Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 25813 |
| ensemblid | ENSG00000100347.15 |
| hgncid | 24276 |
| symbol | SAMM50 |
| name | SAMM50 sorting and assembly machinery component |
| refseq_nuc | NM_015380.5 |
| refseq_prot | NP_056195.3 |
| ensembl_nuc | ENST00000350028.5 |
| ensembl_prot | ENSP00000345445.4 |
| mane_status | MANE Select |
| chr | chr22 |
| start | 43955442 |
| end | 43996529 |
| strand | + |
| ver | v1.2 |
| region | chr22:43955442-43996529 |
| region5000 | chr22:43950442-44001529 |
| regionname0 | SAMM50_chr22_43955442_43996529 |
| regionname5000 | SAMM50_chr22_43950442_44001529 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 469 | 198 | 75 | 25 | 73 | 5 | 20 | 55 | SAMM50_chr22_43950442_44001529 | SAMM50 | MGTVH others(464): Show |
chr22 | 43950442 | 44001529 |
| a0002 | 0/1 | 469 | 100 | 10 | 24 | 54 | 6 | 5 | 40 | SAMM50_chr22_43950442_44001529 | SAMM50 | MGTVH others(464): Show |
chr22 | 43950442 | 44001529 |
| a0003 | 1/0 | 469 | 78 | 9 | 21 | 28 | 5 | 14 | 21 | SAMM50_chr22_43950442_44001529 | SAMM50 | MGTVH others(464): Show |
chr22 | 43950442 | 44001529 |
| a0004 | 0/0 | 469 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | MGTVH others(464): Show |
chr22 | 43950442 | 44001529 |
| a0005 | 0/0 | 469 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | MGTVH others(464): Show |
chr22 | 43950442 | 44001529 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002 | 0/0 | 1407 | 77 | 36 | 6 | 22 | 1 | 12 | SAMM50_chr22_43950442_44001529 | SAMM50 | ATGGG others(1402): Show |
chr22 | 43950442 | 44001529 | ||
| a0001c0004 | 0/0 | 1407 | 73 | 3 | 10 | 50 | 3 | 7 | SAMM50_chr22_43950442_44001529 | SAMM50 | ATGGG others(1402): Show |
chr22 | 43950442 | 44001529 | ||
| a0001c0005 | 0/0 | 1407 | 10 | 10 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | ATGGG others(1402): Show |
chr22 | 43950442 | 44001529 | ||
| a0001c0006 | 0/0 | 1407 | 10 | 7 | 2 | 0 | 0 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | ATGGG others(1402): Show |
chr22 | 43950442 | 44001529 | ||
| a0001c0007 | 0/0 | 1407 | 9 | 3 | 5 | 0 | 1 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | ATGGG others(1402): Show |
chr22 | 43950442 | 44001529 | ||
| a0001c0008 | 0/0 | 1407 | 9 | 8 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | ATGGG others(1402): Show |
chr22 | 43950442 | 44001529 | ||
| a0001c0009 | 0/0 | 1407 | 3 | 2 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | ATGGG others(1402): Show |
chr22 | 43950442 | 44001529 | ||
| a0001c0010 | 0/0 | 1407 | 3 | 3 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | ATGGG others(1402): Show |
chr22 | 43950442 | 44001529 | ||
| a0001c0013 | 0/0 | 1407 | 2 | 2 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | ATGGG others(1402): Show |
chr22 | 43950442 | 44001529 | ||
| a0001c0017 | 0/0 | 1407 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | ATGGG others(1402): Show |
chr22 | 43950442 | 44001529 | ||
| a0001c0020 | 0/0 | 1407 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | ATGGG others(1402): Show |
chr22 | 43950442 | 44001529 | ||
| a0002c0001 | 0/1 | 1407 | 93 | 7 | 22 | 53 | 5 | 5 | SAMM50_chr22_43950442_44001529 | SAMM50 | ATGGG others(1402): Show |
chr22 | 43950442 | 44001529 | ||
| a0002c0011 | 0/0 | 1407 | 3 | 2 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | ATGGG others(1402): Show |
chr22 | 43950442 | 44001529 | ||
| a0002c0012 | 0/0 | 1407 | 3 | 1 | 1 | 0 | 1 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | ATGGG others(1402): Show |
chr22 | 43950442 | 44001529 | ||
| a0002c0018 | 0/0 | 1407 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | ATGGG others(1402): Show |
chr22 | 43950442 | 44001529 | ||
| a0003c0003 | 1/0 | 1407 | 75 | 9 | 21 | 25 | 5 | 14 | SAMM50_chr22_43950442_44001529 | SAMM50 | ATGGG others(1402): Show |
chr22 | 43950442 | 44001529 | ||
| a0003c0014 | 0/0 | 1407 | 2 | 0 | 0 | 2 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | ATGGG others(1402): Show |
chr22 | 43950442 | 44001529 | ||
| a0003c0016 | 0/0 | 1407 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | ATGGG others(1402): Show |
chr22 | 43950442 | 44001529 | ||
| a0004c0015 | 0/0 | 1407 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | ATGGG others(1402): Show |
chr22 | 43950442 | 44001529 | ||
| a0005c0019 | 0/0 | 1407 | 1 | 0 | 0 | 0 | 0 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | ATGGG others(1402): Show |
chr22 | 43950442 | 44001529 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0001 | 0/0 | 1692 | 23 | 14 | 1 | 7 | 0 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | AGTGT others(1687): Show |
chr22 | 43950442 | 44001529 |
| a0001c0002t0002 | 0/0 | 1692 | 53 | 21 | 5 | 15 | 1 | 11 | SAMM50_chr22_43950442_44001529 | SAMM50 | AGTGT others(1687): Show |
chr22 | 43950442 | 44001529 |
| a0001c0002t0004 | 0/0 | 1692 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | AGTGT others(1687): Show |
chr22 | 43950442 | 44001529 |
| a0001c0004t0001 | 0/0 | 1692 | 72 | 3 | 10 | 49 | 3 | 7 | SAMM50_chr22_43950442_44001529 | SAMM50 | AGTGT others(1687): Show |
chr22 | 43950442 | 44001529 |
| a0001c0004t0002 | 0/0 | 1692 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | AGTGT others(1687): Show |
chr22 | 43950442 | 44001529 |
| a0001c0005t0001 | 0/0 | 1692 | 10 | 10 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | AGTGT others(1687): Show |
chr22 | 43950442 | 44001529 |
| a0001c0006t0001 | 0/0 | 1692 | 10 | 7 | 2 | 0 | 0 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | AGTGT others(1687): Show |
chr22 | 43950442 | 44001529 |
| a0001c0007t0001 | 0/0 | 1692 | 7 | 1 | 5 | 0 | 1 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | AGTGT others(1687): Show |
chr22 | 43950442 | 44001529 |
| a0001c0007t0003 | 0/0 | 1692 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | AGTGT others(1687): Show |
chr22 | 43950442 | 44001529 |
| a0001c0007t0005 | 0/0 | 1692 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | AGTGT others(1687): Show |
chr22 | 43950442 | 44001529 |
| a0001c0008t0001 | 0/0 | 1692 | 9 | 8 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | AGTGT others(1687): Show |
chr22 | 43950442 | 44001529 |
| a0001c0009t0001 | 0/0 | 1692 | 3 | 2 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | AGTGT others(1687): Show |
chr22 | 43950442 | 44001529 |
| a0001c0010t0001 | 0/0 | 1692 | 3 | 3 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | AGTGT others(1687): Show |
chr22 | 43950442 | 44001529 |
| a0001c0013t0001 | 0/0 | 1692 | 2 | 2 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | AGTGT others(1687): Show |
chr22 | 43950442 | 44001529 |
| a0001c0017t0006 | 0/0 | 1692 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | AGTGT others(1687): Show |
chr22 | 43950442 | 44001529 |
| a0001c0020t0001 | 0/0 | 1692 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | AGTGT others(1687): Show |
chr22 | 43950442 | 44001529 |
| a0002c0001t0001 | 0/1 | 1692 | 93 | 7 | 22 | 53 | 5 | 5 | SAMM50_chr22_43950442_44001529 | SAMM50 | AGTGT others(1687): Show |
chr22 | 43950442 | 44001529 |
| a0002c0011t0001 | 0/0 | 1692 | 3 | 2 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | AGTGT others(1687): Show |
chr22 | 43950442 | 44001529 |
| a0002c0012t0001 | 0/0 | 1692 | 3 | 1 | 1 | 0 | 1 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | AGTGT others(1687): Show |
chr22 | 43950442 | 44001529 |
| a0002c0018t0001 | 0/0 | 1692 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | AGTGT others(1687): Show |
chr22 | 43950442 | 44001529 |
| a0003c0003t0001 | 1/0 | 1692 | 75 | 9 | 21 | 25 | 5 | 14 | SAMM50_chr22_43950442_44001529 | SAMM50 | AGTGT others(1687): Show |
chr22 | 43950442 | 44001529 |
| a0003c0014t0001 | 0/0 | 1692 | 2 | 0 | 0 | 2 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | AGTGT others(1687): Show |
chr22 | 43950442 | 44001529 |
| a0003c0016t0001 | 0/0 | 1692 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | AGTGT others(1687): Show |
chr22 | 43950442 | 44001529 |
| a0004c0015t0001 | 0/0 | 1692 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | AGTGT others(1687): Show |
chr22 | 43950442 | 44001529 |
| a0005c0019t0007 | 0/0 | 1692 | 1 | 0 | 0 | 0 | 0 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | AGTGT others(1687): Show |
chr22 | 43950442 | 44001529 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0002t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0002t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0002t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0002t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0002t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0002t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0002t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0002t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0002t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0002t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0002t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0002t0001g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0002t0001g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0002t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0002t0002g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0002t0002g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0002t0002g0029 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0002t0002g0030 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0002t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0002t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0002t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0002t0002g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0002t0002g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0002t0002g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0002t0002g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0002t0002g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0002t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0002t0002g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0002t0002g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0002t0002g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0002t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0002t0002g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0002t0002g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0002t0002g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0002t0002g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0002t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0002t0002g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0002t0002g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0002t0002g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0002t0002g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0002t0002g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0002t0002g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0002t0002g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0002t0002g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0002t0002g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0002t0002g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0002t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0002t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0002t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0002t0002g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0002t0002g0300 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0002t0002g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0002t0002g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0002t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0002t0002g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0002t0002g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0002t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0002t0002g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0002t0002g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0002t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0002t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0002t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0002t0002g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0002t0004g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0004t0001g0001 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0004t0001g0015 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0004t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0004t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0004t0001g0018 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0004t0001g0019 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0004t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0004t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0004t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0004t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0004t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0004t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0004t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0004t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0004t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0004t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0004t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0004t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0004t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0004t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0004t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0004t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0004t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0004t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0004t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0004t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0004t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0004t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0004t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0004t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0004t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0004t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0004t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0004t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0004t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0004t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0004t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0004t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0004t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0004t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0004t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0004t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0004t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0004t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0004t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0004t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0004t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0004t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0004t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0004t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0004t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0004t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0004t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0004t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0004t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0004t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0004t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0004t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0004t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0004t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0004t0001g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0004t0001g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0004t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0005t0001g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0005t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0005t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0005t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0005t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0005t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0005t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0005t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0006t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0006t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0006t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0006t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0006t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0006t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0006t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0006t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0006t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0006t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0007t0001g0031 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0007t0001g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0007t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0007t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0007t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0007t0003g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0007t0005g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0008t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0008t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0008t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0008t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0008t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0008t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0008t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0008t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0008t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0009t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0009t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0009t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0010t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0010t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0010t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0013t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0013t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0017t0006g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0001c0020t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0002c0001t0001g0005 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0002c0001t0001g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0002c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0002c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0002c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0002c0001t0001g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0002c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0002c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0002c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0002c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0002c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0002c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0002c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0002c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0002c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0002c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0002c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0002c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0002c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0002c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0002c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0002c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0002c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0002c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0002c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0002c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0002c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0002c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0002c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0002c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0002c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0002c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0002c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0002c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0002c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0002c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0002c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0002c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0002c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0002c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0002c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0002c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0002c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0002c0001t0001g0217 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0002c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0002c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0002c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0002c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0002c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0002c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0002c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0002c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0002c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0002c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0002c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0002c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0002c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0002c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0002c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0002c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0002c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0002c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0002c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0002c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0002c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0002c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0002c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0002c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0002c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0002c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0002c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0002c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0002c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0002c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0002c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0002c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0002c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0002c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0002c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0002c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0002c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0002c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0002c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0002c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0002c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0002c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0002c0011t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0002c0011t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0002c0011t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0002c0012t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0002c0012t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0002c0012t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0002c0018t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0003c0003t0001g0002 | 0/0 | 5 | 0 | 4 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0003c0003t0001g0003 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0003c0003t0001g0004 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0003c0003t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0003c0003t0001g0008 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0003c0003t0001g0009 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0003c0003t0001g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0003c0003t0001g0011 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0003c0003t0001g0012 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0003c0003t0001g0013 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0003c0003t0001g0014 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0003c0003t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0003c0003t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0003c0003t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0003c0003t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0003c0003t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0003c0003t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0003c0003t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0003c0003t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0003c0003t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0003c0003t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0003c0003t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0003c0003t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0003c0003t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0003c0003t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0003c0003t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0003c0003t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0003c0003t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0003c0003t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0003c0003t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0003c0003t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0003c0003t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0003c0003t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0003c0003t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0003c0003t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0003c0003t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0003c0003t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0003c0003t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0003c0003t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0003c0003t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0003c0003t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0003c0003t0001g0085 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0003c0003t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0003c0003t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0003c0003t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0003c0003t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0003c0003t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0003c0003t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0003c0003t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0003c0003t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0003c0003t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0003c0003t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0003c0003t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0003c0003t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0003c0003t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0003c0003t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0003c0003t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0003c0003t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0003c0014t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0003c0014t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0003c0016t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0004c0015t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| a0005c0019t0007g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0004 | t0001 | g0154 | EUR | GBR | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG00099 | hp2 | a0001 | c0002 | t0002 | g0300 | EUR | GBR | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG00140 | hp1 | a0003 | c0003 | t0001 | g0003 | EUR | GBR | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG00140 | hp2 | a0002 | c0001 | t0001 | g0181 | EUR | GBR | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG00280 | hp1 | a0002 | c0012 | t0001 | g0148 | EUR | FIN | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG00280 | hp2 | a0001 | c0007 | t0001 | g0031 | EUR | FIN | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG00323 | hp1 | a0001 | c0004 | t0001 | g0113 | EUR | FIN | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG00323 | hp2 | a0002 | c0001 | t0001 | g0212 | EUR | FIN | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG00408 | hp1 | a0003 | c0014 | t0001 | g0071 | EAS | CHS | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG00408 | hp2 | a0002 | c0001 | t0001 | g0221 | EAS | CHS | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG00423 | hp1 | a0001 | c0002 | t0001 | g0276 | EAS | CHS | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG00423 | hp2 | a0001 | c0004 | t0001 | g0165 | EAS | CHS | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG00438 | hp1 | a0004 | c0015 | t0001 | g0077 | EAS | CHS | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG00438 | hp2 | a0002 | c0001 | t0001 | g0208 | EAS | CHS | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG00544 | hp1 | a0001 | c0002 | t0002 | g0306 | EAS | CHS | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG00544 | hp2 | a0001 | c0004 | t0001 | g0167 | EAS | CHS | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG00558 | hp1 | a0001 | c0002 | t0002 | g0310 | EAS | CHS | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG00558 | hp2 | a0003 | c0003 | t0001 | g0049 | EAS | CHS | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG00609 | hp1 | a0001 | c0004 | t0001 | g0001 | EAS | CHS | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG00609 | hp2 | a0002 | c0001 | t0001 | g0248 | EAS | CHS | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG00621 | hp1 | a0003 | c0003 | t0001 | g0078 | EAS | CHS | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG00621 | hp2 | a0002 | c0001 | t0001 | g0205 | EAS | CHS | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG00639 | hp1 | a0002 | c0011 | t0001 | g0243 | AMR | PUR | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG00639 | hp2 | a0002 | c0001 | t0001 | g0222 | AMR | PUR | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG00642 | hp1 | a0003 | c0003 | t0001 | g0083 | AMR | PUR | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG00642 | hp2 | a0003 | c0003 | t0001 | g0086 | AMR | PUR | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG00733 | hp1 | a0003 | c0003 | t0001 | g0320 | AMR | PUR | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG00733 | hp2 | a0001 | c0007 | t0001 | g0031 | AMR | PUR | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG00735 | hp1 | a0001 | c0004 | t0001 | g0137 | AMR | PUR | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG00735 | hp2 | a0001 | c0002 | t0002 | g0287 | AMR | PUR | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG00738 | hp1 | a0002 | c0001 | t0001 | g0021 | AMR | PUR | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG00738 | hp2 | a0001 | c0004 | t0001 | g0128 | AMR | PUR | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG00741 | hp1 | a0002 | c0001 | t0001 | g0209 | AMR | PUR | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG00741 | hp2 | a0001 | c0004 | t0001 | g0168 | AMR | PUR | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG01070 | hp1 | a0001 | c0002 | t0002 | g0295 | AMR | PUR | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG01070 | hp2 | a0001 | c0007 | t0001 | g0317 | AMR | PUR | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG01071 | hp1 | a0001 | c0007 | t0001 | g0318 | AMR | PUR | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG01071 | hp2 | a0003 | c0003 | t0001 | g0002 | AMR | PUR | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG01074 | hp1 | a0002 | c0001 | t0001 | g0021 | AMR | PUR | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG01074 | hp2 | a0002 | c0001 | t0001 | g0214 | AMR | PUR | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG01081 | hp1 | a0003 | c0003 | t0001 | g0088 | AMR | PUR | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG01081 | hp2 | a0001 | c0004 | t0001 | g0126 | AMR | PUR | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG01099 | hp1 | a0003 | c0003 | t0001 | g0004 | AMR | PUR | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG01099 | hp2 | a0002 | c0001 | t0001 | g0191 | AMR | PUR | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG01109 | hp1 | a0001 | c0007 | t0001 | g0032 | AMR | PUR | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG01109 | hp2 | a0001 | c0008 | t0001 | g0172 | AMR | PUR | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG01167 | hp1 | a0001 | c0006 | t0001 | g0106 | AMR | PUR | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG01167 | hp2 | a0003 | c0003 | t0001 | g0070 | AMR | PUR | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG01169 | hp1 | a0003 | c0003 | t0001 | g0062 | AMR | PUR | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG01169 | hp2 | a0001 | c0006 | t0001 | g0103 | AMR | PUR | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG01175 | hp1 | a0001 | c0004 | t0001 | g0166 | AMR | PUR | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG01175 | hp2 | a0003 | c0003 | t0001 | g0087 | AMR | PUR | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG01192 | hp1 | a0001 | c0002 | t0002 | g0291 | AMR | PUR | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG01192 | hp2 | a0002 | c0001 | t0001 | g0215 | AMR | PUR | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG01243 | hp1 | a0001 | c0002 | t0002 | g0330 | AMR | PUR | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG01243 | hp2 | a0002 | c0001 | t0001 | g0042 | AMR | PUR | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG01255 | hp1 | a0002 | c0001 | t0001 | g0235 | AMR | CLM | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG01255 | hp2 | a0001 | c0007 | t0001 | g0032 | AMR | CLM | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG01257 | hp1 | a0003 | c0003 | t0001 | g0003 | AMR | CLM | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG01257 | hp2 | a0002 | c0001 | t0001 | g0229 | AMR | CLM | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG01258 | hp1 | a0003 | c0003 | t0001 | g0003 | AMR | CLM | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG01258 | hp2 | a0002 | c0001 | t0001 | g0005 | AMR | CLM | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG01261 | hp1 | a0002 | c0001 | t0001 | g0199 | AMR | CLM | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG01261 | hp2 | a0001 | c0002 | t0002 | g0277 | AMR | CLM | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG01346 | hp1 | a0003 | c0003 | t0001 | g0013 | AMR | CLM | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG01346 | hp2 | a0001 | c0004 | t0001 | g0132 | AMR | CLM | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG01358 | hp1 | a0001 | c0004 | t0001 | g0120 | AMR | CLM | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG01358 | hp2 | a0003 | c0003 | t0001 | g0002 | AMR | CLM | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG01361 | hp1 | a0002 | c0001 | t0001 | g0228 | AMR | CLM | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG01361 | hp2 | a0002 | c0001 | t0001 | g0233 | AMR | CLM | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG01433 | hp1 | a0001 | c0009 | t0001 | g0056 | AMR | CLM | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG01433 | hp2 | a0002 | c0012 | t0001 | g0144 | AMR | CLM | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG01496 | hp1 | a0001 | c0004 | t0001 | g0116 | AMR | CLM | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG01496 | hp2 | a0003 | c0003 | t0001 | g0009 | AMR | CLM | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG01515 | hp1 | a0002 | c0001 | t0001 | g0204 | EUR | IBS | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG01515 | hp2 | a0003 | c0003 | t0001 | g0008 | EUR | IBS | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG01517 | hp1 | a0003 | c0003 | t0001 | g0008 | EUR | IBS | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG01517 | hp2 | a0001 | c0004 | t0001 | g0122 | EUR | IBS | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG01891 | hp1 | a0001 | c0002 | t0001 | g0020 | AFR | ACB | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG01891 | hp2 | a0002 | c0001 | t0001 | g0187 | AFR | ACB | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG01934 | hp1 | a0002 | c0001 | t0001 | g0241 | AMR | PEL | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG01934 | hp2 | a0001 | c0002 | t0001 | g0160 | AMR | PEL | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG01943 | hp1 | a0001 | c0004 | t0001 | g0142 | AMR | PEL | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG01943 | hp2 | a0003 | c0003 | t0001 | g0319 | AMR | PEL | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG01952 | hp1 | a0002 | c0001 | t0001 | g0005 | AMR | PEL | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG01952 | hp2 | a0002 | c0001 | t0001 | g0240 | AMR | PEL | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG01978 | hp1 | a0002 | c0001 | t0001 | g0005 | AMR | PEL | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG01978 | hp2 | a0003 | c0003 | t0001 | g0060 | AMR | PEL | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG01981 | hp1 | a0002 | c0001 | t0001 | g0239 | AMR | PEL | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG01981 | hp2 | a0003 | c0003 | t0001 | g0002 | AMR | PEL | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG01993 | hp1 | a0003 | c0003 | t0001 | g0057 | AMR | PEL | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG01993 | hp2 | a0002 | c0001 | t0001 | g0025 | AMR | PEL | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG02015 | hp1 | a0002 | c0001 | t0001 | g0249 | EAS | KHV | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG02015 | hp2 | a0003 | c0003 | t0001 | g0089 | EAS | KHV | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG02027 | hp1 | a0002 | c0001 | t0001 | g0226 | EAS | KHV | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG02027 | hp2 | a0003 | c0003 | t0001 | g0081 | EAS | KHV | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG02040 | hp1 | a0002 | c0001 | t0001 | g0224 | EAS | KHV | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG02040 | hp2 | a0001 | c0002 | t0002 | g0309 | EAS | KHV | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG02055 | hp1 | a0001 | c0006 | t0001 | g0108 | AFR | ACB | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG02055 | hp2 | a0001 | c0005 | t0001 | g0006 | AFR | ACB | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG02056 | hp1 | a0002 | c0001 | t0001 | g0197 | EAS | KHV | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG02056 | hp2 | a0002 | c0001 | t0001 | g0198 | EAS | KHV | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG02071 | hp1 | a0001 | c0002 | t0002 | g0179 | EAS | KHV | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG02071 | hp2 | a0001 | c0004 | t0001 | g0044 | EAS | KHV | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG02074 | hp1 | a0001 | c0004 | t0001 | g0048 | EAS | KHV | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG02074 | hp2 | a0001 | c0004 | t0001 | g0146 | EAS | KHV | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG02080 | hp1 | a0002 | c0001 | t0001 | g0257 | EAS | KHV | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG02080 | hp2 | a0001 | c0004 | t0001 | g0017 | EAS | KHV | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG02083 | hp1 | a0002 | c0018 | t0001 | g0219 | EAS | KHV | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG02083 | hp2 | a0003 | c0003 | t0001 | g0084 | EAS | KHV | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG02129 | hp1 | a0002 | c0001 | t0001 | g0237 | EAS | KHV | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG02129 | hp2 | a0003 | c0003 | t0001 | g0012 | EAS | KHV | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG02132 | hp1 | a0002 | c0001 | t0001 | g0247 | EAS | KHV | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG02132 | hp2 | a0001 | c0002 | t0002 | g0029 | EAS | KHV | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG02135 | hp1 | a0001 | c0004 | t0001 | g0001 | EAS | KHV | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG02135 | hp2 | a0001 | c0002 | t0002 | g0296 | EAS | KHV | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG02145 | hp1 | a0003 | c0003 | t0001 | g0065 | AFR | ACB | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG02145 | hp2 | a0003 | c0003 | t0001 | g0059 | AFR | ACB | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG02155 | hp1 | a0001 | c0002 | t0002 | g0273 | EAS | CDX | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG02155 | hp2 | a0001 | c0004 | t0001 | g0001 | EAS | CDX | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG02257 | hp1 | a0001 | c0008 | t0001 | g0174 | AFR | ACB | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG02257 | hp2 | a0001 | c0004 | t0001 | g0141 | AFR | ACB | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG02258 | hp1 | a0001 | c0002 | t0002 | g0275 | AFR | ACB | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG02258 | hp2 | a0001 | c0002 | t0002 | g0043 | AFR | ACB | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG02280 | hp1 | a0001 | c0009 | t0001 | g0329 | AFR | ACB | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG02280 | hp2 | a0001 | c0002 | t0001 | g0159 | AFR | ACB | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG02293 | hp1 | a0003 | c0003 | t0001 | g0091 | AMR | PEL | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG02293 | hp2 | a0001 | c0004 | t0001 | g0019 | AMR | PEL | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG02300 | hp1 | a0003 | c0003 | t0001 | g0064 | AMR | PEL | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG02300 | hp2 | a0002 | c0001 | t0001 | g0202 | AMR | PEL | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG02451 | hp1 | a0001 | c0006 | t0001 | g0046 | AFR | ACB | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG02451 | hp2 | a0003 | c0003 | t0001 | g0051 | AFR | ACB | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG02572 | hp1 | a0001 | c0002 | t0002 | g0305 | AFR | GWD | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG02572 | hp2 | a0002 | c0001 | t0001 | g0186 | AFR | GWD | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG02602 | hp1 | a0001 | c0004 | t0001 | g0312 | SAS | PJL | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG02602 | hp2 | a0003 | c0003 | t0001 | g0011 | SAS | PJL | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG02615 | hp1 | a0001 | c0010 | t0001 | g0140 | AFR | GWD | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG02615 | hp2 | a0001 | c0005 | t0001 | g0323 | AFR | GWD | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG02622 | hp1 | a0001 | c0002 | t0001 | g0158 | AFR | GWD | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG02622 | hp2 | a0001 | c0002 | t0002 | g0294 | AFR | GWD | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG02630 | hp1 | a0001 | c0002 | t0001 | g0163 | AFR | GWD | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG02630 | hp2 | a0002 | c0001 | t0001 | g0189 | AFR | GWD | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG02647 | hp1 | a0001 | c0002 | t0001 | g0331 | AFR | GWD | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG02647 | hp2 | a0003 | c0003 | t0001 | g0066 | AFR | GWD | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG02683 | hp1 | a0003 | c0003 | t0001 | g0003 | SAS | PJL | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG02683 | hp2 | a0003 | c0003 | t0001 | g0061 | SAS | PJL | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG02698 | hp1 | a0001 | c0002 | t0002 | g0292 | SAS | PJL | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG02698 | hp2 | a0001 | c0002 | t0002 | g0290 | SAS | PJL | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG02717 | hp1 | a0001 | c0008 | t0001 | g0036 | AFR | GWD | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG02717 | hp2 | a0001 | c0002 | t0002 | g0027 | AFR | GWD | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG02723 | hp1 | a0001 | c0002 | t0002 | g0285 | AFR | GWD | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG02723 | hp2 | a0001 | c0013 | t0001 | g0316 | AFR | GWD | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG02738 | hp1 | a0003 | c0003 | t0001 | g0076 | SAS | PJL | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG02738 | hp2 | a0001 | c0004 | t0001 | g0015 | SAS | PJL | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG02809 | hp1 | a0001 | c0002 | t0001 | g0157 | AFR | GWD | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG02809 | hp2 | a0001 | c0007 | t0003 | g0315 | AFR | GWD | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG02818 | hp1 | a0001 | c0006 | t0001 | g0102 | AFR | GWD | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG02818 | hp2 | a0001 | c0002 | t0002 | g0027 | AFR | GWD | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG02886 | hp1 | a0001 | c0005 | t0001 | g0006 | AFR | GWD | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG02886 | hp2 | a0001 | c0004 | t0001 | g0018 | AFR | GWD | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG02895 | hp1 | a0001 | c0010 | t0001 | g0133 | AFR | GWD | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG02895 | hp2 | a0001 | c0002 | t0001 | g0162 | AFR | GWD | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG02896 | hp1 | a0001 | c0002 | t0001 | g0156 | AFR | GWD | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG02896 | hp2 | a0001 | c0002 | t0002 | g0308 | AFR | GWD | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG02897 | hp1 | a0001 | c0002 | t0001 | g0161 | AFR | GWD | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG02897 | hp2 | a0001 | c0002 | t0002 | g0307 | AFR | GWD | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG02922 | hp1 | a0002 | c0011 | t0001 | g0225 | AFR | ESN | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG02922 | hp2 | a0001 | c0002 | t0002 | g0267 | AFR | ESN | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG02965 | hp1 | a0001 | c0005 | t0001 | g0324 | AFR | ESN | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG02965 | hp2 | a0001 | c0002 | t0001 | g0333 | AFR | ESN | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG02970 | hp1 | a0001 | c0005 | t0001 | g0150 | AFR | ESN | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG02970 | hp2 | a0001 | c0002 | t0002 | g0278 | AFR | ESN | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG02976 | hp1 | a0001 | c0002 | t0002 | g0304 | AFR | ESN | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG02976 | hp2 | a0001 | c0004 | t0001 | g0136 | AFR | ESN | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG03017 | hp1 | a0003 | c0003 | t0001 | g0004 | SAS | PJL | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG03017 | hp2 | a0002 | c0001 | t0001 | g0253 | SAS | PJL | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG03041 | hp1 | a0001 | c0008 | t0001 | g0170 | AFR | GWD | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG03041 | hp2 | a0001 | c0005 | t0001 | g0327 | AFR | GWD | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG03098 | hp1 | a0001 | c0006 | t0001 | g0047 | AFR | MSL | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG03098 | hp2 | a0001 | c0020 | t0001 | g0322 | AFR | MSL | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG03130 | hp1 | a0001 | c0005 | t0001 | g0328 | AFR | ESN | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG03130 | hp2 | a0001 | c0002 | t0001 | g0332 | AFR | ESN | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG03139 | hp1 | a0001 | c0002 | t0002 | g0283 | AFR | ESN | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG03139 | hp2 | a0001 | c0005 | t0001 | g0325 | AFR | ESN | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG03195 | hp1 | a0001 | c0007 | t0005 | g0037 | AFR | ESN | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG03195 | hp2 | a0001 | c0002 | t0001 | g0184 | AFR | ESN | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG03209 | hp1 | a0002 | c0001 | t0001 | g0200 | AFR | MSL | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG03209 | hp2 | a0002 | c0001 | t0001 | g0192 | AFR | MSL | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG03225 | hp1 | a0001 | c0002 | t0002 | g0280 | AFR | MSL | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG03225 | hp2 | a0001 | c0002 | t0002 | g0281 | AFR | MSL | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG03453 | hp1 | a0001 | c0002 | t0004 | g0288 | AFR | MSL | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG03453 | hp2 | a0001 | c0013 | t0001 | g0314 | AFR | MSL | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG03486 | hp1 | a0001 | c0002 | t0002 | g0266 | AFR | MSL | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG03486 | hp2 | a0001 | c0008 | t0001 | g0176 | AFR | MSL | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG03490 | hp1 | a0003 | c0003 | t0001 | g0010 | SAS | PJL | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG03490 | hp2 | a0001 | c0002 | t0002 | g0269 | SAS | PJL | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG03491 | hp1 | a0001 | c0002 | t0002 | g0030 | SAS | PJL | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG03491 | hp2 | a0001 | c0006 | t0001 | g0259 | SAS | PJL | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG03492 | hp1 | a0003 | c0003 | t0001 | g0010 | SAS | PJL | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG03492 | hp2 | a0001 | c0002 | t0002 | g0030 | SAS | PJL | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG03516 | hp1 | a0001 | c0007 | t0001 | g0321 | AFR | ESN | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG03516 | hp2 | a0001 | c0002 | t0002 | g0293 | AFR | ESN | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG03540 | hp1 | a0001 | c0006 | t0001 | g0109 | AFR | GWD | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG03540 | hp2 | a0001 | c0005 | t0001 | g0006 | AFR | GWD | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG03579 | hp1 | a0001 | c0002 | t0002 | g0178 | AFR | MSL | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG03579 | hp2 | a0001 | c0002 | t0001 | g0020 | AFR | MSL | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG03654 | hp1 | a0003 | c0003 | t0001 | g0004 | SAS | PJL | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG03654 | hp2 | a0005 | c0019 | t0007 | g0231 | SAS | PJL | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG03669 | hp1 | a0001 | c0004 | t0001 | g0131 | SAS | PJL | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG03669 | hp2 | a0001 | c0004 | t0001 | g0313 | SAS | PJL | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG03688 | hp1 | a0002 | c0001 | t0001 | g0258 | SAS | STU | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG03688 | hp2 | a0003 | c0003 | t0001 | g0012 | SAS | STU | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG03704 | hp1 | a0002 | c0001 | t0001 | g0256 | SAS | PJL | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG03704 | hp2 | a0001 | c0002 | t0002 | g0301 | SAS | PJL | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG03710 | hp1 | a0002 | c0001 | t0001 | g0238 | SAS | PJL | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG03710 | hp2 | a0003 | c0003 | t0001 | g0068 | SAS | PJL | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG03831 | hp1 | a0003 | c0003 | t0001 | g0075 | SAS | BEB | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG03831 | hp2 | a0003 | c0003 | t0001 | g0093 | SAS | BEB | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG03927 | hp1 | a0001 | c0002 | t0002 | g0302 | SAS | BEB | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG03927 | hp2 | a0001 | c0004 | t0001 | g0127 | SAS | BEB | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG03942 | hp1 | a0001 | c0002 | t0002 | g0029 | SAS | BEB | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG03942 | hp2 | a0001 | c0004 | t0001 | g0149 | SAS | BEB | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG04184 | hp1 | a0003 | c0003 | t0001 | g0095 | SAS | BEB | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG04184 | hp2 | a0002 | c0001 | t0001 | g0254 | SAS | BEB | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG04199 | hp1 | a0001 | c0004 | t0001 | g0114 | SAS | STU | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG04199 | hp2 | a0001 | c0002 | t0002 | g0282 | SAS | STU | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG04204 | hp1 | a0001 | c0002 | t0001 | g0264 | SAS | STU | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG04204 | hp2 | a0003 | c0003 | t0001 | g0096 | SAS | STU | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA18522 | hp1 | a0001 | c0005 | t0001 | g0326 | AFR | YRI | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA18522 | hp2 | a0001 | c0010 | t0001 | g0123 | AFR | YRI | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA18747 | hp1 | a0001 | c0004 | t0001 | g0134 | EAS | CHB | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA18747 | hp2 | a0002 | c0001 | t0001 | g0190 | EAS | CHB | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA18906 | hp1 | a0002 | c0001 | t0001 | g0188 | AFR | YRI | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA18906 | hp2 | a0002 | c0001 | t0001 | g0041 | AFR | YRI | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA18939 | hp1 | a0001 | c0002 | t0002 | g0303 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA18939 | hp2 | a0002 | c0001 | t0001 | g0234 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA18940 | hp1 | a0001 | c0004 | t0001 | g0169 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA18940 | hp2 | a0002 | c0001 | t0001 | g0274 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA18943 | hp1 | a0001 | c0004 | t0001 | g0015 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA18943 | hp2 | a0002 | c0001 | t0001 | g0193 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA18945 | hp1 | a0002 | c0001 | t0001 | g0024 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA18945 | hp2 | a0001 | c0004 | t0001 | g0164 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA18946 | hp1 | a0002 | c0001 | t0001 | g0236 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA18946 | hp2 | a0001 | c0004 | t0001 | g0001 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA18947 | hp1 | a0002 | c0001 | t0001 | g0227 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA18947 | hp2 | a0002 | c0001 | t0001 | g0210 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA18949 | hp1 | a0001 | c0004 | t0001 | g0112 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA18949 | hp2 | a0003 | c0003 | t0001 | g0072 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA18951 | hp1 | a0002 | c0001 | t0001 | g0194 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA18951 | hp2 | a0001 | c0004 | t0001 | g0152 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA18952 | hp1 | a0001 | c0004 | t0001 | g0016 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA18952 | hp2 | a0001 | c0004 | t0001 | g0125 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA18953 | hp1 | a0002 | c0001 | t0001 | g0211 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA18953 | hp2 | a0001 | c0004 | t0001 | g0129 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA18959 | hp1 | a0002 | c0001 | t0001 | g0216 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA18959 | hp2 | a0001 | c0004 | t0001 | g0155 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA18963 | hp1 | a0001 | c0004 | t0001 | g0016 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA18963 | hp2 | a0001 | c0002 | t0001 | g0026 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA18965 | hp1 | a0002 | c0001 | t0001 | g0251 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA18965 | hp2 | a0001 | c0002 | t0001 | g0026 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA18966 | hp1 | a0001 | c0004 | t0001 | g0001 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA18966 | hp2 | a0002 | c0001 | t0001 | g0244 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA18968 | hp1 | a0002 | c0001 | t0001 | g0220 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA18968 | hp2 | a0001 | c0004 | t0001 | g0119 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA18969 | hp1 | a0001 | c0004 | t0001 | g0101 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA18969 | hp2 | a0001 | c0002 | t0001 | g0263 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA18970 | hp1 | a0001 | c0002 | t0001 | g0260 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA18970 | hp2 | a0002 | c0001 | t0001 | g0201 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA18971 | hp1 | a0001 | c0004 | t0001 | g0115 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA18971 | hp2 | a0002 | c0001 | t0001 | g0195 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA18972 | hp1 | a0001 | c0002 | t0002 | g0297 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA18972 | hp2 | a0001 | c0004 | t0001 | g0124 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA18979 | hp1 | a0002 | c0001 | t0001 | g0271 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA18979 | hp2 | a0001 | c0004 | t0001 | g0153 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA18980 | hp1 | a0003 | c0003 | t0001 | g0063 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA18980 | hp2 | a0001 | c0004 | t0001 | g0033 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA18981 | hp1 | a0001 | c0004 | t0001 | g0121 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA18981 | hp2 | a0001 | c0002 | t0002 | g0028 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA18986 | hp1 | a0001 | c0004 | t0001 | g0117 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA18986 | hp2 | a0003 | c0003 | t0001 | g0074 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA18987 | hp1 | a0002 | c0001 | t0001 | g0023 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA18987 | hp2 | a0003 | c0016 | t0001 | g0099 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA18990 | hp1 | a0001 | c0004 | t0001 | g0138 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA18990 | hp2 | a0002 | c0001 | t0001 | g0022 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA18991 | hp1 | a0003 | c0003 | t0001 | g0080 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA18991 | hp2 | a0001 | c0017 | t0006 | g0017 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA18992 | hp1 | a0001 | c0004 | t0001 | g0151 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA18992 | hp2 | a0003 | c0003 | t0001 | g0050 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA18993 | hp1 | a0002 | c0001 | t0001 | g0245 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA18993 | hp2 | a0001 | c0004 | t0001 | g0104 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA18994 | hp1 | a0001 | c0004 | t0001 | g0035 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA18994 | hp2 | a0003 | c0003 | t0001 | g0097 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA18997 | hp1 | a0003 | c0003 | t0001 | g0092 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA18997 | hp2 | a0002 | c0001 | t0001 | g0207 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA18999 | hp1 | a0001 | c0002 | t0001 | g0262 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA18999 | hp2 | a0002 | c0001 | t0001 | g0022 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA19001 | hp1 | a0002 | c0001 | t0001 | g0230 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA19001 | hp2 | a0003 | c0003 | t0001 | g0094 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA19002 | hp1 | a0001 | c0002 | t0002 | g0311 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA19002 | hp2 | a0002 | c0001 | t0001 | g0268 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA19003 | hp1 | a0001 | c0004 | t0001 | g0111 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA19003 | hp2 | a0001 | c0002 | t0002 | g0284 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA19004 | hp1 | a0001 | c0004 | t0001 | g0118 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA19004 | hp2 | a0003 | c0014 | t0001 | g0073 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA19006 | hp1 | a0002 | c0001 | t0001 | g0255 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA19006 | hp2 | a0003 | c0003 | t0001 | g0054 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA19007 | hp1 | a0003 | c0003 | t0001 | g0069 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA19007 | hp2 | a0001 | c0002 | t0001 | g0261 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA19010 | hp1 | a0001 | c0002 | t0002 | g0028 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA19010 | hp2 | a0002 | c0001 | t0001 | g0232 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA19011 | hp1 | a0002 | c0001 | t0001 | g0024 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA19011 | hp2 | a0001 | c0004 | t0001 | g0034 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA19012 | hp1 | a0002 | c0001 | t0001 | g0250 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA19012 | hp2 | a0003 | c0003 | t0001 | g0058 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA19030 | hp1 | a0002 | c0012 | t0001 | g0045 | AFR | LWK | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA19030 | hp2 | a0001 | c0002 | t0002 | g0265 | AFR | LWK | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA19043 | hp1 | a0001 | c0002 | t0002 | g0289 | AFR | LWK | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA19043 | hp2 | a0001 | c0006 | t0001 | g0107 | AFR | LWK | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA19055 | hp1 | a0001 | c0004 | t0001 | g0001 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA19055 | hp2 | a0003 | c0003 | t0001 | g0002 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA19056 | hp1 | a0002 | c0001 | t0001 | g0223 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA19056 | hp2 | a0001 | c0004 | t0001 | g0143 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA19057 | hp1 | a0002 | c0001 | t0001 | g0053 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA19057 | hp2 | a0001 | c0004 | t0001 | g0139 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA19062 | hp1 | a0001 | c0004 | t0001 | g0039 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA19062 | hp2 | a0002 | c0001 | t0001 | g0272 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA19063 | hp1 | a0002 | c0001 | t0001 | g0182 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA19063 | hp2 | a0003 | c0003 | t0001 | g0052 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA19066 | hp1 | a0001 | c0002 | t0002 | g0279 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA19066 | hp2 | a0001 | c0004 | t0001 | g0147 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA19068 | hp1 | a0002 | c0001 | t0001 | g0023 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA19068 | hp2 | a0001 | c0002 | t0002 | g0298 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA19077 | hp1 | a0002 | c0001 | t0001 | g0246 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA19077 | hp2 | a0003 | c0003 | t0001 | g0090 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA19080 | hp1 | a0002 | c0001 | t0001 | g0242 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA19080 | hp2 | a0001 | c0004 | t0001 | g0001 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA19082 | hp1 | a0003 | c0003 | t0001 | g0007 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA19082 | hp2 | a0002 | c0001 | t0001 | g0185 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA19085 | hp1 | a0001 | c0004 | t0001 | g0105 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA19085 | hp2 | a0001 | c0004 | t0002 | g0040 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA19086 | hp1 | a0001 | c0004 | t0001 | g0135 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA19086 | hp2 | a0002 | c0001 | t0001 | g0206 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA19087 | hp1 | a0003 | c0003 | t0001 | g0009 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA19087 | hp2 | a0001 | c0004 | t0001 | g0018 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA19088 | hp1 | a0002 | c0001 | t0001 | g0252 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA19088 | hp2 | a0003 | c0003 | t0001 | g0007 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA19089 | hp1 | a0002 | c0001 | t0001 | g0196 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA19089 | hp2 | a0003 | c0003 | t0001 | g0079 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA19090 | hp1 | a0001 | c0004 | t0001 | g0145 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA19090 | hp2 | a0003 | c0003 | t0001 | g0098 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA19091 | hp1 | a0002 | c0001 | t0001 | g0213 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA19091 | hp2 | a0001 | c0004 | t0001 | g0019 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA19240 | hp1 | a0001 | c0006 | t0001 | g0100 | AFR | YRI | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA19240 | hp2 | a0003 | c0003 | t0001 | g0067 | AFR | YRI | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA20752 | hp1 | a0003 | c0003 | t0001 | g0013 | EUR | TSI | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA20752 | hp2 | a0002 | c0001 | t0001 | g0203 | EUR | TSI | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA20805 | hp1 | a0003 | c0003 | t0001 | g0014 | EUR | TSI | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA20805 | hp2 | a0002 | c0001 | t0001 | g0218 | EUR | TSI | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA20905 | hp1 | a0001 | c0002 | t0002 | g0299 | SAS | GIH | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA20905 | hp2 | a0001 | c0002 | t0002 | g0286 | SAS | GIH | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG01123 | hp1 | a0002 | c0001 | t0001 | g0025 | AMR | CLM | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG01123 | hp2 | a0003 | c0003 | t0001 | g0002 | AMR | CLM | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG02109 | hp1 | a0001 | c0008 | t0001 | g0171 | AFR | ACB | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG02109 | hp2 | a0003 | c0003 | t0001 | g0014 | AFR | ACB | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG02486 | hp1 | a0001 | c0002 | t0002 | g0180 | AFR | ACB | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG02486 | hp2 | a0001 | c0008 | t0001 | g0175 | AFR | ACB | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG02559 | hp1 | a0001 | c0008 | t0001 | g0177 | AFR | ACB | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG02559 | hp2 | a0003 | c0003 | t0001 | g0011 | AFR | ACB | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG06807 | hp1 | a0001 | c0008 | t0001 | g0173 | AFR | USA | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| HG06807 | hp2 | a0003 | c0003 | t0001 | g0082 | AFR | USA | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA18955 | hp1 | a0001 | c0004 | t0001 | g0130 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA18955 | hp2 | a0002 | c0001 | t0001 | g0270 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA20300 | hp1 | a0003 | c0003 | t0001 | g0110 | AFR | USA | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA20300 | hp2 | a0002 | c0011 | t0001 | g0038 | AFR | USA | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA21309 | hp1 | a0001 | c0009 | t0001 | g0055 | AFR | LWK | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| NA21309 | hp2 | a0001 | c0002 | t0001 | g0183 | AFR | LWK | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| homoSapiens | chm13v2 | a0002 | c0001 | t0001 | g0217 | REF | REF | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| homoSapiens | grch38p0 | a0003 | c0003 | t0001 | g0085 | REF | REF | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:43972242 | A | G | 2 | a0002 a0005 |
100 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(97): Show |
missense_variant | MODERATE | c.329A>G | p.Asp110Gly | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 5/15 | 465/1692 | 329/1410 | 110/469 | chr22 | 43972242 | |||
| chr22:43972953 | C | T | 1 | a0005 | 1 | HG03654.hp2 | missense_variant | MODERATE | c.512C>T | p.Ser171Leu | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 6/15 | 648/1692 | 512/1410 | 171/469 | chr22 | 43972953 | |||
| chr22:43976772 | G | A | 1 | a0004 | 1 | HG00438.hp1 | missense_variant | MODERATE | c.800G>A | p.Arg267Gln | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 9/15 | 936/1692 | 800/1410 | 267/469 | chr22 | 43976772 | |||
| chr22:43983958 | A | G | 3 | a0001 a0002 a0005 |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(295): Show |
missense_variant | MODERATE | c.1033A>G | p.Ile345Val | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/15 | 1169/1692 | 1033/1410 | 345/469 | chr22 | 43983958 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:43963366 | A | G | 1 | a0001c0020 | 1 | HG03098.hp2 | synonymous_variant | LOW | c.102A>G | p.Glu34Glu | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 2/15 | 238/1692 | 102/1410 | 34/469 | chr22 | 43963366 | |||
| chr22:43972324 | A | G | 10 | a0001c0002 a0001c0004 a0001c0006 others(7): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(267): Show |
synonymous_variant | LOW | c.411A>G | p.Gly137Gly | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 5/15 | 547/1692 | 411/1410 | 137/469 | chr22 | 43972324 | |||
| chr22:43973296 | G | A | 1 | a0001c0008 | 9 | HG01109.hp2 HG02109.hp1 HG02257.hp1 others(6): Show |
synonymous_variant | LOW | c.621G>A | p.Thr207Thr | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 7/15 | 757/1692 | 621/1410 | 207/469 | chr22 | 43973296 | |||
| chr22:43976752 | C | T | 5 | a0001c0002 a0001c0008 a0002c0001 others(2): Show |
180 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(177): Show |
splice_region_variant&synonymous_variant | LOW | c.780C>T | p.His260His | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 9/15 | 916/1692 | 780/1410 | 260/469 | chr22 | 43976752 | |||
| chr22:43983942 | T | C | 13 | a0001c0002 a0001c0004 a0001c0006 others(10): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(279): Show |
synonymous_variant | LOW | c.1017T>C | p.Leu339Leu | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/15 | 1153/1692 | 1017/1410 | 339/469 | chr22 | 43983942 | |||
| chr22:43989148 | C | T | 1 | a0001c0017 | 1 | NA18991.hp2 | synonymous_variant | LOW | c.1113C>T | p.Gly371Gly | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 13/15 | 1249/1692 | 1113/1410 | 371/469 | chr22 | 43989148 | |||
| chr22:43989229 | C | T | 1 | a0001c0010 | 3 | HG02615.hp1 HG02895.hp1 NA18522.hp2 |
synonymous_variant | LOW | c.1194C>T | p.Asn398Asn | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 13/15 | 1330/1692 | 1194/1410 | 398/469 | chr22 | 43989229 | |||
| chr22:43990401 | C | T | 7 | a0001c0004 a0001c0005 a0001c0013 others(4): Show |
90 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(87): Show |
synonymous_variant | LOW | c.1359C>T | p.Gly453Gly | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/15 | 1495/1692 | 1359/1410 | 453/469 | chr22 | 43990401 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:43955453 | T | C | 1 | a0001c0007t0003 | 1 | HG02809.hp2 | 5_prime_UTR_variant | MODIFIER | c.-125T>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/15 | 125 | chr22 | 43955453 | ||||||
| chr22:43955456 | G | T | 1 | a0005c0019t0007 | 1 | HG03654.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-122G>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/15 | chr22 | 43955456 | |||||||
| chr22:43955471 | T | C | 3 | a0001c0002t0002 a0001c0002t0004 a0001c0004t0002 |
55 | HG00099.hp2 HG00544.hp1 HG00558.hp1 others(52): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-107T>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/15 | chr22 | 43955471 | |||||||
| chr22:43996435 | A | C | 1 | a0001c0017t0006 | 1 | NA18991.hp2 | 3_prime_UTR_variant | MODIFIER | c.*52A>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 15/15 | 52 | chr22 | 43996435 | ||||||
| chr22:43996453 | C | T | 2 | a0001c0002t0004 a0001c0007t0005 |
2 | HG03195.hp1 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*70C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 15/15 | 70 | chr22 | 43996453 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:43955691 | G | T | 3 | a0001c0002t0001g0331 a0001c0002t0001g0332 a0001c0002t0001g0333 |
3 | HG02647.hp1 HG02965.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.21+93G>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43955691 | |||||||
| chr22:43955966 | A | G | 1 | a0001c0002t0002g0330 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.21+368A>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43955966 | |||||||
| chr22:43956261 | G | A | 3 | a0001c0004t0001g0033 a0001c0004t0001g0034 a0001c0004t0001g0035 |
3 | NA18980.hp2 NA18994.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.21+663G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43956261 | |||||||
| chr22:43956367 | T | C | 1 | a0001c0008t0001g0036 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.21+769T>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43956367 | |||||||
| chr22:43956633 | C | T | 10 | a0001c0005t0001g0006 a0001c0005t0001g0323 a0001c0005t0001g0324 others(7): Show |
12 | HG02055.hp2 HG02280.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.21+1035C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43956633 | |||||||
| chr22:43956710 | G | A | 1 | a0001c0007t0005g0037 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.21+1112G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43956710 | |||||||
| chr22:43956797 | T | C | 1 | a0002c0011t0001g0038 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.21+1199T>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43956797 | |||||||
| chr22:43956917 | G | A | 2 | a0001c0004t0001g0039 a0001c0004t0002g0040 |
2 | NA19062.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.21+1319G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43956917 | |||||||
| chr22:43956986 | C | T | 3 | a0003c0003t0001g0003 a0003c0003t0001g0319 a0003c0003t0001g0320 |
6 | HG00140.hp1 HG00733.hp1 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.21+1388C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43956986 | |||||||
| chr22:43957185 | T | C | 2 | a0002c0001t0001g0041 a0002c0001t0001g0042 |
2 | HG01243.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.21+1587T>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43957185 | |||||||
| chr22:43957374 | G | C | 1 | a0001c0002t0002g0043 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.21+1776G>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43957374 | |||||||
| chr22:43957567 | C | T | 8 | a0001c0007t0001g0031 a0001c0007t0001g0032 a0001c0007t0001g0317 others(5): Show |
10 | HG00280.hp2 HG00733.hp2 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.21+1969C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43957567 | |||||||
| chr22:43957616 | G | A | 1 | a0001c0004t0001g0044 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.21+2018G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43957616 | |||||||
| chr22:43957760 | A | G | 3 | a0001c0007t0001g0032 a0001c0007t0001g0317 a0001c0007t0001g0318 |
4 | HG01070.hp2 HG01071.hp1 HG01109.hp1 others(1): Show |
intron_variant | MODIFIER | c.21+2162A>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43957760 | |||||||
| chr22:43957766 | T | G | 3 | a0001c0006t0001g0046 a0001c0006t0001g0047 a0002c0012t0001g0045 |
3 | HG02451.hp1 HG03098.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.21+2168T>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43957766 | |||||||
| chr22:43958004 | C | T | 2 | a0001c0004t0001g0312 a0001c0004t0001g0313 |
2 | HG02602.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.21+2406C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43958004 | |||||||
| chr22:43958231 | C | T | 149 | a0001c0002t0001g0026 a0001c0002t0001g0183 a0001c0002t0001g0184 others(146): Show |
161 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(158): Show |
intron_variant | MODIFIER | c.21+2633C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43958231 | |||||||
| chr22:43958412 | A | G | 1 | a0001c0013t0001g0316 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.21+2814A>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43958412 | |||||||
| chr22:43958421 | G | A | 1 | a0001c0004t0001g0048 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.21+2823G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43958421 | |||||||
| chr22:43958476 | C | CT | 16 | a0001c0004t0001g0101 a0001c0004t0001g0104 a0001c0004t0001g0105 others(13): Show |
16 | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.21+2898dupT | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 43958476 | ||||||
| chr22:43958476 | C | CTT | 67 | a0001c0002t0001g0183 a0001c0004t0001g0001 a0001c0004t0001g0015 others(64): Show |
77 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.21+2897_21+2898dup others(2): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 43958476 | ||||||
| chr22:43958476 | C | CTTT | 105 | a0001c0002t0001g0020 a0001c0002t0001g0156 a0001c0002t0001g0157 others(102): Show |
113 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.21+2896_21+2898dup others(3): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 43958476 | ||||||
| chr22:43958476 | C | CTTTT | 22 | a0001c0002t0001g0026 a0001c0002t0001g0260 a0001c0002t0001g0261 others(19): Show |
24 | HG02155.hp1 HG02258.hp2 HG02559.hp1 others(21): Show |
intron_variant | MODIFIER | c.21+2895_21+2898dup others(4): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 43958476 | ||||||
| chr22:43958476 | C | CTTTTT | 40 | a0001c0002t0001g0276 a0001c0002t0002g0028 a0001c0002t0002g0029 others(37): Show |
43 | HG00099.hp2 HG00423.hp1 HG00544.hp1 others(40): Show |
intron_variant | MODIFIER | c.21+2894_21+2898dup others(5): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 43958476 | ||||||
| chr22:43958476 | CT | C | 6 | a0001c0007t0005g0037 a0003c0003t0001g0007 a0003c0003t0001g0049 others(3): Show |
7 | HG00558.hp2 HG02451.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.21+2898delT | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 43958476 | ||||||
| chr22:43958518 | A | G | 255 | a0001c0002t0001g0020 a0001c0002t0001g0026 a0001c0002t0001g0156 others(252): Show |
280 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(277): Show |
intron_variant | MODIFIER | c.21+2920A>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43958518 | |||||||
| chr22:43958718 | C | T | 8 | a0001c0007t0001g0031 a0001c0007t0001g0032 a0001c0007t0001g0317 others(5): Show |
10 | HG00280.hp2 HG00733.hp2 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.21+3120C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43958718 | |||||||
| chr22:43958743 | C | T | 9 | a0001c0008t0001g0036 a0001c0008t0001g0170 a0001c0008t0001g0171 others(6): Show |
9 | HG01109.hp2 HG02109.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.21+3145C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43958743 | |||||||
| chr22:43958880 | G | C | 1 | a0002c0001t0001g0053 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.21+3282G>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43958880 | |||||||
| chr22:43958961 | C | T | 8 | a0001c0005t0001g0006 a0001c0005t0001g0323 a0001c0005t0001g0324 others(5): Show |
10 | HG02055.hp2 HG02280.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.21+3363C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43958961 | |||||||
| chr22:43958985 | A | G | 80 | a0001c0004t0001g0001 a0001c0004t0001g0015 a0001c0004t0001g0016 others(77): Show |
90 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.21+3387A>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43958985 | |||||||
| chr22:43959018 | C | CT | 13 | a0001c0007t0001g0031 a0001c0007t0001g0032 a0001c0007t0001g0317 others(10): Show |
15 | HG00280.hp2 HG00733.hp2 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.21+3438dupT | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 43959018 | ||||||
| chr22:43959018 | CT | C | 218 | a0001c0002t0001g0020 a0001c0002t0001g0157 a0001c0002t0001g0158 others(215): Show |
240 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(237): Show |
intron_variant | MODIFIER | c.21+3438delT | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 43959018 | ||||||
| chr22:43959018 | CTT | C | 16 | a0001c0002t0001g0026 a0001c0002t0001g0156 a0001c0002t0001g0184 others(13): Show |
17 | HG00323.hp1 HG00423.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.21+3437_21+3438del others(2): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 43959018 | ||||||
| chr22:43959270 | C | T | 1 | a0001c0004t0001g0154 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.21+3672C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43959270 | |||||||
| chr22:43959284 | G | A | 1 | a0001c0002t0001g0184 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.21+3686G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43959284 | |||||||
| chr22:43959350 | A | G | 248 | a0001c0002t0001g0020 a0001c0002t0001g0026 a0001c0002t0001g0156 others(245): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.21+3752A>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43959350 | |||||||
| chr22:43959465 | G | C | 1 | a0001c0007t0003g0315 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.22-3821G>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43959465 | |||||||
| chr22:43959507 | T | TAC | 35 | a0001c0020t0001g0322 a0002c0001t0001g0254 a0002c0001t0001g0255 others(32): Show |
42 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(39): Show |
intron_variant | MODIFIER | c.22-3744_22-3743dup others(2): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 43959507 | ||||||
| chr22:43959507 | T | TACAC | 32 | a0001c0002t0001g0156 a0001c0002t0001g0183 a0001c0002t0001g0264 others(29): Show |
36 | HG00558.hp1 HG00609.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.22-3746_22-3743dup others(4): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 43959507 | ||||||
| chr22:43959507 | T | TACACAC | 84 | a0001c0002t0001g0026 a0001c0002t0001g0184 a0001c0002t0001g0260 others(81): Show |
94 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.22-3748_22-3743dup others(6): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 43959507 | ||||||
| chr22:43959507 | T | TACACACA others(1): Show |
38 | a0001c0002t0002g0180 a0001c0002t0002g0269 a0001c0002t0002g0293 others(35): Show |
39 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(36): Show |
intron_variant | MODIFIER | c.22-3750_22-3743dup others(8): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 43959507 | ||||||
| chr22:43959507 | T | TACACACA others(3): Show |
40 | a0001c0002t0002g0028 a0001c0002t0002g0029 a0001c0002t0002g0030 others(37): Show |
45 | HG00099.hp1 HG00280.hp2 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.22-3752_22-3743dup others(10): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 43959507 | ||||||
| chr22:43959507 | T | TACACACA others(5): Show |
38 | a0001c0002t0001g0331 a0001c0002t0001g0332 a0001c0002t0001g0333 others(35): Show |
45 | HG00609.hp1 HG00735.hp1 HG01169.hp2 others(42): Show |
intron_variant | MODIFIER | c.22-3754_22-3743dup others(12): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 43959507 | ||||||
| chr22:43959507 | T | TACACACA others(7): Show |
29 | a0001c0002t0002g0027 a0001c0002t0002g0043 a0001c0002t0002g0178 others(26): Show |
33 | HG00423.hp2 HG00738.hp2 HG01081.hp2 others(30): Show |
intron_variant | MODIFIER | c.22-3756_22-3743dup others(14): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 43959507 | ||||||
| chr22:43959507 | T | TACACACA others(9): Show |
8 | a0001c0004t0001g0117 a0001c0004t0001g0118 a0001c0004t0001g0119 others(5): Show |
8 | HG01070.hp2 HG01071.hp1 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.22-3758_22-3743dup others(16): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 43959507 | ||||||
| chr22:43959507 | T | TACACACA others(11): Show |
3 | a0001c0004t0001g0039 a0001c0004t0001g0115 a0001c0004t0001g0116 |
