Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 84915 |
| ensemblid | ENSG00000139438.6 |
| hgncid | 25915 |
| symbol | FAM222A |
| name | family with sequence similarity 222 member A |
| refseq_nuc | NM_032829.3 |
| refseq_prot | NP_116218.2 |
| ensembl_nuc | ENST00000538780.2 |
| ensembl_prot | ENSP00000443292.1 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 109713825 |
| end | 109770495 |
| strand | + |
| ver | v1.2 |
| region | chr12:109713825-109770495 |
| region5000 | chr12:109708825-109775495 |
| regionname0 | FAM222A_chr12_109713825_109770495 |
| regionname5000 | FAM222A_chr12_109708825_109775495 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 452 | 351 | 85 | 56 | 152 | 16 | 40 | 114 | FAM222A_chr12_109708825_109775495 | FAM222A | MLACL others(447): Show |
chr12 | 109708825 | 109775495 |
| a0002 | 0/0 | 452 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | MLACL others(447): Show |
chr12 | 109708825 | 109775495 |
| a0003 | 0/0 | 452 | 5 | 0 | 0 | 5 | 0 | 0 | 3 | FAM222A_chr12_109708825_109775495 | FAM222A | MLACL others(447): Show |
chr12 | 109708825 | 109775495 |
| a0004 | 0/0 | 452 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | FAM222A_chr12_109708825_109775495 | FAM222A | MLACL others(447): Show |
chr12 | 109708825 | 109775495 |
| a0005 | 0/0 | 452 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAM222A_chr12_109708825_109775495 | FAM222A | MLACL others(447): Show |
chr12 | 109708825 | 109775495 |
| a0006 | 0/0 | 452 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAM222A_chr12_109708825_109775495 | FAM222A | MLACL others(447): Show |
chr12 | 109708825 | 109775495 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1356 | 334 | 76 | 52 | 152 | 15 | 37 | FAM222A_chr12_109708825_109775495 | FAM222A | ATGCT others(1351): Show |
chr12 | 109708825 | 109775495 | ||
| a0001c0002 | 0/0 | 1356 | 7 | 6 | 1 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | ATGCT others(1351): Show |
chr12 | 109708825 | 109775495 | ||
| a0001c0005 | 0/0 | 1356 | 2 | 0 | 0 | 0 | 0 | 2 | FAM222A_chr12_109708825_109775495 | FAM222A | ATGCT others(1351): Show |
chr12 | 109708825 | 109775495 | ||
| a0001c0006 | 0/0 | 1356 | 2 | 2 | 0 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | ATGCT others(1351): Show |
chr12 | 109708825 | 109775495 | ||
| a0001c0007 | 0/0 | 1356 | 2 | 0 | 2 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | ATGCT others(1351): Show |
chr12 | 109708825 | 109775495 | ||
| a0001c0009 | 0/0 | 1356 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | ATGCT others(1351): Show |
chr12 | 109708825 | 109775495 | ||
| a0001c0012 | 0/0 | 1356 | 1 | 0 | 0 | 0 | 1 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | ATGCT others(1351): Show |
chr12 | 109708825 | 109775495 | ||
| a0001c0013 | 0/0 | 1356 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222A_chr12_109708825_109775495 | FAM222A | ATGCT others(1351): Show |
chr12 | 109708825 | 109775495 | ||
| a0001c0015 | 0/0 | 1356 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | ATGCT others(1351): Show |
chr12 | 109708825 | 109775495 | ||
| a0002c0004 | 0/0 | 1356 | 5 | 5 | 0 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | ATGCT others(1351): Show |
chr12 | 109708825 | 109775495 | ||
| a0003c0003 | 0/0 | 1356 | 5 | 0 | 0 | 5 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | ATGCT others(1351): Show |
chr12 | 109708825 | 109775495 | ||
| a0004c0008 | 0/0 | 1356 | 2 | 0 | 0 | 2 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | ATGCT others(1351): Show |
chr12 | 109708825 | 109775495 | ||
| a0004c0010 | 0/0 | 1356 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | ATGCT others(1351): Show |
chr12 | 109708825 | 109775495 | ||
| a0005c0011 | 0/0 | 1356 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | ATGCT others(1351): Show |
chr12 | 109708825 | 109775495 | ||
| a0006c0014 | 0/0 | 1356 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | ATGCT others(1351): Show |
chr12 | 109708825 | 109775495 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 3685 | 171 | 31 | 32 | 76 | 10 | 21 | FAM222A_chr12_109708825_109775495 | FAM222A | AGTCG others(3680): Show |
chr12 | 109708825 | 109775495 |
| a0001c0001t0002 | 0/0 | 3685 | 52 | 17 | 4 | 29 | 1 | 1 | FAM222A_chr12_109708825_109775495 | FAM222A | AGTCG others(3680): Show |
chr12 | 109708825 | 109775495 |
| a0001c0001t0003 | 0/0 | 3685 | 39 | 0 | 0 | 36 | 0 | 3 | FAM222A_chr12_109708825_109775495 | FAM222A | AGTCG others(3680): Show |
chr12 | 109708825 | 109775495 |
| a0001c0001t0004 | 1/0 | 3685 | 23 | 8 | 7 | 4 | 0 | 3 | FAM222A_chr12_109708825_109775495 | FAM222A | AGTCG others(3680): Show |
chr12 | 109708825 | 109775495 |
| a0001c0001t0005 | 0/0 | 3685 | 9 | 9 | 0 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | AGTCG others(3680): Show |
chr12 | 109708825 | 109775495 |
| a0001c0001t0006 | 0/0 | 3685 | 7 | 6 | 0 | 0 | 1 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | AGTCG others(3680): Show |
chr12 | 109708825 | 109775495 |
| a0001c0001t0007 | 0/0 | 3685 | 5 | 1 | 0 | 1 | 1 | 2 | FAM222A_chr12_109708825_109775495 | FAM222A | AGTCG others(3680): Show |
chr12 | 109708825 | 109775495 |
| a0001c0001t0009 | 0/0 | 3685 | 4 | 0 | 4 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | AGTCG others(3680): Show |
chr12 | 109708825 | 109775495 |
| a0001c0001t0010 | 0/0 | 3685 | 3 | 0 | 1 | 0 | 0 | 2 | FAM222A_chr12_109708825_109775495 | FAM222A | AGTCG others(3680): Show |
chr12 | 109708825 | 109775495 |
| a0001c0001t0011 | 0/0 | 3685 | 2 | 0 | 0 | 0 | 0 | 2 | FAM222A_chr12_109708825_109775495 | FAM222A | AGTCG others(3680): Show |
chr12 | 109708825 | 109775495 |
| a0001c0001t0012 | 0/0 | 3685 | 2 | 0 | 0 | 0 | 2 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | AGTCG others(3680): Show |
chr12 | 109708825 | 109775495 |
| a0001c0001t0013 | 0/0 | 3685 | 2 | 0 | 0 | 0 | 0 | 2 | FAM222A_chr12_109708825_109775495 | FAM222A | AGTCG others(3680): Show |
chr12 | 109708825 | 109775495 |
| a0001c0001t0014 | 0/0 | 3667 | 2 | 0 | 2 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | AGTCG others(3662): Show |
chr12 | 109708825 | 109775495 |
| a0001c0001t0015 | 0/0 | 3685 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | AGTCG others(3680): Show |
chr12 | 109708825 | 109775495 |
| a0001c0001t0016 | 0/0 | 3685 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | AGTCG others(3680): Show |
chr12 | 109708825 | 109775495 |
| a0001c0001t0017 | 0/0 | 3685 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222A_chr12_109708825_109775495 | FAM222A | AGTCG others(3680): Show |
chr12 | 109708825 | 109775495 |
| a0001c0001t0018 | 0/0 | 3685 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | AGTCG others(3680): Show |
chr12 | 109708825 | 109775495 |
| a0001c0001t0019 | 0/0 | 3685 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | AGTCG others(3680): Show |
chr12 | 109708825 | 109775495 |
| a0001c0001t0020 | 0/0 | 3685 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | AGTCG others(3680): Show |
chr12 | 109708825 | 109775495 |
| a0001c0001t0021 | 0/0 | 3685 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | AGTCG others(3680): Show |
chr12 | 109708825 | 109775495 |
| a0001c0001t0023 | 0/0 | 3685 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | AGTCG others(3680): Show |
chr12 | 109708825 | 109775495 |
| a0001c0001t0024 | 0/0 | 3685 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | AGTCG others(3680): Show |
chr12 | 109708825 | 109775495 |
| a0001c0001t0025 | 0/0 | 3685 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | AGTCG others(3680): Show |
chr12 | 109708825 | 109775495 |
| a0001c0001t0026 | 0/0 | 3685 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | AGTCG others(3680): Show |
chr12 | 109708825 | 109775495 |
| a0001c0001t0027 | 0/0 | 3667 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | AGTCG others(3662): Show |
chr12 | 109708825 | 109775495 |
| a0001c0001t0028 | 0/0 | 3685 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | AGTCG others(3680): Show |
chr12 | 109708825 | 109775495 |
| a0001c0002t0001 | 0/0 | 3685 | 4 | 4 | 0 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | AGTCG others(3680): Show |
chr12 | 109708825 | 109775495 |
| a0001c0002t0002 | 0/0 | 3685 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | AGTCG others(3680): Show |
chr12 | 109708825 | 109775495 |
| a0001c0002t0006 | 0/0 | 3685 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | AGTCG others(3680): Show |
chr12 | 109708825 | 109775495 |
| a0001c0002t0022 | 0/0 | 3685 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | AGTCG others(3680): Show |
chr12 | 109708825 | 109775495 |
| a0001c0005t0003 | 0/0 | 3685 | 2 | 0 | 0 | 0 | 0 | 2 | FAM222A_chr12_109708825_109775495 | FAM222A | AGTCG others(3680): Show |
chr12 | 109708825 | 109775495 |
| a0001c0006t0002 | 0/0 | 3685 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | AGTCG others(3680): Show |
chr12 | 109708825 | 109775495 |
| a0001c0006t0007 | 0/0 | 3685 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | AGTCG others(3680): Show |
chr12 | 109708825 | 109775495 |
| a0001c0007t0001 | 0/0 | 3685 | 2 | 0 | 2 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | AGTCG others(3680): Show |
chr12 | 109708825 | 109775495 |
| a0001c0009t0004 | 0/0 | 3685 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | AGTCG others(3680): Show |
chr12 | 109708825 | 109775495 |
| a0001c0012t0007 | 0/0 | 3685 | 1 | 0 | 0 | 0 | 1 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | AGTCG others(3680): Show |
chr12 | 109708825 | 109775495 |
| a0001c0013t0001 | 0/0 | 3685 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222A_chr12_109708825_109775495 | FAM222A | AGTCG others(3680): Show |
chr12 | 109708825 | 109775495 |
| a0001c0015t0001 | 0/0 | 3685 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | AGTCG others(3680): Show |
chr12 | 109708825 | 109775495 |
| a0002c0004t0008 | 0/0 | 3684 | 5 | 5 | 0 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | AGTCG others(3679): Show |
chr12 | 109708825 | 109775495 |
| a0003c0003t0001 | 0/0 | 3685 | 4 | 0 | 0 | 4 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | AGTCG others(3680): Show |
chr12 | 109708825 | 109775495 |
| a0003c0003t0003 | 0/0 | 3685 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | AGTCG others(3680): Show |
chr12 | 109708825 | 109775495 |
| a0004c0008t0003 | 0/0 | 3685 | 2 | 0 | 0 | 2 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | AGTCG others(3680): Show |
chr12 | 109708825 | 109775495 |
| a0004c0010t0003 | 0/0 | 3685 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | AGTCG others(3680): Show |
chr12 | 109708825 | 109775495 |
| a0005c0011t0002 | 0/0 | 3685 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | AGTCG others(3680): Show |
chr12 | 109708825 | 109775495 |
| a0006c0014t0001 | 0/0 | 3685 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | AGTCG others(3680): Show |
chr12 | 109708825 | 109775495 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0079 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0002g0002 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0002g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0002g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0002g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0002g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0002g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0002g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0002g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0002g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0002g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0002g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0002g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0002g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0002g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0002g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0002g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0002g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0002g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0002g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0002g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0002g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0002g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0003g0001 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0003g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0003g0013 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0003g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0003g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0003g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0003g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0003g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0003g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0003g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0003g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0003g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0003g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0003g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0003g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0004g0004 | 1/0 | 3 | 0 | 2 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0004g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0004g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0004g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0004g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0004g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0004g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0004g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0004g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0004g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0004g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0004g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0004g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0004g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0004g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0004g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0004g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0004g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0004g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0004g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0004g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0005g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0005g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0005g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0005g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0005g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0005g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0005g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0005g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0006g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0006g0321 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0006g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0006g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0006g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0006g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0007g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0007g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0007g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0007g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0007g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0009g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0009g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0009g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0009g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0010g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0010g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0010g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0011g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0011g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0012g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0012g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0013g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0013g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0014g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0014g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0015g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0016g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0017g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0018g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0019g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0020g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0021g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0023g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0024g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0025g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0026g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0027g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0001t0028g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0002t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0002t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0002t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0002t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0002t0002g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0002t0006g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0002t0022g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0005t0003g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0005t0003g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0006t0002g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0006t0007g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0007t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0007t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0009t0004g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0012t0007g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0013t0001g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0001c0015t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0002c0004t0008g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0002c0004t0008g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0002c0004t0008g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0002c0004t0008g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0002c0004t0008g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0003c0003t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0003c0003t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0003c0003t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0003c0003t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0003c0003t0003g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0004c0008t0003g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0004c0010t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0005c0011t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| a0006c0014t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0335 | EUR | GBR | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG00099 | hp2 | a0001 | c0001 | t0006 | g0321 | EUR | GBR | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0334 | EUR | GBR | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0328 | EUR | GBR | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0276 | EUR | FIN | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0181 | EUR | FIN | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0173 | EUR | FIN | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0109 | EUR | FIN | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG00408 | hp1 | a0001 | c0001 | t0003 | g0242 | EAS | CHS | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG00408 | hp2 | a0001 | c0001 | t0026 | g0278 | EAS | CHS | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG00423 | hp1 | a0001 | c0001 | t0003 | g0229 | EAS | CHS | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG00423 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | CHS | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | CHS | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | CHS | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | CHS | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | CHS | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | CHS | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | CHS | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0284 | EAS | CHS | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | CHS | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG00609 | hp1 | a0001 | c0001 | t0003 | g0247 | EAS | CHS | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0285 | EAS | CHS | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG00639 | hp1 | a0001 | c0001 | t0004 | g0004 | AMR | PUR | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0258 | AMR | PUR | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG00738 | hp1 | a0001 | c0002 | t0022 | g0099 | AMR | PUR | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG00741 | hp1 | a0001 | c0001 | t0004 | g0004 | AMR | PUR | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG00741 | hp2 | a0001 | c0007 | t0001 | g0162 | AMR | PUR | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG01070 | hp1 | a0001 | c0001 | t0004 | g0254 | AMR | PUR | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG01070 | hp2 | a0001 | c0001 | t0014 | g0287 | AMR | PUR | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG01071 | hp1 | a0001 | c0001 | t0004 | g0253 | AMR | PUR | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG01074 | hp2 | a0001 | c0001 | t0009 | g0028 | AMR | PUR | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0308 | AMR | PUR | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0315 | AMR | PUR | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG01167 | hp2 | a0001 | c0001 | t0009 | g0037 | AMR | PUR | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | PUR | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | PUR | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG01169 | hp2 | a0001 | c0001 | t0009 | g0033 | AMR | PUR | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG01175 | hp2 | a0001 | c0001 | t0004 | g0250 | AMR | PUR | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG01192 | hp1 | a0001 | c0001 | t0009 | g0034 | AMR | PUR | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG01192 | hp2 | a0001 | c0001 | t0025 | g0336 | AMR | PUR | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG01256 | hp1 | a0001 | c0001 | t0010 | g0108 | AMR | CLM | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | CLM | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0305 | AMR | CLM | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | CLM | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | CLM | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG01261 | hp2 | a0001 | c0007 | t0001 | g0192 | AMR | CLM | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | CLM | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | CLM | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0329 | AMR | CLM | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0306 | AMR | CLM | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0300 | AMR | CLM | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG01361 | hp2 | a0001 | c0009 | t0004 | g0252 | AMR | CLM | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG01433 | hp1 | a0001 | c0001 | t0004 | g0257 | AMR | CLM | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | CLM | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | CLM | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | CLM | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG01516 | hp1 | a0001 | c0001 | t0007 | g0027 | EUR | IBS | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG01516 | hp2 | a0001 | c0001 | t0012 | g0112 | EUR | IBS | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG01517 | hp1 | a0001 | c0001 | t0012 | g0136 | EUR | IBS | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0121 | EUR | IBS | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | ACB | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG01884 | hp2 | a0001 | c0006 | t0002 | g0304 | AFR | ACB | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG01891 | hp1 | a0001 | c0001 | t0027 | g0313 | AFR | ACB | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG01891 | hp2 | a0002 | c0004 | t0008 | g0054 | AFR | ACB | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG01928 | hp1 | a0001 | c0001 | t0004 | g0066 | AMR | PEL | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | PEL | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG01934 | hp2 | a0001 | c0001 | t0014 | g0286 | AMR | PEL | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0264 | AMR | PEL | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PEL | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PEL | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | PEL | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | PEL | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | PEL | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | KHV | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | KHV | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | KHV | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0275 | EAS | KHV | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | KHV | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG02056 | hp1 | a0001 | c0001 | t0007 | g0025 | EAS | KHV | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG02056 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | KHV | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | KHV | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG02071 | hp2 | a0001 | c0001 | t0028 | g0233 | EAS | KHV | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG02074 | hp1 | a0001 | c0001 | t0003 | g0317 | EAS | KHV | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG02074 | hp2 | a0003 | c0003 | t0001 | g0211 | EAS | KHV | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | KHV | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG02080 | hp2 | a0001 | c0001 | t0019 | g0082 | EAS | KHV | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG02083 | hp1 | a0001 | c0001 | t0003 | g0319 | EAS | KHV | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | KHV | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | KHV | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | KHV | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0277 | EAS | KHV | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG02257 | hp1 | a0001 | c0002 | t0001 | g0309 | AFR | ACB | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0292 | AFR | ACB | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG02258 | hp1 | a0001 | c0001 | t0004 | g0251 | AFR | ACB | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG02258 | hp2 | a0001 | c0001 | t0004 | g0060 | AFR | ACB | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG02280 | hp1 | a0001 | c0001 | t0006 | g0327 | AFR | ACB | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | ACB | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | ACB | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0267 | AFR | ACB | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG02523 | hp1 | a0001 | c0001 | t0003 | g0015 | EAS | KHV | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG02523 | hp2 | a0003 | c0003 | t0001 | g0218 | EAS | KHV | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0295 | AFR | GWD | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG02572 | hp2 | a0001 | c0002 | t0001 | g0183 | AFR | GWD | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG02615 | hp1 | a0001 | c0001 | t0004 | g0061 | AFR | GWD | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG02615 | hp2 | a0001 | c0001 | t0005 | g0044 | AFR | GWD | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0263 | AFR | GWD | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG02630 | hp1 | a0001 | c0001 | t0004 | g0059 | AFR | GWD | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG02630 | hp2 | a0001 | c0001 | t0004 | g0065 | AFR | GWD | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG02647 | hp2 | a0001 | c0002 | t0002 | g0261 | AFR | GWD | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG02698 | hp1 | a0001 | c0013 | t0001 | g0332 | SAS | PJL | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0148 | SAS | PJL | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | GWD | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG02717 | hp2 | a0001 | c0001 | t0006 | g0018 | AFR | GWD | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG02735 | hp1 | a0001 | c0001 | t0010 | g0104 | SAS | PJL | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0171 | SAS | PJL | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG02738 | hp1 | a0001 | c0001 | t0004 | g0069 | SAS | PJL | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0299 | AFR | GWD | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG02809 | hp2 | a0002 | c0004 | t0008 | g0053 | AFR | GWD | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG02818 | hp1 | a0001 | c0001 | t0005 | g0005 | AFR | GWD | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | GWD | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG02886 | hp1 | a0002 | c0004 | t0008 | g0023 | AFR | GWD | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0262 | AFR | GWD | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | GWD | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0266 | AFR | GWD | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | ESN | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG02922 | hp2 | a0001 | c0006 | t0007 | g0030 | AFR | ESN | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | ESN | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG02965 | hp2 | a0001 | c0001 | t0006 | g0323 | AFR | ESN | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG02970 | hp1 | a0001 | c0001 | t0015 | g0020 | AFR | ESN | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | ESN | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0268 | AFR | ESN | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | PJL | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG03017 | hp2 | a0001 | c0001 | t0011 | g0036 | SAS | PJL | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | GWD | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0291 | AFR | GWD | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG03098 | hp1 | a0002 | c0004 | t0008 | g0316 | AFR | MSL | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | MSL | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | ESN | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | ESN | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG03139 | hp1 | a0001 | c0001 | t0005 | g0040 | AFR | ESN | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0260 | AFR | ESN | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG03195 | hp1 | a0001 | c0001 | t0020 | g0022 | AFR | ESN | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0290 | AFR | ESN | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0259 | AFR | MSL | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG03209 | hp2 | a0001 | c0001 | t0016 | g0021 | AFR | MSL | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0303 | AFR | MSL | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0265 | AFR | MSL | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | MSL | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG03453 | hp2 | a0001 | c0001 | t0005 | g0042 | AFR | MSL | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | MSL | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG03486 | hp2 | a0001 | c0001 | t0005 | g0005 | AFR | MSL | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG03491 | hp1 | a0001 | c0001 | t0011 | g0031 | SAS | PJL | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0174 | SAS | PJL | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0196 | SAS | PJL | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG03516 | hp2 | a0001 | c0001 | t0004 | g0058 | AFR | ESN | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG03540 | hp1 | a0001 | c0001 | t0006 | g0018 | AFR | GWD | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG03579 | hp1 | a0001 | c0002 | t0006 | g0324 | AFR | MSL | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | MSL | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG03654 | hp1 | a0001 | c0005 | t0003 | g0234 | SAS | PJL | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0333 | SAS | PJL | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG03669 | hp1 | a0001 | c0001 | t0003 | g0307 | SAS | PJL | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0209 | SAS | PJL | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0130 | SAS | STU | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0337 | SAS | STU | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG03704 | hp1 | a0001 | c0001 | t0004 | g0249 | SAS | PJL | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0246 | SAS | PJL | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG03710 | hp2 | a0001 | c0001 | t0013 | g0256 | SAS | PJL | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG03831 | hp1 | a0001 | c0005 | t0003 | g0227 | SAS | BEB | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG03831 | hp2 | a0001 | c0001 | t0010 | g0120 | SAS | BEB | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0338 | SAS | BEB | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0331 | SAS | BEB | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0203 | SAS | BEB | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG03927 | hp2 | a0001 | c0001 | t0007 | g0029 | SAS | BEB | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0311 | SAS | BEB | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG03942 | hp2 | a0001 | c0001 | t0007 | g0035 | SAS | BEB | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | STU | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG04115 | hp2 | a0001 | c0001 | t0013 | g0255 | SAS | STU | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0296 | SAS | BEB | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | BEB | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG04199 | hp1 | a0001 | c0001 | t0004 | g0248 | SAS | STU | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG04199 | hp2 | a0001 | c0001 | t0003 | g0013 | SAS | STU | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0186 | SAS | STU | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0204 | SAS | STU | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0013 | SAS | STU | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG04228 | hp2 | a0001 | c0001 | t0017 | g0322 | SAS | STU | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA18522 | hp1 | a0001 | c0001 | t0004 | g0330 | AFR | YRI | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | YRI | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA18612 | hp1 | a0001 | c0001 | t0003 | g0236 | EAS | CHB | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | CHB | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | CHB | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA18747 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | CHB | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | YRI | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | YRI | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0271 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA18940 | hp2 | a0004 | c0008 | t0003 | g0012 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA18942 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA18945 | hp2 | a0001 | c0001 | t0021 | g0213 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA18947 | hp1 | a0005 | c0011 | t0002 | g0289 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA18948 | hp2 | a0001 | c0001 | t0004 | g0067 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA18949 | hp2 | a0003 | c0003 | t0001 | g0164 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA18950 | hp2 | a0001 | c0001 | t0003 | g0228 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0270 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA18952 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA18953 | hp2 | a0001 | c0001 | t0003 | g0222 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0294 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA18957 | hp2 | a0003 | c0003 | t0003 | g0226 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA18961 | hp2 | a0004 | c0010 | t0003 | g0237 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA18963 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA18966 | hp1 | a0003 | c0003 | t0001 | g0217 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA18966 | hp2 | a0001 | c0001 | t0003 | g0046 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA18968 | hp1 | a0001 | c0001 | t0003 | g0241 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0301 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA18969 | hp1 | a0001 | c0001 | t0003 | g0232 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA18970 | hp2 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA18971 | hp1 | a0001 | c0001 | t0003 | g0225 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0281 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA18974 | hp1 | a0001 | c0001 | t0003 | g0320 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0279 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA18979 | hp2 | a0001 | c0001 | t0003 | g0231 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA18980 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0269 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0298 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0274 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA18983 | hp2 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0282 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA18986 | hp2 | a0001 | c0001 | t0003 | g0240 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA18990 | hp2 | a0001 | c0001 | t0003 | g0230 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA18992 | hp1 | a0001 | c0001 | t0003 | g0235 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA18995 | hp2 | a0001 | c0001 | t0003 | g0318 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA19006 | hp2 | a0001 | c0001 | t0003 | g0238 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0272 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA19009 | hp1 | a0001 | c0001 | t0004 | g0312 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA19009 | hp2 | a0006 | c0014 | t0001 | g0007 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA19030 | hp1 | a0001 | c0001 | t0005 | g0038 | AFR | LWK | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA19030 | hp2 | a0001 | c0001 | t0004 | g0063 | AFR | LWK | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | LWK | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA19043 | hp2 | a0001 | c0002 | t0001 | g0172 | AFR | LWK | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA19056 | hp1 | a0001 | c0001 | t0004 | g0064 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0293 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA19064 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0280 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA19065 | hp2 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0273 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA19067 | hp2 | a0001 | c0001 | t0003 | g0224 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA19075 | hp1 | a0001 | c0001 | t0018 | g0073 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA19075 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0283 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA19077 | hp2 | a0001 | c0001 | t0003 | g0045 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA19080 | hp1 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA19083 | hp2 | a0001 | c0001 | t0003 | g0239 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA19085 | hp2 | a0004 | c0008 | t0003 | g0012 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA19088 | hp1 | a0001 | c0001 | t0003 | g0223 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0297 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA19090 | hp2 | a0001 | c0001 | t0024 | g0070 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA19091 | hp2 | a0001 | c0001 | t0004 | g0068 | EAS | JPT | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0288 | AFR | YRI | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA19240 | hp2 | a0001 | c0001 | t0005 | g0043 | AFR | YRI | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA20129 | hp1 | a0001 | c0001 | t0005 | g0041 | AFR | ASW | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | ASW | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0200 | EUR | TSI | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0062 | EUR | TSI | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0191 | EUR | TSI | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA20805 | hp2 | a0001 | c0012 | t0007 | g0032 | EUR | TSI | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG01123 | hp1 | a0001 | c0001 | t0023 | g0138 | AMR | CLM | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | ACB | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0314 | AFR | ACB | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG02486 | hp1 | a0002 | c0004 | t0008 | g0056 | AFR | ACB | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | ACB | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG02559 | hp1 | a0001 | c0001 | t0006 | g0325 | AFR | ACB | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG02559 | hp2 | a0001 | c0015 | t0001 | g0310 | AFR | ACB | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG03471 | hp1 | a0001 | c0001 | t0007 | g0019 | AFR | MSL | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG03471 | hp2 | a0001 | c0002 | t0001 | g0151 | AFR | MSL | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0302 | AFR | USA | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| HG06807 | hp2 | a0001 | c0001 | t0006 | g0326 | AFR | USA | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | USA | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | USA | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA21309 | hp1 | a0001 | c0001 | t0005 | g0039 | AFR | LWK | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | LWK | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0079 | REF | REF | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0004 | g0004 | REF | REF | FAM222A_chr12_109708825_109775495 | FAM222A | chr12 | 109708825 | 109775495 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:109768026 | A | G | 1 | a0002 | 5 | HG01891.hp2 HG02486.hp1 HG02809.hp2 others(2): Show |
missense_variant | MODERATE | c.97A>G | p.Ser33Gly | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 3/3 | 1216/3685 | 97/1359 | 33/452 | chr12 | 109768026 | |||
| chr12:109768285 | C | T | 1 | a0003 | 5 | HG02074.hp2 HG02523.hp2 NA18949.hp2 others(2): Show |
missense_variant | MODERATE | c.356C>T | p.Ala119Val | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 3/3 | 1475/3685 | 356/1359 | 119/452 | chr12 | 109768285 | |||
| chr12:109768488 | C | T | 1 | a0004 | 2 | NA18940.hp2 NA19085.hp2 |
missense_variant | MODERATE | c.559C>T | p.Arg187Trp | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 3/3 | 1678/3685 | 559/1359 | 187/452 | chr12 | 109768488 | |||
| chr12:109768489 | G | A | 1 | a0004 | 1 | NA18961.hp2 | missense_variant | MODERATE | c.560G>A | p.Arg187Gln | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 3/3 | 1679/3685 | 560/1359 | 187/452 | chr12 | 109768489 | |||
| chr12:109768764 | G | A | 1 | a0005 | 1 | NA18947.hp1 | missense_variant | MODERATE | c.835G>A | p.Ala279Thr | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 3/3 | 1954/3685 | 835/1359 | 279/452 | chr12 | 109768764 | |||
| chr12:109768830 | C | T | 1 | a0006 | 1 | NA19009.hp2 | missense_variant | MODERATE | c.901C>T | p.Arg301Cys | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 3/3 | 2020/3685 | 901/1359 | 301/452 | chr12 | 109768830 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:109768019 | G | A | 1 | a0001c0009 | 1 | HG01361.hp2 | synonymous_variant | LOW | c.90G>A | p.Ala30Ala | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 3/3 | 1209/3685 | 90/1359 | 30/452 | chr12 | 109768019 | |||
| chr12:109768346 | C | T | 1 | a0001c0015 | 1 | HG02559.hp2 | synonymous_variant | LOW | c.417C>T | p.Ala139Ala | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 3/3 | 1536/3685 | 417/1359 | 139/452 | chr12 | 109768346 | |||
| chr12:109768484 | G | A | 1 | a0001c0005 | 2 | HG03654.hp1 HG03831.hp1 |
synonymous_variant | LOW | c.555G>A | p.Pro185Pro | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 3/3 | 1674/3685 | 555/1359 | 185/452 | chr12 | 109768484 | |||
| chr12:109768682 | C | T | 1 | a0001c0007 | 2 | HG00741.hp2 HG01261.hp2 |
synonymous_variant | LOW | c.753C>T | p.Pro251Pro | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 3/3 | 1872/3685 | 753/1359 | 251/452 | chr12 | 109768682 | |||
| chr12:109768955 | C | A | 1 | a0001c0012 | 1 | NA20805.hp2 | synonymous_variant | LOW | c.1026C>A | p.Gly342Gly | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 3/3 | 2145/3685 | 1026/1359 | 342/452 | chr12 | 109768955 | |||
| chr12:109768973 | G | C | 2 | a0001c0002 a0002c0004 |
12 | HG00738.hp1 HG01891.hp2 HG02257.hp1 others(9): Show |
synonymous_variant | LOW | c.1044G>C | p.Pro348Pro | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 3/3 | 2163/3685 | 1044/1359 | 348/452 | chr12 | 109768973 | |||
| chr12:109769043 | C | T | 1 | a0001c0006 | 2 | HG01884.hp2 HG02922.hp2 |
synonymous_variant | LOW | c.1114C>T | p.Leu372Leu | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 3/3 | 2233/3685 | 1114/1359 | 372/452 | chr12 | 109769043 | |||
| chr12:109769241 | C | T | 1 | a0001c0013 | 1 | HG02698.hp1 | synonymous_variant | LOW | c.1312C>T | p.Leu438Leu | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 3/3 | 2431/3685 | 1312/1359 | 438/452 | chr12 | 109769241 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:109713839 | G | C | 7 | a0001c0001t0007 a0001c0001t0009 a0001c0001t0011 others(4): Show |
15 | HG01074.hp2 HG01167.hp2 HG01169.hp2 others(12): Show |
5_prime_UTR_variant | MODIFIER | c.-1105G>C | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/3 | 30308 | chr12 | 109713839 | ||||||
| chr12:109713859 | C | T | 1 | a0001c0001t0010 | 3 | HG01256.hp1 HG02735.hp1 HG03831.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-1085C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/3 | chr12 | 109713859 | |||||||
| chr12:109713986 | G | C | 1 | a0001c0001t0011 | 2 | HG03017.hp2 HG03491.hp1 |
5_prime_UTR_variant | MODIFIER | c.-958G>C | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/3 | 30161 | chr12 | 109713986 | ||||||
| chr12:109714161 | C | T | 1 | a0001c0001t0028 | 1 | HG02071.hp2 | 5_prime_UTR_variant | MODIFIER | c.-783C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/3 | 29986 | chr12 | 109714161 | ||||||
| chr12:109714190 | G | A | 1 | a0001c0001t0017 | 1 | HG04228.hp2 | 5_prime_UTR_variant | MODIFIER | c.-754G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/3 | 29957 | chr12 | 109714190 | ||||||
| chr12:109714196 | CCCGCTGC others(11): Show |
C | 2 | a0001c0001t0014 a0001c0001t0027 |
3 | HG01070.hp2 HG01891.hp1 HG01934.hp2 |
5_prime_UTR_variant | MODIFIER | c.-731_-714delCGCCGC others(12): Show |
FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/3 | 29917 | INFO_REALIGN_3_PRIME | chr12 | 109714196 | |||||
| chr12:109714207 | CGCCGCCG others(5): Show |
C | 7 | a0001c0001t0007 a0001c0001t0009 a0001c0001t0011 others(4): Show |
15 | HG01074.hp2 HG01167.hp2 HG01169.hp2 others(12): Show |
5_prime_UTR_variant | MODIFIER | c.-723_-712delCCGCCG others(6): Show |
FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/3 | 29915 | INFO_REALIGN_3_PRIME | chr12 | 109714207 | |||||
| chr12:109714353 | G | C | 1 | a0001c0001t0018 | 1 | NA19075.hp1 | 5_prime_UTR_variant | MODIFIER | c.-591G>C | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/3 | 29794 | chr12 | 109714353 | ||||||
| chr12:109714355 | C | T | 7 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0014 others(4): Show |
67 | HG00280.hp1 HG00408.hp2 HG00597.hp1 others(64): Show |
5_prime_UTR_variant | MODIFIER | c.-589C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/3 | 29792 | chr12 | 109714355 | ||||||
| chr12:109714411 | C | T | 1 | a0001c0001t0009 | 4 | HG01074.hp2 HG01167.hp2 HG01169.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-533C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/3 | 29736 | chr12 | 109714411 | ||||||
| chr12:109714495 | C | T | 1 | a0001c0001t0025 | 1 | HG01192.hp2 | 5_prime_UTR_variant | MODIFIER | c.-449C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/3 | 29652 | chr12 | 109714495 | ||||||
| chr12:109714532 | C | G | 1 | a0001c0001t0005 | 9 | HG02615.hp2 HG02818.hp1 HG03139.hp1 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-412C>G | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/3 | 29615 | chr12 | 109714532 | ||||||
