g0128 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-58+5213A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28895891 | |||||||
| chr8:28895988 | T | C | 2 | a0001c0001t0004g0030 a0001c0001t0004g0031 |
2 | HG01975.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-58+5310T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28895988 | |||||||
| chr8:28896004 | CTCCTCAG others(18): Show |
C | 1 | a0001c0001t0003g0114 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-58+5327_-58+5351d others(27): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28896004 | |||||||
| chr8:28896107 | A | G | 1 | a0001c0001t0010g0312 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-58+5429A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28896107 | |||||||
| chr8:28896165 | T | C | 1 | a0001c0001t0010g0312 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-58+5487T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28896165 | |||||||
| chr8:28896176 | T | C | 1 | a0001c0001t0002g0318 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.-58+5498T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28896176 | |||||||
| chr8:28896216 | T | C | 11 | a0001c0001t0007g0005 a0001c0001t0007g0010 a0001c0001t0007g0011 others(8): Show |
11 | HG01261.hp1 HG02622.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.-58+5538T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28896216 | |||||||
| chr8:28896343 | T | G | 7 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 others(4): Show |
7 | HG00423.hp1 HG02071.hp1 NA18947.hp2 others(4): Show |
intron_variant | MODIFIER | c.-58+5665T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28896343 | |||||||
| chr8:28896382 | GTGTGTAG others(231): Show |
G | 12 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0021 others(9): Show |
12 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(9): Show |
intron_variant | MODIFIER | c.-58+5705_-58+5942d others(2): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28896382 | |||||||
| chr8:28896546 | A | G | 1 | a0001c0001t0003g0085 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-58+5868A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28896546 | |||||||
| chr8:28896630 | A | T | 12 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0021 others(9): Show |
12 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(9): Show |
intron_variant | MODIFIER | c.-58+5952A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28896630 | |||||||
| chr8:28896631 | CTGTACTT others(76): Show |
C | 12 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0021 others(9): Show |
12 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(9): Show |
intron_variant | MODIFIER | c.-58+5954_-58+6036d others(85): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28896631 | |||||||
| chr8:28896674 | C | T | 1 | a0001c0001t0002g0265 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.-58+5996C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28896674 | |||||||
| chr8:28896810 | C | T | 4 | a0001c0001t0001g0308 a0001c0001t0001g0309 a0001c0001t0001g0310 others(1): Show |
4 | HG01167.hp2 HG01358.hp1 HG01943.hp2 others(1): Show |
intron_variant | MODIFIER | c.-58+6132C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28896810 | |||||||
| chr8:28896817 | C | T | 5 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(2): Show |
5 | HG02055.hp1 HG02559.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-58+6139C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28896817 | |||||||
| chr8:28896915 | T | C | 1 | a0001c0001t0001g0314 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-58+6237T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28896915 | |||||||
| chr8:28896978 | G | GT | 19 | a0001c0001t0003g0107 a0001c0001t0003g0109 a0001c0001t0003g0119 others(16): Show |
19 | HG02055.hp2 HG02145.hp2 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.-58+6314dupT | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28896978 | ||||||
| chr8:28897078 | A | T | 1 | a0001c0001t0001g0299 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-58+6400A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28897078 | |||||||
| chr8:28897080 | G | T | 1 | a0001c0001t0001g0299 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-58+6402G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28897080 | |||||||
| chr8:28897388 | T | TAAATGAG others(14): Show |
1 | a0001c0001t0003g0114 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-58+6711_-58+6731d others(23): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28897388 | ||||||
| chr8:28897536 | C | T | 1 | a0001c0001t0003g0106 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-58+6858C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28897536 | |||||||
| chr8:28897628 | G | A | 310 | a0001c0001t0001g0072 a0001c0001t0001g0138 a0001c0001t0001g0139 others(307): Show |
311 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(308): Show |
intron_variant | MODIFIER | c.-58+6950G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28897628 | |||||||
| chr8:28898158 | C | CA | 16 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0021 others(13): Show |
16 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(13): Show |
intron_variant | MODIFIER | c.-58+7483dupA | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28898158 | ||||||
| chr8:28898237 | T | C | 318 | a0001c0001t0001g0072 a0001c0001t0001g0138 a0001c0001t0001g0139 others(315): Show |
319 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(316): Show |
intron_variant | MODIFIER | c.-58+7559T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28898237 | |||||||
| chr8:28898238 | A | AC | 15 | a0001c0001t0006g0326 a0001c0001t0006g0328 a0001c0001t0006g0329 others(12): Show |
15 | HG00544.hp1 HG02056.hp1 HG02809.hp2 others(12): Show |
intron_variant | MODIFIER | c.-58+7560_-58+7561i others(3): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28898238 | |||||||
| chr8:28898240 | T | G | 15 | a0001c0001t0006g0326 a0001c0001t0006g0328 a0001c0001t0006g0329 others(12): Show |
15 | HG00544.hp1 HG02056.hp1 HG02809.hp2 others(12): Show |
intron_variant | MODIFIER | c.-58+7562T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28898240 | |||||||
| chr8:28898240 | T | TG | 295 | a0001c0001t0001g0072 a0001c0001t0001g0138 a0001c0001t0001g0139 others(292): Show |
296 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(293): Show |
intron_variant | MODIFIER | c.-58+7562_-58+7563i others(3): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28898240 | |||||||
| chr8:28898248 | G | A | 1 | a0001c0001t0008g0123 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-58+7570G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28898248 | |||||||
| chr8:28898375 | T | G | 3 | a0001c0001t0004g0063 a0001c0001t0004g0064 a0001c0001t0004g0065 |
3 | HG00738.hp2 HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-58+7697T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28898375 | |||||||
| chr8:28898471 | C | T | 200 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 others(197): Show |
201 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(198): Show |
intron_variant | MODIFIER | c.-58+7793C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28898471 | |||||||
| chr8:28898498 | G | C | 3 | a0001c0001t0004g0063 a0001c0001t0004g0064 a0001c0001t0004g0065 |
3 | HG00738.hp2 HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-58+7820G>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28898498 | |||||||
| chr8:28898591 | G | T | 1 | a0001c0001t0003g0298 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-58+7913G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28898591 | |||||||
| chr8:28898671 | C | T | 1 | a0001c0001t0012g0297 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-58+7993C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28898671 | |||||||
| chr8:28898769 | A | G | 310 | a0001c0001t0001g0072 a0001c0001t0001g0138 a0001c0001t0001g0139 others(307): Show |
311 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(308): Show |
intron_variant | MODIFIER | c.-58+8091A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28898769 | |||||||
| chr8:28898874 | G | T | 2 | a0001c0001t0002g0295 a0001c0001t0002g0296 |
2 | NA18968.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.-58+8196G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28898874 | |||||||
| chr8:28898948 | T | A | 2 | a0001c0001t0008g0002 a0001c0001t0008g0003 |
2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-58+8270T>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28898948 | |||||||
| chr8:28898950 | G | A | 2 | a0001c0001t0007g0011 a0001c0001t0007g0018 |
2 | HG02630.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-58+8272G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28898950 | |||||||
| chr8:28899221 | G | A | 225 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 others(222): Show |
226 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(223): Show |
intron_variant | MODIFIER | c.-58+8543G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28899221 | |||||||
| chr8:28899261 | G | C | 1 | a0001c0001t0008g0121 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-58+8583G>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28899261 | |||||||
| chr8:28899730 | T | A | 2 | a0001c0001t0003g0324 a0001c0001t0003g0325 |
2 | HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-58+9052T>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28899730 | |||||||
| chr8:28900115 | A | G | 225 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 others(222): Show |
226 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(223): Show |
intron_variant | MODIFIER | c.-58+9437A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28900115 | |||||||
| chr8:28900152 | G | A | 1 | a0001c0001t0003g0119 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-58+9474G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28900152 | |||||||
| chr8:28900254 | C | CAAA | 6 | a0001c0001t0006g0328 a0001c0001t0006g0329 a0001c0001t0006g0340 others(3): Show |
6 | HG00544.hp1 HG02056.hp1 NA18947.hp1 others(3): Show |
intron_variant | MODIFIER | c.-58+9592_-58+9594d others(5): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28900254 | ||||||
| chr8:28900265 | A | AATATATA others(3): Show |
1 | a0001c0001t0001g0294 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-58+9588_-58+9589i others(12): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28900265 | ||||||
| chr8:28900267 | A | AATATATA others(3): Show |
6 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(3): Show |
6 | HG00423.hp1 HG01123.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.-58+9590_-58+9591i others(12): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28900267 | ||||||
| chr8:28900267 | A | ATAT | 8 | a0001c0001t0004g0021 a0001c0001t0004g0022 a0001c0001t0004g0023 others(5): Show |
8 | HG00140.hp2 HG00323.hp2 HG01069.hp2 others(5): Show |
intron_variant | MODIFIER | c.-58+9589_-58+9590i others(5): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28900267 | |||||||
| chr8:28900267 | A | ATATATAT others(4): Show |
4 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0004g0029 others(1): Show |
4 | HG01070.hp2 HG01516.hp1 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-58+9589_-58+9590i others(13): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28900267 | |||||||
| chr8:28900267 | A | ATATATAT others(6): Show |
1 | a0001c0001t0001g0292 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-58+9589_-58+9590i others(15): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28900267 | |||||||
| chr8:28900267 | A | T | 2 | a0001c0001t0001g0294 a0001c0001t0003g0325 |
2 | HG03041.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.-58+9589A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28900267 | |||||||
| chr8:28900269 | A | AATAT | 27 | a0001c0001t0001g0222 a0001c0001t0002g0133 a0001c0001t0002g0135 others(24): Show |
27 | HG00423.hp2 HG00438.hp2 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.-58+9592_-58+9593i others(6): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28900269 | ||||||
| chr8:28900269 | A | AATATATA others(3): Show |
3 | a0001c0001t0001g0144 a0001c0001t0001g0147 a0001c0001t0001g0307 |
3 | HG02071.hp1 HG02559.hp2 NA18947.hp2 |
intron_variant | MODIFIER | c.-58+9592_-58+9593i others(12): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28900269 | ||||||
| chr8:28900269 | A | AATATATA others(7): Show |
1 | a0001c0001t0001g0223 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-58+9592_-58+9593i others(16): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28900269 | ||||||
| chr8:28900269 | A | AATATATA others(15): Show |
1 | a0001c0001t0001g0315 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-58+9592_-58+9593i others(24): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28900269 | ||||||
| chr8:28900269 | A | AT | 3 | a0001c0001t0001g0226 a0001c0001t0004g0063 a0001c0001t0004g0065 |
3 | HG01243.hp1 HG02004.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.-58+9591_-58+9592i others(3): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28900269 | |||||||
| chr8:28900269 | A | ATATAT | 4 | a0001c0001t0001g0268 a0001c0001t0002g0273 a0001c0001t0002g0341 others(1): Show |
4 | HG03239.hp1 NA19062.hp2 NA19072.hp1 others(1): Show |
intron_variant | MODIFIER | c.-58+9591_-58+9592i others(7): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28900269 | |||||||
| chr8:28900269 | A | ATATATAT others(2): Show |
22 | a0001c0001t0001g0139 a0001c0001t0001g0143 a0001c0001t0001g0146 others(19): Show |
22 | HG00140.hp1 HG00639.hp2 HG01069.hp1 others(19): Show |
intron_variant | MODIFIER | c.-58+9591_-58+9592i others(11): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28900269 | |||||||
| chr8:28900269 | A | ATATATAT others(4): Show |
9 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0234 others(6): Show |
9 | HG00323.hp1 HG01256.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.-58+9591_-58+9592i others(13): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28900269 | |||||||
| chr8:28900269 | A | ATATATAT others(6): Show |
5 | a0001c0001t0001g0227 a0001c0001t0001g0228 a0001c0001t0001g0229 others(2): Show |
5 | HG00735.hp2 HG01109.hp1 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.-58+9591_-58+9592i others(15): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28900269 | |||||||
| chr8:28900269 | A | ATATATAT others(8): Show |
3 | a0001c0001t0001g0154 a0001c0001t0001g0254 a0001c0001t0001g0316 |
3 | HG02040.hp2 HG02451.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-58+9591_-58+9592i others(17): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28900269 | |||||||
| chr8:28900269 | A | ATATATAT others(14): Show |
2 | a0001c0001t0001g0236 a0001c0001t0001g0239 |
2 | HG01175.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-58+9591_-58+9592i others(23): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28900269 | |||||||
| chr8:28900269 | A | T | 27 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(24): Show |
27 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(24): Show |
intron_variant | MODIFIER | c.-58+9591A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28900269 | |||||||
| chr8:28900271 | A | AAAAAT | 8 | a0001c0001t0002g0001 a0001c0001t0003g0008 a0001c0001t0003g0084 others(5): Show |
8 | HG01109.hp2 HG03490.hp2 HG04204.hp1 others(5): Show |
intron_variant | MODIFIER | c.-58+9594_-58+9595i others(7): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28900271 | ||||||
| chr8:28900271 | A | AAAAT | 14 | a0001c0001t0002g0156 a0001c0001t0002g0157 a0001c0001t0002g0163 others(11): Show |
14 | HG02258.hp1 HG02647.hp1 HG03017.hp2 others(11): Show |
intron_variant | MODIFIER | c.-58+9594_-58+9595i others(6): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28900271 | ||||||
| chr8:28900271 | A | AAAT | 6 | a0001c0001t0003g0075 a0001c0001t0003g0134 a0001c0001t0004g0128 others(3): Show |
6 | HG01928.hp2 HG02451.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-58+9594_-58+9595i others(5): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28900271 | ||||||
| chr8:28900271 | A | AAATAT | 34 | a0001c0001t0001g0072 a0001c0001t0002g0001 a0001c0001t0002g0092 others(31): Show |
34 | HG00408.hp2 HG00438.hp1 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.-58+9594_-58+9595i others(7): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28900271 | ||||||
| chr8:28900271 | A | AAATATAT | 6 | a0001c0001t0003g0083 a0001c0001t0003g0102 a0001c0001t0003g0103 others(3): Show |
6 | NA18961.hp2 NA18986.hp1 NA18998.hp2 others(3): Show |
intron_variant | MODIFIER | c.-58+9594_-58+9595i others(9): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28900271 | ||||||
| chr8:28900271 | A | AATAT | 52 | a0001c0001t0001g0169 a0001c0001t0002g0136 a0001c0001t0002g0137 others(49): Show |
52 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(49): Show |
intron_variant | MODIFIER | c.-58+9610_-58+9613d others(6): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28900271 | ||||||
| chr8:28900271 | A | AATATAT | 6 | a0001c0001t0002g0295 a0001c0001t0003g0106 a0001c0001t0005g0176 others(3): Show |
6 | HG00621.hp2 HG02145.hp2 HG02155.hp1 others(3): Show |
intron_variant | MODIFIER | c.-58+9608_-58+9613d others(8): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28900271 | ||||||
| chr8:28900271 | A | AATATATA others(3): Show |
2 | a0001c0001t0001g0221 a0001c0001t0001g0251 |
2 | NA18966.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.-58+9604_-58+9613d others(12): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28900271 | ||||||
| chr8:28900271 | A | ATAT | 4 | a0001c0001t0002g0270 a0001c0001t0002g0274 a0001c0001t0004g0004 others(1): Show |
4 | HG00741.hp2 HG02074.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-58+9593_-58+9594i others(5): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28900271 | |||||||
| chr8:28900271 | A | ATATAT | 7 | a0001c0001t0002g0197 a0001c0001t0002g0206 a0001c0001t0003g0086 others(4): Show |
7 | HG04115.hp1 NA18956.hp2 NA18959.hp2 others(4): Show |
intron_variant | MODIFIER | c.-58+9593_-58+9594i others(7): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28900271 | |||||||
| chr8:28900271 | A | ATATATAT | 4 | a0001c0001t0001g0138 a0001c0001t0001g0231 a0001c0001t0002g0252 others(1): Show |
4 | HG01168.hp2 HG02109.hp1 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.-58+9593_-58+9594i others(9): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28900271 | |||||||
| chr8:28900271 | A | ATATATAT others(2): Show |
9 | a0001c0001t0001g0249 a0001c0001t0001g0299 a0001c0001t0001g0304 others(6): Show |
9 | HG01167.hp2 HG01358.hp1 HG01943.hp2 others(6): Show |
intron_variant | MODIFIER | c.-58+9593_-58+9594i others(11): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28900271 | |||||||
| chr8:28900271 | A | ATATATAT others(4): Show |
6 | a0001c0001t0001g0142 a0001c0001t0001g0237 a0001c0001t0001g0250 others(3): Show |
6 | HG02055.hp1 HG02155.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-58+9593_-58+9594i others(13): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28900271 | |||||||
| chr8:28900271 | A | T | 121 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 others(118): Show |
121 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.-58+9593A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28900271 | |||||||
| chr8:28900273 | T | A | 1 | a0001c0001t0007g0005 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-58+9595T>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28900273 | |||||||
| chr8:28900310 | C | A | 2 | a0001c0001t0007g0005 a0001c0001t0007g0062 |
2 | HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-58+9632C>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28900310 | |||||||
| chr8:28900405 | G | C | 10 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0122 others(7): Show |
10 | HG02280.hp1 HG02572.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.-58+9727G>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28900405 | |||||||
| chr8:28900507 | T | C | 1 | a0001c0001t0005g0151 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-58+9829T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28900507 | |||||||
| chr8:28900529 | C | G | 1 | a0001c0001t0008g0339 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-58+9851C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28900529 | |||||||
| chr8:28900750 | G | A | 1 | a0001c0001t0004g0019 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-58+10072G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28900750 | |||||||
| chr8:28900780 | G | T | 5 | a0001c0001t0003g0102 a0001c0001t0003g0103 a0001c0001t0003g0104 others(2): Show |
5 | NA18986.hp1 NA18998.hp2 NA19009.hp2 others(2): Show |
intron_variant | MODIFIER | c.-58+10102G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28900780 | |||||||
| chr8:28900851 | C | T | 1 | a0001c0001t0008g0123 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-58+10173C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28900851 | |||||||
| chr8:28901169 | A | G | 1 | a0001c0001t0001g0287 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-58+10491A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28901169 | |||||||
| chr8:28901175 | T | C | 5 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0122 others(2): Show |
5 | HG02280.hp1 HG02965.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.-58+10497T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28901175 | |||||||
| chr8:28901543 | T | A | 1 | a0001c0001t0003g0298 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-58+10865T>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28901543 | |||||||
| chr8:28901779 | C | T | 1 | a0001c0001t0005g0286 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-58+11101C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28901779 | |||||||
| chr8:28901936 | G | T | 4 | a0001c0001t0009g0129 a0001c0001t0009g0130 a0001c0001t0009g0131 others(1): Show |
4 | NA18974.hp2 NA18988.hp1 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.-58+11258G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28901936 | |||||||
| chr8:28901937 | T | C | 4 | a0001c0001t0009g0129 a0001c0001t0009g0130 a0001c0001t0009g0131 others(1): Show |
4 | NA18974.hp2 NA18988.hp1 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.-58+11259T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28901937 | |||||||
| chr8:28901950 | T | C | 1 | a0001c0001t0002g0152 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-58+11272T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28901950 | |||||||
| chr8:28901961 | A | G | 318 | a0001c0001t0001g0072 a0001c0001t0001g0138 a0001c0001t0001g0139 others(315): Show |
319 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(316): Show |
intron_variant | MODIFIER | c.-58+11283A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28901961 | |||||||
| chr8:28902537 | C | T | 1 | a0001c0001t0004g0052 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-58+11859C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28902537 | |||||||
| chr8:28902578 | A | G | 1 | a0001c0001t0004g0028 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-58+11900A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28902578 | |||||||
| chr8:28902608 | A | T | 1 | a0001c0001t0003g0101 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.-58+11930A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28902608 | |||||||
| chr8:28902678 | G | A | 1 | a0001c0001t0001g0314 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-58+12000G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28902678 | |||||||
| chr8:28902773 | C | CT | 220 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 others(217): Show |
221 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(218): Show |
intron_variant | MODIFIER | c.-58+12096dupT | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28902773 | ||||||
| chr8:28902902 | C | G | 3 | a0001c0001t0006g0116 a0001c0001t0014g0117 a0001c0001t0014g0118 |
3 | HG02572.hp1 HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-58+12224C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28902902 | |||||||
| chr8:28903106 | T | TAC | 15 | a0001c0001t0003g0153 a0001c0001t0006g0326 a0001c0001t0006g0328 others(12): Show |
15 | HG00544.hp1 HG02056.hp1 HG02809.hp2 others(12): Show |
intron_variant | MODIFIER | c.-58+12444_-58+1244 others(6): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28903106 | ||||||
| chr8:28903124 | T | C | 16 | a0001c0001t0006g0326 a0001c0001t0006g0328 a0001c0001t0006g0329 others(13): Show |
16 | HG00544.hp1 HG02056.hp1 HG02809.hp2 others(13): Show |
intron_variant | MODIFIER | c.-58+12446T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28903124 | |||||||
| chr8:28903220 | C | T | 200 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 others(197): Show |
201 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(198): Show |
intron_variant | MODIFIER | c.-58+12542C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28903220 | |||||||
| chr8:28903447 | G | A | 2 | a0001c0001t0002g0295 a0001c0001t0002g0296 |
2 | NA18968.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.-58+12769G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28903447 | |||||||
| chr8:28903458 | C | T | 3 | a0001c0001t0002g0284 a0001c0001t0002g0285 a0001c0002t0002g0283 |
3 | HG01358.hp2 HG01496.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.-58+12780C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28903458 | |||||||
| chr8:28903556 | G | A | 1 | a0001c0001t0001g0154 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-58+12878G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28903556 | |||||||
| chr8:28903857 | AT | A | 4 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0122 others(1): Show |
4 | HG02280.hp1 HG03195.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-58+13183delT | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28903857 | ||||||
| chr8:28904002 | G | C | 310 | a0001c0001t0001g0072 a0001c0001t0001g0138 a0001c0001t0001g0139 others(307): Show |
311 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(308): Show |
intron_variant | MODIFIER | c.-58+13324G>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28904002 | |||||||
| chr8:28904090 | G | A | 1 | a0001c0001t0006g0066 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.-58+13412G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28904090 | |||||||
| chr8:28904098 | A | G | 3 | a0001c0001t0004g0063 a0001c0001t0004g0064 a0001c0001t0004g0065 |
3 | HG00738.hp2 HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-58+13420A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28904098 | |||||||
| chr8:28904113 | A | G | 1 | a0001c0001t0001g0315 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-58+13435A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28904113 | |||||||
| chr8:28904162 | T | C | 1 | a0001c0001t0002g0155 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-58+13484T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28904162 | |||||||
| chr8:28904212 | A | G | 1 | a0001c0001t0005g0282 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-58+13534A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28904212 | |||||||
| chr8:28904286 | T | C | 1 | a0001c0001t0009g0129 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-58+13608T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28904286 | |||||||
| chr8:28904338 | C | T | 1 | a0001c0001t0006g0116 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-58+13660C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28904338 | |||||||
| chr8:28904357 | C | T | 5 | a0001c0001t0003g0324 a0001c0001t0003g0325 a0001c0001t0006g0116 others(2): Show |
5 | HG02572.hp1 HG02886.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.-58+13679C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28904357 | |||||||
| chr8:28904378 | G | A | 3 | a0001c0001t0004g0063 a0001c0001t0004g0064 a0001c0001t0004g0065 |
3 | HG00738.hp2 HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-58+13700G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28904378 | |||||||
| chr8:28904380 | G | A | 4 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0122 others(1): Show |
4 | HG02280.hp1 HG03195.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-58+13702G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28904380 | |||||||
| chr8:28904526 | C | G | 1 | a0001c0001t0003g0281 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-58+13848C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28904526 | |||||||
| chr8:28904676 | C | A | 1 | a0001c0001t0003g0114 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-58+13998C>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28904676 | |||||||
| chr8:28904679 | A | G | 2 | a0001c0001t0003g0008 a0001c0001t0003g0009 |
2 | HG04199.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.-58+14001A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28904679 | |||||||
| chr8:28905209 | G | A | 1 | a0001c0001t0002g0156 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-58+14531G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28905209 | |||||||
| chr8:28905210 | C | G | 1 | a0001c0001t0002g0156 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-58+14532C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28905210 | |||||||
| chr8:28905211 | A | G | 1 | a0001c0001t0002g0156 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-58+14533A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28905211 | |||||||
| chr8:28905212 | G | A | 10 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0122 others(7): Show |
10 | HG02280.hp1 HG02572.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.-58+14534G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28905212 | |||||||
| chr8:28905233 | G | T | 4 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0288 others(1): Show |
4 | HG00323.hp1 HG01123.hp2 HG01255.hp2 others(1): Show |
intron_variant | MODIFIER | c.-58+14555G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28905233 | |||||||
| chr8:28905281 | A | G | 12 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0021 others(9): Show |
12 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(9): Show |
intron_variant | MODIFIER | c.-58+14603A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28905281 | |||||||
| chr8:28905340 | C | T | 4 | a0001c0001t0004g0124 a0001c0001t0004g0125 a0001c0001t0004g0126 others(1): Show |
4 | HG02109.hp2 HG02896.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.-58+14662C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28905340 | |||||||
| chr8:28905355 | G | GCGCACAC others(7): Show |
5 | a0001c0001t0002g0275 a0001c0001t0002g0276 a0001c0001t0002g0277 others(2): Show |
5 | NA18612.hp1 NA18953.hp1 NA18957.hp1 others(2): Show |
intron_variant | MODIFIER | c.-58+14678_-58+1467 others(18): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28905355 | ||||||
| chr8:28905355 | GCA | G | 17 | a0001c0001t0001g0268 a0001c0001t0002g0260 a0001c0001t0002g0261 others(14): Show |
17 | HG00609.hp2 HG02074.hp2 NA18747.hp1 others(14): Show |
intron_variant | MODIFIER | c.-58+14693_-58+1469 others(6): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28905355 | ||||||
| chr8:28905357 | A | G | 5 | a0001c0001t0002g0275 a0001c0001t0002g0276 a0001c0001t0002g0277 others(2): Show |
5 | NA18612.hp1 NA18953.hp1 NA18957.hp1 others(2): Show |
intron_variant | MODIFIER | c.-58+14679A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28905357 | |||||||
| chr8:28905367 | A | C | 1 | a0001c0001t0004g0027 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.-58+14689A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28905367 | |||||||
| chr8:28905856 | C | A | 1 | a0001c0001t0006g0116 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-58+15178C>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28905856 | |||||||
| chr8:28905969 | A | G | 5 | a0001c0001t0003g0096 a0001c0001t0003g0097 a0001c0001t0003g0098 others(2): Show |
5 | NA18960.hp2 NA18980.hp2 NA19004.hp1 others(2): Show |
intron_variant | MODIFIER | c.-58+15291A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28905969 | |||||||
| chr8:28905974 | A | G | 1 | a0001c0001t0002g0259 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.-58+15296A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28905974 | |||||||
| chr8:28906050 | A | G | 1 | a0001c0001t0021g0343 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-58+15372A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28906050 | |||||||
| chr8:28906108 | C | T | 1 | a0001c0001t0001g0258 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-58+15430C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28906108 | |||||||
| chr8:28906317 | G | T | 4 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0122 others(1): Show |
4 | HG02280.hp1 HG03195.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-58+15639G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28906317 | |||||||
| chr8:28906355 | CTTAG | C | 5 | a0001c0001t0003g0324 a0001c0001t0003g0325 a0001c0001t0006g0116 others(2): Show |
5 | HG02572.hp1 HG02886.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.-58+15681_-58+1568 others(8): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28906355 | ||||||
| chr8:28906374 | A | G | 4 | a0001c0001t0009g0129 a0001c0001t0009g0130 a0001c0001t0009g0131 others(1): Show |
4 | NA18974.hp2 NA18988.hp1 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.-58+15696A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28906374 | |||||||
| chr8:28906506 | T | C | 1 | a0001c0001t0006g0332 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-58+15828T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28906506 | |||||||
| chr8:28906525 | C | A | 114 | a0001c0001t0001g0169 a0001c0001t0001g0268 a0001c0001t0001g0289 others(111): Show |
115 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.-58+15847C>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28906525 | |||||||
| chr8:28906531 | A | T | 1 | a0001c0001t0008g0123 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-58+15853A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28906531 | |||||||
| chr8:28906629 | CCTCAGGC others(24): Show |
C | 1 | a0001c0001t0008g0067 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-58+15956_-58+1598 others(35): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28906629 | ||||||
| chr8:28906643 | A | ATGTCCCT others(4): Show |
1 | a0001c0001t0010g0300 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-58+15965_-58+1596 others(15): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28906643 | |||||||
| chr8:28906664 | A | G | 78 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 others(75): Show |
78 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.-58+15986A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28906664 | |||||||
| chr8:28906839 | G | A | 1 | a0001c0001t0002g0133 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-58+16161G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28906839 | |||||||
| chr8:28906920 | C | G | 1 | a0001c0001t0003g0106 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-58+16242C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28906920 | |||||||
| chr8:28907030 | A | G | 1 | a0001c0001t0002g0156 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-58+16352A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28907030 | |||||||
| chr8:28907044 | ATAAT | A | 54 | a0001c0001t0001g0072 a0001c0001t0002g0092 a0001c0001t0003g0006 others(51): Show |
54 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.-58+16370_-58+1637 others(8): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28907044 | ||||||
| chr8:28907438 | T | G | 1 | a0001c0001t0002g0133 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-58+16760T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28907438 | |||||||
| chr8:28907575 | A | C | 2 | a0001c0001t0003g0122 a0001c0001t0008g0121 |
2 | HG03195.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-58+16897A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28907575 | |||||||
| chr8:28907718 | G | A | 1 | a0001c0001t0002g0157 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-58+17040G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28907718 | |||||||
| chr8:28907805 | C | T | 2 | a0001c0001t0007g0005 a0001c0001t0007g0062 |
2 | HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-58+17127C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28907805 | |||||||
| chr8:28907852 | T | TC | 10 | a0001c0001t0007g0010 a0001c0001t0007g0011 a0001c0001t0007g0012 others(7): Show |
10 | HG01261.hp1 HG02257.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.-58+17174_-58+1717 others(5): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28907852 | |||||||
| chr8:28907853 | T | C | 8 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0288 others(5): Show |
8 | HG00323.hp1 HG01123.hp2 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.-58+17175T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28907853 | |||||||
| chr8:28907877 | G | T | 5 | a0001c0001t0003g0324 a0001c0001t0003g0325 a0001c0001t0006g0116 others(2): Show |
5 | HG02572.hp1 HG02886.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.-58+17199G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28907877 | |||||||
| chr8:28907917 | T | G | 2 | a0001c0001t0001g0220 a0001c0001t0001g0221 |
2 | NA18978.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.-58+17239T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28907917 | |||||||
| chr8:28907976 | T | G | 228 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 others(225): Show |
229 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(226): Show |
intron_variant | MODIFIER | c.-58+17298T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28907976 | |||||||
| chr8:28908128 | C | T | 1 | a0001c0001t0001g0257 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-58+17450C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28908128 | |||||||
| chr8:28908157 | A | G | 1 | a0001c0001t0008g0123 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-58+17479A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28908157 | |||||||
| chr8:28908566 | C | G | 3 | a0001c0001t0003g0119 a0001c0001t0003g0122 a0001c0001t0008g0121 |
3 | HG02280.hp1 HG03195.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-58+17888C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28908566 | |||||||
| chr8:28908616 | A | C | 1 | a0001c0001t0001g0256 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-58+17938A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28908616 | |||||||
| chr8:28908718 | A | T | 1 | a0001c0001t0009g0132 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-58+18040A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28908718 | |||||||
| chr8:28908720 | T | C | 1 | a0001c0001t0003g0119 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-58+18042T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28908720 | |||||||
| chr8:28908726 | A | C | 2 | a0001c0001t0008g0002 a0001c0001t0008g0003 |
2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-58+18048A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28908726 | |||||||
| chr8:28908816 | G | A | 1 | a0001c0001t0001g0222 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-58+18138G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28908816 | |||||||
| chr8:28908921 | G | T | 1 | a0001c0001t0001g0143 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-58+18243G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28908921 | |||||||
| chr8:28908925 | C | T | 1 | a0001c0001t0003g0095 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.-58+18247C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28908925 | |||||||
| chr8:28908958 | C | T | 3 | a0001c0001t0003g0119 a0001c0001t0003g0122 a0001c0001t0008g0121 |
3 | HG02280.hp1 HG03195.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-58+18280C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28908958 | |||||||
| chr8:28909064 | C | T | 9 | a0001c0001t0003g0119 a0001c0001t0003g0122 a0001c0001t0003g0324 others(6): Show |
9 | HG02280.hp1 HG02572.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.-58+18386C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28909064 | |||||||
| chr8:28909076 | C | T | 1 | a0001c0001t0003g0105 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-58+18398C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28909076 | |||||||
| chr8:28909086 | C | A | 2 | a0001c0001t0014g0117 a0001c0001t0014g0118 |
2 | HG02572.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-58+18408C>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28909086 | |||||||
| chr8:28909095 | T | TA | 6 | a0001c0001t0001g0223 a0001c0001t0001g0258 a0001c0001t0001g0319 others(3): Show |
6 | HG02738.hp1 HG02965.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.-58+18435dupA | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28909095 | ||||||
| chr8:28909212 | A | G | 1 | a0001c0001t0008g0094 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-58+18534A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28909212 | |||||||
| chr8:28909256 | A | G | 1 | a0001c0001t0003g0120 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-58+18578A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28909256 | |||||||
| chr8:28909316 | C | A | 1 | a0001c0001t0001g0138 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-58+18638C>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28909316 | |||||||
| chr8:28909329 | C | A | 1 | a0001c0001t0001g0315 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-58+18651C>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28909329 | |||||||
| chr8:28909510 | G | A | 1 | a0001c0001t0001g0224 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-58+18832G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28909510 | |||||||
| chr8:28909773 | C | T | 1 | a0001c0001t0001g0315 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-58+19095C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28909773 | |||||||
| chr8:28910020 | C | T | 1 | a0001c0001t0002g0133 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-58+19342C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28910020 | |||||||
| chr8:28910026 | T | C | 1 | a0001c0001t0006g0328 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-58+19348T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28910026 | |||||||
| chr8:28910152 | T | C | 2 | a0001c0001t0001g0225 a0001c0001t0001g0226 |
2 | HG00140.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.-58+19474T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28910152 | |||||||
| chr8:28910193 | C | G | 1 | a0001c0001t0007g0005 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-58+19515C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28910193 | |||||||
| chr8:28910347 | G | A | 1 | a0001c0001t0008g0123 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-58+19669G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28910347 | |||||||
| chr8:28910456 | C | G | 2 | a0001c0001t0003g0324 a0001c0001t0003g0325 |
2 | HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-58+19778C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28910456 | |||||||
