Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 384 |
| ensemblid | ENSG00000081181.8 |
| hgncid | 664 |
| symbol | ARG2 |
| name | arginase 2 |
| refseq_nuc | NM_001172.4 |
| refseq_prot | NP_001163.1 |
| ensembl_nuc | ENST00000261783.4 |
| ensembl_prot | ENSP00000261783.3 |
| mane_status | MANE Select |
| chr | chr14 |
| start | 67619920 |
| end | 67651708 |
| strand | + |
| ver | v1.2 |
| region | chr14:67619920-67651708 |
| region5000 | chr14:67614920-67656708 |
| regionname0 | ARG2_chr14_67619920_67651708 |
| regionname5000 | ARG2_chr14_67614920_67656708 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 354 | 431 | 91 | 84 | 196 | 16 | 42 | 150 | ARG2_chr14_67614920_67656708 | ARG2 | MSLRG others(349): Show |
chr14 | 67614920 | 67656708 |
| a0002 | 0/0 | 354 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | MSLRG others(349): Show |
chr14 | 67614920 | 67656708 |
| a0003 | 0/0 | 354 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | MSLRG others(349): Show |
chr14 | 67614920 | 67656708 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1062 | 429 | 89 | 84 | 196 | 16 | 42 | ARG2_chr14_67614920_67656708 | ARG2 | ATGTC others(1057): Show |
chr14 | 67614920 | 67656708 | ||
| a0001c0003 | 0/0 | 1062 | 2 | 2 | 0 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | ATGTC others(1057): Show |
chr14 | 67614920 | 67656708 | ||
| a0002c0002 | 0/0 | 1062 | 6 | 6 | 0 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | ATGTC others(1057): Show |
chr14 | 67614920 | 67656708 | ||
| a0003c0004 | 0/0 | 1062 | 1 | 1 | 0 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | ATGTC others(1057): Show |
chr14 | 67614920 | 67656708 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1911 | 239 | 35 | 56 | 100 | 12 | 34 | ARG2_chr14_67614920_67656708 | ARG2 | ACTCC others(1906): Show |
chr14 | 67614920 | 67656708 |
| a0001c0001t0002 | 0/0 | 1910 | 81 | 11 | 14 | 50 | 2 | 4 | ARG2_chr14_67614920_67656708 | ARG2 | ACTCC others(1905): Show |
chr14 | 67614920 | 67656708 |
| a0001c0001t0003 | 0/0 | 1910 | 79 | 14 | 13 | 46 | 2 | 4 | ARG2_chr14_67614920_67656708 | ARG2 | ACTCC others(1905): Show |
chr14 | 67614920 | 67656708 |
| a0001c0001t0004 | 0/0 | 1908 | 19 | 19 | 0 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | ACTCC others(1903): Show |
chr14 | 67614920 | 67656708 |
| a0001c0001t0005 | 0/0 | 1911 | 7 | 7 | 0 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | ACTCC others(1906): Show |
chr14 | 67614920 | 67656708 |
| a0001c0001t0006 | 0/0 | 1914 | 3 | 3 | 0 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | ACTCC others(1909): Show |
chr14 | 67614920 | 67656708 |
| a0001c0001t0007 | 0/0 | 1911 | 1 | 0 | 1 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | ACTCC others(1906): Show |
chr14 | 67614920 | 67656708 |
| a0001c0003t0001 | 0/0 | 1911 | 2 | 2 | 0 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | ACTCC others(1906): Show |
chr14 | 67614920 | 67656708 |
| a0002c0002t0002 | 0/0 | 1910 | 6 | 6 | 0 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | ACTCC others(1905): Show |
chr14 | 67614920 | 67656708 |
| a0003c0004t0001 | 0/0 | 1911 | 1 | 1 | 0 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | ACTCC others(1906): Show |
chr14 | 67614920 | 67656708 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 7 | 1 | 1 | 4 | 0 | 1 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0004 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0005 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0006 | 0/0 | 4 | 1 | 3 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0220 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0303 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0360 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0001g0361 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0002g0002 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0002g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0002g0012 | 0/0 | 3 | 0 | 0 | 2 | 1 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0002g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0002g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0002g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0002g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0002g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0002g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0002g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0002g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0002g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0002g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0002g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0002g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0002g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0002g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0002g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0002g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0002g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0003g0003 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0003g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0003g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0003g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0003g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0003g0023 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0003g0024 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0003g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0003g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0003g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0003g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0003g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0003g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0003g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0003g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0003g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0003g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0003g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0003g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0003g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0003g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0003g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0003g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0003g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0003g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0003g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0003g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0003g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0004g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0004g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0004g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0004g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0004g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0004g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0004g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0004g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0004g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0004g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0004g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0004g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0004g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0004g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0004g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0004g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0004g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0004g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0004g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0005g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0005g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0005g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0005g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0005g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0005g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0005g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0006g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0006g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0006g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0001t0007g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0003t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0001c0003t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0002c0002t0002g0008 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0002c0002t0002g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0002c0002t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| a0003c0004t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0012 | EUR | GBR | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0293 | EUR | GBR | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0219 | EUR | FIN | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0225 | EUR | FIN | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG00323 | hp1 | a0001 | c0001 | t0003 | g0155 | EUR | FIN | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0265 | EUR | FIN | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG00408 | hp1 | a0001 | c0001 | t0003 | g0022 | EAS | CHS | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0145 | EAS | CHS | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | CHS | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG00423 | hp2 | a0001 | c0001 | t0003 | g0090 | EAS | CHS | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | CHS | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | CHS | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0143 | EAS | CHS | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | CHS | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0342 | EAS | CHS | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | CHS | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | CHS | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | CHS | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG00621 | hp2 | a0001 | c0001 | t0003 | g0065 | EAS | CHS | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG00639 | hp2 | a0001 | c0001 | t0003 | g0064 | AMR | PUR | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0152 | AMR | PUR | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0165 | EAS | CHS | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0148 | EAS | CHS | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0136 | AMR | PUR | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | PUR | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0135 | AMR | PUR | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG01069 | hp2 | a0001 | c0001 | t0003 | g0023 | AMR | PUR | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0268 | AMR | PUR | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0240 | AMR | PUR | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG01074 | hp2 | a0001 | c0001 | t0003 | g0024 | AMR | PUR | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0162 | AMR | PUR | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0306 | AMR | PUR | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0274 | AMR | PUR | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0144 | AMR | PUR | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | PUR | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG01167 | hp2 | a0001 | c0001 | t0003 | g0113 | AMR | PUR | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | PUR | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG01169 | hp1 | a0001 | c0001 | t0003 | g0072 | AMR | PUR | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0223 | AMR | PUR | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG01255 | hp1 | a0001 | c0001 | t0003 | g0073 | AMR | CLM | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0215 | AMR | CLM | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0296 | AMR | CLM | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG01256 | hp2 | a0001 | c0001 | t0003 | g0153 | AMR | CLM | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | CLM | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0273 | AMR | CLM | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | CLM | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0324 | AMR | CLM | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0321 | AMR | CLM | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0246 | AMR | CLM | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0229 | AMR | CLM | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0170 | AMR | CLM | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | CLM | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0315 | AMR | CLM | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0283 | AMR | CLM | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0299 | AMR | CLM | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG01433 | hp2 | a0001 | c0001 | t0003 | g0116 | AMR | CLM | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG01496 | hp1 | a0001 | c0001 | t0003 | g0205 | AMR | CLM | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0211 | EUR | IBS | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0262 | EUR | IBS | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0305 | EUR | IBS | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0023 | EUR | IBS | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0304 | EUR | IBS | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0228 | EUR | IBS | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0026 | AFR | ACB | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG01884 | hp2 | a0003 | c0004 | t0001 | g0107 | AFR | ACB | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0126 | AFR | ACB | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG01891 | hp2 | a0001 | c0001 | t0004 | g0200 | AFR | ACB | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PEL | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0269 | AMR | PEL | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | PEL | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG01943 | hp1 | a0001 | c0001 | t0007 | g0166 | AMR | PEL | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0168 | AMR | PEL | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0292 | AMR | PEL | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0167 | AMR | PEL | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0234 | AMR | PEL | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PEL | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG01981 | hp1 | a0001 | c0001 | t0003 | g0253 | AMR | PEL | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0263 | AMR | PEL | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG01993 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | PEL | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0267 | AMR | PEL | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0270 | AMR | PEL | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0134 | EAS | KHV | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG02027 | hp1 | a0001 | c0001 | t0003 | g0096 | EAS | KHV | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0146 | EAS | KHV | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0147 | EAS | KHV | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | ACB | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | ACB | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | KHV | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0132 | EAS | KHV | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0334 | EAS | KHV | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG02071 | hp2 | a0001 | c0001 | t0003 | g0082 | EAS | KHV | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG02074 | hp1 | a0001 | c0001 | t0003 | g0100 | EAS | KHV | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | KHV | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0350 | EAS | KHV | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0314 | EAS | KHV | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG02083 | hp2 | a0001 | c0001 | t0003 | g0091 | EAS | KHV | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0335 | EAS | KHV | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG02129 | hp2 | a0001 | c0001 | t0003 | g0011 | EAS | KHV | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0317 | EAS | KHV | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG02132 | hp2 | a0001 | c0001 | t0003 | g0067 | EAS | KHV | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | KHV | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0339 | EAS | KHV | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | ACB | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG02145 | hp2 | a0001 | c0001 | t0005 | g0349 | AFR | ACB | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0029 | AMR | PEL | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG02148 | hp2 | a0001 | c0001 | t0003 | g0071 | AMR | PEL | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0325 | EAS | CDX | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CDX | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0027 | AFR | ACB | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0294 | AFR | ACB | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0039 | AFR | ACB | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | ACB | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG02273 | hp1 | a0001 | c0001 | t0003 | g0075 | AMR | PEL | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0169 | AMR | PEL | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG02280 | hp1 | a0001 | c0001 | t0004 | g0195 | AFR | ACB | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG02280 | hp2 | a0001 | c0001 | t0004 | g0097 | AFR | ACB | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0363 | AMR | PEL | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | PEL | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0029 | AMR | PEL | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | ACB | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0125 | AFR | ACB | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG02523 | hp1 | a0001 | c0001 | t0003 | g0098 | EAS | KHV | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0124 | EAS | KHV | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0210 | AFR | GWD | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG02572 | hp2 | a0002 | c0002 | t0002 | g0160 | AFR | GWD | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0254 | SAS | PJL | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0191 | AFR | GWD | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | GWD | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG02622 | hp2 | a0001 | c0001 | t0004 | g0181 | AFR | GWD | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG02630 | hp1 | a0001 | c0001 | t0005 | g0203 | AFR | GWD | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0290 | AFR | GWD | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0025 | AFR | GWD | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0277 | SAS | PJL | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0137 | SAS | PJL | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG02698 | hp1 | a0001 | c0001 | t0003 | g0077 | SAS | PJL | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0231 | SAS | PJL | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG02717 | hp1 | a0001 | c0001 | t0004 | g0180 | AFR | GWD | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG02717 | hp2 | a0002 | c0002 | t0002 | g0008 | AFR | GWD | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0028 | AFR | GWD | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0261 | SAS | PJL | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG02735 | hp2 | a0001 | c0001 | t0003 | g0055 | SAS | PJL | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0333 | SAS | PJL | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0233 | SAS | PJL | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | GWD | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG02809 | hp2 | a0001 | c0001 | t0004 | g0186 | AFR | GWD | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG02818 | hp1 | a0001 | c0001 | t0004 | g0187 | AFR | GWD | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0291 | AFR | GWD | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG02886 | hp1 | a0001 | c0001 | t0004 | g0204 | AFR | GWD | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG02886 | hp2 | a0001 | c0001 | t0004 | g0198 | AFR | GWD | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG02895 | hp1 | a0001 | c0001 | t0006 | g0207 | AFR | GWD | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG02895 | hp2 | a0001 | c0003 | t0001 | g0188 | AFR | GWD | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG02896 | hp1 | a0001 | c0001 | t0005 | g0344 | AFR | GWD | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG02896 | hp2 | a0001 | c0001 | t0004 | g0176 | AFR | GWD | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG02897 | hp1 | a0001 | c0001 | t0005 | g0345 | AFR | GWD | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG02897 | hp2 | a0001 | c0003 | t0001 | g0189 | AFR | GWD | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG02922 | hp1 | a0001 | c0001 | t0004 | g0173 | AFR | ESN | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0117 | AFR | ESN | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | ESN | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG02965 | hp2 | a0002 | c0002 | t0002 | g0008 | AFR | ESN | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG02970 | hp1 | a0001 | c0001 | t0005 | g0346 | AFR | ESN | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG02970 | hp2 | a0001 | c0001 | t0003 | g0157 | AFR | ESN | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG02976 | hp1 | a0001 | c0001 | t0004 | g0175 | AFR | ESN | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0087 | AFR | ESN | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0360 | SAS | PJL | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG03041 | hp2 | a0001 | c0001 | t0005 | g0348 | AFR | GWD | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0088 | AFR | MSL | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | MSL | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG03130 | hp1 | a0001 | c0001 | t0003 | g0192 | AFR | ESN | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG03130 | hp2 | a0002 | c0002 | t0002 | g0008 | AFR | ESN | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0026 | AFR | ESN | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG03139 | hp2 | a0001 | c0001 | t0004 | g0174 | AFR | ESN | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG03195 | hp1 | a0001 | c0001 | t0004 | g0178 | AFR | ESN | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG03195 | hp2 | a0001 | c0001 | t0003 | g0209 | AFR | ESN | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG03209 | hp1 | a0001 | c0001 | t0004 | g0182 | AFR | MSL | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | MSL | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | MSL | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | MSL | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0232 | SAS | PJL | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0343 | SAS | PJL | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | MSL | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | MSL | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | MSL | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | MSL | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG03491 | hp1 | a0001 | c0001 | t0003 | g0076 | SAS | PJL | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0329 | SAS | PJL | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG03516 | hp1 | a0001 | c0001 | t0003 | g0099 | AFR | ESN | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | ESN | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | GWD | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | GWD | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG03579 | hp1 | a0001 | c0001 | t0004 | g0190 | AFR | MSL | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0027 | AFR | MSL | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0302 | SAS | PJL | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0284 | SAS | PJL | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0120 | SAS | STU | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | STU | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0241 | SAS | PJL | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0297 | SAS | PJL | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0295 | SAS | PJL | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0361 | SAS | PJL | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0156 | SAS | BEB | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0257 | SAS | BEB | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0108 | SAS | BEB | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0307 | SAS | BEB | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0264 | SAS | BEB | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0109 | SAS | BEB | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0238 | SAS | BEB | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0301 | SAS | BEB | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0133 | SAS | STU | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0287 | SAS | STU | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0121 | SAS | STU | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG04204 | hp2 | a0001 | c0001 | t0003 | g0154 | SAS | STU | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0227 | SAS | STU | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | STU | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA18522 | hp1 | a0001 | c0001 | t0006 | g0206 | AFR | YRI | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA18522 | hp2 | a0001 | c0001 | t0004 | g0179 | AFR | YRI | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0139 | EAS | CHB | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHB | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | CHB | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA18747 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | CHB | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA18906 | hp1 | a0001 | c0001 | t0004 | g0218 | AFR | YRI | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0158 | AFR | YRI | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0355 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA18941 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA18942 | hp1 | a0001 | c0001 | t0003 | g0093 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0354 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA18948 | hp2 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA18949 | hp1 | a0001 | c0001 | t0003 | g0095 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA18951 | hp2 | a0001 | c0001 | t0003 | g0114 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0351 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA18954 | hp1 | a0001 | c0001 | t0003 | g0111 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0341 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA18956 | hp2 | a0001 | c0001 | t0003 | g0119 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA18957 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA18959 | hp1 | a0001 | c0001 | t0003 | g0070 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA18960 | hp1 | a0001 | c0001 | t0003 | g0063 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA18961 | hp2 | a0001 | c0001 | t0003 | g0057 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA18962 | hp1 | a0001 | c0001 | t0003 | g0059 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0362 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA18963 | hp2 | a0001 | c0001 | t0003 | g0079 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0332 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA18968 | hp1 | a0001 | c0001 | t0003 | g0080 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA18971 | hp1 | a0001 | c0001 | t0003 | g0058 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0352 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0358 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA18981 | hp1 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0353 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA18988 | hp1 | a0001 | c0001 | t0003 | g0069 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA18992 | hp2 | a0001 | c0001 | t0003 | g0068 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA18993 | hp2 | a0001 | c0001 | t0003 | g0081 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0338 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA19001 | hp2 | a0001 | c0001 | t0003 | g0092 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA19003 | hp1 | a0001 | c0001 | t0003 | g0062 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA19006 | hp1 | a0001 | c0001 | t0003 | g0060 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA19006 | hp2 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA19007 | hp1 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0357 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA19011 | hp1 | a0001 | c0001 | t0003 | g0094 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | LWK | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | LWK | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA19043 | hp1 | a0001 | c0001 | t0005 | g0347 | AFR | LWK | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA19043 | hp2 | a0001 | c0001 | t0004 | g0193 | AFR | LWK | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA19057 | hp1 | a0001 | c0001 | t0003 | g0078 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA19058 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0340 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA19062 | hp2 | a0001 | c0001 | t0003 | g0056 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA19064 | hp1 | a0001 | c0001 | t0003 | g0083 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA19065 | hp2 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA19067 | hp2 | a0001 | c0001 | t0002 | g0356 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0138 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA19077 | hp2 | a0001 | c0001 | t0003 | g0054 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA19079 | hp2 | a0001 | c0001 | t0003 | g0066 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0359 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA19081 | hp2 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA19084 | hp1 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0331 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0336 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA19089 | hp1 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0337 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | YRI | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA19240 | hp2 | a0002 | c0002 | t0002 | g0008 | AFR | YRI | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | ASW | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0025 | AFR | ASW | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0216 | EUR | TSI | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0150 | EUR | TSI | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0313 | EUR | TSI | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0105 | EUR | TSI | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0259 | SAS | GIH | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0123 | SAS | GIH | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0171 | AMR | CLM | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0226 | AMR | CLM | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG02109 | hp1 | a0002 | c0002 | t0002 | g0159 | AFR | ACB | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG02109 | hp2 | a0001 | c0001 | t0006 | g0208 | AFR | ACB | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0161 | AFR | ACB | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG02486 | hp2 | a0001 | c0001 | t0003 | g0074 | AFR | ACB | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0024 | AFR | ACB | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0028 | AFR | ACB | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | MSL | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | MSL | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | USA | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0177 | AFR | USA | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | USA | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | USA | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0303 | REF | REF | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0220 | REF | REF | ARG2_chr14_67614920_67656708 | ARG2 | chr14 | 67614920 | 67656708 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:67647021 | G | C | 1 | a0002 | 6 | HG02109.hp1 HG02572.hp2 HG02717.hp2 others(3): Show |
missense_variant | MODERATE | c.718G>C | p.Gly240Arg | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 6/8 | 776/1911 | 718/1065 | 240/354 | chr14 | 67647021 | |||
| chr14:67650909 | G | T | 1 | a0003 | 1 | HG01884.hp2 | missense_variant | MODERATE | c.1054G>T | p.Val352Leu | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 8/8 | 1112/1911 | 1054/1065 | 352/354 | chr14 | 67650909 | |||
| chr14:67651703 | TA | T | 2 | a0001 a0002 |
169 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(166): Show |
splice_region_variant | LOW | c.*788delA | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr14 | 67651703 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:67620085 | G | A | 1 | a0001c0003 | 2 | HG02895.hp2 HG02897.hp2 |
synonymous_variant | LOW | c.108G>A | p.Gly36Gly | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 1/8 | 166/1911 | 108/1065 | 36/354 | chr14 | 67620085 | |||
| chr14:67645652 | C | T | 1 | a0003c0004 | 1 | HG01884.hp2 | synonymous_variant | LOW | c.372C>T | p.Ile124Ile | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 4/8 | 430/1911 | 372/1065 | 124/354 | chr14 | 67645652 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:67650941 | G | A | 1 | a0001c0001t0005 | 7 | HG02145.hp2 HG02630.hp1 HG02896.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*21G>A | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 8/8 | 21 | chr14 | 67650941 | ||||||