| chr12:109714679 | C | T | 17 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(14): Show |
123 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(120): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-265C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/3 | chr12 | 109714679 | |||||||
| chr12:109714745 | C | T | 3 | a0001c0001t0006 a0001c0001t0017 a0001c0002t0006 |
9 | HG00099.hp2 HG02280.hp1 HG02559.hp1 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-199C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/3 | 29402 | chr12 | 109714745 | ||||||
| chr12:109714801 | G | C | 41 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(38): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
5_prime_UTR_variant | MODIFIER | c.-143G>C | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/3 | 29346 | chr12 | 109714801 | ||||||
| chr12:109769317 | G | A | 1 | a0001c0001t0015 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*29G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 3/3 | 29 | chr12 | 109769317 | ||||||
| chr12:109769340 | C | T | 1 | a0001c0001t0023 | 1 | HG01123.hp1 | 3_prime_UTR_variant | MODIFIER | c.*52C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 3/3 | 52 | chr12 | 109769340 | ||||||
| chr12:109769367 | G | T | 1 | a0001c0001t0012 | 2 | HG01516.hp2 HG01517.hp1 |
3_prime_UTR_variant | MODIFIER | c.*79G>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 3/3 | 79 | chr12 | 109769367 | ||||||
| chr12:109769429 | G | A | 1 | a0001c0001t0026 | 1 | HG00408.hp2 | 3_prime_UTR_variant | MODIFIER | c.*141G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 3/3 | 141 | chr12 | 109769429 | ||||||
| chr12:109769515 | G | A | 1 | a0001c0001t0019 | 1 | HG02080.hp2 | 3_prime_UTR_variant | MODIFIER | c.*227G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 3/3 | 227 | chr12 | 109769515 | ||||||
| chr12:109769536 | C | T | 1 | a0001c0002t0022 | 1 | HG00738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*248C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 3/3 | 248 | chr12 | 109769536 | ||||||
| chr12:109769727 | C | T | 2 | a0001c0002t0022 a0002c0004t0008 |
6 | HG00738.hp1 HG01891.hp2 HG02486.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*439C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 3/3 | 439 | chr12 | 109769727 | ||||||
| chr12:109770002 | T | C | 2 | a0001c0001t0016 a0001c0001t0020 |
2 | HG03195.hp1 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*714T>C | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 3/3 | 714 | chr12 | 109770002 | ||||||
| chr12:109770023 | A | G | 2 | a0001c0002t0022 a0002c0004t0008 |
6 | HG00738.hp1 HG01891.hp2 HG02486.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*735A>G | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 3/3 | 735 | chr12 | 109770023 | ||||||
| chr12:109770102 | C | T | 1 | a0001c0001t0013 | 2 | HG03710.hp2 HG04115.hp2 |
3_prime_UTR_variant | MODIFIER | c.*814C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 3/3 | 814 | chr12 | 109770102 | ||||||
| chr12:109770166 | C | T | 1 | a0001c0001t0024 | 1 | NA19090.hp2 | 3_prime_UTR_variant | MODIFIER | c.*878C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 3/3 | 878 | chr12 | 109770166 | ||||||
| chr12:109770250 | C | T | 1 | a0001c0002t0022 | 1 | HG00738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*962C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 3/3 | 962 | chr12 | 109770250 | ||||||
| chr12:109770394 | GT | G | 1 | a0002c0004t0008 | 5 | HG01891.hp2 HG02486.hp1 HG02809.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1114delT | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 3/3 | 1114 | INFO_REALIGN_3_PRIME | chr12 | 109770394 | |||||
| chr12:109770402 | T | A | 1 | a0001c0001t0021 | 1 | NA18945.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1114T>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 3/3 | 1114 | chr12 | 109770402 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:109715024 | C | T | 7 | a0001c0001t0001g0333 a0001c0001t0001g0334 a0001c0001t0001g0335 others(4): Show |
7 | HG00099.hp1 HG00140.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.-47+127C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109715024 | |||||||
| chr12:109715151 | C | T | 1 | a0001c0001t0001g0331 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-47+254C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109715151 | |||||||
| chr12:109715201 | C | T | 1 | a0001c0001t0004g0330 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-47+304C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109715201 | |||||||
| chr12:109715625 | C | G | 2 | a0001c0001t0001g0328 a0001c0001t0001g0329 |
2 | HG00140.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.-47+728C>G | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109715625 | |||||||
| chr12:109715631 | G | A | 3 | a0001c0001t0007g0019 a0001c0001t0015g0020 a0001c0001t0016g0021 |
3 | HG02970.hp1 HG03209.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-47+734G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109715631 | |||||||
| chr12:109715687 | C | T | 8 | a0001c0001t0006g0018 a0001c0001t0006g0321 a0001c0001t0006g0323 others(5): Show |
9 | HG00099.hp2 HG02280.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.-47+790C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109715687 | |||||||
| chr12:109715708 | C | A | 1 | a0001c0001t0020g0022 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-47+811C>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109715708 | |||||||
| chr12:109715756 | CAGAGCAA others(9): Show |
C | 1 | a0001c0001t0020g0022 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-47+860_-47+875del others(16): Show |
FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109715756 | |||||||
| chr12:109715870 | C | T | 5 | a0001c0001t0003g0001 a0001c0001t0003g0317 a0001c0001t0003g0318 others(2): Show |
11 | HG00423.hp2 HG02056.hp2 HG02074.hp1 others(8): Show |
intron_variant | MODIFIER | c.-47+973C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109715870 | |||||||
| chr12:109715979 | C | T | 1 | a0002c0004t0008g0316 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-47+1082C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109715979 | |||||||
| chr12:109716005 | G | A | 1 | a0002c0004t0008g0023 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-47+1108G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109716005 | |||||||
| chr12:109716114 | C | T | 1 | a0001c0001t0002g0315 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-47+1217C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109716114 | |||||||
| chr12:109716117 | T | C | 1 | a0001c0001t0001g0024 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-47+1220T>C | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109716117 | |||||||
| chr12:109716132 | G | A | 1 | a0001c0001t0007g0025 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-47+1235G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109716132 | |||||||
| chr12:109716187 | C | T | 2 | a0001c0001t0002g0314 a0001c0001t0002g0315 |
2 | HG01109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.-47+1290C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109716187 | |||||||
| chr12:109716283 | C | T | 1 | a0001c0001t0027g0313 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-47+1386C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109716283 | |||||||
| chr12:109716353 | G | A | 16 | a0001c0001t0001g0026 a0001c0001t0007g0019 a0001c0001t0007g0025 others(13): Show |
16 | HG01074.hp2 HG01167.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.-47+1456G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109716353 | |||||||
| chr12:109716440 | T | G | 8 | a0001c0001t0005g0005 a0001c0001t0005g0038 a0001c0001t0005g0039 others(5): Show |
9 | HG02615.hp2 HG02818.hp1 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.-47+1543T>G | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109716440 | |||||||
| chr12:109716670 | G | A | 2 | a0001c0001t0003g0045 a0001c0001t0003g0046 |
2 | NA18966.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.-47+1773G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109716670 | |||||||
| chr12:109716832 | A | T | 1 | a0001c0001t0004g0312 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-47+1935A>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109716832 | |||||||
| chr12:109717073 | A | G | 8 | a0001c0001t0005g0005 a0001c0001t0005g0038 a0001c0001t0005g0039 others(5): Show |
9 | HG02615.hp2 HG02818.hp1 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.-47+2176A>G | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109717073 | |||||||
| chr12:109717236 | C | T | 1 | a0001c0001t0001g0311 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-47+2339C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109717236 | |||||||
| chr12:109717317 | C | T | 3 | a0001c0001t0001g0308 a0001c0002t0001g0309 a0001c0015t0001g0310 |
3 | HG01081.hp2 HG02257.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.-47+2420C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109717317 | |||||||
| chr12:109717444 | A | C | 1 | a0001c0001t0003g0307 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-47+2547A>C | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109717444 | |||||||
| chr12:109717457 | A | G | 2 | a0001c0001t0001g0305 a0001c0001t0001g0306 |
2 | HG01257.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.-47+2560A>G | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109717457 | |||||||
| chr12:109717547 | G | A | 1 | a0001c0001t0020g0022 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-47+2650G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109717547 | |||||||
| chr12:109717659 | C | G | 69 | a0001c0001t0002g0002 a0001c0001t0002g0016 a0001c0001t0002g0017 others(66): Show |
77 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.-47+2762C>G | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109717659 | |||||||
| chr12:109717725 | G | A | 1 | a0001c0001t0001g0047 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-47+2828G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109717725 | |||||||
| chr12:109717766 | T | C | 327 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(324): Show |
352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.-47+2869T>C | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109717766 | |||||||
| chr12:109717773 | G | A | 1 | a0001c0001t0002g0315 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-47+2876G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109717773 | |||||||
| chr12:109717795 | C | T | 60 | a0001c0001t0002g0002 a0001c0001t0002g0016 a0001c0001t0002g0017 others(57): Show |
67 | HG00280.hp1 HG00408.hp2 HG00597.hp1 others(64): Show |
intron_variant | MODIFIER | c.-47+2898C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109717795 | |||||||
| chr12:109718016 | G | A | 1 | a0001c0001t0020g0022 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-47+3119G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109718016 | |||||||
| chr12:109718186 | C | T | 1 | a0001c0001t0003g0247 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-47+3289C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109718186 | |||||||
| chr12:109718223 | T | C | 1 | a0001c0001t0001g0048 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-47+3326T>C | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109718223 | |||||||
| chr12:109718246 | A | C | 1 | a0001c0001t0001g0246 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-47+3349A>C | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109718246 | |||||||
| chr12:109718299 | C | CCCCA | 6 | a0001c0001t0001g0047 a0001c0001t0006g0018 a0001c0001t0006g0325 others(3): Show |
7 | HG01884.hp1 HG01884.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-47+3416_-47+3419d others(6): Show |
FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 109718299 | ||||||
| chr12:109718299 | C | CCCCACCC others(5): Show |
1 | a0001c0001t0020g0022 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-47+3408_-47+3419d others(14): Show |
FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 109718299 | ||||||
| chr12:109718336 | C | G | 47 | a0001c0001t0002g0002 a0001c0001t0002g0016 a0001c0001t0002g0017 others(44): Show |
53 | HG00280.hp1 HG00408.hp2 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.-47+3439C>G | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109718336 | |||||||
| chr12:109718351 | G | A | 1 | a0001c0013t0001g0332 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-47+3454G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109718351 | |||||||
| chr12:109718356 | G | A | 2 | a0001c0001t0001g0049 a0001c0001t0001g0050 |
2 | NA18953.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.-47+3459G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109718356 | |||||||
| chr12:109718370 | C | T | 3 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0245 |
3 | HG02040.hp1 HG02135.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.-47+3473C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109718370 | |||||||
| chr12:109718534 | GC | G | 35 | a0001c0001t0003g0001 a0001c0001t0003g0011 a0001c0001t0003g0013 others(32): Show |
46 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.-47+3639delC | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 109718534 | ||||||
| chr12:109718551 | C | A | 1 | a0001c0001t0001g0051 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-47+3654C>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109718551 | |||||||
| chr12:109718955 | T | G | 3 | a0001c0001t0005g0038 a0001c0001t0005g0039 a0001c0001t0005g0040 |
3 | HG03139.hp1 NA19030.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-47+4058T>G | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109718955 | |||||||
| chr12:109719231 | C | T | 95 | a0001c0001t0002g0002 a0001c0001t0002g0016 a0001c0001t0002g0017 others(92): Show |
113 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.-47+4334C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109719231 | |||||||
| chr12:109719239 | T | C | 10 | a0001c0001t0001g0048 a0001c0001t0001g0052 a0001c0001t0001g0055 others(7): Show |
10 | HG01081.hp2 HG01891.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.-47+4342T>C | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109719239 | |||||||
| chr12:109719369 | G | C | 1 | a0001c0006t0002g0304 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-47+4472G>C | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109719369 | |||||||
| chr12:109719428 | T | A | 96 | a0001c0001t0001g0057 a0001c0001t0002g0002 a0001c0001t0002g0016 others(93): Show |
114 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.-47+4531T>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109719428 | |||||||
| chr12:109719446 | A | G | 96 | a0001c0001t0001g0057 a0001c0001t0002g0002 a0001c0001t0002g0016 others(93): Show |
114 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.-47+4549A>G | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109719446 | |||||||
| chr12:109719463 | C | T | 1 | a0002c0004t0008g0316 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-47+4566C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109719463 | |||||||
| chr12:109719656 | C | G | 3 | a0001c0001t0001g0219 a0001c0001t0001g0220 a0001c0001t0001g0221 |
3 | HG01168.hp2 HG01169.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.-47+4759C>G | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109719656 | |||||||
| chr12:109719687 | A | G | 92 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0010 others(89): Show |
96 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.-47+4790A>G | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109719687 | |||||||
| chr12:109719826 | A | T | 48 | a0001c0001t0001g0057 a0001c0001t0002g0002 a0001c0001t0002g0016 others(45): Show |
54 | HG00280.hp1 HG00408.hp2 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.-47+4929A>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109719826 | |||||||
| chr12:109719872 | C | G | 1 | a0001c0001t0001g0139 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-47+4975C>G | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109719872 | |||||||
| chr12:109719874 | A | G | 96 | a0001c0001t0001g0057 a0001c0001t0002g0002 a0001c0001t0002g0016 others(93): Show |
114 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.-47+4977A>G | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109719874 | |||||||
| chr12:109719907 | C | T | 8 | a0001c0001t0006g0018 a0001c0001t0006g0321 a0001c0001t0006g0323 others(5): Show |
9 | HG00099.hp2 HG02280.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.-47+5010C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109719907 | |||||||
| chr12:109720111 | G | A | 1 | a0001c0001t0001g0243 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-47+5214G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109720111 | |||||||
| chr12:109720276 | G | T | 8 | a0001c0001t0001g0212 a0001c0001t0001g0214 a0001c0001t0001g0215 others(5): Show |
8 | HG02015.hp1 HG02074.hp2 HG02132.hp1 others(5): Show |
intron_variant | MODIFIER | c.-47+5379G>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109720276 | |||||||
| chr12:109720337 | G | A | 1 | a0001c0001t0003g0222 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-47+5440G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109720337 | |||||||
| chr12:109720355 | G | C | 3 | a0001c0001t0001g0219 a0001c0001t0001g0220 a0001c0001t0001g0221 |
3 | HG01168.hp2 HG01169.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.-47+5458G>C | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109720355 | |||||||
| chr12:109720490 | G | A | 5 | a0001c0001t0004g0058 a0001c0001t0004g0059 a0001c0001t0004g0060 others(2): Show |
5 | HG02258.hp2 HG02615.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.-47+5593G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109720490 | |||||||
| chr12:109720511 | C | T | 96 | a0001c0001t0001g0057 a0001c0001t0002g0002 a0001c0001t0002g0016 others(93): Show |
114 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.-47+5614C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109720511 | |||||||
| chr12:109720552 | A | G | 1 | a0001c0001t0027g0313 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-47+5655A>G | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109720552 | |||||||
| chr12:109720639 | G | A | 9 | a0001c0001t0002g0260 a0001c0001t0002g0262 a0001c0001t0002g0263 others(6): Show |
9 | HG01943.hp1 HG02451.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.-47+5742G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109720639 | |||||||
| chr12:109720759 | G | A | 1 | a0001c0001t0001g0333 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-47+5862G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109720759 | |||||||
| chr12:109720762 | G | C | 1 | a0001c0001t0002g0269 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.-47+5865G>C | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109720762 | |||||||
| chr12:109720769 | C | G | 1 | a0001c0001t0001g0051 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-47+5872C>G | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109720769 | |||||||
| chr12:109720776 | T | C | 107 | a0001c0001t0001g0057 a0001c0001t0001g0219 a0001c0001t0001g0220 others(104): Show |
126 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.-47+5879T>C | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109720776 | |||||||
| chr12:109720816 | T | C | 96 | a0001c0001t0001g0057 a0001c0001t0002g0002 a0001c0001t0002g0016 others(93): Show |
114 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.-47+5919T>C | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109720816 | |||||||
| chr12:109720969 | A | C | 3 | a0001c0001t0001g0219 a0001c0001t0001g0220 a0001c0001t0001g0221 |
3 | HG01168.hp2 HG01169.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.-47+6072A>C | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109720969 | |||||||
| chr12:109721159 | C | CT | 96 | a0001c0001t0001g0057 a0001c0001t0002g0002 a0001c0001t0002g0016 others(93): Show |
114 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.-47+6263dupT | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 109721159 | ||||||
| chr12:109721233 | T | C | 1 | a0001c0001t0001g0062 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-47+6336T>C | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109721233 | |||||||
| chr12:109721288 | C | T | 3 | a0001c0001t0001g0308 a0001c0002t0001g0309 a0001c0015t0001g0310 |
3 | HG01081.hp2 HG02257.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.-47+6391C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109721288 | |||||||
| chr12:109721289 | G | A | 1 | a0001c0001t0001g0139 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-47+6392G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109721289 | |||||||
| chr12:109721296 | C | T | 2 | a0001c0001t0001g0139 a0001c0001t0020g0022 |
2 | HG03130.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-47+6399C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109721296 | |||||||
| chr12:109721302 | T | C | 5 | a0001c0001t0004g0058 a0001c0001t0004g0059 a0001c0001t0004g0060 others(2): Show |
5 | HG02258.hp2 HG02615.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.-47+6405T>C | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109721302 | |||||||
| chr12:109721315 | T | A | 96 | a0001c0001t0001g0057 a0001c0001t0002g0002 a0001c0001t0002g0016 others(93): Show |
114 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.-47+6418T>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109721315 | |||||||
| chr12:109721384 | C | T | 1 | a0001c0001t0001g0210 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.-47+6487C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109721384 | |||||||
| chr12:109721385 | G | T | 3 | a0001c0001t0001g0219 a0001c0001t0001g0220 a0001c0001t0001g0221 |
3 | HG01168.hp2 HG01169.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.-47+6488G>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109721385 | |||||||
| chr12:109721550 | A | G | 1 | a0001c0001t0004g0312 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-47+6653A>G | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109721550 | |||||||
| chr12:109721626 | T | C | 1 | a0001c0001t0006g0321 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-47+6729T>C | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109721626 | |||||||
| chr12:109721652 | G | A | 1 | a0001c0001t0004g0063 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-47+6755G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109721652 | |||||||
| chr12:109721681 | C | T | 35 | a0001c0001t0003g0001 a0001c0001t0003g0011 a0001c0001t0003g0013 others(32): Show |
46 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.-47+6784C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109721681 | |||||||
| chr12:109721690 | T | C | 1 | a0001c0001t0003g0223 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-47+6793T>C | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109721690 | |||||||
| chr12:109722064 | CAG | C | 8 | a0001c0001t0006g0018 a0001c0001t0006g0321 a0001c0001t0006g0323 others(5): Show |
9 | HG00099.hp2 HG02280.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.-47+7169_-47+7170d others(4): Show |
FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 109722064 | ||||||
| chr12:109722108 | T | G | 1 | a0001c0001t0001g0219 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-47+7211T>G | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109722108 | |||||||
| chr12:109722114 | C | T | 1 | a0001c0001t0023g0138 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-47+7217C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109722114 | |||||||
| chr12:109722147 | G | A | 1 | a0001c0001t0001g0026 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-47+7250G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109722147 | |||||||
| chr12:109722367 | C | T | 3 | a0001c0001t0001g0219 a0001c0001t0001g0220 a0001c0001t0001g0221 |
3 | HG01168.hp2 HG01169.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.-47+7470C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109722367 | |||||||
| chr12:109722445 | G | A | 1 | a0001c0001t0001g0140 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-47+7548G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109722445 | |||||||
| chr12:109722456 | A | C | 10 | a0001c0001t0001g0139 a0001c0001t0006g0018 a0001c0001t0006g0321 others(7): Show |
