Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 29902 |
| ensemblid | ENSG00000204856.12 |
| hgncid | 30180 |
| symbol | FAM216A |
| name | family with sequence similarity 216 member A |
| refseq_nuc | NM_013300.3 |
| refseq_prot | NP_037432.2 |
| ensembl_nuc | ENST00000377673.10 |
| ensembl_prot | ENSP00000366901.5 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 110468845 |
| end | 110490385 |
| strand | + |
| ver | v1.2 |
| region | chr12:110468845-110490385 |
| region5000 | chr12:110463845-110495385 |
| regionname0 | FAM216A_chr12_110468845_110490385 |
| regionname5000 | FAM216A_chr12_110463845_110495385 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 273 | 306 | 89 | 60 | 102 | 16 | 37 | 80 | FAM216A_chr12_110463845_110495385 | FAM216A | MLGQL others(268): Show |
chr12 | 110463845 | 110495385 |
| a0002 | 0/0 | 273 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | MLGQL others(268): Show |
chr12 | 110463845 | 110495385 |
| a0003 | 0/0 | 273 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | MLGQL others(268): Show |
chr12 | 110463845 | 110495385 |
| a0004 | 0/0 | 273 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | MLGQL others(268): Show |
chr12 | 110463845 | 110495385 |
| a0005 | 0/0 | 273 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | MLGQL others(268): Show |
chr12 | 110463845 | 110495385 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 819 | 263 | 75 | 56 | 82 | 15 | 33 | FAM216A_chr12_110463845_110495385 | FAM216A | ATGCT others(814): Show |
chr12 | 110463845 | 110495385 | ||
| a0001c0002 | 0/0 | 819 | 35 | 13 | 0 | 18 | 0 | 4 | FAM216A_chr12_110463845_110495385 | FAM216A | ATGCT others(814): Show |
chr12 | 110463845 | 110495385 | ||
| a0001c0003 | 0/0 | 819 | 5 | 0 | 4 | 0 | 1 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | ATGCT others(814): Show |
chr12 | 110463845 | 110495385 | ||
| a0001c0005 | 0/0 | 819 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | ATGCT others(814): Show |
chr12 | 110463845 | 110495385 | ||
| a0001c0008 | 0/0 | 819 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | ATGCT others(814): Show |
chr12 | 110463845 | 110495385 | ||
| a0001c0009 | 0/0 | 819 | 1 | 1 | 0 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | ATGCT others(814): Show |
chr12 | 110463845 | 110495385 | ||
| a0002c0004 | 0/0 | 819 | 1 | 1 | 0 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | ATGCT others(814): Show |
chr12 | 110463845 | 110495385 | ||
| a0003c0006 | 0/0 | 819 | 1 | 1 | 0 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | ATGCT others(814): Show |
chr12 | 110463845 | 110495385 | ||
| a0004c0007 | 0/0 | 819 | 1 | 0 | 0 | 0 | 0 | 1 | FAM216A_chr12_110463845_110495385 | FAM216A | ATGCT others(814): Show |
chr12 | 110463845 | 110495385 | ||
| a0005c0010 | 0/0 | 819 | 1 | 1 | 0 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | ATGCT others(814): Show |
chr12 | 110463845 | 110495385 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1101 | 259 | 75 | 55 | 82 | 15 | 30 | FAM216A_chr12_110463845_110495385 | FAM216A | AGCCT others(1096): Show |
chr12 | 110463845 | 110495385 |
| a0001c0001t0002 | 0/0 | 1101 | 2 | 0 | 0 | 0 | 0 | 2 | FAM216A_chr12_110463845_110495385 | FAM216A | AGCCT others(1096): Show |
chr12 | 110463845 | 110495385 |
| a0001c0001t0003 | 0/0 | 1101 | 1 | 0 | 1 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | AGCCT others(1096): Show |
chr12 | 110463845 | 110495385 |
| a0001c0001t0004 | 0/0 | 1101 | 1 | 0 | 0 | 0 | 0 | 1 | FAM216A_chr12_110463845_110495385 | FAM216A | AGCCT others(1096): Show |
chr12 | 110463845 | 110495385 |
| a0001c0002t0001 | 0/0 | 1101 | 35 | 13 | 0 | 18 | 0 | 4 | FAM216A_chr12_110463845_110495385 | FAM216A | AGCCT others(1096): Show |
chr12 | 110463845 | 110495385 |
| a0001c0003t0001 | 0/0 | 1101 | 5 | 0 | 4 | 0 | 1 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | AGCCT others(1096): Show |
chr12 | 110463845 | 110495385 |
| a0001c0005t0001 | 0/0 | 1101 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | AGCCT others(1096): Show |
chr12 | 110463845 | 110495385 |
| a0001c0008t0001 | 0/0 | 1101 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | AGCCT others(1096): Show |
chr12 | 110463845 | 110495385 |
| a0001c0009t0001 | 0/0 | 1101 | 1 | 1 | 0 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | AGCCT others(1096): Show |
chr12 | 110463845 | 110495385 |
| a0002c0004t0001 | 0/0 | 1101 | 1 | 1 | 0 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | AGCCT others(1096): Show |
chr12 | 110463845 | 110495385 |
| a0003c0006t0001 | 0/0 | 1101 | 1 | 1 | 0 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | AGCCT others(1096): Show |
chr12 | 110463845 | 110495385 |
| a0004c0007t0001 | 0/0 | 1101 | 1 | 0 | 0 | 0 | 0 | 1 | FAM216A_chr12_110463845_110495385 | FAM216A | AGCCT others(1096): Show |
chr12 | 110463845 | 110495385 |
| a0005c0010t0001 | 0/0 | 1101 | 1 | 1 | 0 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | AGCCT others(1096): Show |
chr12 | 110463845 | 110495385 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 8 | 1 | 1 | 6 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0002 | 0/0 | 6 | 5 | 1 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0003 | 0/0 | 4 | 0 | 0 | 3 | 1 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0005 | 0/0 | 4 | 0 | 2 | 0 | 0 | 2 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0006 | 0/0 | 4 | 1 | 0 | 2 | 0 | 1 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0007 | 0/0 | 3 | 0 | 0 | 2 | 1 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0010 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0032 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0118 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0121 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0002g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0003g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0001t0004g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0002t0001g0004 | 0/0 | 4 | 3 | 0 | 1 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0002t0001g0009 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0002t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0002t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0002t0001g0024 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0002t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0002t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0002t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0002t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0002t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0002t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0002t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0002t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0002t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0003t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0003t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0003t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0003t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0003t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0005t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0008t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0001c0009t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0002c0004t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0003c0006t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0004c0007t0001g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| a0005c0010t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0147 | EUR | GBR | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0014 | EUR | GBR | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0108 | EUR | FIN | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | FIN | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0007 | EUR | FIN | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0115 | EUR | FIN | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | CHS | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | CHS | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG00423 | hp2 | a0001 | c0002 | t0001 | g0089 | EAS | CHS | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG00438 | hp1 | a0001 | c0008 | t0001 | g0168 | EAS | CHS | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG00558 | hp2 | a0001 | c0002 | t0001 | g0009 | EAS | CHS | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0214 | AMR | PUR | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG01069 | hp1 | a0001 | c0003 | t0001 | g0066 | AMR | PUR | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG01071 | hp1 | a0001 | c0003 | t0001 | g0067 | AMR | PUR | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0226 | AMR | PUR | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0240 | AMR | PUR | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0246 | AMR | PUR | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | PUR | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0194 | AMR | PUR | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | CLM | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | CLM | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | CLM | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | CLM | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | CLM | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | CLM | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | CLM | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | CLM | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | CLM | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | CLM | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | CLM | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | CLM | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | CLM | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0171 | EUR | IBS | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0138 | EUR | IBS | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0026 | EUR | IBS | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0180 | EUR | IBS | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0026 | EUR | IBS | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0137 | EUR | IBS | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG01884 | hp1 | a0001 | c0002 | t0001 | g0099 | AFR | ACB | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG01884 | hp2 | a0001 | c0002 | t0001 | g0004 | AFR | ACB | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | ACB | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | ACB | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PEL | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | PEL | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0243 | AMR | PEL | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PEL | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | PEL | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG01943 | hp2 | a0001 | c0003 | t0001 | g0065 | AMR | PEL | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PEL | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG02004 | hp1 | a0001 | c0001 | t0003 | g0028 | AMR | PEL | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG02040 | hp2 | a0001 | c0005 | t0001 | g0034 | EAS | KHV | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | ACB | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | ACB | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | KHV | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG02071 | hp2 | a0001 | c0002 | t0001 | g0081 | EAS | KHV | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | KHV | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | KHV | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | KHV | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | KHV | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | KHV | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | KHV | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | KHV | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | ACB | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | ACB | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG02165 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | CDX | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG02165 | hp2 | a0001 | c0002 | t0001 | g0095 | EAS | CDX | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG02257 | hp1 | a0001 | c0002 | t0001 | g0103 | AFR | ACB | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | ACB | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | ACB | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | ACB | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG02293 | hp1 | a0001 | c0003 | t0001 | g0060 | AMR | PEL | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PEL | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG02572 | hp1 | a0001 | c0002 | t0001 | g0083 | AFR | GWD | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | GWD | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0222 | SAS | PJL | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0225 | SAS | PJL | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | GWD | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | GWD | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | GWD | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | GWD | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | GWD | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0229 | SAS | PJL | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG02698 | hp2 | a0001 | c0002 | t0001 | g0009 | SAS | PJL | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0234 | SAS | PJL | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG02735 | hp2 | a0001 | c0001 | t0004 | g0188 | SAS | PJL | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0156 | SAS | PJL | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0201 | SAS | PJL | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG02809 | hp1 | a0002 | c0004 | t0001 | g0043 | AFR | GWD | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | GWD | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | GWD | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | GWD | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG02886 | hp1 | a0001 | c0009 | t0001 | g0023 | AFR | GWD | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | ESN | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG02922 | hp2 | a0003 | c0006 | t0001 | g0048 | AFR | ESN | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ESN | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG02965 | hp2 | a0001 | c0002 | t0001 | g0100 | AFR | ESN | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | ESN | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG02970 | hp2 | a0001 | c0002 | t0001 | g0024 | AFR | ESN | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | ESN | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | ESN | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG03041 | hp1 | a0001 | c0002 | t0001 | g0102 | AFR | GWD | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | GWD | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | MSL | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG03098 | hp2 | a0001 | c0002 | t0001 | g0004 | AFR | MSL | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ESN | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG03139 | hp1 | a0001 | c0002 | t0001 | g0093 | AFR | ESN | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ESN | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | ESN | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | ESN | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | MSL | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | MSL | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | MSL | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | MSL | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG03239 | hp1 | a0004 | c0007 | t0001 | g0001 | SAS | PJL | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | MSL | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | MSL | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | MSL | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | MSL | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0047 | SAS | PJL | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0236 | SAS | PJL | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | ESN | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | ESN | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | MSL | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | MSL | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0166 | SAS | BEB | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0165 | SAS | BEB | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0149 | SAS | BEB | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0223 | SAS | BEB | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0164 | SAS | BEB | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0170 | SAS | BEB | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0238 | SAS | BEB | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0219 | SAS | BEB | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG04115 | hp1 | a0001 | c0002 | t0001 | g0084 | SAS | STU | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0151 | SAS | STU | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | BEB | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0105 | SAS | BEB | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0072 | SAS | STU | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG04199 | hp2 | a0001 | c0002 | t0001 | g0082 | SAS | STU | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | STU | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG04204 | hp2 | a0001 | c0002 | t0001 | g0096 | SAS | STU | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| NA18522 | hp1 | a0001 | c0002 | t0001 | g0098 | AFR | YRI | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | YRI | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | YRI | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | YRI | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| NA18946 | hp1 | a0001 | c0002 | t0001 | g0087 | EAS | JPT | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| NA18947 | hp2 | a0001 | c0002 | t0001 | g0090 | EAS | JPT | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| NA18948 | hp1 | a0001 | c0002 | t0001 | g0088 | EAS | JPT | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| NA18959 | hp1 | a0001 | c0002 | t0001 | g0097 | EAS | JPT | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| NA18973 | hp2 | a0001 | c0002 | t0001 | g0091 | EAS | JPT | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| NA18989 | hp2 | a0001 | c0002 | t0001 | g0022 | EAS | JPT | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| NA19010 | hp1 | a0001 | c0002 | t0001 | g0023 | EAS | JPT | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| NA19030 | hp1 | a0001 | c0002 | t0001 | g0126 | AFR | LWK | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | LWK | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | LWK | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | LWK | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| NA19056 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| NA19063 | hp1 | a0001 | c0002 | t0001 | g0022 | EAS | JPT | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| NA19077 | hp2 | a0001 | c0002 | t0001 | g0024 | EAS | JPT | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| NA19081 | hp1 | a0001 | c0002 | t0001 | g0132 | EAS | JPT | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| NA19088 | hp1 | a0001 | c0002 | t0001 | g0092 | EAS | JPT | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| NA19090 | hp1 | a0001 | c0002 | t0001 | g0130 | EAS | JPT | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | YRI | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | YRI | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ASW | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ASW | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0116 | EUR | TSI | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0030 | EUR | TSI | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| NA20805 | hp1 | a0001 | c0003 | t0001 | g0059 | EUR | TSI | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0227 | EUR | TSI | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0221 | SAS | GIH | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | GIH | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | ACB | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | ACB | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | ACB | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | MSL | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG03471 | hp2 | a0005 | c0010 | t0001 | g0133 | AFR | MSL | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | USA | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | USA | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| NA20300 | hp1 | a0001 | c0002 | t0001 | g0101 | AFR | USA | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | USA | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | LWK | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| NA21309 | hp2 | a0001 | c0002 | t0001 | g0004 | AFR | LWK | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0118 | REF | REF | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0121 | REF | REF | FAM216A_chr12_110463845_110495385 | FAM216A | chr12 | 110463845 | 110495385 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:110468926 | G | C | 1 | a0002 | 1 | HG02809.hp1 | missense_variant | MODERATE | c.51G>C | p.Glu17Asp | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 1/7 | 82/1101 | 51/822 | 17/273 | chr12 | 110468926 | |||