| chr8:28910560 | A | G | 8 | a0001c0001t0007g0011 a0001c0001t0007g0013 a0001c0001t0007g0014 others(5): Show |
8 | HG02257.hp2 HG02622.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.-58+19882A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28910560 | |||||||
| chr8:28910576 | G | A | 1 | a0001c0001t0001g0138 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-58+19898G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28910576 | |||||||
| chr8:28910808 | A | G | 2 | a0001c0001t0001g0322 a0001c0001t0001g0323 |
2 | NA18954.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.-58+20130A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28910808 | |||||||
| chr8:28910876 | C | T | 4 | a0001c0001t0005g0215 a0001c0001t0005g0216 a0001c0001t0005g0217 others(1): Show |
4 | HG02258.hp1 HG02559.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-58+20198C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28910876 | |||||||
| chr8:28910882 | C | T | 1 | a0001c0001t0003g0298 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-58+20204C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28910882 | |||||||
| chr8:28911017 | GTGTTTCA others(7): Show |
G | 1 | a0001c0001t0007g0010 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-58+20341_-58+2035 others(18): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28911017 | ||||||
| chr8:28911164 | C | G | 2 | a0001c0001t0003g0122 a0001c0001t0008g0121 |
2 | HG03195.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-58+20486C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28911164 | |||||||
| chr8:28911238 | A | G | 1 | a0001c0001t0003g0119 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-58+20560A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28911238 | |||||||
| chr8:28911253 | G | A | 1 | a0001c0001t0003g0158 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-58+20575G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28911253 | |||||||
| chr8:28911259 | G | T | 1 | a0001c0001t0005g0282 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-58+20581G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28911259 | |||||||
| chr8:28911365 | G | C | 2 | a0001c0001t0007g0005 a0001c0001t0007g0062 |
2 | HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-58+20687G>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28911365 | |||||||
| chr8:28911403 | T | G | 2 | a0001c0001t0003g0120 a0001c0001t0010g0300 |
2 | HG02055.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-58+20725T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28911403 | |||||||
| chr8:28911484 | TAGCTAGG others(2636): Show |
T | 1 | a0001c0001t0006g0329 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-58+20808_-58+2345 others(4): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28911484 | ||||||
| chr8:28911535 | T | A | 3 | a0001c0001t0003g0119 a0001c0001t0003g0122 a0001c0001t0008g0121 |
3 | HG02280.hp1 HG03195.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-58+20857T>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28911535 | |||||||
| chr8:28911589 | C | G | 2 | a0001c0001t0001g0225 a0001c0001t0001g0226 |
2 | HG00140.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.-58+20911C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28911589 | |||||||
| chr8:28911596 | T | G | 1 | a0001c0001t0008g0123 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-58+20918T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28911596 | |||||||
| chr8:28911617 | A | G | 1 | a0001c0001t0002g0212 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-58+20939A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28911617 | |||||||
| chr8:28911645 | C | T | 1 | a0001c0001t0003g0078 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-58+20967C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28911645 | |||||||
| chr8:28911730 | G | T | 333 | a0001c0001t0001g0072 a0001c0001t0001g0138 a0001c0001t0001g0139 others(330): Show |
334 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(331): Show |
intron_variant | MODIFIER | c.-58+21052G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28911730 | |||||||
| chr8:28911731 | T | C | 12 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0021 others(9): Show |
12 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(9): Show |
intron_variant | MODIFIER | c.-58+21053T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28911731 | |||||||
| chr8:28912164 | T | G | 10 | a0001c0001t0007g0010 a0001c0001t0007g0011 a0001c0001t0007g0012 others(7): Show |
10 | HG01261.hp1 HG02257.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.-58+21486T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28912164 | |||||||
| chr8:28912368 | A | C | 1 | a0001c0001t0010g0312 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-58+21690A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28912368 | |||||||
| chr8:28912404 | A | G | 1 | a0001c0001t0002g0133 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-58+21726A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28912404 | |||||||
| chr8:28912438 | A | G | 1 | a0001c0001t0001g0304 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-58+21760A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28912438 | |||||||
| chr8:28912448 | T | C | 1 | a0001c0001t0003g0119 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-58+21770T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28912448 | |||||||
| chr8:28912615 | C | T | 54 | a0001c0001t0001g0072 a0001c0001t0002g0092 a0001c0001t0003g0006 others(51): Show |
54 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.-58+21937C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28912615 | |||||||
| chr8:28912631 | C | G | 1 | a0001c0001t0003g0071 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-58+21953C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28912631 | |||||||
| chr8:28912697 | T | A | 1 | a0001c0001t0005g0178 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-58+22019T>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28912697 | |||||||
| chr8:28912808 | C | T | 1 | a0001c0001t0010g0312 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-58+22130C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28912808 | |||||||
| chr8:28912901 | A | G | 1 | a0001c0001t0002g0209 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-58+22223A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28912901 | |||||||
| chr8:28912955 | G | T | 12 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0021 others(9): Show |
12 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(9): Show |
intron_variant | MODIFIER | c.-58+22277G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28912955 | |||||||
| chr8:28913342 | A | T | 1 | a0001c0001t0001g0244 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-58+22664A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28913342 | |||||||
| chr8:28913840 | T | C | 1 | a0001c0001t0001g0244 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-58+23162T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28913840 | |||||||
| chr8:28913855 | C | CT | 15 | a0001c0001t0001g0139 a0001c0001t0001g0258 a0001c0001t0002g0001 others(12): Show |
16 | HG02027.hp1 HG02056.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58+23198dupT | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28913855 | ||||||
| chr8:28913855 | CT | C | 13 | a0001c0001t0001g0072 a0001c0001t0001g0306 a0001c0001t0001g0307 others(10): Show |
13 | HG02027.hp2 HG02559.hp2 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.-58+23198delT | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28913855 | ||||||
| chr8:28913855 | CTT | C | 44 | a0001c0001t0002g0092 a0001c0001t0002g0159 a0001c0001t0003g0007 others(41): Show |
44 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.-58+23197_-58+2319 others(6): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28913855 | ||||||
| chr8:28913884 | C | CGG | 5 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0095 others(2): Show |
5 | NA18968.hp2 NA18982.hp1 NA18985.hp1 others(2): Show |
intron_variant | MODIFIER | c.-58+23207_-58+2320 others(6): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28913884 | ||||||
| chr8:28914129 | A | C | 1 | a0001c0001t0006g0329 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-58+23451A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28914129 | |||||||
| chr8:28914321 | C | T | 2 | a0001c0001t0008g0002 a0001c0001t0008g0003 |
2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-58+23643C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28914321 | |||||||
| chr8:28914413 | T | C | 1 | a0001c0001t0004g0004 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-58+23735T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28914413 | |||||||
| chr8:28914450 | A | T | 15 | a0001c0001t0006g0326 a0001c0001t0006g0328 a0001c0001t0006g0329 others(12): Show |
15 | HG00544.hp1 HG02056.hp1 HG02809.hp2 others(12): Show |
intron_variant | MODIFIER | c.-58+23772A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28914450 | |||||||
| chr8:28914619 | A | G | 1 | a0001c0001t0001g0255 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-58+23941A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28914619 | |||||||
| chr8:28914626 | C | T | 310 | a0001c0001t0001g0072 a0001c0001t0001g0138 a0001c0001t0001g0139 others(307): Show |
311 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(308): Show |
intron_variant | MODIFIER | c.-58+23948C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28914626 | |||||||
| chr8:28914721 | G | A | 1 | a0001c0001t0001g0257 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-58+24043G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28914721 | |||||||
| chr8:28915056 | C | A | 1 | a0001c0001t0018g0303 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-58+24378C>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28915056 | |||||||
| chr8:28915140 | C | A | 1 | a0001c0001t0004g0128 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-58+24462C>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28915140 | |||||||
| chr8:28915160 | C | G | 1 | a0001c0001t0003g0100 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-58+24482C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28915160 | |||||||
| chr8:28915279 | T | C | 15 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0122 others(12): Show |
15 | HG00741.hp2 HG02109.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.-58+24601T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28915279 | |||||||
| chr8:28915327 | G | A | 1 | a0001c0001t0008g0068 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-58+24649G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28915327 | |||||||
| chr8:28915332 | C | T | 1 | a0001c0001t0003g0119 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-58+24654C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28915332 | |||||||
| chr8:28915384 | C | G | 1 | a0001c0001t0002g0152 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-58+24706C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28915384 | |||||||
| chr8:28915430 | G | A | 1 | a0001c0001t0001g0258 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-58+24752G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28915430 | |||||||
| chr8:28915556 | C | CA | 24 | a0001c0001t0003g0008 a0001c0001t0003g0069 a0001c0001t0003g0114 others(21): Show |
24 | HG00738.hp1 HG00741.hp2 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.-58+24901dupA | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28915556 | ||||||
| chr8:28915556 | CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0009g0129 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-58+24892_-58+2490 others(14): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28915556 | ||||||
| chr8:28915556 | CAAAAAAA others(4): Show |
C | 193 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 others(190): Show |
194 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.-58+24891_-58+2490 others(15): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28915556 | ||||||
| chr8:28915578 | A | G | 3 | a0001c0001t0004g0063 a0001c0001t0004g0064 a0001c0001t0004g0065 |
3 | HG00738.hp2 HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-58+24900A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28915578 | |||||||
| chr8:28916459 | G | A | 4 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0148 others(1): Show |
4 | NA18947.hp2 NA18990.hp2 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.-58+25781G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28916459 | |||||||
| chr8:28916523 | A | C | 10 | a0001c0001t0007g0010 a0001c0001t0007g0011 a0001c0001t0007g0012 others(7): Show |
10 | HG01261.hp1 HG02257.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.-58+25845A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28916523 | |||||||
| chr8:28916615 | A | G | 15 | a0001c0001t0006g0326 a0001c0001t0006g0328 a0001c0001t0006g0329 others(12): Show |
15 | HG00544.hp1 HG02056.hp1 HG02809.hp2 others(12): Show |
intron_variant | MODIFIER | c.-58+25937A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28916615 | |||||||
| chr8:28916789 | A | C | 3 | a0001c0001t0006g0116 a0001c0001t0014g0117 a0001c0001t0014g0118 |
3 | HG02572.hp1 HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-58+26111A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28916789 | |||||||
| chr8:28916912 | TA | T | 3 | a0001c0001t0002g0259 a0001c0001t0003g0091 a0001c0001t0006g0108 |
3 | NA18949.hp1 NA18949.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.-58+26239delA | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28916912 | ||||||
| chr8:28917066 | C | CA | 67 | a0001c0001t0001g0072 a0001c0001t0001g0227 a0001c0001t0001g0228 others(64): Show |
67 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.-58+26407dupA | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28917066 | ||||||
| chr8:28917103 | T | C | 1 | a0001c0001t0008g0123 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-58+26425T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28917103 | |||||||
| chr8:28917477 | A | G | 1 | a0001c0001t0003g0089 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.-58+26799A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28917477 | |||||||
| chr8:28917623 | T | G | 2 | a0001c0001t0003g0164 a0001c0001t0003g0165 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-58+26945T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28917623 | |||||||
| chr8:28918022 | A | G | 3 | a0001c0001t0006g0116 a0001c0001t0014g0117 a0001c0001t0014g0118 |
3 | HG02572.hp1 HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-58+27344A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28918022 | |||||||
| chr8:28918105 | C | T | 1 | a0001c0001t0001g0315 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-58+27427C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28918105 | |||||||
| chr8:28918595 | A | T | 3 | a0001c0001t0005g0215 a0001c0001t0005g0216 a0001c0001t0005g0217 |
3 | HG02559.hp1 HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-58+27917A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28918595 | |||||||
| chr8:28918596 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-58+27918C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28918596 | |||||||
| chr8:28918611 | C | G | 2 | a0001c0001t0003g0122 a0001c0001t0008g0121 |
2 | HG03195.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-58+27933C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28918611 | |||||||
| chr8:28918717 | C | T | 1 | a0001c0001t0004g0110 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-58+28039C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28918717 | |||||||
| chr8:28918721 | G | A | 1 | a0001c0001t0003g0106 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-58+28043G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28918721 | |||||||
| chr8:28918767 | TAGTA | T | 52 | a0001c0001t0001g0072 a0001c0001t0002g0159 a0001c0001t0002g0259 others(49): Show |
52 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.-58+28094_-58+2809 others(8): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28918767 | ||||||
| chr8:28918966 | T | C | 3 | a0001c0001t0013g0032 a0001c0001t0013g0033 a0001c0001t0020g0053 |
3 | HG02027.hp1 NA18999.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.-58+28288T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28918966 | |||||||
| chr8:28919364 | C | G | 2 | a0001c0001t0004g0026 a0001c0001t0004g0028 |
2 | HG00323.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.-58+28686C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28919364 | |||||||
| chr8:28919392 | T | C | 310 | a0001c0001t0001g0072 a0001c0001t0001g0138 a0001c0001t0001g0139 others(307): Show |
311 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(308): Show |
intron_variant | MODIFIER | c.-58+28714T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28919392 | |||||||
| chr8:28919510 | G | A | 2 | a0001c0001t0014g0117 a0001c0001t0014g0118 |
2 | HG02572.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-58+28832G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28919510 | |||||||
| chr8:28919817 | C | G | 1 | a0001c0001t0006g0116 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-58+29139C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28919817 | |||||||
| chr8:28919971 | T | TTG | 4 | a0001c0001t0003g0069 a0001c0001t0003g0096 a0001c0001t0004g0055 others(1): Show |
4 | HG02145.hp1 HG03540.hp1 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.-58+29323_-58+2932 others(6): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28919971 | ||||||
| chr8:28919971 | TTG | T | 33 | a0001c0001t0001g0222 a0001c0001t0001g0227 a0001c0001t0001g0308 others(30): Show |
33 | HG00544.hp1 HG00609.hp2 HG01943.hp2 others(30): Show |
intron_variant | MODIFIER | c.-58+29323_-58+2932 others(6): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28919971 | ||||||
| chr8:28919971 | TTGTG | T | 174 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 others(171): Show |
175 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.-58+29321_-58+2932 others(8): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28919971 | ||||||
| chr8:28919971 | TTGTGTGT others(1): Show |
T | 4 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0122 others(1): Show |
4 | HG02280.hp1 HG03195.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-58+29317_-58+2932 others(12): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28919971 | ||||||
| chr8:28919971 | TTGTGTGT others(3): Show |
T | 1 | a0001c0001t0001g0254 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-58+29315_-58+2932 others(14): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28919971 | ||||||
| chr8:28920022 | G | C | 2 | a0001c0001t0003g0122 a0001c0001t0008g0121 |
2 | HG03195.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-58+29344G>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28920022 | |||||||
| chr8:28920084 | G | A | 1 | a0001c0001t0001g0315 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-58+29406G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28920084 | |||||||
| chr8:28920160 | T | G | 1 | a0001c0001t0002g0219 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-58+29482T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28920160 | |||||||
| chr8:28920235 | G | A | 1 | a0001c0001t0008g0123 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-58+29557G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28920235 | |||||||
| chr8:28920333 | A | T | 1 | a0001c0001t0006g0116 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-58+29655A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28920333 | |||||||
| chr8:28920525 | C | T | 11 | a0001c0001t0002g0261 a0001c0001t0002g0262 a0001c0001t0002g0265 others(8): Show |
11 | NA18612.hp1 NA18941.hp1 NA18952.hp2 others(8): Show |
intron_variant | MODIFIER | c.-58+29847C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28920525 | |||||||
| chr8:28920579 | C | G | 3 | a0001c0001t0004g0063 a0001c0001t0004g0064 a0001c0001t0004g0065 |
3 | HG00738.hp2 HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-58+29901C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28920579 | |||||||
| chr8:28920715 | G | A | 2 | a0001c0001t0008g0002 a0001c0001t0008g0003 |
2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-58+30037G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28920715 | |||||||
| chr8:28921246 | G | T | 1 | a0001c0001t0014g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-58+30568G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28921246 | |||||||
| chr8:28921312 | G | T | 2 | a0001c0001t0001g0139 a0001c0001t0001g0253 |
2 | HG02486.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-58+30634G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28921312 | |||||||
| chr8:28921344 | C | T | 1 | a0001c0001t0008g0123 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-58+30666C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28921344 | |||||||
| chr8:28921347 | A | T | 4 | a0001c0001t0004g0124 a0001c0001t0004g0125 a0001c0001t0004g0126 others(1): Show |
4 | HG02109.hp2 HG02896.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.-58+30669A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28921347 | |||||||
| chr8:28921367 | A | C | 1 | a0001c0001t0001g0292 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-58+30689A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28921367 | |||||||
| chr8:28921553 | A | G | 3 | a0001c0001t0004g0025 a0001c0001t0004g0026 a0001c0001t0004g0028 |
3 | HG00323.hp2 HG02004.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.-58+30875A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28921553 | |||||||
| chr8:28921686 | A | C | 12 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0021 others(9): Show |
12 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(9): Show |
intron_variant | MODIFIER | c.-58+31008A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28921686 | |||||||
| chr8:28921695 | A | G | 10 | a0001c0001t0007g0010 a0001c0001t0007g0011 a0001c0001t0007g0012 others(7): Show |
10 | HG01261.hp1 HG02257.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.-58+31017A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28921695 | |||||||
| chr8:28921707 | A | T | 1 | a0001c0001t0002g0214 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-58+31029A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28921707 | |||||||
| chr8:28921720 | A | C | 1 | a0001c0001t0017g0213 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-58+31042A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28921720 | |||||||
| chr8:28921805 | A | G | 1 | a0001c0001t0002g0212 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-58+31127A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28921805 | |||||||
| chr8:28921929 | A | G | 1 | a0001c0001t0006g0332 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-58+31251A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28921929 | |||||||
| chr8:28922215 | G | A | 1 | a0001c0001t0002g0157 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-58+31537G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28922215 | |||||||
| chr8:28922283 | C | T | 1 | a0001c0001t0003g0211 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-58+31605C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28922283 | |||||||
| chr8:28922305 | C | T | 1 | a0001c0001t0021g0343 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-58+31627C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28922305 | |||||||
| chr8:28922366 | G | A | 1 | a0001c0001t0004g0004 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-58+31688G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28922366 | |||||||
| chr8:28922562 | C | G | 1 | a0001c0001t0008g0123 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-58+31884C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28922562 | |||||||
| chr8:28922613 | A | G | 2 | a0001c0001t0008g0002 a0001c0001t0008g0003 |
2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-58+31935A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28922613 | |||||||
| chr8:28922841 | G | A | 1 | a0001c0001t0008g0123 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-58+32163G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28922841 | |||||||
| chr8:28922896 | A | G | 1 | a0001c0001t0003g0210 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-58+32218A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28922896 | |||||||
| chr8:28922943 | T | C | 78 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 others(75): Show |
78 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.-58+32265T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28922943 | |||||||
| chr8:28922986 | G | A | 1 | a0001c0001t0005g0301 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-58+32308G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28922986 | |||||||
| chr8:28923216 | T | C | 1 | a0001c0001t0002g0001 | 2 | HG02486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-58+32538T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28923216 | |||||||
| chr8:28923226 | T | A | 1 | a0001c0001t0004g0035 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-58+32548T>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28923226 | |||||||
| chr8:28923272 | G | A | 2 | a0001c0001t0008g0002 a0001c0001t0008g0003 |
2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-58+32594G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28923272 | |||||||
| chr8:28923347 | C | G | 1 | a0001c0001t0002g0209 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-58+32669C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28923347 | |||||||
| chr8:28923443 | A | C | 1 | a0001c0001t0008g0123 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-58+32765A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28923443 | |||||||
| chr8:28923753 | G | A | 1 | a0001c0001t0002g0161 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.-58+33075G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28923753 | |||||||
| chr8:28923831 | T | G | 3 | a0001c0001t0004g0063 a0001c0001t0004g0064 a0001c0001t0004g0065 |
3 | HG00738.hp2 HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-58+33153T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28923831 | |||||||
| chr8:28923861 | T | C | 1 | a0001c0001t0010g0300 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-58+33183T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28923861 | |||||||
| chr8:28924016 | G | T | 1 | a0001c0001t0004g0024 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-58+33338G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28924016 | |||||||
| chr8:28924044 | A | G | 1 | a0001c0001t0004g0051 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-58+33366A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28924044 | |||||||
| chr8:28924050 | C | T | 5 | a0001c0001t0003g0324 a0001c0001t0003g0325 a0001c0001t0006g0116 others(2): Show |
5 | HG02572.hp1 HG02886.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.-58+33372C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28924050 | |||||||
| chr8:28924101 | G | GT | 84 | a0001c0001t0001g0280 a0001c0001t0002g0092 a0001c0001t0002g0133 others(81): Show |
84 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.-58+33432dupT | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28924101 | ||||||
| chr8:28924112 | G | T | 3 | a0001c0001t0001g0315 a0001c0001t0002g0183 a0001c0001t0002g0214 |
3 | HG00642.hp1 NA19043.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.-58+33434G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28924112 | |||||||
| chr8:28924112 | GTT | G | 8 | a0001c0001t0004g0020 a0001c0001t0004g0021 a0001c0001t0004g0022 others(5): Show |
8 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(5): Show |
intron_variant | MODIFIER | c.-58+33445_-58+3344 others(6): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28924112 | ||||||
| chr8:28924175 | T | C | 1 | a0001c0001t0003g0120 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-58+33497T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28924175 | |||||||
| chr8:28924194 | C | T | 2 | a0001c0001t0003g0086 a0001c0001t0003g0087 |
2 | HG02040.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.-58+33516C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28924194 | |||||||
| chr8:28924208 | G | A | 1 | a0001c0001t0004g0036 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-58+33530G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28924208 | |||||||
| chr8:28924359 | C | T | 1 | a0001c0001t0003g0298 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-58+33681C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28924359 | |||||||
| chr8:28924450 | A | AT | 7 | a0001c0001t0002g0208 a0001c0001t0002g0285 a0001c0001t0003g0324 others(4): Show |
7 | HG00741.hp2 HG01358.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.-58+33791dupT | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28924450 | ||||||
| chr8:28924450 | AT | A | 118 | a0001c0001t0001g0072 a0001c0001t0001g0146 a0001c0001t0001g0316 others(115): Show |
118 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.-58+33791delT | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28924450 | ||||||
| chr8:28924451 | T | A | 2 | a0001c0001t0002g0197 a0001c0001t0011g0201 |
2 | NA18956.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.-58+33773T>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28924451 | |||||||
| chr8:28924471 | G | A | 2 | a0001c0001t0003g0070 a0001c0001t0003g0071 |
2 | HG03688.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.-58+33793G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28924471 | |||||||
| chr8:28924471 | G | T | 1 | a0001c0001t0004g0023 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-58+33793G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28924471 | |||||||
| chr8:28924526 | A | G | 1 | a0001c0001t0002g0170 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-58+33848A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28924526 | |||||||
| chr8:28924619 | A | G | 1 | a0001c0001t0003g0087 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-58+33941A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28924619 | |||||||
| chr8:28924698 | C | T | 1 | a0001c0001t0003g0106 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-58+34020C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28924698 | |||||||
| chr8:28924703 | C | T | 8 | a0001c0001t0004g0020 a0001c0001t0004g0021 a0001c0001t0004g0022 others(5): Show |
8 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(5): Show |
intron_variant | MODIFIER | c.-58+34025C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28924703 | |||||||
| chr8:28924768 | G | A | 2 | a0001c0001t0007g0062 a0001c0001t0010g0312 |
2 | HG02630.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-58+34090G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28924768 | |||||||
| chr8:28924800 | C | A | 1 | a0001c0001t0001g0220 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-58+34122C>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28924800 | |||||||
| chr8:28924901 | C | T | 11 | a0001c0001t0003g0134 a0001c0001t0003g0153 a0001c0001t0003g0158 others(8): Show |
11 | HG02257.hp1 HG02280.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.-58+34223C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28924901 | |||||||
| chr8:28924903 | C | T | 1 | a0001c0001t0003g0084 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.-58+34225C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28924903 | |||||||
| chr8:28924913 | CT | C | 8 | a0001c0001t0001g0232 a0001c0001t0002g0185 a0001c0001t0004g0037 others(5): Show |
8 | HG00639.hp2 HG00741.hp1 HG01070.hp1 others(5): Show |
intron_variant | MODIFIER | c.-58+34253delT | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28924913 | ||||||
| chr8:28925002 | C | T | 12 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0021 others(9): Show |
12 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(9): Show |
intron_variant | MODIFIER | c.-58+34324C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28925002 | |||||||
| chr8:28925011 | AT | A | 8 | a0001c0001t0003g0119 a0001c0001t0003g0122 a0001c0001t0004g0004 others(5): Show |
8 | HG00741.hp2 HG01069.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.-58+34346delT | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28925011 | ||||||
| chr8:28925160 | T | C | 14 | a0001c0001t0006g0326 a0001c0001t0006g0328 a0001c0001t0006g0329 others(11): Show |
14 | HG00544.hp1 HG02056.hp1 HG02809.hp2 others(11): Show |
intron_variant | MODIFIER | c.-58+34482T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28925160 | |||||||
| chr8:28925336 | C | G | 1 | a0001c0001t0002g0157 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-58+34658C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28925336 | |||||||
| chr8:28925515 | T | G | 2 | a0001c0001t0004g0026 a0001c0001t0004g0028 |
2 | HG00323.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.-58+34837T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28925515 | |||||||
| chr8:28925640 | GA | G | 229 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 others(226): Show |
230 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(227): Show |
intron_variant | MODIFIER | c.-58+34972delA | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28925640 | ||||||
| chr8:28925761 | A | G | 5 | a0001c0001t0003g0324 a0001c0001t0003g0325 a0001c0001t0006g0116 others(2): Show |
5 | HG02572.hp1 HG02886.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.-58+35083A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28925761 | |||||||
| chr8:28925986 | T | A | 2 | a0001c0001t0014g0117 a0001c0001t0014g0118 |
2 | HG02572.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-58+35308T>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28925986 | |||||||
| chr8:28926178 | T | C | 1 | a0001c0001t0003g0120 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-58+35500T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28926178 | |||||||
| chr8:28926210 | A | G | 6 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0122 others(3): Show |
6 | HG02055.hp2 HG02280.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.-58+35532A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28926210 | |||||||
| chr8:28926219 | C | T | 4 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0148 others(1): Show |
4 | NA18947.hp2 NA18990.hp2 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.-58+35541C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28926219 | |||||||
| chr8:28926282 | GAT | G | 22 | a0001c0001t0002g0209 a0001c0001t0003g0114 a0001c0001t0004g0034 others(19): Show |
22 | HG00544.hp1 HG00738.hp1 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.-58+35626_-58+3562 others(6): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28926282 | ||||||
| chr8:28926300 | T | C | 10 | a0001c0001t0007g0010 a0001c0001t0007g0011 a0001c0001t0007g0012 others(7): Show |
10 | HG01261.hp1 HG02257.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.-58+35622T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28926300 | |||||||
| chr8:28926302 | T | C | 12 | a0001c0001t0007g0010 a0001c0001t0007g0011 a0001c0001t0007g0012 others(9): Show |
12 | HG01261.hp1 HG02257.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.-58+35624T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28926302 | |||||||
| chr8:28926302 | T | TAC | 7 | a0001c0001t0001g0138 a0001c0001t0001g0225 a0001c0001t0001g0226 others(4): Show |
7 | HG00140.hp1 HG00741.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.-58+35625_-58+3562 others(6): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28926302 | ||||||
| chr8:28926302 | T | TACAC | 8 | a0001c0001t0001g0072 a0001c0001t0003g0069 a0001c0001t0003g0089 others(5): Show |
8 | HG02027.hp2 HG03195.hp2 NA18522.hp1 others(5): Show |
intron_variant | MODIFIER | c.-58+35625_-58+3562 others(8): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28926302 | ||||||
| chr8:28926304 | T | C | 175 | a0001c0001t0001g0072 a0001c0001t0001g0138 a0001c0001t0001g0139 others(172): Show |
175 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.-58+35626T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28926304 | |||||||
| chr8:28926304 | T | TAC | 126 | a0001c0001t0001g0142 a0001c0001t0001g0145 a0001c0001t0001g0146 others(123): Show |
127 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(124): Show |
intron_variant | MODIFIER | c.-58+35644_-58+3564 others(6): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28926304 | ||||||
| chr8:28926304 | T | TACAC | 4 | a0001c0001t0002g0208 a0001c0001t0003g0090 a0001c0001t0005g0172 others(1): Show |
4 | HG00280.hp2 HG01123.hp1 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.-58+35642_-58+3564 others(8): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28926304 | ||||||
| chr8:28926304 | T | TACACAC | 3 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0010g0300 |
3 | HG02055.hp2 HG02280.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-58+35640_-58+3564 others(10): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28926304 | ||||||
| chr8:28926304 | T | TATACACA others(7): Show |
1 | a0001c0001t0006g0116 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-58+35627_-58+3562 others(18): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28926304 | ||||||
| chr8:28926304 | T | TATACACA others(9): Show |
2 | a0001c0001t0014g0117 a0001c0001t0014g0118 |
2 | HG02572.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-58+35627_-58+3562 others(20): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28926304 | ||||||
| chr8:28926304 | T | TATATACA others(9): Show |
1 | a0001c0001t0008g0123 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-58+35627_-58+3562 others(20): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28926304 | ||||||
| chr8:28926304 | T | TATATATA others(23): Show |
1 | a0001c0001t0003g0325 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-58+35627_-58+3562 others(34): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28926304 | ||||||
| chr8:28926304 | T | TATATATA others(25): Show |
1 | a0001c0001t0003g0324 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-58+35627_-58+3562 others(36): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28926304 | ||||||
| chr8:28926306 | C | T | 1 | a0001c0001t0004g0049 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-58+35628C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28926306 | |||||||
| chr8:28926324 | T | C | 1 | a0001c0001t0002g0166 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-58+35646T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28926324 | |||||||
| chr8:28926416 | A | C | 2 | a0001c0001t0003g0122 a0001c0001t0008g0121 |
2 | HG03195.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-58+35738A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28926416 | |||||||
| chr8:28926498 | T | C | 198 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 others(195): Show |
199 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.-58+35820T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28926498 | |||||||
| chr8:28926591 | C | A | 3 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 |
3 | NA18975.hp2 NA18998.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.-58+35913C>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28926591 | |||||||
| chr8:28926635 | G | A | 1 | a0001c0001t0001g0236 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-58+35957G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28926635 | |||||||
| chr8:28926705 | C | A | 15 | a0001c0001t0006g0326 a0001c0001t0006g0328 a0001c0001t0006g0329 others(12): Show |
15 | HG00544.hp1 HG02056.hp1 HG02809.hp2 others(12): Show |
intron_variant | MODIFIER | c.-58+36027C>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28926705 | |||||||
| chr8:28926825 | G | A | 1 | a0001c0001t0001g0256 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-58+36147G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28926825 | |||||||
| chr8:28926867 | A | G | 2 | a0001c0001t0003g0084 a0001c0001t0003g0101 |
2 | NA18962.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.-58+36189A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28926867 | |||||||
| chr8:28927047 | A | G | 1 | a0001c0001t0001g0249 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-58+36369A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28927047 | |||||||
| chr8:28927159 | ATAAAATG others(1): Show |
A | 4 | a0001c0001t0003g0119 a0001c0001t0003g0122 a0001c0001t0008g0121 others(1): Show |
4 | HG02280.hp1 HG02965.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-58+36483_-58+3649 others(12): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28927159 | ||||||
| chr8:28927169 | T | G | 4 | a0001c0001t0003g0119 a0001c0001t0003g0122 a0001c0001t0008g0121 others(1): Show |
4 | HG02280.hp1 HG02965.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-58+36491T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28927169 | |||||||
| chr8:28927369 | A | G | 1 | a0001c0001t0010g0230 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-57-36442A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28927369 | |||||||
| chr8:28927389 | T | C | 112 | a0001c0001t0001g0289 a0001c0001t0002g0001 a0001c0001t0002g0092 others(109): Show |
113 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.-57-36422T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28927389 | |||||||
| chr8:28927424 | C | T | 3 | a0001c0001t0006g0116 a0001c0001t0014g0117 a0001c0001t0014g0118 |
3 | HG02572.hp1 HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-57-36387C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28927424 | |||||||
| chr8:28927524 | TAGG | T | 15 | a0001c0001t0006g0326 a0001c0001t0006g0328 a0001c0001t0006g0329 others(12): Show |
15 | HG00544.hp1 HG02056.hp1 HG02809.hp2 others(12): Show |
intron_variant | MODIFIER | c.-57-36276_-57-3627 others(7): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28927524 | ||||||
| chr8:28927696 | A | G | 1 | a0001c0001t0001g0138 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-57-36115A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28927696 | |||||||
| chr8:28927736 | A | C | 2 | a0001c0001t0014g0117 a0001c0001t0014g0118 |
2 | HG02572.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-57-36075A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28927736 | |||||||
| chr8:28927809 | C | A | 1 | a0001c0001t0001g0139 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-57-36002C>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28927809 | |||||||
| chr8:28927831 | C | CA | 98 | a0001c0001t0001g0072 a0001c0001t0001g0139 a0001c0001t0001g0140 others(95): Show |
98 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.-57-35956dupA | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28927831 | ||||||
| chr8:28927831 | C | CAA | 21 | a0001c0001t0001g0138 a0001c0001t0001g0146 a0001c0001t0001g0148 others(18): Show |
21 | HG00423.hp1 HG00642.hp2 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.-57-35957_-57-3595 others(6): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28927831 | ||||||
