Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 203259 |
| ensemblid | ENSG00000164970.15 |
| hgncid | 19920 |
| symbol | FAM219A |
| name | family with sequence similarity 219 member A |
| refseq_nuc | NM_001184940.2 |
| refseq_prot | NP_001171869.1 |
| ensembl_nuc | ENST00000651358.1 |
| ensembl_prot | ENSP00000499069.1 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 34398184 |
| end | 34458570 |
| strand | - |
| ver | v1.2 |
| region | chr9:34398184-34458570 |
| region5000 | chr9:34393184-34463570 |
| regionname0 | FAM219A_chr9_34398184_34458570 |
| regionname5000 | FAM219A_chr9_34393184_34463570 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 555 | 391 | 84 | 72 | 184 | 12 | 37 | FAM219A_chr9_34393184_34463570 | FAM219A | ATGAT others(550): Show |
chr9 | 34393184 | 34463570 | ||
| a0001c0002 | 0/0 | 555 | 3 | 0 | 2 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | ATGAT others(550): Show |
chr9 | 34393184 | 34463570 | ||
| a0001c0003 | 0/0 | 555 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | ATGAT others(550): Show |
chr9 | 34393184 | 34463570 | ||
| a0001c0004 | 0/0 | 555 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | ATGAT others(550): Show |
chr9 | 34393184 | 34463570 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 3645 | 116 | 30 | 13 | 58 | 2 | 12 | FAM219A_chr9_34393184_34463570 | FAM219A | GAGTC others(3640): Show |
chr9 | 34393184 | 34463570 |
| a0001c0001t0002 | 0/1 | 3645 | 107 | 21 | 25 | 39 | 5 | 16 | FAM219A_chr9_34393184_34463570 | FAM219A | GAGTC others(3640): Show |
chr9 | 34393184 | 34463570 |
| a0001c0001t0003 | 0/0 | 3641 | 45 | 1 | 6 | 35 | 0 | 3 | FAM219A_chr9_34393184_34463570 | FAM219A | GAGTC others(3636): Show |
chr9 | 34393184 | 34463570 |
| a0001c0001t0004 | 0/0 | 3645 | 36 | 1 | 11 | 18 | 2 | 4 | FAM219A_chr9_34393184_34463570 | FAM219A | GAGTC others(3640): Show |
chr9 | 34393184 | 34463570 |
| a0001c0001t0005 | 0/0 | 3645 | 29 | 3 | 3 | 23 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | GAGTC others(3640): Show |
chr9 | 34393184 | 34463570 |
| a0001c0001t0006 | 0/0 | 3645 | 14 | 13 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | GAGTC others(3640): Show |
chr9 | 34393184 | 34463570 |
| a0001c0001t0007 | 0/0 | 3645 | 13 | 0 | 9 | 0 | 2 | 2 | FAM219A_chr9_34393184_34463570 | FAM219A | GAGTC others(3640): Show |
chr9 | 34393184 | 34463570 |
| a0001c0001t0008 | 0/0 | 3644 | 4 | 0 | 0 | 4 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | GAGTC others(3639): Show |
chr9 | 34393184 | 34463570 |
| a0001c0001t0009 | 0/0 | 3645 | 4 | 4 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | GAGTC others(3640): Show |
chr9 | 34393184 | 34463570 |
| a0001c0001t0010 | 0/0 | 3645 | 3 | 3 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | GAGTC others(3640): Show |
chr9 | 34393184 | 34463570 |
| a0001c0001t0011 | 0/0 | 3645 | 2 | 2 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | GAGTC others(3640): Show |
chr9 | 34393184 | 34463570 |
| a0001c0001t0012 | 0/0 | 3645 | 2 | 2 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | GAGTC others(3640): Show |
chr9 | 34393184 | 34463570 |
| a0001c0001t0013 | 0/0 | 3645 | 2 | 2 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | GAGTC others(3640): Show |
chr9 | 34393184 | 34463570 |
| a0001c0001t0014 | 0/0 | 3645 | 2 | 0 | 0 | 2 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | GAGTC others(3640): Show |
chr9 | 34393184 | 34463570 |
| a0001c0001t0015 | 0/0 | 3645 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | GAGTC others(3640): Show |
chr9 | 34393184 | 34463570 |
| a0001c0001t0016 | 0/0 | 3645 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | GAGTC others(3640): Show |
chr9 | 34393184 | 34463570 |
| a0001c0001t0017 | 0/0 | 3645 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | GAGTC others(3640): Show |
chr9 | 34393184 | 34463570 |
| a0001c0001t0018 | 0/0 | 3645 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | GAGTC others(3640): Show |
chr9 | 34393184 | 34463570 |
| a0001c0001t0019 | 0/0 | 3645 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | GAGTC others(3640): Show |
chr9 | 34393184 | 34463570 |
| a0001c0001t0020 | 0/0 | 3645 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | GAGTC others(3640): Show |
chr9 | 34393184 | 34463570 |
| a0001c0001t0021 | 0/0 | 3645 | 1 | 0 | 0 | 0 | 1 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | GAGTC others(3640): Show |
chr9 | 34393184 | 34463570 |
| a0001c0001t0022 | 0/0 | 3645 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | GAGTC others(3640): Show |
chr9 | 34393184 | 34463570 |
| a0001c0001t0023 | 0/0 | 3645 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | GAGTC others(3640): Show |
chr9 | 34393184 | 34463570 |
| a0001c0001t0024 | 0/0 | 3645 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | GAGTC others(3640): Show |
chr9 | 34393184 | 34463570 |
| a0001c0001t0025 | 0/0 | 3645 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | GAGTC others(3640): Show |
chr9 | 34393184 | 34463570 |
| a0001c0001t0026 | 0/0 | 3645 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | GAGTC others(3640): Show |
chr9 | 34393184 | 34463570 |
| a0001c0002t0001 | 0/0 | 3645 | 3 | 0 | 2 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | GAGTC others(3640): Show |
chr9 | 34393184 | 34463570 |
| a0001c0003t0001 | 0/0 | 3645 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | GAGTC others(3640): Show |
chr9 | 34393184 | 34463570 |
| a0001c0004t0003 | 0/0 | 3641 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | GAGTC others(3636): Show |
chr9 | 34393184 | 34463570 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0001g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0001g0006 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0001g0195 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0001g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0001g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0001g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0001g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0001g0363 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0001g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0001g0367 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0002g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0002g0008 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0002g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0002g0011 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0002g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0002g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0002g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0002g0220 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0002g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0002g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0002g0316 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0002g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0002g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0002g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0002g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0002g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0002g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0002g0366 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0003g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0003g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0003g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0003g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0003g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0003g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0003g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0003g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0003g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0003g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0003g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0003g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0003g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0003g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0003g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0003g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0003g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0003g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0003g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0003g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0003g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0003g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0003g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0003g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0003g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0003g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0003g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0003g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0003g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0003g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0003g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0003g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0003g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0003g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0003g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0003g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0003g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0004g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0004g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0004g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0004g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0004g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0004g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0004g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0004g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0004g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0004g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0004g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0004g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0004g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0004g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0004g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0004g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0004g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0004g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0004g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0004g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0004g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0004g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0004g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0004g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0004g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0004g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0004g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0004g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0004g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0004g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0004g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0004g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0004g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0004g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0005g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0005g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0005g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0005g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0005g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0005g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0005g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0005g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0005g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0005g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0005g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0005g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0005g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0005g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0005g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0005g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0005g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0005g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0005g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0005g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0005g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0005g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0005g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0005g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0005g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0005g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0005g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0005g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0006g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0006g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0006g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0006g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0006g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0006g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0006g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0006g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0006g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0006g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0006g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0006g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0006g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0006g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0007g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0007g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0007g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0007g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0007g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0007g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0007g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0007g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0007g0350 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0007g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0007g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0007g0353 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0007g0368 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0008g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0008g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0008g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0008g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0009g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0009g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0009g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0009g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0010g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0010g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0010g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0011g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0011g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0012g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0012g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0013g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0013g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0014g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0014g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0015g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0016g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0017g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0018g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0019g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0020g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0021g0354 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0022g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0023g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0024g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0025g0364 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0001t0026g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0002t0001g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0002t0001g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0003t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| a0001c0004t0003g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0007 | g0350 | EUR | GBR | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0151 | EUR | GBR | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0250 | EUR | FIN | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG00280 | hp2 | a0001 | c0001 | t0004 | g0057 | EUR | FIN | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0316 | EUR | FIN | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0135 | EUR | FIN | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG00423 | hp1 | a0001 | c0001 | t0004 | g0214 | EAS | CHS | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | CHS | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0258 | EAS | CHS | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | CHS | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0336 | EAS | CHS | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG00558 | hp1 | a0001 | c0001 | t0005 | g0036 | EAS | CHS | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG00558 | hp2 | a0001 | c0001 | t0003 | g0332 | EAS | CHS | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG00597 | hp1 | a0001 | c0001 | t0014 | g0269 | EAS | CHS | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0181 | EAS | CHS | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0129 | EAS | CHS | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG00621 | hp1 | a0001 | c0001 | t0020 | g0276 | EAS | CHS | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG00621 | hp2 | a0001 | c0001 | t0003 | g0127 | EAS | CHS | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0247 | AMR | PUR | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0013 | AMR | PUR | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0133 | AMR | PUR | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0182 | AMR | PUR | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0018 | EAS | CHS | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0176 | EAS | CHS | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0013 | AMR | PUR | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG00735 | hp2 | a0001 | c0001 | t0003 | g0016 | AMR | PUR | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG00741 | hp1 | a0001 | c0001 | t0007 | g0352 | AMR | PUR | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG00741 | hp2 | a0001 | c0001 | t0007 | g0172 | AMR | PUR | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG01070 | hp1 | a0001 | c0001 | t0007 | g0197 | AMR | PUR | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG01070 | hp2 | a0001 | c0001 | t0007 | g0348 | AMR | PUR | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG01074 | hp1 | a0001 | c0001 | t0004 | g0070 | AMR | PUR | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0274 | AMR | PUR | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG01081 | hp1 | a0001 | c0001 | t0004 | g0065 | AMR | PUR | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0198 | AMR | PUR | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG01099 | hp1 | a0001 | c0001 | t0004 | g0063 | AMR | PUR | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG01099 | hp2 | a0001 | c0002 | t0001 | g0358 | AMR | PUR | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0155 | AMR | PUR | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0186 | AMR | PUR | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0141 | AMR | PUR | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0208 | AMR | PUR | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0123 | AMR | PUR | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG01167 | hp2 | a0001 | c0001 | t0007 | g0347 | AMR | PUR | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | PUR | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0245 | AMR | PUR | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0246 | AMR | PUR | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG01175 | hp1 | a0001 | c0001 | t0004 | g0074 | AMR | PUR | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG01243 | hp2 | a0001 | c0001 | t0004 | g0105 | AMR | PUR | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG01255 | hp1 | a0001 | c0001 | t0026 | g0149 | AMR | CLM | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG01255 | hp2 | a0001 | c0001 | t0024 | g0104 | AMR | CLM | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG01257 | hp1 | a0001 | c0001 | t0004 | g0073 | AMR | CLM | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0175 | AMR | CLM | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG01258 | hp1 | a0001 | c0001 | t0004 | g0064 | AMR | CLM | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | CLM | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0362 | AMR | CLM | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0130 | AMR | CLM | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0126 | AMR | CLM | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0200 | AMR | CLM | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0365 | AMR | CLM | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0140 | AMR | CLM | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0219 | AMR | CLM | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG01361 | hp2 | a0001 | c0002 | t0001 | g0359 | AMR | CLM | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG01433 | hp1 | a0001 | c0001 | t0003 | g0361 | AMR | CLM | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG01433 | hp2 | a0001 | c0001 | t0016 | g0072 | AMR | CLM | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG01496 | hp1 | a0001 | c0001 | t0003 | g0110 | AMR | CLM | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG01496 | hp2 | a0001 | c0001 | t0006 | g0060 | AMR | CLM | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0112 | EUR | IBS | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG01516 | hp2 | a0001 | c0001 | t0021 | g0354 | EUR | IBS | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG01891 | hp1 | a0001 | c0001 | t0010 | g0090 | AFR | ACB | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG01891 | hp2 | a0001 | c0001 | t0011 | g0050 | AFR | ACB | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG01928 | hp1 | a0001 | c0001 | t0005 | g0041 | AMR | PEL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0367 | AMR | PEL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG01934 | hp1 | a0001 | c0001 | t0005 | g0032 | AMR | PEL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG01934 | hp2 | a0001 | c0001 | t0004 | g0058 | AMR | PEL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG01943 | hp1 | a0001 | c0001 | t0007 | g0349 | AMR | PEL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0012 | AMR | PEL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG01952 | hp1 | a0001 | c0001 | t0003 | g0337 | AMR | PEL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG01952 | hp2 | a0001 | c0001 | t0004 | g0069 | AMR | PEL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG01975 | hp1 | a0001 | c0001 | t0003 | g0333 | AMR | PEL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG01978 | hp1 | a0001 | c0001 | t0004 | g0062 | AMR | PEL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG01978 | hp2 | a0001 | c0001 | t0007 | g0202 | AMR | PEL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0120 | AMR | PEL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG01981 | hp2 | a0001 | c0001 | t0025 | g0364 | AMR | PEL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | PEL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0302 | AMR | PEL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG02004 | hp2 | a0001 | c0001 | t0003 | g0016 | AMR | PEL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0221 | EAS | KHV | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | KHV | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG02027 | hp1 | a0001 | c0001 | t0005 | g0028 | EAS | KHV | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG02027 | hp2 | a0001 | c0001 | t0003 | g0314 | EAS | KHV | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | KHV | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0315 | EAS | KHV | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | ACB | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | ACB | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG02056 | hp2 | a0001 | c0001 | t0004 | g0159 | EAS | KHV | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0260 | EAS | KHV | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | KHV | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG02074 | hp1 | a0001 | c0001 | t0005 | g0046 | EAS | KHV | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | KHV | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | KHV | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0163 | EAS | KHV | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG02083 | hp1 | a0001 | c0001 | t0004 | g0224 | EAS | KHV | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | KHV | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0174 | EAS | KHV | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0335 | EAS | KHV | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | KHV | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG02132 | hp2 | a0001 | c0001 | t0003 | g0326 | EAS | KHV | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | KHV | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | KHV | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0215 | AFR | ACB | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0199 | AFR | ACB | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG02155 | hp1 | a0001 | c0001 | t0019 | g0263 | EAS | CDX | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0152 | EAS | CDX | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG02165 | hp1 | a0001 | c0001 | t0003 | g0017 | EAS | CDX | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0183 | EAS | CDX | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG02257 | hp1 | a0001 | c0001 | t0006 | g0081 | AFR | ACB | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | ACB | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0266 | AFR | ACB | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0360 | AFR | ACB | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG02273 | hp1 | a0001 | c0001 | t0005 | g0031 | AMR | PEL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0020 | AMR | PEL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG02280 | hp1 | a0001 | c0001 | t0006 | g0078 | AFR | ACB | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0254 | AFR | ACB | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0244 | AMR | PEL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0154 | AMR | PEL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0020 | AMR | PEL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG02300 | hp2 | a0001 | c0001 | t0007 | g0156 | AMR | PEL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG02451 | hp2 | a0001 | c0001 | t0017 | g0103 | AFR | ACB | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG02523 | hp1 | a0001 | c0001 | t0005 | g0045 | EAS | KHV | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG02523 | hp2 | a0001 | c0001 | t0003 | g0327 | EAS | KHV | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG02572 | hp1 | a0001 | c0001 | t0006 | g0089 | AFR | GWD | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | GWD | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG02602 | hp1 | a0001 | c0001 | t0003 | g0331 | SAS | PJL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0178 | SAS | PJL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0207 | AFR | GWD | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | GWD | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG02622 | hp1 | a0001 | c0001 | t0011 | g0051 | AFR | GWD | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG02622 | hp2 | a0001 | c0001 | t0006 | g0118 | AFR | GWD | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG02630 | hp1 | a0001 | c0001 | t0010 | g0102 | AFR | GWD | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0241 | AFR | GWD | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG02647 | hp1 | a0001 | c0001 | t0018 | g0111 | AFR | GWD | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0226 | AFR | GWD | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0259 | SAS | PJL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0132 | SAS | PJL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0125 | SAS | PJL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG02698 | hp2 | a0001 | c0002 | t0001 | g0196 | SAS | PJL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0253 | AFR | GWD | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0206 | AFR | GWD | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0234 | SAS | PJL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG02735 | hp2 | a0001 | c0001 | t0007 | g0368 | SAS | PJL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0191 | SAS | PJL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0345 | SAS | PJL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | GWD | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0192 | AFR | GWD | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | GWD | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG02818 | hp2 | a0001 | c0001 | t0009 | g0147 | AFR | GWD | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0324 | AFR | GWD | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG02895 | hp2 | a0001 | c0001 | t0006 | g0080 | AFR | GWD | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG02896 | hp1 | a0001 | c0001 | t0006 | g0148 | AFR | GWD | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | GWD | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG02897 | hp1 | a0001 | c0001 | t0006 | g0082 | AFR | GWD | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG02897 | hp2 | a0001 | c0001 | t0006 | g0143 | AFR | GWD | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | ESN | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | ESN | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | ESN | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0079 | AFR | ESN | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0122 | AFR | ESN | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0255 | AFR | ESN | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0121 | SAS | PJL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG03017 | hp2 | a0001 | c0001 | t0004 | g0068 | SAS | PJL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0204 | AFR | GWD | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0267 | AFR | GWD | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | MSL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | MSL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0227 | AFR | ESN | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0291 | AFR | ESN | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG03195 | hp1 | a0001 | c0001 | t0012 | g0053 | AFR | ESN | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0096 | AFR | ESN | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0262 | AFR | MSL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG03225 | hp2 | a0001 | c0001 | t0006 | g0056 | AFR | MSL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0273 | AFR | MSL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0205 | AFR | MSL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0087 | AFR | MSL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | MSL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0235 | SAS | PJL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0201 | SAS | PJL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0366 | SAS | PJL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0286 | SAS | PJL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG03516 | hp1 | a0001 | c0001 | t0013 | g0092 | AFR | ESN | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG03516 | hp2 | a0001 | c0001 | t0012 | g0052 | AFR | ESN | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG03540 | hp1 | a0001 | c0001 | t0010 | g0095 | AFR | GWD | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0209 | AFR | GWD | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0194 | AFR | MSL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG03579 | hp2 | a0001 | c0001 | t0009 | g0144 | AFR | MSL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0268 | SAS | PJL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG03654 | hp2 | a0001 | c0001 | t0007 | g0353 | SAS | PJL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0173 | SAS | PJL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0008 | SAS | PJL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0136 | SAS | STU | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0287 | SAS | STU | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG03704 | hp1 | a0001 | c0001 | t0003 | g0285 | SAS | PJL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0153 | SAS | PJL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG03834 | hp1 | a0001 | c0001 | t0004 | g0071 | SAS | BEB | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0190 | SAS | BEB | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG03927 | hp1 | a0001 | c0001 | t0004 | g0248 | SAS | BEB | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0222 | SAS | BEB | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0233 | SAS | BEB | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0150 | SAS | BEB | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0363 | SAS | STU | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0232 | SAS | STU | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0171 | SAS | BEB | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG04184 | hp2 | a0001 | c0001 | t0003 | g0339 | SAS | BEB | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0281 | SAS | STU | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0203 | SAS | STU | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG04228 | hp1 | a0001 | c0001 | t0004 | g0075 | SAS | STU | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0139 | SAS | STU | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA18747 | hp1 | a0001 | c0001 | t0008 | g0164 | EAS | CHB | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | CHB | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA18906 | hp1 | a0001 | c0001 | t0005 | g0044 | AFR | YRI | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA18906 | hp2 | a0001 | c0001 | t0006 | g0357 | AFR | YRI | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA18939 | hp1 | a0001 | c0001 | t0005 | g0034 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA18939 | hp2 | a0001 | c0001 | t0003 | g0311 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA18940 | hp1 | a0001 | c0001 | t0004 | g0160 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA18940 | hp2 | a0001 | c0001 | t0005 | g0025 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA18941 | hp1 | a0001 | c0001 | t0005 | g0027 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA18944 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA18945 | hp2 | a0001 | c0001 | t0005 | g0049 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA18948 | hp1 | a0001 | c0001 | t0005 | g0033 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA18948 | hp2 | a0001 | c0001 | t0003 | g0328 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0277 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA18950 | hp1 | a0001 | c0001 | t0004 | g0213 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA18950 | hp2 | a0001 | c0001 | t0003 | g0341 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA18952 | hp1 | a0001 | c0001 | t0003 | g0329 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0138 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA18956 | hp1 | a0001 | c0001 | t0003 | g0018 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA18959 | hp1 | a0001 | c0001 | t0005 | g0038 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA18960 | hp2 | a0001 | c0001 | t0003 | g0313 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA18962 | hp2 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA18964 | hp2 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA18965 | hp2 | a0001 | c0001 | t0005 | g0024 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA18967 | hp2 | a0001 | c0001 | t0003 | g0310 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA18971 | hp2 | a0001 | c0001 | t0004 | g0009 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA18974 | hp1 | a0001 | c0001 | t0004 | g0211 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0256 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0238 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA18977 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA18979 | hp1 | a0001 | c0001 | t0003 | g0317 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA18979 | hp2 | a0001 | c0001 | t0015 | g0022 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA18980 | hp2 | a0001 | c0001 | t0005 | g0004 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA18981 | hp1 | a0001 | c0001 | t0003 | g0318 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0165 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA18983 | hp1 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA18983 | hp2 | a0001 | c0001 | t0005 | g0040 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0356 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0292 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA18988 | hp2 | a0001 | c0001 | t0003 | g0312 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA18989 | hp2 | a0001 | c0001 | t0003 | g0319 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA18990 | hp1 | a0001 | c0001 | t0023 | g0162 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA18991 | hp1 | a0001 | c0001 | t0005 | g0029 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0257 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA18992 | hp2 | a0001 | c0001 | t0005 | g0037 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA18994 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA18994 | hp2 | a0001 | c0001 | t0004 | g0076 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA18998 | hp1 | a0001 | c0001 | t0003 | g0322 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA18999 | hp1 | a0001 | c0001 | t0005 | g0047 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA19000 | hp1 | a0001 | c0001 | t0004 | g0114 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA19001 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA19001 | hp2 | a0001 | c0001 | t0003 | g0342 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA19002 | hp1 | a0001 | c0001 | t0004 | g0142 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0355 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA19005 | hp1 | a0001 | c0001 | t0003 | g0320 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA19007 | hp2 | a0001 | c0001 | t0003 | g0321 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA19010 | hp1 | a0001 | c0001 | t0004 | g0210 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0189 | AFR | LWK | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | LWK | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA19043 | hp1 | a0001 | c0001 | t0005 | g0023 | AFR | LWK | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | LWK | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA19054 | hp1 | a0001 | c0001 | t0003 | g0340 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA19055 | hp2 | a0001 | c0001 | t0005 | g0026 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA19057 | hp1 | a0001 | c0001 | t0004 | g0009 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA19060 | hp1 | a0001 | c0001 | t0003 | g0334 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA19060 | hp2 | a0001 | c0001 | t0008 | g0168 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA19062 | hp1 | a0001 | c0001 | t0005 | g0039 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA19063 | hp2 | a0001 | c0001 | t0005 | g0030 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA19065 | hp1 | a0001 | c0001 | t0022 | g0300 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA19067 | hp1 | a0001 | c0001 | t0003 | g0309 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA19067 | hp2 | a0001 | c0001 | t0004 | g0115 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA19068 | hp1 | a0001 | c0001 | t0004 | g0225 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA19068 | hp2 | a0001 | c0001 | t0003 | g0344 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0323 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA19077 | hp1 | a0001 | c0001 | t0003 | g0330 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA19077 | hp2 | a0001 | c0001 | t0008 | g0166 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA19078 | hp2 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA19079 | hp1 | a0001 | c0001 | t0003 | g0338 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA19079 | hp2 | a0001 | c0001 | t0004 | g0212 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA19080 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA19080 | hp2 | a0001 | c0001 | t0014 | g0265 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA19081 | hp1 | a0001 | c0001 | t0008 | g0167 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA19081 | hp2 | a0001 | c0004 | t0003 | g0346 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA19084 | hp1 | a0001 | c0001 | t0005 | g0035 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA19084 | hp2 | a0001 | c0003 | t0001 | g0288 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA19085 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA19087 | hp1 | a0001 | c0001 | t0004 | g0161 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA19087 | hp2 | a0001 | c0001 | t0005 | g0042 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA19088 | hp2 | a0001 | c0001 | t0005 | g0004 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0343 | AFR | YRI | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA19240 | hp2 | a0001 | c0001 | t0013 | g0091 | AFR | YRI | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0325 | AFR | ASW | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA20129 | hp2 | a0001 | c0001 | t0006 | g0077 | AFR | ASW | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0011 | EUR | TSI | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA20752 | hp2 | a0001 | c0001 | t0004 | g0067 | EUR | TSI | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA20805 | hp1 | a0001 | c0001 | t0007 | g0223 | EUR | TSI | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0124 | EUR | TSI | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG01123 | hp1 | a0001 | c0001 | t0004 | g0066 | AMR | CLM | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG01123 | hp2 | a0001 | c0001 | t0007 | g0351 | AMR | CLM | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0010 | AFR | ACB | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG02109 | hp2 | a0001 | c0001 | t0006 | g0061 | AFR | ACB | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG02559 | hp1 | a0001 | c0001 | t0009 | g0145 | AFR | ACB | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG02559 | hp2 | a0001 | c0001 | t0005 | g0048 | AFR | ACB | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG03471 | hp1 | a0001 | c0001 | t0006 | g0093 | AFR | MSL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | MSL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0107 | AFR | USA | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | USA | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA18955 | hp2 | a0001 | c0001 | t0005 | g0043 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0305 | AFR | USA | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0239 | AFR | USA | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA21309 | hp1 | a0001 | c0001 | t0004 | g0098 | AFR | LWK | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| NA21309 | hp2 | a0001 | c0001 | t0009 | g0146 | AFR | LWK | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0220 | REF | REF | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0195 | REF | REF | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:34400982 | G | A | 1 | a0001c0002 | 3 | HG01099.hp2 HG01361.hp2 HG02698.hp2 |
synonymous_variant | LOW | c.540C>T | p.Thr180Thr | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 6/6 | 847/3645 | 540/558 | 180/185 | chr9 | 34400982 | |||
| chr9:34401030 | G | T | 1 | a0001c0003 | 1 | NA19084.hp2 | synonymous_variant | LOW | c.492C>A | p.Pro164Pro | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 6/6 | 799/3645 | 492/558 | 164/185 | chr9 | 34401030 | |||
| chr9:34402706 | T | G | 1 | a0001c0004 | 1 | NA19081.hp2 | splice_region_variant&synonymous_variant | LOW | c.262A>C | p.Arg88Arg | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 3/6 | 569/3645 | 262/558 | 88/185 | chr9 | 34402706 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:34398268 | TA | T | 1 | a0001c0001t0008 | 4 | NA18747.hp1 NA19060.hp2 NA19077.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2695delT | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 6/6 | 2695 | chr9 | 34398268 | ||||||
| chr9:34398587 | G | C | 2 | a0001c0001t0010 a0001c0001t0018 |
4 | HG01891.hp1 HG02630.hp1 HG02647.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2377C>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 6/6 | 2377 | chr9 | 34398587 | ||||||
| chr9:34399004 | C | A | 11 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0005 others(8): Show |
210 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(207): Show |
3_prime_UTR_variant | MODIFIER | c.*1960G>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 6/6 | 1960 | chr9 | 34399004 | ||||||
| chr9:34399172 | G | A | 2 | a0001c0001t0004 a0001c0001t0006 |
50 | HG00280.hp2 HG00423.hp1 HG01074.hp1 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*1792C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 6/6 | 1792 | chr9 | 34399172 | ||||||
| chr9:34399340 | A | G | 2 | a0001c0001t0007 a0001c0001t0021 |
14 | HG00099.hp1 HG00741.hp1 HG00741.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1624T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 6/6 | 1624 | chr9 | 34399340 | ||||||
| chr9:34399504 | C | G | 1 | a0001c0001t0020 | 1 | HG00621.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1460G>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 6/6 | 1460 | chr9 | 34399504 | ||||||
| chr9:34399505 | CCAAA | C | 2 | a0001c0001t0003 a0001c0004t0003 |
46 | HG00558.hp2 HG00621.hp2 HG00673.hp1 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*1455_*1458delTTTG | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 6/6 | 1455 | chr9 | 34399505 | ||||||
| chr9:34399663 | A | C | 1 | a0001c0001t0024 | 1 | HG01255.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1301T>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 6/6 | 1301 | chr9 | 34399663 | ||||||
| chr9:34399683 | A | G | 1 | a0001c0001t0019 | 1 | HG02155.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1281T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 6/6 | 1281 | chr9 | 34399683 | ||||||
| chr9:34399892 | G | A | 1 | a0001c0001t0021 | 1 | HG01516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1072C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 6/6 | 1072 | chr9 | 34399892 | ||||||
| chr9:34400188 | C | A | 1 | a0001c0001t0024 | 1 | HG01255.hp2 | 3_prime_UTR_variant | MODIFIER | c.*776G>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 6/6 | 776 | chr9 | 34400188 | ||||||
| chr9:34400204 | G | A | 1 | a0001c0001t0022 | 1 | NA19065.hp1 | 3_prime_UTR_variant | MODIFIER | c.*760C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 6/6 | 760 | chr9 | 34400204 | ||||||
| chr9:34400251 | G | A | 1 | a0001c0001t0023 | 1 | NA18990.hp1 | 3_prime_UTR_variant | MODIFIER | c.*713C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 6/6 | 713 | chr9 | 34400251 | ||||||
| chr9:34400304 | A | G | 1 | a0001c0001t0018 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*660T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 6/6 | 660 | chr9 | 34400304 | ||||||
| chr9:34400340 | G | A | 1 | a0001c0001t0014 | 2 | HG00597.hp1 NA19080.hp2 |
3_prime_UTR_variant | MODIFIER | c.*624C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 6/6 | 624 | chr9 | 34400340 | ||||||
| chr9:34400475 | T | C | 1 | a0001c0001t0024 | 1 | HG01255.hp2 | 3_prime_UTR_variant | MODIFIER | c.*489A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 6/6 | 489 | chr9 | 34400475 | ||||||
| chr9:34400503 | G | A | 1 | a0001c0001t0025 | 1 | HG01981.hp2 | 3_prime_UTR_variant | MODIFIER | c.*461C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 6/6 | 461 | chr9 | 34400503 | ||||||
| chr9:34400583 | C | T | 7 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0008 others(4): Show |
143 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(140): Show |
3_prime_UTR_variant | MODIFIER | c.*381G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 6/6 | 381 | chr9 | 34400583 | ||||||
| chr9:34400598 | A | G | 1 | a0001c0001t0013 | 2 | HG03516.hp1 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*366T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 6/6 | 366 | chr9 | 34400598 | ||||||
| chr9:34400607 | G | A | 1 | a0001c0001t0004 | 36 | HG00280.hp2 HG00423.hp1 HG01074.hp1 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*357C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 6/6 | 357 | chr9 | 34400607 | ||||||
| chr9:34400687 | A | G | 1 | a0001c0001t0016 | 1 | HG01433.hp2 | 3_prime_UTR_variant | MODIFIER | c.*277T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 6/6 | 277 | chr9 | 34400687 | ||||||
| chr9:34400952 | T | C | 1 | a0001c0001t0026 | 1 | HG01255.hp1 | 3_prime_UTR_variant | MODIFIER | c.*12A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 6/6 | 12 | chr9 | 34400952 | ||||||
| chr9:34458322 | C | T | 1 | a0001c0001t0012 | 2 | HG03195.hp1 HG03516.hp2 |
5_prime_UTR_variant | MODIFIER | c.-59G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/6 | 59 | chr9 | 34458322 | ||||||
| chr9:34458380 | C | G | 2 | a0001c0001t0005 a0001c0001t0011 |
31 | HG00558.hp1 HG01891.hp2 HG01928.hp1 others(28): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-117G>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/6 | chr9 | 34458380 | |||||||
| chr9:34458536 | G | T | 1 | a0001c0001t0015 | 1 | NA18979.hp2 | 5_prime_UTR_variant | MODIFIER | c.-273C>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/6 | 273 | chr9 | 34458536 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:34401184 | C | T | 1 | a0001c0001t0004g0067 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.400-62G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 5/5 | chr9 | 34401184 | |||||||
| chr9:34401372 | C | A | 1 | a0001c0001t0004g0070 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.400-250G>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 5/5 | chr9 | 34401372 | |||||||
| chr9:34401461 | G | A | 1 | a0001c0001t0018g0111 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.399+205C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 5/5 | chr9 | 34401461 | |||||||
| chr9:34401494 | AGGCCAGT others(15): Show |
A | 1 | a0001c0004t0003g0346 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.399+150_399+171del others(22): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 5/5 | chr9 | 34401494 | |||||||
| chr9:34401766 | T | C | 41 | a0001c0001t0001g0345 a0001c0001t0002g0232 a0001c0001t0003g0003 others(38): Show |
48 | HG00558.hp2 HG00621.hp2 HG00673.hp1 others(45): Show |
intron_variant | MODIFIER | c.345-46A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 4/5 | chr9 | 34401766 | |||||||
| chr9:34401970 | A | G | 1 | a0001c0001t0006g0089 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.345-250T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 4/5 | chr9 | 34401970 | |||||||
| chr9:34401972 | CT | C | 140 | a0001c0001t0001g0249 a0001c0001t0001g0301 a0001c0001t0001g0315 others(137): Show |
148 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(145): Show |
intron_variant | MODIFIER | c.345-253delA | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 4/5 | chr9 | 34401972 | |||||||
| chr9:34402096 | T | C | 48 | a0001c0001t0004g0005 a0001c0001t0004g0009 a0001c0001t0004g0057 others(45): Show |
50 | HG00280.hp2 HG00423.hp1 HG01074.hp1 others(47): Show |
intron_variant | MODIFIER | c.344+291A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 4/5 | chr9 | 34402096 | |||||||
| chr9:34402120 | C | T | 1 | a0001c0001t0006g0118 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.344+267G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 4/5 | chr9 | 34402120 | |||||||
| chr9:34402175 | A | G | 365 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(362): Show |
393 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(390): Show |
intron_variant | MODIFIER | c.344+212T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 4/5 | chr9 | 34402175 | |||||||
| chr9:34402486 | G | A | 2 | a0001c0001t0001g0283 a0001c0001t0001g0284 |
2 | HG00423.hp2 HG02015.hp2 |
intron_variant | MODIFIER | c.264-19C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 3/5 | chr9 | 34402486 | |||||||
| chr9:34402665 | C | T | 14 | a0001c0001t0007g0156 a0001c0001t0007g0172 a0001c0001t0007g0197 others(11): Show |
14 | HG00099.hp1 HG00741.hp1 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.263+40G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 3/5 | chr9 | 34402665 | |||||||
| chr9:34402703 | A | T | 1 | a0001c0004t0003g0346 | 1 | NA19081.hp2 | splice_donor_variant&intron_variant | HIGH | c.263+2T>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 3/5 | chr9 | 34402703 | |||||||
| chr9:34402886 | G | T | 1 | a0001c0004t0003g0346 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.161-79C>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 2/5 | chr9 | 34402886 | |||||||
| chr9:34402898 | G | A | 2 | a0001c0001t0001g0360 a0001c0001t0001g0363 |
2 | HG02258.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.161-91C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 2/5 | chr9 | 34402898 | |||||||
| chr9:34402989 | G | A | 1 | a0001c0001t0001g0228 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.161-182C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 2/5 | chr9 | 34402989 | |||||||
| chr9:34403028 | T | C | 1 | a0001c0004t0003g0346 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.161-221A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 2/5 | chr9 | 34403028 | |||||||
| chr9:34403029 | G | T | 1 | a0001c0004t0003g0346 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.161-222C>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 2/5 | chr9 | 34403029 | |||||||
| chr9:34403030 | T | G | 1 | a0001c0004t0003g0346 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.161-223A>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 2/5 | chr9 | 34403030 | |||||||
| chr9:34403033 | T | C | 1 | a0001c0001t0002g0012 | 2 | HG01943.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.161-226A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 2/5 | chr9 | 34403033 | |||||||
| chr9:34403097 | G | A | 3 | a0001c0001t0002g0257 a0001c0001t0002g0258 a0001c0001t0002g0277 |
3 | HG00438.hp1 NA18949.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.161-290C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 2/5 | chr9 | 34403097 | |||||||
| chr9:34403284 | T | C | 1 | a0001c0004t0003g0346 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.161-477A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 2/5 | chr9 | 34403284 | |||||||
| chr9:34403289 | T | C | 1 | a0001c0001t0006g0093 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.161-482A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 2/5 | chr9 | 34403289 | |||||||
| chr9:34403313 | A | G | 4 | a0001c0001t0001g0083 a0001c0001t0001g0267 a0001c0001t0012g0052 others(1): Show |
4 | HG02055.hp2 HG03041.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.161-506T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 2/5 | chr9 | 34403313 | |||||||
| chr9:34403355 | C | T | 1 | a0001c0001t0001g0241 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.161-548G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 2/5 | chr9 | 34403355 | |||||||
| chr9:34403356 | G | A | 1 | a0001c0001t0005g0026 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.161-549C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 2/5 | chr9 | 34403356 | |||||||
| chr9:34403375 | A | G | 4 | a0001c0001t0009g0144 a0001c0001t0009g0145 a0001c0001t0009g0146 others(1): Show |
4 | HG02559.hp1 HG02818.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.161-568T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 2/5 | chr9 | 34403375 | |||||||
| chr9:34403380 | C | G | 1 | a0001c0001t0003g0110 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.161-573G>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 2/5 | chr9 | 34403380 | |||||||
| chr9:34403421 | A | T | 1 | a0001c0004t0003g0346 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.161-614T>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 2/5 | chr9 | 34403421 | |||||||
| chr9:34403426 | C | T | 46 | a0001c0001t0004g0005 a0001c0001t0004g0009 a0001c0001t0004g0057 others(43): Show |
48 | HG00280.hp2 HG00423.hp1 HG01074.hp1 others(45): Show |
intron_variant | MODIFIER | c.161-619G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 2/5 | chr9 | 34403426 | |||||||
| chr9:34403524 | C | T | 2 | a0001c0001t0011g0050 a0001c0001t0011g0051 |
2 | HG01891.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.161-717G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 2/5 | chr9 | 34403524 | |||||||
| chr9:34403603 | C | G | 1 | a0001c0001t0003g0127 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.161-796G>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 2/5 | chr9 | 34403603 | |||||||
| chr9:34403666 | T | A | 1 | a0001c0004t0003g0346 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.161-859A>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 2/5 | chr9 | 34403666 | |||||||