3 | HG01496.hp1 NA18971.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.22-3760_22-3743dup others(18): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 43959507 | ||||||
| chr22:43959507 | T | TACACACA others(13): Show |
1 | a0001c0004t0001g0114 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.22-3762_22-3743dup others(20): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 43959507 | ||||||
| chr22:43959507 | TAC | T | 7 | a0001c0002t0001g0158 a0001c0002t0001g0159 a0003c0003t0001g0088 others(4): Show |
7 | HG01081.hp1 HG02015.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.22-3744_22-3743del others(2): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 43959507 | ||||||
| chr22:43959507 | TACAC | T | 5 | a0001c0002t0001g0020 a0001c0002t0001g0160 a0001c0002t0001g0161 others(2): Show |
6 | HG01891.hp1 HG01934.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.22-3746_22-3743del others(4): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 43959507 | ||||||
| chr22:43959689 | C | T | 69 | a0001c0004t0001g0001 a0001c0004t0001g0015 a0001c0004t0001g0016 others(66): Show |
79 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.22-3597C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43959689 | |||||||
| chr22:43959739 | T | A | 1 | a0002c0001t0001g0053 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.22-3547T>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43959739 | |||||||
| chr22:43959847 | T | G | 1 | a0002c0001t0001g0200 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.22-3439T>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43959847 | |||||||
| chr22:43959902 | A | C | 6 | a0001c0002t0001g0026 a0001c0002t0001g0260 a0001c0002t0001g0261 others(3): Show |
7 | HG00423.hp1 NA18963.hp2 NA18965.hp2 others(4): Show |
intron_variant | MODIFIER | c.22-3384A>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43959902 | |||||||
| chr22:43960007 | C | T | 1 | a0001c0002t0001g0183 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.22-3279C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43960007 | |||||||
| chr22:43960105 | G | T | 2 | a0001c0009t0001g0055 a0001c0009t0001g0056 |
2 | HG01433.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.22-3181G>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43960105 | |||||||
| chr22:43960116 | G | A | 2 | a0001c0002t0002g0028 a0001c0002t0002g0303 |
3 | NA18939.hp1 NA18981.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.22-3170G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43960116 | |||||||
| chr22:43960265 | A | T | 1 | a0001c0002t0001g0184 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.22-3021A>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43960265 | |||||||
| chr22:43960416 | G | A | 3 | a0001c0004t0001g0129 a0001c0004t0001g0138 a0001c0004t0001g0155 |
3 | NA18953.hp2 NA18959.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.22-2870G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43960416 | |||||||
| chr22:43960469 | C | G | 79 | a0001c0004t0001g0001 a0001c0004t0001g0015 a0001c0004t0001g0016 others(76): Show |
89 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.22-2817C>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43960469 | |||||||
| chr22:43960588 | G | A | 89 | a0002c0001t0001g0005 a0002c0001t0001g0021 a0002c0001t0001g0022 others(86): Show |
96 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.22-2698G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43960588 | |||||||
| chr22:43960600 | G | T | 49 | a0001c0002t0002g0027 a0001c0002t0002g0028 a0001c0002t0002g0029 others(46): Show |
53 | HG00099.hp2 HG00544.hp1 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.22-2686G>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43960600 | |||||||
| chr22:43960682 | T | C | 5 | a0001c0007t0001g0031 a0001c0007t0001g0032 a0001c0007t0001g0317 others(2): Show |
7 | HG00280.hp2 HG00733.hp2 HG01070.hp2 others(4): Show |
intron_variant | MODIFIER | c.22-2604T>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43960682 | |||||||
| chr22:43960686 | G | A | 70 | a0001c0004t0001g0001 a0001c0004t0001g0015 a0001c0004t0001g0016 others(67): Show |
80 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(77): Show |
intron_variant | MODIFIER | c.22-2600G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43960686 | |||||||
| chr22:43960773 | C | T | 3 | a0001c0006t0001g0046 a0001c0006t0001g0047 a0002c0012t0001g0045 |
3 | HG02451.hp1 HG03098.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.22-2513C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43960773 | |||||||
| chr22:43961284 | C | T | 3 | a0001c0006t0001g0046 a0001c0006t0001g0047 a0002c0012t0001g0045 |
3 | HG02451.hp1 HG03098.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.22-2002C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43961284 | |||||||
| chr22:43961293 | C | G | 1 | a0003c0003t0001g0082 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.22-1993C>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43961293 | |||||||
| chr22:43961294 | CT | C | 5 | a0001c0002t0002g0027 a0001c0002t0002g0043 a0001c0002t0002g0265 others(2): Show |
6 | HG02258.hp2 HG02717.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.22-1990delT | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 43961294 | ||||||
| chr22:43961332 | G | A | 1 | a0001c0007t0005g0037 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.22-1954G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43961332 | |||||||
| chr22:43962014 | G | T | 148 | a0001c0002t0001g0026 a0001c0002t0001g0183 a0001c0002t0001g0184 others(145): Show |
160 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(157): Show |
intron_variant | MODIFIER | c.22-1272G>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43962014 | |||||||
| chr22:43962020 | G | A | 254 | a0001c0002t0001g0020 a0001c0002t0001g0026 a0001c0002t0001g0156 others(251): Show |
279 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(276): Show |
intron_variant | MODIFIER | c.22-1266G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43962020 | |||||||
| chr22:43962021 | A | G | 1 | a0001c0002t0001g0163 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.22-1265A>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43962021 | |||||||
| chr22:43962048 | A | C | 8 | a0001c0007t0001g0031 a0001c0007t0001g0032 a0001c0007t0001g0317 others(5): Show |
10 | HG00280.hp2 HG00733.hp2 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.22-1238A>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43962048 | |||||||
| chr22:43962048 | A | G | 4 | a0001c0008t0001g0170 a0001c0008t0001g0173 a0001c0008t0001g0176 others(1): Show |
4 | HG02559.hp1 HG03041.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.22-1238A>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43962048 | |||||||
| chr22:43962060 | T | A | 4 | a0001c0007t0001g0031 a0001c0007t0001g0032 a0001c0007t0001g0317 others(1): Show |
6 | HG00280.hp2 HG00733.hp2 HG01070.hp2 others(3): Show |
intron_variant | MODIFIER | c.22-1226T>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43962060 | |||||||
| chr22:43962150 | C | T | 8 | a0001c0007t0001g0031 a0001c0007t0001g0032 a0001c0007t0001g0317 others(5): Show |
10 | HG00280.hp2 HG00733.hp2 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.22-1136C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43962150 | |||||||
| chr22:43962159 | G | A | 1 | a0002c0001t0001g0202 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.22-1127G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43962159 | |||||||
| chr22:43962160 | A | C | 7 | a0001c0006t0001g0100 a0001c0006t0001g0102 a0001c0006t0001g0103 others(4): Show |
7 | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.22-1126A>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43962160 | |||||||
| chr22:43962328 | T | C | 2 | a0001c0013t0001g0314 a0001c0013t0001g0316 |
2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.22-958T>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43962328 | |||||||
| chr22:43962356 | G | A | 1 | a0001c0002t0002g0279 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.22-930G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43962356 | |||||||
| chr22:43962356 | G | T | 9 | a0001c0006t0001g0046 a0001c0006t0001g0047 a0001c0006t0001g0100 others(6): Show |
9 | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.22-930G>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43962356 | |||||||
| chr22:43962386 | C | G | 1 | a0001c0007t0003g0315 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.22-900C>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43962386 | |||||||
| chr22:43962480 | C | G | 7 | a0001c0007t0001g0031 a0001c0007t0001g0032 a0001c0007t0001g0317 others(4): Show |
9 | HG00280.hp2 HG00733.hp2 HG01070.hp2 others(6): Show |
intron_variant | MODIFIER | c.22-806C>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43962480 | |||||||
| chr22:43962881 | A | AT | 47 | a0001c0002t0001g0260 a0001c0002t0001g0261 a0001c0002t0001g0262 others(44): Show |
49 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(46): Show |
intron_variant | MODIFIER | c.22-372dupT | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 43962881 | ||||||
| chr22:43962881 | A | ATT | 12 | a0001c0002t0001g0026 a0001c0004t0001g0121 a0001c0004t0001g0149 others(9): Show |
15 | HG01175.hp2 HG01433.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.22-373_22-372dupTT | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 43962881 | ||||||
| chr22:43962881 | A | ATTT | 7 | a0001c0008t0001g0036 a0001c0008t0001g0174 a0001c0009t0001g0055 others(4): Show |
7 | HG02027.hp2 HG02145.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.22-374_22-372dupTT others(1): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 43962881 | ||||||
| chr22:43962881 | A | ATTTT | 8 | a0001c0002t0001g0331 a0001c0002t0001g0332 a0001c0002t0001g0333 others(5): Show |
8 | HG00140.hp2 HG00323.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.22-375_22-372dupTT others(2): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 43962881 | ||||||
| chr22:43962881 | A | ATTTTT | 39 | a0001c0002t0001g0183 a0001c0008t0001g0173 a0001c0008t0001g0176 others(36): Show |
41 | HG00408.hp2 HG00609.hp2 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.22-376_22-372dupTT others(3): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 43962881 | ||||||
| chr22:43962881 | A | ATTTTTT | 22 | a0001c0008t0001g0170 a0002c0001t0001g0024 a0002c0001t0001g0197 others(19): Show |
23 | HG01257.hp2 HG01361.hp1 HG01361.hp2 others(20): Show |
intron_variant | MODIFIER | c.22-377_22-372dupTT others(4): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 43962881 | ||||||
| chr22:43962881 | A | ATTTTTTT others(1): Show |
7 | a0002c0001t0001g0182 a0002c0001t0001g0198 a0002c0001t0001g0235 others(4): Show |
7 | HG01255.hp1 HG02056.hp2 HG02129.hp1 others(4): Show |
intron_variant | MODIFIER | c.22-379_22-372dupTT others(6): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 43962881 | ||||||
| chr22:43962881 | A | ATTTTTTT others(3): Show |
1 | a0002c0001t0001g0191 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.22-381_22-372dupTT others(8): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 43962881 | ||||||
| chr22:43962881 | A | ATTTTTTT others(6): Show |
2 | a0002c0001t0001g0025 a0002c0001t0001g0253 |
3 | HG01123.hp1 HG01993.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.22-384_22-372dupTT others(11): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 43962881 | ||||||
| chr22:43962881 | A | ATTTTTTT others(7): Show |
3 | a0002c0001t0001g0005 a0002c0001t0001g0239 a0002c0001t0001g0240 |
5 | HG01258.hp2 HG01952.hp1 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.22-385_22-372dupTT others(12): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 43962881 | ||||||
| chr22:43962881 | A | ATTTTTTT others(8): Show |
1 | a0002c0001t0001g0199 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.22-386_22-372dupTT others(13): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 43962881 | ||||||
| chr22:43962881 | A | ATTTTTTT others(12): Show |
1 | a0002c0001t0001g0241 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.22-390_22-372dupTT others(17): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 43962881 | ||||||
| chr22:43962881 | AT | A | 42 | a0001c0002t0002g0027 a0001c0002t0002g0029 a0001c0002t0002g0030 others(39): Show |
46 | HG00544.hp1 HG00735.hp2 HG01070.hp1 others(43): Show |
intron_variant | MODIFIER | c.22-372delT | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 43962881 | ||||||
| chr22:43962881 | ATTTTTTT others(3): Show |
A | 1 | a0002c0001t0001g0203 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.22-381_22-372delTT others(8): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 43962881 | ||||||
| chr22:43962881 | ATTTTTTT others(8): Show |
A | 3 | a0002c0001t0001g0186 a0002c0001t0001g0188 a0002c0001t0001g0189 |
3 | HG02572.hp2 HG02630.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.22-386_22-372delTT others(13): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 43962881 | ||||||
| chr22:43962881 | ATTTTTTT others(9): Show |
A | 5 | a0001c0004t0001g0130 a0001c0007t0001g0031 a0001c0007t0001g0032 others(2): Show |
7 | HG00280.hp2 HG00733.hp2 HG01070.hp2 others(4): Show |
intron_variant | MODIFIER | c.22-387_22-372delTT others(14): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 43962881 | ||||||
| chr22:43962881 | ATTTTTTT others(10): Show |
A | 11 | a0001c0002t0001g0020 a0001c0002t0001g0156 a0001c0002t0001g0157 others(8): Show |
12 | HG01109.hp2 HG01891.hp1 HG01934.hp2 others(9): Show |
intron_variant | MODIFIER | c.22-388_22-372delTT others(15): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 43962881 | ||||||
| chr22:43962882 | T | A | 1 | a0001c0004t0001g0139 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.22-404T>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43962882 | |||||||
| chr22:43962932 | G | A | 72 | a0001c0002t0001g0331 a0001c0002t0001g0332 a0001c0004t0001g0001 others(69): Show |
82 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.22-354G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43962932 | |||||||
| chr22:43962939 | G | C | 8 | a0001c0007t0001g0031 a0001c0007t0001g0032 a0001c0007t0001g0317 others(5): Show |
10 | HG00280.hp2 HG00733.hp2 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.22-347G>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43962939 | |||||||
| chr22:43963117 | A | G | 70 | a0002c0001t0001g0005 a0002c0001t0001g0021 a0002c0001t0001g0022 others(67): Show |
77 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.22-169A>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43963117 | |||||||
| chr22:43963126 | G | A | 1 | a0003c0003t0001g0087 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.22-160G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43963126 | |||||||
| chr22:43963433 | G | T | 2 | a0001c0006t0001g0046 a0001c0006t0001g0047 |
2 | HG02451.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.132+37G>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 2/14 | chr22 | 43963433 | |||||||
| chr22:43963771 | T | C | 8 | a0001c0007t0001g0031 a0001c0007t0001g0032 a0001c0007t0001g0317 others(5): Show |
10 | HG00280.hp2 HG00733.hp2 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.132+375T>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 2/14 | chr22 | 43963771 | |||||||
| chr22:43963835 | C | T | 43 | a0001c0002t0002g0028 a0001c0002t0002g0029 a0001c0002t0002g0030 others(40): Show |
46 | HG00099.hp2 HG00544.hp1 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.132+439C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 2/14 | chr22 | 43963835 | |||||||
| chr22:43963849 | C | T | 8 | a0001c0007t0001g0031 a0001c0007t0001g0032 a0001c0007t0001g0317 others(5): Show |
10 | HG00280.hp2 HG00733.hp2 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.132+453C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 2/14 | chr22 | 43963849 | |||||||
| chr22:43963865 | C | A | 1 | a0001c0002t0002g0290 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.132+469C>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 2/14 | chr22 | 43963865 | |||||||
| chr22:43963904 | T | G | 2 | a0003c0003t0001g0007 a0003c0003t0001g0049 |
3 | HG00558.hp2 NA19082.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.132+508T>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 2/14 | chr22 | 43963904 | |||||||
| chr22:43963909 | T | TTTTTTAT others(324): Show |
2 | a0001c0002t0001g0161 a0001c0002t0001g0162 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.132+517_132+518ins others(331): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr22 | 43963909 | ||||||
| chr22:43963909 | T | TTTTTTAT others(324): Show |
4 | a0001c0002t0001g0020 a0001c0002t0001g0159 a0001c0002t0001g0160 others(1): Show |
5 | HG01891.hp1 HG01934.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.132+517_132+518ins others(331): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr22 | 43963909 | ||||||
| chr22:43963909 | T | TTTTTTAT others(321): Show |
1 | a0001c0002t0001g0157 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.132+517_132+518ins others(328): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr22 | 43963909 | ||||||
| chr22:43963909 | T | TTTTTTAT others(321): Show |
1 | a0001c0002t0001g0156 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.132+517_132+518ins others(328): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr22 | 43963909 | ||||||
| chr22:43963909 | T | TTTTTTAT others(321): Show |
1 | a0001c0002t0001g0158 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.132+517_132+518ins others(328): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr22 | 43963909 | ||||||
| chr22:43963914 | A | T | 9 | a0001c0002t0001g0020 a0001c0002t0001g0156 a0001c0002t0001g0157 others(6): Show |
10 | HG01891.hp1 HG01934.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.132+518A>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 2/14 | chr22 | 43963914 | |||||||
| chr22:43963918 | T | A | 9 | a0001c0002t0001g0020 a0001c0002t0001g0156 a0001c0002t0001g0157 others(6): Show |
10 | HG01891.hp1 HG01934.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.132+522T>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 2/14 | chr22 | 43963918 | |||||||
| chr22:43963965 | C | T | 2 | a0001c0009t0001g0055 a0001c0009t0001g0056 |
2 | HG01433.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.133-487C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 2/14 | chr22 | 43963965 | |||||||
| chr22:43964058 | C | A | 4 | a0001c0007t0001g0031 a0001c0007t0001g0032 a0001c0007t0001g0317 others(1): Show |
6 | HG00280.hp2 HG00733.hp2 HG01070.hp2 others(3): Show |
intron_variant | MODIFIER | c.133-394C>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 2/14 | chr22 | 43964058 | |||||||
| chr22:43964121 | T | C | 2 | a0002c0011t0001g0038 a0002c0011t0001g0243 |
2 | HG00639.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.133-331T>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 2/14 | chr22 | 43964121 | |||||||
| chr22:43964127 | G | A | 69 | a0001c0004t0001g0001 a0001c0004t0001g0015 a0001c0004t0001g0016 others(66): Show |
79 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.133-325G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 2/14 | chr22 | 43964127 | |||||||
| chr22:43964130 | C | A | 69 | a0001c0004t0001g0001 a0001c0004t0001g0015 a0001c0004t0001g0016 others(66): Show |
79 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.133-322C>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 2/14 | chr22 | 43964130 | |||||||
| chr22:43964176 | C | A | 9 | a0001c0002t0001g0020 a0001c0002t0001g0156 a0001c0002t0001g0157 others(6): Show |
10 | HG01891.hp1 HG01934.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.133-276C>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 2/14 | chr22 | 43964176 | |||||||
| chr22:43964243 | A | G | 2 | a0001c0002t0001g0161 a0001c0002t0001g0162 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.133-209A>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 2/14 | chr22 | 43964243 | |||||||
| chr22:43964254 | A | G | 9 | a0001c0008t0001g0036 a0001c0008t0001g0170 a0001c0008t0001g0171 others(6): Show |
9 | HG01109.hp2 HG02109.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.133-198A>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 2/14 | chr22 | 43964254 | |||||||
| chr22:43964362 | C | G | 1 | a0002c0001t0001g0240 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.133-90C>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 2/14 | chr22 | 43964362 | |||||||
| chr22:43964611 | G | A | 2 | a0001c0006t0001g0046 a0001c0006t0001g0047 |
2 | HG02451.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.234+58G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 3/14 | chr22 | 43964611 | |||||||
| chr22:43964656 | C | T | 2 | a0001c0002t0002g0307 a0001c0002t0002g0308 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.234+103C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 3/14 | chr22 | 43964656 | |||||||
| chr22:43964862 | G | A | 1 | a0001c0002t0001g0331 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.234+309G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 3/14 | chr22 | 43964862 | |||||||
| chr22:43964875 | G | C | 3 | a0001c0002t0001g0331 a0001c0002t0001g0332 a0001c0002t0001g0333 |
3 | HG02647.hp1 HG02965.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.234+322G>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 3/14 | chr22 | 43964875 | |||||||
| chr22:43964936 | G | A | 1 | a0003c0003t0001g0319 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.234+383G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 3/14 | chr22 | 43964936 | |||||||
| chr22:43965005 | G | C | 1 | a0002c0001t0001g0198 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.234+452G>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 3/14 | chr22 | 43965005 | |||||||
| chr22:43965184 | T | TA | 257 | a0001c0002t0001g0020 a0001c0002t0001g0026 a0001c0002t0001g0156 others(254): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(279): Show |
intron_variant | MODIFIER | c.234+649dupA | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr22 | 43965184 | ||||||
| chr22:43965184 | T | TAA | 8 | a0001c0002t0002g0284 a0001c0002t0002g0330 a0001c0004t0001g0104 others(5): Show |
8 | HG01243.hp1 HG02257.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.234+648_234+649dup others(2): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr22 | 43965184 | ||||||
| chr22:43965216 | A | T | 1 | a0001c0007t0003g0315 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.234+663A>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 3/14 | chr22 | 43965216 | |||||||
| chr22:43965264 | G | A | 1 | a0002c0001t0001g0191 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.234+711G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 3/14 | chr22 | 43965264 | |||||||
| chr22:43965617 | C | A | 66 | a0001c0004t0001g0001 a0001c0004t0001g0015 a0001c0004t0001g0016 others(63): Show |
76 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.234+1064C>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 3/14 | chr22 | 43965617 | |||||||
| chr22:43965729 | A | AT | 269 | a0001c0002t0001g0020 a0001c0002t0001g0026 a0001c0002t0001g0156 others(266): Show |
296 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(293): Show |
intron_variant | MODIFIER | c.234+1185dupT | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr22 | 43965729 | ||||||
| chr22:43965833 | T | A | 25 | a0001c0007t0001g0031 a0001c0007t0001g0032 a0001c0007t0001g0317 others(22): Show |
28 | HG00280.hp2 HG00621.hp2 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.234+1280T>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 3/14 | chr22 | 43965833 | |||||||
| chr22:43965869 | G | A | 1 | a0001c0007t0001g0321 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.234+1316G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 3/14 | chr22 | 43965869 | |||||||
| chr22:43965962 | C | T | 96 | a0001c0002t0001g0183 a0001c0002t0001g0331 a0001c0002t0001g0332 others(93): Show |
103 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.234+1409C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 3/14 | chr22 | 43965962 | |||||||
| chr22:43966298 | G | A | 8 | a0001c0007t0001g0031 a0001c0007t0001g0032 a0001c0007t0001g0317 others(5): Show |
10 | HG00280.hp2 HG00733.hp2 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.234+1745G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 3/14 | chr22 | 43966298 | |||||||
| chr22:43966379 | C | T | 1 | a0001c0013t0001g0316 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.234+1826C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 3/14 | chr22 | 43966379 | |||||||
| chr22:43966383 | G | C | 2 | a0003c0003t0001g0083 a0003c0003t0001g0088 |
2 | HG00642.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.234+1830G>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 3/14 | chr22 | 43966383 | |||||||
| chr22:43966388 | G | A | 1 | a0002c0001t0001g0245 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.234+1835G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 3/14 | chr22 | 43966388 | |||||||
| chr22:43966605 | C | T | 1 | a0001c0005t0001g0150 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.234+2052C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 3/14 | chr22 | 43966605 | |||||||
| chr22:43966652 | G | A | 246 | a0001c0002t0001g0020 a0001c0002t0001g0026 a0001c0002t0001g0156 others(243): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.235-2079G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 3/14 | chr22 | 43966652 | |||||||
| chr22:43966743 | G | A | 1 | a0002c0001t0001g0216 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.235-1988G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 3/14 | chr22 | 43966743 | |||||||
| chr22:43966808 | A | AT | 199 | a0001c0002t0001g0020 a0001c0002t0001g0026 a0001c0002t0001g0156 others(196): Show |
214 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.235-1912dupT | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr22 | 43966808 | ||||||
| chr22:43966808 | A | ATT | 67 | a0001c0004t0001g0001 a0001c0004t0001g0015 a0001c0004t0001g0016 others(64): Show |
77 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.235-1913_235-1912d others(4): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr22 | 43966808 | ||||||
| chr22:43966907 | A | G | 11 | a0001c0005t0001g0006 a0001c0005t0001g0150 a0001c0005t0001g0323 others(8): Show |
13 | HG02055.hp2 HG02280.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.235-1824A>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 3/14 | chr22 | 43966907 | |||||||
| chr22:43966935 | C | T | 74 | a0001c0004t0001g0001 a0001c0004t0001g0015 a0001c0004t0001g0016 others(71): Show |
84 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(81): Show |
intron_variant | MODIFIER | c.235-1796C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 3/14 | chr22 | 43966935 | |||||||
| chr22:43966961 | C | G | 7 | a0001c0006t0001g0100 a0001c0006t0001g0102 a0001c0006t0001g0103 others(4): Show |
7 | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.235-1770C>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 3/14 | chr22 | 43966961 | |||||||
| chr22:43967138 | A | G | 1 | a0001c0002t0004g0288 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.235-1593A>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 3/14 | chr22 | 43967138 | |||||||
| chr22:43967257 | A | G | 1 | a0002c0001t0001g0238 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.235-1474A>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 3/14 | chr22 | 43967257 | |||||||
| chr22:43967463 | T | G | 1 | a0001c0006t0001g0102 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.235-1268T>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 3/14 | chr22 | 43967463 | |||||||
| chr22:43967585 | C | T | 2 | a0001c0002t0002g0030 a0001c0002t0002g0287 |
3 | HG00735.hp2 HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.235-1146C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 3/14 | chr22 | 43967585 | |||||||
| chr22:43967739 | T | TC | 249 | a0001c0002t0001g0020 a0001c0002t0001g0026 a0001c0002t0001g0156 others(246): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(269): Show |