| chr8:28927831 | CA | C | 106 | a0001c0001t0001g0289 a0001c0001t0002g0001 a0001c0001t0002g0092 others(103): Show |
107 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.-57-35956delA | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28927831 | ||||||
| chr8:28927831 | CAA | C | 9 | a0001c0001t0002g0206 a0001c0001t0002g0260 a0001c0001t0002g0265 others(6): Show |
9 | HG02572.hp1 HG02897.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.-57-35957_-57-3595 others(6): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28927831 | ||||||
| chr8:28927856 | G | A | 7 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 others(4): Show |
7 | HG00423.hp1 HG02071.hp1 NA18947.hp2 others(4): Show |
intron_variant | MODIFIER | c.-57-35955G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28927856 | |||||||
| chr8:28927872 | C | G | 110 | a0001c0001t0001g0289 a0001c0001t0002g0001 a0001c0001t0002g0092 others(107): Show |
111 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.-57-35939C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28927872 | |||||||
| chr8:28927874 | C | T | 12 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0021 others(9): Show |
12 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(9): Show |
intron_variant | MODIFIER | c.-57-35937C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28927874 | |||||||
| chr8:28927893 | T | A | 4 | a0001c0001t0003g0119 a0001c0001t0003g0122 a0001c0001t0008g0121 others(1): Show |
4 | HG02280.hp1 HG02965.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-57-35918T>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28927893 | |||||||
| chr8:28928010 | C | G | 1 | a0001c0001t0003g0119 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-57-35801C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28928010 | |||||||
| chr8:28928093 | C | G | 1 | a0001c0001t0004g0110 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-57-35718C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28928093 | |||||||
| chr8:28928133 | CA | C | 9 | a0001c0001t0003g0119 a0001c0001t0003g0122 a0001c0001t0003g0324 others(6): Show |
9 | HG02280.hp1 HG02572.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.-57-35666delA | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28928133 | ||||||
| chr8:28928468 | A | T | 70 | a0001c0001t0001g0072 a0001c0001t0003g0006 a0001c0001t0003g0007 others(67): Show |
70 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.-57-35343A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28928468 | |||||||
| chr8:28928708 | C | T | 2 | a0001c0001t0008g0067 a0001c0001t0008g0094 |
2 | HG00621.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.-57-35103C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28928708 | |||||||
| chr8:28929150 | G | T | 7 | a0001c0001t0004g0041 a0001c0001t0004g0045 a0001c0001t0004g0046 others(4): Show |
7 | HG00544.hp2 HG00597.hp1 HG02074.hp1 others(4): Show |
intron_variant | MODIFIER | c.-57-34661G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28929150 | |||||||
| chr8:28929160 | A | G | 1 | a0001c0001t0001g0072 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-57-34651A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28929160 | |||||||
| chr8:28929203 | G | A | 2 | a0001c0001t0007g0005 a0001c0001t0007g0062 |
2 | HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-57-34608G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28929203 | |||||||
| chr8:28929256 | C | G | 2 | a0001c0001t0007g0005 a0001c0001t0007g0062 |
2 | HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-57-34555C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28929256 | |||||||
| chr8:28929262 | C | T | 2 | a0001c0001t0007g0005 a0001c0001t0007g0062 |
2 | HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-57-34549C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28929262 | |||||||
| chr8:28929348 | A | T | 1 | a0001c0001t0002g0207 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-57-34463A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28929348 | |||||||
| chr8:28929498 | A | G | 2 | a0001c0001t0002g0186 a0001c0001t0002g0187 |
2 | NA18978.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.-57-34313A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28929498 | |||||||
| chr8:28929585 | T | C | 1 | a0001c0001t0002g0160 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-57-34226T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28929585 | |||||||
| chr8:28929624 | A | C | 1 | a0001c0001t0007g0010 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-57-34187A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28929624 | |||||||
| chr8:28929731 | A | C | 1 | a0001c0001t0004g0019 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-57-34080A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28929731 | |||||||
| chr8:28929846 | G | A | 2 | a0001c0001t0007g0005 a0001c0001t0007g0062 |
2 | HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-57-33965G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28929846 | |||||||
| chr8:28929926 | G | GC | 7 | a0001c0001t0001g0072 a0001c0001t0001g0140 a0001c0001t0001g0304 others(4): Show |
7 | HG02027.hp2 HG02615.hp1 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.-57-33879dupC | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28929926 | ||||||
| chr8:28929933 | G | GC | 24 | a0001c0001t0001g0145 a0001c0001t0001g0238 a0001c0001t0001g0287 others(21): Show |
24 | HG01167.hp1 HG01261.hp1 HG01358.hp2 others(21): Show |
intron_variant | MODIFIER | c.-57-33875dupC | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28929933 | ||||||
| chr8:28929937 | G | A | 2 | a0001c0001t0003g0324 a0001c0001t0003g0325 |
2 | HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-57-33874G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28929937 | |||||||
| chr8:28929937 | G | C | 2 | a0001c0001t0008g0073 a0001c0002t0002g0283 |
2 | HG01496.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.-57-33874G>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28929937 | |||||||
| chr8:28929937 | G | GC | 8 | a0001c0001t0001g0239 a0001c0001t0001g0249 a0001c0001t0001g0253 others(5): Show |
8 | HG00741.hp2 HG01175.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.-57-33868dupC | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28929937 | ||||||
| chr8:28929938 | C | G | 1 | a0001c0001t0008g0073 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-57-33873C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28929938 | |||||||
| chr8:28929942 | C | T | 15 | a0001c0001t0006g0326 a0001c0001t0006g0328 a0001c0001t0006g0329 others(12): Show |
15 | HG00544.hp1 HG02056.hp1 HG02809.hp2 others(12): Show |
intron_variant | MODIFIER | c.-57-33869C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28929942 | |||||||
| chr8:28930008 | C | G | 10 | a0001c0001t0007g0010 a0001c0001t0007g0011 a0001c0001t0007g0012 others(7): Show |
10 | HG01261.hp1 HG02257.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.-57-33803C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28930008 | |||||||
| chr8:28930272 | T | C | 1 | a0001c0001t0004g0026 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-57-33539T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28930272 | |||||||
| chr8:28930296 | G | T | 15 | a0001c0001t0006g0326 a0001c0001t0006g0328 a0001c0001t0006g0329 others(12): Show |
15 | HG00544.hp1 HG02056.hp1 HG02809.hp2 others(12): Show |
intron_variant | MODIFIER | c.-57-33515G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28930296 | |||||||
| chr8:28930325 | A | G | 2 | a0001c0001t0003g0324 a0001c0001t0003g0325 |
2 | HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-57-33486A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28930325 | |||||||
| chr8:28930442 | A | T | 2 | a0001c0001t0004g0125 a0001c0001t0004g0127 |
2 | HG02109.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-57-33369A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28930442 | |||||||
| chr8:28930516 | G | A | 192 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 others(189): Show |
193 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.-57-33295G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28930516 | |||||||
| chr8:28930575 | C | G | 1 | a0001c0001t0004g0110 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-57-33236C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28930575 | |||||||
| chr8:28930815 | A | G | 3 | a0001c0001t0004g0063 a0001c0001t0004g0064 a0001c0001t0004g0065 |
3 | HG00738.hp2 HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-57-32996A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28930815 | |||||||
| chr8:28930840 | C | T | 1 | a0001c0001t0002g0205 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-57-32971C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28930840 | |||||||
| chr8:28930846 | A | G | 6 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0122 others(3): Show |
6 | HG02055.hp2 HG02280.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.-57-32965A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28930846 | |||||||
| chr8:28931124 | T | C | 2 | a0001c0001t0003g0324 a0001c0001t0003g0325 |
2 | HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-57-32687T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28931124 | |||||||
| chr8:28931549 | T | G | 1 | a0001c0001t0012g0297 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-57-32262T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28931549 | |||||||
| chr8:28931581 | A | G | 1 | a0001c0001t0004g0052 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-57-32230A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28931581 | |||||||
| chr8:28931623 | C | T | 2 | a0001c0001t0003g0164 a0001c0001t0003g0165 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-57-32188C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28931623 | |||||||
| chr8:28931734 | C | T | 11 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0122 others(8): Show |
11 | HG02055.hp2 HG02280.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.-57-32077C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28931734 | |||||||
| chr8:28931758 | C | G | 5 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0122 others(2): Show |
5 | HG02055.hp2 HG02280.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.-57-32053C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28931758 | |||||||
| chr8:28931816 | C | T | 109 | a0001c0001t0001g0289 a0001c0001t0002g0001 a0001c0001t0002g0092 others(106): Show |
110 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.-57-31995C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28931816 | |||||||
| chr8:28931833 | A | T | 1 | a0001c0001t0005g0151 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-57-31978A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28931833 | |||||||
| chr8:28932193 | C | T | 1 | a0001c0001t0002g0187 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-57-31618C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28932193 | |||||||
| chr8:28932195 | G | T | 1 | a0001c0001t0002g0187 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-57-31616G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28932195 | |||||||
| chr8:28932200 | A | T | 1 | a0001c0001t0002g0187 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-57-31611A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28932200 | |||||||
| chr8:28932201 | C | T | 1 | a0001c0001t0002g0187 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-57-31610C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28932201 | |||||||
| chr8:28932202 | G | T | 1 | a0001c0001t0002g0187 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-57-31609G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28932202 | |||||||
| chr8:28932209 | G | T | 1 | a0001c0001t0002g0187 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-57-31602G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28932209 | |||||||
| chr8:28932211 | G | T | 1 | a0001c0001t0002g0187 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-57-31600G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28932211 | |||||||
| chr8:28932213 | C | T | 1 | a0001c0001t0002g0187 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-57-31598C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28932213 | |||||||
| chr8:28932214 | T | C | 1 | a0001c0001t0002g0187 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-57-31597T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28932214 | |||||||
| chr8:28932215 | A | T | 1 | a0001c0001t0002g0187 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-57-31596A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28932215 | |||||||
| chr8:28932216 | G | T | 1 | a0001c0001t0002g0187 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-57-31595G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28932216 | |||||||
| chr8:28932217 | G | A | 1 | a0001c0001t0002g0187 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-57-31594G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28932217 | |||||||
| chr8:28932218 | G | T | 1 | a0001c0001t0002g0187 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-57-31593G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28932218 | |||||||
| chr8:28932220 | A | T | 1 | a0001c0001t0002g0187 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-57-31591A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28932220 | |||||||
| chr8:28932221 | T | C | 1 | a0001c0001t0002g0187 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-57-31590T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28932221 | |||||||
| chr8:28932222 | G | C | 1 | a0001c0001t0002g0187 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-57-31589G>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28932222 | |||||||
| chr8:28932223 | G | A | 1 | a0001c0001t0002g0187 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-57-31588G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28932223 | |||||||
| chr8:28932230 | A | C | 1 | a0001c0001t0002g0187 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-57-31581A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28932230 | |||||||
| chr8:28932232 | G | A | 1 | a0001c0001t0002g0187 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-57-31579G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28932232 | |||||||
| chr8:28932233 | G | T | 1 | a0001c0001t0002g0187 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-57-31578G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28932233 | |||||||
| chr8:28932234 | G | T | 1 | a0001c0001t0002g0187 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-57-31577G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28932234 | |||||||
| chr8:28932237 | G | C | 1 | a0001c0001t0002g0187 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-57-31574G>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28932237 | |||||||
| chr8:28932238 | A | T | 1 | a0001c0001t0002g0187 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-57-31573A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28932238 | |||||||
| chr8:28932240 | G | C | 1 | a0001c0001t0002g0187 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-57-31571G>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28932240 | |||||||
| chr8:28932241 | C | A | 1 | a0001c0001t0002g0187 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-57-31570C>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28932241 | |||||||
| chr8:28932243 | A | T | 1 | a0001c0001t0002g0187 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-57-31568A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28932243 | |||||||
| chr8:28932247 | C | G | 1 | a0001c0001t0002g0187 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-57-31564C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28932247 | |||||||
| chr8:28932249 | T | G | 1 | a0001c0001t0002g0187 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-57-31562T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28932249 | |||||||
| chr8:28932252 | A | T | 1 | a0001c0001t0002g0187 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-57-31559A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28932252 | |||||||
| chr8:28932253 | A | G | 1 | a0001c0001t0002g0187 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-57-31558A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28932253 | |||||||
| chr8:28932254 | G | T | 1 | a0001c0001t0002g0187 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-57-31557G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28932254 | |||||||
| chr8:28932255 | G | C | 1 | a0001c0001t0002g0187 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-57-31556G>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28932255 | |||||||
| chr8:28932274 | G | A | 2 | a0001c0001t0008g0002 a0001c0001t0008g0003 |
2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-57-31537G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28932274 | |||||||
| chr8:28932414 | G | A | 2 | a0001c0001t0012g0174 a0001c0001t0012g0297 |
2 | HG02886.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-57-31397G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28932414 | |||||||
| chr8:28932683 | A | G | 1 | a0001c0001t0007g0012 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-57-31128A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28932683 | |||||||
| chr8:28932725 | T | G | 11 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0122 others(8): Show |
11 | HG02055.hp2 HG02280.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.-57-31086T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28932725 | |||||||
| chr8:28932794 | G | T | 1 | a0001c0001t0007g0005 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-57-31017G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28932794 | |||||||
| chr8:28932795 | C | T | 1 | a0001c0001t0007g0005 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-57-31016C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28932795 | |||||||
| chr8:28932810 | C | G | 1 | a0001c0001t0003g0085 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-57-31001C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28932810 | |||||||
| chr8:28933069 | C | T | 1 | a0001c0001t0001g0315 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-57-30742C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28933069 | |||||||
| chr8:28933101 | G | C | 334 | a0001c0001t0001g0072 a0001c0001t0001g0138 a0001c0001t0001g0139 others(331): Show |
335 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(332): Show |
intron_variant | MODIFIER | c.-57-30710G>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28933101 | |||||||
| chr8:28933121 | G | A | 2 | a0001c0001t0001g0290 a0001c0001t0001g0294 |
2 | HG01070.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.-57-30690G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28933121 | |||||||
| chr8:28933378 | C | T | 2 | a0001c0001t0001g0290 a0001c0001t0001g0294 |
2 | HG01070.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.-57-30433C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28933378 | |||||||
| chr8:28933571 | A | G | 2 | a0001c0001t0002g0156 a0001c0001t0002g0163 |
2 | HG03017.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.-57-30240A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28933571 | |||||||
| chr8:28933598 | C | A | 1 | a0001c0001t0005g0151 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-57-30213C>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28933598 | |||||||
| chr8:28933598 | C | G | 1 | a0001c0001t0001g0299 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-57-30213C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28933598 | |||||||
| chr8:28933642 | G | A | 217 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 others(214): Show |
218 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.-57-30169G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28933642 | |||||||
| chr8:28933949 | A | G | 5 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0122 others(2): Show |
5 | HG02055.hp2 HG02280.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.-57-29862A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28933949 | |||||||
| chr8:28933990 | A | C | 2 | a0001c0001t0007g0005 a0001c0001t0007g0062 |
2 | HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-57-29821A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28933990 | |||||||
| chr8:28934281 | T | G | 1 | a0001c0001t0003g0087 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-57-29530T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28934281 | |||||||
| chr8:28934445 | A | G | 1 | a0001c0001t0008g0123 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-57-29366A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28934445 | |||||||
| chr8:28934582 | T | G | 1 | a0001c0001t0007g0013 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-57-29229T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28934582 | |||||||
| chr8:28934647 | C | T | 14 | a0001c0001t0006g0326 a0001c0001t0006g0328 a0001c0001t0006g0329 others(11): Show |
14 | HG00544.hp1 HG02056.hp1 HG02809.hp2 others(11): Show |
intron_variant | MODIFIER | c.-57-29164C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28934647 | |||||||
| chr8:28934705 | C | T | 1 | a0001c0001t0004g0004 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-57-29106C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28934705 | |||||||
| chr8:28934926 | C | CA | 82 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 others(79): Show |
82 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.-57-28868dupA | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28934926 | ||||||
| chr8:28934968 | C | T | 3 | a0001c0001t0006g0116 a0001c0001t0014g0117 a0001c0001t0014g0118 |
3 | HG02572.hp1 HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-57-28843C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28934968 | |||||||
| chr8:28935264 | G | A | 1 | a0001c0001t0001g0305 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-57-28547G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28935264 | |||||||
| chr8:28935385 | A | T | 1 | a0001c0001t0003g0210 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-57-28426A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28935385 | |||||||
| chr8:28935475 | C | T | 2 | a0001c0001t0003g0324 a0001c0001t0003g0325 |
2 | HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-57-28336C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28935475 | |||||||
| chr8:28935505 | T | A | 1 | a0001c0001t0021g0343 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-57-28306T>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28935505 | |||||||
| chr8:28935506 | T | A | 3 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0288 |
3 | HG00323.hp1 HG01123.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.-57-28305T>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28935506 | |||||||
| chr8:28935780 | C | T | 1 | a0001c0001t0021g0343 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-57-28031C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28935780 | |||||||
| chr8:28936390 | G | A | 1 | a0001c0001t0004g0004 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-57-27421G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28936390 | |||||||
| chr8:28936410 | T | C | 204 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 others(201): Show |
205 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(202): Show |
intron_variant | MODIFIER | c.-57-27401T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28936410 | |||||||
| chr8:28936488 | C | T | 2 | a0001c0001t0001g0299 a0001c0001t0003g0119 |
2 | HG02280.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-57-27323C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28936488 | |||||||
| chr8:28936513 | A | T | 1 | a0001c0001t0004g0035 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-57-27298A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28936513 | |||||||
| chr8:28936544 | C | T | 1 | a0001c0001t0007g0062 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-57-27267C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28936544 | |||||||
| chr8:28936799 | T | TA | 122 | a0001c0001t0001g0289 a0001c0001t0002g0001 a0001c0001t0002g0092 others(119): Show |
123 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.-57-26996dupA | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28936799 | ||||||
| chr8:28936799 | TA | T | 6 | a0001c0001t0001g0315 a0001c0001t0003g0324 a0001c0001t0003g0325 others(3): Show |
6 | HG00738.hp2 HG01243.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.-57-26996delA | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28936799 | ||||||
| chr8:28936849 | G | C | 1 | a0001c0001t0008g0123 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-57-26962G>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28936849 | |||||||
| chr8:28936874 | A | T | 3 | a0001c0001t0003g0119 a0001c0001t0003g0122 a0001c0001t0008g0121 |
3 | HG02280.hp1 HG03195.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-57-26937A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28936874 | |||||||
| chr8:28937161 | C | T | 212 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 others(209): Show |
213 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(210): Show |
intron_variant | MODIFIER | c.-57-26650C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28937161 | |||||||
| chr8:28937339 | G | A | 2 | a0001c0001t0001g0249 a0001c0001t0001g0254 |
2 | HG02040.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.-57-26472G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28937339 | |||||||
| chr8:28937505 | A | G | 2 | a0001c0001t0002g0136 a0001c0001t0002g0137 |
2 | HG00558.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.-57-26306A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28937505 | |||||||
| chr8:28937617 | C | T | 3 | a0001c0001t0006g0116 a0001c0001t0014g0117 a0001c0001t0014g0118 |
3 | HG02572.hp1 HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-57-26194C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28937617 | |||||||
| chr8:28937630 | A | G | 1 | a0001c0001t0002g0156 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-57-26181A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28937630 | |||||||
| chr8:28937829 | G | A | 5 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0095 others(2): Show |
5 | NA18968.hp2 NA18982.hp1 NA18985.hp1 others(2): Show |
intron_variant | MODIFIER | c.-57-25982G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28937829 | |||||||
| chr8:28937879 | ATACT | A | 54 | a0001c0001t0001g0072 a0001c0001t0003g0006 a0001c0001t0003g0007 others(51): Show |
54 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.-57-25929_-57-2592 others(8): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28937879 | ||||||
| chr8:28937890 | T | A | 2 | a0001c0001t0012g0174 a0001c0001t0012g0297 |
2 | HG02886.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-57-25921T>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28937890 | |||||||
| chr8:28938058 | A | C | 15 | a0001c0001t0006g0326 a0001c0001t0006g0328 a0001c0001t0006g0329 others(12): Show |
15 | HG00544.hp1 HG02056.hp1 HG02809.hp2 others(12): Show |
intron_variant | MODIFIER | c.-57-25753A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28938058 | |||||||
| chr8:28938320 | T | G | 1 | a0001c0001t0003g0087 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-57-25491T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28938320 | |||||||
| chr8:28938487 | G | A | 1 | a0001c0001t0001g0228 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-57-25324G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28938487 | |||||||
| chr8:28938675 | T | A | 1 | a0001c0001t0003g0119 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-57-25136T>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28938675 | |||||||
| chr8:28938690 | CTTT | C | 6 | a0001c0001t0004g0004 a0001c0001t0004g0124 a0001c0001t0004g0125 others(3): Show |
6 | HG00741.hp2 HG02109.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-57-25120_-57-2511 others(7): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28938690 | |||||||
| chr8:28938714 | G | A | 3 | a0001c0001t0003g0119 a0001c0001t0003g0122 a0001c0001t0008g0121 |
3 | HG02280.hp1 HG03195.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-57-25097G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28938714 | |||||||
| chr8:28938791 | T | TAGC | 228 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 others(225): Show |
229 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(226): Show |
intron_variant | MODIFIER | c.-57-25020_-57-2501 others(7): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28938791 | |||||||
| chr8:28938807 | G | A | 54 | a0001c0001t0001g0072 a0001c0001t0003g0006 a0001c0001t0003g0007 others(51): Show |
54 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.-57-25004G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28938807 | |||||||
| chr8:28938869 | C | T | 1 | a0001c0001t0007g0018 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-57-24942C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28938869 | |||||||
| chr8:28939211 | C | T | 80 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 others(77): Show |
80 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.-57-24600C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28939211 | |||||||
| chr8:28939294 | A | G | 1 | a0001c0001t0001g0315 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-57-24517A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28939294 | |||||||
| chr8:28939304 | A | G | 1 | a0001c0001t0009g0129 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-57-24507A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28939304 | |||||||
| chr8:28939496 | G | C | 1 | a0001c0001t0001g0138 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-57-24315G>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28939496 | |||||||
| chr8:28939511 | T | A | 4 | a0001c0001t0003g0119 a0001c0001t0003g0122 a0001c0001t0008g0121 others(1): Show |
4 | HG02280.hp1 HG02965.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-57-24300T>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28939511 | |||||||
| chr8:28939570 | C | T | 1 | a0001c0001t0004g0060 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-57-24241C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28939570 | |||||||
| chr8:28939576 | C | T | 9 | a0001c0001t0007g0011 a0001c0001t0007g0012 a0001c0001t0007g0013 others(6): Show |
9 | HG01261.hp1 HG02257.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.-57-24235C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28939576 | |||||||
| chr8:28939600 | C | G | 1 | a0001c0001t0002g0133 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-57-24211C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28939600 | |||||||
| chr8:28939674 | T | G | 1 | a0001c0001t0002g0317 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.-57-24137T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28939674 | |||||||
| chr8:28939730 | G | A | 3 | a0001c0001t0003g0119 a0001c0001t0003g0122 a0001c0001t0008g0121 |
3 | HG02280.hp1 HG03195.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-57-24081G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28939730 | |||||||
| chr8:28939735 | C | T | 2 | a0001c0001t0001g0225 a0001c0001t0001g0226 |
2 | HG00140.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.-57-24076C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28939735 | |||||||
| chr8:28939927 | A | C | 3 | a0001c0001t0006g0116 a0001c0001t0014g0117 a0001c0001t0014g0118 |
3 | HG02572.hp1 HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-57-23884A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28939927 | |||||||
| chr8:28939971 | A | G | 1 | a0001c0001t0004g0029 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-57-23840A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28939971 | |||||||
| chr8:28939973 | A | G | 3 | a0001c0001t0006g0116 a0001c0001t0014g0117 a0001c0001t0014g0118 |
3 | HG02572.hp1 HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-57-23838A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28939973 | |||||||
| chr8:28940021 | T | C | 2 | a0001c0001t0003g0122 a0001c0001t0008g0121 |
2 | HG03195.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-57-23790T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28940021 | |||||||
| chr8:28940036 | G | A | 2 | a0001c0001t0007g0005 a0001c0001t0007g0062 |
2 | HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-57-23775G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28940036 | |||||||
| chr8:28940402 | C | T | 1 | a0001c0001t0004g0128 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-57-23409C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28940402 | |||||||
| chr8:28940429 | A | G | 8 | a0001c0001t0004g0054 a0001c0001t0004g0055 a0001c0001t0004g0056 others(5): Show |
8 | HG01884.hp1 HG02145.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.-57-23382A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28940429 | |||||||
| chr8:28940859 | C | T | 3 | a0001c0001t0006g0116 a0001c0001t0014g0117 a0001c0001t0014g0118 |
3 | HG02572.hp1 HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-57-22952C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28940859 | |||||||
| chr8:28940923 | T | A | 1 | a0001c0001t0003g0081 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.-57-22888T>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28940923 | |||||||
| chr8:28940975 | A | G | 2 | a0001c0001t0001g0250 a0001c0001t0001g0251 |
2 | NA18961.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.-57-22836A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28940975 | |||||||
| chr8:28941111 | C | T | 54 | a0001c0001t0001g0072 a0001c0001t0003g0006 a0001c0001t0003g0007 others(51): Show |
54 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.-57-22700C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28941111 | |||||||
| chr8:28941117 | A | T | 1 | a0001c0001t0001g0315 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-57-22694A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28941117 | |||||||
| chr8:28941267 | C | T | 2 | a0001c0001t0001g0225 a0001c0001t0001g0226 |
2 | HG00140.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.-57-22544C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28941267 | |||||||
| chr8:28941276 | G | T | 1 | a0001c0001t0004g0023 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-57-22535G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28941276 | |||||||
| chr8:28941287 | T | C | 1 | a0001c0001t0001g0154 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-57-22524T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28941287 | |||||||
| chr8:28941350 | A | G | 1 | a0001c0001t0002g0156 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-57-22461A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28941350 | |||||||
| chr8:28941388 | T | A | 3 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0268 |
3 | NA18978.hp1 NA19065.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.-57-22423T>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28941388 | |||||||
| chr8:28941718 | T | TA | 9 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0095 others(6): Show |
9 | NA18968.hp2 NA18982.hp1 NA18985.hp1 others(6): Show |
intron_variant | MODIFIER | c.-57-22084dupA | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28941718 | ||||||
| chr8:28941749 | C | T | 21 | a0001c0001t0001g0139 a0001c0001t0001g0222 a0001c0001t0001g0223 others(18): Show |
21 | HG00544.hp1 HG02056.hp1 HG02486.hp2 others(18): Show |
intron_variant | MODIFIER | c.-57-22062C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28941749 | |||||||
| chr8:28941790 | A | G | 3 | a0001c0001t0013g0032 a0001c0001t0013g0033 a0001c0001t0020g0053 |
3 | HG02027.hp1 NA18999.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.-57-22021A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28941790 | |||||||
| chr8:28941940 | G | A | 1 | a0001c0001t0004g0045 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-57-21871G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28941940 | |||||||
| chr8:28941982 | C | T | 2 | a0001c0001t0001g0237 a0001c0001t0001g0247 |
2 | HG02717.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-57-21829C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28941982 | |||||||
| chr8:28942208 | C | T | 1 | a0001c0001t0001g0321 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-57-21603C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28942208 | |||||||
| chr8:28942219 | G | A | 1 | a0001c0001t0004g0040 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-57-21592G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28942219 | |||||||
| chr8:28942248 | G | C | 9 | a0001c0001t0003g0119 a0001c0001t0003g0122 a0001c0001t0003g0324 others(6): Show |
9 | HG02280.hp1 HG02572.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.-57-21563G>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28942248 | |||||||
| chr8:28942252 | T | C | 2 | a0001c0001t0001g0228 a0001c0001t0001g0248 |
2 | HG01109.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.-57-21559T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28942252 | |||||||
| chr8:28942435 | A | C | 6 | a0001c0001t0004g0004 a0001c0001t0004g0124 a0001c0001t0004g0125 others(3): Show |
6 | HG00741.hp2 HG02109.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-57-21376A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28942435 | |||||||
| chr8:28942443 | G | C | 1 | a0001c0001t0007g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-57-21368G>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28942443 | |||||||
| chr8:28942841 | G | A | 1 | a0001c0001t0004g0049 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-57-20970G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28942841 | |||||||
| chr8:28942868 | C | T | 1 | a0001c0001t0002g0212 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-57-20943C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28942868 | |||||||
| chr8:28943092 | A | G | 11 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0122 others(8): Show |
11 | HG02055.hp2 HG02280.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.-57-20719A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28943092 | |||||||
| chr8:28943273 | C | T | 15 | a0001c0001t0006g0326 a0001c0001t0006g0328 a0001c0001t0006g0329 others(12): Show |
15 | HG00544.hp1 HG02056.hp1 HG02809.hp2 others(12): Show |
intron_variant | MODIFIER | c.-57-20538C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28943273 | |||||||
| chr8:28943305 | G | A | 5 | a0001c0001t0003g0102 a0001c0001t0003g0103 a0001c0001t0003g0104 others(2): Show |
5 | NA18986.hp1 NA18998.hp2 NA19009.hp2 others(2): Show |
intron_variant | MODIFIER | c.-57-20506G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28943305 | |||||||
| chr8:28943528 | G | T | 5 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0122 others(2): Show |
5 | HG02055.hp2 HG02280.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.-57-20283G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28943528 | |||||||
| chr8:28943683 | G | C | 1 | a0001c0001t0004g0027 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.-57-20128G>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28943683 | |||||||
| chr8:28943898 | A | C | 3 | a0001c0001t0004g0063 a0001c0001t0004g0064 a0001c0001t0004g0065 |
3 | HG00738.hp2 HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-57-19913A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28943898 | |||||||
| chr8:28943906 | G | T | 1 | a0001c0001t0003g0134 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-57-19905G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28943906 | |||||||
| chr8:28944000 | T | C | 6 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0122 others(3): Show |
6 | HG02055.hp2 HG02280.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.-57-19811T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28944000 | |||||||
| chr8:28944380 | T | C | 1 | a0001c0001t0004g0019 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-57-19431T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28944380 | |||||||
| chr8:28944665 | A | G | 1 | a0001c0001t0002g0185 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-57-19146A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28944665 | |||||||
| chr8:28944974 | G | A | 2 | a0001c0001t0003g0211 a0001c0001t0007g0062 |
2 | HG02723.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-57-18837G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28944974 | |||||||
| chr8:28945018 | T | G | 1 | a0001c0001t0005g0216 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-57-18793T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28945018 | |||||||
| chr8:28945191 | G | A | 2 | a0001c0001t0007g0005 a0001c0001t0007g0062 |
2 | HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-57-18620G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28945191 | |||||||
| chr8:28945235 | T | C | 1 | a0001c0001t0008g0123 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-57-18576T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28945235 | |||||||
| chr8:28945415 | A | G | 236 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 others(233): Show |
237 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(234): Show |
intron_variant | MODIFIER | c.-57-18396A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28945415 | |||||||
| chr8:28945558 | G | C | 192 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 others(189): Show |
193 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.-57-18253G>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28945558 | |||||||
| chr8:28945559 | G | A | 1 | a0001c0001t0002g0271 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-57-18252G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28945559 | |||||||
| chr8:28945698 | T | G | 1 | a0001c0001t0002g0192 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-57-18113T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28945698 | |||||||
| chr8:28945775 | T | A | 2 | a0001c0001t0003g0098 a0001c0001t0003g0100 |
2 | NA18980.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.-57-18036T>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28945775 | |||||||
| chr8:28945799 | A | G | 1 | a0001c0001t0001g0226 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-57-18012A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28945799 | |||||||
| chr8:28945823 | G | A | 2 | a0001c0001t0002g0156 a0001c0001t0002g0163 |
2 | HG03017.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.-57-17988G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28945823 | |||||||
| chr8:28945856 | G | A | 1 | a0001c0001t0001g0142 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-57-17955G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28945856 | |||||||
| chr8:28945881 | T | C | 1 | a0001c0001t0001g0227 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.-57-17930T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28945881 | |||||||
| chr8:28945900 | A | G | 1 | a0001c0001t0004g0048 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-57-17911A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28945900 | |||||||