| chr9:34403813 | C | T | 1 | a0001c0001t0001g0124 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.161-1006G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 2/5 | chr9 | 34403813 | |||||||
| chr9:34403868 | T | A | 1 | a0001c0004t0003g0346 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.161-1061A>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 2/5 | chr9 | 34403868 | |||||||
| chr9:34403906 | T | C | 3 | a0001c0001t0002g0257 a0001c0001t0002g0258 a0001c0001t0002g0277 |
3 | HG00438.hp1 NA18949.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.161-1099A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 2/5 | chr9 | 34403906 | |||||||
| chr9:34403984 | G | C | 1 | a0001c0001t0001g0188 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.161-1177C>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 2/5 | chr9 | 34403984 | |||||||
| chr9:34404417 | A | G | 1 | a0001c0001t0003g0326 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.160+1448T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 2/5 | chr9 | 34404417 | |||||||
| chr9:34404490 | T | A | 1 | a0001c0004t0003g0346 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.160+1375A>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 2/5 | chr9 | 34404490 | |||||||
| chr9:34404578 | C | G | 2 | a0001c0001t0003g0330 a0001c0001t0003g0338 |
2 | NA19077.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.160+1287G>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 2/5 | chr9 | 34404578 | |||||||
| chr9:34404701 | C | CT | 6 | a0001c0001t0001g0059 a0001c0001t0001g0084 a0001c0001t0001g0085 others(3): Show |
6 | HG01175.hp2 HG02818.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.160+1163dupA | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 2/5 | chr9 | 34404701 | |||||||
| chr9:34404709 | AAAC | A | 110 | a0001c0001t0001g0345 a0001c0001t0002g0232 a0001c0001t0003g0003 others(107): Show |
119 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.160+1153_160+1155d others(5): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 2/5 | chr9 | 34404709 | |||||||
| chr9:34404736 | C | A | 1 | a0001c0004t0003g0346 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.160+1129G>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 2/5 | chr9 | 34404736 | |||||||
| chr9:34404737 | A | C | 1 | a0001c0004t0003g0346 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.160+1128T>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 2/5 | chr9 | 34404737 | |||||||
| chr9:34404739 | C | A | 1 | a0001c0004t0003g0346 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.160+1126G>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 2/5 | chr9 | 34404739 | |||||||
| chr9:34404742 | A | C | 1 | a0001c0004t0003g0346 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.160+1123T>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 2/5 | chr9 | 34404742 | |||||||
| chr9:34405013 | G | A | 1 | a0001c0001t0002g0150 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.160+852C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 2/5 | chr9 | 34405013 | |||||||
| chr9:34405620 | G | C | 278 | a0001c0001t0001g0059 a0001c0001t0001g0083 a0001c0001t0001g0084 others(275): Show |
294 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(291): Show |
intron_variant | MODIFIER | c.160+245C>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 2/5 | chr9 | 34405620 | |||||||
| chr9:34405683 | G | C | 19 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0112 others(16): Show |
21 | HG00609.hp2 HG01106.hp2 HG01167.hp1 others(18): Show |
intron_variant | MODIFIER | c.160+182C>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 2/5 | chr9 | 34405683 | |||||||
| chr9:34406161 | C | G | 1 | a0001c0001t0001g0365 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.61-197G>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34406161 | |||||||
| chr9:34406386 | G | A | 156 | a0001c0001t0001g0059 a0001c0001t0001g0084 a0001c0001t0001g0085 others(153): Show |
163 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(160): Show |
intron_variant | MODIFIER | c.61-422C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34406386 | |||||||
| chr9:34406507 | A | C | 2 | a0001c0001t0011g0050 a0001c0001t0011g0051 |
2 | HG01891.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.61-543T>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34406507 | |||||||
| chr9:34406803 | C | CT | 83 | a0001c0001t0001g0015 a0001c0001t0001g0059 a0001c0001t0001g0083 others(80): Show |
91 | HG00099.hp1 HG00544.hp1 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.61-840dupA | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34406803 | |||||||
| chr9:34406803 | CT | C | 189 | a0001c0001t0001g0116 a0001c0001t0001g0119 a0001c0001t0001g0185 others(186): Show |
198 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(195): Show |
intron_variant | MODIFIER | c.61-840delA | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34406803 | |||||||
| chr9:34406895 | C | T | 2 | a0001c0001t0002g0232 a0001c0001t0003g0285 |
2 | HG03704.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.61-931G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34406895 | |||||||
| chr9:34407033 | C | T | 18 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0112 others(15): Show |
20 | HG00609.hp2 HG01106.hp2 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.61-1069G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34407033 | |||||||
| chr9:34407039 | G | C | 1 | a0001c0001t0001g0273 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.61-1075C>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34407039 | |||||||
| chr9:34407043 | C | T | 14 | a0001c0001t0007g0156 a0001c0001t0007g0172 a0001c0001t0007g0197 others(11): Show |
14 | HG00099.hp1 HG00741.hp1 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.61-1079G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34407043 | |||||||
| chr9:34407206 | T | C | 130 | a0001c0001t0001g0059 a0001c0001t0001g0083 a0001c0001t0001g0084 others(127): Show |
139 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(136): Show |
intron_variant | MODIFIER | c.61-1242A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34407206 | |||||||
| chr9:34407241 | A | T | 2 | a0001c0001t0001g0307 a0001c0001t0001g0308 |
2 | NA19054.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.61-1277T>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34407241 | |||||||
| chr9:34407312 | T | C | 41 | a0001c0001t0001g0345 a0001c0001t0002g0232 a0001c0001t0003g0003 others(38): Show |
48 | HG00558.hp2 HG00621.hp2 HG00673.hp1 others(45): Show |
intron_variant | MODIFIER | c.61-1348A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34407312 | |||||||
| chr9:34407333 | G | A | 130 | a0001c0001t0001g0059 a0001c0001t0001g0083 a0001c0001t0001g0084 others(127): Show |
139 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(136): Show |
intron_variant | MODIFIER | c.61-1369C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34407333 | |||||||
| chr9:34407358 | G | T | 2 | a0001c0001t0009g0145 a0001c0001t0009g0147 |
2 | HG02559.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.61-1394C>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34407358 | |||||||
| chr9:34407400 | T | C | 1 | a0001c0001t0002g0192 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.61-1436A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34407400 | |||||||
| chr9:34407425 | C | T | 82 | a0001c0001t0001g0059 a0001c0001t0001g0083 a0001c0001t0001g0084 others(79): Show |
89 | HG00099.hp1 HG00558.hp2 HG00621.hp2 others(86): Show |
intron_variant | MODIFIER | c.61-1461G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34407425 | |||||||
| chr9:34407471 | CAACTT | C | 10 | a0001c0001t0002g0150 a0001c0001t0002g0171 a0001c0001t0002g0174 others(7): Show |
10 | HG01361.hp1 HG01433.hp2 HG02071.hp1 others(7): Show |
intron_variant | MODIFIER | c.61-1512_61-1508del others(5): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34407471 | |||||||
| chr9:34407533 | G | C | 10 | a0001c0001t0002g0150 a0001c0001t0002g0171 a0001c0001t0002g0174 others(7): Show |
10 | HG01361.hp1 HG01433.hp2 HG02071.hp1 others(7): Show |
intron_variant | MODIFIER | c.61-1569C>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34407533 | |||||||
| chr9:34407548 | G | A | 1 | a0001c0001t0003g0344 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.61-1584C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34407548 | |||||||
| chr9:34407574 | G | C | 130 | a0001c0001t0001g0059 a0001c0001t0001g0083 a0001c0001t0001g0084 others(127): Show |
139 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(136): Show |
intron_variant | MODIFIER | c.61-1610C>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34407574 | |||||||
| chr9:34407992 | C | T | 8 | a0001c0001t0001g0059 a0001c0001t0001g0084 a0001c0001t0001g0085 others(5): Show |
8 | HG01175.hp2 HG01891.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.61-2028G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34407992 | |||||||
| chr9:34408052 | C | T | 1 | a0001c0001t0002g0151 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.61-2088G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34408052 | |||||||
| chr9:34408083 | T | C | 2 | a0001c0001t0001g0083 a0001c0001t0024g0104 |
2 | HG01255.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.61-2119A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34408083 | |||||||
| chr9:34408206 | T | G | 277 | a0001c0001t0001g0059 a0001c0001t0001g0083 a0001c0001t0001g0084 others(274): Show |
293 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(290): Show |
intron_variant | MODIFIER | c.61-2242A>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34408206 | |||||||
| chr9:34408387 | T | C | 1 | a0001c0001t0018g0111 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.61-2423A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34408387 | |||||||
| chr9:34408396 | A | G | 130 | a0001c0001t0001g0059 a0001c0001t0001g0083 a0001c0001t0001g0084 others(127): Show |
139 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(136): Show |
intron_variant | MODIFIER | c.61-2432T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34408396 | |||||||
| chr9:34408857 | T | G | 82 | a0001c0001t0001g0059 a0001c0001t0001g0083 a0001c0001t0001g0084 others(79): Show |
89 | HG00099.hp1 HG00558.hp2 HG00621.hp2 others(86): Show |
intron_variant | MODIFIER | c.61-2893A>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34408857 | |||||||
| chr9:34408943 | A | G | 4 | a0001c0001t0009g0144 a0001c0001t0009g0145 a0001c0001t0009g0146 others(1): Show |
4 | HG02559.hp1 HG02818.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.61-2979T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34408943 | |||||||
| chr9:34409174 | C | T | 2 | a0001c0001t0001g0083 a0001c0001t0024g0104 |
2 | HG01255.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.61-3210G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34409174 | |||||||
| chr9:34409382 | C | T | 14 | a0001c0001t0007g0156 a0001c0001t0007g0172 a0001c0001t0007g0197 others(11): Show |
14 | HG00099.hp1 HG00741.hp1 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.61-3418G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34409382 | |||||||
| chr9:34409420 | G | A | 53 | a0001c0001t0001g0059 a0001c0001t0001g0084 a0001c0001t0001g0085 others(50): Show |
60 | HG00558.hp2 HG00621.hp2 HG00673.hp1 others(57): Show |
intron_variant | MODIFIER | c.61-3456C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34409420 | |||||||
| chr9:34409861 | AG | A | 26 | a0001c0001t0002g0158 a0001c0001t0005g0004 a0001c0001t0005g0024 others(23): Show |
27 | HG00558.hp1 HG01928.hp1 HG01934.hp1 others(24): Show |
intron_variant | MODIFIER | c.61-3898delC | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34409861 | |||||||
| chr9:34409979 | C | T | 48 | a0001c0001t0004g0005 a0001c0001t0004g0009 a0001c0001t0004g0057 others(45): Show |
50 | HG00280.hp2 HG00423.hp1 HG01074.hp1 others(47): Show |
intron_variant | MODIFIER | c.61-4015G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34409979 | |||||||
| chr9:34410040 | G | C | 48 | a0001c0001t0004g0005 a0001c0001t0004g0009 a0001c0001t0004g0057 others(45): Show |
50 | HG00280.hp2 HG00423.hp1 HG01074.hp1 others(47): Show |
intron_variant | MODIFIER | c.61-4076C>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34410040 | |||||||
| chr9:34410167 | C | T | 14 | a0001c0001t0007g0156 a0001c0001t0007g0172 a0001c0001t0007g0197 others(11): Show |
14 | HG00099.hp1 HG00741.hp1 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.61-4203G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34410167 | |||||||
| chr9:34410264 | C | T | 365 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(362): Show |
393 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(390): Show |
intron_variant | MODIFIER | c.61-4300G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34410264 | |||||||
| chr9:34410302 | G | T | 4 | a0001c0001t0001g0006 a0001c0001t0001g0106 a0001c0001t0001g0108 others(1): Show |
5 | HG01243.hp1 HG02451.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.61-4338C>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34410302 | |||||||
| chr9:34410336 | G | C | 13 | a0001c0001t0001g0097 a0001c0001t0001g0099 a0001c0001t0001g0100 others(10): Show |
13 | HG01891.hp1 HG02451.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.61-4372C>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34410336 | |||||||
| chr9:34410583 | T | C | 48 | a0001c0001t0004g0005 a0001c0001t0004g0009 a0001c0001t0004g0057 others(45): Show |
50 | HG00280.hp2 HG00423.hp1 HG01074.hp1 others(47): Show |
intron_variant | MODIFIER | c.61-4619A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34410583 | |||||||
| chr9:34410853 | A | G | 1 | a0001c0001t0007g0347 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.61-4889T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34410853 | |||||||
| chr9:34410980 | T | C | 14 | a0001c0001t0007g0156 a0001c0001t0007g0172 a0001c0001t0007g0197 others(11): Show |
14 | HG00099.hp1 HG00741.hp1 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.61-5016A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34410980 | |||||||
| chr9:34411007 | G | A | 1 | a0001c0001t0007g0352 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.61-5043C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34411007 | |||||||
| chr9:34411028 | T | C | 363 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(360): Show |
391 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(388): Show |
intron_variant | MODIFIER | c.61-5064A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34411028 | |||||||
| chr9:34411114 | A | G | 20 | a0001c0001t0001g0083 a0001c0001t0007g0156 a0001c0001t0007g0172 others(17): Show |
20 | HG00099.hp1 HG00741.hp1 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.61-5150T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34411114 | |||||||
| chr9:34411231 | A | T | 1 | a0001c0001t0026g0149 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.61-5267T>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34411231 | |||||||
| chr9:34411358 | C | A | 1 | a0001c0001t0011g0051 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.61-5394G>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34411358 | |||||||
| chr9:34411359 | G | A | 1 | a0001c0001t0005g0048 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.61-5395C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34411359 | |||||||
| chr9:34411417 | C | T | 16 | a0001c0001t0001g0083 a0001c0001t0007g0156 a0001c0001t0007g0172 others(13): Show |
16 | HG00099.hp1 HG00741.hp1 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.61-5453G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34411417 | |||||||
| chr9:34411494 | A | G | 16 | a0001c0001t0001g0083 a0001c0001t0007g0156 a0001c0001t0007g0172 others(13): Show |
16 | HG00099.hp1 HG00741.hp1 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.61-5530T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34411494 | |||||||
| chr9:34411569 | C | T | 16 | a0001c0001t0001g0083 a0001c0001t0007g0156 a0001c0001t0007g0172 others(13): Show |
16 | HG00099.hp1 HG00741.hp1 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.61-5605G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34411569 | |||||||
| chr9:34411609 | G | A | 1 | a0001c0001t0001g0296 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.61-5645C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34411609 | |||||||
| chr9:34411656 | G | A | 2 | a0001c0001t0009g0145 a0001c0001t0009g0147 |
2 | HG02559.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.61-5692C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34411656 | |||||||
| chr9:34411664 | G | A | 1 | a0001c0001t0002g0199 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.61-5700C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34411664 | |||||||
| chr9:34411676 | CA | C | 146 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(143): Show |
153 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(150): Show |
intron_variant | MODIFIER | c.61-5713delT | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34411676 | |||||||
| chr9:34411688 | AAAAAAG | A | 50 | a0001c0001t0001g0059 a0001c0001t0001g0084 a0001c0001t0001g0085 others(47): Show |
57 | HG00558.hp2 HG00673.hp1 HG00735.hp2 others(54): Show |
intron_variant | MODIFIER | c.61-5730_61-5725del others(6): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34411688 | |||||||
| chr9:34411689 | AAAAAG | A | 45 | a0001c0001t0003g0127 a0001c0001t0003g0327 a0001c0001t0003g0328 others(42): Show |
47 | HG00280.hp2 HG00423.hp1 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.61-5730_61-5726del others(5): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34411689 | |||||||
| chr9:34411690 | AAAAG | A | 18 | a0001c0001t0004g0142 a0001c0001t0006g0077 a0001c0001t0006g0078 others(15): Show |
18 | HG00099.hp1 HG00741.hp1 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.61-5730_61-5727del others(4): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34411690 | |||||||
| chr9:34411803 | G | A | 14 | a0001c0001t0007g0156 a0001c0001t0007g0172 a0001c0001t0007g0197 others(11): Show |
14 | HG00099.hp1 HG00741.hp1 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.61-5839C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34411803 | |||||||
| chr9:34411848 | C | A | 8 | a0001c0001t0001g0059 a0001c0001t0001g0084 a0001c0001t0001g0085 others(5): Show |
8 | HG01175.hp2 HG01891.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.61-5884G>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34411848 | |||||||
| chr9:34411900 | T | C | 6 | a0001c0001t0001g0059 a0001c0001t0001g0084 a0001c0001t0001g0085 others(3): Show |
6 | HG01175.hp2 HG02818.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.61-5936A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34411900 | |||||||
| chr9:34412005 | A | C | 1 | a0001c0001t0001g0119 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.61-6041T>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34412005 | |||||||
| chr9:34412399 | A | G | 14 | a0001c0001t0007g0156 a0001c0001t0007g0172 a0001c0001t0007g0197 others(11): Show |
14 | HG00099.hp1 HG00741.hp1 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.61-6435T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34412399 | |||||||
| chr9:34412597 | G | A | 117 | a0001c0001t0001g0059 a0001c0001t0001g0083 a0001c0001t0001g0084 others(114): Show |
126 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.61-6633C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34412597 | |||||||
| chr9:34412602 | G | GA | 111 | a0001c0001t0001g0059 a0001c0001t0001g0084 a0001c0001t0001g0085 others(108): Show |
120 | HG00280.hp2 HG00423.hp1 HG00558.hp2 others(117): Show |
intron_variant | MODIFIER | c.61-6639dupT | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34412602 | |||||||
| chr9:34412602 | G | GAA | 144 | a0001c0001t0001g0116 a0001c0001t0001g0119 a0001c0001t0001g0185 others(141): Show |
151 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.61-6640_61-6639dup others(2): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34412602 | |||||||
| chr9:34412602 | G | GAAA | 8 | a0001c0001t0002g0129 a0001c0001t0002g0150 a0001c0001t0002g0226 others(5): Show |
8 | HG00609.hp2 HG02273.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.61-6641_61-6639dup others(3): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34412602 | |||||||
| chr9:34412608 | A | G | 2 | a0001c0001t0001g0282 a0001c0003t0001g0288 |
2 | NA18993.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.61-6644T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34412608 | |||||||
| chr9:34412733 | T | G | 1 | a0001c0001t0002g0323 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.61-6769A>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34412733 | |||||||
| chr9:34412870 | T | C | 1 | a0001c0001t0007g0350 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.61-6906A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34412870 | |||||||
| chr9:34412914 | G | C | 1 | a0001c0001t0011g0050 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.61-6950C>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34412914 | |||||||
| chr9:34412918 | G | A | 9 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(6): Show |
9 | HG01891.hp1 HG02451.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.61-6954C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34412918 | |||||||
| chr9:34413142 | A | G | 1 | a0001c0001t0017g0103 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.61-7178T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34413142 | |||||||
| chr9:34413409 | G | A | 2 | a0001c0001t0001g0083 a0001c0001t0024g0104 |
2 | HG01255.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.61-7445C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34413409 | |||||||
| chr9:34413422 | G | A | 16 | a0001c0001t0001g0083 a0001c0001t0007g0156 a0001c0001t0007g0172 others(13): Show |
16 | HG00099.hp1 HG00741.hp1 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.61-7458C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34413422 | |||||||
| chr9:34413483 | C | T | 276 | a0001c0001t0001g0059 a0001c0001t0001g0083 a0001c0001t0001g0084 others(273): Show |
292 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(289): Show |
intron_variant | MODIFIER | c.61-7519G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34413483 | |||||||
| chr9:34413511 | C | T | 1 | a0001c0001t0001g0307 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.61-7547G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34413511 | |||||||
| chr9:34413519 | G | C | 1 | a0001c0001t0002g0113 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.61-7555C>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34413519 | |||||||
| chr9:34413675 | T | C | 1 | a0001c0001t0002g0113 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.61-7711A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34413675 | |||||||
| chr9:34413745 | TTTATTTT others(7): Show |
T | 1 | a0001c0001t0002g0113 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.61-7795_61-7782del others(14): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34413745 | |||||||
| chr9:34413758 | G | C | 1 | a0001c0001t0002g0292 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.61-7794C>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34413758 | |||||||
| chr9:34413769 | G | A | 1 | a0001c0001t0003g0314 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.61-7805C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34413769 | |||||||
| chr9:34413804 | C | G | 1 | a0001c0001t0002g0260 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.61-7840G>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34413804 | |||||||
| chr9:34413838 | G | C | 2 | a0001c0001t0004g0211 a0001c0001t0004g0213 |
2 | NA18950.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.61-7874C>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34413838 | |||||||
| chr9:34413849 | A | G | 1 | a0001c0001t0002g0113 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.61-7885T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34413849 | |||||||
| chr9:34413919 | C | A | 48 | a0001c0001t0004g0005 a0001c0001t0004g0009 a0001c0001t0004g0057 others(45): Show |
50 | HG00280.hp2 HG00423.hp1 HG01074.hp1 others(47): Show |
intron_variant | MODIFIER | c.61-7955G>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34413919 | |||||||
| chr9:34413929 | A | G | 39 | a0001c0001t0004g0005 a0001c0001t0004g0009 a0001c0001t0004g0057 others(36): Show |
41 | HG00280.hp2 HG00423.hp1 HG01074.hp1 others(38): Show |
intron_variant | MODIFIER | c.61-7965T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34413929 | |||||||
| chr9:34413937 | C | T | 3 | a0001c0001t0001g0240 a0001c0001t0001g0252 a0001c0001t0001g0274 |
3 | HG01074.hp2 HG02055.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.61-7973G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34413937 | |||||||
| chr9:34414086 | C | G | 276 | a0001c0001t0001g0059 a0001c0001t0001g0083 a0001c0001t0001g0084 others(273): Show |
292 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(289): Show |
intron_variant | MODIFIER | c.61-8122G>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34414086 | |||||||
| chr9:34414291 | C | T | 2 | a0001c0001t0013g0091 a0001c0001t0013g0092 |
2 | HG03516.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.61-8327G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34414291 | |||||||
| chr9:34414341 | C | T | 146 | a0001c0001t0001g0116 a0001c0001t0001g0119 a0001c0001t0001g0185 others(143): Show |
153 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(150): Show |
intron_variant | MODIFIER | c.61-8377G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34414341 | |||||||
| chr9:34414420 | A | G | 16 | a0001c0001t0001g0083 a0001c0001t0007g0156 a0001c0001t0007g0172 others(13): Show |
16 | HG00099.hp1 HG00741.hp1 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.61-8456T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34414420 | |||||||
| chr9:34414499 | G | A | 14 | a0001c0001t0001g0015 a0001c0001t0001g0294 a0001c0001t0001g0295 others(11): Show |
15 | HG00438.hp2 HG00544.hp1 HG01993.hp2 others(12): Show |
intron_variant | MODIFIER | c.61-8535C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34414499 | |||||||
| chr9:34414543 | C | T | 1 | a0001c0001t0002g0173 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.61-8579G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34414543 | |||||||
| chr9:34414654 | G | A | 2 | a0001c0001t0001g0283 a0001c0001t0001g0284 |
2 | HG00423.hp2 HG02015.hp2 |
intron_variant | MODIFIER | c.61-8690C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34414654 | |||||||
| chr9:34414861 | A | G | 2 | a0001c0001t0002g0182 a0001c0001t0002g0215 |
2 | HG00642.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.61-8897T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34414861 | |||||||
| chr9:34415121 | AT | A | 225 | a0001c0001t0001g0083 a0001c0001t0001g0097 a0001c0001t0001g0099 others(222): Show |
240 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(237): Show |
intron_variant | MODIFIER | c.61-9158delA | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34415121 | |||||||
| chr9:34415121 | ATT | A | 21 | a0001c0001t0001g0059 a0001c0001t0001g0084 a0001c0001t0001g0085 others(18): Show |
21 | HG00099.hp1 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.61-9159_61-9158del others(2): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34415121 | |||||||
| chr9:34415224 | G | A | 16 | a0001c0001t0001g0307 a0001c0001t0001g0308 a0001c0001t0007g0156 others(13): Show |
16 | HG00099.hp1 HG00741.hp1 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.61-9260C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34415224 | |||||||
| chr9:34415650 | C | T | 146 | a0001c0001t0001g0116 a0001c0001t0001g0119 a0001c0001t0001g0185 others(143): Show |
153 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(150): Show |
intron_variant | MODIFIER | c.61-9686G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34415650 | |||||||
| chr9:34415714 | T | C | 1 | a0001c0001t0001g0255 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.61-9750A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34415714 | |||||||
| chr9:34415745 | T | G | 1 | a0001c0001t0002g0113 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.61-9781A>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34415745 | |||||||
| chr9:34415787 | G | GTAAAGTT others(33): Show |
1 | a0001c0001t0005g0024 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.61-9824_61-9823ins others(40): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34415787 | |||||||
| chr9:34415883 | G | A | 2 | a0001c0001t0002g0335 a0001c0001t0002g0336 |
2 | HG00544.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.61-9919C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34415883 | |||||||
| chr9:34416173 | G | GAAGAAGA others(3): Show |
1 | a0001c0001t0002g0238 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.61-10210_61-10209i others(12): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416173 | |||||||
| chr9:34416182 | G | A | 2 | a0001c0001t0001g0097 a0001c0001t0002g0238 |
2 | HG02572.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.61-10218C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416182 | |||||||
| chr9:34416182 | GAA | G | 3 | a0001c0001t0002g0134 a0001c0001t0002g0336 a0001c0001t0014g0269 |
