Search by Gene
| Item | Value |
|---|---|
| geneid | 72 |
| ensemblid | ENSG00000163017.14 |
| hgncid | 145 |
| symbol | ACTG2 |
| name | actin gamma 2, smooth muscle |
| refseq_nuc | NM_001615.4 |
| refseq_prot | NP_001606.1 |
| ensembl_nuc | ENST00000345517.8 |
| ensembl_prot | ENSP00000295137.3 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 73893008 |
| end | 73919865 |
| strand | + |
| ver | v1.2 |
| region | chr2:73893008-73919865 |
| region5000 | chr2:73888008-73924865 |
| regionname0 | ACTG2_chr2_73893008_73919865 |
| regionname5000 | ACTG2_chr2_73888008_73924865 |
Multiple Alignments (by translate haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
Multiple Alignments (by aa haplotype frequency)
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 376 | 415 | 96 | 67 | 192 | 14 | 44 | ACTG2_chr2_73888008_73924865 | ACTG2 | MCEEE others(371): Show |
chr2 | 73888008 | 73924865 |
| a0002 | 0/0 | 376 | 1 | 0 | 1 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | MCEEE others(371): Show |
chr2 | 73888008 | 73924865 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1128 | 210 | 38 | 45 | 88 | 8 | 30 | ACTG2_chr2_73888008_73924865 | ACTG2 | ATGTG others(1123): Show |
chr2 | 73888008 | 73924865 | ||
| a0001c0002 | 1/0 | 1128 | 195 | 49 | 21 | 104 | 6 | 14 | ACTG2_chr2_73888008_73924865 | ACTG2 | ATGTG others(1123): Show |
chr2 | 73888008 | 73924865 | ||
| a0001c0003 | 0/0 | 1128 | 9 | 8 | 1 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | ATGTG others(1123): Show |
chr2 | 73888008 | 73924865 | ||
| a0001c0005 | 0/0 | 1128 | 1 | 1 | 0 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | ATGTG others(1123): Show |
chr2 | 73888008 | 73924865 | ||
| a0002c0004 | 0/0 | 1128 | 1 | 0 | 1 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | ATGTG others(1123): Show |
chr2 | 73888008 | 73924865 |
| acthapid | grch38/chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 1501 | 122 | 8 | 29 | 59 | 6 | 19 | ACTG2_chr2_73888008_73924865 | ACTG2 | ACACC others(1496): Show |
chr2 | 73888008 | 73924865 |
| a0001c0001t0002 | 0/0 | 1501 | 3 | 1 | 0 | 2 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | ACACC others(1496): Show |
chr2 | 73888008 | 73924865 |
| a0001c0001t0003 | 0/0 | 1501 | 56 | 12 | 12 | 25 | 1 | 6 | ACTG2_chr2_73888008_73924865 | ACTG2 | ACACC others(1496): Show |
chr2 | 73888008 | 73924865 |
| a0001c0001t0004 | 0/0 | 1501 | 6 | 4 | 0 | 2 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | ACACC others(1496): Show |
chr2 | 73888008 | 73924865 |
| a0001c0001t0005 | 0/0 | 1501 | 19 | 9 | 4 | 0 | 1 | 5 | ACTG2_chr2_73888008_73924865 | ACTG2 | ACACC others(1496): Show |
chr2 | 73888008 | 73924865 |
| a0001c0001t0006 | 0/0 | 1501 | 1 | 1 | 0 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | ACACC others(1496): Show |
chr2 | 73888008 | 73924865 |
| a0001c0001t0007 | 0/0 | 1501 | 1 | 1 | 0 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | ACACC others(1496): Show |
chr2 | 73888008 | 73924865 |
| a0001c0001t0008 | 0/0 | 1501 | 2 | 2 | 0 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | ACACC others(1496): Show |
chr2 | 73888008 | 73924865 |
| a0001c0002t0001 | 0/0 | 1501 | 24 | 7 | 4 | 7 | 3 | 3 | ACTG2_chr2_73888008_73924865 | ACTG2 | ACACC others(1496): Show |
chr2 | 73888008 | 73924865 |
| a0001c0002t0002 | 1/0 | 1501 | 87 | 10 | 5 | 60 | 3 | 8 | ACTG2_chr2_73888008_73924865 | ACTG2 | ACACC others(1496): Show |
chr2 | 73888008 | 73924865 |
| a0001c0002t0003 | 0/0 | 1501 | 33 | 16 | 5 | 12 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | ACACC others(1496): Show |
chr2 | 73888008 | 73924865 |
| a0001c0002t0004 | 0/0 | 1501 | 47 | 13 | 6 | 25 | 0 | 3 | ACTG2_chr2_73888008_73924865 | ACTG2 | ACACC others(1496): Show |
chr2 | 73888008 | 73924865 |
| a0001c0002t0006 | 0/0 | 1501 | 3 | 2 | 1 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | ACACC others(1496): Show |
chr2 | 73888008 | 73924865 |
| a0001c0002t0009 | 0/0 | 1501 | 1 | 1 | 0 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | ACACC others(1496): Show |
chr2 | 73888008 | 73924865 |
| a0001c0003t0001 | 0/0 | 1501 | 1 | 1 | 0 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | ACACC others(1496): Show |
chr2 | 73888008 | 73924865 |
| a0001c0003t0002 | 0/0 | 1501 | 1 | 1 | 0 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | ACACC others(1496): Show |
chr2 | 73888008 | 73924865 |
| a0001c0003t0004 | 0/0 | 1501 | 6 | 6 | 0 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | ACACC others(1496): Show |
chr2 | 73888008 | 73924865 |
| a0001c0003t0007 | 0/0 | 1501 | 1 | 0 | 1 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | ACACC others(1496): Show |
chr2 | 73888008 | 73924865 |
| a0001c0005t0001 | 0/0 | 1501 | 1 | 1 | 0 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | ACACC others(1496): Show |
chr2 | 73888008 | 73924865 |
| a0002c0004t0001 | 0/0 | 1501 | 1 | 0 | 1 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | ACACC others(1496): Show |
chr2 | 73888008 | 73924865 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0085 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0347 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0353 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0355 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0360 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0364 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0382 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0001g0385 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0003g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0003g0010 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0003g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0003g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0003g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0003g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0003g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0003g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0003g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0003g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0003g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0003g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0003g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0003g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0003g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0003g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0003g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0003g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0003g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0003g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0003g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0003g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0003g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0003g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0003g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0003g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0003g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0003g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0003g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0003g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0003g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0003g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0003g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0003g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0003g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0003g0389 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0004g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0004g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0004g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0004g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0004g0390 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0005g0014 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0005g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0005g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0005g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0005g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0005g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0005g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0005g0356 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0005g0357 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0005g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0005g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0005g0372 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0005g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0005g0378 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0005g0379 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0005g0384 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0005g0387 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0005g0388 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0006g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0007g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0008g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0001t0008g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0001g0007 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0001g0381 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0001g0393 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0002g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0002g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0002g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0002g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0002g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0002g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0002g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0002g0157 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0002g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0002g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0002g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0002g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0002g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0002g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0002g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0002g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0002g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0003g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0003g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0003g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0003g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0003g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0003g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0003g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0003g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0003g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0003g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0003g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0003g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0003g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0003g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0003g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0003g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0003g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0003g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0003g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0003g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0003g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0003g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0003g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0003g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0003g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0004g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0004g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0004g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0004g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0004g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0004g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0004g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0004g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0004g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0004g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0004g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0004g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0004g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0004g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0004g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0004g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0004g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0004g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0004g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0004g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0004g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0004g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0004g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0004g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0004g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0004g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0004g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0004g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0004g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0004g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0004g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0004g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0004g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0004g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0004g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0004g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0004g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0004g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0004g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0004g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0004g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0004g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0004g0369 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0004g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0004g0380 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0006g0004 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0006g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0002t0009g0383 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0003t0001g0392 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0003t0002g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0003t0004g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0003t0004g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0003t0004g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0003t0004g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0003t0004g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0003t0004g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0003t0007g0391 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0001c0005t0001g0386 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| a0002c0004t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| sampleid | haplotypeid | ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0347 | EUR | GBR | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG00140 | hp2 | a0001 | c0001 | t0005 | g0102 | EUR | GBR | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0131 | EUR | FIN | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG00280 | hp2 | a0001 | c0002 | t0001 | g0179 | EUR | FIN | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG00408 | hp1 | a0001 | c0002 | t0002 | g0165 | EAS | CHS | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | CHS | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0324 | EAS | CHS | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG00423 | hp2 | a0001 | c0001 | t0003 | g0124 | EAS | CHS | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG00438 | hp1 | a0001 | c0002 | t0003 | g0061 | EAS | CHS | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | CHS | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG00544 | hp2 | a0001 | c0002 | t0002 | g0285 | EAS | CHS | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | CHS | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG00558 | hp2 | a0001 | c0001 | t0003 | g0177 | EAS | CHS | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | CHS | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | CHS | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0121 | EAS | CHS | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG00609 | hp2 | a0001 | c0001 | t0003 | g0235 | EAS | CHS | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | CHS | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG00621 | hp2 | a0001 | c0001 | t0003 | g0067 | EAS | CHS | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG00639 | hp2 | a0001 | c0002 | t0001 | g0095 | AMR | PUR | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG00642 | hp1 | a0001 | c0002 | t0002 | g0096 | AMR | PUR | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG00642 | hp2 | a0001 | c0001 | t0003 | g0011 | AMR | PUR | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG00673 | hp1 | a0001 | c0002 | t0002 | g0237 | EAS | CHS | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG00673 | hp2 | a0001 | c0002 | t0003 | g0178 | EAS | CHS | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG00733 | hp1 | a0001 | c0002 | t0001 | g0099 | AMR | PUR | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG00735 | hp1 | a0001 | c0002 | t0006 | g0004 | AMR | PUR | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG00735 | hp2 | a0001 | c0002 | t0003 | g0066 | AMR | PUR | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG00738 | hp1 | a0001 | c0002 | t0002 | g0118 | AMR | PUR | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0358 | AMR | PUR | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG00741 | hp2 | a0001 | c0002 | t0002 | g0022 | AMR | PUR | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG01070 | hp1 | a0001 | c0002 | t0004 | g0115 | AMR | PUR | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0363 | AMR | PUR | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG01071 | hp1 | a0001 | c0002 | t0004 | g0117 | AMR | PUR | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG01074 | hp2 | a0002 | c0004 | t0001 | g0135 | AMR | PUR | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG01081 | hp1 | a0001 | c0001 | t0003 | g0100 | AMR | PUR | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG01099 | hp1 | a0001 | c0001 | t0003 | g0252 | AMR | PUR | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0265 | AMR | PUR | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0364 | AMR | PUR | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG01109 | hp2 | a0001 | c0001 | t0005 | g0372 | AMR | PUR | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG01167 | hp2 | a0001 | c0001 | t0005 | g0030 | AMR | PUR | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG01168 | hp1 | a0001 | c0002 | t0004 | g0344 | AMR | PUR | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG01169 | hp1 | a0001 | c0001 | t0005 | g0031 | AMR | PUR | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG01169 | hp2 | a0001 | c0002 | t0004 | g0345 | AMR | PUR | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0365 | AMR | PUR | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG01175 | hp2 | a0001 | c0001 | t0003 | g0011 | AMR | PUR | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0037 | AMR | PUR | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG01192 | hp2 | a0001 | c0002 | t0003 | g0087 | AMR | PUR | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG01243 | hp1 | a0001 | c0003 | t0007 | g0391 | AMR | PUR | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG01243 | hp2 | a0001 | c0002 | t0003 | g0025 | AMR | PUR | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG01255 | hp1 | a0001 | c0002 | t0003 | g0108 | AMR | CLM | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG01255 | hp2 | a0001 | c0001 | t0003 | g0194 | AMR | CLM | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | CLM | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG01258 | hp2 | a0001 | c0002 | t0002 | g0059 | AMR | CLM | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG01261 | hp1 | a0001 | c0002 | t0004 | g0082 | AMR | CLM | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG01261 | hp2 | a0001 | c0002 | t0001 | g0007 | AMR | CLM | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0362 | AMR | CLM | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0181 | AMR | CLM | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG01433 | hp1 | a0001 | c0001 | t0003 | g0134 | AMR | CLM | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG01433 | hp2 | a0001 | c0001 | t0003 | g0093 | AMR | CLM | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG01496 | hp1 | a0001 | c0002 | t0001 | g0225 | AMR | CLM | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0212 | AMR | CLM | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG01515 | hp1 | a0001 | c0002 | t0002 | g0097 | EUR | IBS | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG01515 | hp2 | a0001 | c0001 | t0003 | g0201 | EUR | IBS | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0142 | EUR | IBS | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0266 | EUR | IBS | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG01517 | hp1 | a0001 | c0002 | t0002 | g0098 | EUR | IBS | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0267 | EUR | IBS | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG01884 | hp1 | a0001 | c0002 | t0009 | g0383 | AFR | ACB | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG01884 | hp2 | a0001 | c0001 | t0005 | g0388 | AFR | ACB | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG01891 | hp1 | a0001 | c0002 | t0004 | g0006 | AFR | ACB | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG01891 | hp2 | a0001 | c0002 | t0004 | g0349 | AFR | ACB | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | PEL | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG01934 | hp2 | a0001 | c0002 | t0002 | g0164 | AMR | PEL | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PEL | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG01952 | hp2 | a0001 | c0001 | t0003 | g0010 | AMR | PEL | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | PEL | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG01975 | hp2 | a0001 | c0001 | t0005 | g0058 | AMR | PEL | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG01981 | hp1 | a0001 | c0002 | t0004 | g0232 | AMR | PEL | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | PEL | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PEL | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0229 | AMR | PEL | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG02015 | hp1 | a0001 | c0002 | t0002 | g0295 | EAS | KHV | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG02015 | hp2 | a0001 | c0001 | t0003 | g0196 | EAS | KHV | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG02027 | hp1 | a0001 | c0002 | t0002 | g0240 | EAS | KHV | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG02027 | hp2 | a0001 | c0002 | t0003 | g0076 | EAS | KHV | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG02040 | hp2 | a0001 | c0001 | t0003 | g0323 | EAS | KHV | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0261 | AFR | ACB | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG02055 | hp2 | a0001 | c0002 | t0002 | g0033 | AFR | ACB | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG02056 | hp1 | a0001 | c0001 | t0003 | g0010 | EAS | KHV | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | KHV | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG02071 | hp1 | a0001 | c0002 | t0003 | g0063 | EAS | KHV | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG02071 | hp2 | a0001 | c0002 | t0004 | g0159 | EAS | KHV | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG02074 | hp1 | a0001 | c0001 | t0003 | g0084 | EAS | KHV | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG02074 | hp2 | a0001 | c0002 | t0002 | g0219 | EAS | KHV | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG02080 | hp1 | a0001 | c0002 | t0004 | g0298 | EAS | KHV | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG02080 | hp2 | a0001 | c0002 | t0002 | g0303 | EAS | KHV | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG02083 | hp1 | a0001 | c0001 | t0004 | g0114 | EAS | KHV | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG02083 | hp2 | a0001 | c0002 | t0004 | g0166 | EAS | KHV | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | KHV | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG02129 | hp2 | a0001 | c0002 | t0002 | g0137 | EAS | KHV | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG02132 | hp1 | a0001 | c0001 | t0003 | g0125 | EAS | KHV | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | KHV | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | ACB | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG02145 | hp2 | a0001 | c0003 | t0004 | g0052 | AFR | ACB | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG02148 | hp1 | a0001 | c0001 | t0003 | g0366 | AMR | PEL | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | PEL | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | CDX | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG02155 | hp2 | a0001 | c0002 | t0003 | g0175 | EAS | CDX | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG02165 | hp1 | a0001 | c0002 | t0002 | g0160 | EAS | CDX | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG02165 | hp2 | a0001 | c0002 | t0002 | g0309 | EAS | CDX | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG02257 | hp1 | a0001 | c0003 | t0002 | g0262 | AFR | ACB | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG02257 | hp2 | a0001 | c0002 | t0003 | g0330 | AFR | ACB | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG02258 | hp2 | a0001 | c0002 | t0004 | g0113 | AFR | ACB | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0361 | AMR | PEL | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG02273 | hp2 | a0001 | c0002 | t0003 | g0230 | AMR | PEL | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG02280 | hp1 | a0001 | c0002 | t0003 | g0023 | AFR | ACB | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG02280 | hp2 | a0001 | c0001 | t0004 | g0027 | AFR | ACB | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0354 | AMR | PEL | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG02300 | hp2 | a0001 | c0001 | t0003 | g0141 | AMR | PEL | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG02451 | hp1 | a0001 | c0001 | t0005 | g0032 | AFR | ACB | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG02451 | hp2 | a0001 | c0003 | t0004 | g0035 | AFR | ACB | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG02523 | hp1 | a0001 | c0001 | t0003 | g0060 | EAS | KHV | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG02523 | hp2 | a0001 | c0001 | t0004 | g0077 | EAS | KHV | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG02572 | hp1 | a0001 | c0001 | t0008 | g0042 | AFR | GWD | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG02572 | hp2 | a0001 | c0001 | t0005 | g0384 | AFR | GWD | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG02602 | hp1 | a0001 | c0001 | t0005 | g0356 | SAS | PJL | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG02602 | hp2 | a0001 | c0002 | t0004 | g0331 | SAS | PJL | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG02615 | hp1 | a0001 | c0002 | t0006 | g0055 | AFR | GWD | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG02615 | hp2 | a0001 | c0001 | t0005 | g0371 | AFR | GWD | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG02622 | hp1 | a0001 | c0002 | t0002 | g0348 | AFR | GWD | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG02622 | hp2 | a0001 | c0002 | t0002 | g0221 | AFR | GWD | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG02630 | hp1 | a0001 | c0003 | t0004 | g0053 | AFR | GWD | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG02630 | hp2 | a0001 | c0002 | t0002 | g0049 | AFR | GWD | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG02683 | hp2 | a0001 | c0002 | t0002 | g0264 | SAS | PJL | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG02698 | hp1 | a0001 | c0002 | t0004 | g0369 | SAS | PJL | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG02698 | hp2 | a0001 | c0002 | t0004 | g0090 | SAS | PJL | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG02717 | hp1 | a0001 | c0001 | t0006 | g0249 | AFR | GWD | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG02717 | hp2 | a0001 | c0002 | t0002 | g0045 | AFR | GWD | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | GWD | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG02723 | hp2 | a0001 | c0002 | t0004 | g0370 | AFR | GWD | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG02735 | hp1 | a0001 | c0002 | t0002 | g0111 | SAS | PJL | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG02735 | hp2 | a0001 | c0001 | t0003 | g0226 | SAS | PJL | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG02809 | hp1 | a0001 | c0002 | t0002 | g0028 | AFR | GWD | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG02809 | hp2 | a0001 | c0001 | t0003 | g0260 | AFR | GWD | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG02818 | hp1 | a0001 | c0001 | t0005 | g0387 | AFR | GWD | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0343 | AFR | GWD | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG02886 | hp1 | a0001 | c0003 | t0004 | g0050 | AFR | GWD | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG02886 | hp2 | a0001 | c0002 | t0004 | g0056 | AFR | GWD | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG02895 | hp1 | a0001 | c0002 | t0002 | g0005 | AFR | GWD | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG02895 | hp2 | a0001 | c0002 | t0002 | g0223 | AFR | GWD | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG02896 | hp1 | a0001 | c0002 | t0004 | g0380 | AFR | GWD | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG02896 | hp2 | a0001 | c0002 | t0001 | g0020 | AFR | GWD | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG02897 | hp1 | a0001 | c0002 | t0001 | g0020 | AFR | GWD | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG02897 | hp2 | a0001 | c0002 | t0002 | g0005 | AFR | GWD | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG02922 | hp1 | a0001 | c0002 | t0001 | g0393 | AFR | ESN | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG02922 | hp2 | a0001 | c0002 | t0003 | g0297 | AFR | ESN | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG02965 | hp1 | a0001 | c0002 | t0004 | g0038 | AFR | ESN | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG02965 | hp2 | a0001 | c0002 | t0006 | g0004 | AFR | ESN | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG02970 | hp1 | a0001 | c0002 | t0003 | g0257 | AFR | ESN | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG02970 | hp2 | a0001 | c0001 | t0007 | g0036 | AFR | ESN | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG02976 | hp1 | a0001 | c0002 | t0003 | g0373 | AFR | ESN | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG02976 | hp2 | a0001 | c0005 | t0001 | g0386 | AFR | ESN | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0193 | SAS | PJL | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG03017 | hp2 | a0001 | c0002 | t0002 | g0276 | SAS | PJL | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG03041 | hp1 | a0001 | c0002 | t0004 | g0368 | AFR | GWD | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG03041 | hp2 | a0001 | c0002 | t0003 | g0026 | AFR | GWD | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG03098 | hp1 | a0001 | c0002 | t0003 | g0256 | AFR | MSL | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG03098 | hp2 | a0001 | c0002 | t0003 | g0352 | AFR | MSL | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG03130 | hp1 | a0001 | c0001 | t0005 | g0379 | AFR | ESN | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG03130 | hp2 | a0001 | c0002 | t0003 | g0043 | AFR | ESN | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0251 | AFR | ESN | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG03139 | hp2 | a0001 | c0002 | t0001 | g0263 | AFR | ESN | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG03195 | hp1 | a0001 | c0002 | t0004 | g0047 | AFR | ESN | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG03195 | hp2 | a0001 | c0001 | t0005 | g0377 | AFR | ESN | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0002 | AFR | MSL | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0389 | AFR | MSL | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG03225 | hp1 | a0001 | c0002 | t0004 | g0006 | AFR | MSL | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG03225 | hp2 | a0001 | c0003 | t0004 | g0069 | AFR | MSL | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG03239 | hp1 | a0001 | c0001 | t0003 | g0206 | SAS | PJL | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG03239 | hp2 | a0001 | c0002 | t0001 | g0182 | SAS | PJL | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG03453 | hp1 | a0001 | c0002 | t0003 | g0051 | AFR | MSL | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG03453 | hp2 | a0001 | c0002 | t0003 | g0024 | AFR | MSL | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG03486 | hp1 | a0001 | c0002 | t0003 | g0359 | AFR | MSL | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG03486 | hp2 | a0001 | c0001 | t0004 | g0003 | AFR | MSL | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG03490 | hp1 | a0001 | c0001 | t0005 | g0014 | SAS | PJL | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG03490 | hp2 | a0001 | c0002 | t0002 | g0154 | SAS | PJL | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0145 | SAS | PJL | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG03492 | hp2 | a0001 | c0001 | t0005 | g0014 | SAS | PJL | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG03516 | hp1 | a0001 | c0002 | t0003 | g0041 | AFR | ESN | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG03516 | hp2 | a0001 | c0001 | t0003 | g0255 | AFR | ESN | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG03540 | hp1 | a0001 | c0002 | t0002 | g0034 | AFR | GWD | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG03540 | hp2 | a0001 | c0002 | t0003 | g0128 | AFR | GWD | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG03579 | hp1 | a0001 | c0001 | t0008 | g0070 | AFR | MSL | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG03579 | hp2 | a0001 | c0001 | t0004 | g0390 | AFR | MSL | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0216 | SAS | PJL | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | PJL | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG03669 | hp2 | a0001 | c0001 | t0003 | g0315 | SAS | PJL | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG03688 | hp1 | a0001 | c0001 | t0003 | g0210 | SAS | STU | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0353 | SAS | STU | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG03704 | hp1 | a0001 | c0001 | t0005 | g0180 | SAS | PJL | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG03704 | hp2 | a0001 | c0002 | t0001 | g0007 | SAS | PJL | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0109 | SAS | PJL | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0253 | SAS | PJL | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0360 | SAS | BEB | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG03831 | hp2 | a0001 | c0002 | t0002 | g0280 | SAS | BEB | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0214 | SAS | BEB | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG03942 | hp1 | a0001 | c0002 | t0001 | g0091 | SAS | BEB | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG03942 | hp2 | a0001 | c0001 | t0003 | g0153 | SAS | BEB | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0148 | SAS | STU | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG04115 | hp2 | a0001 | c0002 | t0002 | g0222 | SAS | STU | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0143 | SAS | BEB | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG04199 | hp1 | a0001 | c0002 | t0002 | g0270 | SAS | STU | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0138 | SAS | STU | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG04204 | hp1 | a0001 | c0001 | t0005 | g0357 | SAS | STU | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0254 | SAS | STU | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0209 | SAS | STU | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0355 | SAS | STU | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA18522 | hp1 | a0001 | c0001 | t0004 | g0003 | AFR | YRI | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0350 | AFR | YRI | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA18612 | hp1 | a0001 | c0001 | t0003 | g0318 | EAS | CHB | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | CHB | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA18906 | hp1 | a0001 | c0002 | t0004 | g0039 | AFR | YRI | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | YRI | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA18939 | hp2 | a0001 | c0002 | t0002 | g0290 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA18940 | hp2 | a0001 | c0002 | t0001 | g0110 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0336 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA18942 | hp2 | a0001 | c0002 | t0002 | g0013 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0340 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA18944 | hp1 | a0001 | c0002 | t0002 | g0161 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0382 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA18946 | hp1 | a0001 | c0002 | t0002 | g0013 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA18947 | hp1 | a0001 | c0001 | t0003 | g0197 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA18947 | hp2 | a0001 | c0002 | t0002 | g0169 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA18949 | hp2 | a0001 | c0002 | t0002 | g0288 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0374 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA18951 | hp1 | a0001 | c0002 | t0002 | g0120 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA18951 | hp2 | a0001 | c0002 | t0004 | g0287 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0385 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA18956 | hp2 | a0001 | c0002 | t0002 | g0220 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA18957 | hp2 | a0001 | c0002 | t0002 | g0017 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA18960 | hp1 | a0001 | c0002 | t0002 | g0132 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA18960 | hp2 | a0001 | c0002 | t0002 | g0279 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA18961 | hp1 | a0001 | c0002 | t0002 | g0168 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA18961 | hp2 | a0001 | c0002 | t0004 | g0311 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA18963 | hp1 | a0001 | c0002 | t0002 | g0171 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA18963 | hp2 | a0001 | c0002 | t0002 | g0163 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA18964 | hp1 | a0001 | c0002 | t0002 | g0162 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA18964 | hp2 | a0001 | c0002 | t0001 | g0089 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA18967 | hp1 | a0001 | c0002 | t0004 | g0019 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA18968 | hp2 | a0001 | c0002 | t0002 | g0314 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA18969 | hp1 | a0001 | c0002 | t0004 | g0283 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA18969 | hp2 | a0001 | c0002 | t0002 | g0156 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA18970 | hp1 | a0001 | c0002 | t0004 | g0302 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0308 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA18971 | hp1 | a0001 | c0001 | t0003 | g0375 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA18971 | hp2 | a0001 | c0002 | t0004 | g0289 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA18973 | hp1 | a0001 | c0002 | t0002 | g0236 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA18973 | hp2 | a0001 | c0002 | t0004 | g0073 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0337 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA18975 | hp2 | a0001 | c0001 | t0003 | g0322 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA18977 | hp1 | a0001 | c0002 | t0003 | g0244 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0341 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA18978 | hp2 | a0001 | c0002 | t0002 | g0119 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA18980 | hp1 | a0001 | c0002 | t0004 | g0326 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA18980 | hp2 | a0001 | c0002 | t0004 | g0200 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA18981 | hp1 | a0001 | c0002 | t0002 | g0012 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA18981 | hp2 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA18982 | hp2 | a0001 | c0002 | t0002 | g0299 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA18986 | hp1 | a0001 | c0001 | t0003 | g0078 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA18986 | hp2 | a0001 | c0002 | t0002 | g0282 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA18987 | hp1 | a0001 | c0002 | t0002 | g0081 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA18988 | hp1 | a0001 | c0002 | t0002 | g0305 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA18990 | hp1 | a0001 | c0002 | t0004 | g0116 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA18990 | hp2 | a0001 | c0002 | t0004 | g0277 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA18991 | hp1 | a0001 | c0001 | t0003 | g0139 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA18991 | hp2 | a0001 | c0002 | t0003 | g0064 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA18992 | hp1 | a0001 | c0001 | t0003 | g0247 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA18992 | hp2 | a0001 | c0002 | t0003 | g0245 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA18993 | hp1 | a0001 | c0002 | t0002 | g0202 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA18993 | hp2 | a0001 | c0002 | t0002 | g0307 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA18994 | hp1 | a0001 | c0002 | t0002 | g0312 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA18994 | hp2 | a0001 | c0002 | t0004 | g0172 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA18998 | hp1 | a0001 | c0002 | t0002 | g0017 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA18998 | hp2 | a0001 | c0002 | t0001 | g0296 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA18999 | hp2 | a0001 | c0002 | t0002 | g0012 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA19000 | hp1 | a0001 | c0002 | t0002 | g0334 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA19001 | hp1 | a0001 | c0002 | t0004 | g0248 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA19001 | hp2 | a0001 | c0002 | t0004 | g0284 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA19003 | hp1 | a0001 | c0002 | t0002 | g0269 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA19003 | hp2 | a0001 | c0001 | t0003 | g0079 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA19004 | hp1 | a0001 | c0002 | t0003 | g0127 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA19005 | hp2 | a0001 | c0002 | t0002 | g0304 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA19006 | hp2 | a0001 | c0002 | t0002 | g0300 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA19007 | hp1 | a0001 | c0002 | t0004 | g0019 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA19007 | hp2 | a0001 | c0002 | t0003 | g0246 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA19009 | hp2 | a0001 | c0002 | t0004 | g0332 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA19011 | hp1 | a0001 | c0002 | t0004 | g0286 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA19011 | hp2 | a0001 | c0002 | t0001 | g0271 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA19012 | hp2 | a0001 | c0002 | t0002 | g0291 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0231 | AFR | LWK | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA19030 | hp2 | a0001 | c0001 | t0005 | g0367 | AFR | LWK | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA19043 | hp1 | a0001 | c0002 | t0001 | g0258 | AFR | LWK | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA19043 | hp2 | a0001 | c0002 | t0003 | g0346 | AFR | LWK | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA19054 | hp1 | a0001 | c0002 | t0002 | g0278 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA19055 | hp1 | a0001 | c0002 | t0002 | g0274 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0333 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA19057 | hp1 | a0001 | c0002 | t0002 | g0123 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA19057 | hp2 | a0001 | c0001 | t0003 | g0189 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA19058 | hp1 | a0001 | c0002 | t0001 | g0241 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA19058 | hp2 | a0001 | c0002 | t0002 | g0342 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA19060 | hp1 | a0001 | c0002 | t0002 | g0112 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA19060 | hp2 | a0001 | c0002 | t0002 | g0301 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA19063 | hp1 | a0001 | c0002 | t0003 | g0243 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA19063 | hp2 | a0001 | c0002 | t0004 | g0155 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA19064 | hp2 | a0001 | c0002 | t0002 | g0170 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA19065 | hp1 | a0001 | c0002 | t0002 | g0173 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA19065 | hp2 | a0001 | c0001 | t0003 | g0321 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA19067 | hp1 | a0001 | c0002 | t0002 | g0250 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA19067 | hp2 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA19068 | hp1 | a0001 | c0002 | t0004 | g0122 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA19070 | hp2 | a0001 | c0002 | t0002 | g0306 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA19078 | hp1 | a0001 | c0002 | t0001 | g0242 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA19078 | hp2 | a0001 | c0002 | t0002 | g0174 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA19079 | hp1 | a0001 | c0002 | t0004 | g0057 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA19082 | hp1 | a0001 | c0001 | t0003 | g0335 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA19082 | hp2 | a0001 | c0001 | t0003 | g0107 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA19083 | hp1 | a0001 | c0002 | t0002 | g0268 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA19083 | hp2 | a0001 | c0001 | t0003 | g0080 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA19086 | hp2 | a0001 | c0002 | t0004 | g0281 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0339 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA19087 | hp2 | a0001 | c0002 | t0002 | g0083 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA19088 | hp2 | a0001 | c0002 | t0002 | g0328 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA19089 | hp2 | a0001 | c0002 | t0002 | g0158 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA19090 | hp1 | a0001 | c0002 | t0002 | g0167 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA19090 | hp2 | a0001 | c0002 | t0004 | g0310 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA19091 | hp1 | a0001 | c0002 | t0003 | g0106 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0224 | AFR | YRI | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA19240 | hp2 | a0001 | c0001 | t0003 | g0002 | AFR | YRI | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA20129 | hp1 | a0001 | c0002 | t0003 | g0376 | AFR | ASW | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA20129 | hp2 | a0001 | c0003 | t0001 | g0392 | AFR | ASW | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA20752 | hp1 | a0001 | c0002 | t0001 | g0381 | EUR | TSI | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA20752 | hp2 | a0001 | c0002 | t0001 | g0183 | EUR | TSI | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA20805 | hp1 | a0001 | c0002 | t0002 | g0275 | EUR | TSI | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0146 | EUR | TSI | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | GIH | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA20905 | hp2 | a0001 | c0002 | t0002 | g0062 | SAS | GIH | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | CLM | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | CLM | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | ACB | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG02486 | hp2 | a0001 | c0002 | t0004 | g0048 | AFR | ACB | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0002 | AFR | ACB | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | ACB | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG03471 | hp1 | a0001 | c0003 | t0004 | g0054 | AFR | MSL | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG03471 | hp2 | a0001 | c0002 | t0004 | g0046 | AFR | MSL | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG06807 | hp1 | a0001 | c0002 | t0001 | g0329 | AFR | USA | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| HG06807 | hp2 | a0001 | c0001 | t0005 | g0378 | AFR | USA | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0338 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA18955 | hp2 | a0001 | c0002 | t0001 | g0272 | EAS | JPT | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0259 | AFR | USA | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0351 | AFR | USA | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA21309 | hp1 | a0001 | c0002 | t0001 | g0129 | AFR | LWK | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| NA21309 | hp2 | a0001 | c0001 | t0003 | g0105 | AFR | LWK | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0085 | REF | REF | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0002 | g0157 | REF | REF | ACTG2_chr2_73888008_73924865 | ACTG2 | chr2 | 73888008 | 73924865 |