| chr12:110468981 | C | T | 1 | a0005 | 1 | HG03471.hp2 | missense_variant | MODERATE | c.106C>T | p.Pro36Ser | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 1/7 | 137/1101 | 106/822 | 36/273 | chr12 | 110468981 | |||
| chr12:110487913 | A | G | 1 | a0004 | 1 | HG03239.hp1 | missense_variant | MODERATE | c.673A>G | p.Arg225Gly | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 6/7 | 704/1101 | 673/822 | 225/273 | chr12 | 110487913 | |||
| chr12:110490103 | T | C | 1 | a0003 | 1 | HG02922.hp2 | missense_variant | MODERATE | c.788T>C | p.Ile263Thr | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 7/7 | 819/1101 | 788/822 | 263/273 | chr12 | 110490103 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:110485124 | G | T | 2 | a0001c0002 a0001c0009 |
36 | HG00423.hp2 HG00558.hp2 HG01884.hp1 others(33): Show |
synonymous_variant | LOW | c.231G>T | p.Leu77Leu | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 3/7 | 262/1101 | 231/822 | 77/273 | chr12 | 110485124 | |||
| chr12:110486601 | T | G | 1 | a0001c0005 | 1 | HG02040.hp2 | synonymous_variant | LOW | c.504T>G | p.Thr168Thr | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 5/7 | 535/1101 | 504/822 | 168/273 | chr12 | 110486601 | |||
| chr12:110486625 | A | G | 1 | a0001c0008 | 1 | HG00438.hp1 | synonymous_variant | LOW | c.528A>G | p.Arg176Arg | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 5/7 | 559/1101 | 528/822 | 176/273 | chr12 | 110486625 | |||
| chr12:110487927 | A | G | 1 | a0001c0009 | 1 | HG02886.hp1 | synonymous_variant | LOW | c.687A>G | p.Lys229Lys | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 6/7 | 718/1101 | 687/822 | 229/273 | chr12 | 110487927 | |||
| chr12:110490077 | A | G | 1 | a0001c0003 | 5 | HG01069.hp1 HG01071.hp1 HG01943.hp2 others(2): Show |
synonymous_variant | LOW | c.762A>G | p.Leu254Leu | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 7/7 | 793/1101 | 762/822 | 254/273 | chr12 | 110490077 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:110468856 | C | A | 1 | a0001c0001t0003 | 1 | HG02004.hp1 | 5_prime_UTR_variant | MODIFIER | c.-20C>A | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 1/7 | 20 | chr12 | 110468856 | ||||||
| chr12:110490197 | G | A | 1 | a0001c0001t0004 | 1 | HG02735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*60G>A | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 7/7 | 60 | chr12 | 110490197 | ||||||
| chr12:110490343 | T | C | 1 | a0001c0001t0002 | 2 | HG02698.hp1 HG03831.hp2 |
3_prime_UTR_variant | MODIFIER | c.*206T>C | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 7/7 | 206 | chr12 | 110490343 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:110469075 | C | A | 24 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0017 others(21): Show |
33 | HG00323.hp1 HG01167.hp1 HG01175.hp1 others(30): Show |
intron_variant | MODIFIER | c.143+57C>A | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 1/6 | chr12 | 110469075 | |||||||
| chr12:110469139 | G | A | 4 | a0001c0001t0001g0019 a0001c0001t0001g0055 a0001c0001t0001g0056 others(1): Show |
5 | HG02559.hp1 HG03225.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.143+121G>A | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 1/6 | chr12 | 110469139 | |||||||
| chr12:110469186 | G | T | 3 | a0001c0001t0001g0244 a0001c0001t0001g0245 a0001c0001t0001g0246 |
3 | HG01099.hp2 HG02145.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.143+168G>T | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 1/6 | chr12 | 110469186 | |||||||
| chr12:110469363 | A | T | 1 | a0001c0001t0001g0243 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.143+345A>T | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 1/6 | chr12 | 110469363 | |||||||
| chr12:110469730 | G | A | 1 | a0001c0001t0001g0058 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.143+712G>A | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 1/6 | chr12 | 110469730 | |||||||
| chr12:110469768 | C | G | 129 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(126): Show |
159 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.143+750C>G | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 1/6 | chr12 | 110469768 | |||||||
| chr12:110469834 | T | A | 15 | a0001c0001t0001g0007 a0001c0001t0001g0017 a0001c0001t0001g0035 others(12): Show |
18 | HG00323.hp1 HG01175.hp1 HG01361.hp2 others(15): Show |
intron_variant | MODIFIER | c.143+816T>A | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 1/6 | chr12 | 110469834 | |||||||
| chr12:110470103 | G | GT | 18 | a0001c0001t0001g0007 a0001c0001t0001g0017 a0001c0001t0001g0034 others(15): Show |
21 | HG00323.hp1 HG01099.hp1 HG01175.hp1 others(18): Show |
intron_variant | MODIFIER | c.143+1098dupT | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 110470103 | ||||||
| chr12:110470242 | G | A | 2 | a0001c0003t0001g0059 a0001c0003t0001g0060 |
2 | HG02293.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.143+1224G>A | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 1/6 | chr12 | 110470242 | |||||||
| chr12:110470244 | G | C | 2 | a0001c0001t0001g0061 a0001c0001t0001g0062 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.143+1226G>C | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 1/6 | chr12 | 110470244 | |||||||
| chr12:110470298 | C | T | 2 | a0001c0001t0001g0127 a0001c0001t0001g0128 |
2 | HG00741.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.143+1280C>T | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 1/6 | chr12 | 110470298 | |||||||
| chr12:110470408 | G | A | 1 | a0001c0001t0001g0134 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.143+1390G>A | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 1/6 | chr12 | 110470408 | |||||||
| chr12:110470449 | A | C | 42 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0015 others(39): Show |
51 | HG00140.hp2 HG00408.hp1 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.143+1431A>C | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 1/6 | chr12 | 110470449 | |||||||
| chr12:110470475 | A | AT | 8 | a0001c0001t0001g0027 a0001c0001t0001g0123 a0001c0001t0001g0124 others(5): Show |
9 | HG02717.hp2 HG02965.hp1 HG03195.hp1 others(6): Show |
intron_variant | MODIFIER | c.143+1474dupT | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 110470475 | ||||||
| chr12:110470475 | AT | A | 24 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0049 others(21): Show |
30 | HG01069.hp1 HG01071.hp1 HG01099.hp2 others(27): Show |
intron_variant | MODIFIER | c.143+1474delT | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 110470475 | ||||||
| chr12:110470475 | ATT | A | 15 | a0001c0001t0001g0007 a0001c0001t0001g0017 a0001c0001t0001g0035 others(12): Show |
18 | HG00323.hp1 HG01175.hp1 HG01361.hp2 others(15): Show |
intron_variant | MODIFIER | c.143+1473_143+1474d others(4): Show |
FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 110470475 | ||||||
| chr12:110470492 | T | A | 2 | a0001c0001t0001g0135 a0001c0001t0001g0136 |
2 | HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.143+1474T>A | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 1/6 | chr12 | 110470492 | |||||||
| chr12:110470540 | C | T | 1 | a0001c0001t0001g0202 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.143+1522C>T | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 1/6 | chr12 | 110470540 | |||||||
| chr12:110470605 | G | T | 3 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0129 |
3 | HG02630.hp2 HG02976.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.143+1587G>T | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 1/6 | chr12 | 110470605 | |||||||
| chr12:110470818 | T | C | 8 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0001t0001g0208 others(5): Show |
8 | HG00408.hp1 HG02135.hp2 NA18955.hp1 others(5): Show |
intron_variant | MODIFIER | c.143+1800T>C | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 1/6 | chr12 | 110470818 | |||||||
| chr12:110471012 | G | A | 225 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(222): Show |
277 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(274): Show |
intron_variant | MODIFIER | c.143+1994G>A | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 1/6 | chr12 | 110471012 | |||||||
| chr12:110471126 | G | T | 1 | a0001c0001t0001g0237 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.144-1952G>T | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 1/6 | chr12 | 110471126 | |||||||
| chr12:110471374 | T | C | 33 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0017 others(30): Show |
42 | HG00323.hp1 HG00738.hp1 HG01069.hp2 others(39): Show |
intron_variant | MODIFIER | c.144-1704T>C | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 1/6 | chr12 | 110471374 | |||||||
| chr12:110471540 | A | G | 1 | a0001c0001t0001g0201 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.144-1538A>G | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 1/6 | chr12 | 110471540 | |||||||