3 | HG00544.hp2 HG00597.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.61-10220_61-10219d others(4): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416182 | |||||||
| chr9:34416183 | A | AAAAG | 34 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(31): Show |
34 | HG00323.hp1 HG00438.hp1 HG00621.hp2 others(31): Show |
intron_variant | MODIFIER | c.61-10223_61-10220d others(6): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416183 | |||||||
| chr9:34416183 | A | AAAAGAAA others(1): Show |
18 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0106 others(15): Show |
20 | HG01074.hp2 HG01361.hp2 HG02647.hp2 others(17): Show |
intron_variant | MODIFIER | c.61-10227_61-10220d others(10): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416183 | |||||||
| chr9:34416183 | A | AAAAGAAA others(5): Show |
11 | a0001c0001t0001g0108 a0001c0001t0001g0191 a0001c0001t0001g0261 others(8): Show |
11 | HG00673.hp2 HG02027.hp1 HG02155.hp2 others(8): Show |
intron_variant | MODIFIER | c.61-10231_61-10220d others(14): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416183 | |||||||
| chr9:34416183 | A | AAAAGAAA others(9): Show |
1 | a0001c0001t0001g0367 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.61-10235_61-10220d others(18): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416183 | |||||||
| chr9:34416183 | A | AAAAGAAA others(13): Show |
1 | a0001c0002t0001g0358 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.61-10239_61-10220d others(22): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416183 | |||||||
| chr9:34416183 | A | AGAAAGAA others(6): Show |
1 | a0001c0001t0001g0097 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.61-10220_61-10219i others(15): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416183 | |||||||
| chr9:34416183 | AAAAG | A | 18 | a0001c0001t0001g0021 a0001c0001t0001g0109 a0001c0001t0001g0193 others(15): Show |
19 | HG01070.hp1 HG01070.hp2 HG01978.hp2 others(16): Show |
intron_variant | MODIFIER | c.61-10223_61-10220d others(6): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416183 | |||||||
| chr9:34416183 | AAAAGAAA others(1): Show |
A | 12 | a0001c0001t0001g0006 a0001c0001t0001g0234 a0001c0001t0001g0244 others(9): Show |
12 | HG00099.hp1 HG00621.hp1 HG00639.hp1 others(9): Show |
intron_variant | MODIFIER | c.61-10227_61-10220d others(10): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416183 | |||||||
| chr9:34416183 | AAAAGAAA others(5): Show |
A | 13 | a0001c0001t0001g0245 a0001c0001t0001g0246 a0001c0001t0001g0275 others(10): Show |
13 | HG00438.hp2 HG01168.hp2 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.61-10231_61-10220d others(14): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416183 | |||||||
| chr9:34416183 | AAAAGAAA others(9): Show |
A | 7 | a0001c0001t0001g0015 a0001c0001t0001g0280 a0001c0001t0001g0301 others(4): Show |
8 | HG00544.hp1 HG01106.hp2 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.61-10235_61-10220d others(18): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416183 | |||||||
| chr9:34416183 | AAAAGAAA others(13): Show |
A | 5 | a0001c0001t0001g0002 a0001c0001t0001g0083 a0001c0001t0001g0297 others(2): Show |
8 | HG01255.hp2 HG02055.hp2 NA18940.hp1 others(5): Show |
intron_variant | MODIFIER | c.61-10239_61-10220d others(22): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416183 | |||||||
| chr9:34416183 | AAAAGAAA others(17): Show |
A | 1 | a0001c0001t0004g0057 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.61-10243_61-10220d others(26): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416183 | |||||||
| chr9:34416191 | G | T | 1 | a0001c0001t0001g0235 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.61-10227C>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416191 | |||||||
| chr9:34416192 | A | AAAGAAAG others(12): Show |
1 | a0001c0001t0001g0278 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.61-10247_61-10229d others(21): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416192 | |||||||
| chr9:34416195 | G | T | 1 | a0001c0001t0001g0234 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.61-10231C>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416195 | |||||||
| chr9:34416195 | GAAAGAAA others(6): Show |
G | 1 | a0001c0001t0001g0296 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.61-10244_61-10232d others(15): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416195 | |||||||
| chr9:34416205 | A | T | 11 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(8): Show |
14 | HG00323.hp2 HG00639.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.61-10241T>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416205 | |||||||
| chr9:34416212 | A | AAAGAAAG others(14): Show |
1 | a0001c0001t0002g0113 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.61-10249_61-10248i others(23): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416212 | |||||||
| chr9:34416228 | A | G | 5 | a0001c0001t0006g0077 a0001c0001t0006g0078 a0001c0001t0006g0080 others(2): Show |
5 | HG02280.hp1 HG02572.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.61-10264T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416228 | |||||||
| chr9:34416229 | A | G | 5 | a0001c0001t0006g0077 a0001c0001t0006g0078 a0001c0001t0006g0080 others(2): Show |
5 | HG02280.hp1 HG02572.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.61-10265T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416229 | |||||||
| chr9:34416230 | A | G | 5 | a0001c0001t0006g0077 a0001c0001t0006g0078 a0001c0001t0006g0080 others(2): Show |
5 | HG02280.hp1 HG02572.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.61-10266T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416230 | |||||||
| chr9:34416232 | A | G | 1 | a0001c0001t0006g0081 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.61-10268T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416232 | |||||||
| chr9:34416232 | AAAGAAAG others(21): Show |
A | 5 | a0001c0001t0006g0077 a0001c0001t0006g0078 a0001c0001t0006g0080 others(2): Show |
5 | HG02280.hp1 HG02572.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.61-10296_61-10269d others(30): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416232 | |||||||
| chr9:34416233 | A | G | 1 | a0001c0001t0006g0081 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.61-10269T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416233 | |||||||
| chr9:34416234 | A | G | 1 | a0001c0001t0006g0081 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.61-10270T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416234 | |||||||
| chr9:34416236 | A | G | 13 | a0001c0001t0003g0019 a0001c0001t0003g0310 a0001c0001t0003g0317 others(10): Show |
13 | HG01081.hp1 HG01243.hp2 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.61-10272T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416236 | |||||||
| chr9:34416236 | AAAGAAAG others(17): Show |
A | 1 | a0001c0001t0006g0081 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.61-10296_61-10273d others(26): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416236 | |||||||
| chr9:34416237 | A | G | 13 | a0001c0001t0003g0019 a0001c0001t0003g0310 a0001c0001t0003g0317 others(10): Show |
13 | HG01081.hp1 HG01243.hp2 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.61-10273T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416237 | |||||||
| chr9:34416238 | A | G | 13 | a0001c0001t0003g0019 a0001c0001t0003g0310 a0001c0001t0003g0317 others(10): Show |
13 | HG01081.hp1 HG01243.hp2 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.61-10274T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416238 | |||||||
| chr9:34416240 | A | G | 13 | a0001c0001t0002g0121 a0001c0001t0003g0019 a0001c0001t0003g0309 others(10): Show |
14 | HG01074.hp1 HG01099.hp1 HG01175.hp1 others(11): Show |
intron_variant | MODIFIER | c.61-10276T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416240 | |||||||
| chr9:34416240 | AAAGAAAG others(13): Show |
A | 10 | a0001c0001t0004g0009 a0001c0001t0004g0064 a0001c0001t0004g0065 others(7): Show |
10 | HG01081.hp1 HG01243.hp2 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.61-10296_61-10277d others(22): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416240 | |||||||
| chr9:34416241 | A | G | 15 | a0001c0001t0002g0121 a0001c0001t0003g0019 a0001c0001t0003g0309 others(12): Show |
17 | HG01074.hp1 HG01099.hp1 HG01175.hp1 others(14): Show |
intron_variant | MODIFIER | c.61-10277T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416241 | |||||||
| chr9:34416242 | A | G | 15 | a0001c0001t0002g0121 a0001c0001t0003g0019 a0001c0001t0003g0309 others(12): Show |
17 | HG01074.hp1 HG01099.hp1 HG01175.hp1 others(14): Show |
intron_variant | MODIFIER | c.61-10278T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416242 | |||||||
| chr9:34416244 | A | G | 35 | a0001c0001t0002g0007 a0001c0001t0002g0011 a0001c0001t0002g0125 others(32): Show |
37 | HG00558.hp1 HG01123.hp1 HG01168.hp1 others(34): Show |
intron_variant | MODIFIER | c.61-10280T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416244 | |||||||
| chr9:34416244 | AAAGAAAG others(9): Show |
A | 7 | a0001c0001t0002g0121 a0001c0001t0004g0005 a0001c0001t0004g0058 others(4): Show |
8 | HG01074.hp1 HG01099.hp1 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.61-10296_61-10281d others(18): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416244 | |||||||
| chr9:34416245 | A | G | 44 | a0001c0001t0002g0007 a0001c0001t0002g0011 a0001c0001t0002g0125 others(41): Show |
47 | HG00558.hp1 HG01123.hp1 HG01168.hp1 others(44): Show |
intron_variant | MODIFIER | c.61-10281T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416245 | |||||||
| chr9:34416246 | A | AGG | 5 | a0001c0001t0003g0017 a0001c0001t0003g0018 a0001c0001t0003g0338 others(2): Show |
6 | HG00673.hp1 HG02165.hp1 HG04184.hp2 others(3): Show |
intron_variant | MODIFIER | c.61-10283_61-10282i others(4): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416246 | |||||||
| chr9:34416246 | A | G | 44 | a0001c0001t0002g0007 a0001c0001t0002g0011 a0001c0001t0002g0125 others(41): Show |
47 | HG00558.hp1 HG01123.hp1 HG01168.hp1 others(44): Show |
intron_variant | MODIFIER | c.61-10282T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416246 | |||||||
| chr9:34416248 | A | G | 42 | a0001c0001t0001g0084 a0001c0001t0001g0088 a0001c0001t0001g0185 others(39): Show |
44 | HG00423.hp1 HG00609.hp2 HG00642.hp2 others(41): Show |
intron_variant | MODIFIER | c.61-10284T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416248 | |||||||
| chr9:34416248 | AAAGAAAG others(5): Show |
A | 13 | a0001c0001t0002g0007 a0001c0001t0002g0125 a0001c0001t0002g0130 others(10): Show |
13 | HG01123.hp1 HG01258.hp2 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.61-10296_61-10285d others(14): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416248 | |||||||
| chr9:34416249 | A | G | 72 | a0001c0001t0001g0084 a0001c0001t0001g0088 a0001c0001t0001g0185 others(69): Show |
80 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(77): Show |
intron_variant | MODIFIER | c.61-10285T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416249 | |||||||
| chr9:34416250 | A | AGGGG | 11 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0267 others(8): Show |
11 | HG01109.hp1 HG01433.hp1 HG02293.hp2 others(8): Show |
intron_variant | MODIFIER | c.61-10287_61-10286i others(6): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416250 | |||||||
| chr9:34416250 | A | AGGGGGAG others(5): Show |
1 | a0001c0001t0003g0107 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.61-10287_61-10286i others(14): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416250 | |||||||
| chr9:34416250 | A | G | 67 | a0001c0001t0001g0084 a0001c0001t0001g0088 a0001c0001t0001g0185 others(64): Show |
74 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(71): Show |
intron_variant | MODIFIER | c.61-10286T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416250 | |||||||
| chr9:34416252 | A | AAAGAAAG others(3): Show |
1 | a0001c0001t0001g0251 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.61-10289_61-10288i others(12): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416252 | |||||||
| chr9:34416252 | A | G | 34 | a0001c0001t0001g0059 a0001c0001t0001g0085 a0001c0001t0001g0086 others(31): Show |
38 | HG00323.hp2 HG00558.hp2 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.61-10288T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416252 | |||||||
| chr9:34416252 | AAAGAAAG others(1): Show |
A | 27 | a0001c0001t0002g0011 a0001c0001t0002g0123 a0001c0001t0002g0128 others(24): Show |
27 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(24): Show |
intron_variant | MODIFIER | c.61-10296_61-10289d others(10): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416252 | |||||||
| chr9:34416253 | A | G | 88 | a0001c0001t0001g0059 a0001c0001t0001g0084 a0001c0001t0001g0085 others(85): Show |
96 | HG00323.hp2 HG00558.hp2 HG00639.hp2 others(93): Show |
intron_variant | MODIFIER | c.61-10289T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416253 | |||||||
| chr9:34416254 | A | AGGGG | 10 | a0001c0001t0001g0116 a0001c0001t0001g0217 a0001c0001t0001g0230 others(7): Show |
10 | HG01109.hp2 HG02622.hp1 HG02970.hp1 others(7): Show |
intron_variant | MODIFIER | c.61-10291_61-10290i others(6): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416254 | |||||||
| chr9:34416254 | A | G | 83 | a0001c0001t0001g0059 a0001c0001t0001g0084 a0001c0001t0001g0085 others(80): Show |
89 | HG00323.hp2 HG00558.hp2 HG00639.hp2 others(86): Show |
intron_variant | MODIFIER | c.61-10290T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416254 | |||||||
| chr9:34416256 | A | AAAGAAAG others(8): Show |
1 | a0001c0002t0001g0196 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.61-10293_61-10292i others(17): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416256 | |||||||
| chr9:34416256 | A | G | 22 | a0001c0001t0001g0254 a0001c0001t0002g0126 a0001c0001t0002g0136 others(19): Show |
24 | HG00673.hp1 HG01346.hp1 HG01975.hp1 others(21): Show |
intron_variant | MODIFIER | c.61-10292T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416256 | |||||||
| chr9:34416256 | AAAGG | A | 36 | a0001c0001t0001g0084 a0001c0001t0001g0088 a0001c0001t0001g0185 others(33): Show |
40 | HG01081.hp2 HG01106.hp1 HG01169.hp2 others(37): Show |
intron_variant | MODIFIER | c.61-10296_61-10293d others(6): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416256 | |||||||
| chr9:34416257 | A | AAGAAAGA others(3): Show |
1 | a0001c0001t0002g0170 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.61-10294_61-10293i others(12): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416257 | |||||||
| chr9:34416257 | A | G | 73 | a0001c0001t0001g0059 a0001c0001t0001g0085 a0001c0001t0001g0086 others(70): Show |
76 | HG00323.hp2 HG00558.hp2 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.61-10293T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416257 | |||||||
| chr9:34416257 | AAGGG | A | 3 | a0001c0001t0003g0019 a0001c0001t0003g0312 a0001c0001t0003g0321 |
3 | NA18983.hp1 NA18988.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.61-10297_61-10294d others(6): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416257 | |||||||
| chr9:34416258 | A | AGAAAGAA others(13): Show |
1 | a0001c0001t0011g0050 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.61-10295_61-10294i others(22): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416258 | |||||||
| chr9:34416258 | A | G | 73 | a0001c0001t0001g0059 a0001c0001t0001g0085 a0001c0001t0001g0086 others(70): Show |
74 | HG00323.hp2 HG00558.hp2 HG00639.hp2 others(71): Show |
intron_variant | MODIFIER | c.61-10294T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416258 | |||||||
| chr9:34416260 | G | A | 78 | a0001c0001t0001g0059 a0001c0001t0001g0085 a0001c0001t0001g0086 others(75): Show |
79 | HG00323.hp2 HG00558.hp2 HG00639.hp2 others(76): Show |
intron_variant | MODIFIER | c.61-10296C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416260 | |||||||
| chr9:34416261 | G | A | 12 | a0001c0001t0001g0315 a0001c0001t0003g0107 a0001c0001t0003g0313 others(9): Show |
12 | HG01123.hp2 HG02027.hp2 HG02040.hp2 others(9): Show |
intron_variant | MODIFIER | c.61-10297C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416261 | |||||||
| chr9:34416261 | G | GAA | 5 | a0001c0001t0003g0017 a0001c0001t0003g0018 a0001c0001t0003g0338 others(2): Show |
7 | HG00673.hp1 HG02165.hp1 HG04184.hp2 others(4): Show |
intron_variant | MODIFIER | c.61-10298_61-10297i others(4): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416261 | |||||||
| chr9:34416262 | G | A | 4 | a0001c0001t0001g0315 a0001c0001t0007g0156 a0001c0001t0007g0223 others(1): Show |
4 | HG01123.hp2 HG02040.hp2 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.61-10298C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416262 | |||||||
| chr9:34416264 | A | G | 2 | a0001c0001t0001g0315 a0001c0001t0007g0351 |
2 | HG01123.hp2 HG02040.hp2 |
intron_variant | MODIFIER | c.61-10300T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416264 | |||||||
| chr9:34416265 | G | A | 45 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0267 others(42): Show |
51 | HG00642.hp2 HG00673.hp1 HG01109.hp1 others(48): Show |
intron_variant | MODIFIER | c.61-10301C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416265 | |||||||
| chr9:34416265 | G | GGGAAGGA others(1): Show |
6 | a0001c0001t0001g0345 a0001c0001t0003g0329 a0001c0001t0003g0332 others(3): Show |
6 | HG00558.hp2 HG02630.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.61-10302_61-10301i others(10): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416265 | |||||||
| chr9:34416266 | G | A | 2 | a0001c0001t0007g0156 a0001c0001t0007g0223 |
2 | HG02300.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.61-10302C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416266 | |||||||
| chr9:34416268 | A | G | 1 | a0001c0001t0007g0156 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.61-10304T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416268 | |||||||
| chr9:34416269 | G | A | 99 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0116 others(96): Show |
109 | HG00323.hp2 HG00558.hp1 HG00558.hp2 others(106): Show |
intron_variant | MODIFIER | c.61-10305C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416269 | |||||||
| chr9:34416269 | G | GGGAAGGA others(1): Show |
5 | a0001c0001t0002g0136 a0001c0001t0002g0178 a0001c0001t0002g0209 others(2): Show |
5 | HG02129.hp2 HG02602.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.61-10306_61-10305i others(10): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416269 | |||||||
| chr9:34416269 | G | GGGAAGGA others(5): Show |
7 | a0001c0001t0002g0183 a0001c0001t0002g0203 a0001c0001t0002g0206 others(4): Show |
7 | HG01975.hp1 HG02132.hp2 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.61-10306_61-10305i others(14): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416269 | |||||||
| chr9:34416269 | G | GGGAAGGA others(9): Show |
1 | a0001c0001t0002g0173 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.61-10306_61-10305i others(18): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416269 | |||||||
| chr9:34416270 | G | A | 1 | a0001c0001t0007g0223 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.61-10306C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416270 | |||||||
| chr9:34416272 | A | G | 1 | a0001c0001t0007g0223 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.61-10308T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416272 | |||||||
| chr9:34416273 | G | A | 174 | a0001c0001t0001g0059 a0001c0001t0001g0084 a0001c0001t0001g0085 others(171): Show |
188 | HG00323.hp2 HG00423.hp1 HG00558.hp1 others(185): Show |
intron_variant | MODIFIER | c.61-10309C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416273 | |||||||
| chr9:34416273 | G | GGGAA | 11 | a0001c0001t0001g0253 a0001c0001t0002g0132 a0001c0001t0002g0184 others(8): Show |
11 | HG01496.hp2 HG02109.hp2 HG02683.hp2 others(8): Show |
intron_variant | MODIFIER | c.61-10313_61-10310d others(6): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416273 | |||||||
| chr9:34416273 | G | GGGAAGGA others(1): Show |
22 | a0001c0001t0001g0119 a0001c0001t0001g0191 a0001c0001t0001g0218 others(19): Show |
22 | HG00323.hp1 HG00438.hp1 HG02559.hp2 others(19): Show |
intron_variant | MODIFIER | c.61-10317_61-10310d others(10): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416273 | |||||||
| chr9:34416273 | G | GGGAAGGA others(5): Show |
25 | a0001c0001t0001g0097 a0001c0001t0001g0099 a0001c0001t0001g0237 others(22): Show |
25 | HG00099.hp2 HG00544.hp2 HG00597.hp2 others(22): Show |
intron_variant | MODIFIER | c.61-10321_61-10310d others(14): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416273 | |||||||
| chr9:34416273 | G | GGGAAGGA others(9): Show |
9 | a0001c0001t0002g0205 a0001c0001t0002g0221 a0001c0001t0002g0356 others(6): Show |
10 | HG00735.hp2 HG01433.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.61-10325_61-10310d others(18): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416273 | |||||||
| chr9:34416273 | G | GGGAAGGA others(13): Show |
7 | a0001c0001t0002g0165 a0001c0001t0002g0169 a0001c0001t0002g0216 others(4): Show |
7 | HG01496.hp1 NA18955.hp1 NA18982.hp2 others(4): Show |
intron_variant | MODIFIER | c.61-10329_61-10310d others(22): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416273 | |||||||
| chr9:34416273 | G | GGGAGGGA others(9): Show |
1 | a0001c0001t0002g0133 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.61-10310_61-10309i others(18): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416273 | |||||||
| chr9:34416273 | GGGAA | G | 15 | a0001c0001t0001g0015 a0001c0001t0001g0294 a0001c0001t0001g0295 others(12): Show |
16 | HG00438.hp2 HG00544.hp1 HG01993.hp2 others(13): Show |
intron_variant | MODIFIER | c.61-10313_61-10310d others(6): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416273 | |||||||
| chr9:34416273 | GGGAAGGA others(1): Show |
G | 3 | a0001c0001t0009g0144 a0001c0001t0009g0146 a0001c0001t0017g0103 |
3 | HG02451.hp2 HG03579.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.61-10317_61-10310d others(10): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416273 | |||||||
| chr9:34416273 | GGGAAGGA others(9): Show |
G | 2 | a0001c0001t0001g0083 a0001c0001t0024g0104 |
2 | HG01255.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.61-10325_61-10310d others(18): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416273 | |||||||
| chr9:34416277 | A | G | 4 | a0001c0001t0001g0315 a0001c0001t0007g0156 a0001c0001t0007g0223 others(1): Show |
4 | HG01123.hp2 HG02040.hp2 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.61-10313T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416277 | |||||||
| chr9:34416281 | A | G | 2 | a0001c0001t0007g0156 a0001c0001t0007g0223 |
2 | HG02300.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.61-10317T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416281 | |||||||
| chr9:34416285 | A | G | 1 | a0001c0001t0007g0223 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.61-10321T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416285 | |||||||
| chr9:34416298 | GGAAGGAA others(5): Show |
G | 11 | a0001c0001t0007g0172 a0001c0001t0007g0197 a0001c0001t0007g0202 others(8): Show |
11 | HG00099.hp1 HG00741.hp1 HG00741.hp2 others(8): Show |
intron_variant | MODIFIER | c.61-10346_61-10335d others(14): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416298 | |||||||
| chr9:34416310 | C | G | 2 | a0001c0001t0002g0122 a0001c0001t0007g0223 |
2 | HG02970.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.61-10346G>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416310 | |||||||
| chr9:34416311 | G | A | 8 | a0001c0001t0001g0059 a0001c0001t0001g0084 a0001c0001t0001g0085 others(5): Show |
8 | HG01175.hp2 HG01891.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.61-10347C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416311 | |||||||
| chr9:34416314 | G | C | 13 | a0001c0001t0007g0172 a0001c0001t0007g0197 a0001c0001t0007g0202 others(10): Show |
13 | HG00099.hp1 HG00741.hp1 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.61-10350C>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416314 | |||||||
| chr9:34416322 | G | A | 1 | a0001c0001t0003g0321 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.61-10358C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416322 | |||||||
| chr9:34416543 | C | T | 8 | a0001c0001t0001g0059 a0001c0001t0001g0084 a0001c0001t0001g0085 others(5): Show |
8 | HG01175.hp2 HG01891.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.61-10579G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416543 | |||||||
| chr9:34416737 | C | CA | 62 | a0001c0001t0001g0083 a0001c0001t0001g0218 a0001c0001t0004g0005 others(59): Show |
64 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.61-10774dupT | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416737 | |||||||
| chr9:34416756 | T | TA | 276 | a0001c0001t0001g0059 a0001c0001t0001g0083 a0001c0001t0001g0084 others(273): Show |
292 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(289): Show |
intron_variant | MODIFIER | c.61-10793_61-10792i others(3): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416756 | |||||||
| chr9:34416808 | A | AT | 16 | a0001c0001t0001g0006 a0001c0001t0001g0106 a0001c0001t0001g0108 others(13): Show |
17 | HG01099.hp2 HG01243.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.61-10845dupA | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416808 | |||||||
| chr9:34416808 | A | ATG | 121 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(118): Show |
128 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.61-10845_61-10844i others(4): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416808 | |||||||
| chr9:34416808 | A | ATGT | 53 | a0001c0001t0001g0097 a0001c0001t0001g0116 a0001c0001t0001g0188 others(50): Show |
59 | HG00558.hp2 HG00597.hp2 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.61-10845_61-10844i others(5): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416808 | |||||||
| chr9:34416808 | A | ATGTT | 18 | a0001c0001t0001g0059 a0001c0001t0001g0085 a0001c0001t0001g0086 others(15): Show |
19 | HG01175.hp2 HG01433.hp1 HG01496.hp1 others(16): Show |
intron_variant | MODIFIER | c.61-10845_61-10844i others(6): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416808 | |||||||
| chr9:34416808 | A | ATGTTT | 40 | a0001c0001t0001g0084 a0001c0001t0004g0005 a0001c0001t0004g0009 others(37): Show |
42 | HG00280.hp2 HG00423.hp1 HG01081.hp1 others(39): Show |
intron_variant | MODIFIER | c.61-10845_61-10844i others(7): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416808 | |||||||
| chr9:34416808 | A | ATGTTTT | 10 | a0001c0001t0004g0058 a0001c0001t0004g0062 a0001c0001t0004g0067 others(7): Show |
10 | HG01074.hp1 HG01175.hp1 HG01934.hp2 others(7): Show |
intron_variant | MODIFIER | c.61-10845_61-10844i others(8): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416808 | |||||||
| chr9:34416808 | AT | A | 12 | a0001c0001t0001g0014 a0001c0001t0001g0233 a0001c0001t0001g0234 others(9): Show |
13 | HG00280.hp1 HG02155.hp1 HG02735.hp1 others(10): Show |
intron_variant | MODIFIER | c.61-10845delA | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416808 | |||||||
| chr9:34416809 | T | TG | 12 | a0001c0001t0002g0131 a0001c0001t0002g0138 a0001c0001t0002g0165 others(9): Show |
12 | HG01891.hp1 HG02630.hp1 HG03540.hp1 others(9): Show |
intron_variant | MODIFIER | c.61-10846_61-10845i others(3): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416809 | |||||||
| chr9:34416809 | T | TGTTC | 14 | a0001c0001t0001g0083 a0001c0001t0007g0156 a0001c0001t0007g0172 others(11): Show |
14 | HG00099.hp1 HG00741.hp2 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.61-10846_61-10845i others(6): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416809 | |||||||
| chr9:34416810 | T | C | 1 | a0001c0001t0007g0348 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.61-10846A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416810 | |||||||
| chr9:34416813 | T | G | 1 | a0001c0001t0002g0183 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.61-10849A>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416813 | |||||||
| chr9:34416831 | A | T | 1 | a0001c0001t0004g0142 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.61-10867T>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416831 | |||||||
| chr9:34416865 | G | A | 2 | a0001c0001t0001g0254 a0001c0001t0001g0255 |
2 | HG02280.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.61-10901C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416865 | |||||||
| chr9:34416916 | C | T | 1 | a0001c0001t0006g0118 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.61-10952G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416916 | |||||||
| chr9:34416961 | G | A | 2 | a0001c0001t0001g0083 a0001c0001t0024g0104 |
2 | HG01255.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.61-10997C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416961 | |||||||
| chr9:34417000 | CTCCTTCT | C | 3 | a0001c0001t0001g0083 a0001c0001t0005g0027 a0001c0001t0024g0104 |
3 | HG01255.hp2 HG02055.hp2 NA18941.hp1 |
intron_variant | MODIFIER | c.61-11043_61-11037d others(9): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34417000 | |||||||
| chr9:34417070 | CCTT | C | 16 | a0001c0001t0001g0083 a0001c0001t0007g0156 a0001c0001t0007g0172 others(13): Show |