| chr14:67651205 | CTGT | C | 1 | a0001c0001t0004 | 19 | HG01891.hp2 HG02280.hp1 HG02280.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*290_*292delGTT | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 8/8 | 290 | INFO_REALIGN_3_PRIME | chr14 | 67651205 | |||||
| chr14:67651297 | G | C | 1 | a0001c0001t0007 | 1 | HG01943.hp1 | 3_prime_UTR_variant | MODIFIER | c.*377G>C | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 8/8 | 377 | chr14 | 67651297 | ||||||
| chr14:67651415 | C | T | 1 | a0001c0001t0003 | 79 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*495C>T | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 8/8 | 495 | chr14 | 67651415 | ||||||
| chr14:67651647 | G | T | 1 | a0001c0001t0003 | 79 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*727G>T | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 8/8 | 727 | chr14 | 67651647 | ||||||
| chr14:67651654 | A | ACTGT | 1 | a0001c0001t0006 | 3 | HG02109.hp2 HG02895.hp1 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*737_*740dupGTCT | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 8/8 | 741 | INFO_REALIGN_3_PRIME | chr14 | 67651654 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:67620180 | A | T | 1 | a0001c0001t0002g0363 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.111+92A>T | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 1/7 | chr14 | 67620180 | |||||||
| chr14:67620297 | G | A | 1 | a0001c0001t0003g0039 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.111+209G>A | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 1/7 | chr14 | 67620297 | |||||||
| chr14:67620350 | C | G | 15 | a0001c0001t0001g0354 a0001c0001t0001g0360 a0001c0001t0001g0361 others(12): Show |
23 | HG00609.hp1 HG02080.hp1 HG03017.hp2 others(20): Show |
intron_variant | MODIFIER | c.111+262C>G | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 1/7 | chr14 | 67620350 | |||||||
| chr14:67620426 | A | C | 6 | a0001c0001t0005g0344 a0001c0001t0005g0345 a0001c0001t0005g0346 others(3): Show |
6 | HG02145.hp2 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.111+338A>C | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 1/7 | chr14 | 67620426 | |||||||
| chr14:67620487 | A | T | 53 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0038 others(50): Show |
62 | HG00099.hp2 HG00423.hp1 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.111+399A>T | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 1/7 | chr14 | 67620487 | |||||||
| chr14:67620690 | T | C | 166 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0040 others(163): Show |
202 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.112-204T>C | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 1/7 | chr14 | 67620690 | |||||||
| chr14:67620712 | T | G | 2 | a0001c0001t0005g0344 a0001c0001t0005g0345 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.112-182T>G | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 1/7 | chr14 | 67620712 | |||||||
| chr14:67620718 | G | T | 1 | a0001c0001t0001g0172 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.112-176G>T | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 1/7 | chr14 | 67620718 | |||||||
| chr14:67620869 | A | G | 1 | a0001c0001t0001g0292 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.112-25A>G | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 1/7 | chr14 | 67620869 | |||||||
| chr14:67621014 | A | T | 15 | a0001c0001t0001g0354 a0001c0001t0001g0360 a0001c0001t0001g0361 others(12): Show |
23 | HG00609.hp1 HG02080.hp1 HG03017.hp2 others(20): Show |
intron_variant | MODIFIER | c.184+48A>T | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67621014 | |||||||
| chr14:67621085 | C | A | 4 | a0001c0001t0001g0040 a0001c0001t0002g0041 a0001c0001t0002g0042 others(1): Show |
4 | NA18990.hp2 NA18999.hp1 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.184+119C>A | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67621085 | |||||||
| chr14:67621103 | G | A | 203 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0040 others(200): Show |
238 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(235): Show |
intron_variant | MODIFIER | c.184+137G>A | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67621103 | |||||||
| chr14:67621434 | A | G | 15 | a0001c0001t0001g0354 a0001c0001t0001g0360 a0001c0001t0001g0361 others(12): Show |
23 | HG00609.hp1 HG02080.hp1 HG03017.hp2 others(20): Show |
intron_variant | MODIFIER | c.184+468A>G | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67621434 | |||||||
| chr14:67621451 | G | C | 1 | a0001c0001t0001g0211 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.184+485G>C | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67621451 | |||||||
| chr14:67621454 | C | CT | 16 | a0001c0001t0001g0354 a0001c0001t0001g0360 a0001c0001t0001g0361 others(13): Show |
24 | HG00609.hp1 HG00673.hp1 HG02080.hp1 others(21): Show |
intron_variant | MODIFIER | c.184+499dupT | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr14 | 67621454 | ||||||
| chr14:67621461 | T | C | 1 | a0001c0001t0004g0173 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.184+495T>C | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67621461 | |||||||
| chr14:67621536 | A | T | 1 | a0001c0001t0001g0343 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.184+570A>T | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67621536 | |||||||
| chr14:67621550 | G | A | 17 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(14): Show |
17 | HG01175.hp1 HG02622.hp2 HG02717.hp1 others(14): Show |
intron_variant | MODIFIER | c.184+584G>A | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67621550 | |||||||
| chr14:67621626 | G | A | 11 | a0001c0001t0001g0019 a0001c0001t0001g0044 a0001c0001t0001g0045 others(8): Show |
12 | HG02145.hp1 HG02451.hp1 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.184+660G>A | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67621626 | |||||||
| chr14:67621674 | A | G | 2 | a0001c0001t0001g0290 a0001c0001t0001g0291 |
2 | HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.184+708A>G | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67621674 | |||||||
| chr14:67621677 | T | C | 1 | a0001c0001t0001g0053 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.184+711T>C | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67621677 | |||||||
| chr14:67621794 | C | T | 2 | a0001c0001t0001g0163 a0001c0001t0001g0164 |
2 | HG03453.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.184+828C>T | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67621794 | |||||||
| chr14:67621824 | C | T | 1 | a0001c0001t0001g0289 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.184+858C>T | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67621824 | |||||||
| chr14:67621863 | A | G | 158 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0040 others(155): Show |
193 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(190): Show |
intron_variant | MODIFIER | c.184+897A>G | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67621863 | |||||||
| chr14:67621897 | G | A | 1 | a0001c0001t0001g0019 | 2 | HG03225.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.184+931G>A | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67621897 | |||||||
| chr14:67621899 | C | A | 137 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0040 others(134): Show |
161 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.184+933C>A | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67621899 | |||||||
| chr14:67621904 | C | A | 1 | a0001c0001t0002g0158 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.184+938C>A | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67621904 | |||||||
| chr14:67622097 | T | G | 1 | a0001c0001t0003g0054 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.184+1131T>G | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67622097 | |||||||
| chr14:67622122 | G | A | 5 | a0001c0001t0002g0161 a0001c0001t0002g0162 a0002c0002t0002g0008 others(2): Show |
8 | HG01081.hp2 HG02109.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.184+1156G>A | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67622122 | |||||||
| chr14:67622436 | A | T | 158 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0040 others(155): Show |
193 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(190): Show |
intron_variant | MODIFIER | c.184+1470A>T | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67622436 | |||||||
| chr14:67622474 | C | T | 1 | a0001c0001t0003g0039 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.184+1508C>T | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67622474 | |||||||
| chr14:67622614 | C | T | 1 | a0001c0001t0003g0157 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.184+1648C>T | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67622614 | |||||||
| chr14:67622658 | C | T | 143 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0040 others(140): Show |
170 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.184+1692C>T | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67622658 | |||||||
| chr14:67622703 | G | A | 4 | a0001c0001t0001g0293 a0001c0001t0001g0294 a0001c0001t0001g0295 others(1): Show |
4 | HG00099.hp2 HG02257.hp2 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.184+1737G>A | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67622703 | |||||||
| chr14:67622713 | G | A | 203 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0040 others(200): Show |
238 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(235): Show |
intron_variant | MODIFIER | c.184+1747G>A | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67622713 | |||||||
| chr14:67622822 | G | T | 1 | a0001c0001t0001g0288 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.184+1856G>T | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67622822 | |||||||
| chr14:67623106 | T | C | 159 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0040 others(156): Show |
194 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(191): Show |
intron_variant | MODIFIER | c.184+2140T>C | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67623106 | |||||||
| chr14:67623140 | G | T | 1 | a0001c0001t0001g0287 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.184+2174G>T | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67623140 | |||||||
| chr14:67623522 | C | T | 1 | a0001c0001t0002g0156 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.184+2556C>T | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67623522 | |||||||
| chr14:67623534 | C | CT | 92 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(89): Show |
123 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.184+2594dupT | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr14 | 67623534 | ||||||
| chr14:67623534 | C | CTT | 14 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0275 others(11): Show |
16 | HG00621.hp1 HG01361.hp2 HG02683.hp1 others(13): Show |
intron_variant | MODIFIER | c.184+2593_184+2594d others(4): Show |
ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr14 | 67623534 | ||||||
| chr14:67623534 | C | CTTT | 11 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(8): Show |
11 | HG01175.hp1 HG02622.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.184+2592_184+2594d others(5): Show |
ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr14 | 67623534 | ||||||
| chr14:67623534 | C | CTTTT | 11 | a0001c0001t0002g0210 a0001c0001t0003g0205 a0001c0001t0003g0209 others(8): Show |
11 | HG01496.hp1 HG02109.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.184+2591_184+2594d others(6): Show |
ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr14 | 67623534 | ||||||
| chr14:67623534 | CT | C | 13 | a0001c0001t0001g0290 a0001c0001t0001g0291 a0001c0001t0001g0296 others(10): Show |
13 | HG01256.hp1 HG01433.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.184+2594delT | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr14 | 67623534 | ||||||
| chr14:67623534 | CTTT | C | 42 | a0001c0001t0001g0040 a0001c0001t0001g0129 a0001c0001t0001g0130 others(39): Show |
50 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(47): Show |
intron_variant | MODIFIER | c.184+2592_184+2594d others(5): Show |
ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr14 | 67623534 | ||||||
| chr14:67623534 | CTTTT | C | 17 | a0001c0001t0001g0052 a0001c0001t0001g0120 a0001c0001t0001g0121 others(14): Show |
25 | HG00609.hp1 HG02080.hp1 HG03486.hp1 others(22): Show |
intron_variant | MODIFIER | c.184+2591_184+2594d others(6): Show |
ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr14 | 67623534 | ||||||
| chr14:67623534 | CTTTTT | C | 93 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0044 others(90): Show |
112 | HG00408.hp1 HG00423.hp2 HG00621.hp2 others(109): Show |
intron_variant | MODIFIER | c.184+2590_184+2594d others(7): Show |
ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr14 | 67623534 | ||||||
| chr14:67623624 | C | A | 26 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(23): Show |
26 | HG01175.hp1 HG01496.hp1 HG02109.hp2 others(23): Show |
intron_variant | MODIFIER | c.184+2658C>A | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67623624 | |||||||
| chr14:67623747 | G | A | 1 | a0001c0001t0004g0190 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.184+2781G>A | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67623747 | |||||||
| chr14:67623835 | C | G | 1 | a0001c0001t0001g0299 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.184+2869C>G | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67623835 | |||||||
| chr14:67623845 | T | C | 2 | a0001c0001t0001g0360 a0001c0001t0001g0361 |
2 | HG03017.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.184+2879T>C | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67623845 | |||||||
| chr14:67624029 | C | T | 3 | a0001c0001t0001g0035 a0001c0001t0001g0273 a0001c0001t0001g0274 |
4 | HG01106.hp2 HG01257.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.184+3063C>T | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67624029 | |||||||
| chr14:67624251 | G | T | 2 | a0001c0001t0003g0116 a0001c0001t0003g0117 |
2 | HG01433.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.184+3285G>T | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67624251 | |||||||
| chr14:67624256 | T | C | 1 | a0001c0001t0001g0273 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.184+3290T>C | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67624256 | |||||||
| chr14:67624277 | GTGT | G | 100 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0044 others(97): Show |
119 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.184+3316_184+3318d others(5): Show |
ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr14 | 67624277 | ||||||
| chr14:67624368 | G | A | 1 | a0001c0001t0001g0293 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.184+3402G>A | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67624368 | |||||||
| chr14:67624542 | G | A | 1 | a0001c0001t0005g0203 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.184+3576G>A | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67624542 | |||||||
| chr14:67624551 | G | A | 82 | a0001c0001t0001g0006 a0001c0001t0001g0053 a0001c0001t0001g0061 others(79): Show |
97 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.184+3585G>A | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67624551 | |||||||
| chr14:67624580 | G | A | 1 | a0001c0001t0004g0204 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.184+3614G>A | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67624580 | |||||||
| chr14:67624687 | T | C | 15 | a0001c0001t0001g0354 a0001c0001t0001g0360 a0001c0001t0001g0361 others(12): Show |
23 | HG00609.hp1 HG02080.hp1 HG03017.hp2 others(20): Show |
intron_variant | MODIFIER | c.184+3721T>C | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67624687 | |||||||
| chr14:67624697 | A | C | 159 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0040 others(156): Show |
194 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(191): Show |
intron_variant | MODIFIER | c.184+3731A>C | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67624697 | |||||||
| chr14:67624717 | A | G | 159 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0040 others(156): Show |
194 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(191): Show |
intron_variant | MODIFIER | c.184+3751A>G | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67624717 | |||||||
| chr14:67624749 | A | G | 1 | a0001c0001t0001g0115 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.184+3783A>G | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67624749 | |||||||
| chr14:67624854 | A | G | 1 | a0001c0001t0002g0158 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.184+3888A>G | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67624854 | |||||||
| chr14:67624902 | C | T | 2 | a0001c0001t0001g0271 a0001c0001t0001g0272 |
2 | NA18961.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.184+3936C>T | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67624902 | |||||||
| chr14:67624953 | T | C | 17 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(14): Show |
17 | HG01175.hp1 HG02622.hp2 HG02717.hp1 others(14): Show |