| chr12:110471950 | G | A | 1 | a0001c0001t0001g0241 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.144-1128G>A | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 1/6 | chr12 | 110471950 | |||||||
| chr12:110471958 | G | A | 2 | a0001c0001t0001g0137 a0001c0001t0001g0138 |
2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.144-1120G>A | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 1/6 | chr12 | 110471958 | |||||||
| chr12:110471959 | T | A | 1 | a0001c0001t0001g0035 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.144-1119T>A | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 1/6 | chr12 | 110471959 | |||||||
| chr12:110471973 | T | C | 6 | a0001c0001t0001g0007 a0001c0001t0001g0017 a0001c0001t0001g0044 others(3): Show |
9 | HG00323.hp1 HG01175.hp1 HG01361.hp2 others(6): Show |
intron_variant | MODIFIER | c.144-1105T>C | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 1/6 | chr12 | 110471973 | |||||||
| chr12:110472015 | T | C | 1 | a0001c0001t0001g0139 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.144-1063T>C | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 1/6 | chr12 | 110472015 | |||||||
| chr12:110472034 | C | A | 2 | a0001c0001t0001g0061 a0001c0001t0001g0062 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.144-1044C>A | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 1/6 | chr12 | 110472034 | |||||||
| chr12:110472091 | G | A | 1 | a0001c0001t0001g0140 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.144-987G>A | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 1/6 | chr12 | 110472091 | |||||||
| chr12:110472244 | GA | G | 24 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0017 others(21): Show |
33 | HG00323.hp1 HG01167.hp1 HG01175.hp1 others(30): Show |
intron_variant | MODIFIER | c.144-822delA | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 110472244 | ||||||
| chr12:110472251 | A | G | 1 | a0001c0001t0001g0068 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.144-827A>G | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 1/6 | chr12 | 110472251 | |||||||
| chr12:110472397 | A | G | 1 | a0001c0001t0001g0104 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.144-681A>G | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 1/6 | chr12 | 110472397 | |||||||
| chr12:110472474 | G | A | 24 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0017 others(21): Show |
33 | HG00323.hp1 HG01167.hp1 HG01175.hp1 others(30): Show |
intron_variant | MODIFIER | c.144-604G>A | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 1/6 | chr12 | 110472474 | |||||||
| chr12:110472603 | A | G | 5 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0198 others(2): Show |
5 | HG02647.hp2 HG03516.hp2 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.144-475A>G | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 1/6 | chr12 | 110472603 | |||||||
| chr12:110472975 | C | CA | 59 | a0001c0001t0001g0017 a0001c0001t0001g0025 a0001c0001t0001g0028 others(56): Show |
61 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.144-74dupA | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 110472975 | ||||||
| chr12:110472975 | C | CAA | 8 | a0001c0001t0001g0020 a0001c0001t0001g0071 a0001c0001t0001g0072 others(5): Show |
9 | HG00735.hp1 HG01081.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.144-75_144-74dupAA | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 110472975 | ||||||
| chr12:110472975 | CA | C | 34 | a0001c0001t0001g0018 a0001c0001t0001g0047 a0001c0001t0001g0051 others(31): Show |
42 | HG00423.hp2 HG00558.hp2 HG01074.hp1 others(39): Show |
intron_variant | MODIFIER | c.144-74delA | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 110472975 | ||||||
| chr12:110472975 | CAA | C | 5 | a0001c0001t0001g0002 a0001c0001t0001g0053 a0001c0001t0001g0054 others(2): Show |
10 | HG01071.hp1 HG01167.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.144-75_144-74delAA | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 110472975 | ||||||
| chr12:110473031 | A | G | 2 | a0001c0001t0001g0195 a0001c0001t0001g0196 |
2 | HG02258.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.144-47A>G | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 1/6 | chr12 | 110473031 | |||||||
| chr12:110473219 | C | CT | 18 | a0001c0001t0001g0007 a0001c0001t0001g0017 a0001c0001t0001g0035 others(15): Show |
21 | HG00323.hp1 HG00738.hp1 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.184+111dupT | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 110473219 | ||||||
| chr12:110473434 | G | A | 33 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0017 others(30): Show |
42 | HG00323.hp1 HG00738.hp1 HG01069.hp2 others(39): Show |
intron_variant | MODIFIER | c.184+316G>A | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110473434 | |||||||
| chr12:110473502 | A | C | 7 | a0001c0001t0001g0063 a0001c0001t0001g0069 a0001c0001t0001g0070 others(4): Show |
7 | HG01099.hp2 HG02145.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.184+384A>C | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110473502 | |||||||
| chr12:110473652 | C | A | 1 | a0001c0001t0001g0053 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.184+534C>A | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110473652 | |||||||
| chr12:110473852 | G | A | 1 | a0001c0001t0001g0123 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.184+734G>A | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110473852 | |||||||
| chr12:110474076 | A | G | 3 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0129 |
3 | HG02630.hp2 HG02976.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.184+958A>G | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110474076 | |||||||
| chr12:110474126 | A | G | 1 | a0001c0001t0001g0111 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.184+1008A>G | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110474126 | |||||||
| chr12:110474299 | G | A | 2 | a0001c0001t0001g0221 a0001c0001t0001g0234 |
2 | HG02735.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.184+1181G>A | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110474299 | |||||||
| chr12:110474569 | G | A | 1 | a0001c0001t0001g0160 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.184+1451G>A | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110474569 | |||||||
| chr12:110474585 | G | A | 1 | a0003c0006t0001g0048 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.184+1467G>A | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110474585 | |||||||
| chr12:110474628 | G | A | 3 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0129 |
3 | HG02630.hp2 HG02976.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.184+1510G>A | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110474628 | |||||||
| chr12:110474655 | G | C | 1 | a0001c0001t0001g0039 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.184+1537G>C | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110474655 | |||||||
| chr12:110474671 | G | A | 3 | a0001c0001t0001g0028 a0001c0001t0001g0161 a0001c0001t0003g0028 |
3 | HG01934.hp2 HG02004.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.184+1553G>A | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110474671 | |||||||
| chr12:110474690 | T | A | 1 | a0001c0001t0001g0063 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.184+1572T>A | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110474690 | |||||||
| chr12:110474690 | T | C | 1 | a0001c0001t0001g0123 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.184+1572T>C | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110474690 | |||||||
| chr12:110474691 | C | CA | 24 | a0001c0001t0001g0017 a0001c0001t0001g0025 a0001c0001t0001g0035 others(21): Show |
27 | HG00642.hp2 HG00733.hp1 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.184+1601dupA | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 110474691 | ||||||
| chr12:110474691 | CA | C | 111 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(108): Show |
150 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.184+1601delA | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 110474691 | ||||||
| chr12:110474691 | CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0001g0068 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.184+1589_184+1601d others(15): Show |
FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 110474691 | ||||||
| chr12:110474691 | CAAAAAAA others(7): Show |
C | 1 | a0001c0002t0001g0103 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.184+1588_184+1601d others(16): Show |
FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 110474691 | ||||||
| chr12:110474691 | CAAAAAAA others(8): Show |
C | 2 | a0001c0001t0001g0061 a0001c0001t0001g0062 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.184+1587_184+1601d others(17): Show |
FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 110474691 | ||||||
| chr12:110474759 | TG | T | 5 | a0001c0003t0001g0059 a0001c0003t0001g0060 a0001c0003t0001g0065 others(2): Show |
5 | HG01069.hp1 HG01071.hp1 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.184+1644delG | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 110474759 | ||||||
| chr12:110474777 | A | G | 77 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0017 others(74): Show |
94 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.184+1659A>G | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110474777 | |||||||
| chr12:110474932 | C | T | 1 | a0005c0010t0001g0133 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.184+1814C>T | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110474932 | |||||||
| chr12:110474946 | C | G | 3 | a0001c0001t0001g0244 a0001c0001t0001g0245 a0001c0001t0001g0246 |
3 | HG01099.hp2 HG02145.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.184+1828C>G | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110474946 | |||||||
| chr12:110475049 | A | G | 6 | a0001c0002t0001g0093 a0001c0002t0001g0099 a0001c0002t0001g0100 others(3): Show |
6 | HG01884.hp1 HG02257.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.184+1931A>G | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110475049 | |||||||
| chr12:110475176 | T | A | 2 | a0001c0001t0001g0061 a0001c0001t0001g0062 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.184+2058T>A | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110475176 | |||||||