| view | chr:pos | ref | alt | # # of ahapid:amio-acid(protein) level
|
ahapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:73919434 | T | G | 1 | a0002 | 1 | HG01074.hp2 | missense_variant&splice_region_variant | MODERATE | c.990T>G | p.Ile330Met | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 9/9 | 1070/1501 | 990/1131 | 330/376 | chr2 | 73919434 |
| 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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:73902479 | C | T | 1 | a0001c0005 | 1 | HG02976.hp2 | synonymous_variant | LOW | c.246C>T | p.Asp82Asp | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/9 | 326/1501 | 246/1131 | 82/376 | chr2 | 73902479 | |||
| chr2:73908771 | A | G | 3 | a0001c0001a0001c0005a0002c0004 | 211 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
synonymous_variant | LOW | c.354A>G | p.Glu118Glu | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 4/9 | 434/1501 | 354/1131 | 118/376 | chr2 | 73908771 | |||
| chr2:73913489 | C | T | 1 | a0001c0003 | 9 | HG01243.hp1 HG02145.hp2 HG02257.hp1 others(6): Show |
synonymous_variant | LOW | c.456C>T | p.Ile152Ile | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 6/9 | 536/1501 | 456/1131 | 152/376 | chr2 | 73913489 |
| 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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:73901306 | C | T | 11 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(8): Show | 261 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(258): Show |
5_prime_UTR_variant | MODIFIER | c.-6C>T | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 2/9 | 6 | chr2 | 73901306 | ||||||
| chr2:73919583 | A | G | 3 | a0001c0001t0006a0001c0001t0008a0001c0002t0006 | 6 | HG00735.hp1 HG02572.hp1 HG02615.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*8A>G | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 9/9 | 8 | chr2 | 73919583 | ||||||
| chr2:73919742 | G | A | 14 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(11): Show | 234 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(231): Show |
3_prime_UTR_variant | MODIFIER | c.*167G>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 9/9 | 167 | chr2 | 73919742 | ||||||
| chr2:73919779 | C | T | 3 | a0001c0001t0006a0001c0001t0008a0001c0002t0006 | 6 | HG00735.hp1 HG02572.hp1 HG02615.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*204C>T | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 9/9 | 204 | chr2 | 73919779 | ||||||
| chr2:73919801 | G | A | 1 | a0001c0002t0009 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*226G>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 9/9 | 226 | chr2 | 73919801 | ||||||
| chr2:73919802 | A | C | 1 | a0001c0002t0009 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*227A>C | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 9/9 | 227 | chr2 | 73919802 | ||||||
| chr2:73919803 | G | A | 1 | a0001c0002t0009 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*228G>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 9/9 | 228 | chr2 | 73919803 | ||||||
| chr2:73919805 | A | C | 1 | a0001c0002t0009 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*230A>C | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 9/9 | 230 | chr2 | 73919805 | ||||||
| chr2:73919806 | G | A | 1 | a0001c0002t0009 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*231G>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 9/9 | 231 | chr2 | 73919806 | ||||||
| chr2:73919807 | T | A | 1 | a0001c0002t0009 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*232T>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 9/9 | 232 | chr2 | 73919807 | ||||||
| chr2:73919811 | G | C | 1 | a0001c0002t0009 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*236G>C | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 9/9 | 236 | chr2 | 73919811 | ||||||
| chr2:73919814 | C | G | 1 | a0001c0002t0009 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*239C>G | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 9/9 | 239 | chr2 | 73919814 | ||||||
| chr2:73919815 | T | A | 1 | a0001c0002t0009 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*240T>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 9/9 | 240 | chr2 | 73919815 | ||||||
| chr2:73919816 | T | G | 1 | a0001c0002t0009 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*241T>G | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 9/9 | 241 | chr2 | 73919816 | ||||||
| chr2:73919818 | C | A | 1 | a0001c0002t0009 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*243C>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 9/9 | 243 | chr2 | 73919818 | ||||||
| chr2:73919820 | A | G | 1 | a0001c0002t0009 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*245A>G | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 9/9 | 245 | chr2 | 73919820 | ||||||
| chr2:73919822 | G | A | 1 | a0001c0002t0009 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*247G>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 9/9 | 247 | chr2 | 73919822 | ||||||
| chr2:73919824 | T | A | 1 | a0001c0002t0009 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*249T>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 9/9 | 249 | chr2 | 73919824 | ||||||
| chr2:73919825 | C | G | 1 | a0001c0002t0009 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*250C>G | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 9/9 | 250 | chr2 | 73919825 | ||||||
| chr2:73919827 | C | G | 1 | a0001c0002t0009 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*252C>G | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 9/9 | 252 | chr2 | 73919827 | ||||||
| chr2:73919829 | C | G | 1 | a0001c0002t0009 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*254C>G | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 9/9 | 254 | chr2 | 73919829 | ||||||
| chr2:73919837 | A | T | 1 | a0001c0002t0009 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*262A>T | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 9/9 | 262 | chr2 | 73919837 | ||||||
| chr2:73919838 | G | C | 1 | a0001c0002t0009 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*263G>C | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 9/9 | 263 | chr2 | 73919838 | ||||||
| chr2:73919840 | T | A | 1 | a0001c0002t0009 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*265T>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 9/9 | 265 | chr2 | 73919840 | ||||||
| chr2:73919841 | T | C | 1 | a0001c0002t0009 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*266T>C | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 9/9 | 266 | chr2 | 73919841 | ||||||
| chr2:73919844 | A | C | 1 | a0001c0002t0009 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*269A>C | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 9/9 | 269 | chr2 | 73919844 | ||||||
| chr2:73919846 | T | A | 1 | a0001c0002t0009 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*271T>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 9/9 | 271 | chr2 | 73919846 | ||||||
| chr2:73919847 | T | C | 1 | a0001c0002t0009 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*272T>C | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 9/9 | 272 | chr2 | 73919847 | ||||||
| chr2:73919848 | C | A | 1 | a0001c0002t0009 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*273C>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 9/9 | 273 | chr2 | 73919848 | ||||||
| chr2:73919850 | A | C | 1 | a0001c0002t0009 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*275A>C | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 9/9 | 275 | chr2 | 73919850 | ||||||
| chr2:73919850 | A | G | 3 | a0001c0001t0005a0001c0001t0007a0001c0003t0007 | 21 | HG00140.hp2 HG01109.hp2 HG01167.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*275A>G | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 9/9 | 275 | chr2 | 73919850 | ||||||
| chr2:73919852 | T | G | 1 | a0001c0002t0009 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*277T>G | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 9/9 | 277 | chr2 | 73919852 | ||||||
| chr2:73919854 | T | G | 1 | a0001c0002t0009 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*279T>G | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 9/9 | 279 | chr2 | 73919854 | ||||||
| chr2:73919855 | C | G | 1 | a0001c0002t0009 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*280C>G | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 9/9 | 280 | chr2 | 73919855 | ||||||
| chr2:73919858 | A | G | 1 | a0001c0002t0009 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*283A>G | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 9/9 | 283 | chr2 | 73919858 | ||||||
| chr2:73919859 | C | A | 1 | a0001c0002t0009 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*284C>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 9/9 | 284 | chr2 | 73919859 | ||||||
| chr2:73919860 | T | G | 1 | a0001c0002t0009 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*285T>G | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 9/9 | 285 | chr2 | 73919860 | ||||||
| chr2:73919862 | C | A | 1 | a0001c0002t0009 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*287C>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 9/9 | 287 | chr2 | 73919862 |
| 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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:73893054 | A | G | 148 | a0001c0001t0001g0018a0001c0001t0001g0253a0001c0001t0001g0254others(145): Show | 154 | HG00140.hp1 HG00423.hp1 HG00544.hp2 others(151): Show |
splice_region_variant&intron_variant | LOW | c.-37+3A>G | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73893054 | |||||||
| chr2:73893148 | G | A | 2 | a0001c0001t0003g0251a0001c0001t0003g0252 | 2 | HG01099.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-37+97G>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73893148 | |||||||
| chr2:73893173 | C | T | 1 | a0001c0002t0002g0250 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-37+122C>T | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73893173 | |||||||
| chr2:73893223 | G | A | 2 | a0001c0001t0001g0253a0001c0001t0001g0254 | 2 | HG03710.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.-37+172G>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73893223 | |||||||
| chr2:73893239 | G | A | 12 | a0001c0001t0001g0029a0001c0001t0004g0003a0001c0001t0004g0027others(9): Show | 13 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.-37+188G>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73893239 | |||||||
| chr2:73893297 | C | T | 132 | a0001c0001t0001g0018a0001c0001t0001g0253a0001c0001t0001g0254others(129): Show | 136 | HG00140.hp1 HG00423.hp1 HG00544.hp2 others(133): Show |
intron_variant | MODIFIER | c.-37+246C>T | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73893297 | |||||||
| chr2:73893658 | G | A | 110 | a0001c0001t0001g0018a0001c0001t0001g0253a0001c0001t0001g0254others(107): Show | 113 | HG00140.hp1 HG00423.hp1 HG00544.hp2 others(110): Show |
intron_variant | MODIFIER | c.-37+607G>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73893658 | |||||||
| chr2:73893707 | T | C | 30 | a0001c0001t0001g0040a0001c0001t0001g0044a0001c0001t0003g0037others(27): Show | 33 | HG00735.hp1 HG00738.hp2 HG01099.hp1 others(30): Show |
intron_variant | MODIFIER | c.-37+656T>C | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73893707 | |||||||
| chr2:73893782 | C | T | 2 | a0001c0002t0001g0393a0001c0003t0001g0392 | 2 | HG02922.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-37+731C>T | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73893782 | |||||||
| chr2:73893834 | A | G | 40 | a0001c0001t0001g0040a0001c0001t0001g0044a0001c0001t0001g0265others(37): Show | 42 | HG00738.hp2 HG01099.hp1 HG01099.hp2 others(39): Show |
intron_variant | MODIFIER | c.-37+783A>G | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73893834 | |||||||
| chr2:73893856 | T | C | 147 | a0001c0001t0001g0008a0001c0001t0001g0018a0001c0001t0001g0029others(144): Show | 154 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(151): Show |
intron_variant | MODIFIER | c.-37+805T>C | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73893856 | |||||||
| chr2:73893873 | T | C | 128 | a0001c0001t0001g0018a0001c0001t0001g0065a0001c0001t0001g0068others(125): Show | 133 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(130): Show |
intron_variant | MODIFIER | c.-37+822T>C | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73893873 | |||||||
| chr2:73893958 | G | A | 2 | a0001c0002t0002g0268a0001c0002t0004g0057 | 2 | NA19079.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.-37+907G>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73893958 | |||||||
| chr2:73894050 | C | T | 6 | a0001c0001t0003g0247a0001c0002t0003g0243a0001c0002t0003g0244others(3): Show | 6 | NA18977.hp1 NA18992.hp1 NA18992.hp2 others(3): Show |
intron_variant | MODIFIER | c.-37+999C>T | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73894050 | |||||||
| chr2:73894061 | G | A | 1 | a0001c0002t0002g0269 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.-37+1010G>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73894061 | |||||||
| chr2:73894132 | G | A | 1 | a0001c0002t0003g0346 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-37+1081G>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73894132 | |||||||
| chr2:73894151 | T | C | 106 | a0001c0001t0001g0018a0001c0001t0001g0065a0001c0001t0001g0068others(103): Show | 111 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.-37+1100T>C | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73894151 | |||||||
| chr2:73894370 | G | T | 3 | a0001c0002t0001g0258a0001c0002t0003g0256a0001c0002t0003g0257 | 3 | HG02970.hp1 HG03098.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-37+1319G>T | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73894370 | |||||||
| chr2:73894471 | T | C | 1 | a0001c0002t0002g0270 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-37+1420T>C | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73894471 | |||||||
| chr2:73894564 | G | T | 1 | a0001c0002t0004g0331 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-37+1513G>T | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73894564 | |||||||
| chr2:73894568 | C | T | 1 | a0001c0002t0001g0089 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-37+1517C>T | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73894568 | |||||||
| chr2:73894652 | C | T | 8 | a0001c0001t0005g0371a0001c0001t0005g0377a0001c0001t0005g0378others(5): Show | 8 | HG01243.hp1 HG02615.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.-37+1601C>T | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73894652 | |||||||
| chr2:73894705 | GAGCTTGG others(17): Show |
G | 168 | a0001c0001t0001g0018a0001c0001t0001g0029a0001c0001t0001g0068others(165): Show | 175 | HG00423.hp1 HG00544.hp2 HG00597.hp2 others(172): Show |
intron_variant | MODIFIER | c.-37+1666_-37+1689d others(26): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 73894705 | ||||||
| chr2:73894765 | T | C | 2 | a0001c0001t0001g0351a0001c0002t0002g0223 | 2 | HG02895.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-37+1714T>C | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73894765 | |||||||
| chr2:73895053 | T | C | 7 | a0001c0001t0001g0068a0001c0001t0002g0224a0001c0001t0004g0027others(4): Show | 7 | HG02280.hp2 HG02717.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.-37+2002T>C | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73895053 | |||||||
| chr2:73895096 | T | C | 72 | a0001c0001t0001g0008a0001c0001t0001g0068a0001c0001t0001g0071others(69): Show | 75 | HG00140.hp2 HG00639.hp2 HG00642.hp1 others(72): Show |
intron_variant | MODIFIER | c.-37+2045T>C | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73895096 | |||||||
| chr2:73895136 | C | T | 1 | a0001c0002t0002g0222 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-37+2085C>T | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73895136 | |||||||
| chr2:73895191 | A | AG | 8 | a0001c0001t0005g0371a0001c0001t0005g0377a0001c0001t0005g0378others(5): Show | 8 | HG02615.hp2 HG02723.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.-37+2146dupG | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 73895191 | ||||||
| chr2:73895218 | G | A | 129 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0018others(126): Show | 135 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.-37+2167G>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73895218 | |||||||
| chr2:73895223 | G | A | 2 | a0001c0001t0003g0105a0001c0002t0004g0090 | 2 | HG02698.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-37+2172G>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73895223 | |||||||
| chr2:73895292 | G | A | 5 | a0001c0001t0001g0152a0001c0001t0003g0107a0001c0002t0003g0106others(2): Show | 5 | HG02056.hp2 NA18977.hp1 NA19063.hp1 others(2): Show |
intron_variant | MODIFIER | c.-37+2241G>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73895292 | |||||||
| chr2:73895371 | G | T | 1 | a0001c0002t0003g0076 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-37+2320G>T | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73895371 | |||||||
| chr2:73895386 | T | C | 1 | a0001c0002t0001g0296 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-37+2335T>C | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73895386 | |||||||
| chr2:73895443 | G | A | 3 | a0001c0001t0003g0002a0001c0001t0003g0153a0001c0002t0003g0108 | 5 | HG01255.hp1 HG02559.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.-37+2392G>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73895443 | |||||||
| chr2:73895477 | C | T | 2 | a0001c0001t0003g0002a0001c0002t0003g0346 | 4 | HG02559.hp1 HG03209.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.-37+2426C>T | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73895477 | |||||||
| chr2:73895494 | T | C | 2 | a0001c0002t0003g0256a0001c0002t0003g0257 | 2 | HG02970.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-37+2443T>C | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73895494 | |||||||
| chr2:73895508 | G | A | 7 | a0001c0001t0005g0371a0001c0001t0005g0377a0001c0001t0005g0378others(4): Show | 7 | HG02615.hp2 HG02723.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.-37+2457G>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73895508 | |||||||
| chr2:73895576 | G | A | 1 | a0001c0001t0003g0109 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-37+2525G>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73895576 | |||||||
| chr2:73895583 | A | G | 23 | a0001c0001t0003g0251a0001c0001t0003g0252a0001c0001t0003g0255others(20): Show | 25 | HG01099.hp1 HG01261.hp1 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.-37+2532A>G | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73895583 | |||||||
| chr2:73895630 | A | G | 12 | a0001c0001t0002g0224a0001c0001t0003g0231a0001c0001t0003g0389others(9): Show | 13 | HG00735.hp1 HG01884.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.-37+2579A>G | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73895630 | |||||||
| chr2:73895826 | A | G | 259 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(256): Show | 277 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.-37+2775A>G | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73895826 | |||||||
| chr2:73895831 | G | A | 253 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(250): Show | 271 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.-37+2780G>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73895831 | |||||||
| chr2:73895866 | T | C | 1 | a0001c0001t0001g0354 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-37+2815T>C | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73895866 | |||||||
| chr2:73895902 | A | C | 188 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(185): Show | 198 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(195): Show |
intron_variant | MODIFIER | c.-37+2851A>C | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73895902 | |||||||
| chr2:73896179 | T | A | 231 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(228): Show | 246 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.-37+3128T>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73896179 | |||||||
| chr2:73896217 | G | A | 1 | a0001c0002t0002g0111 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-37+3166G>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73896217 | |||||||
| chr2:73896235 | CAGCTCCT others(13): Show |
C | 2 | a0001c0002t0002g0123a0001c0002t0002g0220 | 2 | NA18956.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.-37+3187_-37+3206d others(22): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 73896235 | ||||||
| chr2:73896247 | T | C | 2 | a0001c0002t0004g0159a0001c0002t0004g0166 | 2 | HG02071.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.-37+3196T>C | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73896247 | |||||||
| chr2:73896347 | C | CA | 12 | a0001c0001t0002g0224a0001c0001t0003g0231a0001c0001t0004g0027others(9): Show | 12 | HG02280.hp2 HG02615.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.-37+3314dupA | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 73896347 | ||||||
| chr2:73896347 | C | CAA | 7 | a0001c0001t0003g0389a0001c0001t0005g0367a0001c0001t0005g0387others(4): Show | 8 | HG00735.hp1 HG01884.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.-37+3313_-37+3314d others(4): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 73896347 | ||||||
| chr2:73896347 | CA | C | 82 | a0001c0001t0001g0029a0001c0001t0001g0130a0001c0001t0001g0184others(79): Show | 88 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.-37+3314delA | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 73896347 | ||||||
| chr2:73896347 | CAA | C | 179 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(176): Show | 190 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(187): Show |
intron_variant | MODIFIER | c.-37+3313_-37+3314d others(4): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 73896347 | ||||||
| chr2:73896420 | C | G | 3 | a0001c0002t0002g0173a0001c0002t0002g0174a0001c0002t0002g0250 | 3 | NA19065.hp1 NA19067.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.-37+3369C>G | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73896420 | |||||||
| chr2:73896593 | G | A | 3 | a0001c0001t0003g0078a0001c0001t0003g0079a0001c0001t0003g0080 | 3 | NA18986.hp1 NA19003.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.-37+3542G>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73896593 | |||||||
| chr2:73896700 | C | T | 245 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(242): Show | 261 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.-37+3649C>T | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73896700 | |||||||
| chr2:73896739 | C | T | 4 | a0001c0002t0002g0005a0001c0002t0002g0033a0001c0002t0002g0034others(1): Show | 5 | HG02055.hp2 HG02895.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-37+3688C>T | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73896739 | |||||||
| chr2:73896960 | T | C | 1 | a0001c0001t0004g0077 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-37+3909T>C | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73896960 | |||||||
| chr2:73897015 | C | T | 245 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(242): Show | 261 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.-37+3964C>T | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73897015 | |||||||
| chr2:73897039 | G | A | 18 | a0001c0001t0004g0003a0001c0001t0006g0249a0001c0001t0008g0042others(15): Show | 20 | HG01261.hp1 HG01891.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.-37+3988G>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73897039 | |||||||
| chr2:73897044 | G | A | 232 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(229): Show | 246 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.-37+3993G>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73897044 | |||||||
| chr2:73897068 | T | C | 2 | a0001c0001t0002g0224a0001c0001t0004g0027 | 2 | HG02280.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-37+4017T>C | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73897068 | |||||||
| chr2:73897154 | C | T | 12 | a0001c0001t0003g0259a0001c0001t0003g0260a0001c0001t0003g0261others(9): Show | 12 | HG02055.hp1 HG02257.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.-37+4103C>T | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73897154 | |||||||
| chr2:73897172 | G | A | 13 | a0001c0001t0001g0029a0001c0001t0001g0351a0001c0001t0003g0002others(10): Show | 15 | HG01109.hp2 HG01167.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.-36-4104G>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73897172 | |||||||
| chr2:73897214 | C | A | 1 | a0001c0001t0001g0071 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-36-4062C>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73897214 | |||||||