intron_variant | MODIFIER | c.184+3987T>C | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67624953 | |||||||
| chr14:67625157 | T | TA | 6 | a0001c0001t0001g0275 a0001c0001t0001g0300 a0001c0001t0001g0301 others(3): Show |
6 | HG02735.hp2 HG03654.hp1 HG03942.hp2 others(3): Show |
intron_variant | MODIFIER | c.184+4204dupA | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr14 | 67625157 | ||||||
| chr14:67625157 | TA | T | 9 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0221 others(6): Show |
13 | HG00733.hp1 HG01070.hp1 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.184+4204delA | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr14 | 67625157 | ||||||
| chr14:67625365 | T | A | 1 | a0001c0001t0001g0222 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.184+4399T>A | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67625365 | |||||||
| chr14:67625417 | G | A | 15 | a0001c0001t0001g0354 a0001c0001t0001g0360 a0001c0001t0001g0361 others(12): Show |
23 | HG00609.hp1 HG02080.hp1 HG03017.hp2 others(20): Show |
intron_variant | MODIFIER | c.184+4451G>A | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67625417 | |||||||
| chr14:67625454 | G | A | 2 | a0001c0001t0003g0056 a0001c0001t0003g0057 |
2 | NA18961.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.184+4488G>A | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67625454 | |||||||
| chr14:67625476 | C | T | 53 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0038 others(50): Show |
62 | HG00099.hp2 HG00423.hp1 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.184+4510C>T | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67625476 | |||||||
| chr14:67625481 | C | T | 11 | a0001c0001t0001g0019 a0001c0001t0001g0044 a0001c0001t0001g0045 others(8): Show |
12 | HG02145.hp1 HG02451.hp1 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.184+4515C>T | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67625481 | |||||||
| chr14:67625521 | C | A | 10 | a0001c0001t0001g0194 a0001c0001t0001g0196 a0001c0001t0001g0197 others(7): Show |
10 | HG01891.hp2 HG02280.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.184+4555C>A | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67625521 | |||||||
| chr14:67625522 | A | C | 158 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0040 others(155): Show |
193 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(190): Show |
intron_variant | MODIFIER | c.184+4556A>C | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67625522 | |||||||
| chr14:67625628 | C | T | 159 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0040 others(156): Show |
194 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(191): Show |
intron_variant | MODIFIER | c.184+4662C>T | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67625628 | |||||||
| chr14:67625680 | C | CA | 30 | a0001c0001t0001g0061 a0001c0001t0001g0194 a0001c0001t0001g0196 others(27): Show |
31 | HG01099.hp2 HG01496.hp1 HG01516.hp1 others(28): Show |
intron_variant | MODIFIER | c.184+4734dupA | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr14 | 67625680 | ||||||
| chr14:67625680 | C | CAAA | 22 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0003g0177 others(19): Show |
22 | HG01175.hp1 HG02145.hp2 HG02622.hp2 others(19): Show |
intron_variant | MODIFIER | c.184+4732_184+4734d others(5): Show |
ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr14 | 67625680 | ||||||
| chr14:67625680 | CA | C | 18 | a0001c0001t0001g0019 a0001c0001t0001g0044 a0001c0001t0001g0045 others(15): Show |
19 | HG00323.hp1 HG00323.hp2 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.184+4734delA | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr14 | 67625680 | ||||||
| chr14:67625693 | AAAAAAAA others(58): Show |
A | 13 | a0001c0001t0001g0354 a0001c0001t0001g0360 a0001c0001t0001g0361 others(10): Show |
21 | HG00609.hp1 HG03017.hp2 HG03710.hp2 others(18): Show |
intron_variant | MODIFIER | c.184+4733_184+4797d others(67): Show |
ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr14 | 67625693 | ||||||
| chr14:67625694 | AAAAAAAG others(57): Show |
A | 2 | a0001c0001t0002g0350 a0001c0001t0002g0362 |
2 | HG02080.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.184+4734_184+4797d others(66): Show |
ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr14 | 67625694 | ||||||
| chr14:67625696 | A | G | 2 | a0001c0001t0003g0003 a0001c0001t0005g0203 |
2 | HG02630.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.184+4730A>G | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67625696 | |||||||
| chr14:67625736 | C | CA | 99 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0044 others(96): Show |
117 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.184+4782dupA | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr14 | 67625736 | ||||||
| chr14:67625736 | C | T | 1 | a0001c0001t0003g0011 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.184+4770C>T | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67625736 | |||||||
| chr14:67625946 | C | T | 3 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 |
3 | HG01175.hp1 HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.184+4980C>T | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67625946 | |||||||
| chr14:67626024 | C | T | 100 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0044 others(97): Show |
119 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.184+5058C>T | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67626024 | |||||||
| chr14:67626025 | G | A | 1 | a0001c0001t0005g0346 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.184+5059G>A | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67626025 | |||||||
| chr14:67626082 | G | A | 1 | a0001c0001t0004g0193 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.184+5116G>A | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67626082 | |||||||
| chr14:67626096 | A | C | 15 | a0001c0001t0001g0354 a0001c0001t0001g0360 a0001c0001t0001g0361 others(12): Show |
23 | HG00609.hp1 HG02080.hp1 HG03017.hp2 others(20): Show |
intron_variant | MODIFIER | c.184+5130A>C | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67626096 | |||||||
| chr14:67626167 | T | C | 11 | a0001c0001t0001g0019 a0001c0001t0001g0044 a0001c0001t0001g0045 others(8): Show |
12 | HG02145.hp1 HG02451.hp1 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.184+5201T>C | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67626167 | |||||||
| chr14:67626193 | G | A | 3 | a0001c0001t0003g0021 a0001c0001t0003g0062 a0001c0001t0003g0119 |
4 | NA18948.hp2 NA18956.hp2 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.184+5227G>A | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67626193 | |||||||
| chr14:67626213 | C | T | 10 | a0001c0001t0001g0019 a0001c0001t0001g0045 a0001c0001t0001g0046 others(7): Show |
11 | HG02145.hp1 HG02451.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.184+5247C>T | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67626213 | |||||||
| chr14:67626253 | CAG | C | 15 | a0001c0001t0001g0354 a0001c0001t0001g0360 a0001c0001t0001g0361 others(12): Show |
23 | HG00609.hp1 HG02080.hp1 HG03017.hp2 others(20): Show |
intron_variant | MODIFIER | c.184+5288_184+5289d others(4): Show |
ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67626253 | |||||||
| chr14:67626258 | G | GA | 15 | a0001c0001t0001g0019 a0001c0001t0001g0044 a0001c0001t0001g0045 others(12): Show |
16 | HG01175.hp1 HG01175.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.184+5302dupA | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr14 | 67626258 | ||||||
| chr14:67626268 | A | C | 1 | a0001c0001t0001g0307 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.184+5302A>C | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67626268 | |||||||
| chr14:67626269 | C | A | 3 | a0002c0002t0002g0008 a0002c0002t0002g0159 a0002c0002t0002g0160 |
6 | HG02109.hp1 HG02572.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.184+5303C>A | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67626269 | |||||||
| chr14:67626367 | G | A | 1 | a0001c0001t0003g0056 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.184+5401G>A | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67626367 | |||||||
| chr14:67626472 | T | C | 1 | a0001c0001t0005g0203 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.184+5506T>C | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67626472 | |||||||
| chr14:67626544 | G | A | 1 | a0001c0001t0003g0153 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.184+5578G>A | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67626544 | |||||||
| chr14:67626588 | A | C | 19 | a0001c0001t0001g0006 a0001c0001t0001g0053 a0001c0001t0001g0061 others(16): Show |
22 | HG00639.hp1 HG00735.hp1 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.184+5622A>C | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67626588 | |||||||
| chr14:67626680 | G | T | 1 | a0001c0001t0002g0149 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.184+5714G>T | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67626680 | |||||||
| chr14:67626787 | T | C | 8 | a0001c0001t0002g0210 a0001c0001t0003g0191 a0001c0001t0003g0192 others(5): Show |
8 | HG01496.hp1 HG02109.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.184+5821T>C | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67626787 | |||||||
| chr14:67626868 | T | C | 193 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0040 others(190): Show |
228 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(225): Show |
intron_variant | MODIFIER | c.184+5902T>C | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67626868 | |||||||
| chr14:67627098 | G | T | 1 | a0001c0001t0003g0100 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.184+6132G>T | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67627098 | |||||||
| chr14:67627256 | G | GAT | 139 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(136): Show |
180 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(177): Show |
intron_variant | MODIFIER | c.184+6315_184+6316d others(4): Show |
ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr14 | 67627256 | ||||||
| chr14:67627256 | G | GATAT | 22 | a0001c0001t0001g0031 a0001c0001t0001g0103 a0001c0001t0001g0213 others(19): Show |
24 | HG00323.hp2 HG01123.hp2 HG01167.hp1 others(21): Show |
intron_variant | MODIFIER | c.184+6313_184+6316d others(6): Show |
ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr14 | 67627256 | ||||||
| chr14:67627256 | G | GATATAT | 15 | a0001c0001t0001g0030 a0001c0001t0001g0101 a0001c0001t0001g0102 others(12): Show |
16 | HG01081.hp1 HG01106.hp1 HG01257.hp1 others(13): Show |
intron_variant | MODIFIER | c.184+6311_184+6316d others(8): Show |
ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr14 | 67627256 | ||||||
| chr14:67627256 | G | GATATATA others(1): Show |
14 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0089 others(11): Show |
15 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(12): Show |
intron_variant | MODIFIER | c.184+6309_184+6316d others(10): Show |
ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr14 | 67627256 | ||||||
| chr14:67627256 | G | GATATATA others(3): Show |
15 | a0001c0001t0001g0084 a0001c0001t0001g0184 a0001c0001t0002g0210 others(12): Show |
20 | HG01069.hp2 HG01516.hp2 HG01993.hp1 others(17): Show |
intron_variant | MODIFIER | c.184+6307_184+6316d others(12): Show |
ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr14 | 67627256 | ||||||
| chr14:67627256 | G | GATATATA others(5): Show |
15 | a0001c0001t0003g0021 a0001c0001t0003g0022 a0001c0001t0003g0055 others(12): Show |
17 | HG00408.hp1 HG02145.hp2 HG02698.hp1 others(14): Show |
intron_variant | MODIFIER | c.184+6305_184+6316d others(14): Show |
ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr14 | 67627256 | ||||||
| chr14:67627256 | G | GATATATA others(7): Show |
16 | a0001c0001t0001g0185 a0001c0001t0003g0057 a0001c0001t0003g0059 others(13): Show |
16 | HG01167.hp2 HG01169.hp1 HG01255.hp1 others(13): Show |
intron_variant | MODIFIER | c.184+6303_184+6316d others(16): Show |
ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr14 | 67627256 | ||||||
| chr14:67627256 | G | GATATATA others(9): Show |
10 | a0001c0001t0001g0183 a0001c0001t0001g0212 a0001c0001t0003g0011 others(7): Show |
13 | HG01175.hp1 HG01256.hp2 HG02129.hp2 others(10): Show |
intron_variant | MODIFIER | c.184+6301_184+6316d others(18): Show |
ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr14 | 67627256 | ||||||
| chr14:67627256 | G | GATATATA others(11): Show |
5 | a0001c0001t0003g0065 a0001c0001t0003g0066 a0001c0001t0003g0155 others(2): Show |
5 | HG00323.hp1 HG00621.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.184+6299_184+6316d others(20): Show |
ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr14 | 67627256 | ||||||
| chr14:67627256 | G | GATATATA others(13): Show |
3 | a0001c0001t0001g0164 a0001c0001t0003g0064 a0001c0001t0006g0208 |
3 | HG00639.hp2 HG02109.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.184+6297_184+6316d others(22): Show |
ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr14 | 67627256 | ||||||
| chr14:67627256 | G | GATATATA others(15): Show |
4 | a0001c0001t0001g0163 a0001c0001t0003g0063 a0001c0001t0003g0191 others(1): Show |
4 | HG02615.hp1 HG02895.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.184+6295_184+6316d others(24): Show |
ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr14 | 67627256 | ||||||
| chr14:67627256 | G | GATATATA others(17): Show |
4 | a0001c0001t0003g0058 a0001c0001t0003g0205 a0001c0001t0004g0190 others(1): Show |
4 | HG01496.hp1 HG03579.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.184+6293_184+6316d others(26): Show |
ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr14 | 67627256 | ||||||
| chr14:67627256 | G | GATATATA others(19): Show |
1 | a0001c0001t0003g0056 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.184+6291_184+6316d others(28): Show |
ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr14 | 67627256 | ||||||
| chr14:67627256 | G | GATATATA others(21): Show |
1 | a0001c0001t0005g0203 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.184+6316_184+6317i others(30): Show |
ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr14 | 67627256 | ||||||
| chr14:67627256 | GAT | G | 15 | a0001c0001t0001g0194 a0001c0001t0001g0196 a0001c0001t0001g0197 others(12): Show |
16 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.184+6315_184+6316d others(4): Show |
ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr14 | 67627256 | ||||||
| chr14:67627256 | GATAT | G | 37 | a0001c0001t0001g0040 a0001c0001t0001g0129 a0001c0001t0001g0130 others(34): Show |
44 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.184+6313_184+6316d others(6): Show |
ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr14 | 67627256 | ||||||
| chr14:67627256 | GATATATA others(1): Show |
G | 15 | a0001c0001t0001g0354 a0001c0001t0001g0360 a0001c0001t0001g0361 others(12): Show |
23 | HG00609.hp1 HG02080.hp1 HG03017.hp2 others(20): Show |
intron_variant | MODIFIER | c.184+6309_184+6316d others(10): Show |
ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr14 | 67627256 | ||||||
| chr14:67627337 | T | C | 10 | a0001c0001t0001g0194 a0001c0001t0001g0196 a0001c0001t0001g0197 others(7): Show |
10 | HG01891.hp2 HG02280.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.184+6371T>C | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67627337 | |||||||
| chr14:67627514 | G | A | 5 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(2): Show |
5 | HG02451.hp1 HG02647.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.184+6548G>A | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67627514 | |||||||
| chr14:67627548 | G | C | 100 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0044 others(97): Show |
119 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.184+6582G>C | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67627548 | |||||||
| chr14:67627974 | G | C | 1 | a0001c0001t0001g0312 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.184+7008G>C | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67627974 | |||||||
| chr14:67628053 | G | A | 15 | a0001c0001t0001g0354 a0001c0001t0001g0360 a0001c0001t0001g0361 others(12): Show |
23 | HG00609.hp1 HG02080.hp1 HG03017.hp2 others(20): Show |
intron_variant | MODIFIER | c.184+7087G>A | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67628053 | |||||||
| chr14:67628242 | C | G | 1 | a0001c0001t0003g0154 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.184+7276C>G | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67628242 | |||||||
| chr14:67628349 | A | T | 159 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0040 others(156): Show |
194 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(191): Show |
intron_variant | MODIFIER | c.184+7383A>T | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67628349 | |||||||
| chr14:67628416 | A | G | 2 | a0001c0001t0001g0327 a0001c0001t0001g0328 |
2 | NA18960.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.184+7450A>G | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67628416 | |||||||
| chr14:67628520 | C | T | 1 | a0001c0001t0003g0192 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.184+7554C>T | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67628520 | |||||||