| chr12:110475280 | C | T | 1 | a0001c0001t0001g0212 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.184+2162C>T | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110475280 | |||||||
| chr12:110475391 | G | A | 2 | a0001c0001t0001g0061 a0001c0001t0001g0062 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.184+2273G>A | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110475391 | |||||||
| chr12:110475721 | CA | C | 71 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0017 others(68): Show |
88 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.184+2621delA | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 110475721 | ||||||
| chr12:110476203 | G | GT | 17 | a0001c0001t0001g0007 a0001c0001t0001g0017 a0001c0001t0001g0035 others(14): Show |
20 | HG00323.hp1 HG00738.hp1 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.184+3099dupT | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 110476203 | ||||||
| chr12:110476255 | A | G | 2 | a0001c0001t0001g0049 a0001c0001t0001g0050 |
2 | HG01891.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.184+3137A>G | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110476255 | |||||||
| chr12:110476375 | A | T | 1 | a0001c0001t0001g0123 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.184+3257A>T | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110476375 | |||||||
| chr12:110476472 | C | T | 2 | a0001c0001t0001g0061 a0001c0001t0001g0062 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.184+3354C>T | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110476472 | |||||||
| chr12:110476568 | C | T | 24 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0017 others(21): Show |
33 | HG00323.hp1 HG01167.hp1 HG01175.hp1 others(30): Show |
intron_variant | MODIFIER | c.184+3450C>T | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110476568 | |||||||
| chr12:110476588 | A | G | 1 | a0001c0002t0001g0093 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.184+3470A>G | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110476588 | |||||||
| chr12:110476822 | C | T | 5 | a0001c0003t0001g0059 a0001c0003t0001g0060 a0001c0003t0001g0065 others(2): Show |
5 | HG01069.hp1 HG01071.hp1 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.184+3704C>T | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110476822 | |||||||
| chr12:110476893 | G | A | 15 | a0001c0001t0001g0007 a0001c0001t0001g0017 a0001c0001t0001g0035 others(12): Show |
18 | HG00323.hp1 HG01175.hp1 HG01361.hp2 others(15): Show |
intron_variant | MODIFIER | c.184+3775G>A | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110476893 | |||||||
| chr12:110476953 | C | T | 1 | a0001c0001t0001g0062 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.184+3835C>T | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110476953 | |||||||
| chr12:110477042 | T | G | 2 | a0001c0002t0001g0081 a0001c0002t0001g0089 |
2 | HG00423.hp2 HG02071.hp2 |
intron_variant | MODIFIER | c.184+3924T>G | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110477042 | |||||||
| chr12:110477322 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.184+4204C>T | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110477322 | |||||||
| chr12:110477356 | T | G | 1 | a0001c0001t0001g0215 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.184+4238T>G | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110477356 | |||||||
| chr12:110477422 | G | A | 2 | a0001c0001t0001g0061 a0001c0001t0001g0062 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.184+4304G>A | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110477422 | |||||||
| chr12:110477426 | T | C | 225 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(222): Show |
277 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(274): Show |
intron_variant | MODIFIER | c.184+4308T>C | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110477426 | |||||||
| chr12:110477507 | C | T | 2 | a0001c0001t0001g0061 a0001c0001t0001g0062 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.184+4389C>T | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110477507 | |||||||
| chr12:110477706 | T | C | 1 | a0001c0002t0001g0095 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.184+4588T>C | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110477706 | |||||||
| chr12:110477845 | C | G | 2 | a0001c0001t0001g0157 a0001c0001t0001g0194 |
2 | HG00642.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.184+4727C>G | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110477845 | |||||||
| chr12:110477865 | G | A | 1 | a0001c0001t0001g0115 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.184+4747G>A | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110477865 | |||||||
| chr12:110478058 | T | C | 1 | a0001c0001t0001g0046 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.184+4940T>C | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110478058 | |||||||
| chr12:110478547 | A | G | 2 | a0001c0001t0001g0061 a0001c0001t0001g0062 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.184+5429A>G | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110478547 | |||||||
| chr12:110478708 | C | T | 1 | a0001c0003t0001g0060 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.184+5590C>T | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110478708 | |||||||
| chr12:110478893 | T | C | 1 | a0001c0002t0001g0093 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.184+5775T>C | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110478893 | |||||||
| chr12:110478943 | C | T | 1 | a0001c0001t0001g0156 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.184+5825C>T | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110478943 | |||||||
| chr12:110478953 | CCGAGGCG others(9): Show |
C | 1 | a0001c0002t0001g0098 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.184+5841_184+5856d others(18): Show |
FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 110478953 | ||||||
| chr12:110479045 | C | T | 5 | a0001c0003t0001g0059 a0001c0003t0001g0060 a0001c0003t0001g0065 others(2): Show |
5 | HG01069.hp1 HG01071.hp1 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.184+5927C>T | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110479045 | |||||||
| chr12:110479150 | C | T | 5 | a0001c0001t0001g0063 a0001c0001t0001g0131 a0001c0001t0001g0244 others(2): Show |
5 | HG01099.hp2 HG02055.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.185-5928C>T | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110479150 | |||||||
| chr12:110479163 | C | CA | 12 | a0001c0001t0001g0029 a0001c0001t0001g0063 a0001c0001t0001g0069 others(9): Show |
13 | HG01168.hp1 HG01168.hp2 HG01346.hp1 others(10): Show |
intron_variant | MODIFIER | c.185-5900dupA | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 110479163 | ||||||
| chr12:110479179 | T | A | 6 | a0001c0001t0001g0012 a0001c0001t0001g0143 a0001c0001t0001g0172 others(3): Show |
8 | HG02040.hp1 HG02083.hp1 NA18944.hp1 others(5): Show |
intron_variant | MODIFIER | c.185-5899T>A | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110479179 | |||||||
| chr12:110479205 | C | T | 1 | a0001c0001t0001g0033 | 2 | NA18941.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.185-5873C>T | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110479205 | |||||||
| chr12:110479460 | C | T | 1 | a0001c0001t0001g0208 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.185-5618C>T | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110479460 | |||||||
| chr12:110479531 | G | GA | 28 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0017 others(25): Show |
37 | HG00323.hp1 HG00738.hp1 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.185-5533dupA | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 110479531 | ||||||
| chr12:110479567 | A | G | 48 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0017 others(45): Show |
58 | HG00323.hp1 HG00738.hp1 HG01069.hp1 others(55): Show |
intron_variant | MODIFIER | c.185-5511A>G | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110479567 | |||||||
| chr12:110479831 | C | T | 2 | a0001c0001t0001g0192 a0001c0001t0001g0193 |
2 | NA18955.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.185-5247C>T | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110479831 | |||||||
| chr12:110479848 | A | C | 3 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0129 |
3 | HG02630.hp2 HG02976.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.185-5230A>C | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110479848 | |||||||
| chr12:110479871 | C | A | 6 | a0001c0002t0001g0093 a0001c0002t0001g0099 a0001c0002t0001g0100 others(3): Show |
6 | HG01884.hp1 HG02257.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.185-5207C>A | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110479871 | |||||||
| chr12:110479873 | A | C | 2 | a0001c0002t0001g0102 a0001c0002t0001g0103 |
2 | HG02257.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.185-5205A>C | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110479873 | |||||||
| chr12:110479884 | A | G | 6 | a0001c0002t0001g0093 a0001c0002t0001g0099 a0001c0002t0001g0100 others(3): Show |
6 | HG01884.hp1 HG02257.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.185-5194A>G | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110479884 | |||||||
| chr12:110479887 | A | G | 3 | a0001c0001t0001g0220 a0001c0001t0001g0227 a0001c0001t0001g0232 |
3 | HG00738.hp2 HG01175.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.185-5191A>G | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110479887 | |||||||
| chr12:110480024 | A | G | 1 | a0001c0001t0001g0171 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.185-5054A>G | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110480024 | |||||||
| chr12:110480027 | CT | C | 32 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0017 others(29): Show |
41 | HG00323.hp1 HG01099.hp2 HG01167.hp1 others(38): Show |
intron_variant | MODIFIER | c.185-5040delT | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 110480027 | ||||||
| chr12:110480054 | T | A | 1 | a0001c0001t0001g0174 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.185-5024T>A | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110480054 | |||||||