intron_variant | MODIFIER | c.235-991dupC | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr22 | 43967739 | ||||||
| chr22:43967765 | T | C | 1 | a0001c0004t0001g0136 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.235-966T>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 3/14 | chr22 | 43967765 | |||||||
| chr22:43967777 | G | A | 1 | a0001c0004t0001g0132 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.235-954G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 3/14 | chr22 | 43967777 | |||||||
| chr22:43967856 | C | T | 8 | a0001c0007t0001g0031 a0001c0007t0001g0032 a0001c0007t0001g0317 others(5): Show |
10 | HG00280.hp2 HG00733.hp2 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.235-875C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 3/14 | chr22 | 43967856 | |||||||
| chr22:43967915 | A | C | 1 | a0001c0004t0001g0143 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.235-816A>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 3/14 | chr22 | 43967915 | |||||||
| chr22:43967943 | C | T | 3 | a0001c0002t0001g0020 a0001c0002t0001g0159 a0001c0002t0001g0160 |
4 | HG01891.hp1 HG01934.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.235-788C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 3/14 | chr22 | 43967943 | |||||||
| chr22:43968059 | T | A | 67 | a0001c0004t0001g0001 a0001c0004t0001g0015 a0001c0004t0001g0016 others(64): Show |
77 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.235-672T>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 3/14 | chr22 | 43968059 | |||||||
| chr22:43968104 | G | A | 9 | a0001c0006t0001g0046 a0001c0006t0001g0047 a0001c0006t0001g0100 others(6): Show |
9 | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.235-627G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 3/14 | chr22 | 43968104 | |||||||
| chr22:43968127 | C | T | 1 | a0001c0006t0001g0259 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.235-604C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 3/14 | chr22 | 43968127 | |||||||
| chr22:43968144 | T | A | 3 | a0001c0007t0005g0037 a0001c0013t0001g0314 a0001c0013t0001g0316 |
3 | HG02723.hp2 HG03195.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.235-587T>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 3/14 | chr22 | 43968144 | |||||||
| chr22:43968221 | T | C | 2 | a0001c0004t0001g0112 a0001c0004t0001g0125 |
2 | NA18949.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.235-510T>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 3/14 | chr22 | 43968221 | |||||||
| chr22:43968226 | C | CA | 7 | a0001c0002t0001g0184 a0001c0007t0005g0037 a0001c0008t0001g0174 others(4): Show |
7 | HG02257.hp1 HG02486.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.235-484dupA | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr22 | 43968226 | ||||||
| chr22:43968226 | CA | C | 203 | a0001c0002t0001g0183 a0001c0002t0001g0331 a0001c0002t0001g0332 others(200): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.235-484delA | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr22 | 43968226 | ||||||
| chr22:43968226 | CAA | C | 7 | a0001c0002t0002g0308 a0001c0004t0001g0113 a0002c0001t0001g0200 others(4): Show |
7 | HG00323.hp1 HG01515.hp1 HG02083.hp1 others(4): Show |
intron_variant | MODIFIER | c.235-485_235-484del others(2): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr22 | 43968226 | ||||||
| chr22:43968226 | CAAAAAAA others(8): Show |
C | 11 | a0001c0002t0001g0020 a0001c0002t0001g0156 a0001c0002t0001g0157 others(8): Show |
12 | HG01109.hp2 HG01891.hp1 HG01934.hp2 others(9): Show |
intron_variant | MODIFIER | c.235-498_235-484del others(15): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr22 | 43968226 | ||||||
| chr22:43968239 | AAAAAAAA others(9): Show |
A | 4 | a0001c0008t0001g0170 a0001c0008t0001g0173 a0001c0008t0001g0176 others(1): Show |
4 | HG02559.hp1 HG03041.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.235-484_235-469del others(16): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr22 | 43968239 | ||||||
| chr22:43968264 | A | AAAAAAAA others(10): Show |
1 | a0001c0004t0001g0035 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.235-455_235-454ins others(17): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr22 | 43968264 | ||||||
| chr22:43968447 | G | A | 3 | a0001c0008t0001g0036 a0001c0008t0001g0174 a0001c0008t0001g0175 |
3 | HG02257.hp1 HG02486.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.235-284G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 3/14 | chr22 | 43968447 | |||||||
| chr22:43968487 | C | T | 4 | a0001c0002t0002g0178 a0001c0002t0002g0275 a0001c0002t0002g0278 others(1): Show |
4 | HG02258.hp1 HG02970.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.235-244C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 3/14 | chr22 | 43968487 | |||||||
| chr22:43968534 | G | A | 1 | a0003c0003t0001g0075 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.235-197G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 3/14 | chr22 | 43968534 | |||||||
| chr22:43968615 | T | G | 3 | a0001c0002t0001g0331 a0001c0002t0001g0332 a0001c0002t0001g0333 |
3 | HG02647.hp1 HG02965.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.235-116T>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 3/14 | chr22 | 43968615 | |||||||
| chr22:43968677 | T | C | 3 | a0001c0007t0005g0037 a0001c0013t0001g0314 a0001c0013t0001g0316 |
3 | HG02723.hp2 HG03195.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.235-54T>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 3/14 | chr22 | 43968677 | |||||||
| chr22:43968714 | C | T | 254 | a0001c0002t0001g0020 a0001c0002t0001g0026 a0001c0002t0001g0156 others(251): Show |
279 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(276): Show |
intron_variant | MODIFIER | c.235-17C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 3/14 | chr22 | 43968714 | |||||||
| chr22:43968716 | T | C | 4 | a0001c0004t0001g0039 a0001c0004t0001g0115 a0001c0004t0001g0137 others(1): Show |
4 | HG00735.hp1 NA18971.hp1 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.235-15T>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 3/14 | chr22 | 43968716 | |||||||
| chr22:43968828 | G | T | 1 | a0001c0002t0001g0184 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.322+10G>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 4/14 | chr22 | 43968828 | |||||||
| chr22:43968914 | T | C | 255 | a0001c0002t0001g0020 a0001c0002t0001g0026 a0001c0002t0001g0156 others(252): Show |
280 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(277): Show |
intron_variant | MODIFIER | c.322+96T>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 4/14 | chr22 | 43968914 | |||||||
| chr22:43969187 | C | G | 1 | a0002c0001t0001g0191 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.322+369C>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 4/14 | chr22 | 43969187 | |||||||
| chr22:43969352 | G | C | 256 | a0001c0002t0001g0020 a0001c0002t0001g0026 a0001c0002t0001g0156 others(253): Show |
281 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(278): Show |
intron_variant | MODIFIER | c.322+534G>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 4/14 | chr22 | 43969352 | |||||||
| chr22:43969523 | C | T | 1 | a0003c0014t0001g0073 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.322+705C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 4/14 | chr22 | 43969523 | |||||||
| chr22:43969542 | A | C | 1 | a0001c0002t0002g0286 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.322+724A>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 4/14 | chr22 | 43969542 | |||||||
| chr22:43969635 | C | T | 1 | a0003c0003t0001g0110 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.322+817C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 4/14 | chr22 | 43969635 | |||||||
| chr22:43969808 | T | G | 11 | a0001c0002t0001g0020 a0001c0002t0001g0156 a0001c0002t0001g0157 others(8): Show |
12 | HG01109.hp2 HG01891.hp1 HG01934.hp2 others(9): Show |
intron_variant | MODIFIER | c.322+990T>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 4/14 | chr22 | 43969808 | |||||||
| chr22:43969862 | G | A | 248 | a0001c0002t0001g0020 a0001c0002t0001g0026 a0001c0002t0001g0156 others(245): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.322+1044G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 4/14 | chr22 | 43969862 | |||||||
| chr22:43969899 | T | A | 1 | a0002c0001t0001g0256 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.322+1081T>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 4/14 | chr22 | 43969899 | |||||||
| chr22:43970101 | C | T | 6 | a0001c0002t0001g0026 a0001c0002t0001g0260 a0001c0002t0001g0261 others(3): Show |
7 | HG00423.hp1 NA18963.hp2 NA18965.hp2 others(4): Show |
intron_variant | MODIFIER | c.322+1283C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 4/14 | chr22 | 43970101 | |||||||
| chr22:43970115 | G | A | 1 | a0001c0002t0002g0280 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.322+1297G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 4/14 | chr22 | 43970115 | |||||||
| chr22:43970137 | C | T | 1 | a0001c0004t0001g0152 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.322+1319C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 4/14 | chr22 | 43970137 | |||||||
| chr22:43970255 | G | A | 8 | a0001c0007t0001g0031 a0001c0007t0001g0032 a0001c0007t0001g0317 others(5): Show |
10 | HG00280.hp2 HG00733.hp2 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.322+1437G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 4/14 | chr22 | 43970255 | |||||||
| chr22:43970260 | G | A | 2 | a0003c0003t0001g0058 a0003c0003t0001g0069 |
2 | NA19007.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.322+1442G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 4/14 | chr22 | 43970260 | |||||||
| chr22:43970454 | G | A | 1 | a0001c0004t0001g0034 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.322+1636G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 4/14 | chr22 | 43970454 | |||||||
| chr22:43970797 | C | T | 11 | a0001c0002t0001g0020 a0001c0002t0001g0156 a0001c0002t0001g0157 others(8): Show |
12 | HG01109.hp2 HG01891.hp1 HG01934.hp2 others(9): Show |
intron_variant | MODIFIER | c.323-1439C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 4/14 | chr22 | 43970797 | |||||||
| chr22:43970818 | A | G | 4 | a0001c0005t0001g0323 a0001c0005t0001g0324 a0001c0005t0001g0325 others(1): Show |
4 | HG02615.hp2 HG02965.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.323-1418A>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 4/14 | chr22 | 43970818 | |||||||
| chr22:43970929 | A | G | 258 | a0001c0002t0001g0020 a0001c0002t0001g0026 a0001c0002t0001g0156 others(255): Show |
283 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(280): Show |
intron_variant | MODIFIER | c.323-1307A>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 4/14 | chr22 | 43970929 | |||||||
| chr22:43970994 | G | A | 7 | a0001c0002t0002g0297 a0001c0002t0002g0298 a0001c0002t0002g0311 others(4): Show |
9 | HG00280.hp2 HG00733.hp2 HG01070.hp2 others(6): Show |
intron_variant | MODIFIER | c.323-1242G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 4/14 | chr22 | 43970994 | |||||||
| chr22:43971081 | T | G | 3 | a0001c0002t0002g0030 a0001c0002t0002g0287 a0001c0002t0002g0291 |
4 | HG00735.hp2 HG01192.hp1 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.323-1155T>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 4/14 | chr22 | 43971081 | |||||||
| chr22:43971184 | C | T | 3 | a0001c0006t0001g0046 a0001c0006t0001g0047 a0002c0012t0001g0045 |
3 | HG02451.hp1 HG03098.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.323-1052C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 4/14 | chr22 | 43971184 | |||||||
| chr22:43971322 | C | T | 1 | a0002c0001t0001g0200 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.323-914C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 4/14 | chr22 | 43971322 | |||||||
| chr22:43971323 | G | T | 9 | a0001c0002t0001g0020 a0001c0002t0001g0156 a0001c0002t0001g0157 others(6): Show |
10 | HG01891.hp1 HG01934.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.323-913G>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 4/14 | chr22 | 43971323 | |||||||
| chr22:43971369 | C | T | 58 | a0001c0002t0001g0026 a0001c0002t0001g0184 a0001c0002t0001g0260 others(55): Show |
63 | HG00099.hp2 HG00423.hp1 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.323-867C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 4/14 | chr22 | 43971369 | |||||||
| chr22:43971538 | G | A | 7 | a0001c0006t0001g0100 a0001c0006t0001g0102 a0001c0006t0001g0103 others(4): Show |
7 | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.323-698G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 4/14 | chr22 | 43971538 | |||||||
| chr22:43971749 | C | T | 3 | a0001c0007t0005g0037 a0001c0013t0001g0314 a0001c0013t0001g0316 |
3 | HG02723.hp2 HG03195.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.323-487C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 4/14 | chr22 | 43971749 | |||||||
| chr22:43971943 | C | T | 1 | a0001c0002t0002g0282 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.323-293C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 4/14 | chr22 | 43971943 | |||||||
| chr22:43971992 | CTCAGCCC others(3): Show |
C | 1 | a0001c0004t0001g0135 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.323-242_323-233del others(10): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr22 | 43971992 | ||||||
| chr22:43972159 | T | C | 49 | a0001c0002t0002g0027 a0001c0002t0002g0028 a0001c0002t0002g0029 others(46): Show |
53 | HG00099.hp2 HG00544.hp1 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.323-77T>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 4/14 | chr22 | 43972159 | |||||||
| chr22:43972493 | C | T | 6 | a0001c0002t0001g0020 a0001c0002t0001g0159 a0001c0002t0001g0160 others(3): Show |
7 | HG01891.hp1 HG01934.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.429+151C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 5/14 | chr22 | 43972493 | |||||||
| chr22:43972704 | G | A | 4 | a0001c0007t0001g0031 a0001c0007t0001g0032 a0001c0007t0001g0317 others(1): Show |
6 | HG00280.hp2 HG00733.hp2 HG01070.hp2 others(3): Show |
intron_variant | MODIFIER | c.430-167G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 5/14 | chr22 | 43972704 | |||||||
| chr22:43972848 | A | AT | 175 | a0001c0002t0001g0020 a0001c0002t0001g0026 a0001c0002t0001g0156 others(172): Show |
188 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.430-11dupT | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr22 | 43972848 | ||||||
| chr22:43972861 | C | T | 246 | a0001c0002t0001g0020 a0001c0002t0001g0026 a0001c0002t0001g0156 others(243): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.430-10C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 5/14 | chr22 | 43972861 | |||||||
| chr22:43973153 | G | A | 1 | a0001c0002t0002g0279 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.561-83G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 6/14 | chr22 | 43973153 | |||||||
| chr22:43973357 | G | A | 9 | a0001c0002t0001g0020 a0001c0002t0001g0156 a0001c0002t0001g0157 others(6): Show |
10 | HG01891.hp1 HG01934.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.648+34G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 7/14 | chr22 | 43973357 | |||||||
| chr22:43973411 | G | A | 5 | a0002c0001t0001g0022 a0002c0001t0001g0201 a0002c0001t0001g0205 others(2): Show |
6 | HG00621.hp2 HG04184.hp2 NA18947.hp1 others(3): Show |
intron_variant | MODIFIER | c.648+88G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 7/14 | chr22 | 43973411 | |||||||
| chr22:43973449 | C | T | 151 | a0001c0002t0001g0026 a0001c0002t0001g0183 a0001c0002t0001g0184 others(148): Show |
163 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.648+126C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 7/14 | chr22 | 43973449 | |||||||
| chr22:43973500 | G | T | 9 | a0001c0002t0001g0020 a0001c0002t0001g0156 a0001c0002t0001g0157 others(6): Show |
10 | HG01891.hp1 HG01934.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.648+177G>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 7/14 | chr22 | 43973500 | |||||||
| chr22:43973549 | C | T | 253 | a0001c0002t0001g0020 a0001c0002t0001g0026 a0001c0002t0001g0156 others(250): Show |
278 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(275): Show |
intron_variant | MODIFIER | c.648+226C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 7/14 | chr22 | 43973549 | |||||||
| chr22:43973748 | G | A | 3 | a0001c0010t0001g0123 a0001c0010t0001g0133 a0001c0010t0001g0140 |
3 | HG02615.hp1 HG02895.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.648+425G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 7/14 | chr22 | 43973748 | |||||||
| chr22:43973825 | C | T | 1 | a0001c0007t0005g0037 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.648+502C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 7/14 | chr22 | 43973825 | |||||||
| chr22:43973899 | C | T | 9 | a0003c0003t0001g0052 a0003c0003t0001g0065 a0003c0003t0001g0072 others(6): Show |
9 | HG00621.hp1 HG02145.hp1 NA18949.hp2 others(6): Show |
intron_variant | MODIFIER | c.648+576C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 7/14 | chr22 | 43973899 | |||||||
| chr22:43974024 | CT | C | 245 | a0001c0002t0001g0020 a0001c0002t0001g0026 a0001c0002t0001g0156 others(242): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(267): Show |
intron_variant | MODIFIER | c.648+712delT | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr22 | 43974024 | ||||||
| chr22:43974035 | T | C | 3 | a0001c0002t0001g0331 a0001c0002t0001g0332 a0001c0002t0001g0333 |
3 | HG02647.hp1 HG02965.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.648+712T>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 7/14 | chr22 | 43974035 | |||||||
| chr22:43974047 | C | T | 7 | a0001c0007t0001g0031 a0001c0007t0001g0032 a0001c0007t0001g0317 others(4): Show |
9 | HG00280.hp2 HG00733.hp2 HG01070.hp2 others(6): Show |
intron_variant | MODIFIER | c.648+724C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 7/14 | chr22 | 43974047 | |||||||
| chr22:43974062 | C | T | 3 | a0001c0007t0005g0037 a0001c0013t0001g0314 a0001c0013t0001g0316 |
3 | HG02723.hp2 HG03195.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.648+739C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 7/14 | chr22 | 43974062 | |||||||
| chr22:43974266 | C | G | 1 | a0002c0001t0001g0237 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.648+943C>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 7/14 | chr22 | 43974266 | |||||||
| chr22:43974295 | C | G | 1 | a0001c0004t0001g0135 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.648+972C>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 7/14 | chr22 | 43974295 | |||||||
| chr22:43974295 | C | T | 66 | a0001c0004t0001g0001 a0001c0004t0001g0015 a0001c0004t0001g0016 others(63): Show |
76 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.648+972C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 7/14 | chr22 | 43974295 | |||||||
| chr22:43974357 | A | T | 1 | a0003c0003t0001g0057 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.648+1034A>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 7/14 | chr22 | 43974357 | |||||||
| chr22:43974396 | G | A | 4 | a0001c0008t0001g0170 a0001c0008t0001g0173 a0001c0008t0001g0176 others(1): Show |
4 | HG02559.hp1 HG03041.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.648+1073G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 7/14 | chr22 | 43974396 | |||||||
| chr22:43974456 | T | G | 255 | a0001c0002t0001g0020 a0001c0002t0001g0026 a0001c0002t0001g0156 others(252): Show |
280 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(277): Show |
intron_variant | MODIFIER | c.648+1133T>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 7/14 | chr22 | 43974456 | |||||||
| chr22:43974457 | T | C | 255 | a0001c0002t0001g0020 a0001c0002t0001g0026 a0001c0002t0001g0156 others(252): Show |
280 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(277): Show |
intron_variant | MODIFIER | c.648+1134T>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 7/14 | chr22 | 43974457 | |||||||
| chr22:43974548 | A | C | 2 | a0002c0011t0001g0038 a0002c0011t0001g0243 |
2 | HG00639.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.648+1225A>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 7/14 | chr22 | 43974548 | |||||||
| chr22:43974559 | A | C | 7 | a0001c0007t0001g0031 a0001c0007t0001g0032 a0001c0007t0001g0317 others(4): Show |
9 | HG00280.hp2 HG00733.hp2 HG01070.hp2 others(6): Show |
intron_variant | MODIFIER | c.648+1236A>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 7/14 | chr22 | 43974559 | |||||||
| chr22:43974735 | T | C | 270 | a0001c0002t0001g0020 a0001c0002t0001g0026 a0001c0002t0001g0156 others(267): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(294): Show |
intron_variant | MODIFIER | c.649-1320T>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 7/14 | chr22 | 43974735 | |||||||
| chr22:43974781 | G | A | 2 | a0001c0004t0001g0114 a0001c0004t0001g0127 |
2 | HG03927.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.649-1274G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 7/14 | chr22 | 43974781 | |||||||
| chr22:43974786 | C | T | 1 | a0001c0002t0002g0269 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.649-1269C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 7/14 | chr22 | 43974786 | |||||||
| chr22:43974788 | C | T | 7 | a0001c0006t0001g0100 a0001c0006t0001g0102 a0001c0006t0001g0103 others(4): Show |
7 | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.649-1267C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 7/14 | chr22 | 43974788 | |||||||
| chr22:43975060 | C | T | 1 | a0001c0004t0001g0137 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.649-995C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 7/14 | chr22 | 43975060 | |||||||
| chr22:43975073 | G | T | 1 | a0001c0002t0001g0183 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.649-982G>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 7/14 | chr22 | 43975073 | |||||||
| chr22:43975075 | A | G | 14 | a0001c0006t0001g0100 a0001c0006t0001g0102 a0001c0006t0001g0103 others(11): Show |
16 | HG00280.hp2 HG00733.hp2 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.649-980A>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 7/14 | chr22 | 43975075 | |||||||
| chr22:43975100 | A | G | 1 | a0003c0003t0001g0110 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.649-955A>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 7/14 | chr22 | 43975100 | |||||||
| chr22:43975127 | G | C | 4 | a0002c0001t0001g0235 a0002c0001t0001g0253 a0002c0012t0001g0144 others(1): Show |
4 | HG00280.hp1 HG01255.hp1 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.649-928G>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 7/14 | chr22 | 43975127 | |||||||
| chr22:43975150 | G | A | 4 | a0001c0007t0001g0031 a0001c0007t0001g0032 a0001c0007t0001g0317 others(1): Show |
6 | HG00280.hp2 HG00733.hp2 HG01070.hp2 others(3): Show |
intron_variant | MODIFIER | c.649-905G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 7/14 | chr22 | 43975150 | |||||||
| chr22:43975207 | C | T | 1 | a0001c0004t0001g0137 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.649-848C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 7/14 | chr22 | 43975207 | |||||||
| chr22:43975363 | A | G | 244 | a0001c0002t0001g0020 a0001c0002t0001g0026 a0001c0002t0001g0156 others(241): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.649-692A>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 7/14 | chr22 | 43975363 | |||||||
| chr22:43975408 | C | A | 1 | a0001c0002t0002g0282 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.649-647C>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 7/14 | chr22 | 43975408 | |||||||
| chr22:43975432 | G | A | 244 | a0001c0002t0001g0020 a0001c0002t0001g0026 a0001c0002t0001g0156 others(241): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.649-623G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 7/14 | chr22 | 43975432 | |||||||
| chr22:43975446 | A | C | 3 | a0001c0008t0001g0036 a0001c0008t0001g0174 a0001c0008t0001g0175 |
3 | HG02257.hp1 HG02486.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.649-609A>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 7/14 | chr22 | 43975446 | |||||||
| chr22:43975502 | G | C | 4 | a0001c0002t0001g0183 a0001c0002t0001g0331 a0001c0002t0001g0332 others(1): Show |
4 | HG02647.hp1 HG02965.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.649-553G>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 7/14 | chr22 | 43975502 | |||||||
| chr22:43975526 | A | G | 89 | a0002c0001t0001g0005 a0002c0001t0001g0021 a0002c0001t0001g0022 others(86): Show |
96 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.649-529A>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 7/14 | chr22 | 43975526 | |||||||
| chr22:43975575 | G | C | 1 | a0001c0008t0001g0177 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.649-480G>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 7/14 | chr22 | 43975575 | |||||||
| chr22:43975602 | G | A | 1 | a0003c0003t0001g0068 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.649-453G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 7/14 | chr22 | 43975602 | |||||||
| chr22:43975691 | C | T | 4 | a0003c0003t0001g0002 a0003c0003t0001g0057 a0003c0003t0001g0061 others(1): Show |
8 | HG01071.hp2 HG01123.hp2 HG01358.hp2 others(5): Show |
intron_variant | MODIFIER | c.649-364C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 7/14 | chr22 | 43975691 | |||||||
| chr22:43975845 | C | A | 1 | a0002c0001t0001g0215 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.649-210C>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 7/14 | chr22 | 43975845 | |||||||
| chr22:43975845 | C | G | 246 | a0001c0002t0001g0020 a0001c0002t0001g0026 a0001c0002t0001g0156 others(243): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.649-210C>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 7/14 | chr22 | 43975845 | |||||||
| chr22:43976189 | G | A | 178 | a0001c0002t0001g0020 a0001c0002t0001g0026 a0001c0002t0001g0156 others(175): Show |
191 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(188): Show |
splice_region_variant&intron_variant | LOW | c.777+6G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 8/14 | chr22 | 43976189 | |||||||
| chr22:43976310 | C | T | 177 | a0001c0002t0001g0020 a0001c0002t0001g0026 a0001c0002t0001g0156 others(174): Show |
190 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.777+127C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 8/14 | chr22 | 43976310 | |||||||
| chr22:43976336 | G | T | 1 | a0001c0002t0002g0285 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.777+153G>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 8/14 | chr22 | 43976336 | |||||||
| chr22:43976349 | C | T | 1 | a0001c0004t0001g0127 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.777+166C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 8/14 | chr22 | 43976349 | |||||||
| chr22:43976376 | G | T | 1 | a0001c0007t0003g0315 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.777+193G>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 8/14 | chr22 | 43976376 | |||||||
| chr22:43976406 | C | G | 1 | a0001c0006t0001g0108 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.777+223C>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 8/14 | chr22 | 43976406 | |||||||
| chr22:43976431 | A | G | 3 | a0001c0009t0001g0055 a0001c0009t0001g0056 a0002c0011t0001g0225 |
3 | HG01433.hp1 HG02922.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.777+248A>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 8/14 | chr22 | 43976431 | |||||||
| chr22:43976451 | C | T | 177 | a0001c0002t0001g0020 a0001c0002t0001g0026 a0001c0002t0001g0156 others(174): Show |
190 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.777+268C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 8/14 | chr22 | 43976451 | |||||||
| chr22:43976617 | AAGGGCTC others(22): Show |