| chr14:67628840 | T | C | 1 | a0001c0001t0001g0342 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.184+7874T>C | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67628840 | |||||||
| chr14:67628886 | A | AAAAGG | 7 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0089 others(4): Show |
8 | HG01074.hp2 HG01192.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.184+7922_184+7926d others(7): Show |
ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr14 | 67628886 | ||||||
| chr14:67628919 | T | C | 306 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(303): Show |
372 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(369): Show |
intron_variant | MODIFIER | c.184+7953T>C | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67628919 | |||||||
| chr14:67628948 | T | C | 15 | a0001c0001t0001g0354 a0001c0001t0001g0360 a0001c0001t0001g0361 others(12): Show |
23 | HG00609.hp1 HG02080.hp1 HG03017.hp2 others(20): Show |
intron_variant | MODIFIER | c.184+7982T>C | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67628948 | |||||||
| chr14:67628980 | T | C | 7 | a0001c0001t0004g0190 a0001c0001t0005g0344 a0001c0001t0005g0345 others(4): Show |
7 | HG02145.hp2 HG02896.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.184+8014T>C | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67628980 | |||||||
| chr14:67628997 | A | G | 1 | a0001c0001t0003g0039 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.184+8031A>G | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67628997 | |||||||
| chr14:67629341 | C | T | 8 | a0001c0001t0002g0210 a0001c0001t0003g0191 a0001c0001t0003g0192 others(5): Show |
8 | HG01496.hp1 HG02109.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.184+8375C>T | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67629341 | |||||||
| chr14:67629367 | C | G | 1 | a0001c0001t0003g0154 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.184+8401C>G | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67629367 | |||||||
| chr14:67629379 | G | A | 42 | a0001c0001t0001g0040 a0001c0001t0001g0129 a0001c0001t0001g0130 others(39): Show |
50 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(47): Show |
intron_variant | MODIFIER | c.184+8413G>A | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67629379 | |||||||
| chr14:67629442 | T | A | 2 | a0001c0001t0001g0163 a0001c0001t0001g0164 |
2 | HG03453.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.184+8476T>A | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67629442 | |||||||
| chr14:67629766 | G | A | 15 | a0001c0001t0001g0354 a0001c0001t0001g0360 a0001c0001t0001g0361 others(12): Show |
23 | HG00609.hp1 HG02080.hp1 HG03017.hp2 others(20): Show |
intron_variant | MODIFIER | c.184+8800G>A | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67629766 | |||||||
| chr14:67630146 | C | T | 2 | a0001c0001t0001g0341 a0001c0001t0004g0190 |
2 | HG03579.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.184+9180C>T | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67630146 | |||||||
| chr14:67630380 | C | T | 102 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0044 others(99): Show |
121 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.184+9414C>T | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67630380 | |||||||
| chr14:67630405 | A | G | 1 | a0001c0001t0002g0171 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.184+9439A>G | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67630405 | |||||||
| chr14:67630461 | G | A | 10 | a0001c0001t0001g0019 a0001c0001t0001g0045 a0001c0001t0001g0046 others(7): Show |
11 | HG02145.hp1 HG02451.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.184+9495G>A | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67630461 | |||||||
| chr14:67630497 | G | A | 1 | a0001c0001t0001g0104 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.184+9531G>A | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67630497 | |||||||
| chr14:67630537 | C | T | 4 | a0001c0001t0002g0210 a0001c0001t0006g0206 a0001c0001t0006g0207 others(1): Show |
4 | HG02109.hp2 HG02572.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.184+9571C>T | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67630537 | |||||||
| chr14:67630588 | T | G | 117 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0044 others(114): Show |
144 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.184+9622T>G | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67630588 | |||||||
| chr14:67630665 | C | T | 2 | a0001c0001t0001g0109 a0001c0001t0003g0154 |
2 | HG03927.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.184+9699C>T | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67630665 | |||||||
| chr14:67630694 | T | C | 1 | a0001c0001t0001g0313 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.184+9728T>C | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67630694 | |||||||
| chr14:67630701 | C | T | 1 | a0001c0001t0003g0154 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.184+9735C>T | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67630701 | |||||||
| chr14:67630707 | T | C | 1 | a0001c0001t0001g0214 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.184+9741T>C | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67630707 | |||||||
| chr14:67630757 | T | C | 1 | a0001c0001t0001g0332 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.184+9791T>C | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67630757 | |||||||
| chr14:67630788 | C | T | 1 | a0001c0001t0001g0229 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.184+9822C>T | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67630788 | |||||||
| chr14:67631004 | T | A | 51 | a0001c0001t0001g0040 a0001c0001t0001g0129 a0001c0001t0001g0130 others(48): Show |
60 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.184+10038T>A | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67631004 | |||||||
| chr14:67631252 | T | C | 2 | a0001c0001t0001g0163 a0001c0001t0001g0164 |
2 | HG03453.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.184+10286T>C | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67631252 | |||||||
| chr14:67631406 | A | G | 4 | a0001c0001t0002g0145 a0001c0001t0002g0146 a0001c0001t0002g0147 others(1): Show |
4 | HG00408.hp2 HG00673.hp2 HG02027.hp2 others(1): Show |
intron_variant | MODIFIER | c.184+10440A>G | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67631406 | |||||||
| chr14:67631430 | C | CT | 47 | a0001c0001t0001g0040 a0001c0001t0001g0108 a0001c0001t0001g0109 others(44): Show |
55 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(52): Show |
intron_variant | MODIFIER | c.184+10467dupT | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr14 | 67631430 | ||||||
| chr14:67631430 | C | CTT | 14 | a0001c0001t0001g0361 a0001c0001t0002g0029 a0001c0001t0002g0042 others(11): Show |
15 | HG01109.hp2 HG01123.hp1 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.184+10466_184+1046 others(6): Show |
ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr14 | 67631430 | ||||||
| chr14:67631430 | C | CTTT | 13 | a0001c0001t0001g0354 a0001c0001t0002g0002 a0001c0001t0002g0018 others(10): Show |
21 | HG00609.hp1 HG02080.hp1 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.184+10465_184+1046 others(7): Show |
ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr14 | 67631430 | ||||||
| chr14:67631433 | TC | T | 23 | a0001c0001t0001g0019 a0001c0001t0001g0044 a0001c0001t0001g0046 others(20): Show |
24 | HG00323.hp1 HG01081.hp2 HG01256.hp2 others(21): Show |
intron_variant | MODIFIER | c.184+10468delC | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67631433 | |||||||
| chr14:67631434 | C | T | 185 | a0001c0001t0001g0006 a0001c0001t0001g0040 a0001c0001t0001g0045 others(182): Show |
220 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(217): Show |
intron_variant | MODIFIER | c.184+10468C>T | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67631434 | |||||||
| chr14:67631434 | CT | C | 13 | a0001c0001t0001g0001 a0001c0001t0001g0211 a0001c0001t0001g0212 others(10): Show |
13 | HG00280.hp2 HG01168.hp1 HG01515.hp1 others(10): Show |
intron_variant | MODIFIER | c.184+10487delT | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr14 | 67631434 | ||||||
| chr14:67631460 | G | A | 15 | a0001c0001t0001g0354 a0001c0001t0001g0360 a0001c0001t0001g0361 others(12): Show |
23 | HG00609.hp1 HG02080.hp1 HG03017.hp2 others(20): Show |
intron_variant | MODIFIER | c.184+10494G>A | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67631460 | |||||||
| chr14:67631846 | C | T | 2 | a0001c0001t0005g0344 a0001c0001t0005g0345 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.185-10340C>T | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67631846 | |||||||
| chr14:67631881 | T | A | 4 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0194 others(1): Show |
4 | HG00673.hp1 HG02809.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.185-10305T>A | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67631881 | |||||||
| chr14:67631901 | G | T | 11 | a0001c0001t0001g0019 a0001c0001t0001g0044 a0001c0001t0001g0045 others(8): Show |
12 | HG02145.hp1 HG02451.hp1 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.185-10285G>T | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67631901 | |||||||
| chr14:67631952 | A | G | 50 | a0001c0001t0001g0040 a0001c0001t0001g0129 a0001c0001t0001g0130 others(47): Show |
59 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.185-10234A>G | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67631952 | |||||||
| chr14:67631975 | A | G | 19 | a0001c0001t0001g0006 a0001c0001t0001g0053 a0001c0001t0001g0061 others(16): Show |
22 | HG00639.hp1 HG00735.hp1 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.185-10211A>G | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67631975 | |||||||
| chr14:67632046 | G | A | 1 | a0001c0001t0001g0267 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.185-10140G>A | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67632046 | |||||||
| chr14:67632086 | A | C | 200 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0040 others(197): Show |
236 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(233): Show |
intron_variant | MODIFIER | c.185-10100A>C | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67632086 | |||||||
| chr14:67632279 | G | A | 1 | a0001c0001t0001g0226 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.185-9907G>A | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67632279 | |||||||
| chr14:67632597 | G | T | 1 | a0001c0001t0003g0154 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.185-9589G>T | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67632597 | |||||||
| chr14:67632669 | G | C | 2 | a0001c0001t0002g0161 a0001c0001t0002g0162 |
2 | HG01081.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.185-9517G>C | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67632669 | |||||||
| chr14:67632756 | A | G | 210 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0040 others(207): Show |
246 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(243): Show |
intron_variant | MODIFIER | c.185-9430A>G | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67632756 | |||||||
| chr14:67632771 | CTT | C | 50 | a0001c0001t0001g0040 a0001c0001t0001g0129 a0001c0001t0001g0130 others(47): Show |
59 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.185-9413_185-9412d others(4): Show |
ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr14 | 67632771 | ||||||
| chr14:67632778 | T | G | 1 | a0001c0001t0001g0231 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.185-9408T>G | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67632778 | |||||||
| chr14:67632797 | T | C | 18 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0002g0012 others(15): Show |
20 | HG00099.hp1 HG00408.hp2 HG00642.hp1 others(17): Show |
intron_variant | MODIFIER | c.185-9389T>C | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67632797 | |||||||
| chr14:67632808 | A | AT | 48 | a0001c0001t0001g0001 a0001c0001t0001g0045 a0001c0001t0001g0048 others(45): Show |
53 | HG00408.hp2 HG00558.hp2 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.185-9348dupT | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr14 | 67632808 | ||||||
| chr14:67632808 | A | ATT | 34 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0040 others(31): Show |
37 | HG00597.hp1 HG01074.hp1 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.185-9349_185-9348d others(4): Show |
ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr14 | 67632808 | ||||||
| chr14:67632808 | A | ATTT | 13 | a0001c0001t0001g0006 a0001c0001t0001g0101 a0001c0001t0001g0106 others(10): Show |
15 | HG00639.hp1 HG00735.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.185-9350_185-9348d others(5): Show |
ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr14 | 67632808 | ||||||
| chr14:67632808 | AT | A | 97 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(94): Show |
110 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.185-9348delT | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr14 | 67632808 | ||||||
| chr14:67632808 | ATT | A | 67 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(64): Show |
80 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.185-9349_185-9348d others(4): Show |
ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr14 | 67632808 | ||||||
| chr14:67632808 | ATTT | A | 26 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0194 others(23): Show |
38 | HG00609.hp1 HG01168.hp1 HG02080.hp1 others(35): Show |
intron_variant | MODIFIER | c.185-9350_185-9348d others(5): Show |
ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr14 | 67632808 | ||||||
| chr14:67632808 | ATTTTTTT others(3): Show |
A | 2 | a0001c0001t0002g0141 a0001c0001t0002g0151 |
2 | NA18978.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.185-9357_185-9348d others(12): Show |
ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr14 | 67632808 | ||||||
| chr14:67632808 | ATTTTTTT others(5): Show |
A | 1 | a0001c0001t0001g0257 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.185-9359_185-9348d others(14): Show |
ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr14 | 67632808 | ||||||
| chr14:67632851 | C | T | 1 | a0001c0001t0001g0326 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.185-9335C>T | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67632851 | |||||||
| chr14:67632862 | T | C | 2 | a0001c0001t0001g0129 a0001c0001t0001g0232 |
2 | HG03239.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.185-9324T>C | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67632862 | |||||||
| chr14:67632889 | C | A | 80 | a0001c0001t0001g0006 a0001c0001t0001g0053 a0001c0001t0001g0061 others(77): Show |
95 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.185-9297C>A | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67632889 | |||||||
| chr14:67632922 | A | G | 1 | a0001c0001t0001g0044 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.185-9264A>G | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67632922 | |||||||
| chr14:67632969 | C | T | 1 | a0001c0001t0001g0361 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.185-9217C>T | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67632969 | |||||||
| chr14:67632970 | G | A | 2 | a0001c0001t0001g0049 a0001c0001t0001g0230 |
2 | HG02145.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.185-9216G>A | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67632970 | |||||||
| chr14:67633055 | C | T | 8 | a0001c0001t0002g0210 a0001c0001t0003g0191 a0001c0001t0003g0192 others(5): Show |
8 | HG01496.hp1 HG02109.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.185-9131C>T | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67633055 | |||||||
| chr14:67633111 | C | T | 10 | a0001c0001t0001g0194 a0001c0001t0001g0196 a0001c0001t0001g0197 others(7): Show |
10 | HG01891.hp2 HG02280.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.185-9075C>T | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67633111 | |||||||
| chr14:67633222 | A | G | 1 | a0001c0001t0005g0203 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.185-8964A>G | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67633222 | |||||||
| chr14:67633310 | G | T | 1 | a0001c0001t0004g0180 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.185-8876G>T | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67633310 | |||||||
| chr14:67633366 | T | G | 16 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0016 others(13): Show |
22 | HG00280.hp1 HG00558.hp1 HG00733.hp1 others(19): Show |
intron_variant | MODIFIER | c.185-8820T>G | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67633366 | |||||||
| chr14:67633374 | G | A | 2 | a0001c0001t0001g0163 a0001c0001t0001g0164 |
2 | HG03453.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.185-8812G>A | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67633374 | |||||||
| chr14:67633381 | A | T | 18 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(15): Show |
18 | HG01175.hp1 HG02622.hp2 HG02717.hp1 others(15): Show |
intron_variant | MODIFIER | c.185-8805A>T | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67633381 | |||||||