| chr8:28945937 | G | C | 1 | a0001c0001t0003g0119 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-57-17874G>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28945937 | |||||||
| chr8:28945944 | C | CT | 30 | a0001c0001t0001g0141 a0001c0001t0001g0220 a0001c0001t0001g0239 others(27): Show |
30 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(27): Show |
intron_variant | MODIFIER | c.-57-17849dupT | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28945944 | ||||||
| chr8:28946102 | A | G | 8 | a0001c0001t0004g0054 a0001c0001t0004g0055 a0001c0001t0004g0056 others(5): Show |
8 | HG01884.hp1 HG02145.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.-57-17709A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28946102 | |||||||
| chr8:28946214 | A | G | 12 | a0001c0001t0007g0005 a0001c0001t0007g0010 a0001c0001t0007g0011 others(9): Show |
12 | HG01261.hp1 HG02257.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.-57-17597A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28946214 | |||||||
| chr8:28946227 | A | C | 1 | a0001c0001t0005g0216 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-57-17584A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28946227 | |||||||
| chr8:28946296 | G | A | 1 | a0001c0001t0001g0221 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.-57-17515G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28946296 | |||||||
| chr8:28946579 | A | AT | 7 | a0001c0001t0002g0295 a0001c0001t0002g0296 a0001c0001t0003g0122 others(4): Show |
7 | HG02572.hp1 HG02886.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.-57-17232_-57-1723 others(5): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28946579 | |||||||
| chr8:28946579 | A | T | 87 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 others(84): Show |
88 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.-57-17232A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28946579 | |||||||
| chr8:28946581 | A | AT | 3 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0010g0300 |
3 | HG02055.hp2 HG02280.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-57-17230_-57-1722 others(5): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28946581 | |||||||
| chr8:28946581 | A | T | 200 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 others(197): Show |
201 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(198): Show |
intron_variant | MODIFIER | c.-57-17230A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28946581 | |||||||
| chr8:28946582 | AT | A | 14 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0021 others(11): Show |
14 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.-57-17228delT | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28946582 | |||||||
| chr8:28946805 | G | A | 2 | a0001c0001t0003g0324 a0001c0001t0003g0325 |
2 | HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-57-17006G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28946805 | |||||||
| chr8:28947089 | C | T | 2 | a0001c0001t0003g0324 a0001c0001t0003g0325 |
2 | HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-57-16722C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28947089 | |||||||
| chr8:28947221 | C | T | 1 | a0001c0001t0006g0332 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-57-16590C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28947221 | |||||||
| chr8:28947400 | G | A | 1 | a0001c0001t0017g0213 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-57-16411G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28947400 | |||||||
| chr8:28947636 | A | G | 3 | a0001c0001t0006g0116 a0001c0001t0014g0117 a0001c0001t0014g0118 |
3 | HG02572.hp1 HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-57-16175A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28947636 | |||||||
| chr8:28947797 | C | T | 77 | a0001c0001t0002g0092 a0001c0001t0002g0133 a0001c0001t0002g0135 others(74): Show |
77 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.-57-16014C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28947797 | |||||||
| chr8:28948132 | G | A | 217 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 others(214): Show |
218 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.-57-15679G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28948132 | |||||||
| chr8:28948326 | A | G | 2 | a0001c0001t0003g0093 a0001c0001t0008g0073 |
2 | NA18959.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.-57-15485A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28948326 | |||||||
| chr8:28948340 | A | T | 1 | a0001c0001t0008g0339 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-57-15471A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28948340 | |||||||
| chr8:28948391 | G | A | 16 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0021 others(13): Show |
16 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(13): Show |
intron_variant | MODIFIER | c.-57-15420G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28948391 | |||||||
| chr8:28948609 | C | G | 2 | a0001c0001t0003g0324 a0001c0001t0003g0325 |
2 | HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-57-15202C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28948609 | |||||||
| chr8:28948972 | A | G | 1 | a0001c0001t0003g0122 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-57-14839A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28948972 | |||||||
| chr8:28949284 | G | A | 1 | a0001c0001t0003g0119 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-57-14527G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28949284 | |||||||
| chr8:28949341 | G | T | 1 | a0001c0001t0006g0326 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-57-14470G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28949341 | |||||||
| chr8:28949504 | T | C | 10 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 others(7): Show |
10 | HG00423.hp1 HG02071.hp1 NA18947.hp2 others(7): Show |
intron_variant | MODIFIER | c.-57-14307T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28949504 | |||||||
| chr8:28949797 | A | C | 1 | a0001c0001t0007g0012 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-57-14014A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28949797 | |||||||
| chr8:28949839 | T | G | 221 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 others(218): Show |
222 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.-57-13972T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28949839 | |||||||
| chr8:28949870 | A | G | 1 | a0001c0001t0001g0142 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-57-13941A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28949870 | |||||||
| chr8:28950105 | G | A | 1 | a0001c0001t0001g0256 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-57-13706G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28950105 | |||||||
| chr8:28950383 | A | G | 14 | a0001c0001t0006g0326 a0001c0001t0006g0328 a0001c0001t0006g0329 others(11): Show |
14 | HG00544.hp1 HG02056.hp1 HG02809.hp2 others(11): Show |
intron_variant | MODIFIER | c.-57-13428A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28950383 | |||||||
| chr8:28950881 | A | G | 1 | a0001c0001t0001g0289 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-57-12930A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28950881 | |||||||
| chr8:28950885 | G | A | 2 | a0001c0001t0003g0324 a0001c0001t0003g0325 |
2 | HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-57-12926G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28950885 | |||||||
| chr8:28950925 | G | C | 3 | a0001c0001t0006g0116 a0001c0001t0014g0117 a0001c0001t0014g0118 |
3 | HG02572.hp1 HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-57-12886G>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28950925 | |||||||
| chr8:28951136 | T | C | 6 | a0001c0001t0006g0333 a0001c0001t0006g0335 a0001c0001t0006g0336 others(3): Show |
6 | NA18943.hp2 NA18956.hp1 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.-57-12675T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28951136 | |||||||
| chr8:28951196 | G | A | 1 | a0001c0001t0008g0002 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-57-12615G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28951196 | |||||||
| chr8:28951219 | A | C | 1 | a0001c0001t0002g0204 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.-57-12592A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28951219 | |||||||
| chr8:28951236 | G | A | 1 | a0001c0001t0004g0110 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-57-12575G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28951236 | |||||||
| chr8:28951240 | C | G | 3 | a0001c0001t0003g0119 a0001c0001t0003g0122 a0001c0001t0008g0121 |
3 | HG02280.hp1 HG03195.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-57-12571C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28951240 | |||||||
| chr8:28951277 | C | T | 5 | a0001c0001t0004g0021 a0001c0001t0004g0022 a0001c0001t0004g0025 others(2): Show |
5 | HG00140.hp2 HG00323.hp2 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.-57-12534C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28951277 | |||||||
| chr8:28951289 | C | T | 10 | a0001c0001t0007g0010 a0001c0001t0007g0011 a0001c0001t0007g0012 others(7): Show |
10 | HG01261.hp1 HG02257.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.-57-12522C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28951289 | |||||||
| chr8:28951386 | C | T | 9 | a0001c0001t0003g0119 a0001c0001t0003g0122 a0001c0001t0003g0324 others(6): Show |
9 | HG02280.hp1 HG02572.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.-57-12425C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28951386 | |||||||
| chr8:28951806 | G | A | 15 | a0001c0001t0006g0326 a0001c0001t0006g0328 a0001c0001t0006g0329 others(12): Show |
15 | HG00544.hp1 HG02056.hp1 HG02809.hp2 others(12): Show |
intron_variant | MODIFIER | c.-57-12005G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28951806 | |||||||
| chr8:28951821 | C | G | 4 | a0001c0001t0009g0129 a0001c0001t0009g0130 a0001c0001t0009g0131 others(1): Show |
4 | NA18974.hp2 NA18988.hp1 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57-11990C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28951821 | |||||||
| chr8:28952158 | T | TA | 70 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 others(67): Show |
70 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.-57-11636dupA | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28952158 | ||||||
| chr8:28952158 | TA | T | 15 | a0001c0001t0002g0159 a0001c0001t0002g0318 a0001c0001t0003g0078 others(12): Show |
15 | HG00558.hp2 HG01167.hp1 HG01975.hp2 others(12): Show |
intron_variant | MODIFIER | c.-57-11636delA | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28952158 | ||||||
| chr8:28952279 | G | A | 6 | a0001c0001t0004g0004 a0001c0001t0004g0124 a0001c0001t0004g0125 others(3): Show |
6 | HG00741.hp2 HG02109.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-57-11532G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28952279 | |||||||
| chr8:28952346 | G | C | 1 | a0001c0001t0003g0080 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-57-11465G>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28952346 | |||||||
| chr8:28952394 | C | T | 3 | a0001c0001t0004g0063 a0001c0001t0004g0064 a0001c0001t0004g0065 |
3 | HG00738.hp2 HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-57-11417C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28952394 | |||||||
| chr8:28952400 | A | C | 1 | a0001c0001t0001g0232 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-57-11411A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28952400 | |||||||
| chr8:28952409 | T | A | 3 | a0001c0001t0001g0292 a0001c0001t0008g0002 a0001c0001t0008g0003 |
3 | HG03225.hp2 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-57-11402T>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28952409 | |||||||
| chr8:28952434 | A | G | 197 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 others(194): Show |
198 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(195): Show |
intron_variant | MODIFIER | c.-57-11377A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28952434 | |||||||
| chr8:28953003 | C | A | 3 | a0001c0001t0006g0116 a0001c0001t0014g0117 a0001c0001t0014g0118 |
3 | HG02572.hp1 HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-57-10808C>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28953003 | |||||||
| chr8:28953917 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-57-9894C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28953917 | |||||||
| chr8:28954172 | A | G | 1 | a0001c0001t0001g0231 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-57-9639A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28954172 | |||||||
| chr8:28954494 | C | G | 1 | a0001c0001t0002g0203 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-57-9317C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28954494 | |||||||
| chr8:28954573 | C | G | 1 | a0001c0001t0008g0123 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-57-9238C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28954573 | |||||||
| chr8:28954691 | A | T | 1 | a0001c0001t0002g0270 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-57-9120A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28954691 | |||||||
| chr8:28954956 | A | T | 6 | a0001c0001t0004g0004 a0001c0001t0004g0124 a0001c0001t0004g0125 others(3): Show |
6 | HG00741.hp2 HG02109.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-57-8855A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28954956 | |||||||
| chr8:28954983 | A | G | 1 | a0001c0001t0001g0232 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-57-8828A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28954983 | |||||||
| chr8:28955327 | C | T | 1 | a0001c0001t0002g0252 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-57-8484C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28955327 | |||||||
| chr8:28955366 | A | G | 1 | a0001c0001t0001g0143 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-57-8445A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28955366 | |||||||
| chr8:28955631 | T | A | 1 | a0001c0001t0003g0089 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.-57-8180T>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28955631 | |||||||
| chr8:28955638 | C | T | 218 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 others(215): Show |
219 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.-57-8173C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28955638 | |||||||
| chr8:28955733 | C | T | 1 | a0001c0001t0004g0022 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-57-8078C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28955733 | |||||||
| chr8:28955865 | A | G | 1 | a0001c0001t0001g0246 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-57-7946A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28955865 | |||||||
| chr8:28955924 | A | G | 3 | a0001c0001t0006g0116 a0001c0001t0014g0117 a0001c0001t0014g0118 |
3 | HG02572.hp1 HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-57-7887A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28955924 | |||||||
| chr8:28955926 | T | G | 1 | a0001c0001t0001g0154 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-57-7885T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28955926 | |||||||
| chr8:28955970 | A | AAAAG | 117 | a0001c0001t0001g0072 a0001c0001t0001g0249 a0001c0001t0001g0292 others(114): Show |
117 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.-57-7838_-57-7837i others(6): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28955970 | ||||||
| chr8:28955970 | A | AAAG | 186 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 others(183): Show |
187 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.-57-7839_-57-7838i others(5): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28955970 | ||||||
| chr8:28955970 | A | G | 1 | a0001c0001t0004g0110 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-57-7841A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28955970 | |||||||
| chr8:28956155 | G | A | 10 | a0001c0001t0007g0010 a0001c0001t0007g0011 a0001c0001t0007g0012 others(7): Show |
10 | HG01261.hp1 HG02257.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.-57-7656G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28956155 | |||||||
| chr8:28956242 | G | A | 1 | a0001c0001t0002g0209 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-57-7569G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28956242 | |||||||
| chr8:28956261 | G | C | 22 | a0001c0001t0001g0072 a0001c0001t0003g0008 a0001c0001t0003g0009 others(19): Show |
22 | HG00408.hp2 HG00558.hp2 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.-57-7550G>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28956261 | |||||||
| chr8:28956262 | A | G | 2 | a0001c0001t0002g0204 a0001c0001t0002g0219 |
2 | HG02071.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.-57-7549A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28956262 | |||||||
| chr8:28956317 | A | C | 1 | a0001c0001t0004g0019 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-57-7494A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28956317 | |||||||
| chr8:28956492 | A | G | 2 | a0001c0001t0001g0139 a0001c0001t0001g0253 |
2 | HG02486.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-57-7319A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28956492 | |||||||
| chr8:28956504 | A | AT | 6 | a0001c0001t0004g0004 a0001c0001t0004g0124 a0001c0001t0004g0125 others(3): Show |
6 | HG00741.hp2 HG02109.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-57-7306dupT | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28956504 | ||||||
| chr8:28956517 | TG | T | 3 | a0001c0001t0001g0292 a0001c0001t0008g0002 a0001c0001t0008g0003 |
3 | HG03225.hp2 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-57-7293delG | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28956517 | |||||||
| chr8:28956636 | A | G | 5 | a0001c0001t0003g0324 a0001c0001t0003g0325 a0001c0001t0006g0116 others(2): Show |
5 | HG02572.hp1 HG02886.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.-57-7175A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28956636 | |||||||
| chr8:28956675 | G | C | 338 | a0001c0001t0001g0072 a0001c0001t0001g0138 a0001c0001t0001g0139 others(335): Show |
339 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.-57-7136G>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28956675 | |||||||
| chr8:28956809 | C | G | 1 | a0001c0001t0008g0123 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-57-7002C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28956809 | |||||||
| chr8:28957046 | A | G | 1 | a0001c0001t0008g0123 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-57-6765A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28957046 | |||||||
| chr8:28957346 | T | A | 338 | a0001c0001t0001g0072 a0001c0001t0001g0138 a0001c0001t0001g0139 others(335): Show |
339 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.-57-6465T>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28957346 | |||||||
| chr8:28957378 | T | C | 1 | a0001c0001t0001g0147 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-57-6433T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28957378 | |||||||
| chr8:28957393 | C | T | 5 | a0001c0001t0003g0324 a0001c0001t0003g0325 a0001c0001t0006g0116 others(2): Show |
5 | HG02572.hp1 HG02886.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.-57-6418C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28957393 | |||||||
| chr8:28957425 | C | T | 1 | a0001c0001t0005g0301 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-57-6386C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28957425 | |||||||
| chr8:28957470 | C | A | 1 | a0001c0001t0001g0322 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-57-6341C>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28957470 | |||||||
| chr8:28957537 | C | A | 4 | a0001c0001t0003g0119 a0001c0001t0003g0122 a0001c0001t0008g0121 others(1): Show |
4 | HG02280.hp1 HG02965.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-57-6274C>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28957537 | |||||||
| chr8:28957571 | A | AAAAC | 310 | a0001c0001t0001g0072 a0001c0001t0001g0138 a0001c0001t0001g0139 others(307): Show |
311 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(308): Show |
intron_variant | MODIFIER | c.-57-6236_-57-6233d others(6): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28957571 | ||||||
| chr8:28957583 | T | C | 10 | a0001c0001t0007g0010 a0001c0001t0007g0011 a0001c0001t0007g0012 others(7): Show |
10 | HG01261.hp1 HG02257.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.-57-6228T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28957583 | |||||||
| chr8:28957657 | C | G | 10 | a0001c0001t0007g0010 a0001c0001t0007g0011 a0001c0001t0007g0012 others(7): Show |
10 | HG01261.hp1 HG02257.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.-57-6154C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28957657 | |||||||
| chr8:28957717 | G | T | 8 | a0001c0001t0003g0122 a0001c0001t0003g0324 a0001c0001t0003g0325 others(5): Show |
8 | HG02572.hp1 HG02886.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.-57-6094G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28957717 | |||||||
| chr8:28957973 | C | T | 1 | a0001c0001t0008g0003 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-57-5838C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28957973 | |||||||
| chr8:28958033 | A | G | 1 | a0001c0001t0002g0160 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-57-5778A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28958033 | |||||||
| chr8:28958375 | A | C | 2 | a0001c0001t0014g0117 a0001c0001t0014g0118 |
2 | HG02572.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-57-5436A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28958375 | |||||||
| chr8:28958601 | A | C | 1 | a0001c0001t0003g0084 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.-57-5210A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28958601 | |||||||
| chr8:28958670 | T | G | 2 | a0001c0001t0014g0117 a0001c0001t0014g0118 |
2 | HG02572.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-57-5141T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28958670 | |||||||
| chr8:28958675 | C | A | 1 | a0001c0001t0008g0123 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-57-5136C>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28958675 | |||||||
| chr8:28958677 | A | C | 84 | a0001c0001t0001g0315 a0001c0001t0002g0092 a0001c0001t0002g0133 others(81): Show |
84 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.-57-5134A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28958677 | |||||||
| chr8:28958858 | A | G | 3 | a0001c0001t0006g0116 a0001c0001t0014g0117 a0001c0001t0014g0118 |
3 | HG02572.hp1 HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-57-4953A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28958858 | |||||||
| chr8:28959255 | C | G | 12 | a0001c0001t0007g0005 a0001c0001t0007g0010 a0001c0001t0007g0011 others(9): Show |
12 | HG01261.hp1 HG02257.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.-57-4556C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28959255 | |||||||
| chr8:28959295 | A | G | 15 | a0001c0001t0006g0326 a0001c0001t0006g0328 a0001c0001t0006g0329 others(12): Show |
15 | HG00544.hp1 HG02056.hp1 HG02809.hp2 others(12): Show |
intron_variant | MODIFIER | c.-57-4516A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28959295 | |||||||
| chr8:28959335 | G | A | 218 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 others(215): Show |
219 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.-57-4476G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28959335 | |||||||
| chr8:28959362 | C | G | 2 | a0001c0001t0008g0067 a0001c0001t0008g0094 |
2 | HG00621.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.-57-4449C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28959362 | |||||||
| chr8:28959460 | C | T | 2 | a0001c0001t0001g0222 a0001c0001t0001g0223 |
2 | HG02723.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-57-4351C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28959460 | |||||||
| chr8:28959472 | G | A | 1 | a0001c0001t0010g0230 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-57-4339G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28959472 | |||||||
| chr8:28959520 | A | G | 1 | a0001c0001t0001g0257 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-57-4291A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28959520 | |||||||
| chr8:28959796 | A | G | 2 | a0001c0001t0012g0174 a0001c0001t0012g0297 |
2 | HG02886.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-57-4015A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28959796 | |||||||
| chr8:28959875 | G | GT | 15 | a0001c0001t0006g0326 a0001c0001t0006g0328 a0001c0001t0006g0329 others(12): Show |
15 | HG00544.hp1 HG02056.hp1 HG02809.hp2 others(12): Show |
intron_variant | MODIFIER | c.-57-3932dupT | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28959875 | ||||||
| chr8:28960165 | A | G | 3 | a0001c0001t0005g0215 a0001c0001t0005g0216 a0001c0001t0005g0217 |
3 | HG02559.hp1 HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-57-3646A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28960165 | |||||||
| chr8:28960219 | A | AATATTTA others(372): Show |
8 | a0001c0001t0003g0119 a0001c0001t0003g0122 a0001c0001t0003g0324 others(5): Show |
8 | HG02280.hp1 HG02572.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.-57-3590_-57-3589i others(381): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28960219 | ||||||
| chr8:28960219 | A | AATATTTA others(373): Show |
1 | a0001c0001t0008g0123 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-57-3590_-57-3589i others(382): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28960219 | ||||||
| chr8:28960219 | A | AATATTTA others(372): Show |
1 | a0001c0001t0003g0120 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-57-3590_-57-3589i others(381): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28960219 | ||||||
| chr8:28960427 | T | C | 1 | a0001c0001t0004g0110 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-57-3384T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28960427 | |||||||
| chr8:28960745 | CTCTTTTT others(5): Show |
C | 51 | a0001c0001t0001g0144 a0001c0001t0001g0150 a0001c0001t0001g0154 others(48): Show |
51 | HG00280.hp2 HG00423.hp1 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.-57-3052_-57-3041d others(14): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28960745 | ||||||
| chr8:28960753 | CTTTTTCT others(6): Show |
C | 137 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 others(134): Show |
138 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.-57-3052_-57-3040d others(15): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28960753 | ||||||
| chr8:28960753 | CTTTTTCT others(7): Show |
C | 4 | a0001c0001t0007g0062 a0001c0001t0008g0003 a0001c0001t0008g0123 others(1): Show |
4 | HG02630.hp2 HG02965.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57-3052_-57-3039d others(16): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28960753 | ||||||
| chr8:28960753 | CTTTTTCT others(8): Show |
C | 3 | a0001c0001t0001g0315 a0001c0001t0006g0329 a0001c0001t0008g0002 |
3 | HG02056.hp1 HG03225.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-57-3052_-57-3038d others(17): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28960753 | ||||||
| chr8:28960753 | CTTTTTCT others(9): Show |
C | 24 | a0001c0001t0006g0326 a0001c0001t0006g0328 a0001c0001t0006g0332 others(21): Show |
24 | HG00544.hp1 HG01261.hp1 HG02257.hp2 others(21): Show |
intron_variant | MODIFIER | c.-57-3052_-57-3037d others(18): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28960753 | ||||||
| chr8:28960753 | CTTTTTCT others(11): Show |
C | 1 | a0001c0001t0003g0122 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-57-3052_-57-3035d others(20): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28960753 | ||||||
| chr8:28960753 | CTTTTTCT others(17): Show |
C | 5 | a0001c0001t0003g0324 a0001c0001t0003g0325 a0001c0001t0006g0116 others(2): Show |
5 | HG02572.hp1 HG02886.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.-57-3052_-57-3029d others(26): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28960753 | ||||||
| chr8:28960753 | CTTTTTCT others(27): Show |
C | 12 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0021 others(9): Show |
12 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(9): Show |
intron_variant | MODIFIER | c.-57-3052_-57-3019d others(36): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28960753 | ||||||
| chr8:28960753 | CTTTTTCT others(28): Show |
C | 56 | a0001c0001t0001g0072 a0001c0001t0003g0008 a0001c0001t0003g0009 others(53): Show |
56 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.-57-3052_-57-3018d others(37): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28960753 | ||||||
| chr8:28960753 | CTTTTTCT others(29): Show |
C | 2 | a0001c0001t0003g0006 a0001c0001t0003g0007 |
2 | NA18968.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.-57-3052_-57-3017d others(38): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28960753 | ||||||
| chr8:28960754 | TTTTTCTT others(4): Show |
T | 11 | a0001c0001t0001g0227 a0001c0001t0003g0298 a0001c0001t0004g0063 others(8): Show |
11 | HG01123.hp1 HG01243.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.-57-3052_-57-3042d others(13): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28960754 | ||||||
| chr8:28960765 | C | T | 3 | a0001c0001t0003g0120 a0001c0001t0004g0004 a0001c0001t0004g0126 |
3 | HG00741.hp2 HG02896.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-57-3046C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28960765 | |||||||
| chr8:28960765 | CT | C | 6 | a0001c0001t0004g0030 a0001c0001t0004g0035 a0001c0001t0004g0037 others(3): Show |
6 | HG00639.hp1 HG00738.hp2 HG01070.hp1 others(3): Show |
intron_variant | MODIFIER | c.-57-3007delT | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28960765 | ||||||
| chr8:28960765 | CTTTTTTT others(11): Show |
C | 8 | a0001c0001t0004g0054 a0001c0001t0004g0055 a0001c0001t0004g0056 others(5): Show |
8 | HG01884.hp1 HG02145.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.-57-3024_-57-3007d others(20): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28960765 | ||||||
| chr8:28960779 | T | G | 6 | a0001c0001t0001g0227 a0001c0001t0003g0298 a0001c0001t0005g0217 others(3): Show |
6 | HG01123.hp1 HG02145.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.-57-3032T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28960779 | |||||||
| chr8:28960780 | T | G | 48 | a0001c0001t0001g0144 a0001c0001t0001g0150 a0001c0001t0001g0154 others(45): Show |
48 | HG00280.hp2 HG00423.hp1 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.-57-3031T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28960780 | |||||||
| chr8:28960781 | T | G | 135 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 others(132): Show |
136 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.-57-3030T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28960781 | |||||||
| chr8:28960782 | T | G | 5 | a0001c0001t0001g0315 a0001c0001t0007g0005 a0001c0001t0008g0003 others(2): Show |
5 | HG02630.hp2 HG02965.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.-57-3029T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28960782 | |||||||
| chr8:28960783 | T | G | 3 | a0001c0001t0006g0329 a0001c0001t0007g0062 a0001c0001t0008g0002 |
3 | HG02056.hp1 HG03225.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-57-3028T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28960783 | |||||||
| chr8:28960784 | T | C | 3 | a0001c0001t0006g0116 a0001c0001t0014g0117 a0001c0001t0014g0118 |
3 | HG02572.hp1 HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-57-3027T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28960784 | |||||||
| chr8:28960784 | T | G | 24 | a0001c0001t0006g0326 a0001c0001t0006g0328 a0001c0001t0006g0332 others(21): Show |
24 | HG00544.hp1 HG01261.hp1 HG02257.hp2 others(21): Show |
intron_variant | MODIFIER | c.-57-3027T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28960784 | |||||||
| chr8:28960789 | T | C | 1 | a0001c0001t0001g0309 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-57-3022T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28960789 | |||||||
| chr8:28960792 | T | G | 10 | a0001c0001t0007g0010 a0001c0001t0007g0011 a0001c0001t0007g0012 others(7): Show |
10 | HG01261.hp1 HG02257.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.-57-3019T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28960792 | |||||||
| chr8:28960794 | T | G | 15 | a0001c0001t0006g0326 a0001c0001t0006g0328 a0001c0001t0006g0329 others(12): Show |
15 | HG00544.hp1 HG02056.hp1 HG02809.hp2 others(12): Show |
intron_variant | MODIFIER | c.-57-3017T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28960794 | |||||||
| chr8:28960816 | C | T | 6 | a0001c0001t0004g0004 a0001c0001t0004g0124 a0001c0001t0004g0125 others(3): Show |
6 | HG00741.hp2 HG02109.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-57-2995C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28960816 | |||||||
| chr8:28960943 | T | C | 223 | a0001c0001t0001g0072 a0001c0001t0001g0138 a0001c0001t0001g0139 others(220): Show |
224 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(221): Show |
intron_variant | MODIFIER | c.-57-2868T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28960943 | |||||||
| chr8:28960944 | G | A | 1 | a0001c0001t0002g0262 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-57-2867G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28960944 | |||||||
| chr8:28961312 | A | G | 2 | a0001c0001t0003g0115 a0001c0001t0006g0111 |
2 | NA18945.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.-57-2499A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28961312 | |||||||
| chr8:28961314 | A | G | 1 | a0001c0001t0008g0123 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-57-2497A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28961314 | |||||||
| chr8:28961894 | AT | A | 10 | a0001c0001t0001g0257 a0001c0001t0003g0122 a0001c0001t0003g0298 others(7): Show |
10 | HG02451.hp2 HG03041.hp2 HG03098.hp1 others(7): Show |
intron_variant | MODIFIER | c.-57-1899delT | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28961894 | ||||||
| chr8:28961898 | T | TG | 5 | a0001c0001t0002g0183 a0001c0001t0004g0059 a0001c0001t0006g0116 others(2): Show |
5 | HG02572.hp1 HG02886.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.-57-1913_-57-1912i others(3): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28961898 | |||||||
| chr8:28961899 | T | G | 326 | a0001c0001t0001g0072 a0001c0001t0001g0138 a0001c0001t0001g0139 others(323): Show |
327 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.-57-1912T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28961899 | |||||||
| chr8:28961900 | T | G | 10 | a0001c0001t0001g0257 a0001c0001t0003g0122 a0001c0001t0003g0298 others(7): Show |
10 | HG02451.hp2 HG03041.hp2 HG03098.hp1 others(7): Show |
intron_variant | MODIFIER | c.-57-1911T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28961900 | |||||||
| chr8:28961920 | C | CT | 197 | a0001c0001t0001g0072 a0001c0001t0001g0138 a0001c0001t0001g0139 others(194): Show |
198 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(195): Show |
intron_variant | MODIFIER | c.-57-1878dupT | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28961920 | ||||||
| chr8:28961943 | A | G | 1 | a0001c0001t0015g0233 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-57-1868A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28961943 | |||||||
| chr8:28962448 | A | G | 2 | a0001c0001t0003g0324 a0001c0001t0003g0325 |
2 | HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-57-1363A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28962448 | |||||||
| chr8:28962485 | C | T | 2 | a0001c0001t0007g0005 a0001c0001t0007g0062 |
2 | HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-57-1326C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28962485 | |||||||
| chr8:28962496 | G | T | 15 | a0001c0001t0006g0326 a0001c0001t0006g0328 a0001c0001t0006g0329 others(12): Show |
15 | HG00544.hp1 HG02056.hp1 HG02809.hp2 others(12): Show |
intron_variant | MODIFIER | c.-57-1315G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28962496 | |||||||
| chr8:28962522 | A | G | 4 | a0001c0001t0003g0081 a0001c0001t0003g0084 a0001c0001t0003g0088 others(1): Show |
4 | NA18612.hp2 NA18952.hp1 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.-57-1289A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28962522 | |||||||
| chr8:28962580 | A | G | 1 | a0001c0001t0005g0178 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-57-1231A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28962580 | |||||||
| chr8:28962723 | T | G | 2 | a0001c0001t0003g0006 a0001c0001t0003g0007 |
2 | NA18968.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.-57-1088T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28962723 | |||||||
| chr8:28962897 | A | G | 3 | a0001c0001t0006g0116 a0001c0001t0014g0117 a0001c0001t0014g0118 |
3 | HG02572.hp1 HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-57-914A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28962897 | |||||||
| chr8:28963047 | C | T | 1 | a0001c0001t0001g0305 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-57-764C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28963047 | |||||||
| chr8:28963289 | T | C | 1 | a0001c0001t0001g0146 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-57-522T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28963289 | |||||||
| chr8:28963393 | T | C | 1 | a0001c0001t0010g0312 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-57-418T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28963393 | |||||||
| chr8:28963459 | A | G | 1 | a0001c0001t0004g0054 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-57-352A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28963459 | |||||||
| chr8:28963467 | G | A | 1 | a0001c0001t0003g0120 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-57-344G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28963467 | |||||||
| chr8:28963509 | C | T | 2 | a0001c0001t0002g0136 a0001c0001t0002g0137 |
2 | HG00558.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.-57-302C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28963509 | |||||||
| chr8:28963511 | T | A | 2 | a0001c0001t0002g0136 a0001c0001t0002g0137 |
2 | HG00558.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.-57-300T>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28963511 | |||||||
| chr8:28963620 | A | C | 1 | a0001c0001t0001g0253 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.-57-191A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28963620 | |||||||
| chr8:28964020 | C | A | 1 | a0001c0001t0008g0123 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.23+130C>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 2/9 | chr8 | 28964020 | |||||||
| chr8:28964505 | C | T | 5 | a0001c0001t0004g0124 a0001c0001t0004g0125 a0001c0001t0004g0126 others(2): Show |
5 | HG02109.hp2 HG02896.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.23+615C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 2/9 | chr8 | 28964505 | |||||||
| chr8:28964514 | C | G | 1 | a0001c0001t0007g0010 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.23+624C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 2/9 | chr8 | 28964514 | |||||||
| chr8:28964561 | T | G | 2 | a0001c0001t0002g0188 a0001c0001t0002g0190 |
2 | NA18973.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.23+671T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 2/9 | chr8 | 28964561 | |||||||
| chr8:28964613 | G | C | 3 | a0001c0001t0004g0063 a0001c0001t0004g0064 a0001c0001t0004g0065 |
3 | HG00738.hp2 HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.23+723G>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 2/9 | chr8 | 28964613 | |||||||
| chr8:28964687 | A | G | 1 | a0001c0001t0002g0001 | 2 | HG02486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.23+797A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 2/9 | chr8 | 28964687 | |||||||
| chr8:28964710 | T | C | 10 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0122 others(7): Show |
10 | HG02280.hp1 HG02572.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.23+820T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 2/9 | chr8 | 28964710 | |||||||
| chr8:28964935 | A | G | 1 | a0001c0001t0001g0299 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.23+1045A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 2/9 | chr8 | 28964935 | |||||||
| chr8:28965036 | G | A | 1 | a0001c0001t0008g0074 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.23+1146G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 2/9 | chr8 | 28965036 | |||||||
| chr8:28965157 | C | A | 2 | a0001c0001t0008g0002 a0001c0001t0008g0003 |
2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.23+1267C>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 2/9 | chr8 | 28965157 | |||||||
| chr8:28965317 | T | C | 1 | a0001c0001t0003g0210 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.23+1427T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 2/9 | chr8 | 28965317 | |||||||
| chr8:28965534 | C | T | 191 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 others(188): Show |
192 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.23+1644C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 2/9 | chr8 | 28965534 | |||||||
| chr8:28965578 | A | G | 86 | a0001c0001t0001g0072 a0001c0001t0003g0006 a0001c0001t0003g0007 others(83): Show |
86 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.23+1688A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 2/9 | chr8 | 28965578 | |||||||
| chr8:28965592 | G | T | 2 | a0001c0001t0003g0324 a0001c0001t0003g0325 |
2 | HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.23+1702G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 2/9 | chr8 | 28965592 | |||||||
| chr8:28965636 | G | A | 2 | a0001c0001t0007g0005 a0001c0001t0007g0062 |
2 | HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.23+1746G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 2/9 | chr8 | 28965636 | |||||||
| chr8:28965643 | C | T | 4 | a0001c0001t0002g0263 a0001c0001t0002g0264 a0001c0001t0002g0270 others(1): Show |
4 | HG00609.hp2 HG02074.hp2 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.23+1753C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 2/9 | chr8 | 28965643 | |||||||
| chr8:28965983 | A | G | 5 | a0001c0001t0003g0324 a0001c0001t0003g0325 a0001c0001t0006g0116 others(2): Show |
5 | HG02572.hp1 HG02886.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.23+2093A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 2/9 | chr8 | 28965983 | |||||||
| chr8:28966052 | G | C | 1 | a0001c0001t0010g0312 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.23+2162G>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 2/9 | chr8 | 28966052 | |||||||
| chr8:28966166 | A | G | 1 | a0001c0001t0011g0313 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.23+2276A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 2/9 | chr8 | 28966166 | |||||||
| chr8:28966238 | G | T | 4 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0122 others(1): Show |