16 | HG00099.hp1 HG00741.hp1 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.61-11109_61-11107d others(5): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34417070 | |||||||
| chr9:34417197 | C | T | 1 | a0001c0001t0002g0157 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.61-11233G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34417197 | |||||||
| chr9:34417367 | T | C | 2 | a0001c0001t0002g0232 a0001c0001t0003g0285 |
2 | HG03704.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.61-11403A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34417367 | |||||||
| chr9:34417445 | A | C | 1 | a0001c0001t0002g0113 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.61-11481T>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34417445 | |||||||
| chr9:34417597 | C | T | 48 | a0001c0001t0004g0005 a0001c0001t0004g0009 a0001c0001t0004g0057 others(45): Show |
50 | HG00280.hp2 HG00423.hp1 HG01074.hp1 others(47): Show |
intron_variant | MODIFIER | c.61-11633G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34417597 | |||||||
| chr9:34417752 | C | T | 6 | a0001c0001t0007g0156 a0001c0001t0007g0172 a0001c0001t0007g0197 others(3): Show |
6 | HG00741.hp2 HG01070.hp1 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.61-11788G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34417752 | |||||||
| chr9:34417875 | T | G | 16 | a0001c0001t0001g0083 a0001c0001t0007g0156 a0001c0001t0007g0172 others(13): Show |
16 | HG00099.hp1 HG00741.hp1 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.61-11911A>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34417875 | |||||||
| chr9:34417918 | A | G | 276 | a0001c0001t0001g0059 a0001c0001t0001g0083 a0001c0001t0001g0084 others(273): Show |
292 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(289): Show |
intron_variant | MODIFIER | c.61-11954T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34417918 | |||||||
| chr9:34418200 | T | TA | 10 | a0001c0001t0001g0270 a0001c0001t0002g0055 a0001c0001t0002g0113 others(7): Show |
10 | HG01346.hp2 HG01358.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.61-12237dupT | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34418200 | |||||||
| chr9:34418268 | G | T | 1 | a0001c0001t0002g0194 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.61-12304C>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34418268 | |||||||
| chr9:34418460 | G | C | 1 | a0001c0001t0001g0185 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.61-12496C>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34418460 | |||||||
| chr9:34418554 | C | G | 1 | a0001c0001t0003g0328 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.61-12590G>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34418554 | |||||||
| chr9:34418690 | C | A | 1 | a0001c0001t0003g0309 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.61-12726G>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34418690 | |||||||
| chr9:34418712 | A | C | 1 | a0001c0001t0003g0342 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.61-12748T>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34418712 | |||||||
| chr9:34418776 | A | G | 1 | a0001c0001t0001g0281 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.61-12812T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34418776 | |||||||
| chr9:34418957 | C | T | 45 | a0001c0001t0004g0005 a0001c0001t0004g0009 a0001c0001t0004g0057 others(42): Show |
47 | HG00280.hp2 HG00423.hp1 HG01074.hp1 others(44): Show |
intron_variant | MODIFIER | c.61-12993G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34418957 | |||||||
| chr9:34419073 | T | TCAAA | 15 | a0001c0001t0001g0188 a0001c0001t0001g0304 a0001c0001t0001g0306 others(12): Show |
15 | HG00642.hp1 HG01109.hp1 HG01981.hp1 others(12): Show |
intron_variant | MODIFIER | c.61-13113_61-13110d others(6): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34419073 | |||||||
| chr9:34419073 | TCAAA | T | 14 | a0001c0001t0001g0059 a0001c0001t0001g0083 a0001c0001t0001g0084 others(11): Show |
14 | HG00741.hp2 HG01175.hp2 HG01255.hp2 others(11): Show |
intron_variant | MODIFIER | c.61-13113_61-13110d others(6): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34419073 | |||||||
| chr9:34419166 | T | A | 55 | a0001c0001t0001g0021 a0001c0001t0001g0097 a0001c0001t0001g0345 others(52): Show |
62 | HG00099.hp1 HG00558.hp2 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.61-13202A>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34419166 | |||||||
| chr9:34419167 | A | T | 21 | a0001c0001t0001g0059 a0001c0001t0001g0084 a0001c0001t0001g0085 others(18): Show |
24 | HG00323.hp2 HG00639.hp2 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.61-13203T>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34419167 | |||||||
| chr9:34419191 | G | A | 2 | a0001c0001t0001g0083 a0001c0001t0024g0104 |
2 | HG01255.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.61-13227C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34419191 | |||||||
| chr9:34419297 | T | C | 7 | a0001c0001t0002g0165 a0001c0001t0002g0169 a0001c0001t0002g0216 others(4): Show |
7 | NA18747.hp1 NA18955.hp1 NA18982.hp2 others(4): Show |
intron_variant | MODIFIER | c.61-13333A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34419297 | |||||||
| chr9:34419354 | G | A | 1 | a0001c0001t0001g0250 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.61-13390C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34419354 | |||||||
| chr9:34419583 | T | C | 16 | a0001c0001t0001g0083 a0001c0001t0007g0156 a0001c0001t0007g0172 others(13): Show |
16 | HG00099.hp1 HG00741.hp1 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.61-13619A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34419583 | |||||||
| chr9:34419626 | C | G | 3 | a0001c0001t0001g0014 a0001c0001t0001g0272 a0001c0001t0001g0290 |
4 | NA18960.hp1 NA18975.hp2 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.61-13662G>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34419626 | |||||||
| chr9:34419754 | G | C | 16 | a0001c0001t0001g0083 a0001c0001t0007g0156 a0001c0001t0007g0172 others(13): Show |
16 | HG00099.hp1 HG00741.hp1 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.61-13790C>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34419754 | |||||||
| chr9:34419935 | C | A | 1 | a0001c0001t0017g0103 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.61-13971G>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34419935 | |||||||
| chr9:34420023 | A | G | 1 | a0001c0001t0002g0151 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.61-14059T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34420023 | |||||||
| chr9:34420046 | C | A | 1 | a0001c0001t0002g0178 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.61-14082G>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34420046 | |||||||
| chr9:34420289 | T | C | 19 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(16): Show |
22 | HG00323.hp2 HG00639.hp2 HG00642.hp1 others(19): Show |
intron_variant | MODIFIER | c.61-14325A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34420289 | |||||||
| chr9:34420323 | G | A | 8 | a0001c0001t0001g0059 a0001c0001t0001g0084 a0001c0001t0001g0085 others(5): Show |
8 | HG01175.hp2 HG01891.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.61-14359C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34420323 | |||||||
| chr9:34420415 | G | A | 41 | a0001c0001t0001g0345 a0001c0001t0002g0232 a0001c0001t0003g0003 others(38): Show |
48 | HG00558.hp2 HG00621.hp2 HG00673.hp1 others(45): Show |
intron_variant | MODIFIER | c.61-14451C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34420415 | |||||||
| chr9:34420480 | G | A | 1 | a0001c0001t0001g0217 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.61-14516C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34420480 | |||||||
| chr9:34420690 | A | G | 2 | a0001c0001t0001g0245 a0001c0001t0001g0246 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.61-14726T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34420690 | |||||||
| chr9:34420796 | G | A | 14 | a0001c0001t0007g0156 a0001c0001t0007g0172 a0001c0001t0007g0197 others(11): Show |
14 | HG00099.hp1 HG00741.hp1 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.61-14832C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34420796 | |||||||
| chr9:34420808 | C | G | 1 | a0001c0001t0004g0160 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.61-14844G>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34420808 | |||||||
| chr9:34420821 | A | G | 1 | a0001c0001t0001g0230 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.61-14857T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34420821 | |||||||
| chr9:34420973 | C | CGT | 4 | a0001c0001t0001g0099 a0001c0001t0001g0240 a0001c0001t0002g0020 others(1): Show |
5 | HG02273.hp2 HG02300.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.61-15011_61-15010d others(4): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34420973 | |||||||
| chr9:34420974 | G | A | 1 | a0001c0001t0002g0129 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.61-15010C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34420974 | |||||||
| chr9:34420986 | G | A | 8 | a0001c0001t0001g0059 a0001c0001t0001g0084 a0001c0001t0001g0085 others(5): Show |
8 | HG01175.hp2 HG01891.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.61-15022C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34420986 | |||||||
| chr9:34420992 | A | C | 14 | a0001c0001t0007g0156 a0001c0001t0007g0172 a0001c0001t0007g0197 others(11): Show |
14 | HG00099.hp1 HG00741.hp1 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.61-15028T>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34420992 | |||||||
| chr9:34420992 | A | G | 23 | a0001c0001t0001g0059 a0001c0001t0001g0084 a0001c0001t0001g0085 others(20): Show |
23 | HG01074.hp2 HG01175.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.61-15028T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34420992 | |||||||
| chr9:34420994 | G | A | 12 | a0001c0001t0001g0097 a0001c0001t0001g0100 a0001c0001t0001g0101 others(9): Show |
12 | HG01891.hp1 HG02451.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.61-15030C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34420994 | |||||||
| chr9:34421001 | T | TGAGAGAG others(7): Show |
1 | a0001c0001t0011g0050 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.61-15038_61-15037i others(16): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34421001 | |||||||
| chr9:34421003 | T | A | 3 | a0001c0001t0001g0099 a0001c0001t0011g0050 a0001c0001t0011g0051 |
3 | HG01891.hp2 HG02622.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.61-15039A>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34421003 | |||||||
| chr9:34421003 | T | TGAGAGAG others(1): Show |
6 | a0001c0001t0001g0059 a0001c0001t0001g0084 a0001c0001t0001g0085 others(3): Show |
6 | HG01175.hp2 HG02896.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.61-15040_61-15039i others(10): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34421003 | |||||||
| chr9:34421003 | T | TGAGAGAG others(3): Show |
4 | a0001c0001t0001g0086 a0001c0001t0001g0094 a0001c0001t0010g0090 others(1): Show |
4 | HG01891.hp1 HG02818.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.61-15040_61-15039i others(12): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34421003 | |||||||
| chr9:34421003 | T | TGAGAGAG others(7): Show |
1 | a0001c0001t0001g0100 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.61-15040_61-15039i others(16): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34421003 | |||||||
| chr9:34421005 | T | A | 14 | a0001c0001t0001g0059 a0001c0001t0001g0084 a0001c0001t0001g0085 others(11): Show |
14 | HG01175.hp2 HG01891.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.61-15041A>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34421005 | |||||||
| chr9:34421005 | T | TGAGAGAG others(9): Show |
1 | a0001c0001t0002g0122 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.61-15042_61-15041i others(18): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34421005 | |||||||
| chr9:34421005 | T | TGAGAGAG others(11): Show |
1 | a0001c0001t0002g0132 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.61-15042_61-15041i others(20): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34421005 | |||||||
| chr9:34421007 | T | A | 18 | a0001c0001t0001g0059 a0001c0001t0001g0084 a0001c0001t0001g0085 others(15): Show |
18 | HG01175.hp2 HG01891.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.61-15043A>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34421007 | |||||||
| chr9:34421007 | T | TGAGA | 17 | a0001c0001t0002g0343 a0001c0001t0003g0003 a0001c0001t0003g0016 others(14): Show |
23 | HG00558.hp2 HG00621.hp2 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.61-15044_61-15043i others(6): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34421007 | |||||||
| chr9:34421007 | T | TGAGAGA | 13 | a0001c0001t0001g0267 a0001c0001t0003g0019 a0001c0001t0003g0309 others(10): Show |
14 | HG02559.hp1 HG03041.hp2 HG04184.hp2 others(11): Show |
intron_variant | MODIFIER | c.61-15044_61-15043i others(8): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34421007 | |||||||
| chr9:34421007 | T | TGAGAGAG others(1): Show |
7 | a0001c0001t0003g0311 a0001c0001t0003g0320 a0001c0001t0003g0321 others(4): Show |
7 | HG03516.hp2 NA18939.hp2 NA18950.hp2 others(4): Show |
intron_variant | MODIFIER | c.61-15044_61-15043i others(10): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34421007 | |||||||
| chr9:34421007 | T | TGAGAGAG others(3): Show |
13 | a0001c0001t0002g0079 a0001c0001t0002g0121 a0001c0001t0002g0133 others(10): Show |
13 | HG00642.hp1 HG02559.hp2 HG02965.hp2 others(10): Show |
intron_variant | MODIFIER | c.61-15044_61-15043i others(12): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34421007 | |||||||
| chr9:34421007 | T | TGAGAGAG others(5): Show |
22 | a0001c0001t0002g0007 a0001c0001t0002g0011 a0001c0001t0002g0112 others(19): Show |
24 | HG00323.hp2 HG00558.hp1 HG00609.hp2 others(21): Show |
intron_variant | MODIFIER | c.61-15044_61-15043i others(14): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34421007 | |||||||
| chr9:34421007 | T | TGAGAGAG others(7): Show |
12 | a0001c0001t0002g0125 a0001c0001t0002g0126 a0001c0001t0002g0130 others(9): Show |
12 | HG01081.hp2 HG01106.hp2 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.61-15044_61-15043i others(16): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34421007 | |||||||
| chr9:34421007 | T | TGAGAGAG others(9): Show |
14 | a0001c0001t0002g0008 a0001c0001t0002g0012 a0001c0001t0002g0138 others(11): Show |
17 | HG01255.hp1 HG01346.hp2 HG01928.hp1 others(14): Show |
intron_variant | MODIFIER | c.61-15044_61-15043i others(18): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34421007 | |||||||
| chr9:34421007 | T | TGAGAGAG others(11): Show |
6 | a0001c0001t0002g0010 a0001c0001t0002g0013 a0001c0001t0002g0141 others(3): Show |
8 | HG00639.hp2 HG00735.hp1 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.61-15044_61-15043i others(20): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34421007 | |||||||
| chr9:34421007 | T | TGAGAGAG others(13): Show |
5 | a0001c0001t0002g0096 a0001c0001t0002g0120 a0001c0001t0002g0201 others(2): Show |
5 | HG01981.hp1 HG03195.hp2 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.61-15044_61-15043i others(22): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34421007 | |||||||
| chr9:34421007 | T | TGAGAGAG others(15): Show |
2 | a0001c0001t0002g0087 a0001c0001t0002g0227 |
2 | HG03139.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.61-15044_61-15043i others(24): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34421007 | |||||||
| chr9:34421007 | T | TGAGAGAG others(19): Show |
1 | a0001c0001t0002g0208 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.61-15044_61-15043i others(28): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34421007 | |||||||
| chr9:34421007 | TGTGAGAG others(3): Show |
T | 1 | a0001c0001t0003g0326 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.61-15053_61-15044d others(12): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34421007 | |||||||
| chr9:34421009 | T | A | 139 | a0001c0001t0001g0059 a0001c0001t0001g0084 a0001c0001t0001g0085 others(136): Show |
153 | HG00323.hp2 HG00558.hp1 HG00558.hp2 others(150): Show |
intron_variant | MODIFIER | c.61-15045A>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34421009 | |||||||
| chr9:34421009 | T | TGA | 6 | a0001c0001t0001g0117 a0001c0001t0001g0283 a0001c0001t0001g0289 others(3): Show |
6 | HG00597.hp1 HG01928.hp2 HG02015.hp2 others(3): Show |
intron_variant | MODIFIER | c.61-15047_61-15046d others(4): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34421009 | |||||||
| chr9:34421009 | T | TGAGA | 5 | a0001c0001t0001g0124 a0001c0001t0001g0284 a0001c0001t0002g0153 others(2): Show |
5 | HG00423.hp2 HG01433.hp1 HG02293.hp2 others(2): Show |
intron_variant | MODIFIER | c.61-15049_61-15046d others(6): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34421009 | |||||||
| chr9:34421009 | T | TGAGAGAG others(1): Show |
41 | a0001c0001t0001g0116 a0001c0001t0001g0217 a0001c0001t0001g0228 others(38): Show |
41 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.61-15053_61-15046d others(10): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34421009 | |||||||
| chr9:34421009 | T | TGAGAGAG others(3): Show |
23 | a0001c0001t0001g0119 a0001c0001t0001g0185 a0001c0001t0001g0188 others(20): Show |
23 | HG00099.hp1 HG00597.hp2 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.61-15055_61-15046d others(12): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34421009 | |||||||
| chr9:34421009 | T | TGAGAGAG others(5): Show |
2 | a0001c0001t0002g0256 a0001c0001t0007g0352 |
2 | HG00741.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.61-15057_61-15046d others(14): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34421009 | |||||||
| chr9:34421009 | T | TGAGAGAG others(7): Show |
3 | a0001c0001t0005g0029 a0001c0001t0005g0049 a0001c0001t0021g0354 |
3 | HG01516.hp2 NA18945.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.61-15059_61-15046d others(16): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34421009 | |||||||
| chr9:34421009 | T | TGAGAGAG others(9): Show |
4 | a0001c0001t0002g0189 a0001c0001t0005g0026 a0001c0001t0005g0027 others(1): Show |
4 | HG01943.hp1 NA18941.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.61-15061_61-15046d others(18): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34421009 | |||||||
| chr9:34421009 | T | TGTGAGAG others(3): Show |
7 | a0001c0001t0002g0113 a0001c0001t0004g0057 a0001c0001t0006g0093 others(4): Show |
7 | HG00280.hp2 HG00741.hp2 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.61-15046_61-15045i others(12): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34421009 | |||||||
| chr9:34421009 | T | TGTGAGAG others(5): Show |
1 | a0001c0001t0007g0156 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.61-15046_61-15045i others(14): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34421009 | |||||||
| chr9:34421009 | T | TGTGAGAG others(7): Show |
1 | a0001c0001t0007g0197 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.61-15046_61-15045i others(16): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34421009 | |||||||
| chr9:34421009 | T | TGTGAGAG others(9): Show |
1 | a0001c0001t0001g0083 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.61-15046_61-15045i others(18): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34421009 | |||||||
| chr9:34421009 | T | TGTGAGAG others(11): Show |
1 | a0001c0001t0024g0104 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.61-15046_61-15045i others(20): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34421009 | |||||||
| chr9:34421009 | TGAGAGAG others(3): Show |
T | 1 | a0001c0001t0002g0173 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.61-15055_61-15046d others(12): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34421009 | |||||||
| chr9:34421011 | A | T | 6 | a0001c0001t0001g0006 a0001c0001t0001g0106 a0001c0001t0001g0108 others(3): Show |
7 | HG01243.hp1 HG02040.hp1 HG02074.hp2 others(4): Show |
intron_variant | MODIFIER | c.61-15047T>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34421011 | |||||||
| chr9:34421044 | G | C | 2 | a0001c0001t0004g0057 a0001c0001t0006g0093 |
2 | HG00280.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.61-15080C>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34421044 | |||||||
| chr9:34421044 | G | GAGAGAGA others(3): Show |
20 | a0001c0001t0004g0005 a0001c0001t0004g0009 a0001c0001t0004g0062 others(17): Show |
22 | HG00423.hp1 HG01081.hp1 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.61-15081_61-15080i others(12): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34421044 | |||||||
| chr9:34421044 | G | GAGAGAGA others(5): Show |
6 | a0001c0001t0004g0058 a0001c0001t0004g0069 a0001c0001t0004g0076 others(3): Show |
6 | HG01934.hp2 HG01952.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.61-15081_61-15080i others(14): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34421044 | |||||||
| chr9:34421044 | G | GAGAGAGA others(7): Show |
6 | a0001c0001t0004g0074 a0001c0001t0004g0075 a0001c0001t0004g0248 others(3): Show |
6 | HG01175.hp1 HG02257.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.61-15081_61-15080i others(16): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34421044 | |||||||
| chr9:34421044 | G | GAGAGAGA others(9): Show |
5 | a0001c0001t0004g0070 a0001c0001t0004g0160 a0001c0001t0006g0078 others(2): Show |
5 | HG01074.hp1 HG02280.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.61-15081_61-15080i others(18): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34421044 | |||||||
| chr9:34421044 | G | GAGAGAGA others(13): Show |
4 | a0001c0001t0006g0060 a0001c0001t0006g0061 a0001c0001t0006g0143 others(1): Show |
4 | HG01496.hp2 HG02109.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.61-15081_61-15080i others(22): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34421044 | |||||||
| chr9:34421044 | G | GAGAGAGA others(15): Show |
1 | a0001c0001t0004g0071 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.61-15081_61-15080i others(24): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34421044 | |||||||
| chr9:34421205 | G | A | 38 | a0001c0001t0004g0005 a0001c0001t0004g0009 a0001c0001t0004g0057 others(35): Show |
40 | HG00280.hp2 HG00423.hp1 HG01074.hp1 others(37): Show |
intron_variant | MODIFIER | c.61-15241C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34421205 | |||||||
| chr9:34421217 | C | T | 63 | a0001c0001t0001g0116 a0001c0001t0001g0119 a0001c0001t0001g0185 others(60): Show |
63 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.61-15253G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34421217 | |||||||
| chr9:34421281 | G | A | 4 | a0001c0001t0009g0144 a0001c0001t0009g0145 a0001c0001t0009g0146 others(1): Show |
4 | HG02559.hp1 HG02818.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.61-15317C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34421281 | |||||||
| chr9:34421315 | G | A | 1 | a0001c0001t0001g0266 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.61-15351C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34421315 | |||||||
| chr9:34421473 | C | T | 1 | a0001c0001t0005g0045 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.61-15509G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34421473 | |||||||
| chr9:34421523 | G | T | 4 | a0001c0001t0009g0144 a0001c0001t0009g0145 a0001c0001t0009g0146 others(1): Show |
4 | HG02559.hp1 HG02818.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.61-15559C>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34421523 | |||||||
| chr9:34421553 | G | A | 1 | a0001c0001t0003g0322 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.61-15589C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34421553 | |||||||
| chr9:34421593 | G | C | 271 | a0001c0001t0001g0059 a0001c0001t0001g0083 a0001c0001t0001g0084 others(268): Show |
287 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(284): Show |
intron_variant | MODIFIER | c.61-15629C>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34421593 | |||||||
| chr9:34421668 | C | T | 21 | a0001c0001t0002g0134 a0001c0001t0005g0004 a0001c0001t0005g0024 others(18): Show |
22 | HG00558.hp1 HG02027.hp1 HG02523.hp1 others(19): Show |
intron_variant | MODIFIER | c.61-15704G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34421668 | |||||||
| chr9:34421881 | C | A | 51 | a0001c0001t0004g0005 a0001c0001t0004g0009 a0001c0001t0004g0057 others(48): Show |
53 | HG00280.hp2 HG00423.hp1 HG01074.hp1 others(50): Show |
intron_variant | MODIFIER | c.61-15917G>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34421881 | |||||||
| chr9:34421881 | C | G | 1 | a0001c0001t0002g0221 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.61-15917G>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34421881 | |||||||
| chr9:34422066 | T | C | 15 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(12): Show |
18 | HG00323.hp2 HG00639.hp2 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.61-16102A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34422066 | |||||||
| chr9:34422080 | A | G | 4 | a0001c0001t0009g0144 a0001c0001t0009g0145 a0001c0001t0009g0146 others(1): Show |
4 | HG02559.hp1 HG02818.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.61-16116T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34422080 | |||||||
| chr9:34422113 | G | A | 1 | a0001c0001t0001g0273 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.61-16149C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34422113 | |||||||
| chr9:34422187 | G | A | 121 | a0001c0001t0001g0345 a0001c0001t0002g0007 a0001c0001t0002g0008 others(118): Show |
135 | HG00323.hp2 HG00558.hp1 HG00558.hp2 others(132): Show |
intron_variant | MODIFIER | c.61-16223C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34422187 | |||||||
| chr9:34422215 | T | G | 17 | a0001c0001t0001g0083 a0001c0001t0007g0156 a0001c0001t0007g0172 others(14): Show |
17 | HG00099.hp1 HG00741.hp1 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.61-16251A>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34422215 | |||||||
| chr9:34422248 | A | T | 2 | a0001c0001t0011g0050 a0001c0001t0011g0051 |
2 | HG01891.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.61-16284T>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34422248 | |||||||
| chr9:34422281 | T | C | 1 | a0001c0001t0002g0133 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.61-16317A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34422281 | |||||||
| chr9:34422341 | G | A | 1 | a0001c0001t0003g0107 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.61-16377C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34422341 | |||||||
| chr9:34422457 | T | A | 1 | a0001c0001t0012g0052 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.61-16493A>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34422457 | |||||||
| chr9:34422480 | C | T | 1 | a0001c0001t0001g0244 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.61-16516G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34422480 | |||||||
| chr9:34422492 | T | C | 3 | a0001c0001t0001g0271 a0001c0001t0001g0289 a0001c0001t0001g0315 |
3 | HG02040.hp2 HG02083.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.61-16528A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34422492 | |||||||
| chr9:34422493 | G | T | 2 | a0001c0001t0011g0050 a0001c0001t0011g0051 |
2 | HG01891.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.61-16529C>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34422493 | |||||||
| chr9:34422779 | G | A | 6 | a0001c0001t0001g0059 a0001c0001t0001g0084 a0001c0001t0001g0085 others(3): Show |
6 | HG01175.hp2 HG02818.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.61-16815C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34422779 | |||||||
| chr9:34422832 | G | T | 1 | a0001c0001t0008g0164 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.61-16868C>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34422832 | |||||||
| chr9:34423133 | G | A | 3 | a0001c0001t0001g0267 a0001c0001t0012g0052 a0001c0001t0012g0053 |
3 | HG03041.hp2 HG03195.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.61-17169C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34423133 | |||||||
| chr9:34423207 | G | C | 186 | a0001c0001t0001g0116 a0001c0001t0001g0119 a0001c0001t0001g0185 others(183): Show |
200 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.61-17243C>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34423207 | |||||||
| chr9:34423420 | G | A | 23 | a0001c0001t0002g0134 a0001c0001t0005g0004 a0001c0001t0005g0024 others(20): Show |
24 | HG00558.hp1 HG02027.hp1 HG02074.hp1 others(21): Show |
intron_variant | MODIFIER | c.61-17456C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34423420 | |||||||
| chr9:34423500 | C | T | 53 | a0001c0001t0001g0059 a0001c0001t0001g0084 a0001c0001t0001g0085 others(50): Show |
55 | HG00280.hp2 HG00423.hp1 HG01074.hp1 others(52): Show |
intron_variant | MODIFIER | c.61-17536G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34423500 | |||||||
| chr9:34423743 | A | G | 1 | a0001c0001t0003g0311 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.61-17779T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34423743 | |||||||