| chr14:67633461 | G | T | 1 | a0001c0001t0002g0143 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.185-8725G>T | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67633461 | |||||||
| chr14:67633555 | G | A | 13 | a0001c0001t0001g0354 a0001c0001t0002g0002 a0001c0001t0002g0018 others(10): Show |
21 | HG00609.hp1 HG02080.hp1 NA18612.hp2 others(18): Show |
intron_variant | MODIFIER | c.185-8631G>A | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67633555 | |||||||
| chr14:67633808 | G | A | 15 | a0001c0001t0001g0354 a0001c0001t0001g0360 a0001c0001t0001g0361 others(12): Show |
23 | HG00609.hp1 HG02080.hp1 HG03017.hp2 others(20): Show |
intron_variant | MODIFIER | c.185-8378G>A | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67633808 | |||||||
| chr14:67633959 | T | C | 62 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 others(59): Show |
74 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.185-8227T>C | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67633959 | |||||||
| chr14:67634170 | T | C | 200 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0040 others(197): Show |
236 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(233): Show |
intron_variant | MODIFIER | c.185-8016T>C | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67634170 | |||||||
| chr14:67634212 | C | T | 1 | a0001c0001t0001g0049 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.185-7974C>T | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67634212 | |||||||
| chr14:67634269 | C | T | 1 | a0001c0001t0001g0265 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.185-7917C>T | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67634269 | |||||||
| chr14:67634430 | C | CA | 26 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0194 others(23): Show |
30 | HG00733.hp1 HG01070.hp1 HG01071.hp2 others(27): Show |
intron_variant | MODIFIER | c.185-7736dupA | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr14 | 67634430 | ||||||
| chr14:67634430 | CA | C | 29 | a0001c0001t0001g0213 a0001c0001t0001g0259 a0001c0001t0001g0260 others(26): Show |
37 | HG00323.hp1 HG00609.hp1 HG01167.hp1 others(34): Show |
intron_variant | MODIFIER | c.185-7736delA | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr14 | 67634430 | ||||||
| chr14:67634586 | C | T | 19 | a0001c0001t0001g0006 a0001c0001t0001g0053 a0001c0001t0001g0061 others(16): Show |
22 | HG00639.hp1 HG00735.hp1 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.185-7600C>T | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67634586 | |||||||
| chr14:67634594 | C | CA | 91 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0014 others(88): Show |
108 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.185-7576dupA | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr14 | 67634594 | ||||||
| chr14:67634594 | C | CAA | 9 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0163 others(6): Show |
16 | HG02083.hp1 HG02165.hp2 HG03453.hp1 others(13): Show |
intron_variant | MODIFIER | c.185-7577_185-7576d others(4): Show |
ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr14 | 67634594 | ||||||
| chr14:67634594 | CA | C | 10 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(7): Show |
10 | HG01175.hp1 HG02165.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.185-7576delA | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr14 | 67634594 | ||||||
| chr14:67634635 | G | A | 2 | a0001c0001t0001g0360 a0001c0001t0001g0361 |
2 | HG03017.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.185-7551G>A | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67634635 | |||||||
| chr14:67634737 | G | C | 99 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0044 others(96): Show |
118 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.185-7449G>C | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67634737 | |||||||
| chr14:67634941 | T | C | 5 | a0001c0001t0002g0161 a0001c0001t0002g0162 a0002c0002t0002g0008 others(2): Show |
8 | HG01081.hp2 HG02109.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.185-7245T>C | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67634941 | |||||||
| chr14:67635051 | C | T | 11 | a0001c0001t0001g0019 a0001c0001t0001g0044 a0001c0001t0001g0045 others(8): Show |
12 | HG02145.hp1 HG02451.hp1 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.185-7135C>T | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67635051 | |||||||
| chr14:67635054 | C | T | 1 | a0001c0001t0001g0256 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.185-7132C>T | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67635054 | |||||||
| chr14:67635081 | CAA | C | 10 | a0001c0001t0001g0194 a0001c0001t0001g0196 a0001c0001t0001g0197 others(7): Show |
10 | HG01891.hp2 HG02280.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.185-7099_185-7098d others(4): Show |
ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr14 | 67635081 | ||||||
| chr14:67635088 | A | T | 10 | a0001c0001t0001g0194 a0001c0001t0001g0196 a0001c0001t0001g0197 others(7): Show |
10 | HG01891.hp2 HG02280.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.185-7098A>T | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67635088 | |||||||
| chr14:67635194 | T | C | 15 | a0001c0001t0001g0354 a0001c0001t0001g0360 a0001c0001t0001g0361 others(12): Show |
23 | HG00609.hp1 HG02080.hp1 HG03017.hp2 others(20): Show |
intron_variant | MODIFIER | c.185-6992T>C | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67635194 | |||||||
| chr14:67635377 | C | A | 1 | a0001c0001t0004g0180 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.185-6809C>A | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67635377 | |||||||
| chr14:67635571 | C | A | 1 | a0001c0001t0001g0270 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.185-6615C>A | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67635571 | |||||||
| chr14:67635576 | G | A | 1 | a0001c0001t0005g0203 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.185-6610G>A | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67635576 | |||||||
| chr14:67635714 | G | A | 1 | a0001c0001t0005g0203 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.185-6472G>A | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67635714 | |||||||
| chr14:67635797 | A | G | 10 | a0001c0001t0003g0177 a0001c0001t0004g0174 a0001c0001t0004g0175 others(7): Show |
10 | HG02622.hp2 HG02717.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.185-6389A>G | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67635797 | |||||||
| chr14:67635859 | T | A | 76 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0044 others(73): Show |
90 | HG00323.hp1 HG00408.hp1 HG00621.hp2 others(87): Show |
intron_variant | MODIFIER | c.185-6327T>A | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67635859 | |||||||
| chr14:67635867 | A | T | 53 | a0001c0001t0001g0040 a0001c0001t0001g0129 a0001c0001t0001g0130 others(50): Show |
62 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.185-6319A>T | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67635867 | |||||||
| chr14:67635982 | G | A | 2 | a0001c0001t0003g0092 a0001c0001t0003g0093 |
2 | NA18942.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.185-6204G>A | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67635982 | |||||||
| chr14:67636129 | A | G | 1 | a0001c0001t0001g0201 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.185-6057A>G | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67636129 | |||||||
| chr14:67636140 | G | A | 1 | a0001c0001t0003g0192 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.185-6046G>A | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67636140 | |||||||
| chr14:67636187 | T | C | 6 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0267 others(3): Show |
10 | HG00733.hp1 HG01070.hp1 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.185-5999T>C | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67636187 | |||||||
| chr14:67636261 | CA | C | 17 | a0001c0001t0001g0019 a0001c0001t0001g0046 a0001c0001t0001g0047 others(14): Show |
18 | HG00423.hp2 HG00673.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.185-5914delA | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr14 | 67636261 | ||||||
| chr14:67636272 | A | AAC | 14 | a0001c0001t0001g0354 a0001c0001t0002g0002 a0001c0001t0002g0018 others(11): Show |
22 | HG00609.hp1 HG02080.hp1 HG02132.hp2 others(19): Show |
intron_variant | MODIFIER | c.185-5914_185-5913i others(4): Show |
ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67636272 | |||||||
| chr14:67636439 | C | T | 15 | a0001c0001t0001g0006 a0001c0001t0001g0051 a0001c0001t0001g0053 others(12): Show |
18 | HG00639.hp1 HG00735.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.185-5747C>T | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67636439 | |||||||
| chr14:67636452 | C | T | 1 | a0001c0001t0001g0129 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.185-5734C>T | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67636452 | |||||||
| chr14:67636604 | A | C | 349 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(346): Show |
424 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(421): Show |
intron_variant | MODIFIER | c.185-5582A>C | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67636604 | |||||||
| chr14:67636605 | G | A | 4 | a0001c0001t0005g0346 a0001c0001t0005g0347 a0001c0001t0005g0348 others(1): Show |
4 | HG02145.hp2 HG02970.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.185-5581G>A | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67636605 | |||||||
| chr14:67636678 | G | C | 1 | a0001c0001t0001g0287 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.185-5508G>C | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67636678 | |||||||
| chr14:67636693 | C | T | 2 | a0001c0001t0001g0084 a0001c0001t0001g0255 |
2 | HG02135.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.185-5493C>T | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67636693 | |||||||
| chr14:67636795 | A | G | 1 | a0003c0004t0001g0107 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.185-5391A>G | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67636795 | |||||||
| chr14:67636853 | C | T | 1 | a0001c0001t0001g0164 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.185-5333C>T | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67636853 | |||||||
| chr14:67636948 | ACAGTTAG others(13): Show |
A | 1 | a0001c0001t0001g0254 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.185-5237_185-5218d others(22): Show |
ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67636948 | |||||||
| chr14:67637017 | C | T | 1 | a0003c0004t0001g0107 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.185-5169C>T | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67637017 | |||||||
| chr14:67637063 | C | T | 18 | a0001c0001t0001g0006 a0001c0001t0001g0051 a0001c0001t0001g0053 others(15): Show |
21 | HG00639.hp1 HG00735.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.185-5123C>T | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67637063 | |||||||
| chr14:67637207 | C | T | 4 | a0001c0001t0001g0164 a0001c0001t0002g0137 a0001c0001t0002g0144 others(1): Show |
4 | HG00642.hp1 HG01109.hp2 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.185-4979C>T | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67637207 | |||||||
| chr14:67637276 | G | A | 81 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(78): Show |
103 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.185-4910G>A | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67637276 | |||||||
| chr14:67637323 | G | A | 1 | a0003c0004t0001g0107 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.185-4863G>A | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67637323 | |||||||
| chr14:67637360 | G | A | 87 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(84): Show |
105 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.185-4826G>A | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67637360 | |||||||
| chr14:67637390 | G | A | 11 | a0001c0001t0002g0158 a0001c0001t0002g0161 a0001c0001t0002g0162 others(8): Show |
14 | HG01081.hp2 HG01884.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.185-4796G>A | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67637390 | |||||||
| chr14:67637410 | C | CA | 16 | a0001c0001t0001g0164 a0001c0001t0001g0224 a0001c0001t0001g0290 others(13): Show |
16 | HG00423.hp2 HG02258.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.185-4753dupA | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr14 | 67637410 | ||||||
| chr14:67637410 | C | CAA | 40 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0038 others(37): Show |
49 | HG00099.hp2 HG01099.hp2 HG01261.hp2 others(46): Show |
intron_variant | MODIFIER | c.185-4754_185-4753d others(4): Show |
ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr14 | 67637410 | ||||||
| chr14:67637410 | C | CAAA | 9 | a0001c0001t0001g0296 a0001c0001t0001g0301 a0001c0001t0001g0308 others(6): Show |
9 | HG00423.hp1 HG00597.hp2 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.185-4755_185-4753d others(5): Show |
ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr14 | 67637410 | ||||||
| chr14:67637410 | CA | C | 48 | a0001c0001t0001g0006 a0001c0001t0001g0051 a0001c0001t0001g0061 others(45): Show |
62 | HG00609.hp1 HG00639.hp1 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.185-4753delA | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr14 | 67637410 | ||||||
| chr14:67637410 | CAA | C | 77 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(74): Show |
99 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.185-4754_185-4753d others(4): Show |
ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr14 | 67637410 | ||||||
| chr14:67637410 | CAAAAAAA | C | 26 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(23): Show |
35 | HG00280.hp1 HG00558.hp1 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.185-4759_185-4753d others(9): Show |
ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr14 | 67637410 | ||||||
| chr14:67637410 | CAAAAAAA others(5): Show |
C | 45 | a0001c0001t0001g0040 a0001c0001t0002g0007 a0001c0001t0002g0012 others(42): Show |
52 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(49): Show |
intron_variant | MODIFIER | c.185-4764_185-4753d others(14): Show |
ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr14 | 67637410 | ||||||
| chr14:67637410 | CAAAAAAA others(6): Show |
C | 3 | a0001c0001t0001g0212 a0001c0001t0002g0027 a0001c0001t0002g0028 |
5 | HG02257.hp1 HG02559.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.185-4765_185-4753d others(15): Show |
ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr14 | 67637410 | ||||||
| chr14:67637702 | G | A | 1 | a0001c0001t0002g0118 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.185-4484G>A | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67637702 | |||||||
| chr14:67637714 | A | C | 349 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(346): Show |
424 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(421): Show |
intron_variant | MODIFIER | c.185-4472A>C | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67637714 | |||||||
| chr14:67637719 | A | G | 3 | a0001c0001t0004g0174 a0001c0001t0004g0175 a0001c0001t0004g0186 |
3 | HG02809.hp2 HG02976.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.185-4467A>G | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67637719 | |||||||
| chr14:67637814 | G | T | 3 | a0001c0001t0002g0158 a0001c0001t0002g0161 a0001c0001t0002g0162 |
3 | HG01081.hp2 HG02486.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.185-4372G>T | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67637814 | |||||||
| chr14:67637918 | T | C | 10 | a0001c0001t0002g0158 a0001c0001t0002g0161 a0001c0001t0002g0162 others(7): Show |
13 | HG01081.hp2 HG02109.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.185-4268T>C | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67637918 | |||||||
| chr14:67638039 | G | A | 7 | a0001c0001t0005g0203 a0001c0001t0005g0344 a0001c0001t0005g0345 others(4): Show |
7 | HG02145.hp2 HG02630.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.185-4147G>A | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67638039 | |||||||
| chr14:67638040 | G | A | 1 | a0001c0001t0001g0279 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.185-4146G>A | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67638040 | |||||||
| chr14:67638041 | C | T | 1 | a0001c0001t0001g0279 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.185-4145C>T | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67638041 | |||||||
| chr14:67638213 | A | G | 1 | a0001c0001t0004g0190 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.185-3973A>G | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67638213 | |||||||
| chr14:67638262 | A | G | 1 | a0003c0004t0001g0107 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.185-3924A>G | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67638262 | |||||||
| chr14:67638273 | T | C | 10 | a0001c0001t0002g0158 a0001c0001t0002g0161 a0001c0001t0002g0162 others(7): Show |
13 | HG01081.hp2 HG02109.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.185-3913T>C | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67638273 | |||||||