A | 1 | a0001c0004t0001g0119 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.778-130_778-102del others(29): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr22 | 43976617 | ||||||
| chr22:43976645 | A | G | 7 | a0001c0006t0001g0100 a0001c0006t0001g0102 a0001c0006t0001g0103 others(4): Show |
7 | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.778-105A>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 8/14 | chr22 | 43976645 | |||||||
| chr22:43976941 | T | C | 9 | a0001c0008t0001g0036 a0001c0008t0001g0170 a0001c0008t0001g0171 others(6): Show |
9 | HG01109.hp2 HG02109.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.849+120T>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 9/14 | chr22 | 43976941 | |||||||
| chr22:43977072 | A | G | 2 | a0001c0009t0001g0055 a0001c0009t0001g0056 |
2 | HG01433.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.849+251A>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 9/14 | chr22 | 43977072 | |||||||
| chr22:43977177 | C | T | 1 | a0001c0010t0001g0133 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.849+356C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 9/14 | chr22 | 43977177 | |||||||
| chr22:43977213 | A | G | 2 | a0001c0005t0001g0324 a0001c0005t0001g0325 |
2 | HG02965.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.849+392A>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 9/14 | chr22 | 43977213 | |||||||
| chr22:43977251 | G | A | 3 | a0001c0002t0001g0331 a0001c0002t0001g0332 a0001c0002t0001g0333 |
3 | HG02647.hp1 HG02965.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.849+430G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 9/14 | chr22 | 43977251 | |||||||
| chr22:43977282 | T | G | 1 | a0002c0001t0001g0228 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.849+461T>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 9/14 | chr22 | 43977282 | |||||||
| chr22:43977456 | G | A | 3 | a0001c0007t0005g0037 a0001c0013t0001g0314 a0001c0013t0001g0316 |
3 | HG02723.hp2 HG03195.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.850-416G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 9/14 | chr22 | 43977456 | |||||||
| chr22:43977580 | C | T | 1 | a0001c0005t0001g0150 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.850-292C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 9/14 | chr22 | 43977580 | |||||||
| chr22:43977699 | G | A | 69 | a0001c0004t0001g0001 a0001c0004t0001g0015 a0001c0004t0001g0016 others(66): Show |
79 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.850-173G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 9/14 | chr22 | 43977699 | |||||||
| chr22:43977722 | A | G | 4 | a0001c0006t0001g0046 a0001c0006t0001g0047 a0001c0007t0001g0321 others(1): Show |
4 | HG02451.hp1 HG03098.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.850-150A>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 9/14 | chr22 | 43977722 | |||||||
| chr22:43977779 | C | T | 2 | a0003c0003t0001g0062 a0003c0003t0001g0064 |
2 | HG01169.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.850-93C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 9/14 | chr22 | 43977779 | |||||||
| chr22:43978065 | G | T | 7 | a0001c0006t0001g0100 a0001c0006t0001g0102 a0001c0006t0001g0103 others(4): Show |
7 | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.936+107G>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | chr22 | 43978065 | |||||||
| chr22:43978067 | G | A | 4 | a0001c0007t0001g0031 a0001c0007t0001g0032 a0001c0007t0001g0317 others(1): Show |
6 | HG00280.hp2 HG00733.hp2 HG01070.hp2 others(3): Show |
intron_variant | MODIFIER | c.936+109G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | chr22 | 43978067 | |||||||
| chr22:43978209 | T | G | 1 | a0002c0001t0001g0272 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.936+251T>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | chr22 | 43978209 | |||||||
| chr22:43978315 | G | T | 70 | a0001c0004t0001g0001 a0001c0004t0001g0015 a0001c0004t0001g0016 others(67): Show |
80 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(77): Show |
intron_variant | MODIFIER | c.936+357G>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | chr22 | 43978315 | |||||||
| chr22:43978343 | G | A | 4 | a0001c0008t0001g0170 a0001c0008t0001g0173 a0001c0008t0001g0176 others(1): Show |
4 | HG02559.hp1 HG03041.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.936+385G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | chr22 | 43978343 | |||||||
| chr22:43978378 | T | C | 1 | a0001c0002t0002g0278 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.936+420T>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | chr22 | 43978378 | |||||||
| chr22:43978387 | A | G | 251 | a0001c0002t0001g0020 a0001c0002t0001g0026 a0001c0002t0001g0156 others(248): Show |
274 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(271): Show |
intron_variant | MODIFIER | c.936+429A>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | chr22 | 43978387 | |||||||
| chr22:43978432 | C | CAAAA | 20 | a0001c0002t0001g0263 a0001c0002t0002g0269 a0001c0002t0004g0288 others(17): Show |
20 | HG01496.hp1 HG02027.hp1 HG02080.hp1 others(17): Show |
intron_variant | MODIFIER | c.936+492_936+495dup others(4): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43978432 | ||||||
| chr22:43978432 | C | CAAAAA | 186 | a0001c0002t0001g0026 a0001c0002t0001g0162 a0001c0002t0001g0184 others(183): Show |
208 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(205): Show |
intron_variant | MODIFIER | c.936+491_936+495dup others(5): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43978432 | ||||||
| chr22:43978432 | C | CAAAAAA | 35 | a0001c0002t0001g0020 a0001c0002t0001g0157 a0001c0002t0001g0159 others(32): Show |
36 | HG00438.hp2 HG00544.hp2 HG00621.hp2 others(33): Show |
intron_variant | MODIFIER | c.936+490_936+495dup others(6): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43978432 | ||||||
| chr22:43978432 | CA | C | 7 | a0001c0007t0001g0031 a0001c0007t0001g0032 a0001c0007t0001g0317 others(4): Show |
9 | HG00280.hp2 HG00733.hp2 HG01070.hp2 others(6): Show |
intron_variant | MODIFIER | c.936+495delA | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43978432 | ||||||
| chr22:43978636 | A | T | 7 | a0001c0008t0001g0036 a0001c0008t0001g0170 a0001c0008t0001g0173 others(4): Show |
7 | HG02257.hp1 HG02486.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.936+678A>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | chr22 | 43978636 | |||||||
| chr22:43978636 | AT | A | 9 | a0001c0004t0001g0119 a0001c0004t0001g0135 a0001c0004t0001g0142 others(6): Show |
9 | HG01167.hp2 HG01943.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.936+693delT | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43978636 | ||||||
| chr22:43978637 | T | A | 1 | a0001c0009t0001g0056 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.936+679T>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | chr22 | 43978637 | |||||||
| chr22:43978704 | A | T | 251 | a0001c0002t0001g0020 a0001c0002t0001g0026 a0001c0002t0001g0156 others(248): Show |
274 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(271): Show |
intron_variant | MODIFIER | c.936+746A>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | chr22 | 43978704 | |||||||
| chr22:43978751 | G | A | 1 | a0002c0001t0001g0252 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.936+793G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | chr22 | 43978751 | |||||||
| chr22:43978883 | G | T | 9 | a0001c0002t0001g0020 a0001c0002t0001g0156 a0001c0002t0001g0157 others(6): Show |
10 | HG01891.hp1 HG01934.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.936+925G>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | chr22 | 43978883 | |||||||
| chr22:43979196 | A | C | 1 | a0003c0016t0001g0099 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.936+1238A>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | chr22 | 43979196 | |||||||
| chr22:43979364 | C | T | 251 | a0001c0002t0001g0020 a0001c0002t0001g0026 a0001c0002t0001g0156 others(248): Show |
274 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(271): Show |
intron_variant | MODIFIER | c.936+1406C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | chr22 | 43979364 | |||||||
| chr22:43979367 | A | C | 256 | a0001c0002t0001g0020 a0001c0002t0001g0026 a0001c0002t0001g0156 others(253): Show |
281 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(278): Show |
intron_variant | MODIFIER | c.936+1409A>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | chr22 | 43979367 | |||||||
| chr22:43979395 | C | A | 181 | a0001c0002t0001g0020 a0001c0002t0001g0026 a0001c0002t0001g0156 others(178): Show |
194 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.936+1437C>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | chr22 | 43979395 | |||||||
| chr22:43979558 | C | T | 49 | a0001c0002t0002g0027 a0001c0002t0002g0028 a0001c0002t0002g0029 others(46): Show |
53 | HG00099.hp2 HG00544.hp1 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.936+1600C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | chr22 | 43979558 | |||||||
| chr22:43979582 | T | A | 1 | a0002c0012t0001g0148 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.936+1624T>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | chr22 | 43979582 | |||||||
| chr22:43979601 | G | A | 2 | a0001c0004t0001g0129 a0001c0004t0001g0138 |
2 | NA18953.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.936+1643G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | chr22 | 43979601 | |||||||
| chr22:43979627 | T | C | 251 | a0001c0002t0001g0020 a0001c0002t0001g0026 a0001c0002t0001g0156 others(248): Show |
274 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(271): Show |
intron_variant | MODIFIER | c.936+1669T>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | chr22 | 43979627 | |||||||
| chr22:43979637 | T | C | 1 | a0001c0004t0001g0119 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.936+1679T>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | chr22 | 43979637 | |||||||
| chr22:43979862 | C | T | 181 | a0001c0002t0001g0020 a0001c0002t0001g0026 a0001c0002t0001g0156 others(178): Show |
194 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.937-1529C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | chr22 | 43979862 | |||||||
| chr22:43979981 | A | C | 1 | a0002c0001t0001g0196 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.937-1410A>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | chr22 | 43979981 | |||||||
| chr22:43980022 | C | T | 7 | a0001c0006t0001g0100 a0001c0006t0001g0102 a0001c0006t0001g0103 others(4): Show |
7 | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.937-1369C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | chr22 | 43980022 | |||||||
| chr22:43980065 | C | T | 1 | a0001c0008t0001g0173 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.937-1326C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | chr22 | 43980065 | |||||||
| chr22:43980090 | A | G | 181 | a0001c0002t0001g0020 a0001c0002t0001g0026 a0001c0002t0001g0156 others(178): Show |
194 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.937-1301A>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | chr22 | 43980090 | |||||||
| chr22:43980136 | A | ACACATCC others(623): Show |
1 | a0002c0001t0001g0200 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.937-1253_937-1252i others(632): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | ||||||
| chr22:43980136 | A | ACATCCAT others(593): Show |
1 | a0003c0003t0001g0061 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.937-1228_937-1227i others(602): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | ||||||
| chr22:43980136 | A | ACATCCAT others(597): Show |
3 | a0003c0003t0001g0002 a0003c0003t0001g0057 a0003c0003t0001g0091 |
7 | HG01071.hp2 HG01123.hp2 HG01358.hp2 others(4): Show |
intron_variant | MODIFIER | c.937-1228_937-1227i others(606): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | ||||||
| chr22:43980136 | A | ACATCCAT others(613): Show |
1 | a0002c0001t0001g0053 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.937-1228_937-1227i others(622): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | ||||||
| chr22:43980136 | A | ACATCCAT others(917): Show |
2 | a0001c0007t0001g0031 a0001c0007t0001g0032 |
4 | HG00280.hp2 HG00733.hp2 HG01109.hp1 others(1): Show |
intron_variant | MODIFIER | c.937-1228_937-1227i others(926): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | ||||||
| chr22:43980136 | A | ACATCCAT others(921): Show |
2 | a0001c0007t0001g0317 a0001c0007t0001g0318 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.937-1228_937-1227i others(930): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | ||||||
| chr22:43980136 | A | ACATCCAT others(625): Show |
8 | a0002c0001t0001g0041 a0002c0001t0001g0042 a0002c0001t0001g0201 others(5): Show |
8 | HG00408.hp2 HG01243.hp2 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.937-1228_937-1227i others(634): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | ||||||
| chr22:43980136 | A | ACATCCAT others(625): Show |
1 | a0002c0001t0001g0193 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.937-1228_937-1227i others(634): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | ||||||
| chr22:43980136 | A | ACATCCAT others(617): Show |
3 | a0002c0001t0001g0197 a0002c0001t0001g0209 a0002c0001t0001g0230 |
3 | HG00741.hp1 HG02056.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.937-1228_937-1227i others(626): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | ||||||
| chr22:43980136 | A | ACATCCAT others(621): Show |
2 | a0002c0001t0001g0226 a0002c0001t0001g0247 |
2 | HG02027.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.937-1228_937-1227i others(630): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | ||||||
| chr22:43980136 | A | ACATCCAT others(621): Show |
48 | a0002c0001t0001g0005 a0002c0001t0001g0021 a0002c0001t0001g0022 others(45): Show |
54 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.937-1228_937-1227i others(630): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | ||||||
| chr22:43980136 | A | ACATCCAT others(625): Show |
1 | a0002c0001t0001g0244 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.937-1228_937-1227i others(634): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | ||||||
| chr22:43980136 | A | ACATCCAT others(617): Show |
2 | a0002c0001t0001g0186 a0002c0001t0001g0189 |
2 | HG02572.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.937-1228_937-1227i others(626): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | ||||||
| chr22:43980136 | A | ACATCCAT others(622): Show |
1 | a0002c0001t0001g0255 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.937-1228_937-1227i others(631): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | ||||||
| chr22:43980136 | A | ACATCCAT others(629): Show |
1 | a0002c0001t0001g0257 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.937-1228_937-1227i others(638): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | ||||||
| chr22:43980136 | A | ACATCCAT others(625): Show |
2 | a0002c0001t0001g0195 a0002c0001t0001g0271 |
2 | NA18971.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.937-1228_937-1227i others(634): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | ||||||
| chr22:43980136 | A | ACATCCAT others(617): Show |
1 | a0002c0012t0001g0045 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.937-1228_937-1227i others(626): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | ||||||
| chr22:43980136 | A | ACATCCAT others(621): Show |
1 | a0002c0001t0001g0192 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.937-1228_937-1227i others(630): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | ||||||
| chr22:43980136 | A | ACATCCAT others(617): Show |
5 | a0002c0001t0001g0023 a0002c0001t0001g0236 a0002c0001t0001g0245 others(2): Show |
6 | HG02015.hp1 HG03704.hp1 NA18946.hp1 others(3): Show |
intron_variant | MODIFIER | c.937-1228_937-1227i others(626): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | ||||||
| chr22:43980136 | A | ACATCCAT others(621): Show |
1 | a0001c0006t0001g0109 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.937-1228_937-1227i others(630): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | ||||||
| chr22:43980136 | A | ACATCCAT others(625): Show |
6 | a0002c0001t0001g0198 a0002c0001t0001g0235 a0002c0001t0001g0238 others(3): Show |
6 | HG01255.hp1 HG02056.hp2 HG03017.hp2 others(3): Show |
intron_variant | MODIFIER | c.937-1228_937-1227i others(634): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | ||||||
| chr22:43980136 | A | ACATCCAT others(613): Show |
1 | a0002c0001t0001g0187 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.937-1228_937-1227i others(622): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | ||||||
| chr22:43980136 | A | ACATCCAT others(613): Show |
1 | a0001c0002t0001g0261 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.937-1228_937-1227i others(622): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | ||||||
| chr22:43980136 | A | ACATCCAT others(617): Show |
6 | a0001c0002t0001g0026 a0001c0002t0001g0260 a0001c0002t0001g0262 others(3): Show |
7 | HG00423.hp1 HG04204.hp1 NA18963.hp2 others(4): Show |
intron_variant | MODIFIER | c.937-1228_937-1227i others(626): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | ||||||
| chr22:43980136 | A | ACATCCAT others(617): Show |
1 | a0002c0001t0001g0188 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.937-1228_937-1227i others(626): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | ||||||
| chr22:43980136 | A | ACATCCAT others(617): Show |
1 | a0002c0001t0001g0228 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.937-1228_937-1227i others(626): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | ||||||
| chr22:43980136 | A | ACATCCAT others(609): Show |
1 | a0003c0003t0001g0010 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.937-1228_937-1227i others(618): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | ||||||
| chr22:43980136 | A | ACATCCAT others(605): Show |
4 | a0001c0020t0001g0322 a0003c0003t0001g0059 a0003c0003t0001g0066 others(1): Show |
4 | HG02145.hp2 HG02647.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.937-1228_937-1227i others(614): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | ||||||
| chr22:43980136 | A | ACATCCAT others(601): Show |
1 | a0003c0003t0001g0075 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.937-1228_937-1227i others(610): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | ||||||
| chr22:43980136 | A | ACATCCAT others(617): Show |
3 | a0003c0003t0001g0060 a0003c0003t0001g0083 a0003c0003t0001g0088 |
3 | HG00642.hp1 HG01081.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.937-1228_937-1227i others(626): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | ||||||
| chr22:43980136 | A | ACATCCAT others(613): Show |
26 | a0003c0003t0001g0003 a0003c0003t0001g0004 a0003c0003t0001g0008 others(23): Show |
36 | HG00140.hp1 HG00408.hp1 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.937-1228_937-1227i others(622): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | ||||||
| chr22:43980136 | A | ACATCCAT others(617): Show |
1 | a0003c0003t0001g0076 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.937-1228_937-1227i others(626): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | ||||||
| chr22:43980136 | A | ACATCCAT others(605): Show |
1 | a0004c0015t0001g0077 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.937-1228_937-1227i others(614): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | ||||||
| chr22:43980136 | A | ACATCCAT others(609): Show |
12 | a0003c0003t0001g0007 a0003c0003t0001g0049 a0003c0003t0001g0052 others(9): Show |
13 | HG00558.hp2 HG01169.hp1 HG02015.hp2 others(10): Show |
intron_variant | MODIFIER | c.937-1228_937-1227i others(618): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | ||||||
| chr22:43980136 | A | ACATCCAT others(605): Show |
1 | a0003c0003t0001g0090 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.937-1228_937-1227i others(614): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | ||||||
| chr22:43980136 | A | ACATCCAT others(609): Show |
1 | a0003c0003t0001g0068 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.937-1228_937-1227i others(618): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | ||||||
| chr22:43980136 | A | ACATCCAT others(613): Show |
1 | a0003c0003t0001g0064 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.937-1228_937-1227i others(622): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | ||||||
| chr22:43980136 | A | ACATCCAT others(613): Show |
1 | a0003c0003t0001g0110 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.937-1228_937-1227i others(622): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | ||||||
| chr22:43980136 | A | ACATCCAT others(609): Show |
1 | a0001c0009t0001g0055 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.937-1228_937-1227i others(618): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | ||||||
| chr22:43980136 | A | ACATCCAT others(941): Show |
1 | a0001c0007t0003g0315 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.937-1228_937-1227i others(950): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | ||||||
| chr22:43980136 | A | ACATCCAT others(621): Show |
1 | a0001c0002t0001g0332 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.937-1228_937-1227i others(630): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | ||||||
| chr22:43980136 | A | ACATCCAT others(621): Show |
1 | a0001c0002t0001g0331 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.937-1228_937-1227i others(630): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | ||||||
| chr22:43980136 | A | ACATCCAT others(629): Show |
1 | a0001c0002t0001g0333 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.937-1228_937-1227i others(638): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | ||||||
| chr22:43980136 | A | ACATCCAT others(625): Show |
3 | a0001c0002t0002g0027 a0001c0002t0002g0043 a0001c0002t0002g0267 |
4 | HG02258.hp2 HG02717.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.937-1228_937-1227i others(634): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | ||||||
| chr22:43980136 | A | ACATCCAT others(625): Show |
1 | a0002c0001t0001g0191 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.937-1228_937-1227i others(634): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | ||||||
| chr22:43980136 | A | ACATCCAT others(621): Show |
2 | a0001c0006t0001g0103 a0001c0006t0001g0106 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.937-1228_937-1227i others(630): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | ||||||
| chr22:43980136 | A | ACATCCAT others(625): Show |
4 | a0001c0006t0001g0100 a0001c0006t0001g0102 a0001c0006t0001g0107 others(1): Show |
4 | HG02055.hp1 HG02818.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.937-1228_937-1227i others(634): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | ||||||
| chr22:43980136 | A | ACATCCAT others(625): Show |
1 | a0001c0002t0001g0183 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.937-1228_937-1227i others(634): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | ||||||
| chr22:43980136 | A | ACATCCAT others(629): Show |
1 | a0001c0008t0001g0170 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.937-1228_937-1227i others(638): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | ||||||
| chr22:43980136 | A | ACATCCAT others(625): Show |
1 | a0001c0008t0001g0175 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.937-1228_937-1227i others(634): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | ||||||
| chr22:43980136 | A | ACATCCAT others(585): Show |
1 | a0001c0002t0002g0278 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.937-1228_937-1227i others(594): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | ||||||
| chr22:43980136 | A | ACATCCAT others(581): Show |
1 | a0001c0002t0002g0289 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.937-1228_937-1227i others(590): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | ||||||
| chr22:43980136 | A | ACATCCAT others(581): Show |
2 | a0001c0002t0002g0178 a0001c0002t0002g0275 |
2 | HG02258.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.937-1228_937-1227i others(590): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | ||||||
| chr22:43980136 | A | ACATCCAT others(585): Show |
1 | a0001c0002t0002g0283 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.937-1228_937-1227i others(594): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | ||||||
| chr22:43980136 | A | ACATCCAT others(597): Show |
1 | a0001c0002t0002g0309 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.937-1228_937-1227i others(606): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | ||||||
| chr22:43980136 | A | ACATCCAT others(581): Show |
1 | a0001c0002t0002g0280 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.937-1228_937-1227i others(590): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | ||||||
| chr22:43980136 | A | ACATCCAT others(593): Show |
4 | a0001c0002t0002g0290 a0001c0002t0002g0299 a0001c0002t0002g0300 others(1): Show |
4 | HG00099.hp2 HG01243.hp1 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.937-1228_937-1227i others(602): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | ||||||
| chr22:43980136 | A | ACATCCAT others(581): Show |
10 | a0001c0002t0002g0180 a0001c0002t0002g0281 a0001c0002t0002g0285 others(7): Show |
10 | HG02486.hp1 HG02572.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.937-1228_937-1227i others(590): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | ||||||
| chr22:43980136 | A | ACATCCAT others(597): Show |
18 | a0001c0002t0002g0029 a0001c0002t0002g0030 a0001c0002t0002g0179 others(15): Show |
20 | HG00544.hp1 HG00558.hp1 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.937-1228_937-1227i others(606): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | ||||||
| chr22:43980136 | A | ACATCCAT others(601): Show |
1 | a0001c0002t0002g0292 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.937-1228_937-1227i others(610): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | ||||||
| chr22:43980136 | A | ACATCCAT others(593): Show |
5 | a0001c0002t0002g0028 a0001c0002t0002g0282 a0001c0002t0002g0297 others(2): Show |
6 | HG04199.hp2 NA18972.hp1 NA18981.hp2 others(3): Show |
intron_variant | MODIFIER | c.937-1228_937-1227i others(602): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | ||||||
| chr22:43980136 | A | ACATCCAT others(629): Show |
2 | a0001c0002t0002g0265 a0001c0002t0002g0266 |
2 | HG03486.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.937-1228_937-1227i others(638): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | ||||||
| chr22:43980136 | A | ACATCCAT others(593): Show |
1 | a0001c0004t0001g0048 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.937-1228_937-1227i others(602): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | ||||||
| chr22:43980136 | A | ACATCCAT others(605): Show |
2 | a0002c0011t0001g0038 a0002c0011t0001g0243 |
2 | HG00639.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.937-1228_937-1227i others(614): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | ||||||
| chr22:43980136 | A | ACATCCAT others(605): Show |
1 | a0001c0004t0001g0168 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.937-1228_937-1227i others(614): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | ||||||
| chr22:43980136 | A | ACATCCAT others(593): Show |
1 | a0001c0004t0001g0142 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.937-1228_937-1227i others(602): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | ||||||
| chr22:43980136 | A | ACATCCAT others(597): Show |
1 | a0001c0010t0001g0123 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.937-1228_937-1227i others(606): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | ||||||
| chr22:43980136 | A | ACATCCAT others(601): Show |
2 | a0001c0010t0001g0133 a0001c0010t0001g0140 |
2 | HG02615.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.937-1228_937-1227i others(610): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | ||||||
| chr22:43980136 | A | ACATCCAT others(601): Show |
55 | a0001c0004t0001g0001 a0001c0004t0001g0015 a0001c0004t0001g0016 others(52): Show |