| chr9:34423761 | G | A | 11 | a0001c0001t0007g0156 a0001c0001t0007g0172 a0001c0001t0007g0223 others(8): Show |
11 | HG00099.hp1 HG00741.hp1 HG00741.hp2 others(8): Show |
intron_variant | MODIFIER | c.61-17797C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34423761 | |||||||
| chr9:34423778 | G | A | 1 | a0001c0001t0001g0303 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.61-17814C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34423778 | |||||||
| chr9:34423808 | C | T | 184 | a0001c0001t0001g0116 a0001c0001t0001g0119 a0001c0001t0001g0185 others(181): Show |
198 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(195): Show |
intron_variant | MODIFIER | c.61-17844G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34423808 | |||||||
| chr9:34424095 | C | G | 6 | a0001c0001t0001g0083 a0001c0001t0009g0144 a0001c0001t0009g0145 others(3): Show |
6 | HG01255.hp2 HG02055.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.61-18131G>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34424095 | |||||||
| chr9:34424400 | A | G | 4 | a0001c0001t0009g0144 a0001c0001t0009g0145 a0001c0001t0009g0146 others(1): Show |
4 | HG02559.hp1 HG02818.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.61-18436T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34424400 | |||||||
| chr9:34424443 | T | TGGGCAAG others(11): Show |
62 | a0001c0001t0001g0116 a0001c0001t0001g0119 a0001c0001t0001g0185 others(59): Show |
62 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.61-18497_61-18480d others(20): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34424443 | |||||||
| chr9:34424458 | C | T | 1 | a0001c0001t0011g0050 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.61-18494G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34424458 | |||||||
| chr9:34424651 | C | CGG | 41 | a0001c0001t0001g0345 a0001c0001t0002g0232 a0001c0001t0003g0003 others(38): Show |
48 | HG00558.hp2 HG00621.hp2 HG00673.hp1 others(45): Show |
intron_variant | MODIFIER | c.61-18689_61-18688d others(4): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34424651 | |||||||
| chr9:34424861 | T | G | 1 | a0001c0001t0001g0301 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.61-18897A>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34424861 | |||||||
| chr9:34424949 | T | C | 14 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(11): Show |
17 | HG00323.hp2 HG00639.hp2 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.61-18985A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34424949 | |||||||
| chr9:34424951 | T | C | 1 | a0001c0001t0002g0184 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.61-18987A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34424951 | |||||||
| chr9:34424993 | A | G | 1 | a0001c0001t0002g0170 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.61-19029T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34424993 | |||||||
| chr9:34425005 | C | T | 14 | a0001c0001t0007g0156 a0001c0001t0007g0172 a0001c0001t0007g0223 others(11): Show |
14 | HG00099.hp1 HG00741.hp2 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.61-19041G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34425005 | |||||||
| chr9:34425051 | C | G | 1 | a0001c0001t0004g0248 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.61-19087G>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34425051 | |||||||
| chr9:34425137 | C | T | 4 | a0001c0001t0009g0144 a0001c0001t0009g0145 a0001c0001t0009g0146 others(1): Show |
4 | HG02559.hp1 HG02818.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.61-19173G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34425137 | |||||||
| chr9:34425218 | T | C | 17 | a0001c0001t0001g0083 a0001c0001t0007g0156 a0001c0001t0007g0172 others(14): Show |
17 | HG00099.hp1 HG00741.hp1 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.61-19254A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34425218 | |||||||
| chr9:34425230 | A | T | 54 | a0001c0001t0001g0059 a0001c0001t0001g0084 a0001c0001t0001g0085 others(51): Show |
56 | HG00280.hp2 HG00423.hp1 HG01074.hp1 others(53): Show |
intron_variant | MODIFIER | c.61-19266T>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34425230 | |||||||
| chr9:34425244 | C | G | 1 | a0001c0001t0003g0311 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.61-19280G>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34425244 | |||||||
| chr9:34425246 | A | C | 1 | a0001c0001t0003g0311 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.61-19282T>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34425246 | |||||||
| chr9:34425248 | G | A | 1 | a0001c0001t0003g0311 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.61-19284C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34425248 | |||||||
| chr9:34425317 | C | T | 17 | a0001c0001t0001g0083 a0001c0001t0007g0156 a0001c0001t0007g0172 others(14): Show |
17 | HG00099.hp1 HG00741.hp1 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.61-19353G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34425317 | |||||||
| chr9:34425497 | T | C | 64 | a0001c0001t0001g0116 a0001c0001t0001g0119 a0001c0001t0001g0185 others(61): Show |
64 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.61-19533A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34425497 | |||||||
| chr9:34425577 | G | A | 1 | a0001c0001t0002g0136 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.61-19613C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34425577 | |||||||
| chr9:34425584 | C | T | 2 | a0001c0001t0002g0150 a0001c0001t0002g0219 |
2 | HG01361.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.61-19620G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34425584 | |||||||
| chr9:34425619 | G | A | 183 | a0001c0001t0001g0116 a0001c0001t0001g0119 a0001c0001t0001g0185 others(180): Show |
197 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(194): Show |
intron_variant | MODIFIER | c.61-19655C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34425619 | |||||||
| chr9:34425718 | C | T | 1 | a0001c0001t0007g0353 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.61-19754G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34425718 | |||||||
| chr9:34425800 | A | T | 6 | a0001c0001t0009g0144 a0001c0001t0009g0145 a0001c0001t0009g0146 others(3): Show |
6 | HG02559.hp1 HG02818.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.61-19836T>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34425800 | |||||||
| chr9:34425930 | A | C | 1 | a0001c0001t0006g0056 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.61-19966T>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34425930 | |||||||
| chr9:34426126 | G | C | 256 | a0001c0001t0001g0006 a0001c0001t0001g0059 a0001c0001t0001g0083 others(253): Show |
273 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(270): Show |
intron_variant | MODIFIER | c.61-20162C>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34426126 | |||||||
| chr9:34426189 | T | A | 7 | a0001c0001t0006g0143 a0001c0001t0006g0148 a0001c0001t0009g0144 others(4): Show |
7 | HG02559.hp1 HG02622.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.61-20225A>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34426189 | |||||||
| chr9:34426340 | TG | T | 6 | a0001c0001t0001g0006 a0001c0001t0001g0106 a0001c0001t0001g0108 others(3): Show |
7 | HG01243.hp1 HG02451.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.61-20377delC | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34426340 | |||||||
| chr9:34426590 | G | A | 1 | a0001c0001t0020g0276 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.61-20626C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34426590 | |||||||
| chr9:34426660 | G | C | 72 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0014 others(69): Show |
83 | HG00099.hp1 HG00323.hp2 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.61-20696C>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34426660 | |||||||
| chr9:34426685 | CCAG | C | 2 | a0001c0001t0003g0019 a0001c0004t0003g0346 |
3 | NA18964.hp2 NA18983.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.61-20724_61-20722d others(5): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34426685 | |||||||
| chr9:34426773 | G | A | 19 | a0001c0001t0004g0005 a0001c0001t0004g0057 a0001c0001t0004g0058 others(16): Show |
20 | HG00280.hp2 HG01074.hp1 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.61-20809C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34426773 | |||||||
| chr9:34426774 | G | A | 1 | a0001c0001t0001g0302 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.61-20810C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34426774 | |||||||
| chr9:34426863 | G | A | 4 | a0001c0001t0001g0006 a0001c0001t0001g0106 a0001c0001t0001g0108 others(1): Show |
5 | HG01243.hp1 HG02451.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.61-20899C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34426863 | |||||||
| chr9:34426920 | G | C | 1 | a0001c0001t0006g0357 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.61-20956C>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34426920 | |||||||
| chr9:34426923 | C | T | 1 | a0001c0001t0010g0095 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.61-20959G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34426923 | |||||||
| chr9:34426935 | T | C | 1 | a0001c0001t0024g0104 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.61-20971A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34426935 | |||||||
| chr9:34426984 | G | A | 30 | a0001c0001t0005g0004 a0001c0001t0005g0023 a0001c0001t0005g0024 others(27): Show |
31 | HG00558.hp1 HG01891.hp2 HG01928.hp1 others(28): Show |
intron_variant | MODIFIER | c.61-21020C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34426984 | |||||||
| chr9:34427023 | C | T | 1 | a0001c0001t0024g0104 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.61-21059G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34427023 | |||||||
| chr9:34427048 | C | G | 30 | a0001c0001t0005g0004 a0001c0001t0005g0023 a0001c0001t0005g0024 others(27): Show |
31 | HG00558.hp1 HG01891.hp2 HG01928.hp1 others(28): Show |
intron_variant | MODIFIER | c.61-21084G>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34427048 | |||||||
| chr9:34427194 | C | T | 2 | a0001c0001t0012g0052 a0001c0001t0012g0053 |
2 | HG03195.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.61-21230G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34427194 | |||||||
| chr9:34427199 | C | T | 7 | a0001c0001t0007g0348 a0001c0001t0007g0349 a0001c0001t0007g0350 others(4): Show |
7 | HG00099.hp1 HG00741.hp1 HG01070.hp2 others(4): Show |
intron_variant | MODIFIER | c.61-21235G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34427199 | |||||||
| chr9:34427200 | C | T | 1 | a0001c0001t0002g0194 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.61-21236G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34427200 | |||||||
| chr9:34427333 | G | C | 1 | a0001c0001t0001g0251 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.61-21369C>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34427333 | |||||||
| chr9:34427349 | C | T | 7 | a0001c0001t0007g0348 a0001c0001t0007g0349 a0001c0001t0007g0350 others(4): Show |
7 | HG00099.hp1 HG00741.hp1 HG01070.hp2 others(4): Show |
intron_variant | MODIFIER | c.61-21385G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34427349 | |||||||
| chr9:34427378 | C | T | 47 | a0001c0001t0001g0006 a0001c0001t0001g0106 a0001c0001t0001g0108 others(44): Show |
49 | HG00099.hp1 HG00558.hp1 HG00741.hp1 others(46): Show |
intron_variant | MODIFIER | c.61-21414G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34427378 | |||||||
| chr9:34427495 | T | C | 30 | a0001c0001t0005g0004 a0001c0001t0005g0023 a0001c0001t0005g0024 others(27): Show |
31 | HG00558.hp1 HG01891.hp2 HG01928.hp1 others(28): Show |
intron_variant | MODIFIER | c.61-21531A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34427495 | |||||||
| chr9:34427540 | T | G | 1 | a0001c0001t0002g0209 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.61-21576A>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34427540 | |||||||
| chr9:34428530 | T | C | 1 | a0001c0001t0002g0151 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.61-22566A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34428530 | |||||||
| chr9:34428539 | G | C | 5 | a0001c0001t0001g0116 a0001c0001t0001g0119 a0001c0001t0001g0185 others(2): Show |
5 | NA18949.hp2 NA18953.hp2 NA18985.hp2 others(2): Show |
intron_variant | MODIFIER | c.61-22575C>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34428539 | |||||||
| chr9:34428602 | T | C | 1 | a0001c0001t0001g0250 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.61-22638A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34428602 | |||||||
| chr9:34428990 | G | C | 9 | a0001c0001t0001g0006 a0001c0001t0001g0106 a0001c0001t0001g0108 others(6): Show |
10 | HG01243.hp1 HG01496.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.61-23026C>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34428990 | |||||||
| chr9:34429019 | A | G | 30 | a0001c0001t0005g0004 a0001c0001t0005g0023 a0001c0001t0005g0024 others(27): Show |
31 | HG00558.hp1 HG01891.hp2 HG01928.hp1 others(28): Show |
intron_variant | MODIFIER | c.61-23055T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34429019 | |||||||
| chr9:34429027 | T | G | 1 | a0001c0001t0006g0118 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.61-23063A>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34429027 | |||||||
| chr9:34429077 | C | T | 8 | a0001c0001t0007g0347 a0001c0001t0007g0348 a0001c0001t0007g0349 others(5): Show |
8 | HG00099.hp1 HG00741.hp1 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.61-23113G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34429077 | |||||||
| chr9:34429250 | G | A | 9 | a0001c0001t0001g0006 a0001c0001t0001g0106 a0001c0001t0001g0108 others(6): Show |
10 | HG01243.hp1 HG01496.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.61-23286C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34429250 | |||||||
| chr9:34429352 | T | C | 2 | a0001c0001t0001g0307 a0001c0001t0001g0308 |
2 | NA19054.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.61-23388A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34429352 | |||||||
| chr9:34429480 | G | A | 8 | a0001c0001t0007g0347 a0001c0001t0007g0348 a0001c0001t0007g0349 others(5): Show |
8 | HG00099.hp1 HG00741.hp1 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.61-23516C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34429480 | |||||||
| chr9:34429728 | T | A | 94 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0014 others(91): Show |
105 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.61-23764A>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34429728 | |||||||
| chr9:34429734 | T | C | 8 | a0001c0001t0007g0347 a0001c0001t0007g0348 a0001c0001t0007g0349 others(5): Show |
8 | HG00099.hp1 HG00741.hp1 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.61-23770A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34429734 | |||||||
| chr9:34430101 | C | T | 1 | a0001c0001t0002g0215 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.61-24137G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34430101 | |||||||
| chr9:34430107 | T | G | 1 | a0001c0001t0002g0219 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.61-24143A>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34430107 | |||||||
| chr9:34430204 | C | T | 30 | a0001c0001t0005g0004 a0001c0001t0005g0023 a0001c0001t0005g0024 others(27): Show |
31 | HG00558.hp1 HG01891.hp2 HG01928.hp1 others(28): Show |
intron_variant | MODIFIER | c.61-24240G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34430204 | |||||||
| chr9:34430247 | G | C | 1 | a0001c0001t0002g0186 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.61-24283C>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34430247 | |||||||
| chr9:34430299 | T | C | 25 | a0001c0001t0001g0124 a0001c0001t0002g0007 a0001c0001t0002g0008 others(22): Show |
27 | HG00323.hp2 HG00609.hp2 HG00621.hp2 others(24): Show |
intron_variant | MODIFIER | c.61-24335A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34430299 | |||||||
| chr9:34430632 | G | A | 9 | a0001c0001t0007g0347 a0001c0001t0007g0348 a0001c0001t0007g0349 others(6): Show |
9 | HG00099.hp1 HG00741.hp1 HG01070.hp2 others(6): Show |
intron_variant | MODIFIER | c.61-24668C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34430632 | |||||||
| chr9:34430636 | C | CA | 50 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0001t0001g0085 others(47): Show |
50 | HG00280.hp2 HG01074.hp1 HG01081.hp1 others(47): Show |
intron_variant | MODIFIER | c.61-24673dupT | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34430636 | |||||||
| chr9:34430636 | C | CAA | 85 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0014 others(82): Show |
95 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.61-24674_61-24673d others(4): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34430636 | |||||||
| chr9:34430636 | C | CAAA | 24 | a0001c0001t0001g0021 a0001c0001t0001g0236 a0001c0001t0001g0268 others(21): Show |
26 | HG00099.hp1 HG00597.hp1 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.61-24675_61-24673d others(5): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34430636 | |||||||
| chr9:34430636 | C | CAAAAAAA others(3): Show |
5 | a0001c0001t0005g0024 a0001c0001t0005g0027 a0001c0001t0005g0028 others(2): Show |
5 | HG02027.hp1 NA18941.hp1 NA18945.hp2 others(2): Show |
intron_variant | MODIFIER | c.61-24682_61-24673d others(12): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34430636 | |||||||
| chr9:34430636 | C | CAAAAAAA others(4): Show |
12 | a0001c0001t0005g0023 a0001c0001t0005g0031 a0001c0001t0005g0032 others(9): Show |
12 | HG00558.hp1 HG01934.hp1 HG02273.hp1 others(9): Show |
intron_variant | MODIFIER | c.61-24683_61-24673d others(13): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34430636 | |||||||
| chr9:34430636 | C | CAAAAAAA others(5): Show |
10 | a0001c0001t0005g0004 a0001c0001t0005g0025 a0001c0001t0005g0026 others(7): Show |
11 | HG01891.hp2 HG02074.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.61-24684_61-24673d others(14): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34430636 | |||||||
| chr9:34430636 | C | CAAAAAAA others(6): Show |
3 | a0001c0001t0005g0041 a0001c0001t0005g0042 a0001c0001t0005g0043 |
3 | HG01928.hp1 NA18955.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.61-24685_61-24673d others(15): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34430636 | |||||||
| chr9:34430636 | CA | C | 8 | a0001c0001t0001g0355 a0001c0001t0002g0169 a0001c0001t0002g0170 others(5): Show |
8 | HG01496.hp1 HG02622.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.61-24673delT | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34430636 | |||||||
| chr9:34430846 | T | TAACAACA others(2): Show |
30 | a0001c0001t0005g0004 a0001c0001t0005g0023 a0001c0001t0005g0024 others(27): Show |
31 | HG00558.hp1 HG01891.hp2 HG01928.hp1 others(28): Show |
intron_variant | MODIFIER | c.61-24891_61-24883d others(11): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34430846 | |||||||
| chr9:34430846 | T | TAACAACA others(5): Show |
50 | a0001c0001t0001g0059 a0001c0001t0001g0083 a0001c0001t0001g0084 others(47): Show |
51 | HG00280.hp2 HG01074.hp1 HG01081.hp1 others(48): Show |
intron_variant | MODIFIER | c.61-24894_61-24883d others(14): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34430846 | |||||||
| chr9:34430846 | T | TAACAACA others(8): Show |
2 | a0001c0001t0001g0088 a0001c0001t0017g0103 |
2 | HG02451.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.61-24897_61-24883d others(17): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34430846 | |||||||
| chr9:34430846 | T | TAACAACA others(11): Show |
7 | a0001c0001t0007g0347 a0001c0001t0007g0348 a0001c0001t0007g0350 others(4): Show |
7 | HG00099.hp1 HG00741.hp1 HG01070.hp2 others(4): Show |
intron_variant | MODIFIER | c.61-24900_61-24883d others(20): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34430846 | |||||||
| chr9:34430846 | T | TAACAACA others(14): Show |
3 | a0001c0001t0003g0110 a0001c0001t0012g0052 a0001c0001t0018g0111 |
3 | HG01496.hp1 HG02647.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.61-24883_61-24882i others(23): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34430846 | |||||||
| chr9:34430846 | T | TAACAACA others(17): Show |
2 | a0001c0001t0003g0107 a0001c0001t0012g0053 |
2 | HG03195.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.61-24883_61-24882i others(26): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34430846 | |||||||
| chr9:34430846 | T | TAACAACA others(20): Show |
3 | a0001c0001t0001g0006 a0001c0001t0001g0106 a0001c0001t0001g0108 |
4 | HG01243.hp1 HG02451.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.61-24883_61-24882i others(29): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34430846 | |||||||
| chr9:34430846 | T | TAACAACA others(23): Show |
1 | a0001c0001t0001g0109 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.61-24883_61-24882i others(32): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34430846 | |||||||
| chr9:34430867 | T | C | 9 | a0001c0001t0007g0347 a0001c0001t0007g0348 a0001c0001t0007g0349 others(6): Show |
9 | HG00099.hp1 HG00741.hp1 HG01070.hp2 others(6): Show |
intron_variant | MODIFIER | c.61-24903A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34430867 | |||||||
| chr9:34431081 | C | T | 51 | a0001c0001t0001g0059 a0001c0001t0001g0083 a0001c0001t0001g0084 others(48): Show |
52 | HG00280.hp2 HG01074.hp1 HG01081.hp1 others(49): Show |
intron_variant | MODIFIER | c.61-25117G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34431081 | |||||||
| chr9:34431401 | C | T | 1 | a0001c0001t0021g0354 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.61-25437G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34431401 | |||||||
| chr9:34431485 | T | G | 9 | a0001c0001t0001g0006 a0001c0001t0001g0106 a0001c0001t0001g0108 others(6): Show |
10 | HG01243.hp1 HG01496.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.61-25521A>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34431485 | |||||||
| chr9:34431976 | A | G | 199 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(196): Show |
213 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.61-26012T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34431976 | |||||||
| chr9:34432272 | G | T | 30 | a0001c0001t0005g0004 a0001c0001t0005g0023 a0001c0001t0005g0024 others(27): Show |
31 | HG00558.hp1 HG01891.hp2 HG01928.hp1 others(28): Show |
intron_variant | MODIFIER | c.60+25932C>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34432272 | |||||||
| chr9:34432489 | C | T | 6 | a0001c0001t0006g0143 a0001c0001t0006g0148 a0001c0001t0009g0144 others(3): Show |
6 | HG02559.hp1 HG02818.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.60+25715G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34432489 | |||||||
| chr9:34432500 | T | C | 3 | a0001c0001t0001g0006 a0001c0001t0001g0106 a0001c0001t0001g0108 |
4 | HG01243.hp1 HG02451.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.60+25704A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34432500 | |||||||
| chr9:34432541 | C | T | 36 | a0001c0001t0001g0315 a0001c0001t0002g0316 a0001c0001t0002g0323 others(33): Show |
43 | HG00323.hp1 HG00544.hp2 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.60+25663G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34432541 | |||||||
| chr9:34432554 | C | T | 30 | a0001c0001t0005g0004 a0001c0001t0005g0023 a0001c0001t0005g0024 others(27): Show |
31 | HG00558.hp1 HG01891.hp2 HG01928.hp1 others(28): Show |
intron_variant | MODIFIER | c.60+25650G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34432554 | |||||||
| chr9:34432555 | G | A | 1 | a0001c0001t0001g0097 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.60+25649C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34432555 | |||||||
| chr9:34432639 | C | T | 9 | a0001c0001t0001g0006 a0001c0001t0001g0106 a0001c0001t0001g0108 others(6): Show |
10 | HG01243.hp1 HG01496.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.60+25565G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34432639 | |||||||
| chr9:34432738 | C | T | 9 | a0001c0001t0001g0059 a0001c0001t0001g0083 a0001c0001t0001g0084 others(6): Show |
9 | HG01175.hp2 HG02055.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.60+25466G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34432738 | |||||||
| chr9:34432751 | T | G | 1 | a0001c0001t0024g0104 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.60+25453A>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34432751 | |||||||
| chr9:34432819 | C | G | 9 | a0001c0001t0001g0006 a0001c0001t0001g0106 a0001c0001t0001g0108 others(6): Show |
10 | HG01243.hp1 HG01496.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.60+25385G>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34432819 | |||||||
| chr9:34432903 | G | T | 1 | a0001c0001t0005g0047 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.60+25301C>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34432903 | |||||||
| chr9:34432966 | G | C | 1 | a0001c0001t0001g0280 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.60+25238C>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34432966 | |||||||
| chr9:34432980 | G | A | 1 | a0001c0001t0006g0118 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.60+25224C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34432980 | |||||||
| chr9:34433259 | T | C | 8 | a0001c0001t0007g0347 a0001c0001t0007g0348 a0001c0001t0007g0349 others(5): Show |
8 | HG00099.hp1 HG00741.hp1 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.60+24945A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34433259 | |||||||
| chr9:34433315 | A | G | 94 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0014 others(91): Show |
105 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.60+24889T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34433315 | |||||||
| chr9:34433329 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.60+24875G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34433329 | |||||||
| chr9:34433348 | G | A | 2 | a0001c0001t0003g0019 a0001c0004t0003g0346 |
3 | NA18964.hp2 NA18983.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.60+24856C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34433348 | |||||||
| chr9:34433380 | A | G | 1 | a0001c0001t0005g0027 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.60+24824T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34433380 | |||||||
| chr9:34433818 | G | A | 1 | a0001c0001t0011g0051 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.60+24386C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34433818 | |||||||
| chr9:34433877 | G | C | 30 | a0001c0001t0005g0004 a0001c0001t0005g0023 a0001c0001t0005g0024 others(27): Show |
31 | HG00558.hp1 HG01891.hp2 HG01928.hp1 others(28): Show |
intron_variant | MODIFIER | c.60+24327C>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34433877 | |||||||
| chr9:34433931 | G | A | 3 | a0001c0001t0001g0014 a0001c0001t0001g0272 a0001c0001t0001g0290 |
4 | NA18960.hp1 NA18975.hp2 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.60+24273C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34433931 | |||||||
| chr9:34434030 | G | A | 1 | a0001c0001t0001g0278 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.60+24174C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34434030 | |||||||
| chr9:34434045 | A | T | 1 | a0001c0001t0001g0297 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.60+24159T>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34434045 | |||||||
| chr9:34434046 | C | A | 1 | a0001c0001t0001g0297 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.60+24158G>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34434046 | |||||||
| chr9:34434047 | A | C | 1 | a0001c0001t0001g0297 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.60+24157T>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34434047 | |||||||
| chr9:34434181 | A | G | 1 | a0001c0001t0002g0187 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.60+24023T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34434181 | |||||||
| chr9:34434201 | C | CA | 24 | a0001c0001t0001g0006 a0001c0001t0001g0101 a0001c0001t0001g0108 others(21): Show |
25 | HG01243.hp1 HG01358.hp2 HG01361.hp1 others(22): Show |
intron_variant | MODIFIER | c.60+24002dupT | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34434201 | |||||||
| chr9:34434201 | C | CAA | 6 | a0001c0001t0001g0097 a0001c0001t0001g0106 a0001c0001t0001g0109 others(3): Show |
6 | HG01496.hp1 HG02572.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.60+24001_60+24002d others(4): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34434201 | |||||||
| chr9:34434201 | CA | C | 101 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0014 others(98): Show |
112 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.60+24002delT | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34434201 | |||||||
| chr9:34434201 | CAA | C | 38 | a0001c0001t0001g0249 a0001c0001t0001g0250 a0001c0001t0002g0277 others(35): Show |
40 | HG00280.hp1 HG00558.hp1 HG01081.hp1 others(37): Show |
intron_variant | MODIFIER | c.60+24001_60+24002d others(4): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34434201 | |||||||