| chr2:73897215 | A | G | 249 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(246): Show | 265 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.-36-4061A>G | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73897215 | |||||||
| chr2:73897234 | C | G | 2 | a0001c0001t0001g0044a0001c0002t0003g0330 | 2 | HG00738.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.-36-4042C>G | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73897234 | |||||||
| chr2:73897277 | A | G | 32 | a0001c0001t0001g0029a0001c0001t0001g0351a0001c0001t0003g0002others(29): Show | 36 | HG01109.hp2 HG01167.hp2 HG01169.hp1 others(33): Show |
intron_variant | MODIFIER | c.-36-3999A>G | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73897277 | |||||||
| chr2:73897327 | G | A | 1 | a0001c0001t0005g0014 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-36-3949G>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73897327 | |||||||
| chr2:73897368 | C | T | 3 | a0001c0003t0004g0052a0001c0003t0004g0053a0001c0003t0004g0054 | 3 | HG02145.hp2 HG02630.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-36-3908C>T | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73897368 | |||||||
| chr2:73897401 | T | C | 285 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(282): Show | 304 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(301): Show |
intron_variant | MODIFIER | c.-36-3875T>C | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73897401 | |||||||
| chr2:73897415 | CT | C | 3 | a0001c0001t0004g0003a0001c0001t0006g0249a0001c0003t0001g0392 | 4 | HG02717.hp1 HG03486.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.-36-3858delT | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 73897415 | ||||||
| chr2:73897542 | T | C | 1 | a0001c0001t0006g0249 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-36-3734T>C | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73897542 | |||||||
| chr2:73897600 | A | G | 3 | a0001c0003t0004g0052a0001c0003t0004g0053a0001c0003t0004g0054 | 3 | HG02145.hp2 HG02630.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-36-3676A>G | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73897600 | |||||||
| chr2:73897837 | A | G | 274 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(271): Show | 292 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.-36-3439A>G | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73897837 | |||||||
| chr2:73897933 | G | C | 247 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(244): Show | 263 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.-36-3343G>C | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73897933 | |||||||
| chr2:73897960 | T | A | 1 | a0001c0001t0001g0185 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-36-3316T>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73897960 | |||||||
| chr2:73897966 | T | C | 13 | a0001c0001t0001g0029a0001c0001t0001g0351a0001c0001t0003g0002others(10): Show | 15 | HG01109.hp2 HG01167.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.-36-3310T>C | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73897966 | |||||||
| chr2:73898039 | A | G | 13 | a0001c0001t0001g0029a0001c0001t0001g0351a0001c0001t0003g0002others(10): Show | 15 | HG01109.hp2 HG01167.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.-36-3237A>G | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73898039 | |||||||
| chr2:73898134 | C | A | 247 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(244): Show | 263 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.-36-3142C>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73898134 | |||||||
| chr2:73898192 | C | T | 2 | a0001c0001t0007g0036a0001c0003t0004g0035 | 2 | HG02451.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.-36-3084C>T | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73898192 | |||||||
| chr2:73898201 | G | A | 1 | a0001c0001t0003g0343 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-36-3075G>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73898201 | |||||||
| chr2:73898352 | T | TGCACCTT others(322): Show |
1 | a0001c0001t0001g0186 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-36-2913_-36-2912i others(331): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 73898352 | ||||||
| chr2:73898352 | T | TGCACCTT others(300): Show |
1 | a0001c0001t0001g0187 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.-36-2913_-36-2912i others(309): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 73898352 | ||||||
| chr2:73898352 | T | TGCACCTT others(302): Show |
3 | a0001c0001t0001g0152a0001c0001t0003g0107a0001c0001t0003g0247 | 3 | HG02056.hp2 NA18992.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.-36-2913_-36-2912i others(311): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 73898352 | ||||||
| chr2:73898352 | T | TGCACCTT others(305): Show |
13 | a0001c0001t0001g0009a0001c0001t0001g0185a0001c0001t0001g0188others(10): Show | 14 | HG00438.hp2 NA18941.hp1 NA18943.hp1 others(11): Show |
intron_variant | MODIFIER | c.-36-2913_-36-2912i others(314): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 73898352 | ||||||
| chr2:73898352 | T | TGCACCTT others(306): Show |
1 | a0001c0001t0001g0133 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-36-2913_-36-2912i others(315): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 73898352 | ||||||
| chr2:73898352 | T | TGCACCTT others(307): Show |
4 | a0001c0001t0003g0100a0001c0001t0003g0105a0001c0001t0003g0134others(1): Show | 4 | HG01081.hp1 HG01433.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.-36-2913_-36-2912i others(316): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 73898352 | ||||||
| chr2:73898352 | T | TGCACCTT others(308): Show |
2 | a0001c0001t0001g0293a0001c0001t0001g0317 | 2 | NA18941.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.-36-2913_-36-2912i others(317): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 73898352 | ||||||
| chr2:73898352 | T | TGCACCTT others(310): Show |
2 | a0001c0001t0001g0071a0001c0001t0001g0227 | 2 | HG01934.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.-36-2913_-36-2912i others(319): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 73898352 | ||||||
| chr2:73898352 | T | TGCACCTT others(313): Show |
1 | a0001c0001t0005g0032 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-36-2913_-36-2912i others(322): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 73898352 | ||||||
| chr2:73898352 | T | TGCACCTT others(314): Show |
21 | a0001c0001t0001g0130a0001c0001t0001g0313a0001c0001t0001g0347others(18): Show | 22 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(19): Show |
intron_variant | MODIFIER | c.-36-2913_-36-2912i others(323): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 73898352 | ||||||
| chr2:73898352 | T | TGCACCTT others(315): Show |
1 | a0001c0001t0001g0354 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-36-2913_-36-2912i others(324): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 73898352 | ||||||
| chr2:73898352 | T | TGCACCTT others(315): Show |
17 | a0001c0001t0001g0355a0001c0001t0003g0181a0001c0001t0003g0259others(14): Show | 19 | HG00438.hp1 HG01346.hp2 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.-36-2913_-36-2912i others(324): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 73898352 | ||||||
| chr2:73898352 | T | TGCACCTT others(316): Show |
7 | a0001c0001t0001g0360a0001c0001t0003g0261a0001c0001t0003g0343others(4): Show | 7 | HG02055.hp1 HG02257.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-36-2913_-36-2912i others(325): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 73898352 | ||||||
| chr2:73898352 | T | TGCACCTT others(317): Show |
2 | a0001c0002t0003g0023a0001c0002t0003g0025 | 2 | HG01243.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.-36-2913_-36-2912i others(326): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 73898352 | ||||||
| chr2:73898352 | T | TGCACCTT others(314): Show |
1 | a0001c0001t0001g0361 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.-36-2913_-36-2912i others(323): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 73898352 | ||||||
| chr2:73898352 | T | TGCACCTT others(318): Show |
2 | a0001c0001t0001g0358a0001c0002t0003g0026 | 2 | HG00741.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-36-2913_-36-2912i others(327): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 73898352 | ||||||
| chr2:73898352 | T | TGCACCTT others(319): Show |
1 | a0001c0002t0001g0182 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-36-2913_-36-2912i others(328): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 73898352 | ||||||
| chr2:73898352 | T | TGCACCTT others(320): Show |
1 | a0001c0002t0001g0183 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-36-2913_-36-2912i others(329): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 73898352 | ||||||
| chr2:73898352 | T | TGCACCTT others(321): Show |
5 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0001g0234others(2): Show | 5 | HG02155.hp2 HG03017.hp1 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.-36-2913_-36-2912i others(330): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 73898352 | ||||||
| chr2:73898352 | T | TGCACCTT others(322): Show |
38 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0018others(35): Show | 42 | HG01070.hp2 HG01071.hp2 HG01074.hp1 others(39): Show |
intron_variant | MODIFIER | c.-36-2913_-36-2912i others(331): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 73898352 | ||||||
| chr2:73898352 | T | TGCACCTT others(323): Show |
1 | a0001c0001t0001g0138 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-36-2913_-36-2912i others(332): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 73898352 | ||||||
| chr2:73898352 | T | TGCACCTT others(323): Show |
44 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0065others(41): Show | 49 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.-36-2913_-36-2912i others(332): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 73898352 | ||||||
| chr2:73898352 | T | TGCACCTT others(324): Show |
29 | a0001c0001t0001g0086a0001c0001t0001g0094a0001c0001t0001g0131others(26): Show | 29 | HG00140.hp2 HG00280.hp1 HG00621.hp2 others(26): Show |
intron_variant | MODIFIER | c.-36-2913_-36-2912i others(333): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 73898352 | ||||||
| chr2:73898352 | T | TGCACCTT others(325): Show |
14 | a0001c0001t0001g0044a0001c0001t0001g0103a0001c0001t0001g0104others(11): Show | 14 | HG00544.hp1 HG00639.hp1 HG00733.hp2 others(11): Show |
intron_variant | MODIFIER | c.-36-2913_-36-2912i others(334): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 73898352 | ||||||
| chr2:73898352 | T | TGCACCTT others(326): Show |
5 | a0001c0001t0001g0040a0001c0001t0001g0150a0001c0001t0001g0217others(2): Show | 5 | HG02129.hp1 HG02132.hp2 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.-36-2913_-36-2912i others(335): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 73898352 | ||||||
| chr2:73898352 | T | TGCACCTT others(327): Show |
3 | a0001c0001t0001g0327a0001c0001t0003g0177a0001c0002t0004g0326 | 3 | HG00558.hp2 NA18980.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.-36-2913_-36-2912i others(336): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 73898352 | ||||||
| chr2:73898352 | T | TGCACCTT others(328): Show |
2 | a0001c0001t0003g0060a0001c0002t0002g0328 | 2 | HG02523.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.-36-2913_-36-2912i others(337): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 73898352 | ||||||
| chr2:73898380 | C | T | 17 | a0001c0001t0008g0042a0001c0001t0008g0070a0001c0002t0002g0045others(14): Show | 18 | HG01261.hp1 HG01891.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.-36-2896C>T | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73898380 | |||||||
| chr2:73898423 | G | A | 48 | a0001c0001t0001g0130a0001c0001t0001g0313a0001c0001t0001g0354others(45): Show | 51 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.-36-2853G>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73898423 | |||||||
| chr2:73898534 | C | T | 266 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(263): Show | 284 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(281): Show |
intron_variant | MODIFIER | c.-36-2742C>T | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73898534 | |||||||
| chr2:73898551 | T | C | 1 | a0001c0003t0007g0391 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-36-2725T>C | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73898551 | |||||||
| chr2:73898557 | G | GAAGTGCT others(39): Show |
1 | a0001c0003t0007g0391 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-36-2717_-36-2716i others(48): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 73898557 | ||||||
| chr2:73898591 | A | G | 4 | a0001c0001t0003g0251a0001c0001t0003g0252a0001c0001t0003g0255others(1): Show | 4 | HG01099.hp1 HG03139.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-36-2685A>G | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73898591 | |||||||
| chr2:73898597 | A | G | 1 | a0001c0001t0001g0364 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-36-2679A>G | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73898597 | |||||||
| chr2:73898633 | C | T | 1 | a0001c0001t0003g0389 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-36-2643C>T | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73898633 | |||||||
| chr2:73898669 | C | G | 2 | a0001c0001t0007g0036a0001c0003t0004g0035 | 2 | HG02451.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.-36-2607C>G | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73898669 | |||||||
| chr2:73898686 | C | T | 1 | a0001c0003t0007g0391 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-36-2590C>T | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73898686 | |||||||
| chr2:73898690 | A | G | 265 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(262): Show | 283 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.-36-2586A>G | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73898690 | |||||||
| chr2:73898733 | G | C | 1 | a0001c0001t0003g0201 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-36-2543G>C | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73898733 | |||||||
| chr2:73898741 | G | A | 3 | a0001c0001t0003g0259a0001c0001t0003g0261a0001c0002t0001g0263 | 3 | HG02055.hp1 HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-36-2535G>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73898741 | |||||||
| chr2:73898786 | CTTTTCTT others(4): Show |
C | 51 | a0001c0001t0001g0130a0001c0001t0001g0313a0001c0001t0001g0347others(48): Show | 54 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(51): Show |
intron_variant | MODIFIER | c.-36-2474_-36-2464d others(13): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 73898786 | ||||||
| chr2:73898802 | C | CT | 12 | a0001c0001t0001g0075a0001c0001t0001g0088a0001c0001t0001g0133others(9): Show | 12 | HG02145.hp1 HG02615.hp2 HG03017.hp1 others(9): Show |
intron_variant | MODIFIER | c.-36-2456dupT | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 73898802 | ||||||
| chr2:73898807 | T | C | 1 | a0001c0002t0001g0381 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-36-2469T>C | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73898807 | |||||||
| chr2:73898841 | T | C | 1 | a0001c0003t0004g0035 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-36-2435T>C | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73898841 | |||||||
| chr2:73898872 | G | T | 1 | a0001c0003t0001g0392 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-36-2404G>T | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73898872 | |||||||
| chr2:73898904 | G | A | 1 | a0001c0002t0003g0076 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-36-2372G>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73898904 | |||||||
| chr2:73898927 | C | T | 1 | a0001c0003t0007g0391 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-36-2349C>T | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73898927 | |||||||
| chr2:73898952 | G | A | 1 | a0001c0001t0001g0254 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-36-2324G>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73898952 | |||||||
| chr2:73898954 | C | T | 17 | a0001c0001t0008g0042a0001c0001t0008g0070a0001c0002t0002g0045others(14): Show | 18 | HG01261.hp1 HG01891.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.-36-2322C>T | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73898954 | |||||||
| chr2:73899012 | A | G | 13 | a0001c0001t0001g0185a0001c0001t0001g0190a0001c0001t0001g0191others(10): Show | 13 | NA18941.hp1 NA18943.hp1 NA18950.hp1 others(10): Show |
intron_variant | MODIFIER | c.-36-2264A>G | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73899012 | |||||||
| chr2:73899031 | T | C | 1 | a0001c0001t0001g0355 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-36-2245T>C | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73899031 | |||||||
| chr2:73899032 | G | C | 1 | a0001c0001t0001g0355 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-36-2244G>C | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73899032 | |||||||
| chr2:73899100 | G | A | 4 | a0001c0001t0003g0251a0001c0001t0003g0252a0001c0001t0003g0255others(1): Show | 4 | HG01099.hp1 HG03139.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-36-2176G>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73899100 | |||||||
| chr2:73899174 | T | C | 1 | a0001c0001t0007g0036 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-36-2102T>C | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73899174 | |||||||
| chr2:73899217 | C | G | 1 | a0001c0001t0003g0100 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-36-2059C>G | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73899217 | |||||||
| chr2:73899330 | G | A | 257 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(254): Show | 274 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(271): Show |
intron_variant | MODIFIER | c.-36-1946G>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73899330 | |||||||
| chr2:73899376 | C | T | 253 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(250): Show | 270 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.-36-1900C>T | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73899376 | |||||||
| chr2:73899386 | T | C | 13 | a0001c0001t0003g0231a0001c0001t0003g0389a0001c0001t0005g0367others(10): Show | 14 | HG00735.hp1 HG01243.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.-36-1890T>C | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73899386 | |||||||
| chr2:73899395 | G | A | 1 | a0001c0002t0001g0258 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-36-1881G>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73899395 | |||||||
| chr2:73899468 | T | A | 4 | a0001c0001t0003g0251a0001c0001t0003g0252a0001c0001t0003g0255others(1): Show | 4 | HG01099.hp1 HG03139.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-36-1808T>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73899468 | |||||||
| chr2:73899479 | A | G | 2 | a0001c0002t0002g0290a0001c0003t0007g0391 | 2 | HG01243.hp1 NA18939.hp2 |
intron_variant | MODIFIER | c.-36-1797A>G | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73899479 | |||||||
| chr2:73899483 | C | T | 1 | a0001c0001t0001g0199 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-36-1793C>T | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73899483 | |||||||
| chr2:73899608 | T | C | 1 | a0001c0003t0007g0391 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-36-1668T>C | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73899608 | |||||||
| chr2:73899612 | T | A | 13 | a0001c0001t0001g0029a0001c0001t0001g0351a0001c0001t0003g0002others(10): Show | 15 | HG01109.hp2 HG01167.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.-36-1664T>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73899612 | |||||||
| chr2:73899711 | G | A | 1 | a0001c0001t0007g0036 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-36-1565G>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73899711 | |||||||
| chr2:73899718 | T | C | 2 | a0001c0002t0006g0004a0001c0002t0006g0055 | 3 | HG00735.hp1 HG02615.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-36-1558T>C | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73899718 | |||||||
| chr2:73899811 | T | A | 274 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(271): Show | 292 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.-36-1465T>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73899811 | |||||||
| chr2:73899891 | A | C | 1 | a0001c0002t0002g0049 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-36-1385A>C | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73899891 | |||||||
| chr2:73899990 | G | A | 1 | a0001c0001t0005g0032 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-36-1286G>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73899990 | |||||||
| chr2:73899991 | C | T | 1 | a0001c0003t0007g0391 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-36-1285C>T | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73899991 | |||||||
| chr2:73900107 | C | T | 2 | a0001c0002t0004g0289a0001c0002t0004g0311 | 2 | NA18961.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.-36-1169C>T | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73900107 | |||||||
| chr2:73900159 | G | A | 1 | a0001c0003t0004g0035 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-36-1117G>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73900159 | |||||||
| chr2:73900162 | C | T | 181 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(178): Show | 193 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(190): Show |
intron_variant | MODIFIER | c.-36-1114C>T | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73900162 | |||||||
| chr2:73900217 | G | A | 155 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(152): Show | 165 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(162): Show |
intron_variant | MODIFIER | c.-36-1059G>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73900217 | |||||||
| chr2:73900373 | A | G | 1 | a0001c0002t0002g0264 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-36-903A>G | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73900373 | |||||||
| chr2:73900381 | A | C | 1 | a0001c0002t0002g0250 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-36-895A>C | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73900381 | |||||||
| chr2:73900710 | C | A | 1 | a0001c0002t0002g0269 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.-36-566C>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73900710 | |||||||
| chr2:73900718 | G | T | 156 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(153): Show | 166 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.-36-558G>T | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73900718 | |||||||
| chr2:73900764 | T | A | 1 | a0001c0002t0003g0106 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-36-512T>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73900764 | |||||||
| chr2:73900880 | C | T | 2 | a0001c0002t0002g0005a0001c0002t0002g0223 | 3 | HG02895.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-36-396C>T | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73900880 | |||||||
| chr2:73900930 | T | G | 1 | a0001c0001t0003g0389 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-36-346T>G | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73900930 | |||||||
| chr2:73901160 | G | C | 2 | a0001c0003t0004g0052a0001c0003t0004g0053 | 2 | HG02145.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.-36-116G>C | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73901160 | |||||||
| chr2:73901234 | T | G | 164 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(161): Show | 176 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.-36-42T>G | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73901234 | |||||||
| chr2:73901242 | G | A | 165 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(162): Show | 177 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.-36-34G>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73901242 | |||||||
| chr2:73901264 | G | C | 245 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(242): Show | 261 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.-36-12G>C | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 1/8 | chr2 | 73901264 | |||||||
| chr2:73901532 | A | ATG | 24 | a0001c0002t0001g0091a0001c0002t0002g0005a0001c0002t0002g0083others(21): Show | 25 | HG01168.hp1 HG01169.hp2 HG01515.hp1 others(22): Show |
intron_variant | MODIFIER | c.126+143_126+144dup others(2): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 73901532 | ||||||
| chr2:73901532 | A | ATGTG | 27 | a0001c0001t0004g0114a0001c0002t0002g0017a0001c0002t0002g0062others(24): Show | 29 | HG00673.hp1 HG00738.hp1 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.126+141_126+144dup others(4): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 73901532 | ||||||