4 | HG02280.hp1 HG03195.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.23+2348G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 2/9 | chr8 | 28966238 | |||||||
| chr8:28966306 | T | C | 1 | a0001c0001t0023g0331 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.23+2416T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 2/9 | chr8 | 28966306 | |||||||
| chr8:28966648 | T | C | 1 | a0001c0001t0002g0219 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.23+2758T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 2/9 | chr8 | 28966648 | |||||||
| chr8:28966705 | T | C | 2 | a0001c0001t0003g0324 a0001c0001t0003g0325 |
2 | HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.23+2815T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 2/9 | chr8 | 28966705 | |||||||
| chr8:28966754 | C | T | 3 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0288 |
3 | HG00323.hp1 HG01123.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.23+2864C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 2/9 | chr8 | 28966754 | |||||||
| chr8:28966764 | T | C | 4 | a0001c0001t0002g0092 a0001c0001t0002g0189 a0001c0001t0002g0192 others(1): Show |
4 | NA18946.hp1 NA18990.hp1 NA18992.hp2 others(1): Show |
intron_variant | MODIFIER | c.23+2874T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 2/9 | chr8 | 28966764 | |||||||
| chr8:28967193 | G | A | 3 | a0001c0001t0006g0116 a0001c0001t0014g0117 a0001c0001t0014g0118 |
3 | HG02572.hp1 HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.24-2850G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 2/9 | chr8 | 28967193 | |||||||
| chr8:28967337 | T | A | 2 | a0001c0001t0012g0174 a0001c0001t0012g0297 |
2 | HG02886.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.24-2706T>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 2/9 | chr8 | 28967337 | |||||||
| chr8:28967812 | A | C | 1 | a0001c0001t0008g0068 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.24-2231A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 2/9 | chr8 | 28967812 | |||||||
| chr8:28967905 | C | G | 12 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0021 others(9): Show |
12 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(9): Show |
intron_variant | MODIFIER | c.24-2138C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 2/9 | chr8 | 28967905 | |||||||
| chr8:28967935 | G | A | 1 | a0001c0001t0001g0247 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.24-2108G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 2/9 | chr8 | 28967935 | |||||||
| chr8:28967957 | T | A | 219 | a0001c0001t0001g0072 a0001c0001t0001g0138 a0001c0001t0001g0139 others(216): Show |
220 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.24-2086T>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 2/9 | chr8 | 28967957 | |||||||
| chr8:28968098 | T | C | 1 | a0001c0001t0001g0241 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.24-1945T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 2/9 | chr8 | 28968098 | |||||||
| chr8:28968161 | C | T | 110 | a0001c0001t0001g0255 a0001c0001t0002g0001 a0001c0001t0002g0092 others(107): Show |
111 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.24-1882C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 2/9 | chr8 | 28968161 | |||||||
| chr8:28968271 | A | G | 3 | a0001c0001t0001g0292 a0001c0001t0008g0002 a0001c0001t0008g0003 |
3 | HG03225.hp2 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.24-1772A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 2/9 | chr8 | 28968271 | |||||||
| chr8:28968351 | T | C | 6 | a0001c0001t0004g0004 a0001c0001t0004g0124 a0001c0001t0004g0125 others(3): Show |
6 | HG00741.hp2 HG02109.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.24-1692T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 2/9 | chr8 | 28968351 | |||||||
| chr8:28968561 | G | A | 4 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0234 others(1): Show |
4 | HG00140.hp1 HG01884.hp2 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.24-1482G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 2/9 | chr8 | 28968561 | |||||||
| chr8:28968615 | C | T | 1 | a0001c0001t0008g0123 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.24-1428C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 2/9 | chr8 | 28968615 | |||||||
| chr8:28968686 | A | G | 1 | a0001c0001t0004g0342 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.24-1357A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 2/9 | chr8 | 28968686 | |||||||
| chr8:28968752 | C | T | 4 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0122 others(1): Show |
4 | HG02280.hp1 HG03195.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.24-1291C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 2/9 | chr8 | 28968752 | |||||||
| chr8:28969225 | A | G | 2 | a0001c0001t0001g0236 a0001c0001t0001g0292 |
2 | HG03209.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.24-818A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 2/9 | chr8 | 28969225 | |||||||
| chr8:28969306 | A | G | 3 | a0001c0001t0006g0116 a0001c0001t0014g0117 a0001c0001t0014g0118 |
3 | HG02572.hp1 HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.24-737A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 2/9 | chr8 | 28969306 | |||||||
| chr8:28969541 | CAAA | C | 68 | a0001c0001t0001g0138 a0001c0001t0001g0140 a0001c0001t0001g0141 others(65): Show |
68 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.24-501_24-499delAA others(1): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 2/9 | chr8 | 28969541 | |||||||
| chr8:28970751 | C | G | 6 | a0001c0001t0004g0004 a0001c0001t0004g0124 a0001c0001t0004g0125 others(3): Show |
6 | HG00741.hp2 HG02109.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.500+232C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28970751 | |||||||
| chr8:28970874 | T | G | 195 | a0001c0001t0001g0072 a0001c0001t0001g0138 a0001c0001t0001g0139 others(192): Show |
196 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.500+355T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28970874 | |||||||
| chr8:28970894 | G | A | 10 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0122 others(7): Show |
10 | HG02280.hp1 HG02572.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.500+375G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28970894 | |||||||
| chr8:28970941 | T | TG | 7 | a0001c0001t0002g0092 a0001c0001t0002g0155 a0001c0001t0003g0069 others(4): Show |
7 | HG01175.hp2 HG01928.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.500+426dupG | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr8 | 28970941 | ||||||
| chr8:28970981 | G | GAC | 27 | a0001c0001t0001g0154 a0001c0001t0001g0250 a0001c0001t0002g0135 others(24): Show |
27 | HG00408.hp1 HG00423.hp2 HG00597.hp2 others(24): Show |
intron_variant | MODIFIER | c.500+510_500+511dup others(2): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr8 | 28970981 | ||||||
| chr8:28970981 | G | GACAC | 16 | a0001c0001t0002g0156 a0001c0001t0002g0167 a0001c0001t0002g0206 others(13): Show |
16 | HG01261.hp1 HG01884.hp1 HG01975.hp1 others(13): Show |
intron_variant | MODIFIER | c.500+508_500+511dup others(4): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr8 | 28970981 | ||||||
| chr8:28970981 | GAC | G | 54 | a0001c0001t0001g0072 a0001c0001t0001g0144 a0001c0001t0001g0145 others(51): Show |
54 | HG00280.hp1 HG01081.hp1 HG01123.hp1 others(51): Show |
intron_variant | MODIFIER | c.500+510_500+511del others(2): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr8 | 28970981 | ||||||
| chr8:28970981 | GACAC | G | 88 | a0001c0001t0001g0143 a0001c0001t0001g0146 a0001c0001t0001g0147 others(85): Show |
88 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.500+508_500+511del others(4): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr8 | 28970981 | ||||||
| chr8:28970981 | GACACAC | G | 43 | a0001c0001t0001g0139 a0001c0001t0001g0141 a0001c0001t0001g0142 others(40): Show |
43 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(40): Show |
intron_variant | MODIFIER | c.500+506_500+511del others(6): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr8 | 28970981 | ||||||
| chr8:28970981 | GACACACA others(1): Show |
G | 14 | a0001c0001t0001g0140 a0001c0001t0001g0248 a0001c0001t0001g0316 others(11): Show |
15 | HG00558.hp2 HG01256.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.500+504_500+511del others(8): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr8 | 28970981 | ||||||
| chr8:28970981 | GACACACA others(3): Show |
G | 6 | a0001c0001t0001g0228 a0001c0001t0001g0280 a0001c0001t0003g0158 others(3): Show |
6 | HG01109.hp1 HG01255.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.500+502_500+511del others(10): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr8 | 28970981 | ||||||
| chr8:28970981 | GACACACA others(5): Show |
G | 5 | a0001c0001t0001g0239 a0001c0001t0005g0215 a0001c0001t0005g0216 others(2): Show |
5 | HG01175.hp1 HG02559.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.500+500_500+511del others(12): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr8 | 28970981 | ||||||
| chr8:28970981 | GACACACA others(7): Show |
G | 1 | a0001c0001t0010g0312 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.500+498_500+511del others(14): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr8 | 28970981 | ||||||
| chr8:28970981 | GACACACA others(9): Show |
G | 6 | a0001c0001t0002g0133 a0001c0001t0002g0188 a0001c0001t0002g0190 others(3): Show |
6 | HG00438.hp2 HG01943.hp1 NA18949.hp1 others(3): Show |
intron_variant | MODIFIER | c.500+496_500+511del others(16): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr8 | 28970981 | ||||||
| chr8:28970981 | GACACACA others(11): Show |
G | 1 | a0001c0001t0004g0024 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.500+494_500+511del others(18): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr8 | 28970981 | ||||||
| chr8:28970981 | GACACACA others(13): Show |
G | 3 | a0001c0001t0004g0063 a0001c0001t0004g0064 a0001c0001t0004g0065 |
3 | HG00738.hp2 HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.500+492_500+511del others(20): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr8 | 28970981 | ||||||
| chr8:28971083 | C | G | 2 | a0001c0001t0012g0174 a0001c0001t0012g0297 |
2 | HG02886.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.500+564C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28971083 | |||||||
| chr8:28971086 | CT | C | 43 | a0001c0001t0001g0315 a0001c0001t0002g0156 a0001c0001t0002g0168 others(40): Show |
43 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.500+589delT | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr8 | 28971086 | ||||||
| chr8:28971086 | CTT | C | 253 | a0001c0001t0001g0072 a0001c0001t0001g0138 a0001c0001t0001g0139 others(250): Show |
254 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(251): Show |
intron_variant | MODIFIER | c.500+588_500+589del others(2): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr8 | 28971086 | ||||||
| chr8:28971086 | CTTT | C | 14 | a0001c0001t0001g0240 a0001c0001t0001g0258 a0001c0001t0001g0268 others(11): Show |
14 | HG01496.hp2 HG02647.hp1 HG02738.hp1 others(11): Show |
intron_variant | MODIFIER | c.500+587_500+589del others(3): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr8 | 28971086 | ||||||
| chr8:28971148 | A | G | 1 | a0001c0001t0004g0052 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.500+629A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28971148 | |||||||
| chr8:28971255 | G | A | 1 | a0001c0001t0008g0123 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.500+736G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28971255 | |||||||
| chr8:28971337 | C | T | 3 | a0001c0001t0006g0116 a0001c0001t0014g0117 a0001c0001t0014g0118 |
3 | HG02572.hp1 HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.500+818C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28971337 | |||||||
| chr8:28971338 | G | A | 1 | a0001c0001t0004g0043 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.500+819G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28971338 | |||||||
| chr8:28971642 | G | A | 7 | a0001c0001t0004g0041 a0001c0001t0004g0045 a0001c0001t0004g0046 others(4): Show |
7 | HG00544.hp2 HG00597.hp1 HG02074.hp1 others(4): Show |
intron_variant | MODIFIER | c.500+1123G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28971642 | |||||||
| chr8:28971799 | T | G | 2 | a0001c0001t0003g0324 a0001c0001t0003g0325 |
2 | HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.500+1280T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28971799 | |||||||
| chr8:28971900 | C | A | 12 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0021 others(9): Show |
12 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(9): Show |
intron_variant | MODIFIER | c.500+1381C>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28971900 | |||||||
| chr8:28972213 | T | A | 3 | a0001c0001t0002g0208 a0001c0001t0002g0252 a0001c0001t0017g0213 |
3 | HG00408.hp1 HG01168.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.500+1694T>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28972213 | |||||||
| chr8:28972276 | G | A | 3 | a0001c0001t0001g0139 a0001c0001t0001g0142 a0001c0001t0001g0253 |
3 | HG02486.hp2 HG02897.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.500+1757G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28972276 | |||||||
| chr8:28972287 | A | T | 1 | a0001c0001t0001g0227 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.500+1768A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28972287 | |||||||
| chr8:28972358 | G | C | 2 | a0001c0001t0003g0324 a0001c0001t0003g0325 |
2 | HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.500+1839G>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28972358 | |||||||
| chr8:28972592 | A | G | 1 | a0001c0001t0002g0205 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.500+2073A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28972592 | |||||||
| chr8:28972622 | G | A | 1 | a0001c0001t0001g0315 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.500+2103G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28972622 | |||||||
| chr8:28972783 | C | G | 207 | a0001c0001t0001g0072 a0001c0001t0001g0138 a0001c0001t0001g0139 others(204): Show |
208 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.500+2264C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28972783 | |||||||
| chr8:28972948 | C | T | 1 | a0001c0001t0008g0123 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.500+2429C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28972948 | |||||||
| chr8:28972958 | G | A | 1 | a0001c0001t0001g0150 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.500+2439G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28972958 | |||||||
| chr8:28973192 | A | G | 3 | a0001c0001t0004g0063 a0001c0001t0004g0064 a0001c0001t0004g0065 |
3 | HG00738.hp2 HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.500+2673A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28973192 | |||||||
| chr8:28973568 | A | G | 2 | a0001c0001t0004g0034 a0001c0001t0004g0037 |
2 | HG00738.hp1 HG01070.hp1 |
intron_variant | MODIFIER | c.500+3049A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28973568 | |||||||
| chr8:28973636 | G | T | 2 | a0001c0001t0003g0086 a0001c0001t0003g0087 |
2 | HG02040.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.500+3117G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28973636 | |||||||
| chr8:28973754 | C | T | 1 | a0001c0001t0010g0312 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.500+3235C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28973754 | |||||||
| chr8:28973765 | C | T | 99 | a0001c0001t0001g0315 a0001c0001t0002g0001 a0001c0001t0002g0092 others(96): Show |
100 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.500+3246C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28973765 | |||||||
| chr8:28973787 | C | T | 4 | a0001c0001t0004g0022 a0001c0001t0004g0025 a0001c0001t0004g0026 others(1): Show |
4 | HG00140.hp2 HG00323.hp2 HG02004.hp1 others(1): Show |
intron_variant | MODIFIER | c.500+3268C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28973787 | |||||||
| chr8:28973803 | G | GTTTTTTT others(4): Show |
3 | a0001c0001t0003g0076 a0001c0001t0004g0037 a0001c0001t0004g0048 |
3 | HG01070.hp1 HG02074.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.500+3305_500+3315d others(13): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr8 | 28973803 | ||||||
| chr8:28973803 | G | GTTTTTTT others(5): Show |
8 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0009 others(5): Show |
8 | HG00738.hp1 HG01928.hp2 HG04199.hp2 others(5): Show |
intron_variant | MODIFIER | c.500+3304_500+3315d others(14): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr8 | 28973803 | ||||||
| chr8:28973803 | G | GTTTTTTT others(6): Show |
3 | a0001c0001t0003g0078 a0001c0001t0004g0040 a0001c0001t0004g0046 |
3 | HG00558.hp2 HG03654.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.500+3303_500+3315d others(15): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr8 | 28973803 | ||||||
| chr8:28973803 | G | GTTTTTTT others(7): Show |
3 | a0001c0001t0003g0115 a0001c0001t0004g0030 a0001c0001t0004g0039 |
3 | HG01975.hp1 HG03710.hp1 NA18945.hp2 |
intron_variant | MODIFIER | c.500+3302_500+3315d others(16): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr8 | 28973803 | ||||||
| chr8:28973803 | G | GTTTTTTT others(8): Show |
4 | a0001c0001t0004g0035 a0001c0001t0004g0044 a0001c0001t0004g0049 others(1): Show |
4 | HG00280.hp1 HG01081.hp1 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.500+3301_500+3315d others(17): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr8 | 28973803 | ||||||
| chr8:28973803 | G | GTTTTTTT others(9): Show |
3 | a0001c0001t0004g0038 a0001c0001t0004g0047 a0001c0001t0020g0053 |
3 | HG00544.hp2 HG00741.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.500+3300_500+3315d others(18): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr8 | 28973803 | ||||||
| chr8:28973803 | G | GTTTTTTT others(10): Show |
2 | a0001c0001t0008g0074 a0001c0001t0013g0033 |
2 | HG00735.hp1 HG02027.hp1 |
intron_variant | MODIFIER | c.500+3299_500+3315d others(19): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr8 | 28973803 | ||||||
| chr8:28973803 | G | GTTTTTTT others(13): Show |
2 | a0001c0001t0004g0042 a0001c0001t0004g0043 |
2 | HG00639.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.500+3296_500+3315d others(22): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr8 | 28973803 | ||||||
| chr8:28973803 | G | GTTTTTTT others(14): Show |
1 | a0001c0001t0004g0031 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.500+3295_500+3315d others(23): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr8 | 28973803 | ||||||
| chr8:28973803 | G | GTTTTTTT others(17): Show |
1 | a0001c0001t0004g0052 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.500+3292_500+3315d others(26): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr8 | 28973803 | ||||||
| chr8:28973803 | G | GTTTTTTT others(30): Show |
1 | a0001c0001t0004g0036 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.500+3315_500+3316i others(39): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr8 | 28973803 | ||||||
| chr8:28973803 | GTTTT | G | 16 | a0001c0001t0002g0092 a0001c0001t0002g0160 a0001c0001t0002g0166 others(13): Show |
16 | HG00621.hp1 HG01168.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.500+3312_500+3315d others(6): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr8 | 28973803 | ||||||
| chr8:28973803 | GTTTTT | G | 82 | a0001c0001t0001g0315 a0001c0001t0002g0001 a0001c0001t0002g0133 others(79): Show |
83 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.500+3311_500+3315d others(7): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr8 | 28973803 | ||||||
| chr8:28973803 | GTTTTTTT | G | 7 | a0001c0001t0007g0010 a0001c0001t0007g0011 a0001c0001t0007g0013 others(4): Show |
7 | HG02257.hp2 HG02622.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.500+3309_500+3315d others(9): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr8 | 28973803 | ||||||
| chr8:28973803 | GTTTTTTT others(3): Show |
G | 27 | a0001c0001t0001g0072 a0001c0001t0001g0144 a0001c0001t0001g0145 others(24): Show |
27 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(24): Show |
intron_variant | MODIFIER | c.500+3306_500+3315d others(12): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr8 | 28973803 | ||||||
| chr8:28973803 | GTTTTTTT others(4): Show |
G | 81 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 others(78): Show |
81 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(78): Show |
intron_variant | MODIFIER | c.500+3305_500+3315d others(13): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr8 | 28973803 | ||||||
| chr8:28973803 | GTTTTTTT others(7): Show |
G | 1 | a0001c0001t0003g0107 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.500+3302_500+3315d others(16): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr8 | 28973803 | ||||||
| chr8:28973803 | GTTTTTTT others(8): Show |
G | 8 | a0001c0001t0004g0054 a0001c0001t0004g0055 a0001c0001t0004g0056 others(5): Show |
8 | HG01884.hp1 HG02145.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.500+3301_500+3315d others(17): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr8 | 28973803 | ||||||
| chr8:28973811 | T | TTTTTTTT others(7): Show |
2 | a0001c0001t0003g0089 a0001c0001t0003g0281 |
2 | NA18941.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.500+3305_500+3306i others(16): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr8 | 28973811 | ||||||
| chr8:28973812 | T | TTTTTTTT others(5): Show |
1 | a0001c0001t0003g0158 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.500+3304_500+3305i others(14): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr8 | 28973812 | ||||||
| chr8:28973812 | T | TTTTTTTT others(6): Show |
13 | a0001c0001t0003g0069 a0001c0001t0003g0091 a0001c0001t0003g0093 others(10): Show |
13 | HG01109.hp2 HG02257.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.500+3305_500+3306i others(15): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr8 | 28973812 | ||||||
| chr8:28973812 | T | TTTTTTTT others(7): Show |
2 | a0001c0001t0003g0105 a0001c0001t0006g0066 |
2 | NA18998.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.500+3306_500+3307i others(16): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr8 | 28973812 | ||||||
| chr8:28973813 | T | TGTTTTTT others(5): Show |
1 | a0001c0001t0003g0211 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.500+3294_500+3295i others(14): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28973813 | |||||||
| chr8:28973813 | T | TTTG | 15 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0021 others(12): Show |
15 | HG00323.hp2 HG00642.hp2 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.500+3296_500+3297i others(5): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr8 | 28973813 | ||||||
| chr8:28973813 | T | TTTTTGTT others(5): Show |
2 | a0001c0001t0007g0005 a0001c0001t0007g0062 |
2 | HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.500+3298_500+3299i others(14): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr8 | 28973813 | ||||||
| chr8:28973813 | T | TTTTTTGT others(5): Show |
1 | a0001c0001t0003g0097 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.500+3299_500+3300i others(14): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr8 | 28973813 | ||||||
| chr8:28973813 | T | TTTTTTTT others(5): Show |
37 | a0001c0001t0003g0006 a0001c0001t0003g0070 a0001c0001t0003g0071 others(34): Show |
37 | HG00609.hp1 HG00621.hp2 HG01975.hp2 others(34): Show |
intron_variant | MODIFIER | c.500+3305_500+3306i others(14): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr8 | 28973813 | ||||||
| chr8:28973813 | T | TTTTTTTT others(23): Show |
1 | a0001c0001t0003g0086 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.500+3305_500+3306i others(32): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr8 | 28973813 | ||||||
| chr8:28973813 | T | TTTTTTTT others(6): Show |
1 | a0001c0001t0003g0085 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.500+3306_500+3307i others(15): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr8 | 28973813 | ||||||
| chr8:28973814 | T | G | 1 | a0001c0001t0002g0203 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.500+3295T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28973814 | |||||||
| chr8:28973820 | T | G | 2 | a0001c0001t0007g0005 a0001c0001t0007g0062 |
2 | HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.500+3301T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28973820 | |||||||
| chr8:28973822 | T | G | 1 | a0001c0001t0004g0064 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.500+3303T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28973822 | |||||||
| chr8:28973900 | C | T | 10 | a0001c0001t0007g0010 a0001c0001t0007g0011 a0001c0001t0007g0012 others(7): Show |
10 | HG01261.hp1 HG02257.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.500+3381C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28973900 | |||||||
| chr8:28973917 | C | T | 1 | a0001c0001t0001g0255 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.500+3398C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28973917 | |||||||
| chr8:28973918 | G | A | 2 | a0001c0001t0008g0002 a0001c0001t0008g0003 |
2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.500+3399G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28973918 | |||||||
| chr8:28973920 | T | A | 1 | a0001c0001t0008g0123 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.500+3401T>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28973920 | |||||||
| chr8:28973942 | G | A | 1 | a0001c0001t0001g0315 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.500+3423G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28973942 | |||||||
| chr8:28974034 | A | G | 207 | a0001c0001t0001g0072 a0001c0001t0001g0138 a0001c0001t0001g0139 others(204): Show |
208 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.500+3515A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28974034 | |||||||
| chr8:28974105 | T | C | 310 | a0001c0001t0001g0072 a0001c0001t0001g0138 a0001c0001t0001g0139 others(307): Show |
311 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(308): Show |
intron_variant | MODIFIER | c.500+3586T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28974105 | |||||||
| chr8:28974106 | G | A | 1 | a0001c0001t0004g0128 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.500+3587G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28974106 | |||||||
| chr8:28974248 | A | G | 1 | a0001c0001t0006g0329 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.500+3729A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28974248 | |||||||
| chr8:28974360 | A | C | 8 | a0001c0001t0004g0054 a0001c0001t0004g0055 a0001c0001t0004g0056 others(5): Show |
8 | HG01884.hp1 HG02145.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.500+3841A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28974360 | |||||||
| chr8:28974578 | C | T | 82 | a0001c0001t0001g0072 a0001c0001t0001g0138 a0001c0001t0001g0139 others(79): Show |
82 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.500+4059C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28974578 | |||||||
| chr8:28974726 | T | C | 2 | a0001c0001t0003g0324 a0001c0001t0003g0325 |
2 | HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.500+4207T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28974726 | |||||||
| chr8:28974750 | G | A | 1 | a0001c0001t0004g0061 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.500+4231G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28974750 | |||||||
| chr8:28974771 | T | C | 5 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0122 others(2): Show |
5 | HG02280.hp1 HG02965.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.500+4252T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28974771 | |||||||
| chr8:28974778 | A | T | 1 | a0001c0001t0007g0018 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.500+4259A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28974778 | |||||||
| chr8:28974875 | A | G | 1 | a0001c0001t0001g0146 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.500+4356A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28974875 | |||||||
| chr8:28974987 | C | A | 11 | a0001c0001t0003g0134 a0001c0001t0003g0153 a0001c0001t0003g0158 others(8): Show |
11 | HG02257.hp1 HG02280.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.500+4468C>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28974987 | |||||||
| chr8:28975091 | A | G | 4 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0148 others(1): Show |
4 | NA18947.hp2 NA18990.hp2 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.500+4572A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28975091 | |||||||
| chr8:28975314 | A | C | 1 | a0001c0001t0002g0208 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.501-4757A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28975314 | |||||||
| chr8:28976059 | G | T | 3 | a0001c0001t0002g0273 a0001c0001t0005g0291 a0001c0001t0005g0302 |
3 | HG01516.hp1 HG02145.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.501-4012G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28976059 | |||||||
| chr8:28976264 | T | G | 1 | a0001c0001t0003g0100 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.501-3807T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28976264 | |||||||
| chr8:28976273 | T | A | 1 | a0001c0001t0006g0333 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.501-3798T>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28976273 | |||||||
| chr8:28976283 | T | A | 1 | a0001c0001t0002g0092 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.501-3788T>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28976283 | |||||||
| chr8:28976393 | C | A | 79 | a0001c0001t0001g0072 a0001c0001t0001g0138 a0001c0001t0001g0139 others(76): Show |
79 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.501-3678C>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28976393 | |||||||
| chr8:28976687 | T | C | 69 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(66): Show |
69 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.501-3384T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28976687 | |||||||
| chr8:28976690 | CTTTTCTT others(7): Show |
C | 1 | a0001c0001t0001g0240 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.501-3371_501-3358d others(16): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr8 | 28976690 | ||||||
| chr8:28976709 | C | CT | 7 | a0001c0001t0003g0105 a0001c0001t0006g0116 a0001c0001t0008g0002 others(4): Show |
7 | HG02572.hp1 HG02886.hp2 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.501-3347dupT | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr8 | 28976709 | ||||||
| chr8:28976731 | G | A | 1 | a0001c0001t0003g0076 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.501-3340G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28976731 | |||||||
| chr8:28976738 | A | G | 10 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0122 others(7): Show |
10 | HG02280.hp1 HG02572.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.501-3333A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28976738 | |||||||
| chr8:28977264 | G | A | 3 | a0001c0001t0016g0327 a0001c0001t0016g0330 a0001c0001t0023g0331 |
3 | NA18947.hp1 NA18982.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.501-2807G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28977264 | |||||||
| chr8:28977531 | C | T | 1 | a0001c0001t0006g0116 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.501-2540C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28977531 | |||||||
| chr8:28977681 | C | G | 4 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0122 others(1): Show |
4 | HG02280.hp1 HG03195.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.501-2390C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28977681 | |||||||
| chr8:28977737 | A | G | 310 | a0001c0001t0001g0072 a0001c0001t0001g0138 a0001c0001t0001g0139 others(307): Show |
311 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(308): Show |
intron_variant | MODIFIER | c.501-2334A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28977737 | |||||||
| chr8:28977743 | A | G | 1 | a0001c0001t0001g0228 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.501-2328A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28977743 | |||||||
| chr8:28977875 | C | T | 2 | a0001c0001t0008g0002 a0001c0001t0008g0003 |
2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.501-2196C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28977875 | |||||||
| chr8:28977959 | GA | G | 15 | a0001c0001t0006g0326 a0001c0001t0006g0328 a0001c0001t0006g0329 others(12): Show |
15 | HG00544.hp1 HG02056.hp1 HG02809.hp2 others(12): Show |
intron_variant | MODIFIER | c.501-2109delA | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr8 | 28977959 | ||||||
| chr8:28977972 | A | T | 3 | a0001c0001t0002g0265 a0001c0001t0002g0266 a0001c0001t0002g0267 |
3 | NA18952.hp2 NA18974.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.501-2099A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28977972 | |||||||
| chr8:28978026 | C | A | 1 | a0001c0001t0001g0258 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.501-2045C>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28978026 | |||||||
| chr8:28978052 | G | T | 1 | a0001c0001t0006g0116 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.501-2019G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28978052 | |||||||
| chr8:28978212 | T | G | 6 | a0001c0001t0006g0333 a0001c0001t0006g0335 a0001c0001t0006g0336 others(3): Show |
6 | NA18943.hp2 NA18956.hp1 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.501-1859T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28978212 | |||||||
| chr8:28978286 | T | C | 1 | a0001c0001t0004g0004 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.501-1785T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28978286 | |||||||
| chr8:28978326 | A | T | 1 | a0001c0001t0001g0224 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.501-1745A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28978326 | |||||||
| chr8:28978346 | A | G | 1 | a0001c0001t0001g0224 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.501-1725A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28978346 | |||||||
| chr8:28978564 | C | T | 1 | a0001c0001t0002g0318 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.501-1507C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28978564 | |||||||
| chr8:28978591 | C | T | 1 | a0001c0001t0002g0270 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.501-1480C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28978591 | |||||||
| chr8:28978595 | C | T | 1 | a0001c0001t0010g0312 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.501-1476C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28978595 | |||||||
| chr8:28978645 | G | C | 1 | a0001c0001t0002g0270 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.501-1426G>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28978645 | |||||||
| chr8:28978713 | G | T | 4 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0122 others(1): Show |
4 | HG02280.hp1 HG03195.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.501-1358G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28978713 | |||||||
| chr8:28978786 | C | CA | 276 | a0001c0001t0001g0072 a0001c0001t0001g0138 a0001c0001t0001g0139 others(273): Show |
276 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(273): Show |
intron_variant | MODIFIER | c.501-1265dupA | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr8 | 28978786 | ||||||
| chr8:28978786 | C | CAA | 28 | a0001c0001t0001g0146 a0001c0001t0001g0228 a0001c0001t0001g0310 others(25): Show |
29 | HG01081.hp2 HG01109.hp1 HG01261.hp1 others(26): Show |
intron_variant | MODIFIER | c.501-1266_501-1265d others(4): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr8 | 28978786 | ||||||
| chr8:28978875 | A | C | 4 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0122 others(1): Show |
4 | HG02280.hp1 HG03195.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.501-1196A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28978875 | |||||||
| chr8:28978900 | C | T | 1 | a0001c0001t0003g0298 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.501-1171C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28978900 | |||||||
| chr8:28979104 | C | T | 2 | a0001c0001t0008g0002 a0001c0001t0008g0003 |
2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.501-967C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28979104 | |||||||
| chr8:28979429 | C | T | 1 | a0001c0001t0004g0128 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.501-642C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28979429 | |||||||
| chr8:28979463 | T | C | 5 | a0001c0001t0001g0239 a0001c0001t0001g0241 a0001c0001t0001g0243 others(2): Show |
5 | HG00735.hp2 HG01175.hp1 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.501-608T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28979463 | |||||||
| chr8:28979465 | G | A | 10 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0122 others(7): Show |
10 | HG02280.hp1 HG02572.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.501-606G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28979465 | |||||||
| chr8:28979487 | G | C | 10 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0122 others(7): Show |
10 | HG02280.hp1 HG02572.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.501-584G>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28979487 | |||||||
| chr8:28979567 | G | A | 2 | a0001c0001t0008g0002 a0001c0001t0008g0003 |
2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.501-504G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28979567 | |||||||
| chr8:28979591 | T | C | 3 | a0001c0001t0003g0324 a0001c0001t0003g0325 a0001c0001t0005g0151 |
3 | HG02735.hp2 HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.501-480T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28979591 | |||||||
| chr8:28979718 | C | T | 1 | a0001c0001t0004g0035 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.501-353C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28979718 | |||||||
| chr8:28979757 | T | C | 2 | a0001c0001t0003g0324 a0001c0001t0003g0325 |
2 | HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.501-314T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28979757 | |||||||
| chr8:28979765 | A | G | 1 | a0001c0001t0006g0328 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.501-306A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28979765 | |||||||
| chr8:28979955 | T | G | 1 | a0001c0001t0001g0257 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.501-116T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28979955 | |||||||
| chr8:28979992 | T | C | 1 | a0001c0001t0017g0213 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.501-79T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28979992 | |||||||
| chr8:28980193 | G | A | 1 | a0001c0001t0003g0210 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.586+37G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28980193 | |||||||
| chr8:28980268 | G | C | 1 | a0001c0001t0003g0181 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.586+112G>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28980268 | |||||||
| chr8:28980318 | C | T | 1 | a0001c0001t0002g0207 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.586+162C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28980318 | |||||||
| chr8:28980322 | C | T | 11 | a0001c0001t0003g0134 a0001c0001t0003g0153 a0001c0001t0003g0158 others(8): Show |
11 | HG02257.hp1 HG02280.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.586+166C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28980322 | |||||||
| chr8:28980545 | T | A | 1 | a0001c0001t0021g0343 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.586+389T>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28980545 | |||||||
| chr8:28980820 | C | T | 6 | a0001c0001t0005g0151 a0001c0001t0005g0171 a0001c0001t0005g0172 others(3): Show |
6 | HG00280.hp2 HG01123.hp1 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.586+664C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28980820 | |||||||
| chr8:28980846 | C | T | 6 | a0001c0001t0006g0333 a0001c0001t0006g0335 a0001c0001t0006g0336 others(3): Show |
6 | NA18943.hp2 NA18956.hp1 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.586+690C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28980846 | |||||||
| chr8:28980908 | C | T | 10 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0122 others(7): Show |
10 | HG02280.hp1 HG02572.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.586+752C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28980908 | |||||||
| chr8:28981056 | T | C | 1 | a0001c0001t0001g0143 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.586+900T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28981056 | |||||||
| chr8:28981084 | A | C | 1 | a0001c0001t0003g0119 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.586+928A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28981084 | |||||||
| chr8:28981085 | G | A | 1 | a0001c0001t0003g0119 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.586+929G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28981085 | |||||||
| chr8:28981289 | T | G | 1 | a0001c0001t0001g0139 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.586+1133T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28981289 | |||||||
| chr8:28981382 | T | C | 1 | a0001c0001t0004g0055 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.586+1226T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28981382 | |||||||
| chr8:28981414 | G | T | 2 | a0001c0001t0007g0005 a0001c0001t0007g0062 |
2 | HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.586+1258G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28981414 | |||||||
| chr8:28981590 | T | C | 1 | a0001c0001t0001g0251 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.586+1434T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28981590 | |||||||
| chr8:28981618 | C | T | 10 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0122 others(7): Show |
10 | HG02280.hp1 HG02572.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.586+1462C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28981618 | |||||||
| chr8:28981621 | AT | A | 7 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0122 others(4): Show |
7 | HG02280.hp1 HG03195.hp2 HG03471.hp2 others(4): Show |
intron_variant | MODIFIER | c.586+1476delT | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 28981621 | ||||||
| chr8:28981685 | G | A | 1 | a0001c0001t0003g0158 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.586+1529G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28981685 | |||||||
| chr8:28981963 | C | T | 3 | a0001c0001t0002g0284 a0001c0001t0002g0285 a0001c0002t0002g0283 |
3 | HG01358.hp2 HG01496.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.586+1807C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28981963 | |||||||
| chr8:28981972 | T | C | 1 | a0001c0001t0001g0288 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.586+1816T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28981972 | |||||||