| chr9:34434201 | CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0004g0057 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.60+23990_60+24002d others(15): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34434201 | |||||||
| chr9:34434355 | T | C | 94 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0014 others(91): Show |
105 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.60+23849A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34434355 | |||||||
| chr9:34434434 | A | G | 1 | a0001c0001t0017g0103 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.60+23770T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34434434 | |||||||
| chr9:34434526 | ATCCAGAA others(26): Show |
A | 1 | a0001c0001t0017g0103 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.60+23645_60+23677d others(35): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34434526 | |||||||
| chr9:34434570 | C | T | 30 | a0001c0001t0005g0004 a0001c0001t0005g0023 a0001c0001t0005g0024 others(27): Show |
31 | HG00558.hp1 HG01891.hp2 HG01928.hp1 others(28): Show |
intron_variant | MODIFIER | c.60+23634G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34434570 | |||||||
| chr9:34434680 | T | C | 1 | a0001c0001t0001g0273 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.60+23524A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34434680 | |||||||
| chr9:34434812 | TTTTC | T | 51 | a0001c0001t0001g0059 a0001c0001t0001g0083 a0001c0001t0001g0084 others(48): Show |
52 | HG00280.hp2 HG01074.hp1 HG01081.hp1 others(49): Show |
intron_variant | MODIFIER | c.60+23388_60+23391d others(6): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34434812 | |||||||
| chr9:34434827 | TC | T | 30 | a0001c0001t0005g0004 a0001c0001t0005g0023 a0001c0001t0005g0024 others(27): Show |
31 | HG00558.hp1 HG01891.hp2 HG01928.hp1 others(28): Show |
intron_variant | MODIFIER | c.60+23376delG | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34434827 | |||||||
| chr9:34434832 | T | C | 3 | a0001c0001t0003g0107 a0001c0001t0003g0110 a0001c0001t0018g0111 |
3 | HG01496.hp1 HG02647.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.60+23372A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34434832 | |||||||
| chr9:34434979 | C | G | 1 | a0001c0001t0001g0097 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.60+23225G>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34434979 | |||||||
| chr9:34435011 | G | T | 2 | a0001c0001t0003g0312 a0001c0001t0003g0313 |
2 | NA18960.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.60+23193C>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34435011 | |||||||
| chr9:34435059 | G | A | 1 | a0001c0001t0024g0104 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.60+23145C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34435059 | |||||||
| chr9:34435175 | G | C | 1 | a0001c0001t0004g0225 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.60+23029C>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34435175 | |||||||
| chr9:34435377 | A | G | 1 | a0001c0001t0001g0360 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.60+22827T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34435377 | |||||||
| chr9:34435377 | A | T | 30 | a0001c0001t0005g0004 a0001c0001t0005g0023 a0001c0001t0005g0024 others(27): Show |
31 | HG00558.hp1 HG01891.hp2 HG01928.hp1 others(28): Show |
intron_variant | MODIFIER | c.60+22827T>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34435377 | |||||||
| chr9:34435414 | T | C | 3 | a0001c0001t0003g0107 a0001c0001t0003g0110 a0001c0001t0018g0111 |
3 | HG01496.hp1 HG02647.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.60+22790A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34435414 | |||||||
| chr9:34435425 | A | C | 30 | a0001c0001t0005g0004 a0001c0001t0005g0023 a0001c0001t0005g0024 others(27): Show |
31 | HG00558.hp1 HG01891.hp2 HG01928.hp1 others(28): Show |
intron_variant | MODIFIER | c.60+22779T>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34435425 | |||||||
| chr9:34435430 | GA | G | 30 | a0001c0001t0005g0004 a0001c0001t0005g0023 a0001c0001t0005g0024 others(27): Show |
31 | HG00558.hp1 HG01891.hp2 HG01928.hp1 others(28): Show |
intron_variant | MODIFIER | c.60+22773delT | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34435430 | |||||||
| chr9:34435514 | C | G | 30 | a0001c0001t0005g0004 a0001c0001t0005g0023 a0001c0001t0005g0024 others(27): Show |
31 | HG00558.hp1 HG01891.hp2 HG01928.hp1 others(28): Show |
intron_variant | MODIFIER | c.60+22690G>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34435514 | |||||||
| chr9:34435723 | C | T | 1 | a0001c0001t0017g0103 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.60+22481G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34435723 | |||||||
| chr9:34435813 | C | CT | 94 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0014 others(91): Show |
105 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.60+22390dupA | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34435813 | |||||||
| chr9:34435824 | G | T | 1 | a0001c0001t0017g0103 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.60+22380C>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34435824 | |||||||
| chr9:34435875 | G | A | 2 | a0001c0001t0002g0153 a0001c0001t0002g0154 |
2 | HG02293.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.60+22329C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34435875 | |||||||
| chr9:34435962 | C | T | 1 | a0001c0001t0016g0072 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.60+22242G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34435962 | |||||||
| chr9:34435966 | T | C | 1 | a0001c0001t0001g0231 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.60+22238A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34435966 | |||||||
| chr9:34436004 | C | T | 1 | a0001c0004t0003g0346 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.60+22200G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34436004 | |||||||
| chr9:34436026 | A | G | 7 | a0001c0001t0002g0165 a0001c0001t0002g0169 a0001c0001t0002g0216 others(4): Show |
7 | NA18747.hp1 NA18955.hp1 NA18982.hp2 others(4): Show |
intron_variant | MODIFIER | c.60+22178T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34436026 | |||||||
| chr9:34436095 | G | A | 6 | a0001c0001t0006g0143 a0001c0001t0006g0148 a0001c0001t0009g0144 others(3): Show |
6 | HG02559.hp1 HG02818.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.60+22109C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34436095 | |||||||
| chr9:34436248 | T | C | 1 | a0001c0001t0001g0117 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.60+21956A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34436248 | |||||||
| chr9:34436422 | T | A | 95 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0014 others(92): Show |
106 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.60+21782A>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34436422 | |||||||
| chr9:34436494 | C | T | 1 | a0001c0001t0001g0217 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.60+21710G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34436494 | |||||||
| chr9:34436617 | T | G | 1 | a0001c0001t0001g0345 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.60+21587A>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34436617 | |||||||
| chr9:34436773 | C | CTA | 94 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0014 others(91): Show |
105 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.60+21430_60+21431i others(4): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34436773 | |||||||
| chr9:34436775 | C | T | 94 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0014 others(91): Show |
105 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.60+21429G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34436775 | |||||||
| chr9:34436849 | T | C | 1 | a0001c0001t0017g0103 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.60+21355A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34436849 | |||||||
| chr9:34437026 | C | G | 2 | a0001c0001t0003g0312 a0001c0001t0003g0313 |
2 | NA18960.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.60+21178G>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34437026 | |||||||
| chr9:34437179 | A | ACT | 3 | a0001c0001t0006g0060 a0001c0001t0006g0061 a0001c0001t0006g0357 |
3 | HG01496.hp2 HG02109.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.60+21023_60+21024d others(4): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34437179 | |||||||
| chr9:34437194 | A | G | 30 | a0001c0001t0005g0004 a0001c0001t0005g0023 a0001c0001t0005g0024 others(27): Show |
31 | HG00558.hp1 HG01891.hp2 HG01928.hp1 others(28): Show |
intron_variant | MODIFIER | c.60+21010T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34437194 | |||||||
| chr9:34437471 | G | A | 94 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0014 others(91): Show |
105 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.60+20733C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34437471 | |||||||
| chr9:34437798 | C | A | 1 | a0001c0001t0001g0190 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.60+20406G>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34437798 | |||||||
| chr9:34437895 | G | A | 1 | a0001c0001t0003g0344 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.60+20309C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34437895 | |||||||
| chr9:34437911 | A | G | 1 | a0001c0001t0026g0149 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.60+20293T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34437911 | |||||||
| chr9:34437967 | G | T | 1 | a0001c0001t0004g0075 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.60+20237C>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34437967 | |||||||
| chr9:34437973 | C | G | 30 | a0001c0001t0005g0004 a0001c0001t0005g0023 a0001c0001t0005g0024 others(27): Show |
31 | HG00558.hp1 HG01891.hp2 HG01928.hp1 others(28): Show |
intron_variant | MODIFIER | c.60+20231G>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34437973 | |||||||
| chr9:34437986 | G | A | 30 | a0001c0001t0005g0004 a0001c0001t0005g0023 a0001c0001t0005g0024 others(27): Show |
31 | HG00558.hp1 HG01891.hp2 HG01928.hp1 others(28): Show |
intron_variant | MODIFIER | c.60+20218C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34437986 | |||||||
| chr9:34438004 | G | A | 3 | a0001c0001t0003g0107 a0001c0001t0003g0110 a0001c0001t0018g0111 |
3 | HG01496.hp1 HG02647.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.60+20200C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34438004 | |||||||
| chr9:34438015 | C | G | 3 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 |
3 | HG02615.hp2 HG02809.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.60+20189G>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34438015 | |||||||
| chr9:34438021 | A | G | 50 | a0001c0001t0001g0059 a0001c0001t0001g0083 a0001c0001t0001g0084 others(47): Show |
51 | HG00280.hp2 HG01074.hp1 HG01081.hp1 others(48): Show |
intron_variant | MODIFIER | c.60+20183T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34438021 | |||||||
| chr9:34438113 | C | G | 1 | a0001c0001t0002g0192 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.60+20091G>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34438113 | |||||||
| chr9:34438122 | G | A | 1 | a0001c0001t0001g0191 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.60+20082C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34438122 | |||||||
| chr9:34438144 | G | A | 1 | a0001c0001t0001g0109 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.60+20060C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34438144 | |||||||
| chr9:34438246 | G | A | 193 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(190): Show |
207 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.60+19958C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34438246 | |||||||
| chr9:34438266 | A | G | 1 | a0001c0001t0007g0223 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.60+19938T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34438266 | |||||||
| chr9:34438275 | A | AC | 6 | a0001c0001t0001g0345 a0001c0001t0002g0123 a0001c0001t0002g0138 others(3): Show |
6 | HG01167.hp1 HG02080.hp2 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.60+19928dupG | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34438275 | |||||||
| chr9:34438292 | G | A | 1 | a0001c0001t0002g0239 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.60+19912C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34438292 | |||||||
| chr9:34438309 | A | G | 2 | a0001c0002t0001g0358 a0001c0002t0001g0359 |
2 | HG01099.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.60+19895T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34438309 | |||||||
| chr9:34438315 | G | A | 1 | a0001c0001t0024g0104 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.60+19889C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34438315 | |||||||
| chr9:34438343 | G | A | 1 | a0001c0001t0001g0274 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.60+19861C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34438343 | |||||||
| chr9:34438374 | G | A | 1 | a0001c0001t0002g0155 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.60+19830C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34438374 | |||||||
| chr9:34438378 | C | T | 4 | a0001c0001t0001g0236 a0001c0001t0001g0245 a0001c0001t0001g0246 others(1): Show |
4 | HG00639.hp1 HG01168.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.60+19826G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34438378 | |||||||
| chr9:34438446 | G | C | 1 | a0001c0001t0006g0089 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.60+19758C>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34438446 | |||||||
| chr9:34438456 | T | C | 1 | a0001c0001t0017g0103 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.60+19748A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34438456 | |||||||
| chr9:34438471 | C | G | 72 | a0001c0001t0001g0116 a0001c0001t0001g0119 a0001c0001t0001g0185 others(69): Show |
73 | HG00423.hp1 HG00597.hp2 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.60+19733G>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34438471 | |||||||
| chr9:34438521 | G | GT | 30 | a0001c0001t0005g0004 a0001c0001t0005g0023 a0001c0001t0005g0024 others(27): Show |
31 | HG00558.hp1 HG01891.hp2 HG01928.hp1 others(28): Show |
intron_variant | MODIFIER | c.60+19682dupA | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34438521 | |||||||
| chr9:34438681 | G | A | 32 | a0001c0001t0002g0203 a0001c0001t0005g0004 a0001c0001t0005g0023 others(29): Show |
33 | HG00558.hp1 HG01891.hp1 HG01891.hp2 others(30): Show |
intron_variant | MODIFIER | c.60+19523C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34438681 | |||||||
| chr9:34438799 | G | C | 1 | a0001c0001t0005g0047 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.60+19405C>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34438799 | |||||||
| chr9:34438873 | A | T | 2 | a0001c0002t0001g0358 a0001c0002t0001g0359 |
2 | HG01099.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.60+19331T>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34438873 | |||||||
| chr9:34438885 | T | C | 1 | a0001c0001t0001g0275 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.60+19319A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34438885 | |||||||
| chr9:34439017 | G | A | 4 | a0001c0001t0005g0026 a0001c0001t0005g0028 a0001c0001t0005g0029 others(1): Show |
4 | HG02027.hp1 NA18945.hp2 NA18991.hp1 others(1): Show |
intron_variant | MODIFIER | c.60+19187C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34439017 | |||||||
| chr9:34439068 | C | T | 1 | a0001c0001t0001g0015 | 2 | HG00544.hp1 HG02071.hp2 |
intron_variant | MODIFIER | c.60+19136G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34439068 | |||||||
| chr9:34439175 | C | T | 1 | a0001c0001t0023g0162 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.60+19029G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34439175 | |||||||
| chr9:34439257 | G | A | 1 | a0001c0001t0001g0241 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.60+18947C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34439257 | |||||||
| chr9:34439308 | G | A | 1 | a0001c0001t0001g0291 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.60+18896C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34439308 | |||||||
| chr9:34439342 | A | C | 1 | a0001c0001t0002g0138 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.60+18862T>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34439342 | |||||||
| chr9:34439593 | A | G | 1 | a0001c0001t0002g0122 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.60+18611T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34439593 | |||||||
| chr9:34439662 | G | A | 6 | a0001c0001t0002g0204 a0001c0001t0002g0205 a0001c0001t0002g0206 others(3): Show |
6 | HG01109.hp2 HG02615.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.60+18542C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34439662 | |||||||
| chr9:34439750 | G | A | 1 | a0001c0001t0012g0052 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.60+18454C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34439750 | |||||||
| chr9:34439785 | G | A | 2 | a0001c0001t0001g0230 a0001c0001t0001g0231 |
2 | NA18942.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.60+18419C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34439785 | |||||||
| chr9:34439978 | C | T | 1 | a0001c0001t0002g0122 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.60+18226G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34439978 | |||||||
| chr9:34439994 | G | A | 1 | a0001c0001t0020g0276 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.60+18210C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34439994 | |||||||
| chr9:34440037 | A | T | 1 | a0001c0001t0001g0244 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.60+18167T>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34440037 | |||||||
| chr9:34440078 | A | G | 17 | a0001c0001t0002g0157 a0001c0001t0002g0158 a0001c0001t0003g0309 others(14): Show |
18 | HG00423.hp1 HG02056.hp2 HG02083.hp1 others(15): Show |
intron_variant | MODIFIER | c.60+18126T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34440078 | |||||||
| chr9:34440174 | A | C | 1 | a0001c0001t0001g0099 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.60+18030T>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34440174 | |||||||
| chr9:34440239 | C | T | 1 | a0001c0001t0002g0113 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.60+17965G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34440239 | |||||||
| chr9:34440315 | G | A | 1 | a0001c0001t0015g0022 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.60+17889C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34440315 | |||||||
| chr9:34440477 | T | C | 1 | a0001c0001t0006g0093 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.60+17727A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34440477 | |||||||
| chr9:34440503 | C | T | 3 | a0001c0001t0003g0107 a0001c0001t0003g0110 a0001c0001t0018g0111 |
3 | HG01496.hp1 HG02647.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.60+17701G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34440503 | |||||||
| chr9:34440564 | T | C | 4 | a0001c0001t0004g0210 a0001c0001t0004g0211 a0001c0001t0004g0212 others(1): Show |
4 | NA18950.hp1 NA18974.hp1 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.60+17640A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34440564 | |||||||
| chr9:34440625 | C | T | 9 | a0001c0001t0001g0059 a0001c0001t0001g0083 a0001c0001t0001g0084 others(6): Show |
9 | HG01175.hp2 HG02055.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.60+17579G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34440625 | |||||||
| chr9:34440800 | G | A | 94 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0014 others(91): Show |
105 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.60+17404C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34440800 | |||||||
| chr9:34440844 | C | A | 25 | a0001c0001t0001g0124 a0001c0001t0002g0007 a0001c0001t0002g0008 others(22): Show |
27 | HG00323.hp2 HG00609.hp2 HG00621.hp2 others(24): Show |
intron_variant | MODIFIER | c.60+17360G>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34440844 | |||||||
| chr9:34440850 | C | CA | 16 | a0001c0001t0001g0119 a0001c0001t0001g0278 a0001c0001t0001g0279 others(13): Show |
16 | HG00423.hp1 HG01106.hp1 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.60+17353dupT | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34440850 | |||||||
| chr9:34440850 | CA | C | 16 | a0001c0001t0001g0228 a0001c0001t0001g0242 a0001c0001t0001g0243 others(13): Show |
16 | HG01070.hp2 HG01496.hp1 HG02027.hp1 others(13): Show |
intron_variant | MODIFIER | c.60+17353delT | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34440850 | |||||||
| chr9:34440867 | A | T | 26 | a0001c0001t0005g0004 a0001c0001t0005g0024 a0001c0001t0005g0025 others(23): Show |
27 | HG00558.hp1 HG01928.hp1 HG01934.hp1 others(24): Show |
intron_variant | MODIFIER | c.60+17337T>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34440867 | |||||||
| chr9:34440868 | A | T | 32 | a0001c0001t0001g0355 a0001c0001t0002g0356 a0001c0001t0005g0004 others(29): Show |
33 | HG00558.hp1 HG01891.hp2 HG01928.hp1 others(30): Show |
intron_variant | MODIFIER | c.60+17336T>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34440868 | |||||||
| chr9:34440869 | T | A | 1 | a0001c0001t0017g0103 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.60+17335A>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34440869 | |||||||
| chr9:34441025 | C | T | 2 | a0001c0001t0003g0312 a0001c0001t0003g0313 |
2 | NA18960.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.60+17179G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34441025 | |||||||
| chr9:34441098 | C | T | 2 | a0001c0001t0003g0312 a0001c0001t0003g0313 |
2 | NA18960.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.60+17106G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34441098 | |||||||
| chr9:34441226 | G | T | 1 | a0001c0001t0007g0156 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.60+16978C>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34441226 | |||||||
| chr9:34441268 | C | T | 9 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(6): Show |
9 | HG01891.hp1 HG02615.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.60+16936G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34441268 | |||||||
| chr9:34441288 | A | G | 8 | a0001c0001t0007g0347 a0001c0001t0007g0348 a0001c0001t0007g0349 others(5): Show |
8 | HG00099.hp1 HG00741.hp1 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.60+16916T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34441288 | |||||||
| chr9:34441532 | A | G | 1 | a0001c0001t0002g0155 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.60+16672T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34441532 | |||||||
| chr9:34441582 | C | T | 2 | a0001c0001t0002g0153 a0001c0001t0002g0154 |
2 | HG02293.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.60+16622G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34441582 | |||||||
| chr9:34441653 | T | G | 1 | a0001c0001t0001g0305 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.60+16551A>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34441653 | |||||||
| chr9:34442131 | G | A | 1 | a0001c0001t0002g0215 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.60+16073C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34442131 | |||||||
| chr9:34442346 | A | C | 1 | a0001c0001t0001g0241 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.60+15858T>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34442346 | |||||||
| chr9:34442422 | C | T | 1 | a0001c0001t0001g0217 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.60+15782G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34442422 | |||||||
| chr9:34442633 | C | T | 6 | a0001c0001t0001g0006 a0001c0001t0001g0106 a0001c0001t0001g0108 others(3): Show |
7 | HG01243.hp1 HG02451.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.60+15571G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34442633 | |||||||
| chr9:34442684 | CA | C | 192 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(189): Show |
206 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.60+15519delT | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34442684 | |||||||
| chr9:34442697 | C | A | 3 | a0001c0001t0002g0204 a0001c0001t0002g0207 a0001c0001t0002g0208 |
3 | HG01109.hp2 HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.60+15507G>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34442697 | |||||||
| chr9:34442699 | A | C | 1 | a0001c0001t0003g0107 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.60+15505T>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34442699 | |||||||
| chr9:34442830 | T | A | 9 | a0001c0001t0001g0281 a0001c0001t0001g0282 a0001c0001t0001g0283 others(6): Show |
9 | HG00423.hp2 HG02015.hp2 HG03491.hp2 others(6): Show |
intron_variant | MODIFIER | c.60+15374A>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34442830 | |||||||
| chr9:34442957 | T | G | 1 | a0001c0001t0003g0340 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.60+15247A>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34442957 | |||||||
| chr9:34443193 | T | C | 6 | a0001c0001t0006g0143 a0001c0001t0006g0148 a0001c0001t0009g0144 others(3): Show |
6 | HG02559.hp1 HG02818.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.60+15011A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34443193 | |||||||
| chr9:34443491 | T | G | 94 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0014 others(91): Show |
105 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.60+14713A>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34443491 | |||||||
| chr9:34443528 | A | T | 1 | a0001c0001t0007g0353 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.60+14676T>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34443528 | |||||||
| chr9:34443793 | A | G | 1 | a0001c0001t0001g0240 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.60+14411T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34443793 | |||||||
| chr9:34444171 | T | C | 1 | a0001c0001t0001g0097 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.60+14033A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34444171 | |||||||
| chr9:34444223 | T | C | 1 | a0001c0001t0001g0289 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.60+13981A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34444223 | |||||||
| chr9:34444579 | C | T | 1 | a0001c0001t0017g0103 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.60+13625G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34444579 | |||||||
| chr9:34444587 | A | G | 1 | a0001c0001t0017g0103 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.60+13617T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34444587 | |||||||
| chr9:34444606 | T | C | 3 | a0001c0001t0005g0023 a0001c0001t0005g0048 a0001c0001t0011g0050 |
3 | HG01891.hp2 HG02559.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.60+13598A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34444606 | |||||||
| chr9:34444717 | G | A | 52 | a0001c0001t0001g0059 a0001c0001t0001g0083 a0001c0001t0001g0084 others(49): Show |
53 | HG00280.hp2 HG01074.hp1 HG01081.hp1 others(50): Show |
intron_variant | MODIFIER | c.60+13487C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34444717 | |||||||
| chr9:34444784 | C | A | 30 | a0001c0001t0005g0004 a0001c0001t0005g0023 a0001c0001t0005g0024 others(27): Show |
31 | HG00558.hp1 HG01891.hp2 HG01928.hp1 others(28): Show |
intron_variant | MODIFIER | c.60+13420G>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34444784 | |||||||
| chr9:34444951 | G | C | 1 | a0001c0001t0001g0097 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.60+13253C>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34444951 | |||||||
| chr9:34445176 | T | C | 193 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(190): Show |
207 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.60+13028A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34445176 | |||||||
| chr9:34445187 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.60+13017G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34445187 | |||||||
| chr9:34445262 | T | C | 30 | a0001c0001t0005g0004 a0001c0001t0005g0023 a0001c0001t0005g0024 others(27): Show |
31 | HG00558.hp1 HG01891.hp2 HG01928.hp1 others(28): Show |
intron_variant | MODIFIER | c.60+12942A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34445262 | |||||||
| chr9:34445283 | A | G | 1 | a0001c0001t0004g0058 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.60+12921T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34445283 | |||||||
| chr9:34445564 | T | C | 3 | a0001c0001t0002g0239 a0001c0001t0013g0091 a0001c0001t0013g0092 |
3 | HG03516.hp1 NA19240.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.60+12640A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34445564 | |||||||
| chr9:34445624 | G | A | 1 | a0001c0001t0007g0353 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.60+12580C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34445624 | |||||||