11 | HG00099.hp2 HG02280.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.-47+7559A>C | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109722456 | |||||||
| chr12:109722550 | G | T | 7 | a0001c0001t0001g0048 a0001c0001t0001g0052 a0001c0001t0001g0055 others(4): Show |
7 | HG01891.hp2 HG02486.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.-47+7653G>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109722550 | |||||||
| chr12:109722569 | C | A | 96 | a0001c0001t0001g0057 a0001c0001t0002g0002 a0001c0001t0002g0016 others(93): Show |
114 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.-47+7672C>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109722569 | |||||||
| chr12:109722741 | G | A | 1 | a0001c0002t0006g0324 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-47+7844G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109722741 | |||||||
| chr12:109722816 | G | A | 8 | a0001c0001t0004g0064 a0001c0001t0004g0065 a0001c0001t0004g0066 others(5): Show |
8 | HG01928.hp1 HG02630.hp2 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.-47+7919G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109722816 | |||||||
| chr12:109722935 | G | A | 2 | a0001c0001t0001g0141 a0001c0001t0001g0311 |
2 | HG03017.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.-47+8038G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109722935 | |||||||
| chr12:109723002 | T | TG | 86 | a0001c0001t0001g0008 a0001c0001t0001g0047 a0001c0001t0001g0062 others(83): Show |
87 | HG00544.hp2 HG00558.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.-47+8114dupG | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 109723002 | ||||||
| chr12:109723002 | TG | T | 87 | a0001c0001t0001g0057 a0001c0001t0002g0002 a0001c0001t0002g0016 others(84): Show |
105 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.-47+8114delG | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 109723002 | ||||||
| chr12:109723004 | G | A | 1 | a0001c0001t0001g0071 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-47+8107G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109723004 | |||||||
| chr12:109723004 | G | T | 2 | a0001c0001t0002g0302 a0001c0001t0002g0303 |
2 | HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-47+8107G>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109723004 | |||||||
| chr12:109723005 | G | T | 2 | a0001c0001t0001g0049 a0001c0001t0001g0050 |
2 | NA18953.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.-47+8108G>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109723005 | |||||||
| chr12:109723006 | G | C | 1 | a0001c0001t0002g0270 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.-47+8109G>C | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109723006 | |||||||
| chr12:109723006 | G | T | 2 | a0001c0001t0002g0017 a0001c0001t0002g0301 |
3 | NA18968.hp2 NA19060.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.-47+8109G>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109723006 | |||||||
| chr12:109723007 | G | T | 35 | a0001c0001t0003g0001 a0001c0001t0003g0011 a0001c0001t0003g0013 others(32): Show |
46 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.-47+8110G>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109723007 | |||||||
| chr12:109723012 | A | G | 3 | a0001c0001t0001g0333 a0001c0001t0001g0337 a0001c0001t0001g0338 |
3 | HG03654.hp2 HG03688.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.-47+8115A>G | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109723012 | |||||||
| chr12:109723107 | A | G | 1 | a0001c0001t0001g0114 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-47+8210A>G | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109723107 | |||||||
| chr12:109723404 | G | A | 70 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(67): Show |
72 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.-47+8507G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109723404 | |||||||
| chr12:109723471 | G | A | 8 | a0001c0001t0006g0018 a0001c0001t0006g0321 a0001c0001t0006g0323 others(5): Show |
9 | HG00099.hp2 HG02280.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.-47+8574G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109723471 | |||||||
| chr12:109723507 | G | A | 4 | a0001c0001t0001g0219 a0001c0001t0001g0220 a0001c0001t0001g0221 others(1): Show |
4 | HG01168.hp2 HG01169.hp1 HG02074.hp1 others(1): Show |
intron_variant | MODIFIER | c.-47+8610G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109723507 | |||||||
| chr12:109723517 | C | T | 1 | a0001c0001t0001g0071 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-47+8620C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109723517 | |||||||
| chr12:109723554 | C | CCAT | 109 | a0001c0001t0001g0057 a0001c0001t0001g0139 a0001c0001t0001g0219 others(106): Show |
128 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.-47+8661_-47+8663d others(5): Show |
FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 109723554 | ||||||
| chr12:109723681 | G | A | 3 | a0001c0001t0001g0219 a0001c0001t0001g0220 a0001c0001t0001g0221 |
3 | HG01168.hp2 HG01169.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.-47+8784G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109723681 | |||||||
| chr12:109723834 | C | T | 2 | a0001c0001t0001g0181 a0001c0001t0001g0209 |
2 | HG00280.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.-47+8937C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109723834 | |||||||
| chr12:109723934 | G | GA | 101 | a0001c0001t0001g0049 a0001c0001t0001g0057 a0001c0001t0001g0142 others(98): Show |
119 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.-47+9046dupA | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 109723934 | ||||||
| chr12:109724097 | C | A | 1 | a0001c0001t0001g0072 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-47+9200C>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109724097 | |||||||
| chr12:109724149 | C | G | 1 | a0001c0001t0001g0219 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-47+9252C>G | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109724149 | |||||||
| chr12:109724172 | T | G | 1 | a0001c0001t0001g0144 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-47+9275T>G | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109724172 | |||||||
| chr12:109724331 | CAT | C | 8 | a0001c0001t0006g0018 a0001c0001t0006g0321 a0001c0001t0006g0323 others(5): Show |
9 | HG00099.hp2 HG02280.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.-47+9435_-47+9436d others(4): Show |
FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109724331 | |||||||
| chr12:109724450 | C | A | 1 | a0001c0001t0018g0073 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.-47+9553C>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109724450 | |||||||
| chr12:109724489 | C | T | 1 | a0001c0001t0002g0296 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-47+9592C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109724489 | |||||||
| chr12:109724821 | C | T | 1 | a0002c0004t0008g0316 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-47+9924C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109724821 | |||||||
| chr12:109724828 | T | TTGAA | 3 | a0001c0001t0001g0333 a0001c0001t0001g0337 a0001c0001t0001g0338 |
3 | HG03654.hp2 HG03688.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.-47+9944_-47+9947d others(6): Show |
FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 109724828 | ||||||
| chr12:109724943 | G | C | 333 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(330): Show |
358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.-47+10046G>C | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109724943 | |||||||
| chr12:109724997 | C | T | 9 | a0001c0001t0002g0260 a0001c0001t0002g0262 a0001c0001t0002g0263 others(6): Show |
9 | HG01943.hp1 HG02451.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.-47+10100C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109724997 | |||||||
| chr12:109725322 | G | A | 1 | a0001c0001t0001g0219 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-47+10425G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109725322 | |||||||
| chr12:109725388 | C | T | 1 | a0001c0001t0004g0063 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-47+10491C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109725388 | |||||||
| chr12:109725421 | T | TCTCCCCC others(3): Show |
1 | a0001c0001t0001g0219 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-47+10529_-47+1053 others(14): Show |
FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 109725421 | ||||||
| chr12:109725427 | T | C | 1 | a0001c0001t0001g0219 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-47+10530T>C | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109725427 | |||||||
| chr12:109725427 | T | TCTCCCTC others(3): Show |
187 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(184): Show |
194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.-47+10541_-47+1055 others(14): Show |
FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 109725427 | ||||||
| chr12:109725427 | T | TCTCCCTC others(13): Show |
2 | a0001c0001t0001g0047 a0001c0001t0001g0145 |
2 | HG01081.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.-47+10531_-47+1055 others(24): Show |
FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 109725427 | ||||||
| chr12:109725427 | T | TTTCCCTC others(3): Show |
1 | a0002c0004t0008g0316 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-47+10530_-47+1053 others(14): Show |
FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109725427 | |||||||
| chr12:109725433 | T | TCCCCCTC others(4): Show |
1 | a0001c0001t0018g0073 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.-47+10540_-47+1055 others(15): Show |
FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 109725433 | ||||||
| chr12:109725433 | T | TCCCCTCC others(4): Show |
1 | a0001c0001t0001g0180 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.-47+10540_-47+1054 others(15): Show |
FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 109725433 | ||||||
| chr12:109725735 | A | G | 98 | a0001c0001t0001g0057 a0001c0001t0001g0220 a0001c0001t0001g0221 others(95): Show |
116 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.-47+10838A>G | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109725735 | |||||||
| chr12:109725778 | C | T | 1 | a0001c0001t0001g0110 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-47+10881C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109725778 | |||||||
| chr12:109725794 | C | T | 1 | a0001c0001t0002g0295 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-47+10897C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109725794 | |||||||
| chr12:109725879 | G | A | 1 | a0001c0001t0002g0296 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-47+10982G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109725879 | |||||||
| chr12:109725897 | C | G | 1 | a0002c0004t0008g0316 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-47+11000C>G | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109725897 | |||||||
| chr12:109725920 | G | A | 7 | a0001c0001t0001g0006 a0001c0001t0001g0072 a0001c0001t0001g0074 others(4): Show |
8 | HG01167.hp1 HG02280.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.-47+11023G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109725920 | |||||||
| chr12:109726002 | C | T | 1 | a0001c0001t0003g0242 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-47+11105C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109726002 | |||||||
| chr12:109726119 | T | TA | 167 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(164): Show |
173 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.-47+11244dupA | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 109726119 | ||||||
| chr12:109726119 | T | TAA | 21 | a0001c0001t0001g0024 a0001c0001t0001g0048 a0001c0001t0001g0052 others(18): Show |
21 | HG00597.hp2 HG01081.hp2 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.-47+11243_-47+1124 others(6): Show |
FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 109726119 | ||||||
| chr12:109726119 | TA | T | 56 | a0001c0001t0001g0057 a0001c0001t0001g0219 a0001c0001t0001g0220 others(53): Show |
62 | HG00280.hp1 HG00408.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.-47+11244delA | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 109726119 | ||||||
| chr12:109726119 | TAA | T | 10 | a0001c0001t0002g0268 a0001c0001t0002g0293 a0001c0001t0002g0294 others(7): Show |
11 | HG02280.hp1 HG02559.hp1 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.-47+11243_-47+1124 others(6): Show |
FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 109726119 | ||||||
| chr12:109726143 | T | C | 8 | a0001c0001t0005g0005 a0001c0001t0005g0038 a0001c0001t0005g0039 others(5): Show |
9 | HG02615.hp2 HG02818.hp1 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.-47+11246T>C | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109726143 | |||||||
| chr12:109726161 | A | G | 1 | a0002c0004t0008g0316 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-47+11264A>G | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109726161 | |||||||
| chr12:109726225 | C | T | 2 | a0001c0001t0004g0059 a0001c0001t0004g0061 |
2 | HG02615.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.-47+11328C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109726225 | |||||||
| chr12:109726242 | A | C | 1 | a0001c0001t0001g0170 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-47+11345A>C | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109726242 | |||||||
| chr12:109726427 | A | T | 173 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(170): Show |
179 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.-47+11530A>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109726427 | |||||||
| chr12:109726479 | C | T | 1 | a0001c0001t0002g0314 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-47+11582C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109726479 | |||||||
| chr12:109726511 | C | T | 8 | a0001c0001t0006g0018 a0001c0001t0006g0321 a0001c0001t0006g0323 others(5): Show |
9 | HG00099.hp2 HG02280.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.-47+11614C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109726511 | |||||||
| chr12:109726572 | G | A | 173 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(170): Show |
179 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.-47+11675G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109726572 | |||||||
| chr12:109726650 | C | G | 35 | a0001c0001t0003g0001 a0001c0001t0003g0011 a0001c0001t0003g0013 others(32): Show |
46 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.-47+11753C>G | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109726650 | |||||||
| chr12:109726706 | T | C | 1 | a0001c0001t0001g0219 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-47+11809T>C | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109726706 | |||||||
| chr12:109726735 | C | T | 1 | a0001c0001t0002g0267 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-47+11838C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109726735 | |||||||
| chr12:109726736 | G | A | 5 | a0001c0001t0003g0011 a0001c0001t0003g0045 a0001c0001t0003g0046 others(2): Show |
6 | NA18966.hp2 NA18971.hp1 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.-47+11839G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109726736 | |||||||
| chr12:109726914 | C | A | 63 | a0001c0001t0001g0057 a0001c0001t0001g0220 a0001c0001t0001g0221 others(60): Show |
70 | HG00280.hp1 HG00408.hp2 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.-47+12017C>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109726914 | |||||||
| chr12:109726935 | G | A | 1 | a0001c0001t0001g0219 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-47+12038G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109726935 | |||||||
| chr12:109726946 | C | T | 1 | a0001c0001t0005g0041 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-47+12049C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109726946 | |||||||
| chr12:109726959 | A | G | 1 | a0002c0004t0008g0316 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-47+12062A>G | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109726959 | |||||||
| chr12:109727104 | G | C | 3 | a0001c0001t0001g0147 a0001c0001t0001g0180 a0001c0001t0001g0185 |
3 | NA18952.hp1 NA18985.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.-47+12207G>C | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109727104 | |||||||
| chr12:109727218 | C | G | 1 | a0001c0001t0003g0222 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-47+12321C>G | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109727218 | |||||||
| chr12:109727318 | G | A | 1 | a0001c0001t0003g0222 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-47+12421G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109727318 | |||||||
| chr12:109727352 | T | A | 1 | a0001c0001t0001g0186 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-47+12455T>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109727352 | |||||||
| chr12:109727422 | G | C | 2 | a0001c0001t0002g0260 a0001c0001t0002g0268 |
2 | HG02976.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-47+12525G>C | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109727422 | |||||||
| chr12:109727495 | A | G | 2 | a0001c0001t0002g0291 a0001c0001t0002g0292 |
2 | HG02257.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.-47+12598A>G | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109727495 | |||||||
| chr12:109727504 | A | T | 1 | a0001c0001t0003g0222 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-47+12607A>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109727504 | |||||||
| chr12:109727895 | T | G | 1 | a0002c0004t0008g0316 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-47+12998T>G | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109727895 | |||||||
| chr12:109727899 | T | C | 1 | a0002c0004t0008g0316 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-47+13002T>C | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109727899 | |||||||
| chr12:109727900 | C | T | 1 | a0002c0004t0008g0316 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-47+13003C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109727900 | |||||||
| chr12:109727902 | A | G | 4 | a0001c0001t0002g0290 a0001c0001t0002g0291 a0001c0001t0002g0292 others(1): Show |
4 | HG01361.hp1 HG02257.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-47+13005A>G | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109727902 | |||||||
| chr12:109727989 | G | A | 1 | a0001c0001t0001g0141 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-47+13092G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109727989 | |||||||
| chr12:109727990 | C | T | 1 | a0003c0003t0001g0217 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-47+13093C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109727990 | |||||||
| chr12:109728001 | G | C | 4 | a0001c0001t0001g0119 a0001c0001t0001g0121 a0001c0001t0010g0108 others(1): Show |
4 | HG01256.hp1 HG01517.hp2 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.-47+13104G>C | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109728001 | |||||||
| chr12:109728152 | G | C | 99 | a0001c0001t0001g0057 a0001c0001t0001g0114 a0001c0001t0001g0220 others(96): Show |
117 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.-47+13255G>C | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109728152 | |||||||
| chr12:109728318 | G | A | 1 | a0001c0001t0001g0219 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-47+13421G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109728318 | |||||||
| chr12:109728322 | GGGGTCCC others(1): Show |
G | 9 | a0001c0001t0001g0171 a0001c0001t0006g0018 a0001c0001t0006g0321 others(6): Show |
10 | HG00099.hp2 HG02280.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.-47+13442_-47+1344 others(12): Show |
FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 109728322 | ||||||
| chr12:109728359 | G | T | 8 | a0001c0001t0006g0018 a0001c0001t0006g0321 a0001c0001t0006g0323 others(5): Show |
9 | HG00099.hp2 HG02280.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.-47+13462G>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109728359 | |||||||
| chr12:109728419 | C | T | 12 | a0001c0001t0001g0062 a0001c0001t0001g0111 a0001c0001t0001g0113 others(9): Show |
12 | HG00099.hp1 HG00140.hp1 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.-47+13522C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109728419 | |||||||
| chr12:109728420 | G | A | 97 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0002g0002 others(94): Show |
115 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.-47+13523G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109728420 | |||||||
| chr12:109728468 | G | C | 1 | a0001c0001t0003g0222 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-47+13571G>C | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109728468 | |||||||
| chr12:109728469 | C | G | 1 | a0001c0001t0003g0222 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-47+13572C>G | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109728469 | |||||||
| chr12:109728567 | C | T | 1 | a0001c0001t0013g0256 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-47+13670C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109728567 | |||||||
| chr12:109728568 | G | A | 1 | a0003c0003t0001g0211 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-47+13671G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109728568 | |||||||
| chr12:109728822 | G | A | 1 | a0001c0001t0001g0148 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-47+13925G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109728822 | |||||||
| chr12:109728894 | T | C | 4 | a0001c0001t0002g0290 a0001c0001t0002g0291 a0001c0001t0002g0292 others(1): Show |
4 | HG01361.hp1 HG02257.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-47+13997T>C | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109728894 | |||||||
| chr12:109728898 | C | T | 1 | a0001c0001t0001g0107 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-47+14001C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109728898 | |||||||
| chr12:109728906 | T | A | 1 | a0001c0001t0001g0219 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-47+14009T>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109728906 | |||||||
| chr12:109728973 | T | TA | 26 | a0001c0001t0001g0026 a0001c0001t0001g0055 a0001c0001t0001g0116 others(23): Show |
27 | HG00639.hp2 HG01074.hp2 HG01081.hp2 others(24): Show |
intron_variant | MODIFIER | c.-47+14088dupA | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 109728973 | ||||||
| chr12:109728973 | T | TAA | 223 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(220): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.-47+14087_-47+1408 others(6): Show |
FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 109728973 | ||||||
| chr12:109729233 | G | GTTTTTA | 226 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0009 others(223): Show |
249 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.-47+14341_-47+1434 others(10): Show |
FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 109729233 | ||||||
| chr12:109729374 | C | T | 1 | a0001c0001t0001g0215 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-47+14477C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109729374 | |||||||
| chr12:109729411 | C | T | 1 | a0001c0001t0004g0068 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.-47+14514C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109729411 | |||||||
| chr12:109729629 | A | C | 1 | a0001c0001t0002g0294 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-46-14472A>C | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109729629 | |||||||
| chr12:109729642 | G | A | 1 | a0001c0001t0001g0123 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-46-14459G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109729642 | |||||||
| chr12:109729645 | C | T | 1 | a0001c0001t0001g0219 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-46-14456C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109729645 | |||||||
| chr12:109729700 | A | AC | 10 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0147 others(7): Show |
10 | HG01928.hp2 HG02004.hp1 HG02074.hp1 others(7): Show |
intron_variant | MODIFIER | c.-46-14396dupC | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 109729700 | ||||||
| chr12:109729741 | C | T | 6 | a0001c0001t0007g0025 a0001c0001t0007g0027 a0001c0001t0007g0035 others(3): Show |