65 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.937-1228_937-1227i others(610): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | ||||||
| chr22:43980136 | A | ACATCCAT others(605): Show |
2 | a0001c0004t0001g0145 a0002c0012t0001g0144 |
2 | HG01433.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.937-1228_937-1227i others(614): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | ||||||
| chr22:43980136 | A | ACATCCAT others(597): Show |
2 | a0001c0004t0001g0141 a0001c0004t0002g0040 |
2 | HG02257.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.937-1228_937-1227i others(606): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | ||||||
| chr22:43980136 | A | ACATCCAT others(597): Show |
1 | a0001c0009t0001g0056 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.937-1228_937-1227i others(606): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | ||||||
| chr22:43980136 | A | ACATCCAT others(617): Show |
4 | a0001c0005t0001g0006 a0001c0005t0001g0324 a0001c0005t0001g0325 others(1): Show |
6 | HG02055.hp2 HG02886.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.937-1228_937-1227i others(626): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | ||||||
| chr22:43980136 | A | ACATCCAT others(613): Show |
4 | a0001c0005t0001g0323 a0001c0005t0001g0326 a0001c0005t0001g0327 others(1): Show |
4 | HG02280.hp1 HG02615.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.937-1228_937-1227i others(622): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | ||||||
| chr22:43980136 | A | ACATCCAT others(597): Show |
1 | a0002c0011t0001g0225 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.937-1228_937-1227i others(606): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | ||||||
| chr22:43980136 | A | ACATCCAT others(901): Show |
1 | a0001c0004t0001g0154 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.937-1228_937-1227i others(910): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | ||||||
| chr22:43980136 | A | ACATCCAT others(613): Show |
1 | a0001c0005t0001g0150 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.937-1228_937-1227i others(622): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | ||||||
| chr22:43980136 | A | ACATCCAT others(606): Show |
1 | a0001c0004t0001g0119 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.937-1228_937-1227i others(615): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | ||||||
| chr22:43980136 | A | ACATCCAT others(605): Show |
2 | a0001c0002t0001g0020 a0001c0002t0001g0159 |
3 | HG01891.hp1 HG02280.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.937-1228_937-1227i others(614): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | ||||||
| chr22:43980136 | A | ACATCCAT others(609): Show |
2 | a0001c0002t0001g0161 a0001c0002t0001g0162 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.937-1228_937-1227i others(618): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | ||||||
| chr22:43980136 | A | ACATCCAT others(597): Show |
1 | a0001c0008t0001g0171 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.937-1228_937-1227i others(606): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | ||||||
| chr22:43980136 | A | ACATCCAT others(605): Show |
3 | a0001c0002t0001g0156 a0001c0002t0001g0163 a0001c0008t0001g0172 |
3 | HG01109.hp2 HG02630.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.937-1228_937-1227i others(614): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | ||||||
| chr22:43980136 | A | ACATCCAT others(609): Show |
2 | a0001c0002t0001g0157 a0001c0002t0001g0158 |
2 | HG02622.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.937-1228_937-1227i others(618): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | ||||||
| chr22:43980136 | A | ACATCCAT others(613): Show |
1 | a0001c0013t0001g0316 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.937-1228_937-1227i others(622): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | ||||||
| chr22:43980136 | A | ACATCCAT others(621): Show |
1 | a0001c0007t0005g0037 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.937-1228_937-1227i others(630): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | ||||||
| chr22:43980136 | A | ACATCCAT others(629): Show |
2 | a0001c0008t0001g0173 a0001c0008t0001g0177 |
2 | HG02559.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.937-1228_937-1227i others(638): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | ||||||
| chr22:43980136 | A | ACATCCAT others(633): Show |
3 | a0001c0008t0001g0036 a0001c0008t0001g0174 a0001c0008t0001g0176 |
3 | HG02257.hp1 HG02717.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.937-1228_937-1227i others(642): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | ||||||
| chr22:43980136 | A | ACATCCAT others(625): Show |
1 | a0001c0013t0001g0314 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.937-1228_937-1227i others(634): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | ||||||
| chr22:43980136 | A | ACATCCAT others(625): Show |
1 | a0001c0007t0001g0321 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.937-1228_937-1227i others(634): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | ||||||
| chr22:43980136 | A | ACATCCAT others(629): Show |
1 | a0001c0006t0001g0046 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.937-1228_937-1227i others(638): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | ||||||
| chr22:43980136 | A | ACATCCAT others(625): Show |
1 | a0001c0006t0001g0047 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.937-1228_937-1227i others(634): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | ||||||
| chr22:43980136 | A | ACATCCAT others(605): Show |
3 | a0001c0004t0001g0132 a0001c0004t0001g0151 a0001c0004t0001g0153 |
3 | HG01346.hp2 NA18979.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.937-1228_937-1227i others(614): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | ||||||
| chr22:43980136 | A | ACATCCAT others(609): Show |
1 | a0001c0002t0001g0160 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.937-1228_937-1227i others(618): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | ||||||
| chr22:43980139 | T | TCCATCCA others(605): Show |
3 | a0003c0003t0001g0013 a0003c0003t0001g0051 a0003c0003t0001g0086 |
4 | HG00642.hp2 HG01346.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.937-1228_937-1227i others(614): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980139 | ||||||
| chr22:43980139 | T | TCCATCCA others(613): Show |
1 | a0003c0003t0001g0087 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.937-1228_937-1227i others(622): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980139 | ||||||
| chr22:43980139 | T | TCCATCCA others(609): Show |
1 | a0001c0002t0001g0184 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.937-1228_937-1227i others(618): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980139 | ||||||
| chr22:43980161 | C | CATCCATC others(609): Show |
1 | a0003c0003t0001g0054 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.937-1228_937-1227i others(618): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980161 | ||||||
| chr22:43980455 | C | T | 186 | a0001c0002t0001g0020 a0001c0002t0001g0026 a0001c0002t0001g0156 others(183): Show |
201 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.937-936C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | chr22 | 43980455 | |||||||
| chr22:43980479 | G | A | 1 | a0001c0004t0001g0119 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.937-912G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | chr22 | 43980479 | |||||||
| chr22:43980512 | C | T | 1 | a0003c0003t0001g0076 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.937-879C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | chr22 | 43980512 | |||||||
| chr22:43980582 | C | A | 11 | a0001c0002t0001g0020 a0001c0002t0001g0156 a0001c0002t0001g0157 others(8): Show |
12 | HG01109.hp2 HG01891.hp1 HG01934.hp2 others(9): Show |
intron_variant | MODIFIER | c.937-809C>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | chr22 | 43980582 | |||||||
| chr22:43980595 | G | A | 1 | a0001c0005t0001g0150 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.937-796G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | chr22 | 43980595 | |||||||
| chr22:43980610 | T | A | 11 | a0001c0002t0001g0026 a0001c0002t0001g0184 a0001c0002t0001g0260 others(8): Show |
12 | HG00423.hp1 HG02451.hp1 HG03098.hp1 others(9): Show |
intron_variant | MODIFIER | c.937-781T>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | chr22 | 43980610 | |||||||
| chr22:43980634 | G | C | 1 | a0001c0007t0003g0315 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.937-757G>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | chr22 | 43980634 | |||||||
| chr22:43980903 | G | T | 1 | a0001c0004t0001g0119 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.937-488G>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | chr22 | 43980903 | |||||||
| chr22:43980944 | T | C | 1 | a0001c0004t0001g0048 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.937-447T>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | chr22 | 43980944 | |||||||
| chr22:43981015 | A | T | 1 | a0001c0004t0001g0119 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.937-376A>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | chr22 | 43981015 | |||||||
| chr22:43981133 | G | A | 9 | a0001c0005t0001g0006 a0001c0005t0001g0323 a0001c0005t0001g0324 others(6): Show |
11 | HG02055.hp2 HG02280.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.937-258G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | chr22 | 43981133 | |||||||
| chr22:43981144 | G | A | 1 | a0001c0004t0001g0135 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.937-247G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | chr22 | 43981144 | |||||||
| chr22:43981155 | G | A | 1 | a0001c0008t0001g0172 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.937-236G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | chr22 | 43981155 | |||||||
| chr22:43981297 | C | T | 1 | a0001c0002t0001g0264 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.937-94C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | chr22 | 43981297 | |||||||
| chr22:43981341 | G | T | 4 | a0001c0007t0001g0031 a0001c0007t0001g0032 a0001c0007t0001g0317 others(1): Show |
6 | HG00280.hp2 HG00733.hp2 HG01070.hp2 others(3): Show |
intron_variant | MODIFIER | c.937-50G>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | chr22 | 43981341 | |||||||
| chr22:43981562 | A | G | 187 | a0001c0002t0001g0020 a0001c0002t0001g0026 a0001c0002t0001g0156 others(184): Show |
202 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.1007+101A>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 11/14 | chr22 | 43981562 | |||||||
| chr22:43981563 | T | C | 2 | a0003c0003t0001g0075 a0003c0003t0001g0095 |
2 | HG03831.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.1007+102T>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 11/14 | chr22 | 43981563 | |||||||
| chr22:43981677 | A | C | 63 | a0001c0002t0001g0026 a0001c0002t0001g0184 a0001c0002t0001g0260 others(60): Show |
68 | HG00099.hp2 HG00423.hp1 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.1007+216A>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 11/14 | chr22 | 43981677 | |||||||
| chr22:43981680 | G | A | 1 | a0001c0004t0001g0134 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1007+219G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 11/14 | chr22 | 43981680 | |||||||
| chr22:43981842 | A | C | 3 | a0001c0009t0001g0055 a0001c0009t0001g0056 a0002c0011t0001g0225 |
3 | HG01433.hp1 HG02922.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1007+381A>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 11/14 | chr22 | 43981842 | |||||||
| chr22:43982072 | G | A | 1 | a0002c0001t0001g0198 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1007+611G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 11/14 | chr22 | 43982072 | |||||||
| chr22:43982103 | A | C | 4 | a0003c0003t0001g0002 a0003c0003t0001g0057 a0003c0003t0001g0061 others(1): Show |
8 | HG01071.hp2 HG01123.hp2 HG01358.hp2 others(5): Show |
intron_variant | MODIFIER | c.1007+642A>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 11/14 | chr22 | 43982103 | |||||||
| chr22:43982119 | C | T | 114 | a0001c0002t0001g0020 a0001c0002t0001g0156 a0001c0002t0001g0157 others(111): Show |
122 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.1007+658C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 11/14 | chr22 | 43982119 | |||||||
| chr22:43982342 | C | T | 1 | a0002c0001t0001g0228 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1007+881C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 11/14 | chr22 | 43982342 | |||||||
| chr22:43982350 | G | A | 2 | a0001c0006t0001g0103 a0001c0006t0001g0106 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1007+889G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 11/14 | chr22 | 43982350 | |||||||
| chr22:43982426 | T | G | 1 | a0003c0003t0001g0076 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1007+965T>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 11/14 | chr22 | 43982426 | |||||||
| chr22:43982447 | G | A | 4 | a0001c0004t0001g0039 a0001c0004t0001g0115 a0001c0004t0001g0137 others(1): Show |
4 | HG00735.hp1 NA18971.hp1 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.1007+986G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 11/14 | chr22 | 43982447 | |||||||
| chr22:43982488 | C | T | 2 | a0001c0004t0001g0016 a0001c0004t0001g0118 |
3 | NA18952.hp1 NA18963.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1007+1027C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 11/14 | chr22 | 43982488 | |||||||
| chr22:43982522 | C | T | 2 | a0003c0003t0001g0083 a0003c0003t0001g0088 |
2 | HG00642.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.1007+1061C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 11/14 | chr22 | 43982522 | |||||||
| chr22:43982626 | T | C | 2 | a0001c0002t0002g0265 a0001c0002t0002g0266 |
2 | HG03486.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1007+1165T>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 11/14 | chr22 | 43982626 | |||||||
| chr22:43982704 | C | T | 1 | a0002c0001t0001g0214 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1008-1229C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 11/14 | chr22 | 43982704 | |||||||
| chr22:43982790 | C | T | 3 | a0002c0001t0001g0191 a0002c0001t0001g0199 a0002c0001t0001g0204 |
3 | HG01099.hp2 HG01261.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.1008-1143C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 11/14 | chr22 | 43982790 | |||||||
| chr22:43982792 | C | A | 111 | a0001c0002t0001g0020 a0001c0002t0001g0156 a0001c0002t0001g0157 others(108): Show |
119 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.1008-1141C>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 11/14 | chr22 | 43982792 | |||||||
| chr22:43982824 | C | A | 1 | a0001c0007t0003g0315 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1008-1109C>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 11/14 | chr22 | 43982824 | |||||||
| chr22:43982929 | C | T | 114 | a0001c0002t0001g0020 a0001c0002t0001g0156 a0001c0002t0001g0157 others(111): Show |
122 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.1008-1004C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 11/14 | chr22 | 43982929 | |||||||
| chr22:43982958 | C | T | 1 | a0002c0001t0001g0240 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1008-975C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 11/14 | chr22 | 43982958 | |||||||
| chr22:43983171 | G | A | 7 | a0001c0006t0001g0100 a0001c0006t0001g0102 a0001c0006t0001g0103 others(4): Show |
7 | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.1008-762G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 11/14 | chr22 | 43983171 | |||||||
| chr22:43983251 | A | C | 1 | a0001c0004t0001g0125 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1008-682A>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 11/14 | chr22 | 43983251 | |||||||
| chr22:43983627 | C | G | 2 | a0001c0013t0001g0314 a0001c0013t0001g0316 |
2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1008-306C>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 11/14 | chr22 | 43983627 | |||||||
| chr22:43983685 | G | C | 128 | a0001c0002t0001g0020 a0001c0002t0001g0156 a0001c0002t0001g0157 others(125): Show |
138 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.1008-248G>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 11/14 | chr22 | 43983685 | |||||||
| chr22:43983772 | T | C | 2 | a0002c0001t0001g0218 a0002c0001t0001g0229 |
2 | HG01257.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1008-161T>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 11/14 | chr22 | 43983772 | |||||||
| chr22:43983851 | CAT | C | 9 | a0001c0006t0001g0046 a0001c0006t0001g0047 a0001c0006t0001g0100 others(6): Show |
9 | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1008-81_1008-80del others(2): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 11/14 | chr22 | 43983851 | |||||||
| chr22:43983860 | C | A | 114 | a0001c0002t0001g0020 a0001c0002t0001g0156 a0001c0002t0001g0157 others(111): Show |
122 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.1008-73C>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 11/14 | chr22 | 43983860 | |||||||
| chr22:43984043 | G | A | 1 | a0002c0011t0001g0243 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1075+43G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | chr22 | 43984043 | |||||||
| chr22:43984129 | A | G | 113 | a0001c0002t0001g0020 a0001c0002t0001g0156 a0001c0002t0001g0157 others(110): Show |
121 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(118): Show |
intron_variant | MODIFIER | c.1075+129A>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | chr22 | 43984129 | |||||||
| chr22:43984153 | T | C | 60 | a0001c0002t0001g0026 a0001c0002t0001g0184 a0001c0002t0001g0260 others(57): Show |
65 | HG00099.hp2 HG00423.hp1 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.1075+153T>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | chr22 | 43984153 | |||||||
| chr22:43984290 | G | GCTTC | 115 | a0001c0002t0001g0020 a0001c0002t0001g0156 a0001c0002t0001g0157 others(112): Show |
123 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.1075+293_1075+296d others(6): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 43984290 | ||||||
| chr22:43984301 | T | C | 1 | a0002c0001t0001g0187 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1075+301T>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | chr22 | 43984301 | |||||||
| chr22:43984312 | A | G | 1 | a0001c0008t0001g0170 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1075+312A>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | chr22 | 43984312 | |||||||
| chr22:43984373 | C | T | 2 | a0001c0002t0001g0184 a0001c0007t0001g0321 |
2 | HG03195.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1075+373C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | chr22 | 43984373 | |||||||
| chr22:43984721 | C | T | 2 | a0001c0002t0002g0277 a0001c0002t0002g0292 |
2 | HG01261.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.1075+721C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | chr22 | 43984721 | |||||||
| chr22:43984754 | G | A | 1 | a0001c0009t0001g0055 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1075+754G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | chr22 | 43984754 | |||||||
| chr22:43984769 | C | T | 11 | a0001c0002t0001g0020 a0001c0002t0001g0156 a0001c0002t0001g0157 others(8): Show |
12 | HG01109.hp2 HG01891.hp1 HG01934.hp2 others(9): Show |
intron_variant | MODIFIER | c.1075+769C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | chr22 | 43984769 | |||||||
| chr22:43984776 | A | G | 18 | a0001c0002t0001g0020 a0001c0002t0001g0156 a0001c0002t0001g0157 others(15): Show |
19 | HG01109.hp2 HG01891.hp1 HG01934.hp2 others(16): Show |
intron_variant | MODIFIER | c.1075+776A>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | chr22 | 43984776 | |||||||
| chr22:43984831 | TATGTTGG others(1403): Show |
T | 7 | a0001c0006t0001g0100 a0001c0006t0001g0102 a0001c0006t0001g0103 others(4): Show |
7 | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.1075+843_1075+2252 others(3): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 43984831 | ||||||
| chr22:43984887 | T | C | 114 | a0001c0002t0001g0020 a0001c0002t0001g0156 a0001c0002t0001g0157 others(111): Show |
122 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.1075+887T>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | chr22 | 43984887 | |||||||
| chr22:43985008 | C | T | 3 | a0001c0006t0001g0046 a0001c0006t0001g0047 a0002c0012t0001g0045 |
3 | HG02451.hp1 HG03098.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1075+1008C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | chr22 | 43985008 | |||||||
| chr22:43985131 | AC | A | 4 | a0001c0002t0001g0183 a0001c0002t0001g0331 a0001c0002t0001g0332 others(1): Show |
4 | HG02647.hp1 HG02965.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1075+1136delC | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 43985131 | ||||||
| chr22:43985297 | T | A | 1 | a0003c0003t0001g0094 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1075+1297T>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | chr22 | 43985297 | |||||||
| chr22:43985343 | G | C | 321 | a0001c0002t0001g0020 a0001c0002t0001g0026 a0001c0002t0001g0156 others(318): Show |
364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
intron_variant | MODIFIER | c.1075+1343G>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | chr22 | 43985343 | |||||||
| chr22:43985415 | C | A | 1 | a0003c0003t0001g0094 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1075+1415C>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | chr22 | 43985415 | |||||||
| chr22:43985460 | T | C | 115 | a0001c0002t0001g0020 a0001c0002t0001g0156 a0001c0002t0001g0157 others(112): Show |
123 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.1075+1460T>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | chr22 | 43985460 | |||||||
| chr22:43985602 | C | T | 88 | a0001c0002t0002g0273 a0002c0001t0001g0005 a0002c0001t0001g0021 others(85): Show |
95 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.1075+1602C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | chr22 | 43985602 | |||||||
| chr22:43985665 | C | T | 250 | a0001c0002t0001g0020 a0001c0002t0001g0026 a0001c0002t0001g0156 others(247): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(272): Show |
intron_variant | MODIFIER | c.1075+1665C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | chr22 | 43985665 | |||||||
| chr22:43985983 | C | T | 3 | a0001c0008t0001g0036 a0001c0008t0001g0174 a0001c0008t0001g0175 |
3 | HG02257.hp1 HG02486.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1075+1983C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | chr22 | 43985983 | |||||||
| chr22:43986012 | T | TTTTA | 11 | a0001c0002t0001g0020 a0001c0002t0001g0156 a0001c0002t0001g0157 others(8): Show |
12 | HG01109.hp2 HG01891.hp1 HG01934.hp2 others(9): Show |
intron_variant | MODIFIER | c.1075+2028_1075+203 others(8): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 43986012 | ||||||
| chr22:43986021 | T | G | 1 | a0003c0003t0001g0079 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1075+2021T>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | chr22 | 43986021 | |||||||
| chr22:43986043 | C | CT | 14 | a0001c0004t0001g0001 a0001c0004t0001g0015 a0001c0004t0001g0017 others(11): Show |
16 | HG00609.hp1 HG01175.hp1 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.1075+2060dupT | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 43986043 | ||||||
| chr22:43986045 | T | TTC | 12 | a0001c0002t0001g0020 a0001c0002t0001g0156 a0001c0002t0001g0157 others(9): Show |
13 | HG01109.hp2 HG01891.hp1 HG01934.hp2 others(10): Show |
intron_variant | MODIFIER | c.1075+2046_1075+204 others(6): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 43986045 | ||||||
| chr22:43986046 | T | TC | 162 | a0001c0002t0001g0026 a0001c0002t0001g0162 a0001c0002t0001g0183 others(159): Show |
174 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.1075+2046_1075+204 others(5): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | chr22 | 43986046 | |||||||
| chr22:43986064 | ATGGAGTC others(6): Show |
A | 177 | a0001c0002t0001g0020 a0001c0002t0001g0026 a0001c0002t0001g0156 others(174): Show |
190 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.1075+2067_1075+207 others(17): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 43986064 | ||||||
| chr22:43986124 | C | A | 173 | a0001c0002t0001g0020 a0001c0002t0001g0026 a0001c0002t0001g0156 others(170): Show |
186 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.1075+2124C>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | chr22 | 43986124 | |||||||
| chr22:43986191 | G | A | 1 | a0001c0002t0001g0183 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1075+2191G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | chr22 | 43986191 | |||||||
| chr22:43986192 | C | T | 39 | a0001c0002t0001g0020 a0001c0002t0001g0156 a0001c0002t0001g0157 others(36): Show |
40 | HG01109.hp2 HG01243.hp1 HG01891.hp1 others(37): Show |
intron_variant | MODIFIER | c.1075+2192C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | chr22 | 43986192 | |||||||
| chr22:43986254 | C | A | 1 | a0002c0001t0001g0222 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1075+2254C>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | chr22 | 43986254 | |||||||
| chr22:43986276 | G | A | 3 | a0001c0009t0001g0056 a0001c0013t0001g0314 a0001c0013t0001g0316 |
3 | HG01433.hp1 HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1075+2276G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | chr22 | 43986276 | |||||||
| chr22:43986287 | G | A | 1 | a0001c0010t0001g0140 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1075+2287G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | chr22 | 43986287 | |||||||
| chr22:43986367 | A | C | 53 | a0001c0002t0002g0027 a0001c0002t0002g0028 a0001c0002t0002g0029 others(50): Show |
57 | HG00099.hp2 HG00544.hp1 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.1075+2367A>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | chr22 | 43986367 | |||||||
| chr22:43986455 | A | G | 1 | a0001c0007t0003g0315 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1075+2455A>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | chr22 | 43986455 | |||||||
| chr22:43986457 | A | G | 3 | a0001c0004t0001g0039 a0001c0004t0001g0115 a0001c0004t0002g0040 |
3 | NA18971.hp1 NA19062.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.1075+2457A>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | chr22 | 43986457 | |||||||
| chr22:43986653 | C | T | 173 | a0001c0002t0001g0020 a0001c0002t0001g0026 a0001c0002t0001g0156 others(170): Show |
187 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.1076-2458C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | chr22 | 43986653 | |||||||
| chr22:43986804 | T | C | 186 | a0001c0002t0001g0020 a0001c0002t0001g0026 a0001c0002t0001g0156 others(183): Show |
202 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.1076-2307T>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | chr22 | 43986804 | |||||||
| chr22:43986825 | T | G | 18 | a0001c0002t0001g0020 a0001c0002t0001g0156 a0001c0002t0001g0157 others(15): Show |
19 | HG01109.hp2 HG01891.hp1 HG01934.hp2 others(16): Show |
intron_variant | MODIFIER | c.1076-2286T>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | chr22 | 43986825 | |||||||
| chr22:43986844 | C | T | 1 | a0001c0002t0002g0030 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1076-2267C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | chr22 | 43986844 | |||||||
| chr22:43986899 | T | C | 1 | a0002c0001t0001g0257 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1076-2212T>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | chr22 | 43986899 | |||||||
| chr22:43986973 | G | A | 61 | a0001c0002t0001g0026 a0001c0002t0001g0184 a0001c0002t0001g0260 others(58): Show |
66 | HG00099.hp2 HG00423.hp1 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.1076-2138G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | chr22 | 43986973 | |||||||