| chr8:28982054 | G | A | 1 | a0001c0001t0003g0079 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.586+1898G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28982054 | |||||||
| chr8:28982093 | C | T | 2 | a0001c0001t0004g0036 a0001c0001t0004g0039 |
2 | HG03710.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.586+1937C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28982093 | |||||||
| chr8:28982168 | G | A | 10 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0122 others(7): Show |
10 | HG02280.hp1 HG02572.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.586+2012G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28982168 | |||||||
| chr8:28982398 | T | C | 1 | a0001c0001t0002g0170 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.586+2242T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28982398 | |||||||
| chr8:28982405 | G | C | 225 | a0001c0001t0001g0072 a0001c0001t0001g0138 a0001c0001t0001g0139 others(222): Show |
226 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(223): Show |
intron_variant | MODIFIER | c.586+2249G>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28982405 | |||||||
| chr8:28982498 | A | G | 1 | a0001c0001t0003g0090 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.586+2342A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28982498 | |||||||
| chr8:28982712 | G | A | 78 | a0001c0001t0001g0072 a0001c0001t0001g0138 a0001c0001t0001g0139 others(75): Show |
78 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.586+2556G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28982712 | |||||||
| chr8:28982753 | G | A | 1 | a0001c0001t0004g0128 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.586+2597G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28982753 | |||||||
| chr8:28982812 | C | T | 1 | a0001c0001t0004g0034 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.586+2656C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28982812 | |||||||
| chr8:28982815 | G | A | 5 | a0001c0001t0002g0133 a0001c0001t0002g0188 a0001c0001t0002g0190 others(2): Show |
5 | HG00438.hp2 NA18949.hp1 NA18973.hp2 others(2): Show |
intron_variant | MODIFIER | c.586+2659G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28982815 | |||||||
| chr8:28982828 | C | T | 1 | a0001c0001t0004g0004 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.586+2672C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28982828 | |||||||
| chr8:28983129 | A | G | 2 | a0001c0001t0007g0005 a0001c0001t0007g0062 |
2 | HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.586+2973A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28983129 | |||||||
| chr8:28983151 | A | G | 1 | a0001c0001t0002g0318 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.586+2995A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28983151 | |||||||
| chr8:28983581 | A | G | 1 | a0001c0001t0004g0048 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.586+3425A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28983581 | |||||||
| chr8:28983879 | C | T | 4 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0122 others(1): Show |
4 | HG02280.hp1 HG03195.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.586+3723C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28983879 | |||||||
| chr8:28984040 | G | A | 3 | a0001c0001t0006g0116 a0001c0001t0014g0117 a0001c0001t0014g0118 |
3 | HG02572.hp1 HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.586+3884G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28984040 | |||||||
| chr8:28984065 | C | T | 2 | a0001c0001t0002g0272 a0001c0001t0002g0273 |
2 | NA19072.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.586+3909C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28984065 | |||||||
| chr8:28984161 | G | A | 1 | a0001c0001t0005g0175 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.586+4005G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28984161 | |||||||
| chr8:28984304 | G | A | 182 | a0001c0001t0001g0072 a0001c0001t0001g0138 a0001c0001t0001g0139 others(179): Show |
183 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.586+4148G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28984304 | |||||||
| chr8:28984789 | T | A | 1 | a0001c0001t0021g0343 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.586+4633T>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28984789 | |||||||
| chr8:28985034 | A | G | 5 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0122 others(2): Show |
5 | HG02280.hp1 HG02965.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.586+4878A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28985034 | |||||||
| chr8:28985307 | T | C | 1 | a0001c0001t0003g0211 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.586+5151T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28985307 | |||||||
| chr8:28985359 | T | C | 10 | a0001c0001t0007g0010 a0001c0001t0007g0011 a0001c0001t0007g0012 others(7): Show |
10 | HG01261.hp1 HG02257.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.586+5203T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28985359 | |||||||
| chr8:28985468 | G | A | 1 | a0001c0001t0002g0212 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.586+5312G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28985468 | |||||||
| chr8:28985540 | C | T | 1 | a0001c0001t0001g0316 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.586+5384C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28985540 | |||||||
| chr8:28985585 | T | C | 1 | a0001c0001t0001g0321 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.586+5429T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28985585 | |||||||
| chr8:28985849 | A | G | 4 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0122 others(1): Show |
4 | HG02280.hp1 HG03195.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.586+5693A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28985849 | |||||||
| chr8:28985919 | A | G | 1 | a0001c0001t0004g0040 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.586+5763A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28985919 | |||||||
| chr8:28986113 | T | C | 2 | a0001c0001t0005g0291 a0001c0001t0005g0302 |
2 | HG01516.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.586+5957T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28986113 | |||||||
| chr8:28986204 | G | A | 207 | a0001c0001t0001g0072 a0001c0001t0001g0138 a0001c0001t0001g0139 others(204): Show |
208 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.586+6048G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28986204 | |||||||
| chr8:28986271 | ATAT | A | 179 | a0001c0001t0001g0072 a0001c0001t0001g0138 a0001c0001t0001g0139 others(176): Show |
180 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.586+6117_586+6119d others(5): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 28986271 | ||||||
| chr8:28986305 | A | G | 1 | a0001c0001t0003g0086 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.586+6149A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28986305 | |||||||
| chr8:28986316 | G | A | 2 | a0001c0001t0005g0291 a0001c0001t0005g0302 |
2 | HG01516.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.586+6160G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28986316 | |||||||
| chr8:28986367 | A | G | 1 | a0001c0001t0003g0100 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.586+6211A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28986367 | |||||||
| chr8:28986666 | A | T | 3 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0288 |
3 | HG00323.hp1 HG01123.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.586+6510A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28986666 | |||||||
| chr8:28986877 | A | G | 1 | a0001c0001t0003g0107 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.586+6721A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28986877 | |||||||
| chr8:28987082 | A | G | 1 | a0001c0001t0003g0097 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.586+6926A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28987082 | |||||||
| chr8:28987214 | T | A | 2 | a0001c0001t0002g0197 a0001c0001t0011g0201 |
2 | NA18956.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.586+7058T>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28987214 | |||||||
| chr8:28987227 | A | G | 2 | a0001c0001t0002g0186 a0001c0001t0002g0187 |
2 | NA18978.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.586+7071A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28987227 | |||||||
| chr8:28987319 | G | A | 2 | a0001c0001t0008g0002 a0001c0001t0008g0003 |
2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.586+7163G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28987319 | |||||||
| chr8:28987417 | C | T | 13 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0021 others(10): Show |
13 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.586+7261C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28987417 | |||||||
| chr8:28987525 | C | T | 2 | a0001c0001t0008g0002 a0001c0001t0008g0003 |
2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.586+7369C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28987525 | |||||||
| chr8:28987878 | G | C | 1 | a0001c0001t0003g0182 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.586+7722G>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28987878 | |||||||
| chr8:28988031 | T | C | 16 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0021 others(13): Show |
16 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(13): Show |
intron_variant | MODIFIER | c.586+7875T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28988031 | |||||||
| chr8:28988134 | A | G | 6 | a0001c0001t0004g0004 a0001c0001t0004g0124 a0001c0001t0004g0125 others(3): Show |
6 | HG00741.hp2 HG02109.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.586+7978A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28988134 | |||||||
| chr8:28988157 | T | C | 1 | a0001c0001t0003g0069 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.586+8001T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28988157 | |||||||
| chr8:28988291 | A | G | 10 | a0001c0001t0007g0010 a0001c0001t0007g0011 a0001c0001t0007g0012 others(7): Show |
10 | HG01261.hp1 HG02257.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.586+8135A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28988291 | |||||||
| chr8:28988463 | G | C | 1 | a0001c0001t0006g0338 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.586+8307G>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28988463 | |||||||
| chr8:28988482 | G | A | 73 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(70): Show |
73 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(70): Show |
intron_variant | MODIFIER | c.586+8326G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28988482 | |||||||
| chr8:28988531 | A | G | 10 | a0001c0001t0002g0261 a0001c0001t0002g0262 a0001c0001t0002g0265 others(7): Show |
10 | NA18612.hp1 NA18941.hp1 NA18952.hp2 others(7): Show |
intron_variant | MODIFIER | c.586+8375A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28988531 | |||||||
| chr8:28988886 | A | G | 1 | a0001c0001t0003g0085 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.586+8730A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28988886 | |||||||
| chr8:28988911 | A | T | 1 | a0001c0001t0003g0112 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.586+8755A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28988911 | |||||||
| chr8:28989044 | G | A | 182 | a0001c0001t0001g0072 a0001c0001t0001g0138 a0001c0001t0001g0139 others(179): Show |
183 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.586+8888G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28989044 | |||||||
| chr8:28989133 | A | G | 182 | a0001c0001t0001g0072 a0001c0001t0001g0138 a0001c0001t0001g0139 others(179): Show |
183 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.586+8977A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28989133 | |||||||
| chr8:28989362 | C | A | 6 | a0001c0001t0001g0139 a0001c0001t0001g0222 a0001c0001t0001g0223 others(3): Show |
6 | HG02486.hp2 HG02723.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.586+9206C>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28989362 | |||||||
| chr8:28989953 | A | G | 334 | a0001c0001t0001g0072 a0001c0001t0001g0138 a0001c0001t0001g0139 others(331): Show |
335 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(332): Show |
intron_variant | MODIFIER | c.586+9797A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28989953 | |||||||
| chr8:28990161 | G | A | 98 | a0001c0001t0002g0001 a0001c0001t0002g0092 a0001c0001t0002g0133 others(95): Show |
99 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.586+10005G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28990161 | |||||||
| chr8:28990166 | T | C | 13 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0021 others(10): Show |
13 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.586+10010T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28990166 | |||||||
| chr8:28990252 | T | C | 1 | a0001c0001t0006g0116 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.586+10096T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28990252 | |||||||
| chr8:28990256 | C | T | 2 | a0001c0001t0008g0002 a0001c0001t0008g0003 |
2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.586+10100C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28990256 | |||||||
| chr8:28990341 | T | C | 1 | a0001c0001t0002g0219 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.586+10185T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28990341 | |||||||
| chr8:28990628 | TTTTTTTG others(5): Show |
T | 1 | a0001c0001t0001g0258 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.586+10483_586+1049 others(16): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 28990628 | ||||||
| chr8:28990686 | T | A | 1 | a0001c0001t0010g0300 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.586+10530T>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28990686 | |||||||
| chr8:28990883 | A | G | 5 | a0001c0001t0003g0324 a0001c0001t0003g0325 a0001c0001t0006g0116 others(2): Show |
5 | HG02572.hp1 HG02886.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.586+10727A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28990883 | |||||||
| chr8:28991022 | G | T | 16 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0021 others(13): Show |
16 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(13): Show |
intron_variant | MODIFIER | c.586+10866G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28991022 | |||||||
| chr8:28991027 | G | A | 1 | a0001c0001t0002g0341 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.586+10871G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28991027 | |||||||
| chr8:28991055 | G | A | 2 | a0001c0001t0005g0175 a0001c0001t0005g0177 |
2 | HG02922.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.586+10899G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28991055 | |||||||
| chr8:28991293 | T | C | 1 | a0001c0001t0003g0119 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.586+11137T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28991293 | |||||||
| chr8:28991509 | C | T | 1 | a0001c0001t0008g0121 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.586+11353C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28991509 | |||||||
| chr8:28991535 | C | T | 3 | a0001c0001t0004g0063 a0001c0001t0004g0064 a0001c0001t0004g0065 |
3 | HG00738.hp2 HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.586+11379C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28991535 | |||||||
| chr8:28991698 | T | G | 10 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0122 others(7): Show |
10 | HG02280.hp1 HG02572.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.586+11542T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28991698 | |||||||
| chr8:28991727 | C | T | 1 | a0001c0001t0008g0123 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.586+11571C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28991727 | |||||||
| chr8:28991754 | G | T | 1 | a0001c0001t0007g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.586+11598G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28991754 | |||||||
| chr8:28992125 | G | A | 1 | a0001c0001t0001g0231 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.586+11969G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28992125 | |||||||
| chr8:28992200 | A | G | 1 | a0001c0001t0008g0123 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.586+12044A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28992200 | |||||||
| chr8:28992203 | G | C | 1 | a0001c0001t0008g0123 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.586+12047G>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28992203 | |||||||
| chr8:28992372 | T | C | 1 | a0001c0001t0002g0133 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.586+12216T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28992372 | |||||||
| chr8:28992391 | C | G | 4 | a0001c0001t0005g0173 a0001c0001t0005g0175 a0001c0001t0005g0176 others(1): Show |
4 | HG02922.hp2 HG02965.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.586+12235C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28992391 | |||||||
| chr8:28992413 | C | G | 1 | a0001c0001t0003g0211 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.586+12257C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28992413 | |||||||
| chr8:28992528 | T | A | 2 | a0001c0001t0005g0173 a0001c0001t0005g0176 |
2 | HG02965.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.586+12372T>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28992528 | |||||||
| chr8:28992597 | G | A | 1 | a0001c0001t0001g0231 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.586+12441G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28992597 | |||||||
| chr8:28992602 | G | T | 2 | a0001c0001t0003g0324 a0001c0001t0003g0325 |
2 | HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.586+12446G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28992602 | |||||||
| chr8:28992635 | C | G | 1 | a0001c0001t0004g0041 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.586+12479C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28992635 | |||||||
| chr8:28992869 | C | CA | 166 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 others(163): Show |
166 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.586+12738dupA | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 28992869 | ||||||
| chr8:28992869 | C | CAA | 121 | a0001c0001t0001g0072 a0001c0001t0001g0147 a0001c0001t0001g0148 others(118): Show |
122 | HG00280.hp2 HG00423.hp2 HG00558.hp1 others(119): Show |
intron_variant | MODIFIER | c.586+12737_586+1273 others(6): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 28992869 | ||||||
| chr8:28992869 | C | CAAA | 21 | a0001c0001t0002g0133 a0001c0001t0002g0155 a0001c0001t0002g0170 others(18): Show |
21 | HG00438.hp1 HG00438.hp2 HG00642.hp1 others(18): Show |
intron_variant | MODIFIER | c.586+12736_586+1273 others(7): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 28992869 | ||||||
| chr8:28992869 | CAAAAAAA others(3): Show |
C | 2 | a0001c0001t0002g0161 a0001c0001t0002g0206 |
2 | NA18950.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.586+12729_586+1273 others(14): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 28992869 | ||||||
| chr8:28992869 | CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0002g0274 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.586+12728_586+1273 others(15): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 28992869 | ||||||
| chr8:28992869 | CAAAAAAA others(5): Show |
C | 2 | a0001c0001t0003g0324 a0001c0001t0003g0325 |
2 | HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.586+12727_586+1273 others(16): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 28992869 | ||||||
| chr8:28993049 | GT | G | 308 | a0001c0001t0001g0072 a0001c0001t0001g0138 a0001c0001t0001g0139 others(305): Show |
309 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(306): Show |
intron_variant | MODIFIER | c.586+12904delT | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 28993049 | ||||||
| chr8:28993099 | A | G | 10 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0122 others(7): Show |
10 | HG02280.hp1 HG02572.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.586+12943A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28993099 | |||||||
| chr8:28993660 | A | C | 114 | a0001c0001t0002g0001 a0001c0001t0002g0092 a0001c0001t0002g0133 others(111): Show |
115 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.586+13504A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28993660 | |||||||
| chr8:28993706 | C | T | 2 | a0001c0001t0008g0002 a0001c0001t0008g0003 |
2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.586+13550C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28993706 | |||||||
| chr8:28994014 | G | A | 8 | a0001c0001t0007g0011 a0001c0001t0007g0013 a0001c0001t0007g0014 others(5): Show |
8 | HG02257.hp2 HG02622.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.586+13858G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28994014 | |||||||
| chr8:28994023 | C | T | 2 | a0001c0001t0002g0156 a0001c0001t0002g0163 |
2 | HG03017.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.586+13867C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28994023 | |||||||
| chr8:28994111 | G | A | 2 | a0001c0001t0012g0174 a0001c0001t0012g0297 |
2 | HG02886.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.586+13955G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28994111 | |||||||
| chr8:28994167 | C | CA | 97 | a0001c0001t0001g0072 a0001c0001t0001g0138 a0001c0001t0001g0139 others(94): Show |
97 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.586+14024dupA | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 28994167 | ||||||
| chr8:28994221 | C | T | 4 | a0001c0001t0001g0305 a0001c0001t0001g0306 a0001c0001t0001g0307 others(1): Show |
4 | HG02055.hp1 HG02559.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.586+14065C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28994221 | |||||||
| chr8:28994701 | A | G | 1 | a0001c0001t0004g0029 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.587-14371A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28994701 | |||||||
| chr8:28994817 | G | A | 1 | a0001c0001t0001g0307 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.587-14255G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28994817 | |||||||
| chr8:28994837 | C | A | 97 | a0001c0001t0002g0001 a0001c0001t0002g0092 a0001c0001t0002g0133 others(94): Show |
98 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.587-14235C>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28994837 | |||||||
| chr8:28994911 | G | A | 1 | a0001c0001t0009g0129 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.587-14161G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28994911 | |||||||
| chr8:28994934 | A | G | 2 | a0001c0001t0001g0139 a0001c0001t0001g0253 |
2 | HG02486.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.587-14138A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28994934 | |||||||
| chr8:28995238 | C | T | 1 | a0001c0001t0003g0119 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.587-13834C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28995238 | |||||||
| chr8:28995440 | A | G | 2 | a0001c0001t0008g0067 a0001c0001t0008g0094 |
2 | HG00621.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.587-13632A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28995440 | |||||||
| chr8:28995545 | T | G | 5 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0122 others(2): Show |
5 | HG02280.hp1 HG02965.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.587-13527T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28995545 | |||||||
| chr8:28995575 | A | C | 1 | a0001c0001t0002g0170 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.587-13497A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28995575 | |||||||
| chr8:28995703 | T | C | 1 | a0001c0001t0007g0010 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.587-13369T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28995703 | |||||||
| chr8:28995868 | C | T | 1 | a0001c0001t0001g0149 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.587-13204C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28995868 | |||||||
| chr8:28995869 | G | A | 1 | a0001c0001t0003g0080 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.587-13203G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28995869 | |||||||
| chr8:28995874 | G | A | 1 | a0001c0001t0004g0043 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.587-13198G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28995874 | |||||||
| chr8:28996031 | G | A | 1 | a0001c0001t0001g0305 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.587-13041G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28996031 | |||||||
| chr8:28996070 | C | T | 1 | a0001c0001t0004g0022 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.587-13002C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28996070 | |||||||
| chr8:28996269 | CAAG | C | 69 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(66): Show |
69 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(66): Show |
intron_variant | MODIFIER | c.587-12802_587-1280 others(7): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28996269 | |||||||
| chr8:28996275 | G | A | 69 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(66): Show |
69 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(66): Show |
intron_variant | MODIFIER | c.587-12797G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28996275 | |||||||
| chr8:28996276 | A | C | 69 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(66): Show |
69 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(66): Show |
intron_variant | MODIFIER | c.587-12796A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28996276 | |||||||
| chr8:28996278 | T | TA | 69 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(66): Show |
69 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(66): Show |
intron_variant | MODIFIER | c.587-12794_587-1279 others(5): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28996278 | |||||||
| chr8:28996279 | T | A | 69 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(66): Show |
69 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(66): Show |
intron_variant | MODIFIER | c.587-12793T>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28996279 | |||||||
| chr8:28996280 | C | A | 69 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(66): Show |
69 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(66): Show |
intron_variant | MODIFIER | c.587-12792C>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28996280 | |||||||
| chr8:28996281 | T | C | 69 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(66): Show |
69 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(66): Show |
intron_variant | MODIFIER | c.587-12791T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28996281 | |||||||
| chr8:28996434 | T | C | 10 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0122 others(7): Show |
10 | HG02280.hp1 HG02572.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.587-12638T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28996434 | |||||||
| chr8:28996509 | T | C | 1 | a0001c0001t0004g0004 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.587-12563T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28996509 | |||||||
| chr8:28996722 | G | C | 10 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0122 others(7): Show |
10 | HG02280.hp1 HG02572.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.587-12350G>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28996722 | |||||||
| chr8:28996736 | G | A | 12 | a0001c0001t0007g0005 a0001c0001t0007g0010 a0001c0001t0007g0011 others(9): Show |
12 | HG01261.hp1 HG02257.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.587-12336G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28996736 | |||||||
| chr8:28996901 | T | C | 1 | a0001c0001t0008g0123 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.587-12171T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28996901 | |||||||
| chr8:28997359 | T | A | 2 | a0001c0001t0007g0005 a0001c0001t0007g0062 |
2 | HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.587-11713T>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28997359 | |||||||
| chr8:28997482 | T | A | 1 | a0001c0001t0004g0027 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.587-11590T>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28997482 | |||||||
| chr8:28997545 | G | A | 1 | a0001c0001t0010g0300 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.587-11527G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28997545 | |||||||
| chr8:28997585 | C | T | 198 | a0001c0001t0001g0072 a0001c0001t0001g0138 a0001c0001t0001g0139 others(195): Show |
199 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.587-11487C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28997585 | |||||||
| chr8:28997702 | C | T | 4 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0122 others(1): Show |
4 | HG02280.hp1 HG03195.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.587-11370C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28997702 | |||||||
| chr8:28997792 | C | G | 1 | a0001c0001t0002g0264 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.587-11280C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28997792 | |||||||
| chr8:28998009 | C | T | 182 | a0001c0001t0001g0072 a0001c0001t0001g0138 a0001c0001t0001g0139 others(179): Show |
183 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.587-11063C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28998009 | |||||||
| chr8:28998265 | A | G | 1 | a0001c0001t0002g0167 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.587-10807A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28998265 | |||||||
| chr8:28998368 | C | G | 1 | a0001c0001t0003g0095 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.587-10704C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28998368 | |||||||
| chr8:28998374 | C | T | 1 | a0001c0001t0001g0305 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.587-10698C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28998374 | |||||||
| chr8:28998689 | A | C | 1 | a0001c0001t0008g0123 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.587-10383A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28998689 | |||||||
| chr8:28998776 | C | T | 1 | a0001c0001t0008g0339 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.587-10296C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28998776 | |||||||
| chr8:28999341 | C | T | 3 | a0001c0001t0007g0011 a0001c0001t0007g0018 a0001c0001t0007g0218 |
3 | HG02257.hp2 HG02630.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.587-9731C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28999341 | |||||||
| chr8:28999393 | A | G | 3 | a0001c0001t0007g0011 a0001c0001t0007g0018 a0001c0001t0007g0218 |
3 | HG02257.hp2 HG02630.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.587-9679A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28999393 | |||||||
| chr8:29000064 | A | G | 1 | a0001c0001t0003g0105 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.587-9008A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29000064 | |||||||
| chr8:29000076 | G | A | 1 | a0001c0001t0001g0154 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.587-8996G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29000076 | |||||||
| chr8:29000212 | C | G | 3 | a0001c0001t0006g0116 a0001c0001t0014g0117 a0001c0001t0014g0118 |
3 | HG02572.hp1 HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.587-8860C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29000212 | |||||||
| chr8:29000276 | G | A | 10 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0122 others(7): Show |
10 | HG02280.hp1 HG02572.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.587-8796G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29000276 | |||||||
| chr8:29000290 | T | C | 2 | a0001c0001t0003g0070 a0001c0001t0003g0071 |
2 | HG03688.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.587-8782T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29000290 | |||||||
| chr8:29000333 | C | T | 12 | a0001c0001t0007g0005 a0001c0001t0007g0010 a0001c0001t0007g0011 others(9): Show |
12 | HG01261.hp1 HG02257.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.587-8739C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29000333 | |||||||
| chr8:29000943 | T | G | 1 | a0001c0001t0008g0339 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.587-8129T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29000943 | |||||||
| chr8:29001057 | A | C | 2 | a0001c0001t0002g0188 a0001c0001t0002g0190 |
2 | NA18973.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.587-8015A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29001057 | |||||||
| chr8:29001060 | C | A | 97 | a0001c0001t0002g0001 a0001c0001t0002g0092 a0001c0001t0002g0133 others(94): Show |
98 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.587-8012C>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29001060 | |||||||
| chr8:29001376 | C | T | 1 | a0001c0001t0003g0099 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.587-7696C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29001376 | |||||||
| chr8:29001476 | G | A | 1 | a0001c0001t0003g0119 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.587-7596G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29001476 | |||||||
| chr8:29001510 | G | A | 3 | a0001c0001t0001g0290 a0001c0001t0001g0294 a0001c0001t0007g0012 |
3 | HG01070.hp2 HG01261.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.587-7562G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29001510 | |||||||
| chr8:29001512 | G | T | 2 | a0001c0001t0006g0335 a0001c0001t0006g0336 |
2 | NA18943.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.587-7560G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29001512 | |||||||
| chr8:29001536 | C | T | 11 | a0001c0001t0003g0134 a0001c0001t0003g0153 a0001c0001t0003g0158 others(8): Show |
11 | HG02257.hp1 HG02280.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.587-7536C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29001536 | |||||||
| chr8:29001537 | G | A | 1 | a0001c0001t0003g0324 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.587-7535G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29001537 | |||||||
| chr8:29001547 | C | G | 2 | a0001c0001t0003g0324 a0001c0001t0003g0325 |
2 | HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.587-7525C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29001547 | |||||||
| chr8:29001549 | C | CAAACAAA others(3): Show |
1 | a0001c0001t0004g0061 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.587-7486_587-7477d others(12): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 29001549 | ||||||
| chr8:29001549 | CAAACA | C | 112 | a0001c0001t0001g0140 a0001c0001t0001g0222 a0001c0001t0001g0246 others(109): Show |
112 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.587-7481_587-7477d others(7): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 29001549 | ||||||
| chr8:29001549 | CAAACAAA others(3): Show |
C | 185 | a0001c0001t0001g0072 a0001c0001t0001g0138 a0001c0001t0001g0139 others(182): Show |
186 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.587-7486_587-7477d others(12): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 29001549 | ||||||
| chr8:29001549 | CAAACAAA others(8): Show |
C | 4 | a0001c0001t0001g0306 a0001c0001t0001g0307 a0001c0001t0014g0117 others(1): Show |
4 | HG02559.hp2 HG02572.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.587-7491_587-7477d others(17): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 29001549 | ||||||
| chr8:29001718 | A | C | 1 | a0001c0001t0010g0300 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.587-7354A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29001718 | |||||||
| chr8:29002114 | G | T | 1 | a0001c0001t0010g0312 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.587-6958G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29002114 | |||||||
| chr8:29002294 | G | A | 10 | a0001c0001t0007g0010 a0001c0001t0007g0011 a0001c0001t0007g0012 others(7): Show |
10 | HG01261.hp1 HG02257.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.587-6778G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29002294 | |||||||
| chr8:29002863 | A | G | 2 | a0001c0001t0004g0036 a0001c0001t0004g0039 |
2 | HG03710.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.587-6209A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29002863 | |||||||
| chr8:29002901 | C | A | 1 | a0001c0001t0006g0328 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.587-6171C>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29002901 | |||||||
| chr8:29003084 | C | CT | 67 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(64): Show |
67 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.587-5977dupT | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 29003084 | ||||||
| chr8:29003084 | CT | C | 14 | a0001c0001t0001g0237 a0001c0001t0002g0183 a0001c0001t0004g0019 others(11): Show |
14 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.587-5977delT | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 29003084 | ||||||
| chr8:29003140 | T | C | 6 | a0001c0001t0004g0004 a0001c0001t0004g0124 a0001c0001t0004g0125 others(3): Show |
6 | HG00741.hp2 HG02109.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.587-5932T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29003140 | |||||||
| chr8:29003342 | T | C | 2 | a0001c0001t0007g0005 a0001c0001t0007g0062 |
2 | HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.587-5730T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29003342 | |||||||
| chr8:29003496 | GTA | G | 101 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(98): Show |
101 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.587-5556_587-5555d others(4): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 29003496 | ||||||
| chr8:29003496 | GTATA | G | 208 | a0001c0001t0001g0072 a0001c0001t0001g0138 a0001c0001t0001g0139 others(205): Show |
209 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(206): Show |
intron_variant | MODIFIER | c.587-5558_587-5555d others(6): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 29003496 | ||||||
| chr8:29003500 | A | G | 17 | a0001c0001t0003g0085 a0001c0001t0004g0019 a0001c0001t0004g0020 others(14): Show |
17 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(14): Show |
intron_variant | MODIFIER | c.587-5572A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29003500 | |||||||
| chr8:29003543 | T | A | 1 | a0001c0001t0002g0284 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.587-5529T>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29003543 | |||||||
| chr8:29003545 | T | A | 1 | a0001c0001t0002g0284 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.587-5527T>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29003545 | |||||||
| chr8:29003547 | C | A | 1 | a0001c0001t0002g0284 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.587-5525C>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29003547 | |||||||
| chr8:29003549 | G | A | 1 | a0001c0001t0002g0284 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.587-5523G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29003549 | |||||||
| chr8:29003552 | T | TATATATA others(4): Show |
1 | a0001c0001t0002g0284 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.587-5520_587-5519i others(13): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29003552 | |||||||
| chr8:29003555 | A | AAT | 10 | a0001c0001t0004g0036 a0001c0001t0004g0039 a0001c0001t0004g0048 others(7): Show |
10 | HG02074.hp1 HG02572.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.587-5496_587-5495d others(4): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 29003555 | ||||||
| chr8:29003555 | A | AATAAATA others(9): Show |
1 | a0001c0001t0003g0084 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.587-5514_587-5513i others(18): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 29003555 | ||||||
| chr8:29003555 | A | AATAT | 7 | a0001c0001t0001g0238 a0001c0001t0001g0244 a0001c0001t0001g0245 others(4): Show |
7 | HG02040.hp2 HG02738.hp2 NA18964.hp1 others(4): Show |
intron_variant | MODIFIER | c.587-5498_587-5495d others(6): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 29003555 | ||||||
| chr8:29003555 | A | AATATAT | 8 | a0001c0001t0001g0227 a0001c0001t0004g0020 a0001c0001t0004g0021 others(5): Show |
8 | HG00140.hp2 HG00642.hp2 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.587-5500_587-5495d others(8): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 29003555 | ||||||
| chr8:29003555 | A | AATATATA others(1): Show |
8 | a0001c0001t0001g0315 a0001c0001t0003g0102 a0001c0001t0003g0103 others(5): Show |
8 | HG01069.hp2 HG02717.hp1 NA18986.hp1 others(5): Show |
intron_variant | MODIFIER | c.587-5502_587-5495d others(10): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 29003555 | ||||||
| chr8:29003555 | A | AATATATA others(3): Show |
8 | a0001c0001t0002g0168 a0001c0001t0002g0184 a0001c0001t0003g0008 others(5): Show |
8 | HG00735.hp1 HG02896.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.587-5504_587-5495d others(12): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 29003555 | ||||||
| chr8:29003555 | A | AATATATA others(5): Show |
28 | a0001c0001t0002g0156 a0001c0001t0003g0009 a0001c0001t0003g0069 others(25): Show |
28 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(25): Show |
intron_variant | MODIFIER | c.587-5506_587-5495d others(14): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 29003555 | ||||||
| chr8:29003555 | A | AATATATA others(7): Show |
16 | a0001c0001t0001g0226 a0001c0001t0001g0229 a0001c0001t0001g0234 others(13): Show |
16 | HG01167.hp2 HG01884.hp2 HG01943.hp2 others(13): Show |
intron_variant | MODIFIER | c.587-5508_587-5495d others(16): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 29003555 | ||||||
| chr8:29003555 | A | AATATATA others(9): Show |
25 | a0001c0001t0001g0072 a0001c0001t0001g0140 a0001c0001t0001g0141 others(22): Show |
25 | HG00140.hp1 HG00639.hp2 HG00741.hp2 others(22): Show |
intron_variant | MODIFIER | c.587-5510_587-5495d others(18): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 29003555 | ||||||
| chr8:29003555 | A | AATATATA others(11): Show |
15 | a0001c0001t0001g0138 a0001c0001t0001g0145 a0001c0001t0001g0147 others(12): Show |
15 | HG00323.hp1 HG00423.hp1 HG00609.hp1 others(12): Show |
intron_variant | MODIFIER | c.587-5512_587-5495d others(20): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 29003555 | ||||||
| chr8:29003555 | A | AATATATA others(13): Show |
17 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0235 others(14): Show |
17 | HG00735.hp2 HG00738.hp2 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.587-5514_587-5495d others(22): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 29003555 | ||||||
| chr8:29003555 | A | AATATATA others(15): Show |
12 | a0001c0001t0001g0139 a0001c0001t0001g0221 a0001c0001t0001g0222 others(9): Show |