6 | HG01516.hp1 HG02056.hp1 HG03017.hp2 others(3): Show |
intron_variant | MODIFIER | c.-46-14360C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109729741 | |||||||
| chr12:109729785 | C | T | 96 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0220 others(93): Show |
114 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.-46-14316C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109729785 | |||||||
| chr12:109729838 | C | T | 2 | a0001c0001t0001g0139 a0001c0001t0020g0022 |
2 | HG03130.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-46-14263C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109729838 | |||||||
| chr12:109729933 | G | A | 1 | a0001c0001t0001g0149 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-46-14168G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109729933 | |||||||
| chr12:109729939 | G | A | 9 | a0001c0001t0001g0009 a0001c0001t0001g0052 a0001c0001t0001g0142 others(6): Show |
10 | HG02572.hp2 HG02647.hp1 HG02970.hp2 others(7): Show |
intron_variant | MODIFIER | c.-46-14162G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109729939 | |||||||
| chr12:109729956 | G | A | 61 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0220 others(58): Show |
68 | HG00280.hp1 HG00408.hp2 HG00597.hp1 others(65): Show |
intron_variant | MODIFIER | c.-46-14145G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109729956 | |||||||
| chr12:109730198 | T | C | 1 | a0001c0001t0001g0114 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-46-13903T>C | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109730198 | |||||||
| chr12:109730400 | G | C | 1 | a0001c0001t0001g0190 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-46-13701G>C | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109730400 | |||||||
| chr12:109730406 | CG | C | 275 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(272): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.-46-13684delG | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 109730406 | ||||||
| chr12:109730412 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-46-13689G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109730412 | |||||||
| chr12:109730460 | C | G | 1 | a0001c0002t0001g0309 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-46-13641C>G | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109730460 | |||||||
| chr12:109730655 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-46-13446G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109730655 | |||||||
| chr12:109731023 | T | C | 2 | a0001c0001t0001g0308 a0001c0015t0001g0310 |
2 | HG01081.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.-46-13078T>C | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109731023 | |||||||
| chr12:109731173 | C | G | 1 | a0001c0001t0001g0121 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-46-12928C>G | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109731173 | |||||||
| chr12:109731203 | G | A | 1 | a0001c0001t0001g0155 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-46-12898G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109731203 | |||||||
| chr12:109731239 | G | A | 2 | a0001c0001t0001g0139 a0001c0001t0020g0022 |
2 | HG03130.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-46-12862G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109731239 | |||||||
| chr12:109731245 | G | T | 8 | a0001c0001t0004g0064 a0001c0001t0004g0065 a0001c0001t0004g0066 others(5): Show |
8 | HG01928.hp1 HG02630.hp2 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.-46-12856G>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109731245 | |||||||
| chr12:109731279 | C | T | 1 | a0001c0001t0001g0026 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-46-12822C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109731279 | |||||||
| chr12:109731307 | G | A | 16 | a0001c0001t0002g0258 a0001c0001t0007g0019 a0001c0001t0007g0025 others(13): Show |
16 | HG00639.hp2 HG01074.hp2 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.-46-12794G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109731307 | |||||||
| chr12:109731341 | T | C | 123 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0009 others(120): Show |
128 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.-46-12760T>C | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109731341 | |||||||
| chr12:109731348 | C | A | 6 | a0001c0001t0005g0005 a0001c0001t0005g0038 a0001c0001t0005g0039 others(3): Show |
7 | HG02615.hp2 HG02818.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.-46-12753C>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109731348 | |||||||
| chr12:109731353 | C | T | 1 | a0001c0001t0027g0313 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-46-12748C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109731353 | |||||||
| chr12:109731423 | G | C | 1 | a0002c0004t0008g0316 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-46-12678G>C | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109731423 | |||||||
| chr12:109731444 | T | G | 3 | a0001c0001t0001g0139 a0001c0001t0001g0219 a0001c0001t0020g0022 |
3 | HG02717.hp1 HG03130.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-46-12657T>G | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109731444 | |||||||
| chr12:109731506 | G | T | 1 | a0001c0001t0017g0322 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-46-12595G>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109731506 | |||||||
| chr12:109731697 | C | A | 1 | a0001c0001t0001g0219 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-46-12404C>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109731697 | |||||||
| chr12:109731706 | C | A | 1 | a0001c0001t0001g0080 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-46-12395C>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109731706 | |||||||
| chr12:109731749 | G | T | 1 | a0001c0001t0001g0080 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-46-12352G>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109731749 | |||||||
| chr12:109731900 | G | A | 1 | a0001c0001t0001g0122 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-46-12201G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109731900 | |||||||
| chr12:109731918 | T | C | 81 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0024 others(78): Show |
84 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.-46-12183T>C | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109731918 | |||||||
| chr12:109732223 | G | A | 69 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0026 others(66): Show |
71 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.-46-11878G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109732223 | |||||||
| chr12:109732383 | G | T | 16 | a0001c0001t0002g0258 a0001c0001t0004g0063 a0001c0001t0007g0019 others(13): Show |
16 | HG00639.hp2 HG01074.hp2 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.-46-11718G>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109732383 | |||||||
| chr12:109732495 | C | T | 26 | a0001c0001t0001g0006 a0001c0001t0001g0047 a0001c0001t0001g0062 others(23): Show |
27 | HG00099.hp1 HG00140.hp1 HG01167.hp1 others(24): Show |
intron_variant | MODIFIER | c.-46-11606C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109732495 | |||||||
| chr12:109732519 | A | G | 1 | a0001c0001t0027g0313 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-46-11582A>G | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109732519 | |||||||
| chr12:109732648 | C | T | 1 | a0001c0001t0004g0067 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-46-11453C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109732648 | |||||||
| chr12:109732652 | T | C | 1 | a0001c0001t0001g0026 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-46-11449T>C | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109732652 | |||||||
| chr12:109732656 | C | T | 11 | a0001c0001t0001g0003 a0001c0001t0001g0165 a0001c0001t0001g0166 others(8): Show |
13 | HG01099.hp1 HG01123.hp2 HG01433.hp2 others(10): Show |
intron_variant | MODIFIER | c.-46-11445C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109732656 | |||||||
| chr12:109732677 | AGGGGAGG others(7): Show |
A | 1 | a0001c0006t0002g0304 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-46-11414_-46-1140 others(18): Show |
FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 109732677 | ||||||
| chr12:109732847 | C | T | 2 | a0001c0001t0001g0026 a0001c0001t0027g0313 |
2 | HG01891.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-46-11254C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109732847 | |||||||
| chr12:109732892 | C | G | 1 | a0001c0001t0020g0022 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-46-11209C>G | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109732892 | |||||||
| chr12:109732892 | C | T | 22 | a0001c0001t0001g0109 a0001c0001t0001g0133 a0001c0001t0001g0190 others(19): Show |
22 | HG00323.hp2 HG00639.hp2 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.-46-11209C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109732892 | |||||||
| chr12:109732912 | G | A | 1 | a0001c0001t0013g0255 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-46-11189G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109732912 | |||||||
| chr12:109732923 | G | A | 32 | a0001c0001t0001g0007 a0001c0001t0001g0080 a0001c0001t0001g0085 others(29): Show |
32 | HG00323.hp2 HG00438.hp2 HG00544.hp2 others(29): Show |
intron_variant | MODIFIER | c.-46-11178G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109732923 | |||||||
| chr12:109732936 | A | C | 1 | a0001c0001t0020g0022 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-46-11165A>C | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109732936 | |||||||
| chr12:109732965 | G | C | 1 | a0005c0011t0002g0289 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.-46-11136G>C | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109732965 | |||||||
| chr12:109733231 | C | T | 90 | a0001c0001t0001g0006 a0001c0001t0001g0051 a0001c0001t0001g0052 others(87): Show |
109 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(106): Show |
intron_variant | MODIFIER | c.-46-10870C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109733231 | |||||||
| chr12:109733265 | C | T | 2 | a0001c0001t0001g0219 a0002c0004t0008g0023 |
2 | HG02717.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-46-10836C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109733265 | |||||||
| chr12:109733336 | A | G | 5 | a0003c0003t0001g0164 a0003c0003t0001g0211 a0003c0003t0001g0217 others(2): Show |
5 | HG02074.hp2 HG02523.hp2 NA18949.hp2 others(2): Show |
intron_variant | MODIFIER | c.-46-10765A>G | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109733336 | |||||||
| chr12:109733405 | A | AT | 11 | a0001c0001t0001g0026 a0001c0001t0001g0219 a0001c0001t0002g0259 others(8): Show |
17 | HG00423.hp2 HG01891.hp1 HG02056.hp2 others(14): Show |
intron_variant | MODIFIER | c.-46-10682dupT | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 109733405 | ||||||
| chr12:109733405 | AT | A | 12 | a0001c0001t0001g0085 a0001c0001t0002g0002 a0001c0001t0002g0017 others(9): Show |
17 | NA18940.hp1 NA18945.hp1 NA18957.hp2 others(14): Show |
intron_variant | MODIFIER | c.-46-10682delT | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 109733405 | ||||||
| chr12:109733523 | C | T | 1 | a0001c0001t0003g0229 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-46-10578C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109733523 | |||||||
| chr12:109733553 | G | A | 1 | a0001c0001t0002g0259 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-46-10548G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109733553 | |||||||
| chr12:109733595 | G | C | 1 | a0001c0001t0001g0026 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-46-10506G>C | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109733595 | |||||||
| chr12:109733597 | G | T | 1 | a0001c0001t0001g0186 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-46-10504G>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109733597 | |||||||
| chr12:109733706 | C | T | 1 | a0001c0001t0007g0025 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-46-10395C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109733706 | |||||||
| chr12:109733807 | G | A | 1 | a0001c0001t0004g0069 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-46-10294G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109733807 | |||||||
| chr12:109734171 | G | A | 1 | a0001c0001t0003g0230 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.-46-9930G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109734171 | |||||||
| chr12:109734208 | C | CA | 42 | a0001c0001t0001g0062 a0001c0001t0001g0077 a0001c0001t0001g0090 others(39): Show |
42 | HG00323.hp2 HG00639.hp2 HG01070.hp2 others(39): Show |
intron_variant | MODIFIER | c.-46-9875dupA | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 109734208 | ||||||
| chr12:109734260 | A | G | 1 | a0002c0004t0008g0316 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-46-9841A>G | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109734260 | |||||||
| chr12:109734328 | C | T | 27 | a0001c0001t0001g0062 a0001c0001t0001g0077 a0001c0001t0001g0092 others(24): Show |
27 | HG00323.hp2 HG00639.hp2 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.-46-9773C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109734328 | |||||||
| chr12:109734344 | C | T | 1 | a0001c0001t0004g0069 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-46-9757C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109734344 | |||||||
| chr12:109734345 | G | A | 2 | a0001c0001t0001g0090 a0001c0001t0001g0093 |
2 | NA18962.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.-46-9756G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109734345 | |||||||
| chr12:109734382 | C | T | 2 | a0001c0001t0001g0208 a0001c0001t0004g0066 |
2 | HG01433.hp2 HG01928.hp1 |
intron_variant | MODIFIER | c.-46-9719C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109734382 | |||||||
| chr12:109734416 | G | A | 97 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0010 others(94): Show |
107 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(104): Show |
intron_variant | MODIFIER | c.-46-9685G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109734416 | |||||||
| chr12:109734488 | G | A | 1 | a0001c0001t0001g0181 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-46-9613G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109734488 | |||||||
| chr12:109734494 | A | G | 27 | a0001c0001t0001g0062 a0001c0001t0001g0077 a0001c0001t0001g0092 others(24): Show |
27 | HG00323.hp2 HG00639.hp2 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.-46-9607A>G | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109734494 | |||||||
| chr12:109734523 | C | G | 1 | a0001c0001t0006g0321 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-46-9578C>G | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109734523 | |||||||
| chr12:109734597 | TA | T | 106 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0010 others(103): Show |
116 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.-46-9489delA | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 109734597 | ||||||
| chr12:109734708 | C | A | 4 | a0001c0001t0001g0333 a0001c0001t0001g0337 a0001c0001t0001g0338 others(1): Show |
4 | HG02698.hp1 HG03654.hp2 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.-46-9393C>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109734708 | |||||||
| chr12:109734817 | G | A | 27 | a0001c0001t0001g0062 a0001c0001t0001g0077 a0001c0001t0001g0092 others(24): Show |
27 | HG00323.hp2 HG00639.hp2 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.-46-9284G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109734817 | |||||||
| chr12:109735032 | C | T | 1 | a0001c0001t0001g0026 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-46-9069C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109735032 | |||||||
| chr12:109735040 | C | T | 1 | a0001c0001t0002g0279 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-46-9061C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109735040 | |||||||
| chr12:109735045 | C | A | 4 | a0002c0004t0008g0023 a0002c0004t0008g0053 a0002c0004t0008g0054 others(1): Show |
4 | HG01891.hp2 HG02486.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.-46-9056C>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109735045 | |||||||
| chr12:109735169 | C | T | 134 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0010 others(131): Show |
144 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.-46-8932C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109735169 | |||||||
| chr12:109735230 | G | T | 3 | a0001c0001t0004g0250 a0001c0001t0004g0251 a0001c0001t0010g0104 |
3 | HG01175.hp2 HG02258.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.-46-8871G>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109735230 | |||||||
| chr12:109735358 | C | T | 1 | a0001c0001t0001g0219 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-46-8743C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109735358 | |||||||
| chr12:109735374 | C | G | 1 | a0004c0010t0003g0237 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.-46-8727C>G | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109735374 | |||||||
| chr12:109735457 | T | C | 1 | a0001c0001t0001g0329 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-46-8644T>C | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109735457 | |||||||
| chr12:109735481 | C | T | 27 | a0001c0001t0001g0062 a0001c0001t0001g0077 a0001c0001t0001g0092 others(24): Show |
27 | HG00323.hp2 HG00639.hp2 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.-46-8620C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109735481 | |||||||
| chr12:109735488 | C | T | 7 | a0001c0001t0002g0259 a0001c0001t0002g0290 a0001c0001t0002g0291 others(4): Show |
7 | HG01361.hp1 HG02257.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.-46-8613C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109735488 | |||||||
| chr12:109735493 | C | A | 1 | a0001c0005t0003g0227 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-46-8608C>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109735493 | |||||||
| chr12:109735728 | C | T | 1 | a0001c0001t0001g0026 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-46-8373C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109735728 | |||||||
| chr12:109735759 | T | C | 97 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0010 others(94): Show |
107 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(104): Show |
intron_variant | MODIFIER | c.-46-8342T>C | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109735759 | |||||||
| chr12:109735823 | T | C | 1 | a0001c0001t0002g0271 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-46-8278T>C | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109735823 | |||||||
| chr12:109735874 | G | A | 97 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0010 others(94): Show |
107 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(104): Show |
intron_variant | MODIFIER | c.-46-8227G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109735874 | |||||||
| chr12:109735959 | G | A | 1 | a0001c0001t0001g0329 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-46-8142G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109735959 | |||||||
| chr12:109736040 | G | A | 2 | a0001c0001t0002g0259 a0001c0006t0007g0030 |
2 | HG02922.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-46-8061G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109736040 | |||||||
| chr12:109736082 | G | C | 2 | a0001c0001t0001g0181 a0001c0001t0001g0209 |
2 | HG00280.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.-46-8019G>C | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109736082 | |||||||
| chr12:109736103 | C | T | 1 | a0001c0001t0001g0026 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-46-7998C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109736103 | |||||||
| chr12:109736224 | C | G | 5 | a0001c0001t0002g0290 a0001c0001t0002g0291 a0001c0001t0002g0292 others(2): Show |
5 | HG01361.hp1 HG02257.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.-46-7877C>G | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109736224 | |||||||
| chr12:109736408 | T | C | 1 | a0001c0001t0027g0313 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-46-7693T>C | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109736408 | |||||||
| chr12:109736446 | C | T | 1 | a0001c0001t0005g0041 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-46-7655C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109736446 | |||||||
| chr12:109736582 | G | A | 1 | a0001c0013t0001g0332 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-46-7519G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109736582 | |||||||
| chr12:109736739 | G | A | 1 | a0001c0001t0001g0128 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-46-7362G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109736739 | |||||||
| chr12:109736759 | C | T | 34 | a0001c0001t0001g0062 a0001c0001t0001g0077 a0001c0001t0001g0092 others(31): Show |
34 | HG00323.hp2 HG00639.hp2 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.-46-7342C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109736759 | |||||||
| chr12:109736819 | G | A | 2 | a0001c0001t0001g0308 a0001c0015t0001g0310 |
2 | HG01081.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.-46-7282G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109736819 | |||||||
| chr12:109736885 | C | T | 4 | a0002c0004t0008g0023 a0002c0004t0008g0053 a0002c0004t0008g0054 others(1): Show |
4 | HG01891.hp2 HG02486.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.-46-7216C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109736885 | |||||||
| chr12:109737057 | C | T | 1 | a0001c0001t0001g0181 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-46-7044C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109737057 | |||||||
| chr12:109737113 | C | G | 1 | a0001c0001t0004g0330 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-46-6988C>G | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109737113 | |||||||
| chr12:109737166 | G | A | 1 | a0001c0001t0001g0137 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-46-6935G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109737166 | |||||||
| chr12:109737585 | TA | T | 181 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0010 others(178): Show |
201 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.-46-6500delA | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 109737585 | ||||||
| chr12:109737602 | G | A | 1 | a0001c0001t0001g0203 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-46-6499G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109737602 | |||||||
| chr12:109737612 | C | T | 1 | a0001c0001t0001g0329 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-46-6489C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109737612 | |||||||
| chr12:109737732 | G | A | 97 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0010 others(94): Show |
107 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(104): Show |
intron_variant | MODIFIER | c.-46-6369G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109737732 | |||||||
| chr12:109737801 | C | T | 8 | a0001c0001t0001g0052 a0001c0001t0001g0071 a0001c0001t0004g0058 others(5): Show |
8 | HG02258.hp2 HG02615.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.-46-6300C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109737801 | |||||||
| chr12:109737906 | C | T | 27 | a0001c0001t0001g0062 a0001c0001t0001g0077 a0001c0001t0001g0092 others(24): Show |
27 | HG00323.hp2 HG00639.hp2 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.-46-6195C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109737906 | |||||||
| chr12:109738018 | A | G | 27 | a0001c0001t0001g0062 a0001c0001t0001g0077 a0001c0001t0001g0092 others(24): Show |
27 | HG00323.hp2 HG00639.hp2 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.-46-6083A>G | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109738018 | |||||||
| chr12:109738028 | G | C | 1 | a0001c0001t0004g0063 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-46-6073G>C | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109738028 | |||||||
| chr12:109738125 | C | T | 27 | a0001c0001t0001g0062 a0001c0001t0001g0077 a0001c0001t0001g0092 others(24): Show |
27 | HG00323.hp2 HG00639.hp2 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.-46-5976C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109738125 | |||||||