| chr12:110480062 | G | T | 1 | a0001c0001t0001g0231 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.185-5016G>T | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110480062 | |||||||
| chr12:110480193 | AT | A | 71 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0013 others(68): Show |
86 | HG00280.hp1 HG00323.hp2 HG00642.hp1 others(83): Show |
intron_variant | MODIFIER | c.185-4857delT | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 110480193 | ||||||
| chr12:110480193 | ATT | A | 111 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(108): Show |
145 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.185-4858_185-4857d others(4): Show |
FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 110480193 | ||||||
| chr12:110480193 | ATTT | A | 8 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0123 others(5): Show |
8 | HG00738.hp1 HG01069.hp2 HG01167.hp2 others(5): Show |
intron_variant | MODIFIER | c.185-4859_185-4857d others(5): Show |
FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 110480193 | ||||||
| chr12:110480193 | ATTTT | A | 17 | a0001c0001t0001g0020 a0001c0001t0001g0035 a0001c0001t0001g0044 others(14): Show |
18 | HG01069.hp1 HG01071.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.185-4860_185-4857d others(6): Show |
FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 110480193 | ||||||
| chr12:110480193 | ATTTTT | A | 27 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0017 others(24): Show |
36 | HG00323.hp1 HG01099.hp2 HG01167.hp1 others(33): Show |
intron_variant | MODIFIER | c.185-4861_185-4857d others(7): Show |
FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 110480193 | ||||||
| chr12:110480266 | C | T | 1 | a0001c0001t0001g0026 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.185-4812C>T | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110480266 | |||||||
| chr12:110480304 | C | T | 1 | a0001c0001t0001g0154 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.185-4774C>T | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110480304 | |||||||
| chr12:110480358 | C | G | 2 | a0001c0001t0001g0061 a0001c0001t0001g0062 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.185-4720C>G | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110480358 | |||||||
| chr12:110480369 | A | G | 1 | a0001c0001t0001g0144 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.185-4709A>G | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110480369 | |||||||
| chr12:110480419 | G | C | 1 | a0001c0001t0001g0170 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.185-4659G>C | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110480419 | |||||||
| chr12:110480424 | C | T | 32 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0017 others(29): Show |
41 | HG00323.hp1 HG01099.hp2 HG01167.hp1 others(38): Show |
intron_variant | MODIFIER | c.185-4654C>T | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110480424 | |||||||
| chr12:110480449 | C | T | 1 | a0001c0001t0001g0184 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.185-4629C>T | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110480449 | |||||||
| chr12:110480450 | G | A | 3 | a0001c0001t0001g0013 a0001c0001t0001g0159 a0001c0001t0001g0185 |
5 | HG01123.hp2 HG01928.hp2 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.185-4628G>A | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110480450 | |||||||
| chr12:110480759 | G | A | 24 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0017 others(21): Show |
33 | HG00323.hp1 HG01167.hp1 HG01175.hp1 others(30): Show |
intron_variant | MODIFIER | c.185-4319G>A | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110480759 | |||||||
| chr12:110480868 | G | A | 34 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0017 others(31): Show |
43 | HG00323.hp1 HG00738.hp1 HG01069.hp2 others(40): Show |
intron_variant | MODIFIER | c.185-4210G>A | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110480868 | |||||||
| chr12:110480916 | T | G | 32 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0017 others(29): Show |
41 | HG00323.hp1 HG01099.hp2 HG01167.hp1 others(38): Show |
intron_variant | MODIFIER | c.185-4162T>G | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110480916 | |||||||
| chr12:110480931 | C | T | 1 | a0001c0001t0001g0245 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.185-4147C>T | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110480931 | |||||||
| chr12:110481053 | A | T | 5 | a0001c0003t0001g0059 a0001c0003t0001g0060 a0001c0003t0001g0065 others(2): Show |
5 | HG01069.hp1 HG01071.hp1 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.185-4025A>T | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110481053 | |||||||
| chr12:110481457 | G | A | 1 | a0001c0001t0001g0225 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.185-3621G>A | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110481457 | |||||||
| chr12:110481477 | T | C | 2 | a0001c0002t0001g0081 a0001c0002t0001g0089 |
2 | HG00423.hp2 HG02071.hp2 |
intron_variant | MODIFIER | c.185-3601T>C | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110481477 | |||||||
| chr12:110481493 | T | A | 1 | a0001c0001t0001g0202 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.185-3585T>A | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110481493 | |||||||
| chr12:110481528 | G | T | 1 | a0001c0001t0001g0189 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.185-3550G>T | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110481528 | |||||||
| chr12:110481650 | C | T | 1 | a0001c0001t0001g0183 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.185-3428C>T | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110481650 | |||||||
| chr12:110482086 | CT | C | 8 | a0001c0001t0001g0020 a0001c0001t0001g0064 a0001c0001t0001g0071 others(5): Show |
9 | HG01081.hp1 HG01943.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.185-2979delT | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 110482086 | ||||||
| chr12:110482089 | T | TC | 139 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(136): Show |
172 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.185-2989_185-2988i others(3): Show |
FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110482089 | |||||||
| chr12:110482123 | C | G | 1 | a0001c0001t0001g0245 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.185-2955C>G | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110482123 | |||||||
| chr12:110482123 | C | T | 5 | a0001c0003t0001g0059 a0001c0003t0001g0060 a0001c0003t0001g0065 others(2): Show |
5 | HG01069.hp1 HG01071.hp1 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.185-2955C>T | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110482123 | |||||||
| chr12:110482150 | C | T | 3 | a0001c0001t0001g0035 a0001c0001t0001g0037 a0002c0004t0001g0043 |
3 | HG02055.hp2 HG02809.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.185-2928C>T | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110482150 | |||||||
| chr12:110482151 | G | A | 1 | a0001c0001t0001g0230 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.185-2927G>A | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110482151 | |||||||
| chr12:110482167 | C | T | 1 | a0001c0001t0001g0208 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.185-2911C>T | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110482167 | |||||||
| chr12:110482186 | A | G | 1 | a0001c0001t0001g0149 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.185-2892A>G | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110482186 | |||||||
| chr12:110482234 | A | G | 2 | a0001c0001t0001g0061 a0001c0001t0001g0062 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.185-2844A>G | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110482234 | |||||||
| chr12:110482377 | C | T | 32 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0017 others(29): Show |
41 | HG00323.hp1 HG01099.hp2 HG01167.hp1 others(38): Show |
intron_variant | MODIFIER | c.185-2701C>T | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110482377 | |||||||
| chr12:110482591 | C | T | 5 | a0001c0001t0001g0010 a0001c0001t0001g0111 a0001c0001t0001g0114 others(2): Show |
7 | HG01071.hp2 HG01081.hp2 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.185-2487C>T | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110482591 | |||||||
| chr12:110482792 | C | T | 2 | a0001c0001t0001g0072 a0001c0001t0001g0073 |
2 | HG03710.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.185-2286C>T | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110482792 | |||||||
| chr12:110482794 | C | CA | 15 | a0001c0001t0001g0020 a0001c0001t0001g0049 a0001c0001t0001g0050 others(12): Show |
16 | HG00423.hp2 HG01081.hp1 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.185-2269dupA | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 110482794 | ||||||
| chr12:110483052 | G | A | 1 | a0001c0001t0001g0223 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.185-2026G>A | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110483052 | |||||||
| chr12:110483088 | G | A | 2 | a0001c0002t0001g0082 a0001c0002t0001g0096 |
2 | HG04199.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.185-1990G>A | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110483088 | |||||||
| chr12:110483096 | C | T | 2 | a0001c0002t0001g0082 a0001c0002t0001g0096 |
2 | HG04199.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.185-1982C>T | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110483096 | |||||||
| chr12:110483100 | C | T | 2 | a0001c0002t0001g0082 a0001c0002t0001g0096 |
2 | HG04199.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.185-1978C>T | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110483100 | |||||||
| chr12:110483101 | A | G | 2 | a0001c0002t0001g0082 a0001c0002t0001g0096 |
2 | HG04199.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.185-1977A>G | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110483101 | |||||||
| chr12:110483122 | A | G | 2 | a0001c0002t0001g0082 a0001c0002t0001g0096 |
2 | HG04199.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.185-1956A>G | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110483122 | |||||||
| chr12:110483130 | A | C | 2 | a0001c0002t0001g0082 a0001c0002t0001g0096 |