12 | HG01123.hp2 HG01496.hp2 HG02155.hp1 others(9): Show |
intron_variant | MODIFIER | c.587-5516_587-5495d others(24): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 29003555 | ||||||
| chr8:29003555 | A | AATATATA others(17): Show |
12 | a0001c0001t0001g0146 a0001c0001t0001g0236 a0001c0001t0001g0241 others(9): Show |
12 | HG00408.hp1 HG01243.hp1 HG01358.hp1 others(9): Show |
intron_variant | MODIFIER | c.587-5495_587-5494i others(26): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 29003555 | ||||||
| chr8:29003555 | A | AATATATA others(19): Show |
17 | a0001c0001t0001g0223 a0001c0001t0001g0251 a0001c0001t0001g0257 others(14): Show |
17 | HG00438.hp2 HG01070.hp2 HG01123.hp1 others(14): Show |
intron_variant | MODIFIER | c.587-5495_587-5494i others(28): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 29003555 | ||||||
| chr8:29003555 | A | AATATATA others(21): Show |
22 | a0001c0001t0001g0258 a0001c0001t0001g0292 a0001c0001t0001g0306 others(19): Show |
22 | HG00621.hp2 HG02055.hp2 HG02056.hp1 others(19): Show |
intron_variant | MODIFIER | c.587-5495_587-5494i others(30): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 29003555 | ||||||
| chr8:29003555 | A | AATATATA others(23): Show |
18 | a0001c0001t0001g0240 a0001c0001t0001g0247 a0001c0001t0001g0323 others(15): Show |
18 | HG00280.hp2 HG00558.hp1 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.587-5495_587-5494i others(32): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 29003555 | ||||||
| chr8:29003555 | A | AATATATA others(25): Show |
32 | a0001c0001t0001g0224 a0001c0001t0001g0299 a0001c0001t0001g0320 others(29): Show |
32 | HG00597.hp2 HG00642.hp1 HG01358.hp2 others(29): Show |
intron_variant | MODIFIER | c.587-5495_587-5494i others(34): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 29003555 | ||||||
| chr8:29003555 | A | AATATATA others(27): Show |
15 | a0001c0001t0001g0319 a0001c0001t0002g0135 a0001c0001t0002g0137 others(12): Show |
15 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(12): Show |
intron_variant | MODIFIER | c.587-5495_587-5494i others(36): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 29003555 | ||||||
| chr8:29003555 | A | AATATATA others(29): Show |
8 | a0001c0001t0001g0169 a0001c0001t0001g0305 a0001c0001t0002g0001 others(5): Show |
9 | HG01168.hp1 HG01175.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.587-5495_587-5494i others(38): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 29003555 | ||||||
| chr8:29003555 | A | AATATATA others(31): Show |
11 | a0001c0001t0001g0237 a0001c0001t0002g0170 a0001c0001t0002g0188 others(8): Show |
11 | HG00544.hp1 HG00621.hp1 HG02056.hp2 others(8): Show |
intron_variant | MODIFIER | c.587-5495_587-5494i others(40): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 29003555 | ||||||
| chr8:29003555 | A | AATATATA others(33): Show |
1 | a0001c0001t0002g0198 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.587-5495_587-5494i others(42): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 29003555 | ||||||
| chr8:29003555 | A | AATATATA others(35): Show |
1 | a0001c0001t0002g0202 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.587-5495_587-5494i others(44): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 29003555 | ||||||
| chr8:29003555 | A | ATATATAT others(22): Show |
3 | a0001c0001t0005g0215 a0001c0001t0006g0332 a0001c0001t0009g0132 |
3 | HG02559.hp1 NA19062.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.587-5517_587-5516i others(31): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29003555 | |||||||
| chr8:29003555 | A | ATATATAT others(28): Show |
1 | a0001c0001t0002g0262 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.587-5517_587-5516i others(37): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29003555 | |||||||
| chr8:29003555 | A | T | 1 | a0001c0001t0002g0284 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.587-5517A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29003555 | |||||||
| chr8:29003555 | AATAT | A | 11 | a0001c0001t0003g0134 a0001c0001t0003g0153 a0001c0001t0003g0158 others(8): Show |
11 | HG02257.hp1 HG02280.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.587-5498_587-5495d others(6): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 29003555 | ||||||
| chr8:29003555 | AATATATA others(3): Show |
A | 3 | a0001c0001t0002g0157 a0001c0001t0002g0186 a0001c0001t0002g0187 |
3 | NA18943.hp1 NA18978.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.587-5504_587-5495d others(12): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 29003555 | ||||||
| chr8:29003565 | T | TATATATA others(13): Show |
1 | a0001c0001t0001g0220 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.587-5495_587-5494i others(22): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 29003565 | ||||||
| chr8:29003700 | G | A | 10 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0122 others(7): Show |
10 | HG02280.hp1 HG02572.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.587-5372G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29003700 | |||||||
| chr8:29003774 | G | T | 2 | a0001c0001t0003g0122 a0001c0001t0008g0121 |
2 | HG03195.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.587-5298G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29003774 | |||||||
| chr8:29003799 | A | G | 1 | a0001c0001t0006g0329 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.587-5273A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29003799 | |||||||
| chr8:29003866 | A | G | 1 | a0001c0001t0001g0248 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.587-5206A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29003866 | |||||||
| chr8:29003884 | A | G | 4 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0122 others(1): Show |
4 | HG02280.hp1 HG03195.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.587-5188A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29003884 | |||||||
| chr8:29003943 | G | A | 1 | a0001c0001t0010g0312 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.587-5129G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29003943 | |||||||
| chr8:29004292 | T | C | 10 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0122 others(7): Show |
10 | HG02280.hp1 HG02572.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.587-4780T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29004292 | |||||||
| chr8:29004433 | G | C | 1 | a0001c0001t0001g0232 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.587-4639G>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29004433 | |||||||
| chr8:29004670 | A | T | 3 | a0001c0001t0002g0157 a0001c0001t0002g0186 a0001c0001t0002g0187 |
3 | NA18943.hp1 NA18978.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.587-4402A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29004670 | |||||||
| chr8:29004776 | G | T | 3 | a0001c0001t0016g0327 a0001c0001t0016g0330 a0001c0001t0023g0331 |
3 | NA18947.hp1 NA18982.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.587-4296G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29004776 | |||||||
| chr8:29004809 | A | C | 1 | a0001c0001t0003g0086 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.587-4263A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29004809 | |||||||
| chr8:29004855 | C | T | 2 | a0001c0001t0002g0186 a0001c0001t0002g0187 |
2 | NA18978.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.587-4217C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29004855 | |||||||
| chr8:29004856 | G | A | 2 | a0001c0001t0014g0117 a0001c0001t0014g0118 |
2 | HG02572.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.587-4216G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29004856 | |||||||
| chr8:29004886 | A | G | 1 | a0001c0001t0001g0315 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.587-4186A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29004886 | |||||||
| chr8:29005213 | T | G | 2 | a0001c0001t0003g0122 a0001c0001t0008g0121 |
2 | HG03195.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.587-3859T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29005213 | |||||||
| chr8:29005420 | G | T | 207 | a0001c0001t0001g0072 a0001c0001t0001g0138 a0001c0001t0001g0139 others(204): Show |
208 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.587-3652G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29005420 | |||||||
| chr8:29005786 | G | A | 1 | a0001c0001t0003g0075 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.587-3286G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29005786 | |||||||
| chr8:29005911 | A | G | 1 | a0001c0001t0003g0119 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.587-3161A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29005911 | |||||||
| chr8:29005990 | A | AT | 93 | a0001c0001t0001g0140 a0001c0001t0001g0148 a0001c0001t0001g0220 others(90): Show |
93 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.587-3062dupT | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 29005990 | ||||||
| chr8:29006021 | G | A | 2 | a0001c0001t0003g0324 a0001c0001t0003g0325 |
2 | HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.587-3051G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29006021 | |||||||
| chr8:29006210 | G | C | 334 | a0001c0001t0001g0072 a0001c0001t0001g0138 a0001c0001t0001g0139 others(331): Show |
335 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(332): Show |
intron_variant | MODIFIER | c.587-2862G>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29006210 | |||||||
| chr8:29006241 | C | A | 1 | a0001c0001t0003g0120 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.587-2831C>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29006241 | |||||||
| chr8:29006266 | T | A | 1 | a0001c0001t0004g0128 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.587-2806T>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29006266 | |||||||
| chr8:29006285 | G | T | 2 | a0001c0001t0003g0324 a0001c0001t0003g0325 |
2 | HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.587-2787G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29006285 | |||||||
| chr8:29006292 | C | T | 1 | a0001c0001t0008g0121 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.587-2780C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29006292 | |||||||
| chr8:29006558 | C | T | 179 | a0001c0001t0001g0072 a0001c0001t0001g0138 a0001c0001t0001g0139 others(176): Show |
180 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.587-2514C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29006558 | |||||||
| chr8:29006681 | T | G | 1 | a0001c0001t0001g0299 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.587-2391T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29006681 | |||||||
| chr8:29006708 | C | T | 1 | a0001c0001t0007g0013 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.587-2364C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29006708 | |||||||
| chr8:29006756 | G | C | 12 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0021 others(9): Show |
12 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(9): Show |
intron_variant | MODIFIER | c.587-2316G>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29006756 | |||||||
| chr8:29006795 | A | G | 2 | a0001c0001t0002g0159 a0001c0001t0002g0193 |
2 | NA19004.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.587-2277A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29006795 | |||||||
| chr8:29007016 | C | T | 1 | a0001c0001t0008g0002 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.587-2056C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29007016 | |||||||
| chr8:29007158 | G | A | 1 | a0001c0001t0001g0140 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.587-1914G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29007158 | |||||||
| chr8:29007421 | A | G | 1 | a0001c0001t0001g0315 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.587-1651A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29007421 | |||||||
| chr8:29007640 | G | A | 1 | a0001c0001t0008g0003 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.587-1432G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29007640 | |||||||
| chr8:29007749 | G | A | 2 | a0001c0001t0004g0029 a0001c0001t0004g0342 |
2 | HG00642.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.587-1323G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29007749 | |||||||
| chr8:29007831 | T | C | 1 | a0001c0001t0008g0123 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.587-1241T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29007831 | |||||||
| chr8:29007930 | C | G | 2 | a0001c0001t0014g0117 a0001c0001t0014g0118 |
2 | HG02572.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.587-1142C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29007930 | |||||||
| chr8:29007984 | T | C | 1 | a0001c0001t0001g0072 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.587-1088T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29007984 | |||||||
| chr8:29008087 | G | A | 1 | a0001c0001t0004g0058 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.587-985G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29008087 | |||||||
| chr8:29008468 | T | C | 3 | a0001c0001t0004g0063 a0001c0001t0004g0064 a0001c0001t0004g0065 |
3 | HG00738.hp2 HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.587-604T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29008468 | |||||||
| chr8:29008740 | G | A | 1 | a0001c0001t0001g0249 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.587-332G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29008740 | |||||||
| chr8:29009267 | T | G | 1 | a0001c0001t0012g0297 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.697+85T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29009267 | |||||||
| chr8:29009343 | A | T | 3 | a0001c0001t0004g0020 a0001c0001t0004g0029 a0001c0001t0004g0342 |
3 | HG00642.hp2 HG01081.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.697+161A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29009343 | |||||||
| chr8:29009380 | AG | A | 10 | a0001c0001t0007g0010 a0001c0001t0007g0011 a0001c0001t0007g0012 others(7): Show |
10 | HG01261.hp1 HG02257.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.697+199delG | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29009380 | |||||||
| chr8:29009457 | C | T | 4 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0122 others(1): Show |
4 | HG02280.hp1 HG03195.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.697+275C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29009457 | |||||||
| chr8:29009465 | ATGTT | A | 53 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(50): Show |
53 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.697+284_697+287del others(4): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29009465 | |||||||
| chr8:29009506 | C | T | 1 | a0001c0001t0001g0256 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.697+324C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29009506 | |||||||
| chr8:29009516 | C | T | 1 | a0001c0001t0003g0077 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.697+334C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29009516 | |||||||
| chr8:29009523 | CT | C | 240 | a0001c0001t0001g0072 a0001c0001t0001g0138 a0001c0001t0001g0139 others(237): Show |
240 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(237): Show |
intron_variant | MODIFIER | c.697+362delT | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr8 | 29009523 | ||||||
| chr8:29009523 | CTT | C | 37 | a0001c0001t0001g0221 a0001c0001t0001g0306 a0001c0001t0002g0214 others(34): Show |
37 | HG00140.hp2 HG00323.hp2 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.697+361_697+362del others(2): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr8 | 29009523 | ||||||
| chr8:29009523 | CTTTTTTT others(1): Show |
C | 7 | a0001c0001t0003g0324 a0001c0001t0003g0325 a0001c0001t0006g0116 others(4): Show |
7 | HG02055.hp2 HG02572.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.697+355_697+362del others(8): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr8 | 29009523 | ||||||
| chr8:29009619 | C | G | 1 | a0001c0001t0008g0121 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.697+437C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29009619 | |||||||
| chr8:29009929 | C | T | 81 | a0001c0001t0001g0072 a0001c0001t0001g0138 a0001c0001t0001g0139 others(78): Show |
81 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.697+747C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29009929 | |||||||
| chr8:29010285 | C | T | 2 | a0001c0001t0001g0139 a0001c0001t0001g0253 |
2 | HG02486.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.697+1103C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29010285 | |||||||
| chr8:29010563 | A | T | 26 | a0001c0001t0001g0149 a0001c0001t0001g0224 a0001c0001t0003g0006 others(23): Show |
26 | HG00642.hp2 HG00738.hp2 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.697+1381A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29010563 | |||||||
| chr8:29010915 | T | G | 1 | a0001c0001t0003g0119 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.697+1733T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29010915 | |||||||
| chr8:29010918 | A | G | 1 | a0001c0001t0010g0312 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.697+1736A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29010918 | |||||||
| chr8:29011000 | T | G | 1 | a0001c0001t0003g0075 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.697+1818T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29011000 | |||||||
| chr8:29011188 | T | C | 2 | a0001c0001t0008g0002 a0001c0001t0008g0003 |
2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.697+2006T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29011188 | |||||||
| chr8:29011711 | C | T | 1 | a0001c0001t0008g0123 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.697+2529C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29011711 | |||||||
| chr8:29011714 | G | T | 1 | a0001c0001t0003g0119 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.697+2532G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29011714 | |||||||
| chr8:29011724 | T | A | 1 | a0001c0001t0001g0288 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.697+2542T>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29011724 | |||||||
| chr8:29012014 | A | G | 14 | a0001c0001t0006g0326 a0001c0001t0006g0328 a0001c0001t0006g0329 others(11): Show |
14 | HG00544.hp1 HG02056.hp1 HG02809.hp2 others(11): Show |
intron_variant | MODIFIER | c.697+2832A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29012014 | |||||||
| chr8:29012109 | G | A | 1 | a0001c0001t0008g0339 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.697+2927G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29012109 | |||||||
| chr8:29012120 | C | T | 222 | a0001c0001t0001g0072 a0001c0001t0001g0138 a0001c0001t0001g0139 others(219): Show |
223 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.697+2938C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29012120 | |||||||
| chr8:29012418 | T | C | 1 | a0001c0001t0008g0123 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.697+3236T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29012418 | |||||||
| chr8:29012427 | A | G | 2 | a0001c0001t0008g0002 a0001c0001t0008g0003 |
2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.697+3245A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29012427 | |||||||
| chr8:29012454 | A | G | 2 | a0001c0001t0004g0036 a0001c0001t0004g0039 |
2 | HG03710.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.697+3272A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29012454 | |||||||
| chr8:29012570 | A | C | 1 | a0001c0001t0009g0129 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.697+3388A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29012570 | |||||||
| chr8:29012596 | G | A | 2 | a0001c0001t0007g0005 a0001c0001t0007g0062 |
2 | HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.697+3414G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29012596 | |||||||
| chr8:29012611 | G | A | 50 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(47): Show |
50 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.697+3429G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29012611 | |||||||
| chr8:29013053 | A | C | 1 | a0001c0001t0007g0015 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.697+3871A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29013053 | |||||||
| chr8:29013245 | C | T | 1 | a0001c0001t0002g0189 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.697+4063C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29013245 | |||||||
| chr8:29013267 | C | T | 1 | a0001c0001t0002g0219 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.697+4085C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29013267 | |||||||
| chr8:29013282 | C | T | 1 | a0001c0001t0003g0093 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.697+4100C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29013282 | |||||||
| chr8:29013335 | C | G | 10 | a0001c0001t0007g0010 a0001c0001t0007g0011 a0001c0001t0007g0012 others(7): Show |
10 | HG01261.hp1 HG02257.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.697+4153C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29013335 | |||||||
| chr8:29013362 | C | T | 1 | a0001c0001t0002g0001 | 2 | HG02486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.697+4180C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29013362 | |||||||
| chr8:29013386 | G | A | 1 | a0001c0001t0008g0123 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.697+4204G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29013386 | |||||||
| chr8:29013474 | T | G | 10 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0122 others(7): Show |
10 | HG02280.hp1 HG02572.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.697+4292T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29013474 | |||||||
| chr8:29013640 | G | A | 1 | a0001c0001t0004g0022 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.697+4458G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29013640 | |||||||
| chr8:29013730 | T | A | 1 | a0001c0001t0001g0294 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.697+4548T>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29013730 | |||||||
| chr8:29014086 | TC | T | 334 | a0001c0001t0001g0072 a0001c0001t0001g0138 a0001c0001t0001g0139 others(331): Show |
335 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(332): Show |
intron_variant | MODIFIER | c.698-4670delC | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr8 | 29014086 | ||||||
| chr8:29014126 | T | C | 1 | a0001c0001t0004g0029 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.698-4634T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29014126 | |||||||
| chr8:29014208 | A | G | 1 | a0001c0001t0007g0015 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.698-4552A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29014208 | |||||||
| chr8:29014212 | G | T | 15 | a0001c0001t0006g0326 a0001c0001t0006g0328 a0001c0001t0006g0329 others(12): Show |
15 | HG00544.hp1 HG02056.hp1 HG02809.hp2 others(12): Show |
intron_variant | MODIFIER | c.698-4548G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29014212 | |||||||
| chr8:29014270 | GA | G | 119 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(116): Show |
119 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.698-4484delA | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr8 | 29014270 | ||||||
| chr8:29014286 | A | G | 1 | a0001c0001t0001g0143 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.698-4474A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29014286 | |||||||
| chr8:29014336 | T | A | 3 | a0001c0001t0005g0215 a0001c0001t0005g0216 a0001c0001t0005g0217 |
3 | HG02559.hp1 HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.698-4424T>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29014336 | |||||||
| chr8:29014573 | C | T | 2 | a0001c0001t0003g0122 a0001c0001t0008g0121 |
2 | HG03195.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.698-4187C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29014573 | |||||||
| chr8:29014719 | G | A | 4 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0122 others(1): Show |
4 | HG02280.hp1 HG03195.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.698-4041G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29014719 | |||||||
| chr8:29014780 | A | G | 2 | a0001c0001t0002g0133 a0001c0001t0002g0259 |
2 | HG00438.hp2 NA18949.hp1 |
intron_variant | MODIFIER | c.698-3980A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29014780 | |||||||
| chr8:29014943 | G | A | 6 | a0001c0001t0004g0004 a0001c0001t0004g0124 a0001c0001t0004g0125 others(3): Show |
6 | HG00741.hp2 HG02109.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.698-3817G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29014943 | |||||||
| chr8:29014975 | C | T | 1 | a0001c0001t0003g0097 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.698-3785C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29014975 | |||||||
| chr8:29015058 | T | C | 1 | a0001c0001t0003g0119 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.698-3702T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29015058 | |||||||
| chr8:29015305 | T | C | 1 | a0001c0001t0003g0122 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.698-3455T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29015305 | |||||||
| chr8:29015365 | A | G | 1 | a0001c0001t0004g0019 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.698-3395A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29015365 | |||||||
| chr8:29015395 | C | G | 1 | a0001c0001t0003g0122 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.698-3365C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29015395 | |||||||
| chr8:29015438 | A | G | 1 | a0001c0001t0003g0165 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.698-3322A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29015438 | |||||||
| chr8:29015466 | T | C | 1 | a0001c0001t0001g0309 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.698-3294T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29015466 | |||||||
| chr8:29015472 | C | T | 1 | a0001c0001t0001g0146 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.698-3288C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29015472 | |||||||
| chr8:29015527 | C | T | 6 | a0001c0001t0006g0333 a0001c0001t0006g0335 a0001c0001t0006g0336 others(3): Show |
6 | NA18943.hp2 NA18956.hp1 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.698-3233C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29015527 | |||||||
| chr8:29015701 | G | A | 1 | a0001c0001t0008g0123 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.698-3059G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29015701 | |||||||
| chr8:29015774 | G | C | 1 | a0001c0001t0007g0010 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.698-2986G>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29015774 | |||||||
| chr8:29016113 | T | C | 1 | a0001c0001t0001g0234 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.698-2647T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29016113 | |||||||
| chr8:29016114 | T | C | 1 | a0001c0001t0001g0246 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.698-2646T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29016114 | |||||||
| chr8:29016232 | T | C | 1 | a0001c0001t0001g0138 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.698-2528T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29016232 | |||||||
| chr8:29016995 | A | C | 15 | a0001c0001t0006g0326 a0001c0001t0006g0328 a0001c0001t0006g0329 others(12): Show |
15 | HG00544.hp1 HG02056.hp1 HG02809.hp2 others(12): Show |
intron_variant | MODIFIER | c.698-1765A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29016995 | |||||||
| chr8:29017001 | A | G | 4 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0122 others(1): Show |
4 | HG02280.hp1 HG03195.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.698-1759A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29017001 | |||||||
| chr8:29017309 | A | G | 1 | a0001c0001t0007g0012 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.698-1451A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29017309 | |||||||
| chr8:29017581 | A | T | 1 | a0001c0001t0003g0085 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.698-1179A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29017581 | |||||||
| chr8:29017914 | C | T | 4 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0122 others(1): Show |
4 | HG02280.hp1 HG03195.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.698-846C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29017914 | |||||||
| chr8:29017991 | G | C | 2 | a0001c0001t0002g0191 a0001c0001t0002g0195 |
2 | HG00438.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.698-769G>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29017991 | |||||||
| chr8:29018399 | A | G | 1 | a0001c0001t0003g0181 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.698-361A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29018399 | |||||||
| chr8:29018704 | T | C | 163 | a0001c0001t0001g0148 a0001c0001t0003g0006 a0001c0001t0003g0007 others(160): Show |
163 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(160): Show |
intron_variant | MODIFIER | c.698-56T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29018704 | |||||||
| chr8:29018935 | G | A | 1 | a0001c0001t0001g0229 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.851+22G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29018935 | |||||||
| chr8:29019049 | A | G | 2 | a0001c0001t0003g0324 a0001c0001t0003g0325 |
2 | HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.851+136A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29019049 | |||||||
| chr8:29019076 | C | G | 244 | a0001c0001t0001g0072 a0001c0001t0001g0138 a0001c0001t0001g0139 others(241): Show |
244 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.851+163C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29019076 | |||||||
| chr8:29019119 | C | T | 1 | a0001c0001t0001g0287 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.851+206C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29019119 | |||||||
| chr8:29019345 | A | T | 12 | a0001c0001t0003g0134 a0001c0001t0003g0153 a0001c0001t0003g0158 others(9): Show |
12 | HG02257.hp1 HG02280.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.851+432A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29019345 | |||||||
| chr8:29019436 | C | T | 2 | a0001c0001t0003g0324 a0001c0001t0003g0325 |
2 | HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.851+523C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29019436 | |||||||
| chr8:29019671 | C | T | 1 | a0001c0001t0007g0062 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.851+758C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29019671 | |||||||
| chr8:29019773 | T | C | 14 | a0001c0001t0006g0326 a0001c0001t0006g0328 a0001c0001t0006g0329 others(11): Show |
14 | HG00544.hp1 HG02056.hp1 HG02809.hp2 others(11): Show |
intron_variant | MODIFIER | c.851+860T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29019773 | |||||||
| chr8:29019788 | T | C | 5 | a0001c0001t0002g0275 a0001c0001t0002g0276 a0001c0001t0002g0277 others(2): Show |
5 | NA18612.hp1 NA18953.hp1 NA18957.hp1 others(2): Show |
intron_variant | MODIFIER | c.851+875T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29019788 | |||||||
| chr8:29019872 | G | A | 2 | a0001c0001t0005g0291 a0001c0001t0005g0302 |
2 | HG01516.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.851+959G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29019872 | |||||||
| chr8:29020109 | A | G | 3 | a0001c0001t0002g0092 a0001c0001t0002g0192 a0001c0001t0019g0162 |
3 | NA18990.hp1 NA18992.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.851+1196A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29020109 | |||||||
| chr8:29020188 | A | G | 1 | a0001c0001t0008g0121 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.851+1275A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29020188 | |||||||
| chr8:29020243 | G | A | 4 | a0001c0001t0004g0124 a0001c0001t0004g0125 a0001c0001t0004g0126 others(1): Show |
4 | HG02109.hp2 HG02896.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.851+1330G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29020243 | |||||||
| chr8:29020480 | C | T | 1 | a0001c0001t0005g0301 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.851+1567C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29020480 | |||||||
| chr8:29020562 | A | G | 12 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0021 others(9): Show |
12 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(9): Show |
intron_variant | MODIFIER | c.851+1649A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29020562 | |||||||
| chr8:29020753 | A | G | 4 | a0001c0001t0001g0072 a0001c0001t0001g0140 a0001c0001t0001g0141 others(1): Show |
4 | HG02027.hp2 NA18975.hp2 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.851+1840A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29020753 | |||||||
| chr8:29021574 | G | A | 1 | a0001c0001t0003g0120 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.851+2661G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29021574 | |||||||
| chr8:29021621 | C | T | 1 | a0001c0001t0001g0154 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.851+2708C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29021621 | |||||||
| chr8:29021622 | G | A | 1 | a0001c0001t0001g0221 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.851+2709G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29021622 | |||||||
| chr8:29021631 | G | A | 2 | a0001c0001t0002g0295 a0001c0001t0002g0296 |
2 | NA18968.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.851+2718G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29021631 | |||||||
| chr8:29021638 | G | A | 1 | a0001c0001t0001g0145 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.851+2725G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29021638 | |||||||
| chr8:29021717 | G | T | 3 | a0001c0001t0003g0120 a0001c0001t0003g0122 a0001c0001t0008g0121 |
3 | HG03195.hp2 HG03471.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.851+2804G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29021717 | |||||||
| chr8:29021728 | C | T | 1 | a0001c0001t0010g0300 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.851+2815C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29021728 | |||||||
| chr8:29021801 | G | A | 10 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0122 others(7): Show |
10 | HG02280.hp1 HG02572.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.851+2888G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29021801 | |||||||
| chr8:29021859 | C | CA | 123 | a0001c0001t0001g0145 a0001c0001t0001g0148 a0001c0001t0001g0315 others(120): Show |
123 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.851+2963dupA | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr8 | 29021859 | ||||||
| chr8:29021859 | C | CAA | 16 | a0001c0001t0003g0097 a0001c0001t0003g0134 a0001c0001t0003g0153 others(13): Show |
16 | HG01069.hp2 HG01167.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.851+2962_851+2963d others(4): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr8 | 29021859 | ||||||
| chr8:29021989 | T | TGGGC | 80 | a0001c0001t0001g0072 a0001c0001t0001g0138 a0001c0001t0001g0139 others(77): Show |
80 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.851+3077_851+3080d others(6): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr8 | 29021989 | ||||||
| chr8:29022182 | T | A | 2 | a0001c0001t0003g0122 a0001c0001t0008g0121 |
2 | HG03195.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.851+3269T>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29022182 | |||||||
| chr8:29022234 | T | C | 1 | a0001c0001t0007g0017 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.851+3321T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29022234 | |||||||
| chr8:29022494 | A | G | 31 | a0001c0001t0004g0030 a0001c0001t0004g0031 a0001c0001t0004g0034 others(28): Show |
31 | HG00280.hp1 HG00544.hp2 HG00597.hp1 others(28): Show |
intron_variant | MODIFIER | c.851+3581A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29022494 | |||||||
| chr8:29022524 | G | A | 1 | a0001c0001t0004g0128 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.851+3611G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29022524 | |||||||
| chr8:29022643 | C | T | 10 | a0001c0001t0007g0010 a0001c0001t0007g0011 a0001c0001t0007g0012 others(7): Show |
10 | HG01261.hp1 HG02257.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.851+3730C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29022643 | |||||||
| chr8:29022882 | A | G | 1 | a0001c0001t0004g0110 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.851+3969A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29022882 | |||||||
| chr8:29023060 | T | TAA | 6 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0075 others(3): Show |
6 | HG00735.hp1 HG01928.hp2 HG02300.hp1 others(3): Show |
intron_variant | MODIFIER | c.851+4149_851+4150d others(4): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr8 | 29023060 | ||||||
| chr8:29023235 | T | C | 244 | a0001c0001t0001g0072 a0001c0001t0001g0138 a0001c0001t0001g0139 others(241): Show |
244 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.851+4322T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29023235 | |||||||
| chr8:29023514 | C | T | 14 | a0001c0001t0003g0079 a0001c0001t0003g0080 a0001c0001t0003g0081 others(11): Show |
14 | HG00609.hp1 HG02080.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.851+4601C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29023514 | |||||||
| chr8:29023543 | C | CA | 5 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0122 others(2): Show |
5 | HG02280.hp1 HG02965.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.851+4631dupA | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr8 | 29023543 | ||||||
| chr8:29023646 | C | T | 6 | a0001c0001t0004g0004 a0001c0001t0004g0124 a0001c0001t0004g0125 others(3): Show |
6 | HG00741.hp2 HG02109.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.851+4733C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29023646 | |||||||
| chr8:29023662 | A | G | 2 | a0001c0001t0007g0005 a0001c0001t0007g0062 |
2 | HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.851+4749A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29023662 | |||||||
| chr8:29023744 | C | A | 2 | a0001c0001t0002g0261 a0001c0001t0002g0262 |
2 | NA18941.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.851+4831C>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29023744 | |||||||
| chr8:29023763 | A | T | 3 | a0001c0001t0016g0327 a0001c0001t0016g0330 a0001c0001t0023g0331 |
3 | NA18947.hp1 NA18982.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.851+4850A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29023763 | |||||||
| chr8:29023811 | A | C | 259 | a0001c0001t0001g0072 a0001c0001t0001g0138 a0001c0001t0001g0139 others(256): Show |
260 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.851+4898A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29023811 | |||||||
| chr8:29024393 | G | A | 79 | a0001c0001t0001g0072 a0001c0001t0001g0138 a0001c0001t0001g0139 others(76): Show |
79 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.851+5480G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29024393 | |||||||
| chr8:29024412 | G | C | 1 | a0001c0001t0004g0064 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.851+5499G>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29024412 | |||||||
| chr8:29024612 | T | C | 12 | a0001c0001t0003g0134 a0001c0001t0003g0153 a0001c0001t0003g0158 others(9): Show |
12 | HG02257.hp1 HG02280.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.851+5699T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29024612 | |||||||
| chr8:29024920 | C | T | 12 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0021 others(9): Show |
12 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(9): Show |
intron_variant | MODIFIER | c.851+6007C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29024920 | |||||||
| chr8:29024984 | G | A | 1 | a0001c0001t0001g0315 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.851+6071G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29024984 | |||||||
| chr8:29025093 | A | G | 2 | a0001c0001t0001g0222 a0001c0001t0001g0223 |
2 | HG02723.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.851+6180A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29025093 | |||||||
| chr8:29025398 | A | G | 1 | a0001c0001t0009g0082 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.851+6485A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29025398 | |||||||
| chr8:29025473 | GTTA | G | 10 | a0001c0001t0007g0010 a0001c0001t0007g0011 a0001c0001t0007g0012 others(7): Show |
10 | HG01261.hp1 HG02257.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.851+6565_851+6567d others(5): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr8 | 29025473 | ||||||
| chr8:29025871 | C | A | 1 | a0001c0001t0008g0339 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.851+6958C>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29025871 | |||||||
| chr8:29025897 | T | C | 2 | a0001c0001t0008g0002 a0001c0001t0008g0003 |
2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.851+6984T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29025897 | |||||||
| chr8:29026043 | T | TAC | 12 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0288 others(9): Show |
12 | HG00323.hp1 HG01123.hp2 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.851+7168_851+7169d others(4): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr8 | 29026043 | ||||||
| chr8:29026043 | T | TACAC | 7 | a0001c0001t0001g0315 a0001c0001t0002g0135 a0001c0001t0002g0170 others(4): Show |
7 | HG00423.hp2 HG01943.hp1 HG02056.hp2 others(4): Show |
intron_variant | MODIFIER | c.851+7166_851+7169d others(6): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr8 | 29026043 | ||||||
| chr8:29026043 | T | TACACACA others(5): Show |
1 | a0001c0001t0003g0120 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.851+7158_851+7169d others(14): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr8 | 29026043 | ||||||
| chr8:29026043 | TAC | T | 149 | a0001c0001t0001g0072 a0001c0001t0001g0138 a0001c0001t0001g0139 others(146): Show |
150 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(147): Show |
intron_variant | MODIFIER | c.851+7168_851+7169d others(4): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr8 | 29026043 | ||||||
| chr8:29026043 | TACAC | T | 48 | a0001c0001t0002g0152 a0001c0001t0002g0166 a0001c0001t0002g0295 others(45): Show |
48 | HG00544.hp1 HG00735.hp1 HG00738.hp2 others(45): Show |
intron_variant | MODIFIER | c.851+7166_851+7169d others(6): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr8 | 29026043 | ||||||
| chr8:29026043 | TACACAC | T | 43 | a0001c0001t0004g0004 a0001c0001t0004g0019 a0001c0001t0004g0020 others(40): Show |
43 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(40): Show |
intron_variant | MODIFIER | c.851+7164_851+7169d others(8): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr8 | 29026043 | ||||||