| chr2:73901532 | A | ATGTGTG | 23 | a0001c0001t0002g0121a0001c0002t0002g0028a0001c0002t0002g0081others(20): Show | 23 | HG00408.hp1 HG00544.hp2 HG00609.hp1 others(20): Show |
intron_variant | MODIFIER | c.126+139_126+144dup others(6): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 73901532 | ||||||
| chr2:73901532 | A | ATGTGTGT others(1): Show |
7 | a0001c0002t0002g0169a0001c0002t0002g0170a0001c0002t0002g0219others(4): Show | 7 | HG02074.hp2 NA18947.hp2 NA18951.hp2 others(4): Show |
intron_variant | MODIFIER | c.126+137_126+144dup others(8): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 73901532 | ||||||
| chr2:73901532 | A | ATGTGTGT others(3): Show |
5 | a0001c0001t0002g0308a0001c0002t0002g0059a0001c0002t0002g0171others(2): Show | 5 | HG01258.hp2 HG02165.hp2 NA18949.hp2 others(2): Show |
intron_variant | MODIFIER | c.126+135_126+144dup others(10): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 73901532 | ||||||
| chr2:73901532 | A | ATGTGTGT others(5): Show |
1 | a0001c0002t0004g0310 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.126+133_126+144dup others(12): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 73901532 | ||||||
| chr2:73901532 | ATG | A | 14 | a0001c0002t0002g0034a0001c0002t0002g0096a0001c0002t0002g0112others(11): Show | 14 | HG00642.hp1 HG01891.hp2 HG02080.hp1 others(11): Show |
intron_variant | MODIFIER | c.126+143_126+144del others(2): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 73901532 | ||||||
| chr2:73901532 | ATGTG | A | 11 | a0001c0001t0004g0003a0001c0001t0004g0390a0001c0002t0002g0033others(8): Show | 12 | HG02015.hp1 HG02055.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.126+141_126+144del others(4): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 73901532 | ||||||
| chr2:73901532 | ATGTGTG | A | 7 | a0001c0001t0002g0224a0001c0001t0004g0027a0001c0002t0002g0274others(4): Show | 7 | HG02280.hp2 HG02896.hp1 NA18977.hp1 others(4): Show |
intron_variant | MODIFIER | c.126+139_126+144del others(6): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 73901532 | ||||||
| chr2:73901532 | ATGTGTGT others(5): Show |
A | 1 | a0001c0002t0002g0269 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.126+133_126+144del others(12): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 73901532 | ||||||
| chr2:73901532 | ATGTGTGT others(15): Show |
A | 1 | a0001c0003t0001g0392 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.126+123_126+144del others(22): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 73901532 | ||||||
| chr2:73901532 | ATGTGTGT others(37): Show |
A | 2 | a0001c0002t0002g0012a0001c0002t0002g0334 | 3 | NA18981.hp1 NA18999.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.126+101_126+144del others(44): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 73901532 | ||||||
| chr2:73901533 | TGTGTGTG others(42): Show |
T | 51 | a0001c0001t0001g0130a0001c0001t0001g0313a0001c0001t0001g0351others(48): Show | 54 | HG00280.hp2 HG00438.hp1 HG00733.hp1 others(51): Show |
intron_variant | MODIFIER | c.126+97_126+145delG others(48): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 2/8 | chr2 | 73901533 | |||||||
| chr2:73901533 | TGTGTGTG others(44): Show |
T | 3 | a0001c0002t0003g0023a0001c0002t0003g0025a0001c0002t0003g0026 | 3 | HG01243.hp2 HG02280.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.126+97_126+147delG others(50): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 2/8 | chr2 | 73901533 | |||||||
| chr2:73901533 | TGTGTGTG others(46): Show |
T | 6 | a0001c0002t0001g0095a0001c0002t0001g0129a0001c0002t0003g0024others(3): Show | 6 | HG00639.hp2 HG02922.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.126+97_126+149delG others(52): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 2/8 | chr2 | 73901533 | |||||||
| chr2:73901537 | TGTGTGTG others(43): Show |
T | 2 | a0001c0001t0003g0259a0001c0002t0002g0132 | 2 | NA18960.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.126+119_126+168del others(50): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 73901537 | ||||||
| chr2:73901539 | TGTGTGTG others(41): Show |
T | 164 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(161): Show | 177 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.126+121_126+168del others(48): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 73901539 | ||||||
| chr2:73901541 | TGTGTGTG others(39): Show |
T | 11 | a0001c0001t0001g0151a0001c0001t0001g0199a0001c0001t0001g0217others(8): Show | 11 | HG00673.hp2 HG01168.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.126+123_126+168del others(46): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 73901541 | ||||||
| chr2:73901543 | TGTGTGTG others(37): Show |
T | 1 | a0001c0002t0002g0137 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.126+125_126+168del others(44): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 73901543 | ||||||
| chr2:73901578 | G | C | 1 | a0001c0002t0003g0051 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.126+141G>C | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 2/8 | chr2 | 73901578 | |||||||
| chr2:73901582 | C | G | 6 | a0001c0001t0008g0070a0001c0002t0004g0038a0001c0002t0004g0039others(3): Show | 6 | HG01261.hp1 HG02723.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.126+145C>G | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 2/8 | chr2 | 73901582 | |||||||
| chr2:73901584 | G | C | 3 | a0001c0001t0008g0070a0001c0002t0004g0038a0001c0002t0004g0082 | 3 | HG01261.hp1 HG02965.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.126+147G>C | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 2/8 | chr2 | 73901584 | |||||||
| chr2:73901587 | C | T | 66 | a0001c0001t0001g0130a0001c0001t0001g0313a0001c0001t0001g0351others(63): Show | 69 | HG00280.hp2 HG00438.hp1 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.126+150C>T | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 2/8 | chr2 | 73901587 | |||||||
| chr2:73901587 | CGT | C | 12 | a0001c0001t0008g0042a0001c0002t0002g0045a0001c0002t0002g0348others(9): Show | 13 | HG01891.hp1 HG01891.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.126+167_126+168del others(2): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 73901587 | ||||||
| chr2:73901589 | T | C | 5 | a0001c0001t0008g0070a0001c0002t0004g0038a0001c0002t0004g0039others(2): Show | 5 | HG01261.hp1 HG02965.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.126+152T>C | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 2/8 | chr2 | 73901589 | |||||||
| chr2:73901608 | G | A | 1 | a0001c0001t0003g0194 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.126+171G>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 2/8 | chr2 | 73901608 | |||||||
| chr2:73901670 | G | C | 1 | a0001c0001t0008g0070 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.126+233G>C | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 2/8 | chr2 | 73901670 | |||||||
| chr2:73901778 | G | A | 251 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(248): Show | 268 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.126+341G>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 2/8 | chr2 | 73901778 | |||||||
| chr2:73901984 | A | T | 3 | a0001c0002t0003g0023a0001c0002t0003g0025a0001c0002t0003g0026 | 3 | HG01243.hp2 HG02280.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.127-376A>T | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 2/8 | chr2 | 73901984 | |||||||
| chr2:73901998 | TGAG | T | 9 | a0001c0001t0001g0029a0001c0001t0003g0231a0001c0001t0003g0366others(6): Show | 9 | HG01109.hp2 HG01167.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.127-356_127-354del others(3): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 73901998 | ||||||
| chr2:73902012 | A | G | 2 | a0001c0002t0004g0122a0001c0002t0004g0310 | 2 | NA19068.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.127-348A>G | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 2/8 | chr2 | 73902012 | |||||||
| chr2:73902018 | C | CGT | 59 | a0001c0001t0001g0130a0001c0001t0001g0313a0001c0001t0001g0354others(56): Show | 62 | HG00280.hp2 HG00438.hp1 HG00639.hp2 others(59): Show |
intron_variant | MODIFIER | c.127-321_127-320dup others(2): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 73902018 | ||||||
| chr2:73902019 | GTGTGTGT others(15): Show |
G | 5 | a0001c0001t0003g0231a0001c0001t0005g0032a0001c0001t0007g0036others(2): Show | 5 | HG02451.hp1 HG02970.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.127-311_127-290del others(22): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 73902019 | ||||||
| chr2:73902035 | G | GTGTGTGT others(3): Show |
4 | a0001c0003t0002g0262a0001c0003t0004g0052a0001c0003t0004g0053others(1): Show | 4 | HG01243.hp1 HG02145.hp2 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-320_127-319ins others(10): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 73902035 | ||||||
| chr2:73902037 | G | GTGTGTGT others(1): Show |
5 | a0001c0001t0001g0351a0001c0001t0002g0224a0001c0001t0004g0027others(2): Show | 5 | HG02280.hp2 HG03225.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.127-320_127-319ins others(8): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 73902037 | ||||||
| chr2:73902037 | G | GTGTGTGT others(3): Show |
2 | a0001c0001t0004g0003a0001c0003t0001g0392 | 3 | HG03486.hp2 NA18522.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.127-320_127-319ins others(10): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 73902037 | ||||||
| chr2:73902037 | G | GTGTGTGT others(5): Show |
4 | a0001c0001t0001g0151a0001c0001t0003g0084a0001c0001t0003g0125others(1): Show | 4 | HG01515.hp2 HG02074.hp1 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-320_127-319ins others(12): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 73902037 | ||||||
| chr2:73902039 | G | GTGTGTGT others(1): Show |
4 | a0001c0001t0001g0149a0001c0001t0001g0214a0001c0001t0001g0324others(1): Show | 5 | HG00423.hp1 HG00735.hp1 HG01123.hp2 others(2): Show |
intron_variant | MODIFIER | c.127-320_127-319ins others(8): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 73902039 | ||||||
| chr2:73902039 | G | GTGTGTGT others(3): Show |
145 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(142): Show | 155 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(152): Show |
intron_variant | MODIFIER | c.127-320_127-319ins others(10): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 73902039 | ||||||
| chr2:73902039 | G | GTGTGTGT others(5): Show |
19 | a0001c0001t0001g0016a0001c0001t0001g0126a0001c0001t0001g0142others(16): Show | 22 | HG00140.hp1 HG00408.hp2 HG00621.hp1 others(19): Show |
intron_variant | MODIFIER | c.127-320_127-319ins others(12): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 73902039 | ||||||
| chr2:73902039 | G | GTGTGTGT others(7): Show |
1 | a0001c0001t0001g0216 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.127-320_127-319ins others(14): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 73902039 | ||||||
| chr2:73902039 | G | GTGTGTGT others(9): Show |
1 | a0001c0002t0002g0049 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.127-320_127-319ins others(16): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 73902039 | ||||||
| chr2:73902041 | C | G | 185 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(182): Show | 200 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.127-319C>G | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 2/8 | chr2 | 73902041 | |||||||
| chr2:73902041 | CTG | C | 5 | a0001c0001t0001g0029a0001c0001t0005g0030a0001c0001t0005g0031others(2): Show | 5 | HG01109.hp2 HG01167.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.127-299_127-298del others(2): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 73902041 | ||||||
| chr2:73902047 | G | GTGTGTGT others(3): Show |
1 | a0001c0003t0004g0035 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.127-304_127-303ins others(10): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 73902047 | ||||||
| chr2:73902262 | T | C | 56 | a0001c0001t0001g0130a0001c0001t0001g0313a0001c0001t0001g0354others(53): Show | 59 | HG00280.hp2 HG00438.hp1 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.127-98T>C | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 2/8 | chr2 | 73902262 | |||||||
| chr2:73902347 | T | C | 196 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(193): Show | 211 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.127-13T>C | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 2/8 | chr2 | 73902347 | |||||||
| chr2:73902537 | A | G | 196 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(193): Show | 211 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.255+49A>G | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | chr2 | 73902537 | |||||||
| chr2:73902585 | C | G | 189 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(186): Show | 204 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.255+97C>G | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | chr2 | 73902585 | |||||||
| chr2:73902616 | C | A | 1 | a0001c0003t0004g0069 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.255+128C>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | chr2 | 73902616 | |||||||
| chr2:73902667 | T | A | 1 | a0001c0001t0003g0335 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.255+179T>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | chr2 | 73902667 | |||||||
| chr2:73902768 | G | A | 188 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(185): Show | 203 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.255+280G>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | chr2 | 73902768 | |||||||
| chr2:73902828 | G | A | 1 | a0001c0001t0001g0203 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.255+340G>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | chr2 | 73902828 | |||||||
| chr2:73902839 | C | T | 1 | a0001c0002t0002g0049 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.255+351C>T | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | chr2 | 73902839 | |||||||
| chr2:73902897 | C | A | 187 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(184): Show | 202 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.255+409C>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | chr2 | 73902897 | |||||||
| chr2:73903032 | G | A | 8 | a0001c0001t0001g0029a0001c0001t0003g0231a0001c0001t0005g0030others(5): Show | 8 | HG01109.hp2 HG01167.hp2 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.255+544G>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | chr2 | 73903032 | |||||||
| chr2:73903086 | A | G | 3 | a0001c0001t0003g0002a0001c0001t0003g0259a0001c0001t0003g0261 | 5 | HG02055.hp1 HG02559.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.255+598A>G | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | chr2 | 73903086 | |||||||
| chr2:73903095 | T | G | 1 | a0001c0001t0003g0315 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.255+607T>G | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | chr2 | 73903095 | |||||||
| chr2:73903113 | G | A | 185 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(182): Show | 199 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.255+625G>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | chr2 | 73903113 | |||||||
| chr2:73903395 | G | A | 4 | a0001c0002t0002g0171a0001c0002t0002g0282a0001c0002t0002g0288others(1): Show | 4 | NA18949.hp2 NA18963.hp1 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.255+907G>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | chr2 | 73903395 | |||||||
| chr2:73903430 | C | G | 184 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(181): Show | 198 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.255+942C>G | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | chr2 | 73903430 | |||||||
| chr2:73903542 | A | G | 195 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(192): Show | 210 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.255+1054A>G | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | chr2 | 73903542 | |||||||
| chr2:73903679 | T | C | 256 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(253): Show | 274 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(271): Show |
intron_variant | MODIFIER | c.255+1191T>C | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | chr2 | 73903679 | |||||||
| chr2:73903715 | G | A | 1 | a0001c0002t0003g0087 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.255+1227G>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | chr2 | 73903715 | |||||||
| chr2:73903718 | G | T | 1 | a0001c0001t0001g0145 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.255+1230G>T | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | chr2 | 73903718 | |||||||
| chr2:73903796 | T | A | 1 | a0001c0003t0002g0262 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.255+1308T>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | chr2 | 73903796 | |||||||
| chr2:73903888 | C | T | 11 | a0001c0001t0002g0224a0001c0001t0004g0003a0001c0001t0004g0027others(8): Show | 12 | HG01243.hp1 HG02145.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.255+1400C>T | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | chr2 | 73903888 | |||||||
| chr2:73903926 | T | A | 1 | a0001c0002t0002g0049 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.255+1438T>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | chr2 | 73903926 | |||||||
| chr2:73903937 | CTCA | C | 2 | a0001c0002t0006g0004a0001c0002t0006g0055 | 3 | HG00735.hp1 HG02615.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.255+1450_255+1452d others(5): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | chr2 | 73903937 | |||||||
| chr2:73903939 | C | A | 1 | a0001c0002t0002g0049 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.255+1451C>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | chr2 | 73903939 | |||||||
| chr2:73903939 | C | CA | 14 | a0001c0001t0004g0027a0001c0002t0002g0012a0001c0002t0002g0137others(11): Show | 15 | HG00735.hp2 HG01934.hp2 HG02080.hp1 others(12): Show |
intron_variant | MODIFIER | c.255+1471dupA | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 73903939 | ||||||
| chr2:73903939 | CA | C | 50 | a0001c0001t0001g0130a0001c0001t0001g0354a0001c0001t0001g0355others(47): Show | 53 | HG00280.hp2 HG00639.hp2 HG00733.hp1 others(50): Show |
intron_variant | MODIFIER | c.255+1471delA | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 73903939 | ||||||
| chr2:73903939 | CAA | C | 14 | a0001c0001t0001g0029a0001c0001t0005g0371a0001c0001t0005g0377others(11): Show | 14 | HG00438.hp1 HG00673.hp2 HG02071.hp1 others(11): Show |
intron_variant | MODIFIER | c.255+1470_255+1471d others(4): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 73903939 | ||||||
| chr2:73903939 | CAAAAAAA others(2): Show |
C | 18 | a0001c0001t0008g0042a0001c0001t0008g0070a0001c0002t0002g0045others(15): Show | 19 | HG01261.hp1 HG01891.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.255+1463_255+1471d others(11): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 73903939 | ||||||
| chr2:73903943 | A | G | 7 | a0001c0003t0002g0262a0001c0003t0004g0035a0001c0003t0004g0052others(4): Show | 7 | HG01243.hp1 HG02145.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.255+1455A>G | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | chr2 | 73903943 | |||||||
| chr2:73903950 | A | C | 6 | a0001c0001t0001g0088a0001c0001t0001g0186a0001c0001t0001g0187others(3): Show | 6 | NA18612.hp2 NA18940.hp1 NA18942.hp1 others(3): Show |
intron_variant | MODIFIER | c.255+1462A>C | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | chr2 | 73903950 | |||||||
| chr2:73903953 | A | C | 4 | a0001c0001t0005g0014a0001c0001t0005g0180a0001c0001t0005g0356others(1): Show | 5 | HG02602.hp1 HG03490.hp1 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.255+1465A>C | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | chr2 | 73903953 | |||||||
| chr2:73903954 | A | C | 1 | a0001c0002t0002g0306 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.255+1466A>C | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | chr2 | 73903954 | |||||||
| chr2:73903957 | A | C | 9 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0361others(6): Show | 10 | HG01070.hp2 HG01175.hp1 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.255+1469A>C | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | chr2 | 73903957 | |||||||
| chr2:73903958 | A | C | 151 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0015others(148): Show | 163 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.255+1470A>C | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | chr2 | 73903958 | |||||||
| chr2:73903958 | AAC | A | 15 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0361others(12): Show | 16 | HG01070.hp2 HG01175.hp1 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.255+1472_255+1473d others(4): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 73903958 | ||||||
| chr2:73903959 | A | C | 12 | a0001c0001t0001g0176a0001c0001t0001g0336a0001c0001t0001g0341others(9): Show | 12 | HG00544.hp1 HG00558.hp2 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.255+1471A>C | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | chr2 | 73903959 | |||||||
| chr2:73903959 | AC | A | 152 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0015others(149): Show | 164 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.255+1472delC | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | chr2 | 73903959 | |||||||
| chr2:73903960 | C | A | 35 | a0001c0001t0001g0176a0001c0001t0001g0336a0001c0001t0001g0341others(32): Show | 38 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.255+1472C>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | chr2 | 73903960 | |||||||
| chr2:73903970 | A | C | 1 | a0001c0001t0003g0177 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.255+1482A>C | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | chr2 | 73903970 | |||||||
| chr2:73904128 | G | A | 1 | a0001c0001t0001g0103 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.255+1640G>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | chr2 | 73904128 | |||||||
| chr2:73904205 | C | T | 15 | a0001c0001t0001g0009a0001c0001t0001g0185a0001c0001t0001g0188others(12): Show | 16 | HG00438.hp2 NA18941.hp1 NA18943.hp1 others(13): Show |
intron_variant | MODIFIER | c.255+1717C>T | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | chr2 | 73904205 | |||||||
| chr2:73904248 | C | CA | 13 | a0001c0001t0001g0351a0001c0001t0004g0390a0001c0002t0001g0091others(10): Show | 13 | HG01168.hp1 HG01169.hp2 HG02683.hp2 others(10): Show |
intron_variant | MODIFIER | c.255+1784dupA | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 73904248 | ||||||
| chr2:73904248 | CA | C | 51 | a0001c0001t0001g0126a0001c0001t0001g0130a0001c0001t0001g0133others(48): Show | 52 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.255+1784delA | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 73904248 | ||||||
| chr2:73904248 | CAA | C | 172 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(169): Show | 187 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.255+1783_255+1784d others(4): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 73904248 | ||||||
| chr2:73904248 | CAAAAAAA others(7): Show |
C | 1 | a0001c0001t0001g0187 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.255+1771_255+1784d others(16): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 73904248 | ||||||
| chr2:73904248 | CAAAAAAA others(9): Show |
C | 1 | a0001c0001t0003g0235 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.255+1769_255+1784d others(18): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 73904248 | ||||||
| chr2:73904265 | A | G | 1 | a0001c0002t0004g0287 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.255+1777A>G | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | chr2 | 73904265 | |||||||
| chr2:73904659 | AT | A | 195 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(192): Show | 210 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.255+2180delT | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 73904659 | ||||||
| chr2:73904661 | T | A | 26 | a0001c0001t0008g0042a0001c0001t0008g0070a0001c0002t0002g0045others(23): Show | 27 | HG00673.hp2 HG01261.hp1 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.255+2173T>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | chr2 | 73904661 | |||||||
| chr2:73904662 | T | A | 3 | a0001c0001t0002g0224a0001c0001t0004g0003a0001c0001t0004g0027 | 4 | HG02280.hp2 HG03486.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.255+2174T>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | chr2 | 73904662 | |||||||
| chr2:73904668 | T | A | 184 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(181): Show | 198 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.255+2180T>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | chr2 | 73904668 | |||||||
| chr2:73904669 | A | T | 1 | a0001c0002t0002g0028 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.255+2181A>T | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | chr2 | 73904669 | |||||||