| chr12:109738212 | C | T | 1 | a0001c0001t0001g0026 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-46-5889C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109738212 | |||||||
| chr12:109738385 | C | T | 1 | a0001c0001t0001g0105 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-46-5716C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109738385 | |||||||
| chr12:109738391 | C | G | 1 | a0002c0004t0008g0316 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-46-5710C>G | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109738391 | |||||||
| chr12:109738456 | G | A | 97 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0010 others(94): Show |
107 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(104): Show |
intron_variant | MODIFIER | c.-46-5645G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109738456 | |||||||
| chr12:109738553 | G | T | 106 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0010 others(103): Show |
117 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(114): Show |
intron_variant | MODIFIER | c.-46-5548G>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109738553 | |||||||
| chr12:109738637 | G | A | 1 | a0001c0001t0001g0185 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.-46-5464G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109738637 | |||||||
| chr12:109738763 | T | C | 108 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0010 others(105): Show |
119 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(116): Show |
intron_variant | MODIFIER | c.-46-5338T>C | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109738763 | |||||||
| chr12:109738928 | C | G | 1 | a0001c0001t0026g0278 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-46-5173C>G | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109738928 | |||||||
| chr12:109739260 | C | T | 1 | a0001c0001t0001g0051 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-46-4841C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109739260 | |||||||
| chr12:109739324 | A | T | 3 | a0001c0001t0002g0314 a0001c0001t0002g0315 a0001c0001t0005g0043 |
3 | HG01109.hp1 HG02109.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-46-4777A>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109739324 | |||||||
| chr12:109739389 | T | C | 1 | a0001c0001t0001g0219 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-46-4712T>C | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109739389 | |||||||
| chr12:109739393 | G | A | 1 | a0001c0001t0007g0027 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-46-4708G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109739393 | |||||||
| chr12:109739469 | G | C | 8 | a0001c0001t0001g0048 a0001c0001t0001g0055 a0001c0001t0001g0078 others(5): Show |
9 | HG01168.hp2 HG01169.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.-46-4632G>C | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109739469 | |||||||
| chr12:109739491 | G | A | 1 | a0001c0001t0001g0142 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-46-4610G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109739491 | |||||||
| chr12:109739566 | T | C | 1 | a0002c0004t0008g0316 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-46-4535T>C | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109739566 | |||||||
| chr12:109739671 | A | G | 1 | a0001c0001t0007g0027 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-46-4430A>G | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109739671 | |||||||
| chr12:109739824 | C | G | 2 | a0001c0001t0001g0308 a0001c0015t0001g0310 |
2 | HG01081.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.-46-4277C>G | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109739824 | |||||||
| chr12:109739885 | G | A | 1 | a0001c0001t0001g0095 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.-46-4216G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109739885 | |||||||
| chr12:109739896 | G | A | 1 | a0001c0001t0004g0312 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-46-4205G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109739896 | |||||||
| chr12:109739939 | G | C | 1 | a0001c0001t0004g0249 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-46-4162G>C | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109739939 | |||||||
| chr12:109740067 | C | T | 1 | a0001c0001t0005g0041 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-46-4034C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109740067 | |||||||
| chr12:109740120 | C | T | 1 | a0001c0001t0001g0203 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-46-3981C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109740120 | |||||||
| chr12:109740371 | C | T | 1 | a0001c0001t0001g0114 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-46-3730C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109740371 | |||||||
| chr12:109740456 | G | A | 23 | a0001c0001t0001g0062 a0001c0001t0001g0077 a0001c0001t0001g0113 others(20): Show |
23 | HG00639.hp2 HG01070.hp2 HG01074.hp2 others(20): Show |
intron_variant | MODIFIER | c.-46-3645G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109740456 | |||||||
| chr12:109740605 | G | C | 96 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0024 others(93): Show |
105 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(102): Show |
intron_variant | MODIFIER | c.-46-3496G>C | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109740605 | |||||||
| chr12:109740692 | T | C | 232 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(229): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.-46-3409T>C | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109740692 | |||||||
| chr12:109740773 | C | T | 2 | a0001c0002t0001g0151 a0001c0002t0001g0183 |
2 | HG02572.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-46-3328C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109740773 | |||||||
| chr12:109740940 | C | T | 1 | a0001c0006t0007g0030 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-46-3161C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109740940 | |||||||
| chr12:109741093 | G | C | 1 | a0004c0008t0003g0012 | 2 | NA18940.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.-46-3008G>C | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109741093 | |||||||
| chr12:109741163 | C | G | 1 | a0001c0001t0003g0238 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.-46-2938C>G | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109741163 | |||||||
| chr12:109741560 | C | T | 5 | a0001c0001t0001g0026 a0001c0001t0001g0308 a0001c0001t0002g0314 others(2): Show |
5 | HG01081.hp2 HG01109.hp1 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.-46-2541C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109741560 | |||||||
| chr12:109741653 | G | C | 2 | a0001c0001t0013g0255 a0001c0001t0013g0256 |
2 | HG03710.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.-46-2448G>C | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109741653 | |||||||
| chr12:109741760 | G | T | 1 | a0001c0001t0003g0240 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-46-2341G>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109741760 | |||||||
| chr12:109741844 | C | G | 1 | a0001c0001t0007g0029 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-46-2257C>G | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109741844 | |||||||
| chr12:109742346 | A | G | 247 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(244): Show |
259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.-46-1755A>G | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109742346 | |||||||
| chr12:109742372 | G | A | 1 | a0002c0004t0008g0316 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-46-1729G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109742372 | |||||||
| chr12:109742414 | G | A | 32 | a0001c0001t0001g0052 a0001c0001t0001g0062 a0001c0001t0001g0071 others(29): Show |
32 | HG00323.hp2 HG00639.hp2 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.-46-1687G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109742414 | |||||||
| chr12:109742592 | A | ACT | 16 | a0001c0001t0001g0009 a0001c0001t0001g0047 a0001c0001t0001g0076 others(13): Show |
17 | HG01884.hp1 HG01891.hp2 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.-46-1495_-46-1494d others(4): Show |
FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 109742592 | ||||||
| chr12:109742606 | T | G | 1 | a0002c0004t0008g0316 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-46-1495T>G | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109742606 | |||||||
| chr12:109742608 | G | T | 1 | a0002c0004t0008g0316 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-46-1493G>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109742608 | |||||||
| chr12:109742611 | C | CT | 241 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(238): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.-46-1477dupT | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 109742611 | ||||||
| chr12:109742753 | T | C | 1 | a0001c0001t0001g0081 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-46-1348T>C | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109742753 | |||||||
| chr12:109742783 | G | A | 1 | a0001c0006t0002g0304 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-46-1318G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109742783 | |||||||
| chr12:109743087 | G | A | 1 | a0002c0004t0008g0316 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-46-1014G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109743087 | |||||||
| chr12:109743206 | T | C | 245 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(242): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.-46-895T>C | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109743206 | |||||||
| chr12:109743304 | G | A | 1 | a0001c0001t0001g0329 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-46-797G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109743304 | |||||||
| chr12:109743326 | C | T | 107 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(104): Show |
110 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(107): Show |
intron_variant | MODIFIER | c.-46-775C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109743326 | |||||||
| chr12:109743340 | A | G | 9 | a0001c0001t0001g0062 a0001c0001t0001g0109 a0001c0001t0001g0113 others(6): Show |
9 | HG00323.hp2 HG01074.hp2 HG01167.hp2 others(6): Show |
intron_variant | MODIFIER | c.-46-761A>G | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109743340 | |||||||
| chr12:109743358 | T | C | 3 | a0001c0001t0003g0013 a0001c0005t0003g0227 a0001c0005t0003g0234 |
4 | HG03654.hp1 HG03831.hp1 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.-46-743T>C | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109743358 | |||||||
| chr12:109743373 | C | T | 1 | a0002c0004t0008g0054 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-46-728C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109743373 | |||||||
| chr12:109743375 | C | T | 6 | a0001c0001t0001g0208 a0001c0001t0004g0066 a0001c0001t0004g0068 others(3): Show |
6 | HG01433.hp2 HG01928.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.-46-726C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109743375 | |||||||
| chr12:109743433 | T | A | 11 | a0001c0001t0001g0006 a0001c0001t0001g0051 a0001c0001t0001g0072 others(8): Show |
12 | HG01167.hp1 HG02280.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.-46-668T>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109743433 | |||||||
| chr12:109743522 | C | T | 2 | a0001c0001t0001g0090 a0001c0001t0001g0093 |
2 | NA18962.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.-46-579C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109743522 | |||||||
| chr12:109743590 | G | A | 1 | a0001c0001t0001g0047 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-46-511G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109743590 | |||||||
| chr12:109743610 | G | A | 1 | a0001c0001t0002g0279 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-46-491G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109743610 | |||||||
| chr12:109743876 | G | T | 1 | a0001c0001t0002g0277 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-46-225G>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109743876 | |||||||
| chr12:109743947 | C | T | 2 | a0001c0001t0002g0259 a0001c0006t0007g0030 |
2 | HG02922.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-46-154C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 1/2 | chr12 | 109743947 | |||||||
| chr12:109744287 | A | G | 1 | a0001c0001t0001g0149 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.82+59A>G | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109744287 | |||||||
| chr12:109744287 | A | T | 1 | a0002c0004t0008g0316 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.82+59A>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109744287 | |||||||
| chr12:109744345 | C | A | 1 | a0002c0004t0008g0316 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.82+117C>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109744345 | |||||||
| chr12:109744518 | C | T | 1 | a0001c0001t0002g0017 | 2 | NA19060.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.82+290C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109744518 | |||||||
| chr12:109744836 | A | G | 17 | a0001c0001t0001g0057 a0001c0001t0001g0214 a0001c0001t0001g0215 others(14): Show |
18 | HG00558.hp2 HG00597.hp1 HG00609.hp2 others(15): Show |
intron_variant | MODIFIER | c.82+608A>G | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109744836 | |||||||
| chr12:109744905 | C | A | 1 | a0001c0001t0001g0157 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.82+677C>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109744905 | |||||||
| chr12:109744946 | C | T | 1 | a0001c0001t0001g0329 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.82+718C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109744946 | |||||||
| chr12:109744949 | C | A | 1 | a0001c0001t0001g0194 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.82+721C>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109744949 | |||||||
| chr12:109744957 | T | C | 4 | a0001c0001t0001g0094 a0001c0001t0001g0147 a0001c0001t0001g0180 others(1): Show |
4 | NA18952.hp1 NA18985.hp2 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.82+729T>C | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109744957 | |||||||
| chr12:109745021 | A | T | 1 | a0001c0001t0001g0137 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.82+793A>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109745021 | |||||||
| chr12:109745143 | G | A | 93 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0024 others(90): Show |
102 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.82+915G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109745143 | |||||||
| chr12:109745226 | T | A | 1 | a0001c0001t0001g0139 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.82+998T>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109745226 | |||||||
| chr12:109745336 | T | C | 1 | a0001c0013t0001g0332 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.82+1108T>C | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109745336 | |||||||
| chr12:109745477 | G | A | 1 | a0001c0001t0027g0313 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.82+1249G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109745477 | |||||||
| chr12:109745572 | A | G | 1 | a0001c0001t0005g0043 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.82+1344A>G | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109745572 | |||||||
| chr12:109745778 | T | A | 40 | a0001c0001t0001g0168 a0001c0001t0001g0177 a0001c0001t0001g0216 others(37): Show |
51 | HG00408.hp1 HG00423.hp2 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.82+1550T>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109745778 | |||||||
| chr12:109745883 | ACTAAT | A | 94 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0024 others(91): Show |
103 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.82+1659_82+1663del others(5): Show |
FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 109745883 | ||||||
| chr12:109745980 | C | T | 94 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0024 others(91): Show |
103 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.82+1752C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109745980 | |||||||
| chr12:109746046 | C | T | 1 | a0002c0004t0008g0316 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.82+1818C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109746046 | |||||||
| chr12:109746177 | G | T | 3 | a0001c0001t0001g0216 a0001c0001t0003g0247 a0001c0001t0021g0213 |
3 | HG00609.hp1 NA18942.hp2 NA18945.hp2 |
intron_variant | MODIFIER | c.82+1949G>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109746177 | |||||||
| chr12:109746291 | C | T | 7 | a0001c0001t0005g0005 a0001c0001t0005g0038 a0001c0001t0005g0039 others(4): Show |
8 | HG02615.hp2 HG02818.hp1 HG03139.hp1 others(5): Show |
intron_variant | MODIFIER | c.82+2063C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109746291 | |||||||
| chr12:109746406 | T | C | 96 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0024 others(93): Show |
105 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(102): Show |
intron_variant | MODIFIER | c.82+2178T>C | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109746406 | |||||||
| chr12:109746468 | A | G | 96 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0024 others(93): Show |
105 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(102): Show |
intron_variant | MODIFIER | c.82+2240A>G | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109746468 | |||||||
| chr12:109746472 | G | A | 1 | a0001c0001t0001g0195 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.82+2244G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109746472 | |||||||
| chr12:109746575 | A | G | 2 | a0001c0001t0001g0308 a0001c0015t0001g0310 |
2 | HG01081.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.82+2347A>G | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109746575 | |||||||
| chr12:109746633 | G | A | 243 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(240): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.82+2405G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109746633 | |||||||
| chr12:109747309 | G | A | 3 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0200 |
3 | HG01256.hp2 HG01261.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.82+3081G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109747309 | |||||||
| chr12:109747320 | C | T | 7 | a0001c0001t0001g0145 a0001c0001t0001g0152 a0001c0001t0001g0153 others(4): Show |
7 | HG00323.hp1 HG00738.hp2 HG01074.hp1 others(4): Show |
intron_variant | MODIFIER | c.82+3092C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109747320 | |||||||
| chr12:109747399 | A | G | 1 | a0001c0001t0002g0296 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.82+3171A>G | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109747399 | |||||||
| chr12:109747690 | G | GTTAAGT | 243 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(240): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.82+3465_82+3466ins others(6): Show |
FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 109747690 | ||||||
| chr12:109747757 | G | A | 1 | a0001c0001t0003g0222 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.82+3529G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109747757 | |||||||
| chr12:109747797 | C | T | 1 | a0001c0001t0002g0258 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.82+3569C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109747797 | |||||||
| chr12:109747802 | T | TTAA | 3 | a0001c0001t0002g0262 a0001c0001t0002g0263 a0001c0001t0002g0264 |
3 | HG01943.hp1 HG02622.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.82+3574_82+3575ins others(3): Show |
FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109747802 | |||||||
| chr12:109747812 | A | G | 1 | a0001c0001t0004g0065 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.82+3584A>G | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109747812 | |||||||
| chr12:109747832 | C | T | 3 | a0001c0001t0004g0250 a0001c0001t0004g0251 a0001c0001t0010g0104 |
3 | HG01175.hp2 HG02258.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.82+3604C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109747832 | |||||||
| chr12:109747955 | C | T | 94 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0024 others(91): Show |
103 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.82+3727C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109747955 | |||||||
| chr12:109748067 | T | C | 1 | a0001c0001t0021g0213 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.82+3839T>C | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109748067 | |||||||
| chr12:109748154 | T | C | 1 | a0001c0001t0001g0026 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.82+3926T>C | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109748154 | |||||||
| chr12:109748303 | T | C | 1 | a0001c0001t0001g0106 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.82+4075T>C | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109748303 | |||||||
| chr12:109748326 | TTTTC | T | 3 | a0001c0001t0001g0116 a0001c0001t0010g0108 a0001c0013t0001g0332 |
3 | HG01167.hp1 HG01256.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.82+4106_82+4109del others(4): Show |
FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 109748326 | ||||||
| chr12:109748331 | TTTC | T | 86 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(83): Show |
89 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(86): Show |
intron_variant | MODIFIER | c.82+4106_82+4108del others(3): Show |
FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 109748331 | ||||||
| chr12:109748332 | TTC | T | 18 | a0001c0001t0001g0007 a0001c0001t0001g0075 a0001c0001t0001g0080 others(15): Show |
18 | HG00544.hp2 HG00558.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.82+4106_82+4107del others(2): Show |
FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 109748332 | ||||||
| chr12:109748334 | C | CT | 89 | a0001c0001t0001g0168 a0001c0001t0001g0177 a0001c0001t0001g0203 others(86): Show |
103 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(100): Show |
intron_variant | MODIFIER | c.82+4126dupT | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 109748334 | ||||||
| chr12:109748334 | C | CTT | 6 | a0001c0001t0001g0114 a0001c0001t0002g0291 a0001c0001t0002g0292 others(3): Show |
6 | HG00609.hp1 HG01891.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.82+4125_82+4126dup others(2): Show |
FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 109748334 | ||||||
| chr12:109748334 | CTTT | C | 93 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0024 others(90): Show |
102 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.82+4124_82+4126del others(3): Show |
FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 109748334 | ||||||
| chr12:109748341 | T | C | 93 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0024 others(90): Show |
102 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.82+4113T>C | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109748341 | |||||||
| chr12:109748748 | T | C | 33 | a0001c0001t0001g0052 a0001c0001t0001g0062 a0001c0001t0001g0071 others(30): Show |
33 | HG00099.hp2 HG00323.hp2 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.82+4520T>C | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109748748 | |||||||
| chr12:109748972 | G | A | 1 | a0001c0001t0002g0271 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.82+4744G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109748972 | |||||||
| chr12:109749003 | T | C | 1 | a0001c0001t0005g0043 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.82+4775T>C | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109749003 | |||||||
| chr12:109749173 | C | A | 1 | a0001c0001t0007g0029 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.82+4945C>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109749173 | |||||||
| chr12:109749250 | G | A | 95 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0024 others(92): Show |
104 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.82+5022G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109749250 | |||||||
| chr12:109749295 | G | A | 5 | a0001c0001t0001g0026 a0001c0001t0001g0308 a0001c0001t0002g0314 others(2): Show |
5 | HG01081.hp2 HG01109.hp1 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.82+5067G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109749295 | |||||||