| chr8:29026043 | TACACACA others(7): Show |
T | 2 | a0001c0001t0003g0324 a0001c0001t0003g0325 |
2 | HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.851+7156_851+7169d others(16): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr8 | 29026043 | ||||||
| chr8:29026179 | C | G | 1 | a0001c0001t0002g0156 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.851+7266C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29026179 | |||||||
| chr8:29026235 | A | G | 1 | a0001c0001t0008g0123 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.851+7322A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29026235 | |||||||
| chr8:29026398 | T | C | 1 | a0001c0001t0008g0121 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.851+7485T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29026398 | |||||||
| chr8:29026445 | G | T | 1 | a0001c0001t0002g0212 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.851+7532G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29026445 | |||||||
| chr8:29026517 | T | C | 1 | a0001c0001t0008g0123 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.851+7604T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29026517 | |||||||
| chr8:29027037 | G | T | 1 | a0001c0001t0002g0161 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.851+8124G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29027037 | |||||||
| chr8:29027131 | C | T | 1 | a0001c0001t0003g0325 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.851+8218C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29027131 | |||||||
| chr8:29027178 | G | C | 1 | a0001c0001t0004g0019 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.851+8265G>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29027178 | |||||||
| chr8:29027236 | G | A | 1 | a0001c0001t0002g0155 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.851+8323G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29027236 | |||||||
| chr8:29027289 | C | G | 2 | a0001c0001t0006g0335 a0001c0001t0006g0336 |
2 | NA18943.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.851+8376C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29027289 | |||||||
| chr8:29027374 | G | A | 1 | a0001c0001t0001g0220 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.851+8461G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29027374 | |||||||
| chr8:29027396 | G | T | 2 | a0001c0001t0002g0317 a0001c0001t0003g0078 |
2 | HG00558.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.851+8483G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29027396 | |||||||
| chr8:29027953 | T | C | 80 | a0001c0001t0001g0072 a0001c0001t0001g0138 a0001c0001t0001g0139 others(77): Show |
80 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.851+9040T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29027953 | |||||||
| chr8:29028087 | A | T | 7 | a0001c0001t0001g0227 a0001c0001t0001g0238 a0001c0001t0001g0244 others(4): Show |
7 | HG02040.hp2 NA18964.hp1 NA18980.hp1 others(4): Show |
intron_variant | MODIFIER | c.851+9174A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29028087 | |||||||
| chr8:29028112 | C | T | 2 | a0001c0001t0003g0324 a0001c0001t0003g0325 |
2 | HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.851+9199C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29028112 | |||||||
| chr8:29028144 | T | C | 118 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(115): Show |
118 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.851+9231T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29028144 | |||||||
| chr8:29028387 | A | G | 1 | a0001c0001t0002g0208 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.851+9474A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29028387 | |||||||
| chr8:29028462 | T | C | 11 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0122 others(8): Show |
11 | HG02280.hp1 HG02572.hp1 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.851+9549T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29028462 | |||||||
| chr8:29028559 | A | G | 2 | a0001c0001t0003g0324 a0001c0001t0003g0325 |
2 | HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.851+9646A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29028559 | |||||||
| chr8:29028573 | CT | C | 4 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0122 others(1): Show |
4 | HG02280.hp1 HG03195.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.851+9661delT | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29028573 | |||||||
| chr8:29028577 | C | G | 1 | a0001c0001t0003g0119 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.851+9664C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29028577 | |||||||
| chr8:29028766 | G | A | 2 | a0001c0001t0002g0136 a0001c0001t0002g0137 |
2 | HG00558.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.851+9853G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29028766 | |||||||
| chr8:29028774 | T | A | 11 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0122 others(8): Show |
11 | HG02280.hp1 HG02572.hp1 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.851+9861T>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29028774 | |||||||
| chr8:29028832 | G | A | 1 | a0001c0001t0001g0315 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.851+9919G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29028832 | |||||||
| chr8:29029106 | C | T | 3 | a0001c0001t0006g0116 a0001c0001t0014g0117 a0001c0001t0014g0118 |
3 | HG02572.hp1 HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.851+10193C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29029106 | |||||||
| chr8:29029486 | C | G | 2 | a0001c0001t0002g0261 a0001c0001t0002g0262 |
2 | NA18941.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.851+10573C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29029486 | |||||||
| chr8:29029578 | G | A | 1 | a0001c0001t0007g0017 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.851+10665G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29029578 | |||||||
| chr8:29029611 | G | C | 1 | a0001c0001t0001g0143 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.851+10698G>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29029611 | |||||||
| chr8:29029666 | A | G | 1 | a0001c0001t0004g0060 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.851+10753A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29029666 | |||||||
| chr8:29029706 | C | T | 4 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0122 others(1): Show |
4 | HG02280.hp1 HG03195.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.851+10793C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29029706 | |||||||
| chr8:29029713 | G | C | 3 | a0001c0001t0006g0116 a0001c0001t0014g0117 a0001c0001t0014g0118 |
3 | HG02572.hp1 HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.851+10800G>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29029713 | |||||||
| chr8:29029743 | T | G | 1 | a0001c0001t0006g0326 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.851+10830T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29029743 | |||||||
| chr8:29029903 | T | C | 1 | a0001c0001t0006g0332 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.851+10990T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29029903 | |||||||
| chr8:29029943 | CT | C | 14 | a0001c0001t0006g0326 a0001c0001t0006g0328 a0001c0001t0006g0329 others(11): Show |
14 | HG00544.hp1 HG02056.hp1 HG02809.hp2 others(11): Show |
intron_variant | MODIFIER | c.851+11039delT | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr8 | 29029943 | ||||||
| chr8:29030008 | T | C | 5 | a0001c0001t0003g0324 a0001c0001t0003g0325 a0001c0001t0006g0116 others(2): Show |
5 | HG02572.hp1 HG02886.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.851+11095T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29030008 | |||||||
| chr8:29030169 | T | A | 12 | a0001c0001t0006g0328 a0001c0001t0006g0329 a0001c0001t0006g0333 others(9): Show |
12 | HG00544.hp1 HG02056.hp1 NA18943.hp2 others(9): Show |
intron_variant | MODIFIER | c.851+11256T>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29030169 | |||||||
| chr8:29030179 | G | GT | 122 | a0001c0001t0001g0148 a0001c0001t0002g0259 a0001c0001t0003g0006 others(119): Show |
122 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.851+11282dupT | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr8 | 29030179 | ||||||
| chr8:29030179 | G | GTT | 11 | a0001c0001t0003g0079 a0001c0001t0003g0086 a0001c0001t0003g0179 others(8): Show |
11 | HG00642.hp2 HG01261.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.851+11281_851+1128 others(6): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr8 | 29030179 | ||||||
| chr8:29030179 | GT | G | 9 | a0001c0001t0001g0146 a0001c0001t0001g0299 a0001c0001t0003g0119 others(6): Show |
9 | HG01167.hp2 HG02280.hp1 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.851+11282delT | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr8 | 29030179 | ||||||
| chr8:29030185 | T | G | 1 | a0001c0001t0008g0123 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.851+11272T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29030185 | |||||||
| chr8:29030239 | C | T | 1 | a0001c0001t0003g0098 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.851+11326C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29030239 | |||||||
| chr8:29030299 | C | T | 14 | a0001c0001t0006g0326 a0001c0001t0006g0328 a0001c0001t0006g0329 others(11): Show |
14 | HG00544.hp1 HG02056.hp1 HG02809.hp2 others(11): Show |
intron_variant | MODIFIER | c.851+11386C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29030299 | |||||||
| chr8:29030428 | A | G | 14 | a0001c0001t0006g0326 a0001c0001t0006g0328 a0001c0001t0006g0329 others(11): Show |
14 | HG00544.hp1 HG02056.hp1 HG02809.hp2 others(11): Show |
intron_variant | MODIFIER | c.851+11515A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29030428 | |||||||
| chr8:29030518 | C | T | 1 | a0001c0001t0001g0315 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.851+11605C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29030518 | |||||||
| chr8:29030531 | A | G | 3 | a0001c0001t0006g0116 a0001c0001t0014g0117 a0001c0001t0014g0118 |
3 | HG02572.hp1 HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.851+11618A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29030531 | |||||||
| chr8:29030572 | A | G | 1 | a0001c0001t0004g0022 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.851+11659A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29030572 | |||||||
| chr8:29030940 | A | G | 10 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0122 others(7): Show |
10 | HG02280.hp1 HG02572.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.851+12027A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29030940 | |||||||
| chr8:29031192 | A | G | 1 | a0001c0001t0003g0181 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.851+12279A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29031192 | |||||||
| chr8:29031372 | T | C | 69 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(66): Show |
69 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.851+12459T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29031372 | |||||||
| chr8:29031513 | T | C | 1 | a0001c0001t0001g0138 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.851+12600T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29031513 | |||||||
| chr8:29031532 | A | AT | 70 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(67): Show |
70 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.851+12631dupT | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr8 | 29031532 | ||||||
| chr8:29031643 | T | C | 1 | a0001c0001t0005g0282 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.851+12730T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29031643 | |||||||
| chr8:29031649 | A | G | 146 | a0001c0001t0001g0148 a0001c0001t0003g0006 a0001c0001t0003g0007 others(143): Show |
146 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.851+12736A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29031649 | |||||||
| chr8:29032224 | T | C | 1 | a0001c0001t0003g0070 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.852-13137T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29032224 | |||||||
| chr8:29032280 | A | C | 1 | a0001c0001t0001g0249 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.852-13081A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29032280 | |||||||
| chr8:29032352 | A | C | 3 | a0001c0001t0004g0023 a0001c0001t0004g0024 a0001c0001t0004g0027 |
3 | HG01069.hp2 HG01167.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.852-13009A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29032352 | |||||||
| chr8:29032418 | C | T | 2 | a0001c0001t0001g0322 a0001c0001t0001g0323 |
2 | NA18954.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.852-12943C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29032418 | |||||||
| chr8:29032442 | A | C | 5 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0122 others(2): Show |
5 | HG02280.hp1 HG02965.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.852-12919A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29032442 | |||||||
| chr8:29032697 | G | A | 1 | a0001c0001t0001g0148 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.852-12664G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29032697 | |||||||
| chr8:29032802 | T | C | 1 | a0001c0001t0002g0135 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.852-12559T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29032802 | |||||||
| chr8:29032862 | G | A | 1 | a0001c0001t0004g0052 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.852-12499G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29032862 | |||||||
| chr8:29032923 | GATA | G | 8 | a0001c0001t0004g0020 a0001c0001t0004g0021 a0001c0001t0004g0022 others(5): Show |
8 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(5): Show |
intron_variant | MODIFIER | c.852-12429_852-1242 others(7): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr8 | 29032923 | ||||||
| chr8:29033023 | A | G | 1 | a0001c0001t0008g0339 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.852-12338A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29033023 | |||||||
| chr8:29033099 | C | CTAT | 7 | a0001c0001t0001g0227 a0001c0001t0001g0238 a0001c0001t0001g0244 others(4): Show |
7 | HG02040.hp2 NA18964.hp1 NA18980.hp1 others(4): Show |
intron_variant | MODIFIER | c.852-12261_852-1225 others(7): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr8 | 29033099 | ||||||
| chr8:29033200 | G | A | 2 | a0001c0001t0001g0222 a0001c0001t0001g0223 |
2 | HG02723.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.852-12161G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29033200 | |||||||
| chr8:29033267 | G | A | 2 | a0001c0001t0002g0274 a0001c0001t0005g0282 |
2 | HG02258.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.852-12094G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29033267 | |||||||
| chr8:29033270 | A | C | 123 | a0001c0001t0001g0148 a0001c0001t0003g0006 a0001c0001t0003g0007 others(120): Show |
123 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.852-12091A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29033270 | |||||||
| chr8:29033425 | A | G | 4 | a0001c0001t0002g0152 a0001c0001t0002g0166 a0001c0001t0002g0183 others(1): Show |
4 | HG02165.hp2 NA18965.hp2 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.852-11936A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29033425 | |||||||
| chr8:29033646 | C | T | 2 | a0001c0001t0003g0324 a0001c0001t0003g0325 |
2 | HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.852-11715C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29033646 | |||||||
| chr8:29033769 | G | A | 14 | a0001c0001t0006g0326 a0001c0001t0006g0328 a0001c0001t0006g0329 others(11): Show |
14 | HG00544.hp1 HG02056.hp1 HG02809.hp2 others(11): Show |
intron_variant | MODIFIER | c.852-11592G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29033769 | |||||||
| chr8:29034092 | C | A | 1 | a0001c0001t0001g0315 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.852-11269C>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29034092 | |||||||
| chr8:29034260 | C | T | 1 | a0001c0001t0001g0315 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.852-11101C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29034260 | |||||||
| chr8:29034521 | T | C | 1 | a0001c0001t0008g0339 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.852-10840T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29034521 | |||||||
| chr8:29034573 | G | A | 53 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(50): Show |
53 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.852-10788G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29034573 | |||||||
| chr8:29034586 | G | A | 3 | a0001c0001t0006g0116 a0001c0001t0014g0117 a0001c0001t0014g0118 |
3 | HG02572.hp1 HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.852-10775G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29034586 | |||||||
| chr8:29034837 | G | A | 1 | a0001c0001t0008g0339 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.852-10524G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29034837 | |||||||
| chr8:29034862 | A | AAAAT | 4 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0122 others(1): Show |
4 | HG02280.hp1 HG03195.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.852-10483_852-1048 others(8): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr8 | 29034862 | ||||||
| chr8:29034885 | A | G | 6 | a0001c0001t0005g0151 a0001c0001t0005g0171 a0001c0001t0005g0172 others(3): Show |
6 | HG00280.hp2 HG01123.hp1 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.852-10476A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29034885 | |||||||
| chr8:29034906 | T | A | 2 | a0001c0001t0003g0070 a0001c0001t0003g0071 |
2 | HG03688.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.852-10455T>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29034906 | |||||||
| chr8:29034991 | A | G | 3 | a0001c0001t0006g0116 a0001c0001t0014g0117 a0001c0001t0014g0118 |
3 | HG02572.hp1 HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.852-10370A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29034991 | |||||||
| chr8:29035030 | C | T | 2 | a0001c0001t0008g0002 a0001c0001t0008g0003 |
2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.852-10331C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29035030 | |||||||
| chr8:29035140 | G | T | 1 | a0001c0001t0002g0271 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.852-10221G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29035140 | |||||||
| chr8:29035194 | G | C | 1 | a0001c0001t0002g0183 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.852-10167G>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29035194 | |||||||
| chr8:29035362 | A | T | 2 | a0001c0001t0004g0040 a0001c0001t0008g0339 |
2 | HG03209.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.852-9999A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29035362 | |||||||
| chr8:29035376 | T | G | 160 | a0001c0001t0001g0148 a0001c0001t0003g0006 a0001c0001t0003g0007 others(157): Show |
160 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(157): Show |
intron_variant | MODIFIER | c.852-9985T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29035376 | |||||||
| chr8:29035629 | G | A | 1 | a0001c0001t0003g0081 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.852-9732G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29035629 | |||||||
| chr8:29035890 | A | G | 1 | a0001c0001t0008g0339 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.852-9471A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29035890 | |||||||
| chr8:29036023 | C | T | 1 | a0001c0001t0008g0123 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.852-9338C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29036023 | |||||||
| chr8:29036156 | G | T | 3 | a0001c0001t0006g0116 a0001c0001t0014g0117 a0001c0001t0014g0118 |
3 | HG02572.hp1 HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.852-9205G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29036156 | |||||||
| chr8:29036256 | A | G | 1 | a0001c0001t0003g0087 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.852-9105A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29036256 | |||||||
| chr8:29036619 | C | T | 2 | a0001c0001t0002g0261 a0001c0001t0002g0262 |
2 | NA18941.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.852-8742C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29036619 | |||||||
| chr8:29036720 | C | T | 118 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(115): Show |
118 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.852-8641C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29036720 | |||||||
| chr8:29036774 | A | G | 1 | a0001c0001t0008g0339 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.852-8587A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29036774 | |||||||
| chr8:29036869 | A | C | 4 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0122 others(1): Show |
4 | HG02280.hp1 HG03195.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.852-8492A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29036869 | |||||||
| chr8:29036878 | C | T | 80 | a0001c0001t0001g0072 a0001c0001t0001g0138 a0001c0001t0001g0139 others(77): Show |
80 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.852-8483C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29036878 | |||||||
| chr8:29037062 | C | T | 13 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0021 others(10): Show |
13 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.852-8299C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29037062 | |||||||
| chr8:29037161 | G | T | 1 | a0001c0001t0001g0315 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.852-8200G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29037161 | |||||||
| chr8:29037317 | G | T | 1 | a0001c0001t0001g0238 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.852-8044G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29037317 | |||||||
| chr8:29037472 | C | T | 14 | a0001c0001t0006g0326 a0001c0001t0006g0328 a0001c0001t0006g0329 others(11): Show |
14 | HG00544.hp1 HG02056.hp1 HG02809.hp2 others(11): Show |
intron_variant | MODIFIER | c.852-7889C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29037472 | |||||||
| chr8:29037474 | G | A | 146 | a0001c0001t0001g0315 a0001c0001t0003g0006 a0001c0001t0003g0007 others(143): Show |
146 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.852-7887G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29037474 | |||||||
| chr8:29037612 | T | C | 5 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0122 others(2): Show |
5 | HG02280.hp1 HG02965.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.852-7749T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29037612 | |||||||
| chr8:29037651 | G | A | 4 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0122 others(1): Show |
4 | HG02280.hp1 HG03195.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.852-7710G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29037651 | |||||||
| chr8:29037741 | TTGTTTTG others(992): Show |
T | 1 | a0001c0001t0002g0135 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.852-7617_852-6619d others(2): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr8 | 29037741 | ||||||
| chr8:29037904 | T | C | 1 | a0001c0001t0001g0248 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.852-7457T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29037904 | |||||||
| chr8:29038048 | C | T | 1 | a0001c0001t0010g0300 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.852-7313C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29038048 | |||||||
| chr8:29038184 | AC | A | 6 | a0001c0001t0005g0173 a0001c0001t0005g0175 a0001c0001t0005g0176 others(3): Show |
6 | HG02647.hp1 HG02809.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.852-7176delC | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29038184 | |||||||
| chr8:29038258 | T | C | 4 | a0001c0001t0004g0124 a0001c0001t0004g0125 a0001c0001t0004g0126 others(1): Show |
4 | HG02109.hp2 HG02896.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.852-7103T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29038258 | |||||||
| chr8:29038299 | T | C | 1 | a0001c0001t0002g0163 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.852-7062T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29038299 | |||||||
| chr8:29038464 | A | G | 1 | a0001c0001t0003g0119 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.852-6897A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29038464 | |||||||
| chr8:29038985 | G | A | 2 | a0001c0001t0003g0115 a0001c0001t0006g0111 |
2 | NA18945.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.852-6376G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29038985 | |||||||
| chr8:29038997 | T | C | 80 | a0001c0001t0001g0072 a0001c0001t0001g0138 a0001c0001t0001g0139 others(77): Show |
80 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.852-6364T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29038997 | |||||||
| chr8:29039203 | T | C | 1 | a0001c0001t0001g0256 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.852-6158T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29039203 | |||||||
| chr8:29039345 | T | G | 5 | a0001c0001t0003g0324 a0001c0001t0003g0325 a0001c0001t0006g0116 others(2): Show |
5 | HG02572.hp1 HG02886.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.852-6016T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29039345 | |||||||
| chr8:29039491 | T | A | 1 | a0001c0001t0003g0119 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.852-5870T>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29039491 | |||||||
| chr8:29039654 | T | C | 2 | a0001c0001t0005g0291 a0001c0001t0005g0302 |
2 | HG01516.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.852-5707T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29039654 | |||||||
| chr8:29039912 | G | T | 1 | a0001c0001t0003g0075 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.852-5449G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29039912 | |||||||
| chr8:29040310 | A | T | 5 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0122 others(2): Show |
5 | HG02280.hp1 HG02965.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.852-5051A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29040310 | |||||||
| chr8:29040347 | T | C | 1 | a0001c0001t0004g0110 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.852-5014T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29040347 | |||||||
| chr8:29040729 | T | A | 1 | a0001c0001t0001g0315 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.852-4632T>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29040729 | |||||||
| chr8:29040916 | C | T | 259 | a0001c0001t0001g0072 a0001c0001t0001g0138 a0001c0001t0001g0139 others(256): Show |
260 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.852-4445C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29040916 | |||||||
| chr8:29041006 | C | G | 8 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0122 others(5): Show |
8 | HG02280.hp1 HG02572.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.852-4355C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29041006 | |||||||
| chr8:29041012 | A | G | 2 | a0001c0001t0003g0324 a0001c0001t0003g0325 |
2 | HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.852-4349A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29041012 | |||||||
| chr8:29041126 | GTGTT | G | 53 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(50): Show |
53 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.852-4233_852-4230d others(6): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr8 | 29041126 | ||||||
| chr8:29041181 | T | A | 1 | a0001c0001t0006g0116 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.852-4180T>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29041181 | |||||||
| chr8:29041182 | A | T | 58 | a0001c0001t0001g0148 a0001c0001t0003g0006 a0001c0001t0003g0007 others(55): Show |
58 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.852-4179A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29041182 | |||||||
| chr8:29041310 | G | A | 1 | a0001c0001t0004g0019 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.852-4051G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29041310 | |||||||
| chr8:29041340 | C | G | 2 | a0001c0001t0002g0186 a0001c0001t0002g0187 |
2 | NA18978.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.852-4021C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29041340 | |||||||
| chr8:29041818 | T | G | 3 | a0001c0001t0005g0215 a0001c0001t0005g0216 a0001c0001t0005g0217 |
3 | HG02559.hp1 HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.852-3543T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29041818 | |||||||
| chr8:29041820 | C | G | 243 | a0001c0001t0001g0072 a0001c0001t0001g0138 a0001c0001t0001g0139 others(240): Show |
243 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.852-3541C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29041820 | |||||||
| chr8:29042083 | C | T | 2 | a0001c0001t0003g0070 a0001c0001t0003g0071 |
2 | HG03688.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.852-3278C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29042083 | |||||||
| chr8:29042106 | A | G | 14 | a0001c0001t0006g0326 a0001c0001t0006g0328 a0001c0001t0006g0329 others(11): Show |
14 | HG00544.hp1 HG02056.hp1 HG02809.hp2 others(11): Show |
intron_variant | MODIFIER | c.852-3255A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29042106 | |||||||
| chr8:29042146 | A | G | 1 | a0001c0001t0004g0022 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.852-3215A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29042146 | |||||||
| chr8:29042180 | C | G | 159 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(156): Show |
159 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.852-3181C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29042180 | |||||||
| chr8:29042257 | G | A | 8 | a0001c0001t0004g0054 a0001c0001t0004g0055 a0001c0001t0004g0056 others(5): Show |
8 | HG01884.hp1 HG02145.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.852-3104G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29042257 | |||||||
| chr8:29042277 | A | G | 1 | a0001c0001t0003g0325 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.852-3084A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29042277 | |||||||
| chr8:29042455 | G | C | 1 | a0001c0001t0008g0339 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.852-2906G>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29042455 | |||||||
| chr8:29042480 | G | A | 122 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(119): Show |
122 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.852-2881G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29042480 | |||||||
| chr8:29042514 | A | C | 14 | a0001c0001t0006g0326 a0001c0001t0006g0328 a0001c0001t0006g0329 others(11): Show |
14 | HG00544.hp1 HG02056.hp1 HG02809.hp2 others(11): Show |
intron_variant | MODIFIER | c.852-2847A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29042514 | |||||||
| chr8:29042570 | T | C | 149 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(146): Show |
149 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.852-2791T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29042570 | |||||||
| chr8:29043049 | A | G | 1 | a0001c0001t0002g0259 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.852-2312A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29043049 | |||||||
| chr8:29043150 | A | C | 1 | a0001c0001t0004g0019 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.852-2211A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29043150 | |||||||
| chr8:29043295 | C | T | 1 | a0001c0001t0003g0298 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.852-2066C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29043295 | |||||||
| chr8:29043297 | TC | T | 16 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0021 others(13): Show |
16 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(13): Show |
intron_variant | MODIFIER | c.852-2062delC | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr8 | 29043297 | ||||||
| chr8:29043790 | A | T | 1 | a0001c0001t0003g0078 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.852-1571A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29043790 | |||||||
| chr8:29043826 | A | C | 81 | a0001c0001t0001g0072 a0001c0001t0001g0138 a0001c0001t0001g0139 others(78): Show |
81 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.852-1535A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29043826 | |||||||
| chr8:29043869 | G | A | 1 | a0001c0001t0002g0212 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.852-1492G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29043869 | |||||||
| chr8:29043985 | C | G | 1 | a0001c0001t0001g0288 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.852-1376C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29043985 | |||||||
| chr8:29044175 | G | A | 3 | a0001c0001t0001g0169 a0001c0001t0001g0232 a0001c0001t0015g0233 |
3 | HG00639.hp2 HG01069.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.852-1186G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29044175 | |||||||
| chr8:29044260 | G | C | 69 | a0001c0001t0001g0072 a0001c0001t0001g0138 a0001c0001t0001g0140 others(66): Show |
69 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.852-1101G>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29044260 | |||||||
| chr8:29044310 | C | G | 2 | a0001c0001t0002g0183 a0001c0001t0011g0313 |
2 | NA18965.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.852-1051C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29044310 | |||||||
| chr8:29044352 | T | C | 1 | a0001c0001t0004g0058 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.852-1009T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29044352 | |||||||
| chr8:29044453 | G | C | 1 | a0001c0001t0001g0244 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.852-908G>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29044453 | |||||||
| chr8:29044793 | ACT | A | 3 | a0001c0001t0006g0116 a0001c0001t0014g0117 a0001c0001t0014g0118 |
3 | HG02572.hp1 HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.852-565_852-564del others(2): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr8 | 29044793 | ||||||
| chr8:29045005 | TC | T | 3 | a0001c0001t0001g0169 a0001c0001t0001g0232 a0001c0001t0015g0233 |
3 | HG00639.hp2 HG01069.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.852-354delC | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr8 | 29045005 | ||||||
| chr8:29045242 | C | T | 31 | a0001c0001t0004g0030 a0001c0001t0004g0031 a0001c0001t0004g0034 others(28): Show |
31 | HG00280.hp1 HG00544.hp2 HG00597.hp1 others(28): Show |
intron_variant | MODIFIER | c.852-119C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29045242 | |||||||
| chr8:29045298 | G | T | 1 | a0001c0001t0001g0254 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.852-63G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29045298 | |||||||
| chr8:29046496 | A | T | 1 | a0001c0001t0004g0021 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.935-862A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 7/9 | chr8 | 29046496 | |||||||
| chr8:29046569 | G | T | 117 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(114): Show |
117 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(114): Show |
intron_variant | MODIFIER | c.935-789G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 7/9 | chr8 | 29046569 | |||||||
| chr8:29046706 | T | G | 2 | a0001c0001t0001g0225 a0001c0001t0001g0226 |
2 | HG00140.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.935-652T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 7/9 | chr8 | 29046706 | |||||||
| chr8:29046785 | A | C | 1 | a0001c0001t0006g0116 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.935-573A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 7/9 | chr8 | 29046785 | |||||||
| chr8:29047018 | T | A | 1 | a0001c0001t0002g0187 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.935-340T>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 7/9 | chr8 | 29047018 | |||||||
| chr8:29047258 | C | T | 1 | a0001c0001t0002g0191 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.935-100C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 7/9 | chr8 | 29047258 | |||||||
| chr8:29047501 | G | A | 1 | a0001c0001t0002g0212 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1030+48G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 8/9 | chr8 | 29047501 | |||||||
| chr8:29047527 | A | G | 4 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0122 others(1): Show |
4 | HG02280.hp1 HG03195.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1030+74A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 8/9 | chr8 | 29047527 | |||||||
| chr8:29047539 | G | A | 1 | a0001c0001t0002g0001 | 2 | HG02486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1030+86G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 8/9 | chr8 | 29047539 | |||||||
| chr8:29047564 | C | CT | 30 | a0001c0001t0001g0148 a0001c0001t0001g0228 a0001c0001t0002g0209 others(27): Show |
30 | HG00544.hp1 HG01109.hp1 HG02056.hp1 others(27): Show |
intron_variant | MODIFIER | c.1030+131dupT | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr8 | 29047564 | ||||||
| chr8:29047564 | CT | C | 70 | a0001c0001t0001g0144 a0001c0001t0001g0169 a0001c0001t0001g0240 others(67): Show |
70 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.1030+131delT | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr8 | 29047564 | ||||||
| chr8:29047602 | T | C | 1 | a0001c0001t0001g0239 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1030+149T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 8/9 | chr8 | 29047602 | |||||||
| chr8:29047830 | A | G | 161 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(158): Show |
161 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(158): Show |
intron_variant | MODIFIER | c.1030+377A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 8/9 | chr8 | 29047830 | |||||||
| chr8:29048029 | C | G | 1 | a0001c0001t0001g0255 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1030+576C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 8/9 | chr8 | 29048029 | |||||||
| chr8:29048113 | C | T | 1 | a0001c0001t0008g0068 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1030+660C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 8/9 | chr8 | 29048113 | |||||||
| chr8:29048228 | AAT | A | 3 | a0001c0001t0006g0116 a0001c0001t0014g0117 a0001c0001t0014g0118 |
3 | HG02572.hp1 HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1031-723_1031-722d others(4): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr8 | 29048228 | ||||||
| chr8:29048234 | G | A | 1 | a0001c0001t0008g0339 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1031-720G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 8/9 | chr8 | 29048234 | |||||||
| chr8:29048440 | T | C | 1 | a0001c0001t0008g0339 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1031-514T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 8/9 | chr8 | 29048440 | |||||||
| chr8:29048440 | T | G | 2 | a0001c0001t0012g0174 a0001c0001t0012g0297 |
2 | HG02886.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1031-514T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 8/9 | chr8 | 29048440 | |||||||
| chr8:29048735 | C | T | 1 | a0001c0001t0008g0339 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1031-219C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 8/9 | chr8 | 29048735 | |||||||
| chr8:29049300 | A | C | 3 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 |
3 | NA18975.hp2 NA18998.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.1125+252A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 9/9 | chr8 | 29049300 | |||||||
| chr8:29049718 | C | T | 7 | a0001c0001t0004g0036 a0001c0001t0004g0039 a0001c0001t0007g0011 others(4): Show |
7 | HG02257.hp2 HG02630.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.1125+670C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 9/9 | chr8 | 29049718 | |||||||
| chr8:29049894 | T | C | 1 | a0001c0001t0008g0121 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1125+846T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 9/9 | chr8 | 29049894 | |||||||
| chr8:29049910 | C | T | 1 | a0001c0001t0002g0135 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1125+862C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 9/9 | chr8 | 29049910 | |||||||
| chr8:29049916 | T | A | 68 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(65): Show |
68 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.1125+868T>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 9/9 | chr8 | 29049916 | |||||||
| chr8:29050224 | T | G | 1 | a0001c0001t0003g0009 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1126-794T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 9/9 | chr8 | 29050224 | |||||||
| chr8:29050245 | A | T | 1 | a0001c0001t0001g0221 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1126-773A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 9/9 | chr8 | 29050245 | |||||||
| chr8:29050404 | C | T | 2 | a0001c0001t0003g0324 a0001c0001t0003g0325 |
2 | HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1126-614C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 9/9 | chr8 | 29050404 | |||||||
| chr8:29050459 | C | T | 1 | a0001c0001t0002g0195 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1126-559C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 9/9 | chr8 | 29050459 | |||||||
| chr8:29050460 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1126-558G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 9/9 | chr8 | 29050460 | |||||||
| chr8:29050466 | G | A | 2 | a0001c0001t0012g0174 a0001c0001t0012g0297 |
2 | HG02886.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1126-552G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 9/9 | chr8 | 29050466 | |||||||
| chr8:29050503 | ATTCTTTT others(1): Show |
A | 8 | a0001c0001t0004g0054 a0001c0001t0004g0055 a0001c0001t0004g0056 others(5): Show |
8 | HG01884.hp1 HG02145.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1126-504_1126-497d others(10): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr8 | 29050503 | ||||||
| chr8:29050550 | G | A | 11 | a0001c0001t0002g0261 a0001c0001t0002g0262 a0001c0001t0002g0265 others(8): Show |
11 | NA18612.hp1 NA18941.hp1 NA18952.hp2 others(8): Show |
intron_variant | MODIFIER | c.1126-468G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 9/9 | chr8 | 29050550 | |||||||
| chr8:29050704 | G | C | 1 | a0001c0001t0010g0300 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1126-314G>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 9/9 | chr8 | 29050704 | |||||||
| chr8:29050879 | A | G | 1 | a0001c0001t0008g0339 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1126-139A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 9/9 | chr8 | 29050879 | |||||||
| chr8:29050904 | C | T | 1 | a0001c0001t0001g0254 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1126-114C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 9/9 | chr8 | 29050904 |