| chr2:73904737 | CATTGTGT | C | 2 | a0001c0002t0006g0004a0001c0002t0006g0055 | 3 | HG00735.hp1 HG02615.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.255+2250_255+2256d others(9): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | chr2 | 73904737 | |||||||
| chr2:73904739 | T | TTG | 6 | a0001c0002t0002g0250a0001c0002t0002g0301a0001c0002t0002g0306others(3): Show | 6 | HG02071.hp2 NA18970.hp1 NA19004.hp1 others(3): Show |
intron_variant | MODIFIER | c.255+2289_255+2290d others(4): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 73904739 | ||||||
| chr2:73904739 | TTG | T | 9 | a0001c0002t0002g0154a0001c0002t0002g0174a0001c0002t0002g0222others(6): Show | 9 | HG02015.hp1 HG02698.hp2 HG03490.hp2 others(6): Show |
intron_variant | MODIFIER | c.255+2289_255+2290d others(4): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 73904739 | ||||||
| chr2:73904739 | TTGTG | T | 4 | a0001c0002t0002g0096a0001c0002t0002g0137a0001c0002t0002g0275others(1): Show | 4 | HG00642.hp1 HG02129.hp2 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.255+2287_255+2290d others(6): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 73904739 | ||||||
| chr2:73904765 | GTGTGTGT others(13): Show |
G | 5 | a0001c0001t0001g0103a0001c0001t0001g0140a0001c0001t0001g0319others(2): Show | 5 | HG01074.hp2 HG03516.hp2 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.255+2279_255+2298d others(22): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 73904765 | ||||||
| chr2:73904765 | GTGTGTGT others(15): Show |
G | 13 | a0001c0001t0001g0009a0001c0001t0001g0185a0001c0001t0001g0188others(10): Show | 14 | HG00438.hp2 HG01168.hp2 NA18941.hp1 others(11): Show |
intron_variant | MODIFIER | c.255+2279_255+2300d others(24): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 73904765 | ||||||
| chr2:73904767 | GTGTGTGT others(7): Show |
G | 1 | a0001c0002t0003g0330 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.255+2281_255+2294d others(16): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 73904767 | ||||||
| chr2:73904767 | GTGTGTGT others(9): Show |
G | 6 | a0001c0001t0001g0142a0001c0001t0001g0233a0001c0001t0001g0265others(3): Show | 6 | HG01099.hp2 HG01516.hp1 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.255+2281_255+2296d others(18): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 73904767 | ||||||
| chr2:73904767 | GTGTGTGT others(11): Show |
G | 16 | a0001c0001t0001g0072a0001c0001t0001g0186a0001c0001t0001g0203others(13): Show | 16 | HG00140.hp1 HG00423.hp1 HG00558.hp2 others(13): Show |
intron_variant | MODIFIER | c.255+2281_255+2298d others(20): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 73904767 | ||||||
| chr2:73904767 | GTGTGTGT others(13): Show |
G | 105 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(102): Show | 113 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.255+2281_255+2300d others(22): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 73904767 | ||||||
| chr2:73904767 | GTGTGTGT others(15): Show |
G | 5 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0292others(2): Show | 6 | HG01257.hp1 HG01257.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.255+2281_255+2302d others(24): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 73904767 | ||||||
| chr2:73904767 | GTGTGTGT others(17): Show |
G | 2 | a0001c0001t0003g0231a0001c0001t0005g0032 | 2 | HG02451.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.255+2281_255+2304d others(26): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 73904767 | ||||||
| chr2:73904769 | GTGTGTGT others(5): Show |
G | 1 | a0001c0001t0001g0353 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.255+2283_255+2294d others(14): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 73904769 | ||||||
| chr2:73904769 | GTGTGTGT others(7): Show |
G | 2 | a0001c0002t0003g0043a0001c0002t0003g0346 | 2 | HG03130.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.255+2283_255+2296d others(16): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 73904769 | ||||||
| chr2:73904769 | GTGTGTGT others(9): Show |
G | 1 | a0001c0001t0003g0060 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.255+2283_255+2298d others(18): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 73904769 | ||||||
| chr2:73904769 | GTGTGTGT others(11): Show |
G | 6 | a0001c0001t0001g0184a0001c0001t0003g0100a0001c0001t0003g0134others(3): Show | 6 | HG00733.hp2 HG01081.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.255+2283_255+2300d others(20): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 73904769 | ||||||
| chr2:73904769 | GTGTGTGT others(13): Show |
G | 10 | a0001c0001t0001g0068a0001c0001t0001g0204a0001c0001t0001g0350others(7): Show | 10 | HG00558.hp1 HG01175.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.255+2283_255+2302d others(22): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 73904769 | ||||||
| chr2:73904769 | GTGTGTGT others(15): Show |
G | 4 | a0001c0002t0002g0005a0001c0002t0002g0033a0001c0003t0001g0392others(1): Show | 5 | HG02055.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.255+2283_255+2304d others(24): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 73904769 | ||||||
| chr2:73904771 | GTGTGTGT others(13): Show |
G | 2 | a0001c0003t0004g0052a0001c0003t0004g0054 | 2 | HG02145.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.255+2285_255+2304d others(22): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 73904771 | ||||||
| chr2:73904771 | GTGTGTGT others(17): Show |
G | 3 | a0001c0001t0001g0351a0001c0001t0004g0390a0001c0001t0007g0036 | 3 | HG02970.hp2 HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.255+2285_255+2308d others(26): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 73904771 | ||||||
| chr2:73904773 | G | A | 1 | a0001c0002t0003g0376 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.255+2285G>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | chr2 | 73904773 | |||||||
| chr2:73904773 | G | GTATATAT others(1): Show |
3 | a0001c0002t0002g0221a0001c0002t0003g0256a0001c0002t0003g0257 | 3 | HG02622.hp2 HG02970.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.255+2286_255+2287i others(10): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 73904773 | ||||||
| chr2:73904773 | GTGTGTAT others(9): Show |
G | 4 | a0001c0001t0005g0371a0001c0001t0005g0377a0001c0001t0005g0378others(1): Show | 4 | HG02615.hp2 HG03130.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.255+2287_255+2302d others(18): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 73904773 | ||||||
| chr2:73904773 | GTGTGTAT others(11): Show |
G | 1 | a0001c0003t0007g0391 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.255+2287_255+2304d others(20): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 73904773 | ||||||
| chr2:73904773 | GTGTGTAT others(15): Show |
G | 3 | a0001c0001t0002g0224a0001c0001t0004g0003a0001c0001t0004g0027 | 4 | HG02280.hp2 HG03486.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.255+2287_255+2308d others(24): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 73904773 | ||||||
| chr2:73904775 | G | A | 6 | a0001c0002t0002g0022a0001c0002t0002g0221a0001c0002t0003g0256others(3): Show | 6 | HG00741.hp2 HG02622.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.255+2287G>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | chr2 | 73904775 | |||||||
| chr2:73904775 | G | GTA | 3 | a0001c0001t0002g0121a0001c0002t0002g0017a0001c0002t0002g0304 | 3 | HG00609.hp1 NA18957.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.255+2288_255+2289i others(4): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 73904775 | ||||||
| chr2:73904775 | G | GTATA | 6 | a0001c0002t0001g0329a0001c0002t0002g0171a0001c0002t0002g0288others(3): Show | 6 | HG06807.hp1 NA18949.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.255+2288_255+2289i others(6): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 73904775 | ||||||
| chr2:73904775 | G | GTATATA | 3 | a0001c0002t0002g0161a0001c0002t0002g0165a0001c0002t0004g0283 | 3 | HG00408.hp1 NA18944.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.255+2288_255+2289i others(8): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 73904775 | ||||||
| chr2:73904775 | G | GTATATAT others(3): Show |
2 | a0001c0002t0002g0236a0001c0002t0003g0023 | 2 | HG02280.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.255+2288_255+2289i others(12): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 73904775 | ||||||
| chr2:73904775 | GTGTATA | G | 3 | a0001c0002t0003g0025a0001c0002t0003g0026a0001c0002t0004g0286 | 3 | HG01243.hp2 HG03041.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.255+2289_255+2294d others(8): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 73904775 | ||||||
| chr2:73904775 | GTGTATAT others(11): Show |
G | 2 | a0001c0002t0002g0049a0001c0003t0004g0035 | 2 | HG02451.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.255+2289_255+2306d others(20): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 73904775 | ||||||
| chr2:73904775 | GTGTATAT others(13): Show |
G | 5 | a0001c0001t0001g0029a0001c0001t0005g0030a0001c0001t0005g0031others(2): Show | 5 | HG01109.hp2 HG01167.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.255+2289_255+2308d others(22): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 73904775 | ||||||
| chr2:73904777 | G | A | 28 | a0001c0001t0001g0360a0001c0001t0002g0121a0001c0002t0001g0329others(25): Show | 28 | HG00408.hp1 HG00609.hp1 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.255+2289G>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | chr2 | 73904777 | |||||||
| chr2:73904777 | G | GTA | 21 | a0001c0002t0001g0089a0001c0002t0002g0013a0001c0002t0002g0017others(18): Show | 22 | HG00735.hp2 HG01168.hp1 HG02080.hp1 others(19): Show |
intron_variant | MODIFIER | c.255+2326_255+2327d others(4): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 73904777 | ||||||
| chr2:73904777 | G | GTATA | 8 | a0001c0002t0002g0081a0001c0002t0002g0123a0001c0002t0002g0164others(5): Show | 8 | HG00673.hp1 HG01934.hp2 HG02273.hp2 others(5): Show |
intron_variant | MODIFIER | c.255+2324_255+2327d others(6): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 73904777 | ||||||
| chr2:73904777 | G | GTATATA | 6 | a0001c0001t0001g0355a0001c0002t0001g0263a0001c0002t0002g0012others(3): Show | 7 | HG00544.hp2 HG03139.hp2 HG04228.hp2 others(4): Show |
intron_variant | MODIFIER | c.255+2322_255+2327d others(8): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 73904777 | ||||||
| chr2:73904777 | G | GTATATAT others(1): Show |
3 | a0001c0001t0001g0354a0001c0002t0002g0240a0001c0002t0002g0303 | 3 | HG02027.hp1 HG02080.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.255+2320_255+2327d others(10): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 73904777 | ||||||
| chr2:73904777 | G | GTATATAT others(3): Show |
4 | a0001c0002t0003g0041a0001c0002t0004g0019a0001c0002t0004g0172others(1): Show | 4 | HG01884.hp1 HG03516.hp1 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.255+2318_255+2327d others(12): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 73904777 | ||||||
| chr2:73904777 | G | GTATATAT others(5): Show |
2 | a0001c0002t0002g0111a0001c0002t0002g0163 | 2 | HG02735.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.255+2316_255+2327d others(14): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 73904777 | ||||||
| chr2:73904777 | G | GTATATAT others(7): Show |
1 | a0001c0002t0001g0091 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.255+2314_255+2327d others(16): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 73904777 | ||||||
| chr2:73904777 | G | GTGTA | 3 | a0001c0002t0002g0062a0001c0002t0002g0119a0001c0002t0004g0345 | 3 | HG01169.hp2 NA18978.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.255+2290_255+2291i others(6): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 73904777 | ||||||
| chr2:73904777 | G | GTGTATAT others(3): Show |
3 | a0001c0001t0001g0130a0001c0002t0002g0264a0001c0002t0002g0270 | 3 | HG01167.hp1 HG02683.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.255+2290_255+2291i others(12): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 73904777 | ||||||
| chr2:73904777 | G | GTGTATAT others(5): Show |
1 | a0001c0001t0003g0181 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.255+2290_255+2291i others(14): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 73904777 | ||||||
| chr2:73904777 | G | GTGTGTAT others(7): Show |
2 | a0001c0001t0005g0014a0001c0001t0005g0180 | 3 | HG03490.hp1 HG03492.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.255+2290_255+2291i others(16): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 73904777 | ||||||
| chr2:73904777 | G | GTGTGTGT others(9): Show |
1 | a0001c0001t0005g0356 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.255+2290_255+2291i others(18): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 73904777 | ||||||
| chr2:73904777 | G | GTGTGTGT others(11): Show |
2 | a0001c0001t0005g0387a0001c0001t0005g0388 | 2 | HG01884.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.255+2290_255+2291i others(20): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 73904777 | ||||||
| chr2:73904777 | G | GTGTGTGT others(15): Show |
1 | a0001c0001t0005g0367 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.255+2290_255+2291i others(24): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 73904777 | ||||||
| chr2:73904777 | G | GTGTGTGT others(17): Show |
1 | a0001c0001t0005g0357 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.255+2290_255+2291i others(26): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 73904777 | ||||||
| chr2:73904777 | GTA | G | 13 | a0001c0001t0008g0070a0001c0002t0002g0223a0001c0002t0002g0299others(10): Show | 13 | HG02886.hp1 HG02895.hp2 HG03195.hp1 others(10): Show |
intron_variant | MODIFIER | c.255+2326_255+2327d others(4): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 73904777 | ||||||
| chr2:73904777 | GTATA | G | 10 | a0001c0002t0002g0045a0001c0002t0002g0348a0001c0002t0004g0038others(7): Show | 10 | HG01261.hp1 HG02486.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.255+2324_255+2327d others(6): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 73904777 | ||||||
| chr2:73904777 | GTATATAT others(7): Show |
G | 3 | a0001c0002t0003g0063a0001c0002t0006g0004a0001c0002t0006g0055 | 4 | HG00735.hp1 HG02071.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.255+2314_255+2327d others(16): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 73904777 | ||||||
| chr2:73904777 | GTATATAT others(9): Show |
G | 3 | a0001c0002t0003g0061a0001c0002t0003g0106a0001c0002t0003g0178 | 3 | HG00438.hp1 HG00673.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.255+2312_255+2327d others(18): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 73904777 | ||||||
| chr2:73904777 | GTATATAT others(11): Show |
G | 10 | a0001c0002t0001g0110a0001c0002t0001g0241a0001c0002t0001g0242others(7): Show | 10 | HG02027.hp2 HG02257.hp1 NA18940.hp2 others(7): Show |
intron_variant | MODIFIER | c.255+2310_255+2327d others(20): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 73904777 | ||||||
| chr2:73904777 | GTATATAT others(13): Show |
G | 20 | a0001c0001t0001g0313a0001c0002t0001g0007a0001c0002t0001g0020others(17): Show | 22 | HG00280.hp2 HG00639.hp2 HG00733.hp1 others(19): Show |
intron_variant | MODIFIER | c.255+2308_255+2327d others(22): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 73904777 | ||||||
| chr2:73904777 | GTATATAT others(15): Show |
G | 1 | a0001c0002t0001g0183 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.255+2306_255+2327d others(24): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 73904777 | ||||||
| chr2:73904779 | A | G | 16 | a0001c0002t0002g0167a0001c0002t0002g0169a0001c0002t0002g0219others(13): Show | 17 | HG01070.hp1 HG01071.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.255+2291A>G | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | chr2 | 73904779 | |||||||
| chr2:73904781 | A | G | 8 | a0001c0001t0008g0070a0001c0002t0002g0223a0001c0002t0003g0051others(5): Show | 9 | HG01891.hp1 HG02886.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.255+2293A>G | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | chr2 | 73904781 | |||||||
| chr2:73904783 | A | G | 12 | a0001c0002t0002g0045a0001c0002t0004g0038a0001c0002t0004g0039others(9): Show | 12 | HG01261.hp1 HG02486.hp2 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.255+2295A>G | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | chr2 | 73904783 | |||||||
| chr2:73904785 | A | G | 1 | a0001c0001t0008g0042 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.255+2297A>G | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | chr2 | 73904785 | |||||||
| chr2:73904787 | A | G | 1 | a0001c0002t0001g0258 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.255+2299A>G | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | chr2 | 73904787 | |||||||
| chr2:73904793 | A | G | 1 | a0001c0002t0003g0063 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.255+2305A>G | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | chr2 | 73904793 | |||||||
| chr2:73904795 | A | G | 6 | a0001c0002t0003g0061a0001c0002t0003g0063a0001c0002t0003g0106others(3): Show | 7 | HG00438.hp1 HG00673.hp2 HG00735.hp1 others(4): Show |
intron_variant | MODIFIER | c.255+2307A>G | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | chr2 | 73904795 | |||||||
| chr2:73904797 | A | G | 13 | a0001c0002t0001g0110a0001c0002t0001g0241a0001c0002t0001g0242others(10): Show | 13 | HG00438.hp1 HG00673.hp2 HG02027.hp2 others(10): Show |
intron_variant | MODIFIER | c.255+2309A>G | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | chr2 | 73904797 | |||||||
| chr2:73904799 | A | G | 33 | a0001c0001t0001g0313a0001c0002t0001g0007a0001c0002t0001g0020others(30): Show | 35 | HG00280.hp2 HG00438.hp1 HG00639.hp2 others(32): Show |
intron_variant | MODIFIER | c.255+2311A>G | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | chr2 | 73904799 | |||||||
| chr2:73904801 | A | G | 3 | a0001c0001t0001g0313a0001c0002t0001g0183a0001c0002t0003g0373 | 3 | HG02976.hp1 NA19000.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.255+2313A>G | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | chr2 | 73904801 | |||||||
| chr2:73904803 | A | G | 1 | a0001c0001t0001g0313 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.255+2315A>G | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | chr2 | 73904803 | |||||||
| chr2:73904818 | C | T | 5 | a0001c0001t0001g0018a0001c0001t0001g0234a0001c0001t0001g0239others(2): Show | 6 | HG00597.hp2 NA18939.hp1 NA18962.hp2 others(3): Show |
intron_variant | MODIFIER | c.255+2330C>T | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | chr2 | 73904818 | |||||||
| chr2:73904872 | A | G | 2 | a0001c0001t0001g0351a0001c0001t0004g0390 | 2 | HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.255+2384A>G | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | chr2 | 73904872 | |||||||
| chr2:73905200 | C | G | 13 | a0001c0001t0001g0029a0001c0001t0001g0351a0001c0001t0002g0224others(10): Show | 14 | HG01109.hp2 HG01167.hp2 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.255+2712C>G | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | chr2 | 73905200 | |||||||
| chr2:73905635 | T | TTTTTTTT others(27): Show |
1 | a0001c0002t0002g0081 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.256-3038_256-3037i others(36): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | chr2 | 73905635 | |||||||
| chr2:73905636 | C | A | 1 | a0001c0002t0002g0081 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.256-3037C>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | chr2 | 73905636 | |||||||
| chr2:73905679 | A | T | 2 | a0001c0001t0003g0231a0001c0001t0005g0032 | 2 | HG02451.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.256-2994A>T | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | chr2 | 73905679 | |||||||
| chr2:73905767 | A | G | 2 | a0001c0001t0001g0149a0001c0001t0001g0214 | 2 | HG01123.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.256-2906A>G | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | chr2 | 73905767 | |||||||
| chr2:73905829 | T | G | 1 | a0001c0002t0002g0173 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.256-2844T>G | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | chr2 | 73905829 | |||||||
| chr2:73906103 | A | T | 1 | a0001c0001t0001g0273 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.256-2570A>T | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | chr2 | 73906103 | |||||||
| chr2:73906178 | G | A | 6 | a0001c0001t0005g0371a0001c0001t0005g0377a0001c0001t0005g0378others(3): Show | 6 | HG02615.hp2 HG03098.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.256-2495G>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | chr2 | 73906178 | |||||||
| chr2:73906179 | C | T | 2 | a0001c0001t0001g0351a0001c0001t0004g0390 | 2 | HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.256-2494C>T | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | chr2 | 73906179 | |||||||
| chr2:73906221 | G | T | 7 | a0001c0001t0001g0029a0001c0001t0001g0351a0001c0001t0004g0390others(4): Show | 7 | HG01109.hp2 HG01167.hp2 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.256-2452G>T | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | chr2 | 73906221 | |||||||
| chr2:73906462 | T | TAATAAAT others(1): Show |
4 | a0001c0001t0001g0146a0001c0001t0001g0351a0001c0001t0004g0390others(1): Show | 4 | HG02970.hp2 HG03579.hp2 NA20300.hp2 others(1): Show |
intron_variant | MODIFIER | c.256-2209_256-2208i others(10): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 73906462 | ||||||
| chr2:73906462 | T | TAATAAAT others(5): Show |
12 | a0001c0001t0001g0029a0001c0001t0003g0231a0001c0001t0004g0003others(9): Show | 13 | HG01109.hp2 HG01167.hp2 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.256-2209_256-2208i others(14): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 73906462 | ||||||
| chr2:73906462 | T | TAATAAAT others(9): Show |
2 | a0001c0002t0002g0049a0001c0002t0006g0055 | 2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.256-2209_256-2208i others(18): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 73906462 | ||||||
| chr2:73906462 | T | TAATAAAT others(13): Show |
1 | a0001c0002t0006g0004 | 2 | HG00735.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.256-2209_256-2208i others(22): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 73906462 | ||||||
| chr2:73906465 | A | T | 193 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(190): Show | 207 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.256-2208A>T | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | chr2 | 73906465 | |||||||
| chr2:73906469 | T | A | 1 | a0001c0002t0001g0020 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.256-2204T>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | chr2 | 73906469 | |||||||
| chr2:73906483 | A | AATAAATA others(9): Show |
1 | a0001c0001t0003g0206 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.256-2187_256-2186i others(18): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 73906483 | ||||||
| chr2:73906483 | A | AATAAATA others(5): Show |
2 | a0001c0001t0001g0044a0001c0001t0001g0150 | 2 | HG00738.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.256-2187_256-2186i others(14): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 73906483 | ||||||
| chr2:73906483 | A | AATAAATA others(1): Show |
159 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(156): Show | 171 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.256-2187_256-2186i others(10): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 73906483 | ||||||
| chr2:73906706 | G | A | 1 | a0001c0001t0001g0075 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.256-1967G>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | chr2 | 73906706 | |||||||
| chr2:73906848 | G | T | 255 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(252): Show | 272 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.256-1825G>T | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | chr2 | 73906848 | |||||||
| chr2:73906853 | C | A | 1 | a0001c0001t0001g0044 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.256-1820C>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | chr2 | 73906853 | |||||||
| chr2:73906888 | A | G | 2 | a0001c0002t0006g0004a0001c0002t0006g0055 | 3 | HG00735.hp1 HG02615.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.256-1785A>G | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | chr2 | 73906888 | |||||||
| chr2:73907021 | A | G | 195 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(192): Show | 209 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.256-1652A>G | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | chr2 | 73907021 | |||||||
| chr2:73907122 | G | A | 2 | a0001c0002t0006g0004a0001c0002t0006g0055 | 3 | HG00735.hp1 HG02615.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.256-1551G>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | chr2 | 73907122 | |||||||
| chr2:73907149 | T | A | 8 | a0001c0003t0001g0392a0001c0003t0002g0262a0001c0003t0004g0035others(5): Show | 8 | HG01243.hp1 HG02145.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.256-1524T>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | chr2 | 73907149 | |||||||