2 | HG04199.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.185-1948A>C | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110483130 | |||||||
| chr12:110483134 | G | T | 1 | a0001c0001t0001g0155 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.185-1944G>T | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110483134 | |||||||
| chr12:110483141 | C | T | 2 | a0001c0002t0001g0082 a0001c0002t0001g0096 |
2 | HG04199.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.185-1937C>T | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110483141 | |||||||
| chr12:110483142 | A | G | 2 | a0001c0002t0001g0082 a0001c0002t0001g0096 |
2 | HG04199.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.185-1936A>G | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110483142 | |||||||
| chr12:110483150 | G | C | 2 | a0001c0002t0001g0082 a0001c0002t0001g0096 |
2 | HG04199.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.185-1928G>C | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110483150 | |||||||
| chr12:110483153 | G | A | 1 | a0001c0001t0001g0044 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.185-1925G>A | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110483153 | |||||||
| chr12:110483160 | C | G | 2 | a0001c0002t0001g0082 a0001c0002t0001g0096 |
2 | HG04199.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.185-1918C>G | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110483160 | |||||||
| chr12:110483161 | T | A | 2 | a0001c0002t0001g0082 a0001c0002t0001g0096 |
2 | HG04199.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.185-1917T>A | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110483161 | |||||||
| chr12:110483169 | C | A | 2 | a0001c0002t0001g0082 a0001c0002t0001g0096 |
2 | HG04199.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.185-1909C>A | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110483169 | |||||||
| chr12:110483175 | C | T | 2 | a0001c0002t0001g0082 a0001c0002t0001g0096 |
2 | HG04199.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.185-1903C>T | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110483175 | |||||||
| chr12:110483180 | T | C | 2 | a0001c0002t0001g0082 a0001c0002t0001g0096 |
2 | HG04199.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.185-1898T>C | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110483180 | |||||||
| chr12:110483181 | G | A | 2 | a0001c0002t0001g0082 a0001c0002t0001g0096 |
2 | HG04199.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.185-1897G>A | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110483181 | |||||||
| chr12:110483182 | G | A | 2 | a0001c0002t0001g0082 a0001c0002t0001g0096 |
2 | HG04199.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.185-1896G>A | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110483182 | |||||||
| chr12:110483185 | G | A | 2 | a0001c0002t0001g0082 a0001c0002t0001g0096 |
2 | HG04199.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.185-1893G>A | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110483185 | |||||||
| chr12:110483193 | G | A | 2 | a0001c0002t0001g0082 a0001c0002t0001g0096 |
2 | HG04199.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.185-1885G>A | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110483193 | |||||||
| chr12:110483197 | A | G | 2 | a0001c0002t0001g0082 a0001c0002t0001g0096 |
2 | HG04199.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.185-1881A>G | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110483197 | |||||||
| chr12:110483324 | C | G | 1 | a0001c0001t0001g0068 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.185-1754C>G | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110483324 | |||||||
| chr12:110483330 | C | CAAAAAAA others(3): Show |
8 | a0001c0001t0001g0047 a0001c0002t0001g0090 a0001c0002t0001g0093 others(5): Show |
8 | HG01884.hp1 HG02257.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.185-1744_185-1735d others(12): Show |
FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 110483330 | ||||||
| chr12:110483330 | C | CAAAAAAA others(4): Show |
50 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0017 others(47): Show |
66 | HG00323.hp1 HG00558.hp2 HG01069.hp2 others(63): Show |
intron_variant | MODIFIER | c.185-1745_185-1735d others(13): Show |
FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 110483330 | ||||||
| chr12:110483330 | C | CAAAAAAA others(5): Show |
17 | a0001c0001t0001g0020 a0001c0001t0001g0053 a0001c0001t0001g0062 others(14): Show |
18 | HG00423.hp2 HG00738.hp1 HG01069.hp1 others(15): Show |
intron_variant | MODIFIER | c.185-1746_185-1735d others(14): Show |
FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 110483330 | ||||||
| chr12:110483330 | C | CAAAAAAA others(6): Show |
2 | a0001c0001t0001g0244 a0001c0002t0001g0096 |
2 | HG02145.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.185-1747_185-1735d others(15): Show |
FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 110483330 | ||||||
| chr12:110483354 | G | A | 2 | a0001c0001t0001g0061 a0001c0001t0001g0062 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.185-1724G>A | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110483354 | |||||||
| chr12:110483410 | A | G | 1 | a0001c0001t0001g0049 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.185-1668A>G | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110483410 | |||||||
| chr12:110483655 | C | G | 10 | a0001c0001t0001g0031 a0001c0001t0001g0152 a0001c0001t0001g0153 others(7): Show |
11 | HG00438.hp1 HG02132.hp1 HG02135.hp2 others(8): Show |
intron_variant | MODIFIER | c.185-1423C>G | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110483655 | |||||||
| chr12:110483838 | C | CA | 8 | a0001c0001t0001g0063 a0001c0001t0001g0069 a0001c0001t0001g0070 others(5): Show |
8 | HG01099.hp2 HG02055.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.185-1234dupA | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 110483838 | ||||||
| chr12:110483948 | A | G | 1 | a0001c0001t0001g0119 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.185-1130A>G | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110483948 | |||||||
| chr12:110483971 | C | T | 1 | a0001c0001t0001g0068 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.185-1107C>T | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110483971 | |||||||
| chr12:110484005 | C | T | 1 | a0001c0002t0001g0098 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.185-1073C>T | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110484005 | |||||||
| chr12:110484084 | C | T | 2 | a0001c0001t0001g0209 a0001c0001t0001g0211 |
2 | NA18969.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.185-994C>T | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110484084 | |||||||
| chr12:110484166 | C | T | 1 | a0001c0001t0001g0164 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.185-912C>T | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110484166 | |||||||
| chr12:110484200 | G | A | 1 | a0001c0001t0001g0069 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.185-878G>A | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110484200 | |||||||
| chr12:110484319 | C | T | 1 | a0001c0001t0001g0039 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.185-759C>T | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110484319 | |||||||
| chr12:110484350 | T | C | 2 | a0001c0001t0001g0061 a0001c0001t0001g0062 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.185-728T>C | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110484350 | |||||||
| chr12:110484426 | C | CA | 29 | a0001c0001t0001g0021 a0001c0001t0001g0057 a0001c0001t0001g0058 others(26): Show |
30 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.185-623dupA | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 110484426 | ||||||
| chr12:110484426 | CA | C | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(104): Show |
141 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.185-623delA | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 110484426 | ||||||
| chr12:110484426 | CAA | C | 20 | a0001c0001t0001g0017 a0001c0001t0001g0038 a0001c0001t0001g0041 others(17): Show |
21 | HG01099.hp1 HG01099.hp2 HG01175.hp1 others(18): Show |
intron_variant | MODIFIER | c.185-624_185-623del others(2): Show |
FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 110484426 | ||||||
| chr12:110484426 | CAAA | C | 7 | a0001c0001t0001g0007 a0001c0001t0001g0036 a0001c0001t0001g0039 others(4): Show |
9 | HG00323.hp1 HG02886.hp2 HG03209.hp1 others(6): Show |
intron_variant | MODIFIER | c.185-625_185-623del others(3): Show |
FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 110484426 | ||||||
| chr12:110484426 | CAAAAAAA others(9): Show |
C | 2 | a0001c0001t0001g0061 a0001c0001t0001g0062 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.185-638_185-623del others(16): Show |
FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 110484426 | ||||||
| chr12:110484443 | A | C | 2 | a0001c0002t0001g0087 a0001c0002t0001g0097 |
2 | NA18946.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.185-635A>C | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110484443 | |||||||
| chr12:110484447 | A | C | 17 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0049 others(14): Show |
23 | HG01099.hp2 HG01167.hp1 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.185-631A>C | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110484447 | |||||||
| chr12:110484531 | C | T | 5 | a0001c0001t0001g0020 a0001c0001t0001g0064 a0001c0001t0001g0071 others(2): Show |
6 | HG01943.hp1 HG02647.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.185-547C>T | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110484531 | |||||||
| chr12:110484845 | C | T | 3 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0129 |
3 | HG02630.hp2 HG02976.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.185-233C>T | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110484845 | |||||||
| chr12:110484851 | C | T | 1 | a0001c0001t0001g0148 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.185-227C>T | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110484851 | |||||||
| chr12:110484937 | T | C | 9 | a0001c0001t0001g0030 a0001c0001t0001g0149 a0001c0001t0001g0151 others(6): Show |