| chr12:109749471 | A | G | 1 | a0001c0002t0006g0324 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.82+5243A>G | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109749471 | |||||||
| chr12:109749475 | T | C | 40 | a0001c0001t0001g0168 a0001c0001t0001g0177 a0001c0001t0001g0216 others(37): Show |
51 | HG00408.hp1 HG00423.hp2 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.82+5247T>C | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109749475 | |||||||
| chr12:109749528 | A | G | 5 | a0001c0001t0001g0026 a0001c0001t0001g0308 a0001c0001t0002g0314 others(2): Show |
5 | HG01081.hp2 HG01109.hp1 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.82+5300A>G | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109749528 | |||||||
| chr12:109749994 | C | T | 1 | a0001c0001t0003g0229 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.82+5766C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109749994 | |||||||
| chr12:109750114 | T | C | 1 | a0001c0001t0001g0062 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.82+5886T>C | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109750114 | |||||||
| chr12:109750158 | T | C | 1 | a0001c0001t0001g0092 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.82+5930T>C | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109750158 | |||||||
| chr12:109750187 | C | A | 80 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0024 others(77): Show |
88 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.82+5959C>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109750187 | |||||||
| chr12:109750261 | A | T | 1 | a0001c0001t0001g0190 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.82+6033A>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109750261 | |||||||
| chr12:109750350 | G | C | 96 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0024 others(93): Show |
105 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(102): Show |
intron_variant | MODIFIER | c.82+6122G>C | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109750350 | |||||||
| chr12:109750541 | G | C | 3 | a0001c0001t0002g0281 a0001c0001t0002g0298 a0001c0001t0003g0235 |
3 | NA18973.hp1 NA18982.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.82+6313G>C | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109750541 | |||||||
| chr12:109750573 | A | G | 94 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0024 others(91): Show |
103 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.82+6345A>G | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109750573 | |||||||
| chr12:109750883 | AT | A | 241 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(238): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.82+6662delT | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 109750883 | ||||||
| chr12:109751008 | T | G | 33 | a0001c0001t0001g0052 a0001c0001t0001g0062 a0001c0001t0001g0071 others(30): Show |
33 | HG00099.hp2 HG00323.hp2 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.82+6780T>G | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109751008 | |||||||
| chr12:109751088 | C | G | 1 | a0001c0001t0001g0084 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.82+6860C>G | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109751088 | |||||||
| chr12:109751216 | A | AT | 22 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0047 others(19): Show |
24 | HG01167.hp1 HG01884.hp1 HG02280.hp2 others(21): Show |
intron_variant | MODIFIER | c.82+6997dupT | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 109751216 | ||||||
| chr12:109751509 | C | G | 1 | a0001c0001t0004g0065 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.82+7281C>G | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109751509 | |||||||
| chr12:109751553 | A | G | 7 | a0001c0001t0001g0094 a0001c0001t0001g0147 a0001c0001t0001g0159 others(4): Show |
7 | NA18948.hp1 NA18952.hp1 NA18985.hp2 others(4): Show |
intron_variant | MODIFIER | c.82+7325A>G | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109751553 | |||||||
| chr12:109751599 | T | C | 1 | a0001c0001t0001g0165 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.82+7371T>C | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109751599 | |||||||
| chr12:109751678 | T | C | 1 | a0001c0001t0001g0047 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.82+7450T>C | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109751678 | |||||||
| chr12:109752402 | C | T | 94 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0024 others(91): Show |
103 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.82+8174C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109752402 | |||||||
| chr12:109752403 | G | A | 1 | a0001c0001t0001g0026 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.82+8175G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109752403 | |||||||
| chr12:109752442 | G | A | 2 | a0001c0001t0006g0325 a0001c0001t0006g0326 |
2 | HG02559.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.82+8214G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109752442 | |||||||
| chr12:109752475 | TTGTCCC | T | 94 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0024 others(91): Show |
103 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.82+8251_82+8256del others(6): Show |
FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 109752475 | ||||||
| chr12:109752638 | CTG | C | 94 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0024 others(91): Show |
103 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.82+8412_82+8413del others(2): Show |
FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 109752638 | ||||||
| chr12:109752731 | G | A | 1 | a0001c0001t0020g0022 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.82+8503G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109752731 | |||||||
| chr12:109752856 | C | T | 1 | a0001c0001t0001g0219 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.82+8628C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109752856 | |||||||
| chr12:109752925 | C | T | 2 | a0001c0001t0001g0114 a0001c0001t0027g0313 |
2 | HG01891.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.82+8697C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109752925 | |||||||
| chr12:109752981 | A | G | 7 | a0001c0001t0002g0277 a0001c0001t0003g0001 a0001c0001t0003g0236 others(4): Show |
13 | HG00423.hp2 HG02056.hp2 HG02074.hp1 others(10): Show |
intron_variant | MODIFIER | c.82+8753A>G | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109752981 | |||||||
| chr12:109753153 | G | A | 1 | a0001c0001t0001g0026 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.82+8925G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109753153 | |||||||
| chr12:109753278 | T | A | 1 | a0001c0001t0002g0265 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.82+9050T>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109753278 | |||||||
| chr12:109753386 | C | T | 3 | a0002c0004t0008g0053 a0002c0004t0008g0054 a0002c0004t0008g0056 |
3 | HG01891.hp2 HG02486.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.82+9158C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109753386 | |||||||
| chr12:109753400 | A | G | 4 | a0001c0001t0001g0169 a0001c0001t0006g0325 a0001c0001t0006g0326 others(1): Show |
4 | HG02559.hp1 HG02886.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.82+9172A>G | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109753400 | |||||||
| chr12:109753407 | A | G | 91 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0024 others(88): Show |
100 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.82+9179A>G | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109753407 | |||||||
| chr12:109753412 | G | C | 1 | a0001c0001t0001g0168 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.82+9184G>C | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109753412 | |||||||
| chr12:109753547 | GCC | G | 234 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(231): Show |
246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.82+9325_82+9326del others(2): Show |
FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 109753547 | ||||||
| chr12:109753559 | CG | C | 92 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0024 others(89): Show |
101 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(98): Show |
intron_variant | MODIFIER | c.82+9340delG | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 109753559 | ||||||
| chr12:109753561 | G | T | 1 | a0001c0001t0003g0318 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.82+9333G>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109753561 | |||||||
| chr12:109753562 | G | C | 1 | a0001c0001t0001g0111 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.82+9334G>C | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109753562 | |||||||
| chr12:109753570 | G | A | 141 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(138): Show |
144 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(141): Show |
intron_variant | MODIFIER | c.82+9342G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109753570 | |||||||
| chr12:109753700 | G | C | 91 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0024 others(88): Show |
100 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.82+9472G>C | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109753700 | |||||||
| chr12:109753716 | G | A | 91 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0024 others(88): Show |
100 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.82+9488G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109753716 | |||||||
| chr12:109753728 | C | G | 1 | a0001c0001t0001g0091 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.82+9500C>G | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109753728 | |||||||
| chr12:109753853 | A | G | 5 | a0001c0001t0001g0026 a0001c0001t0001g0308 a0001c0001t0002g0314 others(2): Show |
5 | HG01081.hp2 HG01109.hp1 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.82+9625A>G | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109753853 | |||||||
| chr12:109754014 | A | G | 4 | a0001c0001t0001g0169 a0001c0001t0006g0325 a0001c0001t0006g0326 others(1): Show |
4 | HG02559.hp1 HG02886.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.82+9786A>G | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109754014 | |||||||
| chr12:109754137 | C | A | 1 | a0001c0001t0002g0283 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.82+9909C>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109754137 | |||||||
| chr12:109754296 | A | G | 1 | a0001c0001t0001g0219 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.82+10068A>G | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109754296 | |||||||
| chr12:109754362 | T | C | 33 | a0001c0001t0001g0052 a0001c0001t0001g0062 a0001c0001t0001g0071 others(30): Show |
33 | HG00099.hp2 HG00323.hp2 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.82+10134T>C | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109754362 | |||||||
| chr12:109754377 | A | G | 1 | a0004c0010t0003g0237 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.82+10149A>G | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109754377 | |||||||
| chr12:109754404 | A | G | 1 | a0002c0004t0008g0316 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.82+10176A>G | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109754404 | |||||||
| chr12:109754462 | T | C | 2 | a0001c0001t0002g0259 a0001c0006t0007g0030 |
2 | HG02922.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.82+10234T>C | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109754462 | |||||||
| chr12:109754634 | C | G | 1 | a0001c0015t0001g0310 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.82+10406C>G | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109754634 | |||||||
| chr12:109754649 | G | A | 6 | a0001c0001t0001g0003 a0001c0001t0001g0165 a0001c0001t0001g0166 others(3): Show |
8 | HG01099.hp1 HG01123.hp2 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.82+10421G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109754649 | |||||||
| chr12:109754666 | CT | C | 96 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0024 others(93): Show |
105 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(102): Show |
intron_variant | MODIFIER | c.82+10453delT | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 109754666 | ||||||
| chr12:109754679 | T | G | 1 | a0001c0015t0001g0310 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.82+10451T>G | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109754679 | |||||||
| chr12:109754722 | C | T | 4 | a0001c0001t0001g0026 a0001c0001t0002g0314 a0001c0001t0002g0315 others(1): Show |
4 | HG01109.hp1 HG02109.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.82+10494C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109754722 | |||||||
| chr12:109754738 | G | A | 2 | a0001c0001t0001g0114 a0001c0001t0027g0313 |
2 | HG01891.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.82+10510G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109754738 | |||||||
| chr12:109754972 | G | A | 1 | a0001c0001t0010g0120 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.82+10744G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109754972 | |||||||
| chr12:109755109 | G | A | 2 | a0001c0001t0001g0208 a0001c0001t0004g0066 |
2 | HG01433.hp2 HG01928.hp1 |
intron_variant | MODIFIER | c.82+10881G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109755109 | |||||||
| chr12:109755284 | CTTCTTTT others(13): Show |
C | 1 | a0002c0004t0008g0316 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.82+11059_82+11078d others(22): Show |
FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 109755284 | ||||||
| chr12:109755287 | CT | C | 15 | a0001c0001t0002g0016 a0001c0001t0002g0268 a0001c0001t0002g0284 others(12): Show |
15 | HG00597.hp1 HG01070.hp1 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.82+11101delT | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 109755287 | ||||||
| chr12:109755287 | CTT | C | 7 | a0001c0001t0001g0208 a0001c0001t0002g0260 a0001c0001t0002g0283 others(4): Show |
7 | HG00609.hp2 HG01433.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.82+11100_82+11101d others(4): Show |
FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 109755287 | ||||||
| chr12:109755287 | CTTTTTTT others(5): Show |
C | 2 | a0001c0001t0005g0005 a0001c0001t0005g0038 |
2 | HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.82+11090_82+11101d others(14): Show |
FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 109755287 | ||||||
| chr12:109755287 | CTTTTTTT others(6): Show |
C | 17 | a0001c0001t0001g0329 a0001c0001t0003g0001 a0001c0001t0003g0011 others(14): Show |
19 | HG00423.hp2 HG01358.hp1 HG02056.hp2 others(16): Show |
intron_variant | MODIFIER | c.82+11089_82+11101d others(15): Show |
FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 109755287 | ||||||
| chr12:109755287 | CTTTTTTT others(7): Show |
C | 31 | a0001c0001t0001g0168 a0001c0001t0001g0177 a0001c0001t0001g0216 others(28): Show |
39 | HG00408.hp1 HG00609.hp1 HG02074.hp1 others(36): Show |
intron_variant | MODIFIER | c.82+11088_82+11101d others(16): Show |
FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 109755287 | ||||||
| chr12:109755287 | CTTTTTTT others(8): Show |
C | 44 | a0001c0001t0001g0052 a0001c0001t0001g0062 a0001c0001t0001g0075 others(41): Show |
44 | HG00099.hp2 HG00323.hp2 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.82+11087_82+11101d others(17): Show |
FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 109755287 | ||||||
| chr12:109755287 | CTTTTTTT others(9): Show |
C | 100 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(97): Show |
102 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(99): Show |
intron_variant | MODIFIER | c.82+11086_82+11101d others(18): Show |
FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 109755287 | ||||||
| chr12:109755287 | CTTTTTTT others(10): Show |
C | 13 | a0001c0001t0001g0006 a0001c0001t0001g0085 a0001c0001t0001g0090 others(10): Show |
13 | HG02976.hp2 HG03540.hp2 HG03942.hp1 others(10): Show |
intron_variant | MODIFIER | c.82+11085_82+11101d others(19): Show |
FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 109755287 | ||||||
| chr12:109755287 | CTTTTTTT others(11): Show |
C | 84 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0024 others(81): Show |
93 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.82+11084_82+11101d others(20): Show |
FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 109755287 | ||||||
| chr12:109755287 | CTTTTTTT others(12): Show |
C | 3 | a0001c0001t0001g0160 a0001c0001t0002g0282 a0001c0001t0018g0073 |
3 | NA18986.hp1 NA19074.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.82+11083_82+11101d others(21): Show |
FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 109755287 | ||||||
| chr12:109755287 | CTTTTTTT others(13): Show |
C | 1 | a0001c0001t0004g0004 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.82+11082_82+11101d others(22): Show |
FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 109755287 | ||||||
| chr12:109755287 | CTTTTTTT others(15): Show |
C | 2 | a0001c0005t0003g0227 a0001c0005t0003g0234 |
2 | HG03654.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.82+11080_82+11101d others(24): Show |
FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 109755287 | ||||||
| chr12:109755287 | CTTTTTTT others(18): Show |
C | 1 | a0001c0001t0002g0303 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.82+11077_82+11101d others(27): Show |
FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 109755287 | ||||||
| chr12:109755372 | GCGCAATC others(9): Show |
G | 2 | a0001c0001t0002g0259 a0001c0006t0007g0030 |
2 | HG02922.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.82+11166_82+11181d others(18): Show |
FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 109755372 | ||||||
| chr12:109755414 | T | TGCCTCCC others(25): Show |
8 | a0001c0001t0001g0095 a0001c0001t0001g0103 a0001c0001t0001g0117 others(5): Show |
8 | HG00438.hp1 HG02080.hp2 HG02132.hp2 others(5): Show |
intron_variant | MODIFIER | c.82+11198_82+11229d others(34): Show |
FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 109755414 | ||||||
| chr12:109755482 | C | A | 1 | a0002c0004t0008g0316 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.82+11254C>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109755482 | |||||||
| chr12:109755691 | G | A | 1 | a0002c0004t0008g0316 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.82+11463G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109755691 | |||||||
| chr12:109755697 | C | T | 1 | a0001c0001t0002g0302 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.82+11469C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109755697 | |||||||
| chr12:109755734 | A | G | 1 | a0001c0001t0001g0124 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.82+11506A>G | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109755734 | |||||||
| chr12:109755814 | T | C | 2 | a0001c0001t0002g0259 a0001c0006t0007g0030 |
2 | HG02922.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.82+11586T>C | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109755814 | |||||||
| chr12:109756098 | C | T | 5 | a0001c0001t0002g0290 a0001c0001t0002g0291 a0001c0001t0002g0292 others(2): Show |
5 | HG01361.hp1 HG02257.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.82+11870C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109756098 | |||||||
| chr12:109756290 | T | G | 1 | a0001c0001t0001g0026 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.83-11722T>G | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109756290 | |||||||
| chr12:109756392 | C | CT | 20 | a0001c0001t0001g0140 a0001c0001t0001g0143 a0001c0001t0001g0170 others(17): Show |
21 | HG01169.hp1 HG01884.hp2 HG02074.hp1 others(18): Show |
intron_variant | MODIFIER | c.83-11603dupT | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 109756392 | ||||||
| chr12:109756392 | C | CTT | 84 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0024 others(81): Show |
93 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.83-11604_83-11603d others(4): Show |
FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 109756392 | ||||||
| chr12:109756392 | C | CTTT | 6 | a0001c0001t0001g0141 a0001c0001t0001g0190 a0001c0001t0001g0205 others(3): Show |
6 | HG02004.hp2 HG03017.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.83-11605_83-11603d others(5): Show |
FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 109756392 | ||||||
| chr12:109756392 | CT | C | 15 | a0001c0001t0001g0009 a0001c0001t0001g0047 a0001c0001t0001g0076 others(12): Show |
16 | HG01884.hp1 HG02559.hp1 HG02647.hp1 others(13): Show |
intron_variant | MODIFIER | c.83-11603delT | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 109756392 | ||||||
| chr12:109756392 | CTT | C | 130 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(127): Show |
132 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(129): Show |
intron_variant | MODIFIER | c.83-11604_83-11603d others(4): Show |
FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 109756392 | ||||||
| chr12:109756392 | CTTT | C | 6 | a0001c0001t0001g0026 a0001c0001t0001g0114 a0001c0001t0002g0314 others(3): Show |
6 | HG01109.hp1 HG01891.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.83-11605_83-11603d others(5): Show |
FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 109756392 | ||||||
| chr12:109756513 | G | A | 2 | a0001c0007t0001g0162 a0001c0007t0001g0192 |
2 | HG00741.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.83-11499G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109756513 | |||||||
| chr12:109756618 | G | T | 147 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(144): Show |
150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): Show |
intron_variant | MODIFIER | c.83-11394G>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109756618 | |||||||
| chr12:109757295 | G | A | 92 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0024 others(89): Show |
101 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(98): Show |
intron_variant | MODIFIER | c.83-10717G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109757295 | |||||||
| chr12:109757509 | C | T | 1 | a0001c0001t0020g0022 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.83-10503C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109757509 | |||||||
| chr12:109757931 | G | A | 9 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0002g0016 others(6): Show |
10 | HG00597.hp1 HG00609.hp2 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.83-10081G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109757931 | |||||||
| chr12:109758068 | G | T | 1 | a0001c0001t0001g0102 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.83-9944G>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109758068 | |||||||
| chr12:109758108 | C | T | 91 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0024 others(88): Show |
100 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.83-9904C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109758108 | |||||||
| chr12:109758353 | G | A | 1 | a0001c0001t0001g0114 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.83-9659G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109758353 | |||||||
| chr12:109758366 | C | T | 1 | a0001c0001t0001g0128 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.83-9646C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109758366 | |||||||
| chr12:109758401 | C | T | 2 | a0001c0001t0015g0020 a0001c0001t0016g0021 |
2 | HG02970.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.83-9611C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109758401 | |||||||
| chr12:109758402 | G | A | 1 | a0001c0006t0002g0304 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.83-9610G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109758402 | |||||||
| chr12:109758521 | T | C | 3 | a0001c0001t0002g0262 a0001c0001t0002g0263 a0001c0001t0002g0264 |
3 | HG01943.hp1 HG02622.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.83-9491T>C | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109758521 | |||||||
| chr12:109758620 | TCTGCCCT others(16): Show |
T | 2 | a0001c0001t0014g0286 a0001c0001t0014g0287 |
2 | HG01070.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.83-9385_83-9363del others(23): Show |
FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 109758620 | ||||||
| chr12:109758794 | C | T | 80 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0057 others(77): Show |