| chr2:73907214 | C | T | 1 | a0001c0002t0002g0049 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.256-1459C>T | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | chr2 | 73907214 | |||||||
| chr2:73907247 | T | C | 1 | a0001c0002t0002g0028 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.256-1426T>C | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | chr2 | 73907247 | |||||||
| chr2:73907284 | G | A | 2 | a0001c0001t0001g0374a0001c0001t0003g0196 | 2 | HG02015.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.256-1389G>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | chr2 | 73907284 | |||||||
| chr2:73907302 | C | T | 1 | a0001c0001t0007g0036 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.256-1371C>T | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | chr2 | 73907302 | |||||||
| chr2:73907671 | A | C | 200 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(197): Show | 215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.256-1002A>C | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | chr2 | 73907671 | |||||||
| chr2:73907968 | G | A | 1 | a0001c0001t0005g0384 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.256-705G>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | chr2 | 73907968 | |||||||
| chr2:73907984 | G | T | 3 | a0001c0002t0002g0264a0001c0002t0004g0344a0001c0002t0004g0345 | 3 | HG01168.hp1 HG01169.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.256-689G>T | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | chr2 | 73907984 | |||||||
| chr2:73907995 | T | C | 8 | a0001c0003t0001g0392a0001c0003t0002g0262a0001c0003t0004g0035others(5): Show | 8 | HG01243.hp1 HG02145.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.256-678T>C | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | chr2 | 73907995 | |||||||
| chr2:73908030 | C | T | 2 | a0001c0002t0002g0005a0001c0002t0002g0033 | 3 | HG02055.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.256-643C>T | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | chr2 | 73908030 | |||||||
| chr2:73908151 | G | A | 1 | a0001c0002t0002g0137 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.256-522G>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | chr2 | 73908151 | |||||||
| chr2:73908208 | G | C | 1 | a0001c0002t0002g0049 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.256-465G>C | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | chr2 | 73908208 | |||||||
| chr2:73908228 | A | G | 6 | a0001c0003t0004g0035a0001c0003t0004g0052a0001c0003t0004g0053others(3): Show | 6 | HG01243.hp1 HG02145.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.256-445A>G | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | chr2 | 73908228 | |||||||
| chr2:73908253 | G | A | 173 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(170): Show | 186 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.256-420G>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | chr2 | 73908253 | |||||||
| chr2:73908266 | T | G | 1 | a0001c0002t0003g0376 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.256-407T>G | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | chr2 | 73908266 | |||||||
| chr2:73908457 | AT | A | 3 | a0001c0001t0003g0231a0001c0001t0005g0032a0001c0001t0007g0036 | 3 | HG02451.hp1 HG02970.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.256-215delT | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | chr2 | 73908457 | |||||||
| chr2:73908474 | G | A | 1 | a0001c0002t0004g0047 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.256-199G>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | chr2 | 73908474 | |||||||
| chr2:73908605 | G | A | 197 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(194): Show | 211 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.256-68G>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | chr2 | 73908605 | |||||||
| chr2:73908670 | T | C | 198 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(195): Show | 212 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(209): Show |
splice_region_variant&intron_variant | LOW | c.256-3T>C | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 3/8 | chr2 | 73908670 | |||||||
| chr2:73908921 | G | A | 2 | a0001c0001t0002g0224a0001c0001t0004g0027 | 2 | HG02280.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.367-134G>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 4/8 | chr2 | 73908921 | |||||||
| chr2:73909230 | A | C | 8 | a0001c0003t0001g0392a0001c0003t0002g0262a0001c0003t0004g0035others(5): Show | 8 | HG01243.hp1 HG02145.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.451+91A>C | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 5/8 | chr2 | 73909230 | |||||||
| chr2:73909280 | A | C | 1 | a0001c0002t0002g0049 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.451+141A>C | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 5/8 | chr2 | 73909280 | |||||||
| chr2:73909382 | A | T | 1 | a0001c0001t0001g0068 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.451+243A>T | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 5/8 | chr2 | 73909382 | |||||||
| chr2:73909476 | T | C | 2 | a0001c0002t0006g0004a0001c0002t0006g0055 | 3 | HG00735.hp1 HG02615.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.451+337T>C | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 5/8 | chr2 | 73909476 | |||||||
| chr2:73909511 | T | C | 2 | a0001c0001t0001g0215a0001c0001t0001g0216 | 2 | HG02486.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.451+372T>C | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 5/8 | chr2 | 73909511 | |||||||
| chr2:73909571 | C | T | 209 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(206): Show | 223 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.451+432C>T | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 5/8 | chr2 | 73909571 | |||||||
| chr2:73909572 | G | A | 1 | a0001c0002t0002g0303 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.451+433G>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 5/8 | chr2 | 73909572 | |||||||
| chr2:73909636 | T | C | 5 | a0001c0002t0002g0221a0001c0002t0003g0041a0001c0002t0003g0256others(2): Show | 5 | HG01884.hp1 HG02622.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.451+497T>C | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 5/8 | chr2 | 73909636 | |||||||
| chr2:73909703 | C | T | 1 | a0001c0001t0001g0214 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.451+564C>T | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 5/8 | chr2 | 73909703 | |||||||
| chr2:73909781 | A | C | 7 | a0001c0003t0002g0262a0001c0003t0004g0035a0001c0003t0004g0052others(4): Show | 7 | HG01243.hp1 HG02145.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.451+642A>C | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 5/8 | chr2 | 73909781 | |||||||
| chr2:73909783 | G | A | 2 | a0001c0002t0003g0041a0001c0002t0009g0383 | 2 | HG01884.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.451+644G>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 5/8 | chr2 | 73909783 | |||||||
| chr2:73909990 | G | A | 1 | a0001c0002t0002g0309 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.451+851G>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 5/8 | chr2 | 73909990 | |||||||
| chr2:73910033 | G | A | 2 | a0001c0002t0004g0113a0001c0002t0004g0331 | 2 | HG02258.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.451+894G>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 5/8 | chr2 | 73910033 | |||||||
| chr2:73910171 | C | T | 1 | a0001c0001t0001g0213 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.451+1032C>T | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 5/8 | chr2 | 73910171 | |||||||
| chr2:73910202 | G | A | 196 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(193): Show | 210 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.451+1063G>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 5/8 | chr2 | 73910202 | |||||||
| chr2:73910224 | G | GTA | 186 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(183): Show | 199 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.451+1097_451+1098d others(4): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 73910224 | ||||||
| chr2:73910224 | G | GTATA | 12 | a0001c0001t0001g0130a0001c0001t0001g0354a0001c0001t0001g0355others(9): Show | 13 | HG01167.hp1 HG01346.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.451+1095_451+1098d others(6): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 73910224 | ||||||
| chr2:73910365 | C | CT | 15 | a0001c0001t0001g0092a0001c0001t0001g0147a0001c0001t0001g0199others(12): Show | 16 | HG00639.hp1 HG00673.hp1 HG00735.hp1 others(13): Show |
intron_variant | MODIFIER | c.451+1246dupT | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 73910365 | ||||||
| chr2:73910365 | C | CTT | 135 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(132): Show | 146 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.451+1245_451+1246d others(4): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 73910365 | ||||||
| chr2:73910365 | C | CTTT | 52 | a0001c0001t0001g0065a0001c0001t0001g0075a0001c0001t0001g0086others(49): Show | 55 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(52): Show |
intron_variant | MODIFIER | c.451+1244_451+1246d others(5): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 73910365 | ||||||
| chr2:73910365 | CT | C | 44 | a0001c0002t0001g0007a0001c0002t0001g0020a0001c0002t0001g0095others(41): Show | 46 | HG00280.hp2 HG00438.hp1 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.451+1246delT | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 73910365 | ||||||
| chr2:73910428 | G | A | 2 | a0001c0002t0006g0004a0001c0002t0006g0055 | 3 | HG00735.hp1 HG02615.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.451+1289G>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 5/8 | chr2 | 73910428 | |||||||
| chr2:73910436 | G | A | 1 | a0001c0001t0003g0366 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.451+1297G>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 5/8 | chr2 | 73910436 | |||||||
| chr2:73910455 | C | T | 1 | a0001c0001t0005g0388 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.451+1316C>T | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 5/8 | chr2 | 73910455 | |||||||
| chr2:73910461 | C | G | 197 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(194): Show | 211 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.451+1322C>G | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 5/8 | chr2 | 73910461 | |||||||
| chr2:73910492 | A | G | 3 | a0001c0002t0002g0049a0001c0002t0006g0004a0001c0002t0006g0055 | 4 | HG00735.hp1 HG02615.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.451+1353A>G | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 5/8 | chr2 | 73910492 | |||||||
| chr2:73910496 | C | CT | 36 | a0001c0001t0001g0088a0001c0001t0001g0144a0001c0001t0001g0149others(33): Show | 37 | HG00280.hp2 HG00438.hp1 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.451+1377dupT | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 73910496 | ||||||
| chr2:73910496 | CT | C | 26 | a0001c0001t0001g0029a0001c0001t0001g0130a0001c0001t0001g0148others(23): Show | 27 | HG01109.hp2 HG01167.hp1 HG01167.hp2 others(24): Show |
intron_variant | MODIFIER | c.451+1377delT | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 73910496 | ||||||
| chr2:73910671 | G | GTCTTT | 197 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(194): Show | 211 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.451+1533_451+1537d others(7): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 73910671 | ||||||
| chr2:73910717 | G | A | 197 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(194): Show | 211 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.451+1578G>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 5/8 | chr2 | 73910717 | |||||||
| chr2:73910766 | G | C | 197 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(194): Show | 211 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.451+1627G>C | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 5/8 | chr2 | 73910766 | |||||||
| chr2:73910794 | T | C | 197 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(194): Show | 211 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.451+1655T>C | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 5/8 | chr2 | 73910794 | |||||||
| chr2:73910858 | C | A | 1 | a0001c0001t0001g0148 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.451+1719C>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 5/8 | chr2 | 73910858 | |||||||
| chr2:73910870 | G | T | 255 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(252): Show | 272 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.451+1731G>T | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 5/8 | chr2 | 73910870 | |||||||
| chr2:73910966 | T | TAC | 198 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(195): Show | 212 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.451+1831_451+1832d others(4): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 73910966 | ||||||
| chr2:73911007 | A | G | 3 | a0001c0002t0003g0043a0001c0002t0003g0330a0001c0002t0003g0346 | 3 | HG02257.hp2 HG03130.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.451+1868A>G | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 5/8 | chr2 | 73911007 | |||||||
| chr2:73911011 | C | T | 198 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(195): Show | 212 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.451+1872C>T | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 5/8 | chr2 | 73911011 | |||||||
| chr2:73911025 | C | T | 1 | a0001c0001t0003g0231 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.451+1886C>T | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 5/8 | chr2 | 73911025 | |||||||
| chr2:73911259 | C | T | 176 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(173): Show | 189 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.451+2120C>T | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 5/8 | chr2 | 73911259 | |||||||
| chr2:73911266 | G | A | 5 | a0001c0003t0004g0052a0001c0003t0004g0053a0001c0003t0004g0054others(2): Show | 5 | HG01243.hp1 HG02145.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.451+2127G>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 5/8 | chr2 | 73911266 | |||||||
| chr2:73911302 | C | G | 1 | a0001c0003t0004g0035 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.451+2163C>G | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 5/8 | chr2 | 73911302 | |||||||
| chr2:73911422 | A | G | 1 | a0001c0002t0002g0049 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.452-2063A>G | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 5/8 | chr2 | 73911422 | |||||||
| chr2:73911547 | T | C | 198 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(195): Show | 212 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.452-1938T>C | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 5/8 | chr2 | 73911547 | |||||||
| chr2:73911585 | T | C | 2 | a0001c0001t0002g0224a0001c0001t0004g0027 | 2 | HG02280.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.452-1900T>C | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 5/8 | chr2 | 73911585 | |||||||
| chr2:73911661 | G | A | 24 | a0001c0001t0001g0029a0001c0001t0001g0130a0001c0001t0001g0176others(21): Show | 25 | HG00544.hp1 HG01109.hp2 HG01167.hp1 others(22): Show |
intron_variant | MODIFIER | c.452-1824G>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 5/8 | chr2 | 73911661 | |||||||
| chr2:73911732 | A | G | 7 | a0001c0003t0002g0262a0001c0003t0004g0035a0001c0003t0004g0052others(4): Show | 7 | HG01243.hp1 HG02145.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.452-1753A>G | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 5/8 | chr2 | 73911732 | |||||||
| chr2:73911826 | G | A | 1 | a0001c0001t0005g0356 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.452-1659G>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 5/8 | chr2 | 73911826 | |||||||
| chr2:73912109 | A | G | 1 | a0001c0002t0001g0129 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.452-1376A>G | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 5/8 | chr2 | 73912109 | |||||||
| chr2:73912131 | G | A | 2 | a0001c0002t0006g0004a0001c0002t0006g0055 | 3 | HG00735.hp1 HG02615.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.452-1354G>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 5/8 | chr2 | 73912131 | |||||||
| chr2:73912182 | C | T | 198 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(195): Show | 212 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.452-1303C>T | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 5/8 | chr2 | 73912182 | |||||||
| chr2:73912251 | G | A | 5 | a0001c0001t0003g0343a0001c0002t0003g0043a0001c0002t0003g0330others(2): Show | 5 | HG02257.hp2 HG02818.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.452-1234G>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 5/8 | chr2 | 73912251 | |||||||
| chr2:73912271 | C | T | 1 | a0001c0002t0004g0073 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.452-1214C>T | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 5/8 | chr2 | 73912271 | |||||||
| chr2:73912282 | C | T | 3 | a0001c0002t0002g0049a0001c0002t0006g0004a0001c0002t0006g0055 | 4 | HG00735.hp1 HG02615.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.452-1203C>T | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 5/8 | chr2 | 73912282 | |||||||
| chr2:73912365 | C | T | 4 | a0001c0002t0003g0043a0001c0002t0003g0330a0001c0002t0003g0346others(1): Show | 4 | HG02257.hp2 HG03130.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.452-1120C>T | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 5/8 | chr2 | 73912365 | |||||||
| chr2:73912406 | C | A | 198 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(195): Show | 212 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.452-1079C>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 5/8 | chr2 | 73912406 | |||||||
| chr2:73912408 | T | C | 198 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(195): Show | 212 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.452-1077T>C | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 5/8 | chr2 | 73912408 | |||||||
| chr2:73912427 | C | G | 198 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(195): Show | 212 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.452-1058C>G | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 5/8 | chr2 | 73912427 | |||||||
| chr2:73912448 | C | T | 198 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(195): Show | 212 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.452-1037C>T | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 5/8 | chr2 | 73912448 | |||||||
| chr2:73912502 | G | A | 200 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(197): Show | 214 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.452-983G>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 5/8 | chr2 | 73912502 | |||||||
| chr2:73912523 | G | T | 210 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(207): Show | 224 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.452-962G>T | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 5/8 | chr2 | 73912523 | |||||||
| chr2:73912583 | C | A | 198 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(195): Show | 212 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.452-902C>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 5/8 | chr2 | 73912583 | |||||||
| chr2:73912640 | A | G | 8 | a0001c0003t0001g0392a0001c0003t0002g0262a0001c0003t0004g0035others(5): Show | 8 | HG01243.hp1 HG02145.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.452-845A>G | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 5/8 | chr2 | 73912640 | |||||||
| chr2:73912723 | A | G | 9 | a0001c0003t0001g0392a0001c0003t0002g0262a0001c0003t0004g0035others(6): Show | 9 | HG01243.hp1 HG02145.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.452-762A>G | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 5/8 | chr2 | 73912723 | |||||||
| chr2:73912824 | G | A | 206 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(203): Show | 220 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.452-661G>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 5/8 | chr2 | 73912824 | |||||||
| chr2:73912830 | G | C | 22 | a0001c0001t0001g0029a0001c0001t0001g0130a0001c0001t0001g0351others(19): Show | 23 | HG01109.hp2 HG01167.hp1 HG01167.hp2 others(20): Show |
intron_variant | MODIFIER | c.452-655G>C | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 5/8 | chr2 | 73912830 | |||||||
| chr2:73912869 | T | C | 207 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(204): Show | 221 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.452-616T>C | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 5/8 | chr2 | 73912869 | |||||||
| chr2:73912883 | T | C | 207 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(204): Show | 221 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.452-602T>C | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 5/8 | chr2 | 73912883 | |||||||
| chr2:73912944 | A | G | 274 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(271): Show | 293 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.452-541A>G | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 5/8 | chr2 | 73912944 | |||||||
| chr2:73913022 | A | G | 198 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(195): Show | 212 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.452-463A>G | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 5/8 | chr2 | 73913022 | |||||||
| chr2:73913025 | C | T | 207 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(204): Show | 221 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.452-460C>T | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 5/8 | chr2 | 73913025 | |||||||
| chr2:73913103 | A | G | 207 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(204): Show | 221 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.452-382A>G | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 5/8 | chr2 | 73913103 | |||||||
| chr2:73913117 | C | T | 1 | a0001c0002t0003g0330 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.452-368C>T | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 5/8 | chr2 | 73913117 | |||||||
| chr2:73913163 | CT | C | 3 | a0001c0002t0003g0023a0001c0002t0003g0025a0001c0002t0003g0026 | 3 | HG01243.hp2 HG02280.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.452-321delT | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 5/8 | chr2 | 73913163 | |||||||
| chr2:73913170 | C | CA | 6 | a0001c0002t0003g0023a0001c0002t0003g0025a0001c0002t0003g0026others(3): Show | 7 | HG00735.hp1 HG01243.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.452-299dupA | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 73913170 | ||||||
| chr2:73913170 | C | CAAA | 8 | a0001c0003t0001g0392a0001c0003t0002g0262a0001c0003t0004g0050others(5): Show | 8 | HG01243.hp1 HG02145.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.452-301_452-299dup others(3): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 73913170 | ||||||
| chr2:73913170 | C | CAAAAA | 179 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(176): Show | 193 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.452-303_452-299dup others(5): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 73913170 | ||||||
| chr2:73913170 | C | CAAAAAA | 14 | a0001c0001t0001g0133a0001c0001t0001g0152a0001c0001t0001g0211others(11): Show | 14 | HG01081.hp2 HG01433.hp1 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.452-304_452-299dup others(6): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 73913170 | ||||||
| chr2:73913454 | A | T | 206 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(203): Show | 220 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.452-31A>T | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 5/8 | chr2 | 73913454 | |||||||
| chr2:73913654 | G | T | 5 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0093others(2): Show | 7 | HG00642.hp2 HG01175.hp2 HG01433.hp2 others(4): Show |
splice_region_variant&intron_variant | LOW | c.613+8G>T | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 6/8 | chr2 | 73913654 | |||||||
| chr2:73913662 | T | C | 207 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(204): Show | 221 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.613+16T>C | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 6/8 | chr2 | 73913662 | |||||||
| chr2:73913761 | A | C | 178 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(175): Show | 191 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.613+115A>C | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 6/8 | chr2 | 73913761 | |||||||
| chr2:73913849 | G | C | 1 | a0001c0002t0004g0155 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.613+203G>C | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 6/8 | chr2 | 73913849 | |||||||