| chr14:67638278 | C | T | 1 | a0003c0004t0001g0107 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.185-3908C>T | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67638278 | |||||||
| chr14:67638314 | A | C | 1 | a0001c0001t0002g0152 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.185-3872A>C | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67638314 | |||||||
| chr14:67638369 | CA | C | 261 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(258): Show |
318 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(315): Show |
intron_variant | MODIFIER | c.185-3807delA | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr14 | 67638369 | ||||||
| chr14:67638424 | G | A | 1 | a0003c0004t0001g0107 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.185-3762G>A | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67638424 | |||||||
| chr14:67638617 | T | G | 1 | a0003c0004t0001g0107 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.185-3569T>G | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67638617 | |||||||
| chr14:67638653 | G | A | 1 | a0001c0001t0002g0352 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.185-3533G>A | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67638653 | |||||||
| chr14:67638659 | A | G | 1 | a0001c0001t0002g0352 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.185-3527A>G | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67638659 | |||||||
| chr14:67638660 | G | A | 1 | a0001c0001t0002g0352 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.185-3526G>A | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67638660 | |||||||
| chr14:67638697 | A | C | 1 | a0003c0004t0001g0107 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.185-3489A>C | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67638697 | |||||||
| chr14:67638840 | G | T | 3 | a0002c0002t0002g0008 a0002c0002t0002g0159 a0002c0002t0002g0160 |
6 | HG02109.hp1 HG02572.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.185-3346G>T | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67638840 | |||||||
| chr14:67639004 | C | T | 1 | a0003c0004t0001g0107 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.185-3182C>T | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67639004 | |||||||
| chr14:67639045 | TA | T | 41 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(38): Show |
52 | HG00609.hp1 HG01081.hp2 HG01175.hp1 others(49): Show |
intron_variant | MODIFIER | c.185-3139delA | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr14 | 67639045 | ||||||
| chr14:67639109 | A | G | 1 | a0001c0001t0004g0190 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.185-3077A>G | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67639109 | |||||||
| chr14:67639136 | C | T | 13 | a0001c0001t0002g0002 a0001c0001t0002g0018 a0001c0001t0002g0337 others(10): Show |
21 | HG00609.hp1 HG02080.hp1 NA18612.hp2 others(18): Show |
intron_variant | MODIFIER | c.185-3050C>T | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67639136 | |||||||
| chr14:67639226 | C | T | 2 | a0001c0001t0001g0085 a0001c0001t0001g0086 |
2 | HG03209.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.185-2960C>T | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67639226 | |||||||
| chr14:67639347 | T | C | 1 | a0001c0001t0001g0317 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.185-2839T>C | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67639347 | |||||||
| chr14:67639475 | T | A | 1 | a0001c0001t0004g0173 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.185-2711T>A | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67639475 | |||||||
| chr14:67639537 | G | A | 1 | a0001c0001t0001g0236 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.185-2649G>A | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67639537 | |||||||
| chr14:67639629 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.185-2557C>T | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67639629 | |||||||
| chr14:67639639 | C | G | 17 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(14): Show |
17 | HG01175.hp1 HG02280.hp2 HG02622.hp2 others(14): Show |
intron_variant | MODIFIER | c.185-2547C>G | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67639639 | |||||||
| chr14:67639687 | G | A | 48 | a0001c0001t0001g0040 a0001c0001t0002g0007 a0001c0001t0002g0012 others(45): Show |
57 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.185-2499G>A | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67639687 | |||||||
| chr14:67639817 | T | C | 1 | a0001c0001t0005g0347 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.185-2369T>C | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67639817 | |||||||
| chr14:67639818 | G | T | 1 | a0001c0001t0005g0347 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.185-2368G>T | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67639818 | |||||||
| chr14:67639878 | T | C | 80 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(77): Show |
102 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.185-2308T>C | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67639878 | |||||||
| chr14:67639924 | C | CA | 77 | a0001c0001t0001g0040 a0001c0001t0001g0053 a0001c0001t0001g0101 others(74): Show |
90 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.185-2237dupA | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr14 | 67639924 | ||||||
| chr14:67639924 | C | CAA | 45 | a0001c0001t0001g0120 a0001c0001t0002g0131 a0001c0001t0002g0132 others(42): Show |
55 | HG00408.hp1 HG00408.hp2 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.185-2238_185-2237d others(4): Show |
ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr14 | 67639924 | ||||||
| chr14:67639924 | CA | C | 125 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(122): Show |
150 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.185-2237delA | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr14 | 67639924 | ||||||
| chr14:67639924 | CAAAAA | C | 10 | a0001c0001t0002g0002 a0001c0001t0002g0018 a0001c0001t0002g0337 others(7): Show |
18 | HG00609.hp1 HG02080.hp1 NA18612.hp2 others(15): Show |
intron_variant | MODIFIER | c.185-2241_185-2237d others(7): Show |
ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr14 | 67639924 | ||||||
| chr14:67639949 | A | G | 1 | a0003c0004t0001g0107 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.185-2237A>G | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67639949 | |||||||
| chr14:67640096 | A | T | 18 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(15): Show |
18 | HG01175.hp1 HG01884.hp2 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.185-2090A>T | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67640096 | |||||||
| chr14:67640115 | A | T | 349 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(346): Show |
424 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(421): Show |
intron_variant | MODIFIER | c.185-2071A>T | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67640115 | |||||||
| chr14:67640116 | A | T | 1 | a0001c0001t0002g0137 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.185-2070A>T | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67640116 | |||||||
| chr14:67640453 | G | C | 48 | a0001c0001t0001g0040 a0001c0001t0002g0007 a0001c0001t0002g0012 others(45): Show |
57 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.185-1733G>C | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67640453 | |||||||
| chr14:67640522 | T | C | 1 | a0003c0004t0001g0107 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.185-1664T>C | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67640522 | |||||||
| chr14:67640630 | C | T | 1 | a0003c0004t0001g0107 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.185-1556C>T | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67640630 | |||||||
| chr14:67640662 | A | G | 2 | a0001c0001t0002g0161 a0001c0001t0002g0162 |
2 | HG01081.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.185-1524A>G | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67640662 | |||||||
| chr14:67640773 | C | T | 17 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(14): Show |
17 | HG01175.hp1 HG02280.hp2 HG02622.hp2 others(14): Show |
intron_variant | MODIFIER | c.185-1413C>T | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67640773 | |||||||
| chr14:67640783 | G | A | 1 | a0003c0004t0001g0107 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.185-1403G>A | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67640783 | |||||||
| chr14:67641095 | T | C | 10 | a0001c0001t0002g0158 a0001c0001t0002g0161 a0001c0001t0002g0162 others(7): Show |
13 | HG01081.hp2 HG02109.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.185-1091T>C | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67641095 | |||||||
| chr14:67641187 | A | C | 1 | a0003c0004t0001g0107 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.185-999A>C | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67641187 | |||||||
| chr14:67641376 | C | T | 1 | a0003c0004t0001g0107 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.185-810C>T | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67641376 | |||||||
| chr14:67641495 | C | T | 1 | a0001c0001t0001g0261 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.185-691C>T | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67641495 | |||||||
| chr14:67641562 | T | C | 3 | a0001c0001t0005g0203 a0001c0001t0005g0344 a0001c0001t0005g0345 |
3 | HG02630.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.185-624T>C | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67641562 | |||||||
| chr14:67641694 | C | A | 2 | a0001c0001t0003g0087 a0001c0001t0003g0088 |
2 | HG02976.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.185-492C>A | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67641694 | |||||||
| chr14:67641711 | G | A | 17 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(14): Show |
17 | HG01175.hp1 HG02280.hp2 HG02622.hp2 others(14): Show |
intron_variant | MODIFIER | c.185-475G>A | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67641711 | |||||||
| chr14:67641711 | G | C | 1 | a0001c0001t0001g0212 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.185-475G>C | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67641711 | |||||||
| chr14:67641806 | CTT | C | 7 | a0001c0001t0005g0203 a0001c0001t0005g0344 a0001c0001t0005g0345 others(4): Show |
7 | HG02145.hp2 HG02630.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.185-378_185-377del others(2): Show |
ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr14 | 67641806 | ||||||
| chr14:67641878 | G | A | 1 | a0003c0004t0001g0107 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.185-308G>A | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67641878 | |||||||
| chr14:67642030 | G | A | 82 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(79): Show |
104 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.185-156G>A | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | chr14 | 67642030 | |||||||
| chr14:67642373 | G | A | 1 | a0001c0001t0001g0051 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.362+10G>A | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 3/7 | chr14 | 67642373 | |||||||
| chr14:67642381 | C | T | 1 | a0001c0001t0004g0200 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.362+18C>T | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 3/7 | chr14 | 67642381 | |||||||
| chr14:67642750 | A | G | 1 | a0003c0004t0001g0107 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.362+387A>G | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 3/7 | chr14 | 67642750 | |||||||
| chr14:67642752 | T | C | 3 | a0001c0001t0003g0025 a0001c0001t0003g0116 a0001c0001t0003g0117 |
4 | HG01433.hp2 HG02647.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.362+389T>C | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 3/7 | chr14 | 67642752 | |||||||
| chr14:67642793 | C | CT | 69 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(66): Show |
90 | HG00099.hp2 HG00423.hp1 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.362+457dupT | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr14 | 67642793 | ||||||
| chr14:67642793 | C | CTT | 32 | a0001c0001t0001g0016 a0001c0001t0001g0038 a0001c0001t0001g0129 others(29): Show |
37 | HG00609.hp1 HG01167.hp1 HG01192.hp2 others(34): Show |
intron_variant | MODIFIER | c.362+456_362+457dup others(2): Show |
ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr14 | 67642793 | ||||||
| chr14:67642793 | C | CTTT | 77 | a0001c0001t0001g0120 a0001c0001t0001g0230 a0001c0001t0002g0007 others(74): Show |
96 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.362+455_362+457dup others(3): Show |
ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr14 | 67642793 | ||||||
| chr14:67642793 | C | CTTTT | 33 | a0001c0001t0001g0040 a0001c0001t0002g0028 a0001c0001t0002g0041 others(30): Show |
34 | HG00423.hp2 HG00558.hp2 HG00621.hp2 others(31): Show |
intron_variant | MODIFIER | c.362+454_362+457dup others(4): Show |
ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr14 | 67642793 | ||||||
| chr14:67642793 | C | CTTTTTT | 33 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(30): Show |
45 | HG00597.hp2 HG00621.hp1 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.362+452_362+457dup others(6): Show |
ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr14 | 67642793 | ||||||
| chr14:67642793 | C | CTTTTTTT | 22 | a0001c0001t0001g0009 a0001c0001t0001g0031 a0001c0001t0001g0032 others(19): Show |
31 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(28): Show |
intron_variant | MODIFIER | c.362+451_362+457dup others(7): Show |
ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr14 | 67642793 | ||||||
| chr14:67642793 | C | CTTTTTTT others(1): Show |
12 | a0001c0001t0001g0163 a0001c0001t0001g0211 a0001c0001t0001g0223 others(9): Show |
12 | HG01175.hp2 HG01257.hp2 HG01515.hp1 others(9): Show |
intron_variant | MODIFIER | c.362+450_362+457dup others(8): Show |
ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr14 | 67642793 | ||||||
| chr14:67642793 | C | CTTTTTTT others(2): Show |
6 | a0001c0001t0001g0250 a0001c0001t0001g0272 a0001c0001t0001g0274 others(3): Show |
6 | HG01106.hp2 HG03654.hp2 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.362+449_362+457dup others(9): Show |
ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr14 | 67642793 | ||||||
| chr14:67642793 | C | CTTTTTTT others(5): Show |
3 | a0001c0001t0004g0173 a0001c0001t0004g0174 a0001c0001t0004g0175 |
3 | HG02922.hp1 HG02976.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.362+446_362+457dup others(12): Show |
ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr14 | 67642793 | ||||||
| chr14:67642793 | C | CTTTTTTT others(6): Show |
3 | a0001c0001t0001g0183 a0001c0001t0004g0097 a0001c0001t0004g0186 |
3 | HG01175.hp1 HG02280.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.362+445_362+457dup others(13): Show |
ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr14 | 67642793 | ||||||
| chr14:67642793 | C | CTTTTTTT others(7): Show |
4 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0004g0181 others(1): Show |
4 | HG02622.hp2 HG02818.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.362+444_362+457dup others(14): Show |
ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr14 | 67642793 | ||||||
| chr14:67642793 | CT | C | 9 | a0001c0001t0002g0158 a0001c0001t0002g0162 a0001c0001t0002g0210 others(6): Show |
12 | HG01081.hp2 HG02109.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.362+457delT | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr14 | 67642793 | ||||||
| chr14:67642793 | CTTTTT | C | 7 | a0001c0001t0001g0106 a0001c0001t0004g0176 a0001c0001t0004g0178 others(4): Show |
7 | HG01168.hp2 HG01884.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.362+453_362+457del others(5): Show |
ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr14 | 67642793 | ||||||
| chr14:67642793 | CTTTTTT | C | 15 | a0001c0001t0001g0006 a0001c0001t0001g0051 a0001c0001t0001g0053 others(12): Show |
18 | HG00639.hp1 HG00735.hp1 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.362+452_362+457del others(6): Show |
ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr14 | 67642793 | ||||||
| chr14:67642803 | T | TTTTTC | 11 | a0001c0001t0001g0019 a0001c0001t0001g0045 a0001c0001t0001g0046 others(8): Show |
12 | HG02145.hp1 HG02451.hp1 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.362+444_362+445ins others(5): Show |
ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr14 | 67642803 | ||||||
| chr14:67642888 | T | C | 1 | a0003c0004t0001g0107 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.362+525T>C | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 3/7 | chr14 | 67642888 | |||||||
| chr14:67642926 | C | A | 14 | a0001c0001t0002g0002 a0001c0001t0002g0018 a0001c0001t0002g0337 others(11): Show |
22 | HG00609.hp1 HG02080.hp1 NA18612.hp2 others(19): Show |
intron_variant | MODIFIER | c.362+563C>A | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 3/7 | chr14 | 67642926 | |||||||
| chr14:67643010 | C | T | 10 | a0001c0001t0002g0158 a0001c0001t0002g0161 a0001c0001t0002g0162 others(7): Show |
13 | HG01081.hp2 HG02109.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.362+647C>T | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 3/7 | chr14 | 67643010 | |||||||