81 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(78): Show |
intron_variant | MODIFIER | c.83-9218C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109758794 | |||||||
| chr12:109758831 | A | T | 1 | a0001c0001t0003g0011 | 2 | NA18983.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.83-9181A>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109758831 | |||||||
| chr12:109758942 | G | A | 1 | a0001c0001t0001g0328 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.83-9070G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109758942 | |||||||
| chr12:109759188 | C | A | 91 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0024 others(88): Show |
100 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.83-8824C>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109759188 | |||||||
| chr12:109759255 | A | T | 1 | a0002c0004t0008g0316 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.83-8757A>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109759255 | |||||||
| chr12:109759280 | T | C | 245 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(242): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.83-8732T>C | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109759280 | |||||||
| chr12:109759323 | C | T | 2 | a0001c0001t0002g0259 a0001c0006t0007g0030 |
2 | HG02922.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.83-8689C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109759323 | |||||||
| chr12:109759324 | G | A | 1 | a0001c0001t0001g0329 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.83-8688G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109759324 | |||||||
| chr12:109759357 | G | A | 9 | a0001c0001t0001g0048 a0001c0001t0001g0055 a0001c0001t0001g0078 others(6): Show |
10 | HG01168.hp2 HG01169.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.83-8655G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109759357 | |||||||
| chr12:109759677 | G | A | 2 | a0001c0001t0001g0117 a0001c0001t0001g0182 |
2 | NA18949.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.83-8335G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109759677 | |||||||
| chr12:109759918 | A | C | 1 | a0001c0001t0005g0043 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.83-8094A>C | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109759918 | |||||||
| chr12:109759943 | C | T | 1 | a0001c0001t0001g0171 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.83-8069C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109759943 | |||||||
| chr12:109759971 | G | C | 91 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0024 others(88): Show |
100 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.83-8041G>C | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109759971 | |||||||
| chr12:109760155 | A | G | 245 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(242): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.83-7857A>G | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109760155 | |||||||
| chr12:109760156 | T | C | 149 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(146): Show |
152 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(149): Show |
intron_variant | MODIFIER | c.83-7856T>C | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109760156 | |||||||
| chr12:109760364 | G | A | 2 | a0001c0002t0001g0172 a0001c0002t0002g0261 |
2 | HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.83-7648G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109760364 | |||||||
| chr12:109760450 | A | G | 2 | a0001c0001t0001g0155 a0001c0001t0002g0301 |
2 | NA18968.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.83-7562A>G | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109760450 | |||||||
| chr12:109760468 | G | A | 148 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(145): Show |
151 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(148): Show |
intron_variant | MODIFIER | c.83-7544G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109760468 | |||||||
| chr12:109760613 | GC | G | 108 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(105): Show |
111 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(108): Show |
intron_variant | MODIFIER | c.83-7396delC | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 109760613 | ||||||
| chr12:109760725 | A | T | 149 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(146): Show |
152 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(149): Show |
intron_variant | MODIFIER | c.83-7287A>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109760725 | |||||||
| chr12:109760760 | G | A | 239 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(236): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.83-7252G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109760760 | |||||||
| chr12:109760762 | G | A | 1 | a0002c0004t0008g0316 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.83-7250G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109760762 | |||||||
| chr12:109760792 | G | A | 1 | a0001c0001t0001g0201 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.83-7220G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109760792 | |||||||
| chr12:109760826 | T | C | 1 | a0002c0004t0008g0316 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.83-7186T>C | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109760826 | |||||||
| chr12:109760948 | G | A | 1 | a0002c0004t0008g0316 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.83-7064G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109760948 | |||||||
| chr12:109761197 | A | T | 1 | a0001c0001t0001g0101 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.83-6815A>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109761197 | |||||||
| chr12:109761204 | C | G | 1 | a0001c0001t0001g0101 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.83-6808C>G | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109761204 | |||||||
| chr12:109761205 | C | G | 1 | a0001c0001t0001g0101 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.83-6807C>G | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109761205 | |||||||
| chr12:109761281 | C | T | 92 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0024 others(89): Show |
101 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(98): Show |
intron_variant | MODIFIER | c.83-6731C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109761281 | |||||||
| chr12:109761302 | C | G | 2 | a0001c0001t0001g0144 a0001c0001t0001g0176 |
2 | NA18962.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.83-6710C>G | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109761302 | |||||||
| chr12:109761353 | C | A | 1 | a0002c0004t0008g0316 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.83-6659C>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109761353 | |||||||
| chr12:109761449 | A | T | 2 | a0001c0001t0001g0009 a0001c0001t0001g0150 |
3 | HG03516.hp1 NA18522.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.83-6563A>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109761449 | |||||||
| chr12:109761596 | G | A | 148 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(145): Show |
151 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(148): Show |
intron_variant | MODIFIER | c.83-6416G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109761596 | |||||||
| chr12:109761610 | G | A | 1 | a0001c0001t0001g0091 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.83-6402G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109761610 | |||||||
| chr12:109761810 | G | A | 1 | a0001c0001t0001g0328 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.83-6202G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109761810 | |||||||
| chr12:109761844 | T | C | 94 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0024 others(91): Show |
103 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.83-6168T>C | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109761844 | |||||||
| chr12:109761981 | G | A | 1 | a0001c0001t0001g0131 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.83-6031G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109761981 | |||||||
| chr12:109762130 | G | A | 1 | a0001c0001t0002g0267 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.83-5882G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109762130 | |||||||
| chr12:109762154 | C | T | 17 | a0001c0001t0001g0216 a0001c0001t0002g0281 a0001c0001t0002g0298 others(14): Show |
19 | HG00408.hp1 HG00609.hp1 HG02523.hp1 others(16): Show |
intron_variant | MODIFIER | c.83-5858C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109762154 | |||||||
| chr12:109762246 | C | T | 1 | a0001c0001t0002g0259 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.83-5766C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109762246 | |||||||
| chr12:109762263 | C | T | 94 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0024 others(91): Show |
103 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.83-5749C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109762263 | |||||||
| chr12:109762518 | C | T | 1 | a0001c0001t0002g0267 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.83-5494C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109762518 | |||||||
| chr12:109762558 | A | C | 1 | a0001c0001t0001g0205 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.83-5454A>C | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109762558 | |||||||
| chr12:109762841 | C | T | 107 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(104): Show |
110 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(107): Show |
intron_variant | MODIFIER | c.83-5171C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109762841 | |||||||
| chr12:109762879 | C | T | 1 | a0001c0001t0006g0325 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.83-5133C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109762879 | |||||||
| chr12:109762887 | C | T | 1 | a0001c0001t0027g0313 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.83-5125C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109762887 | |||||||
| chr12:109762930 | C | T | 2 | a0001c0001t0001g0114 a0001c0001t0027g0313 |
2 | HG01891.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.83-5082C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109762930 | |||||||
| chr12:109762931 | G | A | 1 | a0001c0001t0019g0082 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.83-5081G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109762931 | |||||||
| chr12:109763326 | G | A | 3 | a0001c0001t0001g0147 a0001c0001t0001g0180 a0001c0001t0001g0185 |
3 | NA18952.hp1 NA18985.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.83-4686G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109763326 | |||||||
| chr12:109763518 | A | G | 1 | a0002c0004t0008g0316 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.83-4494A>G | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109763518 | |||||||
| chr12:109763629 | A | G | 1 | a0001c0001t0004g0248 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.83-4383A>G | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109763629 | |||||||
| chr12:109763645 | G | A | 2 | a0001c0001t0002g0260 a0001c0001t0002g0268 |
2 | HG02976.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.83-4367G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109763645 | |||||||
| chr12:109763800 | T | C | 98 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0024 others(95): Show |
107 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(104): Show |
intron_variant | MODIFIER | c.83-4212T>C | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109763800 | |||||||
| chr12:109763949 | G | A | 1 | a0001c0006t0002g0304 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.83-4063G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109763949 | |||||||
| chr12:109763960 | A | C | 2 | a0001c0001t0001g0115 a0001c0001t0001g0116 |
2 | HG01167.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.83-4052A>C | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109763960 | |||||||
| chr12:109764004 | A | T | 1 | a0002c0004t0008g0316 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.83-4008A>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109764004 | |||||||
| chr12:109764091 | G | A | 1 | a0001c0001t0007g0027 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.83-3921G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109764091 | |||||||
| chr12:109764222 | C | CAAAAAAA | 80 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0024 others(77): Show |
89 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.83-3781_83-3775dup others(7): Show |
FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 109764222 | ||||||
| chr12:109764222 | C | CAAAAAAA others(1): Show |
12 | a0001c0001t0001g0049 a0001c0001t0001g0144 a0001c0001t0001g0146 others(9): Show |
12 | HG01074.hp1 HG01175.hp1 HG01346.hp2 others(9): Show |
intron_variant | MODIFIER | c.83-3782_83-3775dup others(8): Show |
FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 109764222 | ||||||
| chr12:109764222 | C | CAAAAAAA others(3): Show |
127 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(124): Show |
129 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(126): Show |
intron_variant | MODIFIER | c.83-3784_83-3775dup others(10): Show |
FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 109764222 | ||||||
| chr12:109764222 | C | CAAAAAAA others(4): Show |
18 | a0001c0001t0001g0009 a0001c0001t0001g0026 a0001c0001t0001g0047 others(15): Show |
19 | HG00544.hp2 HG01109.hp1 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.83-3785_83-3775dup others(11): Show |
FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 109764222 | ||||||
| chr12:109764222 | C | CAAAAAAA others(6): Show |
2 | a0001c0001t0001g0111 a0001c0001t0001g0114 |
2 | HG02486.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.83-3787_83-3775dup others(13): Show |
FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 109764222 | ||||||
| chr12:109764222 | C | CAAAAAAA others(8): Show |
1 | a0001c0001t0020g0022 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.83-3789_83-3775dup others(15): Show |
FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 109764222 | ||||||
| chr12:109764573 | A | G | 2 | a0001c0001t0002g0314 a0001c0001t0002g0315 |
2 | HG01109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.83-3439A>G | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109764573 | |||||||
| chr12:109764643 | C | G | 1 | a0001c0001t0027g0313 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.83-3369C>G | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109764643 | |||||||
| chr12:109764643 | C | T | 147 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(144): Show |
151 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(148): Show |
intron_variant | MODIFIER | c.83-3369C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109764643 | |||||||
| chr12:109764645 | G | A | 84 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0024 others(81): Show |
92 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.83-3367G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109764645 | |||||||
| chr12:109764734 | G | A | 1 | a0002c0004t0008g0316 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.83-3278G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109764734 | |||||||
| chr12:109764909 | C | T | 1 | a0001c0001t0001g0049 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.83-3103C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109764909 | |||||||
| chr12:109765012 | G | A | 18 | a0001c0001t0001g0050 a0001c0001t0001g0216 a0001c0001t0002g0281 others(15): Show |
20 | HG00408.hp1 HG00609.hp1 HG02523.hp1 others(17): Show |
intron_variant | MODIFIER | c.83-3000G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109765012 | |||||||
| chr12:109765113 | A | C | 1 | a0001c0001t0001g0009 | 2 | HG03516.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.83-2899A>C | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109765113 | |||||||
| chr12:109765227 | T | A | 1 | a0001c0001t0001g0142 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.83-2785T>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109765227 | |||||||
| chr12:109765229 | C | T | 1 | a0001c0006t0002g0304 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.83-2783C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109765229 | |||||||
| chr12:109765291 | C | G | 10 | a0001c0001t0001g0048 a0001c0001t0001g0055 a0001c0001t0001g0078 others(7): Show |
11 | HG01168.hp2 HG01169.hp1 HG01943.hp1 others(8): Show |
intron_variant | MODIFIER | c.83-2721C>G | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109765291 | |||||||
| chr12:109765331 | T | A | 212 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(209): Show |
221 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.83-2681T>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109765331 | |||||||
| chr12:109765370 | G | C | 80 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0047 others(77): Show |
89 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.83-2642G>C | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109765370 | |||||||
| chr12:109765401 | C | A | 1 | a0002c0004t0008g0023 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.83-2611C>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109765401 | |||||||
| chr12:109765403 | G | A | 1 | a0001c0001t0001g0114 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.83-2609G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109765403 | |||||||
| chr12:109765408 | C | T | 3 | a0001c0001t0001g0154 a0001c0001t0001g0187 a0001c0001t0002g0259 |
3 | HG01496.hp1 HG02004.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.83-2604C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109765408 | |||||||
| chr12:109765430 | T | C | 12 | a0001c0001t0001g0078 a0001c0001t0002g0260 a0001c0001t0002g0263 others(9): Show |
13 | HG02109.hp1 HG02615.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.83-2582T>C | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109765430 | |||||||
| chr12:109765459 | C | T | 1 | a0001c0001t0001g0048 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.83-2553C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109765459 | |||||||
| chr12:109765464 | T | C | 1 | a0001c0001t0001g0097 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.83-2548T>C | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109765464 | |||||||
| chr12:109765538 | T | C | 1 | a0001c0001t0001g0338 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.83-2474T>C | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109765538 | |||||||
| chr12:109765710 | GA | G | 6 | a0001c0001t0005g0005 a0001c0001t0005g0038 a0001c0001t0005g0039 others(3): Show |
7 | HG02615.hp2 HG02818.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.83-2300delA | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 109765710 | ||||||
| chr12:109766008 | A | T | 2 | a0001c0001t0001g0121 a0001c0001t0023g0138 |
2 | HG01123.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.83-2004A>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109766008 | |||||||
| chr12:109766097 | C | T | 3 | a0001c0001t0001g0024 a0001c0001t0001g0175 a0001c0001t0001g0193 |
3 | NA18747.hp1 NA19056.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.83-1915C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109766097 | |||||||
| chr12:109766331 | C | T | 16 | a0001c0001t0001g0010 a0001c0001t0001g0080 a0001c0001t0001g0105 others(13): Show |
22 | HG02040.hp2 HG02080.hp1 HG02083.hp2 others(19): Show |
intron_variant | MODIFIER | c.83-1681C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109766331 | |||||||
| chr12:109766456 | C | T | 1 | a0001c0001t0001g0185 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.83-1556C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109766456 | |||||||
| chr12:109766553 | G | A | 5 | a0002c0004t0008g0023 a0002c0004t0008g0053 a0002c0004t0008g0054 others(2): Show |
5 | HG01891.hp2 HG02486.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.83-1459G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109766553 | |||||||
| chr12:109766679 | G | A | 1 | a0001c0001t0001g0202 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.83-1333G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109766679 | |||||||
| chr12:109766739 | C | T | 6 | a0001c0001t0001g0047 a0001c0001t0001g0076 a0001c0001t0001g0142 others(3): Show |
6 | HG01884.hp1 HG01891.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.83-1273C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109766739 | |||||||
| chr12:109766750 | G | A | 5 | a0001c0001t0002g0290 a0001c0001t0002g0291 a0001c0001t0002g0292 others(2): Show |
5 | HG01361.hp1 HG02257.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.83-1262G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109766750 | |||||||
| chr12:109766795 | C | T | 1 | a0001c0001t0011g0031 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.83-1217C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109766795 | |||||||
| chr12:109766817 | C | T | 5 | a0001c0001t0016g0021 a0001c0002t0001g0151 a0001c0002t0001g0183 others(2): Show |
5 | HG02257.hp1 HG02572.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.83-1195C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109766817 | |||||||
| chr12:109766844 | G | A | 1 | a0001c0001t0018g0073 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.83-1168G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109766844 | |||||||
| chr12:109766935 | G | A | 1 | a0001c0001t0020g0022 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.83-1077G>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109766935 | |||||||
| chr12:109767062 | C | CT | 181 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0024 others(178): Show |
201 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.83-926dupT | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 109767062 | ||||||
| chr12:109767062 | C | CTT | 18 | a0001c0001t0001g0047 a0001c0001t0001g0076 a0001c0001t0001g0092 others(15): Show |
18 | HG01358.hp2 HG01516.hp1 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.83-927_83-926dupTT | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 109767062 | ||||||
| chr12:109767062 | CT | C | 6 | a0001c0001t0001g0119 a0001c0001t0001g0167 a0001c0001t0001g0308 others(3): Show |
6 | HG01081.hp2 HG02015.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.83-926delT | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 109767062 | ||||||
| chr12:109767062 | CTTTTTTT others(1): Show |
C | 11 | a0001c0001t0001g0159 a0001c0001t0001g0185 a0001c0001t0001g0214 others(8): Show |
12 | HG00597.hp1 HG00609.hp2 HG02015.hp1 others(9): Show |
intron_variant | MODIFIER | c.83-933_83-926delTT others(6): Show |
FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 109767062 | ||||||
| chr12:109767116 | C | T | 7 | a0001c0001t0001g0047 a0001c0001t0001g0076 a0001c0001t0001g0142 others(4): Show |
7 | HG01884.hp1 HG01891.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.83-896C>T | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109767116 | |||||||
| chr12:109767421 | A | G | 4 | a0001c0001t0001g0149 a0001c0001t0001g0154 a0001c0001t0001g0187 others(1): Show |
4 | HG01192.hp2 HG01496.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.83-591A>G | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109767421 | |||||||
| chr12:109767454 | C | G | 80 | a0001c0001t0001g0010 a0001c0001t0001g0024 a0001c0001t0001g0026 others(77): Show |
97 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.83-558C>G | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109767454 | |||||||
| chr12:109767504 | C | A | 1 | a0001c0001t0001g0153 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.83-508C>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109767504 | |||||||
| chr12:109767509 | A | G | 16 | a0001c0001t0001g0006 a0001c0001t0001g0047 a0001c0001t0001g0051 others(13): Show |
17 | HG01167.hp1 HG01884.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.83-503A>G | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109767509 | |||||||
| chr12:109767951 | C | A | 1 | a0001c0001t0001g0331 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.83-61C>A | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109767951 | |||||||
| chr12:109767970 | A | C | 6 | a0001c0002t0022g0099 a0002c0004t0008g0023 a0002c0004t0008g0053 others(3): Show |
6 | HG00738.hp1 HG01891.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.83-42A>C | FAM222A | ENSG00000139438.6 | transcript | ENST00000538780.2 | protein_coding | 2/2 | chr12 | 109767970 |