| chr2:73914019 | C | T | 22 | a0001c0002t0001g0263a0001c0002t0001g0329a0001c0002t0002g0005others(19): Show | 24 | HG01261.hp1 HG01891.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.613+373C>T | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 6/8 | chr2 | 73914019 | |||||||
| chr2:73914118 | C | A | 1 | a0001c0001t0003g0105 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.613+472C>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 6/8 | chr2 | 73914118 | |||||||
| chr2:73914190 | G | A | 199 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(196): Show | 215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.614-490G>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 6/8 | chr2 | 73914190 | |||||||
| chr2:73914231 | G | A | 1 | a0001c0002t0003g0376 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.614-449G>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 6/8 | chr2 | 73914231 | |||||||
| chr2:73914286 | G | A | 194 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(191): Show | 210 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.614-394G>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 6/8 | chr2 | 73914286 | |||||||
| chr2:73914297 | C | T | 2 | a0001c0001t0003g0078a0001c0001t0003g0079 | 2 | NA18986.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.614-383C>T | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 6/8 | chr2 | 73914297 | |||||||
| chr2:73914420 | T | C | 1 | a0001c0001t0003g0206 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.614-260T>C | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 6/8 | chr2 | 73914420 | |||||||
| chr2:73914427 | C | T | 5 | a0001c0001t0001g0068a0001c0001t0001g0350a0001c0001t0003g0260others(2): Show | 6 | HG02717.hp1 HG02723.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.614-253C>T | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 6/8 | chr2 | 73914427 | |||||||
| chr2:73914489 | G | A | 6 | a0001c0002t0003g0061a0001c0002t0003g0063a0001c0002t0003g0064others(3): Show | 6 | HG00438.hp1 HG00673.hp2 HG02071.hp1 others(3): Show |
intron_variant | MODIFIER | c.614-191G>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 6/8 | chr2 | 73914489 | |||||||
| chr2:73914558 | C | CA | 38 | a0001c0001t0001g0133a0001c0001t0001g0147a0001c0001t0001g0149others(35): Show | 40 | HG00408.hp1 HG00639.hp1 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.614-103dupA | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 73914558 | ||||||
| chr2:73914558 | CA | C | 26 | a0001c0001t0001g0267a0001c0001t0001g0319a0001c0001t0003g0107others(23): Show | 28 | HG01169.hp2 HG01517.hp2 HG01891.hp1 others(25): Show |
intron_variant | MODIFIER | c.614-103delA | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 73914558 | ||||||
| chr2:73914558 | CAA | C | 6 | a0001c0002t0004g0038a0001c0002t0004g0039a0001c0002t0004g0082others(3): Show | 6 | HG01261.hp1 HG02723.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.614-104_614-103del others(2): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 73914558 | ||||||
| chr2:73914558 | CAAAAAAA others(3): Show |
C | 65 | a0001c0001t0001g0029a0001c0001t0001g0130a0001c0001t0001g0351others(62): Show | 68 | HG00280.hp2 HG00438.hp1 HG00639.hp2 others(65): Show |
intron_variant | MODIFIER | c.614-112_614-103del others(10): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 73914558 | ||||||
| chr2:73914984 | G | A | 3 | a0001c0002t0003g0243a0001c0002t0003g0244a0001c0002t0003g0246 | 3 | NA18977.hp1 NA19007.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.805+113G>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 7/8 | chr2 | 73914984 | |||||||
| chr2:73915015 | A | C | 2 | a0001c0001t0001g0130a0001c0001t0003g0181 | 2 | HG01167.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.805+144A>C | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 7/8 | chr2 | 73915015 | |||||||
| chr2:73915037 | GA | G | 225 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(222): Show | 240 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.805+171delA | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr2 | 73915037 | ||||||
| chr2:73915087 | G | A | 1 | a0001c0002t0004g0047 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.805+216G>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 7/8 | chr2 | 73915087 | |||||||
| chr2:73915106 | ATGAAACT others(22): Show |
A | 1 | a0001c0001t0003g0251 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.805+236_805+264del others(29): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 7/8 | chr2 | 73915106 | |||||||
| chr2:73915121 | G | C | 8 | a0001c0003t0001g0392a0001c0003t0004g0035a0001c0003t0004g0050others(5): Show | 8 | HG01243.hp1 HG02145.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.805+250G>C | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 7/8 | chr2 | 73915121 | |||||||
| chr2:73915148 | C | T | 1 | a0001c0002t0002g0303 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.805+277C>T | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 7/8 | chr2 | 73915148 | |||||||
| chr2:73915192 | A | G | 1 | a0001c0001t0007g0036 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.805+321A>G | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 7/8 | chr2 | 73915192 | |||||||
| chr2:73915257 | C | T | 18 | a0001c0001t0001g0029a0001c0001t0001g0354a0001c0001t0001g0355others(15): Show | 19 | HG01109.hp2 HG01167.hp2 HG01169.hp1 others(16): Show |
intron_variant | MODIFIER | c.805+386C>T | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 7/8 | chr2 | 73915257 | |||||||
| chr2:73915264 | A | AATCCCAG others(286): Show |
23 | a0001c0001t0001g0029a0001c0001t0001g0351a0001c0001t0001g0354others(20): Show | 24 | HG01109.hp2 HG01167.hp2 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.805+413_805+414ins others(293): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr2 | 73915264 | ||||||
| chr2:73915264 | A | AATCCCAG others(286): Show |
10 | a0001c0001t0005g0371a0001c0001t0007g0036a0001c0003t0001g0392others(7): Show | 10 | HG01243.hp1 HG02145.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.805+413_805+414ins others(293): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr2 | 73915264 | ||||||
| chr2:73915292 | G | A | 17 | a0001c0001t0001g0009a0001c0001t0001g0185a0001c0001t0001g0188others(14): Show | 18 | HG00438.hp2 HG00597.hp1 NA18939.hp1 others(15): Show |
intron_variant | MODIFIER | c.805+421G>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 7/8 | chr2 | 73915292 | |||||||
| chr2:73915299 | C | A | 43 | a0001c0001t0001g0029a0001c0001t0001g0216a0001c0001t0001g0351others(40): Show | 46 | HG01109.hp2 HG01167.hp2 HG01169.hp1 others(43): Show |
intron_variant | MODIFIER | c.805+428C>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 7/8 | chr2 | 73915299 | |||||||
| chr2:73915326 | A | C | 59 | a0001c0001t0001g0029a0001c0001t0001g0068a0001c0001t0001g0216others(56): Show | 63 | HG00280.hp2 HG00733.hp1 HG00741.hp1 others(60): Show |
intron_variant | MODIFIER | c.805+455A>C | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 7/8 | chr2 | 73915326 | |||||||
| chr2:73915330 | G | T | 57 | a0001c0001t0001g0029a0001c0001t0001g0068a0001c0001t0001g0216others(54): Show | 61 | HG00280.hp2 HG00733.hp1 HG00741.hp1 others(58): Show |
intron_variant | MODIFIER | c.805+459G>T | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 7/8 | chr2 | 73915330 | |||||||
| chr2:73915387 | G | A | 32 | a0001c0001t0001g0068a0001c0001t0003g0231a0001c0001t0004g0003others(29): Show | 35 | HG01261.hp1 HG01891.hp1 HG01891.hp2 others(32): Show |
intron_variant | MODIFIER | c.805+516G>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 7/8 | chr2 | 73915387 | |||||||
| chr2:73915388 | T | G | 49 | a0001c0001t0001g0148a0001c0001t0001g0213a0001c0001t0001g0215others(46): Show | 50 | HG00438.hp1 HG00639.hp2 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.805+517T>G | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 7/8 | chr2 | 73915388 | |||||||
| chr2:73915444 | G | A | 5 | a0001c0002t0001g0020a0001c0002t0001g0258a0001c0002t0001g0393others(2): Show | 7 | HG00735.hp1 HG02615.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.805+573G>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 7/8 | chr2 | 73915444 | |||||||
| chr2:73915519 | C | CA | 174 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(171): Show | 187 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.805+666dupA | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr2 | 73915519 | ||||||
| chr2:73915519 | CA | C | 31 | a0001c0001t0001g0265a0001c0001t0001g0267a0001c0001t0001g0351others(28): Show | 33 | HG01099.hp2 HG01169.hp1 HG01243.hp1 others(30): Show |
intron_variant | MODIFIER | c.805+666delA | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr2 | 73915519 | ||||||
| chr2:73915543 | G | A | 15 | a0001c0001t0003g0231a0001c0001t0003g0259a0001c0001t0003g0261others(12): Show | 16 | HG01243.hp2 HG01884.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.805+672G>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 7/8 | chr2 | 73915543 | |||||||
| chr2:73915583 | G | A | 15 | a0001c0001t0003g0231a0001c0001t0003g0259a0001c0001t0003g0261others(12): Show | 16 | HG01243.hp2 HG01884.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.805+712G>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 7/8 | chr2 | 73915583 | |||||||
| chr2:73915596 | T | G | 1 | a0001c0001t0005g0377 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.805+725T>G | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 7/8 | chr2 | 73915596 | |||||||
| chr2:73915601 | T | C | 38 | a0001c0001t0001g0351a0001c0001t0003g0343a0001c0001t0004g0390others(35): Show | 40 | HG01109.hp2 HG01167.hp2 HG01169.hp1 others(37): Show |
intron_variant | MODIFIER | c.805+730T>C | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 7/8 | chr2 | 73915601 | |||||||
| chr2:73915656 | T | G | 80 | a0001c0001t0001g0351a0001c0001t0003g0067a0001c0001t0003g0100others(77): Show | 83 | HG00438.hp1 HG00621.hp2 HG00738.hp1 others(80): Show |
intron_variant | MODIFIER | c.805+785T>G | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 7/8 | chr2 | 73915656 | |||||||
| chr2:73915675 | C | T | 11 | a0001c0002t0002g0005a0001c0002t0002g0028a0001c0002t0002g0033others(8): Show | 12 | HG02055.hp2 HG02145.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.805+804C>T | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 7/8 | chr2 | 73915675 | |||||||
| chr2:73915753 | A | G | 1 | a0001c0001t0001g0092 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.806-831A>G | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 7/8 | chr2 | 73915753 | |||||||
| chr2:73915855 | A | G | 43 | a0001c0001t0001g0351a0001c0001t0003g0259a0001c0001t0003g0261others(40): Show | 45 | HG01243.hp2 HG01261.hp1 HG01884.hp1 others(42): Show |
intron_variant | MODIFIER | c.806-729A>G | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 7/8 | chr2 | 73915855 | |||||||
| chr2:73915863 | T | A | 1 | a0001c0002t0004g0006 | 2 | HG01891.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.806-721T>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 7/8 | chr2 | 73915863 | |||||||
| chr2:73915875 | G | A | 13 | a0001c0001t0001g0351a0001c0001t0004g0390a0001c0002t0001g0020others(10): Show | 14 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.806-709G>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 7/8 | chr2 | 73915875 | |||||||
| chr2:73915881 | G | A | 1 | a0001c0001t0001g0068 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.806-703G>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 7/8 | chr2 | 73915881 | |||||||
| chr2:73915961 | G | A | 1 | a0001c0001t0003g0318 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.806-623G>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 7/8 | chr2 | 73915961 | |||||||
| chr2:73916013 | C | A | 21 | a0001c0001t0005g0014a0001c0001t0005g0030a0001c0001t0005g0031others(18): Show | 23 | HG00735.hp1 HG01109.hp2 HG01167.hp2 others(20): Show |
intron_variant | MODIFIER | c.806-571C>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 7/8 | chr2 | 73916013 | |||||||
| chr2:73916047 | C | T | 3 | a0001c0002t0004g0038a0001c0002t0004g0082a0001c0002t0004g0368 | 3 | HG01261.hp1 HG02965.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.806-537C>T | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 7/8 | chr2 | 73916047 | |||||||
| chr2:73916085 | A | G | 180 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(177): Show | 191 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.806-499A>G | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 7/8 | chr2 | 73916085 | |||||||
| chr2:73916114 | G | A | 175 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(172): Show | 186 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.806-470G>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 7/8 | chr2 | 73916114 | |||||||
| chr2:73916251 | T | C | 178 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(175): Show | 189 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.806-333T>C | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 7/8 | chr2 | 73916251 | |||||||
| chr2:73916296 | A | C | 1 | a0001c0001t0005g0357 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.806-288A>C | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 7/8 | chr2 | 73916296 | |||||||
| chr2:73916311 | G | T | 176 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(173): Show | 187 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.806-273G>T | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 7/8 | chr2 | 73916311 | |||||||
| chr2:73916374 | G | GA | 9 | a0001c0001t0008g0042a0001c0001t0008g0070a0001c0002t0002g0033others(6): Show | 10 | HG00735.hp1 HG01884.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.806-194dupA | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr2 | 73916374 | ||||||
| chr2:73916374 | GA | G | 6 | a0001c0001t0001g0195a0001c0001t0001g0364a0001c0001t0005g0031others(3): Show | 6 | HG01109.hp1 HG01169.hp1 NA18951.hp2 others(3): Show |
intron_variant | MODIFIER | c.806-194delA | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr2 | 73916374 | ||||||
| chr2:73916374 | GAA | G | 170 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(167): Show | 181 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(178): Show |
intron_variant | MODIFIER | c.806-195_806-194del others(2): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr2 | 73916374 | ||||||
| chr2:73916376 | A | G | 1 | a0001c0001t0001g0195 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.806-208A>G | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 7/8 | chr2 | 73916376 | |||||||
| chr2:73916394 | C | A | 1 | a0001c0001t0001g0233 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.806-190C>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 7/8 | chr2 | 73916394 | |||||||
| chr2:73916396 | A | G | 16 | a0001c0002t0001g0183a0001c0002t0001g0263a0001c0002t0001g0329others(13): Show | 17 | HG01261.hp1 HG01891.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.806-188A>G | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 7/8 | chr2 | 73916396 | |||||||
| chr2:73916441 | G | T | 1 | a0001c0001t0006g0249 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.806-143G>T | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 7/8 | chr2 | 73916441 | |||||||
| chr2:73916443 | A | C | 179 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(176): Show | 190 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.806-141A>C | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 7/8 | chr2 | 73916443 | |||||||
| chr2:73916556 | G | A | 2 | a0001c0001t0005g0372a0001c0001t0005g0384 | 2 | HG01109.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.806-28G>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 7/8 | chr2 | 73916556 | |||||||
| chr2:73916821 | T | C | 4 | a0001c0001t0008g0042a0001c0001t0008g0070a0001c0002t0006g0004others(1): Show | 5 | HG00735.hp1 HG02572.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.987+56T>C | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 8/8 | chr2 | 73916821 | |||||||
| chr2:73916863 | T | A | 176 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(173): Show | 187 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.987+98T>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 8/8 | chr2 | 73916863 | |||||||
| chr2:73916881 | A | G | 9 | a0001c0001t0001g0088a0001c0001t0001g0186a0001c0001t0001g0187others(6): Show | 9 | HG02083.hp2 NA18612.hp2 NA18940.hp1 others(6): Show |
intron_variant | MODIFIER | c.987+116A>G | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 8/8 | chr2 | 73916881 | |||||||
| chr2:73916913 | G | A | 176 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(173): Show | 187 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.987+148G>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 8/8 | chr2 | 73916913 | |||||||
| chr2:73916922 | T | A | 8 | a0001c0001t0003g0259a0001c0001t0003g0261a0001c0001t0003g0389others(5): Show | 8 | HG01243.hp2 HG02055.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.987+157T>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 8/8 | chr2 | 73916922 | |||||||
| chr2:73916983 | A | C | 178 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(175): Show | 189 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.987+218A>C | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 8/8 | chr2 | 73916983 | |||||||
| chr2:73917188 | A | AAAAT | 180 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(177): Show | 192 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.987+441_987+444dup others(4): Show |
ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 73917188 | ||||||
| chr2:73917195 | A | T | 1 | a0001c0002t0004g0380 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.987+430A>T | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 8/8 | chr2 | 73917195 | |||||||
| chr2:73917262 | A | G | 1 | a0001c0002t0004g0380 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.987+497A>G | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 8/8 | chr2 | 73917262 | |||||||
| chr2:73917306 | C | T | 177 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(174): Show | 188 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.987+541C>T | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 8/8 | chr2 | 73917306 | |||||||
| chr2:73917392 | T | C | 4 | a0001c0001t0005g0371a0001c0001t0005g0387a0001c0001t0005g0388others(1): Show | 4 | HG01884.hp2 HG02615.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.987+627T>C | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 8/8 | chr2 | 73917392 | |||||||
| chr2:73917413 | C | T | 1 | a0001c0001t0008g0070 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.987+648C>T | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 8/8 | chr2 | 73917413 | |||||||
| chr2:73917416 | A | T | 177 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(174): Show | 188 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.987+651A>T | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 8/8 | chr2 | 73917416 | |||||||
| chr2:73917461 | C | T | 3 | a0001c0001t0001g0351a0001c0001t0004g0390a0001c0002t0001g0129 | 3 | HG03579.hp2 NA20300.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.987+696C>T | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 8/8 | chr2 | 73917461 | |||||||
| chr2:73917505 | G | T | 1 | a0001c0001t0003g0318 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.987+740G>T | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 8/8 | chr2 | 73917505 | |||||||
| chr2:73917553 | G | C | 3 | a0001c0001t0001g0351a0001c0001t0004g0390a0001c0002t0001g0129 | 3 | HG03579.hp2 NA20300.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.987+788G>C | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 8/8 | chr2 | 73917553 | |||||||
| chr2:73917633 | G | A | 3 | a0001c0001t0001g0147a0001c0002t0001g0091a0001c0002t0004g0369 | 3 | HG00639.hp1 HG02698.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.987+868G>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 8/8 | chr2 | 73917633 | |||||||
| chr2:73917724 | C | T | 14 | a0001c0001t0005g0014a0001c0001t0005g0030a0001c0001t0005g0031others(11): Show | 15 | HG00140.hp2 HG01109.hp2 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.987+959C>T | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 8/8 | chr2 | 73917724 | |||||||
| chr2:73917761 | C | A | 176 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(173): Show | 187 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.987+996C>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 8/8 | chr2 | 73917761 | |||||||
| chr2:73918106 | C | T | 2 | a0001c0002t0001g0241a0001c0002t0001g0242 | 2 | NA19058.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.988-1326C>T | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 8/8 | chr2 | 73918106 | |||||||
| chr2:73918107 | G | A | 1 | a0001c0001t0003g0107 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.988-1325G>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 8/8 | chr2 | 73918107 | |||||||
| chr2:73918154 | G | A | 14 | a0001c0001t0003g0259a0001c0001t0003g0261a0001c0001t0003g0389others(11): Show | 14 | HG01243.hp2 HG01884.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.988-1278G>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 8/8 | chr2 | 73918154 | |||||||
| chr2:73918209 | G | A | 1 | a0001c0001t0001g0188 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.988-1223G>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 8/8 | chr2 | 73918209 | |||||||
| chr2:73918224 | G | C | 4 | a0001c0002t0002g0005a0001c0002t0002g0033a0001c0002t0002g0034others(1): Show | 5 | HG02055.hp2 HG02717.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.988-1208G>C | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 8/8 | chr2 | 73918224 | |||||||
| chr2:73918232 | G | A | 1 | a0001c0002t0002g0119 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.988-1200G>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 8/8 | chr2 | 73918232 | |||||||
| chr2:73918269 | G | A | 2 | a0001c0001t0001g0382a0001c0001t0001g0385 | 2 | NA18944.hp2 NA18956.hp1 |
intron_variant | MODIFIER | c.988-1163G>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 8/8 | chr2 | 73918269 | |||||||
| chr2:73918313 | C | T | 2 | a0001c0002t0004g0344a0001c0002t0004g0345 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.988-1119C>T | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 8/8 | chr2 | 73918313 | |||||||
| chr2:73918456 | C | A | 1 | a0001c0002t0002g0163 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.988-976C>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 8/8 | chr2 | 73918456 | |||||||
| chr2:73918496 | A | C | 185 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(182): Show | 197 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.988-936A>C | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 8/8 | chr2 | 73918496 | |||||||
| chr2:73918626 | A | T | 3 | a0001c0001t0001g0351a0001c0001t0004g0390a0001c0002t0001g0129 | 3 | HG03579.hp2 NA20300.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.988-806A>T | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 8/8 | chr2 | 73918626 | |||||||
| chr2:73918706 | T | G | 1 | a0001c0002t0002g0049 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.988-726T>G | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 8/8 | chr2 | 73918706 | |||||||
| chr2:73918881 | G | A | 2 | a0001c0001t0003g0197a0001c0001t0003g0335 | 2 | NA18947.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.988-551G>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 8/8 | chr2 | 73918881 | |||||||
| chr2:73918901 | CA | C | 6 | a0001c0001t0003g0060a0001c0001t0003g0177a0001c0002t0002g0167others(3): Show | 6 | HG00558.hp2 HG00673.hp1 HG02074.hp2 others(3): Show |
intron_variant | MODIFIER | c.988-528delA | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 73918901 | ||||||
| chr2:73918960 | C | T | 1 | a0001c0001t0003g0315 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.988-472C>T | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 8/8 | chr2 | 73918960 | |||||||
| chr2:73919001 | A | G | 5 | a0001c0001t0006g0249a0001c0001t0008g0042a0001c0001t0008g0070others(2): Show | 6 | HG00735.hp1 HG02572.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.988-431A>G | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 8/8 | chr2 | 73919001 | |||||||
| chr2:73919115 | G | A | 1 | a0001c0002t0002g0062 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.988-317G>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 8/8 | chr2 | 73919115 | |||||||
| chr2:73919145 | G | A | 1 | a0001c0002t0004g0116 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.988-287G>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 8/8 | chr2 | 73919145 | |||||||
| chr2:73919224 | C | T | 1 | a0001c0003t0004g0052 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.988-208C>T | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 8/8 | chr2 | 73919224 | |||||||
| chr2:73919278 | G | A | 1 | a0001c0001t0001g0029 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.988-154G>A | ACTG2 | ENSG00000163017.14 | transcript | ENST00000345517.8 | protein_coding | 8/8 | chr2 | 73919278 |