| chr22:43987190 | T | C | 8 | a0001c0007t0001g0031 a0001c0007t0001g0032 a0001c0007t0001g0317 others(5): Show |
10 | HG00280.hp2 HG00733.hp2 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.1076-1921T>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | chr22 | 43987190 | |||||||
| chr22:43987242 | A | G | 1 | a0001c0008t0001g0170 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1076-1869A>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | chr22 | 43987242 | |||||||
| chr22:43987508 | G | A | 1 | a0001c0004t0001g0151 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1076-1603G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | chr22 | 43987508 | |||||||
| chr22:43987520 | C | T | 186 | a0001c0002t0001g0020 a0001c0002t0001g0026 a0001c0002t0001g0156 others(183): Show |
202 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.1076-1591C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | chr22 | 43987520 | |||||||
| chr22:43987523 | G | C | 4 | a0003c0003t0001g0002 a0003c0003t0001g0057 a0003c0003t0001g0061 others(1): Show |
8 | HG01071.hp2 HG01123.hp2 HG01358.hp2 others(5): Show |
intron_variant | MODIFIER | c.1076-1588G>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | chr22 | 43987523 | |||||||
| chr22:43987552 | G | C | 186 | a0001c0002t0001g0020 a0001c0002t0001g0026 a0001c0002t0001g0156 others(183): Show |
202 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.1076-1559G>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | chr22 | 43987552 | |||||||
| chr22:43987560 | G | A | 1 | a0001c0004t0001g0143 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1076-1551G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | chr22 | 43987560 | |||||||
| chr22:43987622 | T | C | 8 | a0001c0007t0001g0031 a0001c0007t0001g0032 a0001c0007t0001g0317 others(5): Show |
10 | HG00280.hp2 HG00733.hp2 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.1076-1489T>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | chr22 | 43987622 | |||||||
| chr22:43987737 | C | G | 194 | a0001c0002t0001g0020 a0001c0002t0001g0026 a0001c0002t0001g0156 others(191): Show |
210 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.1076-1374C>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | chr22 | 43987737 | |||||||
| chr22:43987793 | A | T | 2 | a0001c0004t0001g0016 a0001c0004t0001g0118 |
3 | NA18952.hp1 NA18963.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1076-1318A>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | chr22 | 43987793 | |||||||
| chr22:43987880 | A | AG | 4 | a0001c0007t0003g0315 a0001c0010t0001g0123 a0001c0010t0001g0133 others(1): Show |
4 | HG02615.hp1 HG02809.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1076-1230dupG | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 43987880 | ||||||
| chr22:43987898 | G | GTA | 17 | a0001c0004t0001g0131 a0001c0005t0001g0006 a0001c0005t0001g0323 others(14): Show |
22 | HG00280.hp2 HG00733.hp2 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.1076-1198_1076-119 others(6): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 43987898 | ||||||
| chr22:43987898 | G | GTATA | 142 | a0001c0002t0001g0026 a0001c0002t0001g0260 a0001c0002t0001g0261 others(139): Show |
153 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.1076-1200_1076-119 others(8): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 43987898 | ||||||
| chr22:43987898 | G | GTATATA | 16 | a0001c0002t0001g0020 a0001c0002t0001g0159 a0001c0002t0001g0160 others(13): Show |
17 | HG00639.hp1 HG01099.hp2 HG01261.hp1 others(14): Show |
intron_variant | MODIFIER | c.1076-1202_1076-119 others(10): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 43987898 | ||||||
| chr22:43987898 | G | GTATATAT others(1): Show |
3 | a0001c0002t0001g0183 a0001c0008t0001g0174 a0001c0008t0001g0175 |
3 | HG02257.hp1 HG02486.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1076-1204_1076-119 others(12): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 43987898 | ||||||
| chr22:43987898 | G | GTATATAT others(3): Show |
2 | a0001c0002t0004g0288 a0001c0008t0001g0036 |
2 | HG02717.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1076-1206_1076-119 others(14): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 43987898 | ||||||
| chr22:43987898 | G | GTATATAT others(5): Show |
3 | a0001c0002t0001g0156 a0001c0002t0001g0157 a0001c0002t0001g0158 |
3 | HG02622.hp1 HG02809.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1076-1208_1076-119 others(16): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 43987898 | ||||||
| chr22:43987898 | G | GTATATAT others(7): Show |
2 | a0001c0008t0001g0171 a0001c0008t0001g0172 |
2 | HG01109.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.1076-1210_1076-119 others(18): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 43987898 | ||||||
| chr22:43987898 | G | GTGTA | 3 | a0002c0001t0001g0022 a0002c0001t0001g0201 a0002c0001t0001g0227 |
4 | NA18947.hp1 NA18970.hp2 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.1076-1212_1076-121 others(8): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 43987898 | ||||||
| chr22:43987913 | T | C | 9 | a0003c0003t0001g0052 a0003c0003t0001g0065 a0003c0003t0001g0072 others(6): Show |
9 | HG00621.hp1 HG02145.hp1 NA18949.hp2 others(6): Show |
intron_variant | MODIFIER | c.1076-1198T>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | chr22 | 43987913 | |||||||
| chr22:43987913 | T | TATACAC | 4 | a0001c0008t0001g0170 a0001c0008t0001g0173 a0001c0008t0001g0176 others(1): Show |
4 | HG02559.hp1 HG03041.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1076-1197_1076-119 others(10): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 43987913 | ||||||
| chr22:43987913 | T | TATATATA others(7): Show |
1 | a0001c0007t0005g0037 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1076-1197_1076-119 others(18): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 43987913 | ||||||
| chr22:43987921 | C | G | 1 | a0001c0004t0001g0313 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1076-1190C>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | chr22 | 43987921 | |||||||
| chr22:43988017 | T | A | 1 | a0001c0004t0001g0113 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1076-1094T>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | chr22 | 43988017 | |||||||
| chr22:43988399 | C | G | 51 | a0001c0002t0002g0027 a0001c0002t0002g0028 a0001c0002t0002g0029 others(48): Show |
55 | HG00099.hp2 HG00544.hp1 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.1076-712C>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | chr22 | 43988399 | |||||||
| chr22:43988488 | G | GT | 5 | a0003c0003t0001g0004 a0003c0003t0001g0008 a0003c0003t0001g0010 others(2): Show |
9 | HG01099.hp1 HG01167.hp2 HG01515.hp2 others(6): Show |
intron_variant | MODIFIER | c.1076-618dupT | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 43988488 | ||||||
| chr22:43988545 | G | A | 2 | a0002c0001t0001g0041 a0002c0001t0001g0042 |
2 | HG01243.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1076-566G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | chr22 | 43988545 | |||||||
| chr22:43988741 | T | G | 7 | a0001c0008t0001g0036 a0001c0008t0001g0170 a0001c0008t0001g0173 others(4): Show |
7 | HG02257.hp1 HG02486.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1076-370T>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | chr22 | 43988741 | |||||||
| chr22:43988920 | C | T | 2 | a0001c0002t0004g0288 a0001c0007t0005g0037 |
2 | HG03195.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1076-191C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | chr22 | 43988920 | |||||||
| chr22:43989001 | G | C | 60 | a0001c0002t0001g0026 a0001c0002t0001g0184 a0001c0002t0001g0260 others(57): Show |
65 | HG00099.hp2 HG00423.hp1 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.1076-110G>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | chr22 | 43989001 | |||||||
| chr22:43989268 | C | T | 4 | a0003c0003t0001g0002 a0003c0003t0001g0057 a0003c0003t0001g0061 others(1): Show |
8 | HG01071.hp2 HG01123.hp2 HG01358.hp2 others(5): Show |
intron_variant | MODIFIER | c.1222+11C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 13/14 | chr22 | 43989268 | |||||||
| chr22:43989276 | A | T | 1 | a0003c0003t0001g0061 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1222+19A>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 13/14 | chr22 | 43989276 | |||||||
| chr22:43989339 | C | CT | 69 | a0001c0002t0001g0026 a0001c0002t0001g0184 a0001c0002t0001g0260 others(66): Show |
74 | HG00099.hp2 HG00423.hp1 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.1222+98dupT | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr22 | 43989339 | ||||||
| chr22:43989339 | C | CTT | 115 | a0001c0002t0001g0020 a0001c0002t0001g0156 a0001c0002t0001g0157 others(112): Show |
126 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.1222+97_1222+98dup others(2): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr22 | 43989339 | ||||||
| chr22:43989661 | A | G | 1 | a0003c0003t0001g0067 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1222+404A>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 13/14 | chr22 | 43989661 | |||||||
| chr22:43989703 | T | C | 8 | a0001c0007t0001g0031 a0001c0007t0001g0032 a0001c0007t0001g0317 others(5): Show |
10 | HG00280.hp2 HG00733.hp2 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.1222+446T>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 13/14 | chr22 | 43989703 | |||||||
| chr22:43989714 | A | G | 98 | a0001c0002t0001g0183 a0001c0002t0001g0331 a0001c0002t0001g0332 others(95): Show |
106 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.1222+457A>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 13/14 | chr22 | 43989714 | |||||||
| chr22:43989788 | C | T | 1 | a0002c0001t0001g0200 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1223-477C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 13/14 | chr22 | 43989788 | |||||||
| chr22:43989799 | CTGTT | C | 29 | a0001c0002t0002g0028 a0001c0002t0002g0029 a0001c0002t0002g0030 others(26): Show |
32 | HG00099.hp2 HG00544.hp1 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.1223-462_1223-459d others(6): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr22 | 43989799 | ||||||
| chr22:43990409 | A | ACGTGTTG others(9): Show |
1 | a0001c0002t0001g0183 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1364+4_1364+19dupC others(15): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr22 | 43990409 | ||||||
| chr22:43990549 | T | C | 2 | a0001c0002t0004g0288 a0001c0007t0005g0037 |
2 | HG03195.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1364+143T>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43990549 | |||||||
| chr22:43990758 | G | A | 20 | a0001c0002t0001g0020 a0001c0002t0001g0156 a0001c0002t0001g0157 others(17): Show |
21 | HG01109.hp2 HG01891.hp1 HG01934.hp2 others(18): Show |
intron_variant | MODIFIER | c.1364+352G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43990758 | |||||||
| chr22:43990980 | A | AT | 250 | a0001c0002t0001g0020 a0001c0002t0001g0026 a0001c0002t0001g0157 others(247): Show |
278 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(275): Show |
intron_variant | MODIFIER | c.1364+588dupT | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr22 | 43990980 | ||||||
| chr22:43990980 | A | ATT | 9 | a0001c0002t0001g0184 a0001c0004t0001g0166 a0001c0006t0001g0100 others(6): Show |
9 | HG01167.hp1 HG01169.hp2 HG01175.hp1 others(6): Show |
intron_variant | MODIFIER | c.1364+587_1364+588d others(4): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr22 | 43990980 | ||||||
| chr22:43991061 | C | G | 1 | a0001c0007t0005g0037 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1364+655C>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43991061 | |||||||
| chr22:43991186 | C | G | 2 | a0001c0009t0001g0055 a0001c0009t0001g0056 |
2 | HG01433.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1364+780C>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43991186 | |||||||
| chr22:43991212 | G | A | 1 | a0002c0001t0001g0191 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1364+806G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43991212 | |||||||
| chr22:43991228 | A | G | 185 | a0001c0002t0001g0020 a0001c0002t0001g0026 a0001c0002t0001g0156 others(182): Show |
201 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.1364+822A>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43991228 | |||||||
| chr22:43991267 | C | T | 1 | a0002c0001t0001g0194 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1364+861C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43991267 | |||||||
| chr22:43991275 | A | AT | 23 | a0001c0002t0002g0027 a0001c0002t0002g0043 a0001c0002t0002g0180 others(20): Show |
24 | HG00438.hp2 HG00558.hp2 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.1364+890dupT | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr22 | 43991275 | ||||||
| chr22:43991275 | AT | A | 8 | a0001c0002t0002g0295 a0001c0002t0002g0296 a0001c0002t0002g0304 others(5): Show |
8 | HG00621.hp1 HG01070.hp1 HG01167.hp2 others(5): Show |
intron_variant | MODIFIER | c.1364+890delT | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr22 | 43991275 | ||||||
| chr22:43991324 | C | G | 2 | a0001c0006t0001g0046 a0001c0006t0001g0047 |
2 | HG02451.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1364+918C>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43991324 | |||||||
| chr22:43991411 | G | A | 3 | a0002c0001t0001g0209 a0002c0001t0001g0222 a0002c0001t0001g0233 |
3 | HG00639.hp2 HG00741.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.1364+1005G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43991411 | |||||||
| chr22:43991418 | C | T | 8 | a0001c0007t0001g0031 a0001c0007t0001g0032 a0001c0007t0001g0317 others(5): Show |
10 | HG00280.hp2 HG00733.hp2 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.1364+1012C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43991418 | |||||||
| chr22:43991426 | G | A | 1 | a0002c0001t0001g0223 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1364+1020G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43991426 | |||||||
| chr22:43991501 | C | G | 3 | a0002c0001t0001g0191 a0002c0001t0001g0199 a0002c0001t0001g0204 |
3 | HG01099.hp2 HG01261.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.1364+1095C>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43991501 | |||||||
| chr22:43991837 | CTCT | C | 3 | a0001c0008t0001g0036 a0001c0008t0001g0174 a0001c0008t0001g0175 |
3 | HG02257.hp1 HG02486.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1364+1436_1364+143 others(7): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr22 | 43991837 | ||||||
| chr22:43991873 | C | T | 1 | a0002c0001t0001g0186 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1364+1467C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43991873 | |||||||
| chr22:43992052 | C | CTA | 186 | a0001c0002t0001g0020 a0001c0002t0001g0026 a0001c0002t0001g0156 others(183): Show |
202 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.1364+1647_1364+164 others(6): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr22 | 43992052 | ||||||
| chr22:43992064 | T | C | 5 | a0001c0008t0001g0036 a0001c0008t0001g0171 a0001c0008t0001g0172 others(2): Show |
5 | HG01109.hp2 HG02109.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.1364+1658T>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43992064 | |||||||
| chr22:43992116 | G | C | 276 | a0001c0002t0001g0020 a0001c0002t0001g0026 a0001c0002t0001g0156 others(273): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(301): Show |
intron_variant | MODIFIER | c.1364+1710G>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43992116 | |||||||
| chr22:43992239 | T | C | 6 | a0001c0002t0001g0020 a0001c0002t0001g0159 a0001c0002t0001g0160 others(3): Show |
7 | HG01891.hp1 HG01934.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1364+1833T>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43992239 | |||||||
| chr22:43992328 | C | T | 331 | a0001c0002t0001g0020 a0001c0002t0001g0026 a0001c0002t0001g0156 others(328): Show |
375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.1364+1922C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43992328 | |||||||
| chr22:43992366 | G | A | 12 | a0001c0002t0001g0020 a0001c0002t0001g0156 a0001c0002t0001g0157 others(9): Show |
13 | HG01891.hp1 HG01934.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.1364+1960G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43992366 | |||||||
| chr22:43992367 | C | T | 1 | a0002c0012t0001g0144 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1364+1961C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43992367 | |||||||
| chr22:43992390 | G | A | 1 | a0001c0002t0002g0309 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1364+1984G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43992390 | |||||||
| chr22:43992401 | G | T | 3 | a0001c0004t0001g0120 a0001c0004t0001g0312 a0001c0004t0001g0313 |
3 | HG01358.hp1 HG02602.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.1364+1995G>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43992401 | |||||||
| chr22:43992438 | G | A | 7 | a0001c0005t0001g0006 a0001c0005t0001g0323 a0001c0005t0001g0324 others(4): Show |
9 | HG02055.hp2 HG02615.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.1364+2032G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43992438 | |||||||
| chr22:43992457 | G | A | 78 | a0001c0004t0001g0001 a0001c0004t0001g0015 a0001c0004t0001g0016 others(75): Show |
90 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.1364+2051G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43992457 | |||||||
| chr22:43992537 | A | G | 186 | a0001c0002t0001g0020 a0001c0002t0001g0026 a0001c0002t0001g0156 others(183): Show |
202 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.1364+2131A>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43992537 | |||||||
| chr22:43992728 | C | A | 3 | a0001c0008t0001g0036 a0001c0008t0001g0174 a0001c0008t0001g0175 |
3 | HG02257.hp1 HG02486.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1364+2322C>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43992728 | |||||||
| chr22:43992797 | G | A | 2 | a0001c0002t0004g0288 a0001c0007t0005g0037 |
2 | HG03195.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1364+2391G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43992797 | |||||||
| chr22:43992937 | T | C | 97 | a0001c0002t0001g0331 a0001c0002t0001g0332 a0001c0002t0001g0333 others(94): Show |
105 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.1364+2531T>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43992937 | |||||||
| chr22:43993017 | A | G | 1 | a0001c0008t0001g0170 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1364+2611A>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43993017 | |||||||
| chr22:43993018 | G | A | 1 | a0001c0002t0002g0309 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1364+2612G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43993018 | |||||||
| chr22:43993039 | A | G | 2 | a0003c0003t0001g0062 a0003c0003t0001g0064 |
2 | HG01169.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.1364+2633A>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43993039 | |||||||
| chr22:43993085 | G | A | 2 | a0001c0002t0001g0184 a0001c0007t0001g0321 |
2 | HG03195.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1364+2679G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43993085 | |||||||
| chr22:43993229 | C | G | 1 | a0002c0001t0001g0190 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1364+2823C>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43993229 | |||||||
| chr22:43993274 | G | A | 7 | a0001c0002t0001g0026 a0001c0002t0001g0260 a0001c0002t0001g0261 others(4): Show |
8 | HG00423.hp1 HG04204.hp1 NA18963.hp2 others(5): Show |
intron_variant | MODIFIER | c.1364+2868G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43993274 | |||||||
| chr22:43993373 | CGGCTTTT others(27): Show |
C | 1 | a0001c0006t0001g0046 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1365-2963_1365-293 others(38): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr22 | 43993373 | ||||||
| chr22:43993512 | G | A | 57 | a0001c0002t0001g0026 a0001c0002t0001g0184 a0001c0002t0001g0260 others(54): Show |
62 | HG00099.hp2 HG00423.hp1 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.1365-2826G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43993512 | |||||||
| chr22:43993520 | C | T | 3 | a0001c0008t0001g0036 a0001c0008t0001g0174 a0001c0008t0001g0175 |
3 | HG02257.hp1 HG02486.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1365-2818C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43993520 | |||||||
| chr22:43993634 | T | C | 185 | a0001c0002t0001g0020 a0001c0002t0001g0026 a0001c0002t0001g0156 others(182): Show |
201 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.1365-2704T>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43993634 | |||||||
| chr22:43993638 | C | T | 6 | a0001c0002t0002g0269 a0001c0002t0002g0295 a0001c0002t0002g0299 others(3): Show |
6 | HG00099.hp2 HG01070.hp1 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.1365-2700C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43993638 | |||||||
| chr22:43993676 | C | T | 1 | a0001c0002t0001g0183 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1365-2662C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43993676 | |||||||
| chr22:43993914 | G | A | 2 | a0001c0002t0002g0269 a0001c0004t0001g0146 |
2 | HG02074.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.1365-2424G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43993914 | |||||||
| chr22:43993929 | C | T | 3 | a0001c0008t0001g0173 a0001c0008t0001g0176 a0001c0008t0001g0177 |
3 | HG02559.hp1 HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1365-2409C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43993929 | |||||||
| chr22:43993982 | C | T | 1 | a0002c0001t0001g0242 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1365-2356C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43993982 | |||||||
| chr22:43994145 | A | AGC | 3 | a0001c0010t0001g0123 a0001c0010t0001g0133 a0001c0010t0001g0140 |
3 | HG02615.hp1 HG02895.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1365-2192_1365-219 others(6): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr22 | 43994145 | ||||||
| chr22:43994168 | G | A | 57 | a0001c0002t0001g0026 a0001c0002t0001g0184 a0001c0002t0001g0260 others(54): Show |
62 | HG00099.hp2 HG00423.hp1 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.1365-2170G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43994168 | |||||||
| chr22:43994195 | G | C | 1 | a0005c0019t0007g0231 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1365-2143G>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43994195 | |||||||
| chr22:43994247 | C | T | 1 | a0001c0002t0002g0284 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1365-2091C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43994247 | |||||||
| chr22:43994341 | GT | G | 12 | a0001c0002t0001g0020 a0001c0002t0001g0156 a0001c0002t0001g0157 others(9): Show |
13 | HG01891.hp1 HG01934.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.1365-1996delT | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43994341 | |||||||
| chr22:43994356 | T | C | 273 | a0001c0002t0001g0020 a0001c0002t0001g0026 a0001c0002t0001g0156 others(270): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(298): Show |
intron_variant | MODIFIER | c.1365-1982T>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43994356 | |||||||
| chr22:43994405 | C | T | 2 | a0001c0004t0001g0129 a0001c0004t0001g0138 |
2 | NA18953.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.1365-1933C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43994405 | |||||||
| chr22:43994457 | G | A | 1 | a0001c0006t0001g0259 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1365-1881G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43994457 | |||||||
| chr22:43994475 | T | G | 1 | a0001c0002t0001g0276 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1365-1863T>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43994475 | |||||||
| chr22:43994486 | A | G | 287 | a0001c0002t0001g0020 a0001c0002t0001g0026 a0001c0002t0001g0156 others(284): Show |
322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.1365-1852A>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43994486 | |||||||
| chr22:43994666 | C | T | 2 | a0001c0002t0004g0288 a0001c0007t0005g0037 |
2 | HG03195.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1365-1672C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43994666 | |||||||
| chr22:43994667 | G | A | 69 | a0001c0004t0001g0001 a0001c0004t0001g0015 a0001c0004t0001g0016 others(66): Show |
79 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.1365-1671G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43994667 | |||||||
| chr22:43994688 | C | T | 173 | a0001c0002t0001g0020 a0001c0002t0001g0026 a0001c0002t0001g0156 others(170): Show |
187 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(184): Show |
intron_variant | MODIFIER | c.1365-1650C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43994688 | |||||||
| chr22:43995036 | C | G | 1 | a0002c0001t0001g0212 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1365-1302C>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43995036 | |||||||
| chr22:43995145 | T | C | 288 | a0001c0002t0001g0020 a0001c0002t0001g0026 a0001c0002t0001g0156 others(285): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(313): Show |
intron_variant | MODIFIER | c.1365-1193T>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43995145 | |||||||
| chr22:43995179 | C | T | 3 | a0001c0002t0001g0331 a0001c0002t0001g0332 a0001c0002t0001g0333 |
3 | HG02647.hp1 HG02965.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1365-1159C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43995179 | |||||||
| chr22:43995349 | CAAGGGCA others(15): Show |
C | 2 | a0001c0002t0004g0288 a0001c0007t0005g0037 |
2 | HG03195.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1365-984_1365-963d others(24): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr22 | 43995349 | ||||||
| chr22:43995354 | G | A | 93 | a0001c0002t0001g0331 a0001c0002t0001g0332 a0001c0002t0001g0333 others(90): Show |
101 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.1365-984G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43995354 | |||||||
| chr22:43995517 | C | T | 11 | a0001c0005t0001g0006 a0001c0005t0001g0150 a0001c0005t0001g0323 others(8): Show |
13 | HG02055.hp2 HG02615.hp2 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.1365-821C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43995517 | |||||||
| chr22:43995708 | T | C | 176 | a0001c0002t0001g0020 a0001c0002t0001g0026 a0001c0002t0001g0156 others(173): Show |
190 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.1365-630T>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43995708 | |||||||
| chr22:43995806 | G | A | 111 | a0001c0002t0001g0020 a0001c0002t0001g0156 a0001c0002t0001g0157 others(108): Show |
120 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.1365-532G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43995806 | |||||||
| chr22:43995969 | C | A | 1 | a0001c0008t0001g0176 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1365-369C>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43995969 | |||||||
| chr22:43996049 | G | A | 6 | a0001c0002t0001g0020 a0001c0002t0001g0159 a0001c0002t0001g0160 others(3): Show |
7 | HG01891.hp1 HG01934.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1365-289G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43996049 | |||||||
| chr22:43996189 | G | A | 2 | a0001c0002t0004g0288 a0001c0007t0005g0037 |
2 | HG03195.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1365-149G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43996189 | |||||||
| chr22:43996223 | G | A | 1 | a0003c0003t0001g0096 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1365-115G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43996223 | |||||||
| chr22:43996240 | C | T | 1 | a0001c0002t0002g0300 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1365-98C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43996240 |