10 | HG00642.hp1 HG01167.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.185-141T>C | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110484937 | |||||||
| chr12:110484994 | C | A | 2 | a0001c0001t0001g0061 a0001c0001t0001g0062 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.185-84C>A | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110484994 | |||||||
| chr12:110484996 | G | A | 4 | a0001c0001t0001g0027 a0001c0001t0001g0124 a0001c0001t0001g0125 others(1): Show |
5 | HG02717.hp2 HG02965.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.185-82G>A | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 2/6 | chr12 | 110484996 | |||||||
| chr12:110485207 | A | G | 2 | a0001c0001t0001g0181 a0001c0001t0001g0184 |
2 | HG00408.hp2 HG02132.hp2 |
splice_region_variant&intron_variant | LOW | c.306+8A>G | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 3/6 | chr12 | 110485207 | |||||||
| chr12:110485290 | A | G | 5 | a0001c0001t0001g0019 a0001c0001t0001g0055 a0001c0001t0001g0056 others(2): Show |
6 | HG02559.hp1 HG02622.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.306+91A>G | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 3/6 | chr12 | 110485290 | |||||||
| chr12:110485341 | T | C | 1 | a0001c0002t0001g0083 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.306+142T>C | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 3/6 | chr12 | 110485341 | |||||||
| chr12:110485357 | T | C | 2 | a0001c0001t0001g0061 a0001c0001t0001g0062 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.306+158T>C | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 3/6 | chr12 | 110485357 | |||||||
| chr12:110485696 | G | A | 2 | a0001c0001t0001g0063 a0001c0001t0001g0131 |
2 | HG02055.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.306+497G>A | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 3/6 | chr12 | 110485696 | |||||||
| chr12:110486066 | G | A | 34 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0017 others(31): Show |
43 | HG00323.hp1 HG00738.hp1 HG01069.hp2 others(40): Show |
intron_variant | MODIFIER | c.307-259G>A | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 3/6 | chr12 | 110486066 | |||||||
| chr12:110486128 | G | A | 1 | a0001c0001t0001g0123 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.307-197G>A | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 3/6 | chr12 | 110486128 | |||||||
| chr12:110486196 | C | T | 6 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0156 others(3): Show |
6 | HG01261.hp1 HG01515.hp2 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.307-129C>T | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 3/6 | chr12 | 110486196 | |||||||
| chr12:110486242 | G | A | 2 | a0001c0001t0001g0181 a0001c0001t0001g0184 |
2 | HG00408.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.307-83G>A | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 3/6 | chr12 | 110486242 | |||||||
| chr12:110486932 | A | C | 1 | a0001c0001t0001g0171 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.620+215A>C | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 5/6 | chr12 | 110486932 | |||||||
| chr12:110487011 | G | A | 1 | a0005c0010t0001g0133 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.620+294G>A | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 5/6 | chr12 | 110487011 | |||||||
| chr12:110487086 | A | G | 1 | a0001c0001t0001g0042 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.620+369A>G | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 5/6 | chr12 | 110487086 | |||||||
| chr12:110487129 | G | C | 1 | a0001c0001t0001g0151 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.620+412G>C | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 5/6 | chr12 | 110487129 | |||||||
| chr12:110487195 | C | T | 1 | a0001c0001t0001g0144 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.620+478C>T | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 5/6 | chr12 | 110487195 | |||||||
| chr12:110487268 | T | A | 9 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0049 others(6): Show |
15 | HG01167.hp1 HG01891.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.620+551T>A | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 5/6 | chr12 | 110487268 | |||||||
| chr12:110487416 | T | C | 1 | a0001c0001t0001g0058 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.621-445T>C | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 5/6 | chr12 | 110487416 | |||||||
| chr12:110487543 | A | T | 3 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0129 |
3 | HG02630.hp2 HG02976.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.621-318A>T | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 5/6 | chr12 | 110487543 | |||||||
| chr12:110487561 | A | G | 1 | a0001c0001t0001g0149 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.621-300A>G | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 5/6 | chr12 | 110487561 | |||||||
| chr12:110488098 | G | A | 2 | a0001c0001t0001g0187 a0001c0001t0001g0190 |
2 | HG02615.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.703+155G>A | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 6/6 | chr12 | 110488098 | |||||||
| chr12:110488140 | C | T | 1 | a0001c0001t0001g0179 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.703+197C>T | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 6/6 | chr12 | 110488140 | |||||||
| chr12:110488304 | G | A | 2 | a0001c0001t0001g0056 a0001c0001t0001g0057 |
2 | HG03225.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.703+361G>A | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 6/6 | chr12 | 110488304 | |||||||
| chr12:110488342 | C | T | 1 | a0001c0001t0001g0229 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.703+399C>T | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 6/6 | chr12 | 110488342 | |||||||
| chr12:110488405 | C | T | 4 | a0001c0001t0001g0027 a0001c0001t0001g0124 a0001c0001t0001g0125 others(1): Show |
5 | HG02717.hp2 HG02965.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.703+462C>T | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 6/6 | chr12 | 110488405 | |||||||
| chr12:110488410 | C | CA | 8 | a0001c0001t0001g0075 a0001c0001t0001g0135 a0001c0001t0001g0136 others(5): Show |
8 | HG00735.hp1 HG01081.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.703+484dupA | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 110488410 | ||||||
| chr12:110488410 | CA | C | 7 | a0001c0001t0001g0053 a0001c0001t0001g0144 a0001c0001t0001g0172 others(4): Show |
7 | HG02976.hp1 HG03491.hp2 HG03834.hp2 others(4): Show |
intron_variant | MODIFIER | c.703+484delA | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 110488410 | ||||||
| chr12:110488454 | T | A | 5 | a0001c0003t0001g0059 a0001c0003t0001g0060 a0001c0003t0001g0065 others(2): Show |
5 | HG01069.hp1 HG01071.hp1 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.703+511T>A | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 6/6 | chr12 | 110488454 | |||||||
| chr12:110488733 | T | C | 1 | a0001c0001t0001g0145 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.703+790T>C | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 6/6 | chr12 | 110488733 | |||||||
| chr12:110488750 | T | C | 1 | a0001c0001t0001g0177 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.703+807T>C | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 6/6 | chr12 | 110488750 | |||||||
| chr12:110488921 | G | A | 2 | a0001c0001t0001g0061 a0001c0001t0001g0062 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.703+978G>A | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 6/6 | chr12 | 110488921 | |||||||
| chr12:110489015 | A | G | 2 | a0001c0001t0001g0061 a0001c0001t0001g0062 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.704-1004A>G | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 6/6 | chr12 | 110489015 | |||||||
| chr12:110489027 | C | T | 2 | a0001c0001t0001g0151 a0001c0001t0001g0166 |
2 | HG03831.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.704-992C>T | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 6/6 | chr12 | 110489027 | |||||||
| chr12:110489294 | C | T | 1 | a0001c0001t0001g0164 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.704-725C>T | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 6/6 | chr12 | 110489294 | |||||||
| chr12:110489311 | C | G | 2 | a0001c0001t0001g0061 a0001c0001t0001g0062 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.704-708C>G | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 6/6 | chr12 | 110489311 | |||||||
| chr12:110489480 | C | CA | 37 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0017 others(34): Show |
46 | HG00323.hp1 HG01099.hp2 HG01167.hp1 others(43): Show |
intron_variant | MODIFIER | c.704-525dupA | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 110489480 | ||||||
| chr12:110489661 | G | T | 3 | a0001c0002t0001g0100 a0001c0002t0001g0102 a0001c0002t0001g0103 |
3 | HG02257.hp1 HG02965.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.704-358G>T | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 6/6 | chr12 | 110489661 | |||||||
| chr12:110489666 | G | A | 2 | a0001c0001t0001g0061 a0001c0001t0001g0062 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.704-353G>A | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 6/6 | chr12 | 110489666 | |||||||
| chr12:110489669 | G | T | 1 | a0001c0001t0001g0245 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.704-350G>T | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 6/6 | chr12 | 110489669 | |||||||
| chr12:110489719 | A | G | 8 | a0001c0001t0001g0020 a0001c0001t0001g0064 a0001c0001t0001g0071 others(5): Show |
9 | HG01081.hp1 HG01943.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.704-300A>G | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 6/6 | chr12 | 110489719 | |||||||
| chr12:110489824 | A | G | 1 | a0001c0001t0001g0111 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.704-195A>G | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 6/6 | chr12 | 110489824 | |||||||
| chr12:110489928 | C | G | 3 | a0001c0001t0001g0105 a0001c0001t0001g0115 a0001c0001t0001g0119 |
3 | HG00323.hp2 HG02258.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.704-91C>G | FAM216A | ENSG00000204856.12 | transcript | ENST00000377673.10 | protein_coding | 6/6 | chr12 | 110489928 |