| chr9:34445719 | C | A | 1 | a0001c0001t0002g0216 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.60+12485G>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34445719 | |||||||
| chr9:34445734 | C | T | 8 | a0001c0001t0007g0347 a0001c0001t0007g0348 a0001c0001t0007g0349 others(5): Show |
8 | HG00099.hp1 HG00741.hp1 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.60+12470G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34445734 | |||||||
| chr9:34445875 | A | T | 1 | a0001c0001t0002g0239 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.60+12329T>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34445875 | |||||||
| chr9:34446164 | C | T | 2 | a0001c0001t0002g0120 a0001c0001t0002g0141 |
2 | HG01109.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.60+12040G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34446164 | |||||||
| chr9:34446172 | C | CA | 8 | a0001c0001t0001g0116 a0001c0001t0001g0217 a0001c0001t0001g0218 others(5): Show |
8 | HG01358.hp2 HG01361.hp1 HG03942.hp2 others(5): Show |
intron_variant | MODIFIER | c.60+12031dupT | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34446172 | |||||||
| chr9:34446172 | C | CAA | 6 | a0001c0001t0006g0143 a0001c0001t0006g0148 a0001c0001t0009g0144 others(3): Show |
6 | HG02559.hp1 HG02818.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.60+12030_60+12031d others(4): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34446172 | |||||||
| chr9:34446172 | CA | C | 177 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0014 others(174): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.60+12031delT | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34446172 | |||||||
| chr9:34446201 | G | T | 8 | a0001c0001t0007g0347 a0001c0001t0007g0348 a0001c0001t0007g0349 others(5): Show |
8 | HG00099.hp1 HG00741.hp1 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.60+12003C>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34446201 | |||||||
| chr9:34446209 | A | G | 4 | a0001c0001t0001g0315 a0001c0001t0002g0316 a0001c0001t0003g0314 others(1): Show |
4 | HG00323.hp1 HG02027.hp2 HG02040.hp2 others(1): Show |
intron_variant | MODIFIER | c.60+11995T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34446209 | |||||||
| chr9:34446273 | A | T | 2 | a0001c0001t0001g0237 a0001c0001t0002g0238 |
2 | NA18957.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.60+11931T>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34446273 | |||||||
| chr9:34446324 | G | A | 1 | a0001c0001t0011g0050 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.60+11880C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34446324 | |||||||
| chr9:34446355 | T | C | 30 | a0001c0001t0005g0004 a0001c0001t0005g0023 a0001c0001t0005g0024 others(27): Show |
31 | HG00558.hp1 HG01891.hp2 HG01928.hp1 others(28): Show |
intron_variant | MODIFIER | c.60+11849A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34446355 | |||||||
| chr9:34446646 | C | G | 8 | a0001c0001t0007g0347 a0001c0001t0007g0348 a0001c0001t0007g0349 others(5): Show |
8 | HG00099.hp1 HG00741.hp1 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.60+11558G>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34446646 | |||||||
| chr9:34446721 | C | G | 25 | a0001c0001t0001g0124 a0001c0001t0002g0007 a0001c0001t0002g0008 others(22): Show |
27 | HG00323.hp2 HG00609.hp2 HG00621.hp2 others(24): Show |
intron_variant | MODIFIER | c.60+11483G>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34446721 | |||||||
| chr9:34446979 | T | C | 30 | a0001c0001t0005g0004 a0001c0001t0005g0023 a0001c0001t0005g0024 others(27): Show |
31 | HG00558.hp1 HG01891.hp2 HG01928.hp1 others(28): Show |
intron_variant | MODIFIER | c.60+11225A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34446979 | |||||||
| chr9:34447342 | C | T | 25 | a0001c0001t0001g0124 a0001c0001t0002g0007 a0001c0001t0002g0008 others(22): Show |
27 | HG00323.hp2 HG00609.hp2 HG00621.hp2 others(24): Show |
intron_variant | MODIFIER | c.60+10862G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34447342 | |||||||
| chr9:34447361 | T | C | 94 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0014 others(91): Show |
105 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.60+10843A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34447361 | |||||||
| chr9:34447384 | C | T | 1 | a0001c0001t0024g0104 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.60+10820G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34447384 | |||||||
| chr9:34447457 | T | C | 94 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0014 others(91): Show |
105 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.60+10747A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34447457 | |||||||
| chr9:34447506 | G | A | 8 | a0001c0001t0007g0347 a0001c0001t0007g0348 a0001c0001t0007g0349 others(5): Show |
8 | HG00099.hp1 HG00741.hp1 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.60+10698C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34447506 | |||||||
| chr9:34447560 | G | A | 95 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0014 others(92): Show |
106 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.60+10644C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34447560 | |||||||
| chr9:34447569 | G | T | 1 | a0001c0001t0004g0057 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.60+10635C>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34447569 | |||||||
| chr9:34447825 | A | G | 1 | a0001c0001t0024g0104 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.60+10379T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34447825 | |||||||
| chr9:34447876 | AT | A | 48 | a0001c0001t0001g0006 a0001c0001t0001g0097 a0001c0001t0001g0106 others(45): Show |
50 | HG00099.hp1 HG00558.hp1 HG00741.hp1 others(47): Show |
intron_variant | MODIFIER | c.60+10327delA | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34447876 | |||||||
| chr9:34447921 | G | C | 94 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0014 others(91): Show |
105 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.60+10283C>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34447921 | |||||||
| chr9:34447991 | C | T | 1 | a0001c0001t0002g0151 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.60+10213G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34447991 | |||||||
| chr9:34448038 | C | G | 30 | a0001c0001t0005g0004 a0001c0001t0005g0023 a0001c0001t0005g0024 others(27): Show |
31 | HG00558.hp1 HG01891.hp2 HG01928.hp1 others(28): Show |
intron_variant | MODIFIER | c.60+10166G>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34448038 | |||||||
| chr9:34448072 | TG | T | 30 | a0001c0001t0005g0004 a0001c0001t0005g0023 a0001c0001t0005g0024 others(27): Show |
31 | HG00558.hp1 HG01891.hp2 HG01928.hp1 others(28): Show |
intron_variant | MODIFIER | c.60+10131delC | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34448072 | |||||||
| chr9:34448248 | C | A | 1 | a0001c0001t0002g0221 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.60+9956G>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34448248 | |||||||
| chr9:34448306 | C | T | 3 | a0001c0001t0001g0015 a0001c0001t0001g0293 a0001c0001t0001g0294 |
4 | HG00438.hp2 HG00544.hp1 HG02071.hp2 others(1): Show |
intron_variant | MODIFIER | c.60+9898G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34448306 | |||||||
| chr9:34448443 | C | T | 8 | a0001c0001t0007g0347 a0001c0001t0007g0348 a0001c0001t0007g0349 others(5): Show |
8 | HG00099.hp1 HG00741.hp1 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.60+9761G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34448443 | |||||||
| chr9:34448612 | C | A | 1 | a0001c0001t0001g0097 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.60+9592G>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34448612 | |||||||
| chr9:34448764 | A | C | 1 | a0001c0001t0002g0150 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.60+9440T>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34448764 | |||||||
| chr9:34448779 | G | T | 1 | a0001c0001t0001g0002 | 4 | NA18964.hp1 NA18985.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.60+9425C>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34448779 | |||||||
| chr9:34448861 | G | A | 16 | a0001c0001t0002g0335 a0001c0001t0002g0336 a0001c0001t0003g0016 others(13): Show |
19 | HG00544.hp2 HG00558.hp2 HG00673.hp1 others(16): Show |
intron_variant | MODIFIER | c.60+9343C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34448861 | |||||||
| chr9:34448973 | C | T | 1 | a0001c0001t0003g0312 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.60+9231G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34448973 | |||||||
| chr9:34448993 | G | GA | 10 | a0001c0001t0003g0110 a0001c0001t0007g0347 a0001c0001t0007g0348 others(7): Show |
10 | HG00099.hp1 HG00741.hp1 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.60+9210_60+9211ins others(1): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34448993 | |||||||
| chr9:34448993 | G | GAA | 7 | a0001c0001t0001g0006 a0001c0001t0001g0100 a0001c0001t0001g0106 others(4): Show |
8 | HG01243.hp1 HG02451.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.60+9210_60+9211ins others(2): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34448993 | |||||||
| chr9:34448993 | G | GAAA | 10 | a0001c0001t0001g0099 a0001c0001t0001g0101 a0001c0001t0001g0109 others(7): Show |
10 | HG01255.hp2 HG01891.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.60+9210_60+9211ins others(3): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34448993 | |||||||
| chr9:34448994 | G | A | 152 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(149): Show |
165 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(162): Show |
intron_variant | MODIFIER | c.60+9210C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34448994 | |||||||
| chr9:34448994 | G | GA | 10 | a0001c0001t0002g0141 a0001c0001t0002g0222 a0001c0001t0002g0343 others(7): Show |
11 | HG00673.hp1 HG01109.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.60+9209dupT | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34448994 | |||||||
| chr9:34448994 | G | GAAA | 33 | a0001c0001t0001g0059 a0001c0001t0001g0083 a0001c0001t0001g0084 others(30): Show |
34 | HG00280.hp2 HG01074.hp1 HG01081.hp1 others(31): Show |
intron_variant | MODIFIER | c.60+9207_60+9209dup others(3): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34448994 | |||||||
| chr9:34448994 | G | GAAAA | 7 | a0001c0001t0002g0079 a0001c0001t0004g0076 a0001c0001t0006g0077 others(4): Show |
7 | HG02257.hp1 HG02280.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.60+9206_60+9209dup others(4): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34448994 | |||||||
| chr9:34449005 | A | C | 30 | a0001c0001t0005g0004 a0001c0001t0005g0023 a0001c0001t0005g0024 others(27): Show |
31 | HG00558.hp1 HG01891.hp2 HG01928.hp1 others(28): Show |
intron_variant | MODIFIER | c.60+9199T>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34449005 | |||||||
| chr9:34449006 | A | AAG | 92 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0014 others(89): Show |
103 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.60+9197_60+9198ins others(2): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34449006 | |||||||
| chr9:34449009 | C | A | 193 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(190): Show |
207 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.60+9195G>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34449009 | |||||||
| chr9:34449330 | G | A | 199 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(196): Show |
213 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.60+8874C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34449330 | |||||||
| chr9:34449470 | T | C | 1 | a0001c0001t0006g0093 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.60+8734A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34449470 | |||||||
| chr9:34449505 | C | G | 2 | a0001c0001t0003g0312 a0001c0001t0003g0313 |
2 | NA18960.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.60+8699G>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34449505 | |||||||
| chr9:34449530 | C | T | 3 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 |
3 | HG02615.hp2 HG02809.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.60+8674G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34449530 | |||||||
| chr9:34449842 | G | A | 1 | a0001c0001t0007g0223 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.60+8362C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34449842 | |||||||
| chr9:34450049 | C | T | 1 | a0001c0001t0026g0149 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.60+8155G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34450049 | |||||||
| chr9:34450091 | C | G | 30 | a0001c0001t0005g0004 a0001c0001t0005g0023 a0001c0001t0005g0024 others(27): Show |
31 | HG00558.hp1 HG01891.hp2 HG01928.hp1 others(28): Show |
intron_variant | MODIFIER | c.60+8113G>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34450091 | |||||||
| chr9:34450091 | C | T | 6 | a0001c0001t0006g0143 a0001c0001t0006g0148 a0001c0001t0009g0144 others(3): Show |
6 | HG02559.hp1 HG02818.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.60+8113G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34450091 | |||||||
| chr9:34450221 | G | A | 8 | a0001c0001t0007g0347 a0001c0001t0007g0348 a0001c0001t0007g0349 others(5): Show |
8 | HG00099.hp1 HG00741.hp1 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.60+7983C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34450221 | |||||||
| chr9:34450245 | G | T | 1 | a0001c0001t0001g0236 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.60+7959C>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34450245 | |||||||
| chr9:34450293 | A | T | 94 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0014 others(91): Show |
105 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.60+7911T>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34450293 | |||||||
| chr9:34450308 | C | CA | 71 | a0001c0001t0001g0059 a0001c0001t0001g0083 a0001c0001t0001g0084 others(68): Show |
73 | HG00280.hp2 HG00558.hp1 HG01074.hp1 others(70): Show |
intron_variant | MODIFIER | c.60+7895dupT | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34450308 | |||||||
| chr9:34450308 | C | CAA | 10 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(7): Show |
10 | HG01891.hp1 HG02615.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.60+7894_60+7895dup others(2): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34450308 | |||||||
| chr9:34450308 | CA | C | 94 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0014 others(91): Show |
105 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.60+7895delT | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34450308 | |||||||
| chr9:34450505 | C | T | 1 | a0001c0001t0004g0142 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.60+7699G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34450505 | |||||||
| chr9:34450534 | T | C | 1 | a0001c0001t0002g0292 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.60+7670A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34450534 | |||||||
| chr9:34450570 | C | T | 3 | a0001c0001t0001g0233 a0001c0001t0001g0234 a0001c0001t0001g0235 |
3 | HG02735.hp1 HG03490.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.60+7634G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34450570 | |||||||
| chr9:34450597 | T | G | 1 | a0001c0001t0006g0093 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.60+7607A>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34450597 | |||||||
| chr9:34450646 | C | T | 1 | a0001c0001t0017g0103 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.60+7558G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34450646 | |||||||
| chr9:34450707 | C | T | 1 | a0001c0001t0003g0314 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.60+7497G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34450707 | |||||||
| chr9:34450757 | G | A | 1 | a0001c0001t0002g0227 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.60+7447C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34450757 | |||||||
| chr9:34450772 | C | G | 9 | a0001c0001t0001g0006 a0001c0001t0001g0106 a0001c0001t0001g0108 others(6): Show |
10 | HG01243.hp1 HG01496.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.60+7432G>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34450772 | |||||||
| chr9:34450799 | T | C | 1 | a0001c0001t0001g0116 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.60+7405A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34450799 | |||||||
| chr9:34450942 | A | G | 8 | a0001c0001t0007g0347 a0001c0001t0007g0348 a0001c0001t0007g0349 others(5): Show |
8 | HG00099.hp1 HG00741.hp1 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.60+7262T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34450942 | |||||||
| chr9:34450943 | T | C | 30 | a0001c0001t0005g0004 a0001c0001t0005g0023 a0001c0001t0005g0024 others(27): Show |
31 | HG00558.hp1 HG01891.hp2 HG01928.hp1 others(28): Show |
intron_variant | MODIFIER | c.60+7261A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34450943 | |||||||
| chr9:34450963 | C | T | 2 | a0001c0001t0005g0024 a0001c0001t0005g0025 |
2 | NA18940.hp2 NA18965.hp2 |
intron_variant | MODIFIER | c.60+7241G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34450963 | |||||||
| chr9:34451009 | G | A | 50 | a0001c0001t0001g0059 a0001c0001t0001g0083 a0001c0001t0001g0084 others(47): Show |
51 | HG00280.hp2 HG01074.hp1 HG01081.hp1 others(48): Show |
intron_variant | MODIFIER | c.60+7195C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34451009 | |||||||
| chr9:34451118 | A | G | 1 | a0001c0001t0005g0023 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.60+7086T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34451118 | |||||||
| chr9:34451225 | A | G | 1 | a0001c0001t0003g0344 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.60+6979T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34451225 | |||||||
| chr9:34451347 | A | C | 30 | a0001c0001t0005g0004 a0001c0001t0005g0023 a0001c0001t0005g0024 others(27): Show |
31 | HG00558.hp1 HG01891.hp2 HG01928.hp1 others(28): Show |
intron_variant | MODIFIER | c.60+6857T>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34451347 | |||||||
| chr9:34451385 | C | G | 8 | a0001c0001t0007g0347 a0001c0001t0007g0348 a0001c0001t0007g0349 others(5): Show |
8 | HG00099.hp1 HG00741.hp1 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.60+6819G>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34451385 | |||||||
| chr9:34451414 | G | A | 1 | a0001c0001t0017g0103 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.60+6790C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34451414 | |||||||
| chr9:34451574 | G | A | 4 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0001g0230 others(1): Show |
4 | NA18747.hp2 NA18942.hp2 NA18952.hp2 others(1): Show |
intron_variant | MODIFIER | c.60+6630C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34451574 | |||||||
| chr9:34451810 | C | A | 30 | a0001c0001t0005g0004 a0001c0001t0005g0023 a0001c0001t0005g0024 others(27): Show |
31 | HG00558.hp1 HG01891.hp2 HG01928.hp1 others(28): Show |
intron_variant | MODIFIER | c.60+6394G>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34451810 | |||||||
| chr9:34451952 | G | C | 50 | a0001c0001t0001g0059 a0001c0001t0001g0083 a0001c0001t0001g0084 others(47): Show |
51 | HG00280.hp2 HG01074.hp1 HG01081.hp1 others(48): Show |
intron_variant | MODIFIER | c.60+6252C>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34451952 | |||||||
| chr9:34452034 | C | A | 1 | a0001c0001t0001g0094 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.60+6170G>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34452034 | |||||||
| chr9:34452098 | TAAC | T | 94 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0014 others(91): Show |
105 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.60+6103_60+6105del others(3): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34452098 | |||||||
| chr9:34452270 | G | C | 193 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(190): Show |
207 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.60+5934C>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34452270 | |||||||
| chr9:34452290 | A | G | 1 | a0001c0001t0006g0056 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.60+5914T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34452290 | |||||||
| chr9:34452533 | C | T | 2 | a0001c0001t0012g0052 a0001c0001t0012g0053 |
2 | HG03195.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.60+5671G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34452533 | |||||||
| chr9:34452650 | C | G | 2 | a0001c0001t0003g0312 a0001c0001t0003g0313 |
2 | NA18960.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.60+5554G>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34452650 | |||||||
| chr9:34452707 | T | C | 1 | a0001c0001t0021g0354 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.60+5497A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34452707 | |||||||
| chr9:34452928 | C | T | 1 | a0001c0001t0003g0311 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.60+5276G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34452928 | |||||||
| chr9:34452977 | A | C | 25 | a0001c0001t0001g0124 a0001c0001t0002g0007 a0001c0001t0002g0008 others(22): Show |
27 | HG00323.hp2 HG00609.hp2 HG00621.hp2 others(24): Show |
intron_variant | MODIFIER | c.60+5227T>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34452977 | |||||||
| chr9:34453006 | G | A | 1 | a0001c0001t0003g0344 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.60+5198C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34453006 | |||||||
| chr9:34453009 | T | C | 94 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0014 others(91): Show |
105 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.60+5195A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34453009 | |||||||
| chr9:34453105 | A | G | 1 | a0001c0001t0002g0232 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.60+5099T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34453105 | |||||||
| chr9:34453269 | T | C | 1 | a0001c0001t0001g0345 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.60+4935A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34453269 | |||||||
| chr9:34453279 | G | A | 8 | a0001c0001t0007g0347 a0001c0001t0007g0348 a0001c0001t0007g0349 others(5): Show |
8 | HG00099.hp1 HG00741.hp1 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.60+4925C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34453279 | |||||||
| chr9:34453295 | G | A | 1 | a0001c0001t0011g0051 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.60+4909C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34453295 | |||||||
| chr9:34453592 | G | A | 94 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0014 others(91): Show |
105 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.60+4612C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34453592 | |||||||
| chr9:34454166 | G | A | 1 | a0001c0001t0017g0103 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.60+4038C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34454166 | |||||||
| chr9:34454219 | T | C | 2 | a0001c0001t0002g0096 a0001c0001t0010g0095 |
2 | HG03195.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.60+3985A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34454219 | |||||||
| chr9:34454584 | A | G | 1 | a0001c0001t0001g0119 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.60+3620T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34454584 | |||||||
| chr9:34454585 | A | G | 1 | a0001c0001t0001g0106 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.60+3619T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34454585 | |||||||
| chr9:34454799 | A | T | 1 | a0001c0001t0006g0077 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.60+3405T>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34454799 | |||||||
| chr9:34454968 | C | T | 1 | a0001c0001t0006g0118 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.60+3236G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34454968 | |||||||
| chr9:34455005 | C | T | 8 | a0001c0001t0007g0347 a0001c0001t0007g0348 a0001c0001t0007g0349 others(5): Show |
8 | HG00099.hp1 HG00741.hp1 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.60+3199G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34455005 | |||||||
| chr9:34455036 | G | A | 1 | a0001c0001t0017g0103 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.60+3168C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34455036 | |||||||
| chr9:34455069 | T | G | 1 | a0001c0001t0024g0104 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.60+3135A>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34455069 | |||||||
| chr9:34455252 | C | G | 9 | a0001c0001t0001g0006 a0001c0001t0001g0106 a0001c0001t0001g0108 others(6): Show |
10 | HG01243.hp1 HG01496.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.60+2952G>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34455252 | |||||||
| chr9:34455297 | CGAG | C | 2 | a0001c0001t0003g0019 a0001c0004t0003g0346 |
3 | NA18964.hp2 NA18983.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.60+2904_60+2906del others(3): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34455297 | |||||||
| chr9:34455448 | T | G | 30 | a0001c0001t0005g0004 a0001c0001t0005g0023 a0001c0001t0005g0024 others(27): Show |
31 | HG00558.hp1 HG01891.hp2 HG01928.hp1 others(28): Show |
intron_variant | MODIFIER | c.60+2756A>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34455448 | |||||||
| chr9:34455465 | A | AT | 66 | a0001c0001t0001g0006 a0001c0001t0001g0083 a0001c0001t0001g0084 others(63): Show |
68 | HG00558.hp1 HG01243.hp1 HG01496.hp1 others(65): Show |
intron_variant | MODIFIER | c.60+2738dupA | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34455465 | |||||||
| chr9:34455465 | A | ATT | 25 | a0001c0001t0001g0059 a0001c0001t0004g0005 a0001c0001t0004g0057 others(22): Show |
26 | HG00280.hp2 HG01074.hp1 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.60+2737_60+2738dup others(2): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34455465 | |||||||
| chr9:34455814 | G | A | 15 | a0001c0001t0001g0015 a0001c0001t0001g0293 a0001c0001t0001g0294 others(12): Show |
16 | HG00438.hp2 HG00544.hp1 HG01993.hp2 others(13): Show |
intron_variant | MODIFIER | c.60+2390C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34455814 | |||||||
| chr9:34456054 | G | A | 2 | a0001c0001t0001g0307 a0001c0001t0001g0308 |
2 | NA19054.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.60+2150C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34456054 | |||||||
| chr9:34456107 | C | T | 1 | a0001c0001t0006g0056 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.60+2097G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34456107 | |||||||
| chr9:34456184 | C | A | 1 | a0001c0001t0004g0105 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.60+2020G>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34456184 | |||||||
| chr9:34456272 | T | G | 43 | a0001c0001t0001g0315 a0001c0001t0001g0324 a0001c0001t0001g0345 others(40): Show |
50 | HG00323.hp1 HG00544.hp2 HG00558.hp2 others(47): Show |
intron_variant | MODIFIER | c.60+1932A>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34456272 | |||||||
| chr9:34456580 | G | A | 8 | a0001c0001t0007g0347 a0001c0001t0007g0348 a0001c0001t0007g0349 others(5): Show |
8 | HG00099.hp1 HG00741.hp1 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.60+1624C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34456580 | |||||||
| chr9:34456600 | A | C | 52 | a0001c0001t0001g0059 a0001c0001t0001g0083 a0001c0001t0001g0084 others(49): Show |
53 | HG00280.hp2 HG01074.hp1 HG01081.hp1 others(50): Show |
intron_variant | MODIFIER | c.60+1604T>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34456600 | |||||||
| chr9:34456720 | A | G | 2 | a0001c0001t0002g0054 a0001c0001t0002g0055 |
2 | NA18947.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.60+1484T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34456720 | |||||||
| chr9:34456726 | G | A | 2 | a0001c0001t0001g0355 a0001c0001t0002g0356 |
2 | NA18984.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.60+1478C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34456726 | |||||||
| chr9:34456886 | C | T | 30 | a0001c0001t0005g0004 a0001c0001t0005g0023 a0001c0001t0005g0024 others(27): Show |
31 | HG00558.hp1 HG01891.hp2 HG01928.hp1 others(28): Show |
intron_variant | MODIFIER | c.60+1318G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34456886 | |||||||
| chr9:34457198 | G | A | 1 | a0001c0001t0006g0357 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.60+1006C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34457198 | |||||||
| chr9:34457262 | C | G | 2 | a0001c0001t0002g0054 a0001c0001t0002g0055 |
2 | NA18947.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.60+942G>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34457262 | |||||||
| chr9:34457854 | C | A | 12 | a0001c0001t0001g0021 a0001c0001t0001g0360 a0001c0001t0001g0362 others(9): Show |
14 | HG01099.hp2 HG01261.hp1 HG01358.hp1 others(11): Show |
intron_variant | MODIFIER | c.60+350G>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34457854 | |||||||
| chr9:34458075 | T | C | 1 | a0001c0001t0007g0368 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.60+129A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34458075 |