| chr14:67643095 | G | A | 14 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(11): Show |
14 | HG01175.hp1 HG02280.hp2 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.362+732G>A | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 3/7 | chr14 | 67643095 | |||||||
| chr14:67643292 | C | T | 3 | a0001c0001t0002g0026 a0001c0001t0002g0125 a0001c0001t0002g0126 |
4 | HG01884.hp1 HG01891.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.362+929C>T | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 3/7 | chr14 | 67643292 | |||||||
| chr14:67643293 | A | G | 48 | a0001c0001t0001g0040 a0001c0001t0002g0007 a0001c0001t0002g0012 others(45): Show |
57 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.362+930A>G | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 3/7 | chr14 | 67643293 | |||||||
| chr14:67643552 | A | G | 1 | a0001c0001t0001g0089 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.362+1189A>G | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 3/7 | chr14 | 67643552 | |||||||
| chr14:67643571 | C | T | 5 | a0001c0001t0004g0097 a0001c0001t0004g0173 a0001c0001t0004g0181 others(2): Show |
5 | HG02280.hp2 HG02622.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.362+1208C>T | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 3/7 | chr14 | 67643571 | |||||||
| chr14:67643616 | G | A | 1 | a0001c0001t0001g0278 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.362+1253G>A | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 3/7 | chr14 | 67643616 | |||||||
| chr14:67643712 | G | A | 3 | a0001c0001t0001g0035 a0001c0001t0001g0273 a0001c0001t0001g0274 |
4 | HG01106.hp2 HG01257.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.362+1349G>A | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 3/7 | chr14 | 67643712 | |||||||
| chr14:67643726 | A | C | 1 | a0001c0001t0003g0075 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.362+1363A>C | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 3/7 | chr14 | 67643726 | |||||||
| chr14:67643772 | C | G | 1 | a0001c0001t0001g0227 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.362+1409C>G | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 3/7 | chr14 | 67643772 | |||||||
| chr14:67643835 | A | G | 61 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0012 others(58): Show |
78 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.362+1472A>G | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 3/7 | chr14 | 67643835 | |||||||
| chr14:67643852 | T | TA | 12 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0291 others(9): Show |
12 | HG02015.hp1 HG02109.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.362+1519dupA | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr14 | 67643852 | ||||||
| chr14:67643852 | T | TAA | 33 | a0001c0001t0002g0012 a0001c0001t0002g0028 a0001c0001t0002g0042 others(30): Show |
39 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.362+1518_362+1519d others(4): Show |
ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr14 | 67643852 | ||||||
| chr14:67643852 | T | TAAA | 20 | a0001c0001t0002g0007 a0001c0001t0002g0026 a0001c0001t0002g0027 others(17): Show |
25 | HG00597.hp1 HG00642.hp1 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.362+1517_362+1519d others(5): Show |
ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr14 | 67643852 | ||||||
| chr14:67643852 | T | TAAAA | 6 | a0001c0001t0002g0029 a0001c0001t0002g0127 a0001c0001t0002g0128 others(3): Show |
7 | HG01358.hp1 HG02027.hp2 HG02148.hp1 others(4): Show |
intron_variant | MODIFIER | c.362+1516_362+1519d others(6): Show |
ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr14 | 67643852 | ||||||
| chr14:67643852 | TA | T | 39 | a0001c0001t0001g0006 a0001c0001t0001g0051 a0001c0001t0001g0061 others(36): Show |
50 | HG00609.hp1 HG00639.hp1 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.362+1519delA | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr14 | 67643852 | ||||||
| chr14:67643852 | TAA | T | 69 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(66): Show |
87 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.362+1518_362+1519d others(4): Show |
ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr14 | 67643852 | ||||||
| chr14:67643852 | TAAAAAAA others(3): Show |
T | 1 | a0001c0001t0002g0151 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.362+1510_362+1519d others(12): Show |
ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr14 | 67643852 | ||||||
| chr14:67643852 | TAAAAAAA others(6): Show |
T | 5 | a0001c0001t0001g0089 a0001c0001t0001g0248 a0001c0001t0001g0276 others(2): Show |
5 | HG01192.hp1 HG01261.hp2 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.362+1507_362+1519d others(15): Show |
ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr14 | 67643852 | ||||||
| chr14:67643852 | TAAAAAAA others(7): Show |
T | 145 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(142): Show |
179 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.362+1506_362+1519d others(16): Show |
ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr14 | 67643852 | ||||||
| chr14:67643852 | TAAAAAAA others(8): Show |
T | 3 | a0001c0001t0001g0247 a0001c0001t0003g0059 a0001c0001t0003g0078 |
3 | NA18962.hp1 NA19003.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.362+1505_362+1519d others(17): Show |
ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr14 | 67643852 | ||||||
| chr14:67643852 | TAAAAAAA others(9): Show |
T | 1 | a0001c0001t0004g0190 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.362+1504_362+1519d others(18): Show |
ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr14 | 67643852 | ||||||
| chr14:67643852 | TAAAAAAA others(10): Show |
T | 1 | a0001c0001t0004g0204 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.362+1503_362+1519d others(19): Show |
ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr14 | 67643852 | ||||||
| chr14:67643883 | G | T | 83 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(80): Show |
105 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.362+1520G>T | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 3/7 | chr14 | 67643883 | |||||||
| chr14:67643910 | C | G | 1 | a0001c0001t0001g0211 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.362+1547C>G | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 3/7 | chr14 | 67643910 | |||||||
| chr14:67643951 | A | T | 1 | a0003c0004t0001g0107 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.362+1588A>T | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 3/7 | chr14 | 67643951 | |||||||
| chr14:67643953 | C | T | 1 | a0003c0004t0001g0107 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.362+1590C>T | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 3/7 | chr14 | 67643953 | |||||||
| chr14:67643995 | G | A | 1 | a0001c0001t0001g0255 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.362+1632G>A | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 3/7 | chr14 | 67643995 | |||||||
| chr14:67644020 | T | G | 87 | a0001c0001t0001g0033 a0001c0001t0001g0250 a0001c0001t0001g0256 others(84): Show |
105 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.363-1623T>G | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 3/7 | chr14 | 67644020 | |||||||
| chr14:67644328 | T | C | 1 | a0001c0001t0001g0047 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.363-1315T>C | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 3/7 | chr14 | 67644328 | |||||||
| chr14:67644408 | T | C | 6 | a0001c0001t0002g0158 a0001c0001t0002g0161 a0001c0001t0002g0162 others(3): Show |
9 | HG01081.hp2 HG02109.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.363-1235T>C | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 3/7 | chr14 | 67644408 | |||||||
| chr14:67644444 | C | A | 2 | a0001c0001t0003g0023 a0001c0001t0003g0064 |
3 | HG00639.hp2 HG01069.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.363-1199C>A | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 3/7 | chr14 | 67644444 | |||||||
| chr14:67644486 | A | G | 20 | a0001c0001t0004g0097 a0001c0001t0004g0173 a0001c0001t0004g0174 others(17): Show |
20 | HG01884.hp2 HG01891.hp2 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.363-1157A>G | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 3/7 | chr14 | 67644486 | |||||||
| chr14:67644532 | C | T | 24 | a0001c0001t0002g0012 a0001c0001t0002g0123 a0001c0001t0002g0128 others(21): Show |
26 | HG00099.hp1 HG00408.hp2 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.363-1111C>T | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 3/7 | chr14 | 67644532 | |||||||
| chr14:67644830 | T | C | 356 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(353): Show |
431 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(428): Show |
intron_variant | MODIFIER | c.363-813T>C | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 3/7 | chr14 | 67644830 | |||||||
| chr14:67644988 | A | G | 1 | a0001c0001t0003g0039 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.363-655A>G | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 3/7 | chr14 | 67644988 | |||||||
| chr14:67644997 | T | TA | 18 | a0001c0001t0001g0243 a0001c0001t0002g0002 a0001c0001t0002g0018 others(15): Show |
26 | HG00609.hp1 HG02080.hp1 HG02258.hp1 others(23): Show |
intron_variant | MODIFIER | c.363-628dupA | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr14 | 67644997 | ||||||
| chr14:67644997 | T | TAA | 46 | a0001c0001t0002g0007 a0001c0001t0002g0012 a0001c0001t0002g0026 others(43): Show |
55 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(52): Show |
intron_variant | MODIFIER | c.363-629_363-628dup others(2): Show |
ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr14 | 67644997 | ||||||
| chr14:67644997 | TA | T | 15 | a0001c0001t0001g0213 a0001c0001t0001g0241 a0001c0001t0001g0316 others(12): Show |
18 | HG01081.hp2 HG01167.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.363-628delA | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr14 | 67644997 | ||||||
| chr14:67645015 | AT | A | 64 | a0001c0001t0003g0003 a0001c0001t0003g0011 a0001c0001t0003g0020 others(61): Show |
76 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.363-626delT | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr14 | 67645015 | ||||||
| chr14:67645016 | T | A | 2 | a0001c0001t0003g0039 a0001c0001t0003g0069 |
2 | HG02258.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.363-627T>A | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 3/7 | chr14 | 67645016 | |||||||
| chr14:67645018 | G | A | 69 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(66): Show |
90 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.363-625G>A | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 3/7 | chr14 | 67645018 | |||||||
| chr14:67645090 | A | AT | 62 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0012 others(59): Show |
79 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.363-552dupT | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr14 | 67645090 | ||||||
| chr14:67645096 | T | G | 62 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0012 others(59): Show |
79 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.363-547T>G | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 3/7 | chr14 | 67645096 | |||||||
| chr14:67645145 | T | C | 1 | a0001c0001t0001g0104 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.363-498T>C | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 3/7 | chr14 | 67645145 | |||||||
| chr14:67645210 | G | C | 350 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(347): Show |
425 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(422): Show |
intron_variant | MODIFIER | c.363-433G>C | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 3/7 | chr14 | 67645210 | |||||||
| chr14:67645299 | C | T | 62 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0012 others(59): Show |
79 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.363-344C>T | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 3/7 | chr14 | 67645299 | |||||||
| chr14:67645317 | C | T | 4 | a0001c0001t0004g0193 a0001c0001t0004g0195 a0001c0001t0004g0198 others(1): Show |
4 | HG01891.hp2 HG02280.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.363-326C>T | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 3/7 | chr14 | 67645317 | |||||||
| chr14:67645318 | T | C | 2 | a0001c0001t0003g0072 a0001c0001t0003g0113 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.363-325T>C | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 3/7 | chr14 | 67645318 | |||||||
| chr14:67646066 | A | C | 61 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0012 others(58): Show |
78 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.522+264A>C | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 4/7 | chr14 | 67646066 | |||||||
| chr14:67646099 | C | A | 1 | a0001c0001t0004g0187 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.522+297C>A | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 4/7 | chr14 | 67646099 | |||||||
| chr14:67646144 | G | A | 1 | a0001c0001t0001g0212 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.522+342G>A | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 4/7 | chr14 | 67646144 | |||||||
| chr14:67646255 | C | T | 2 | a0001c0001t0001g0249 a0001c0001t0001g0275 |
2 | NA18940.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.523-389C>T | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 4/7 | chr14 | 67646255 | |||||||
| chr14:67646297 | A | G | 2 | a0001c0001t0002g0161 a0001c0001t0002g0162 |
2 | HG01081.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.523-347A>G | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 4/7 | chr14 | 67646297 | |||||||
| chr14:67646483 | G | T | 1 | a0001c0001t0001g0319 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.523-161G>T | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 4/7 | chr14 | 67646483 | |||||||
| chr14:67646576 | G | A | 83 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(80): Show |
101 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.523-68G>A | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 4/7 | chr14 | 67646576 | |||||||
| chr14:67647937 | T | C | 1 | a0001c0001t0004g0187 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.723-110T>C | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 6/7 | chr14 | 67647937 | |||||||
| chr14:67647957 | T | C | 1 | a0001c0001t0002g0139 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.723-90T>C | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 6/7 | chr14 | 67647957 | |||||||
| chr14:67648199 | G | A | 2 | a0001c0001t0001g0327 a0001c0001t0001g0328 |
2 | NA18960.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.859+16G>A | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 7/7 | chr14 | 67648199 | |||||||
| chr14:67648284 | A | G | 28 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(25): Show |
37 | HG00280.hp1 HG00558.hp1 HG00733.hp1 others(34): Show |
intron_variant | MODIFIER | c.859+101A>G | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 7/7 | chr14 | 67648284 | |||||||
| chr14:67648324 | G | C | 2 | a0001c0001t0001g0225 a0001c0001t0001g0259 |
2 | HG00280.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.859+141G>C | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 7/7 | chr14 | 67648324 | |||||||
| chr14:67648340 | A | G | 1 | a0001c0001t0001g0226 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.859+157A>G | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 7/7 | chr14 | 67648340 | |||||||
| chr14:67648450 | T | C | 67 | a0001c0001t0003g0003 a0001c0001t0003g0011 a0001c0001t0003g0020 others(64): Show |
79 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.859+267T>C | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 7/7 | chr14 | 67648450 | |||||||
| chr14:67648465 | T | C | 1 | a0001c0001t0001g0244 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.859+282T>C | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 7/7 | chr14 | 67648465 | |||||||
| chr14:67648502 | CAAGAT | C | 19 | a0001c0001t0004g0097 a0001c0001t0004g0173 a0001c0001t0004g0174 others(16): Show |
19 | HG01891.hp2 HG02280.hp1 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.859+329_859+333del others(5): Show |
ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr14 | 67648502 | ||||||
| chr14:67648691 | T | A | 1 | a0001c0001t0001g0245 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.859+508T>A | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 7/7 | chr14 | 67648691 | |||||||
| chr14:67648742 | T | C | 61 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0012 others(58): Show |
78 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.859+559T>C | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 7/7 | chr14 | 67648742 | |||||||
| chr14:67648759 | C | T | 81 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(78): Show |
103 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.859+576C>T | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 7/7 | chr14 | 67648759 | |||||||
| chr14:67649296 | A | G | 1 | a0001c0001t0001g0291 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.859+1113A>G | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 7/7 | chr14 | 67649296 | |||||||
| chr14:67649419 | T | C | 1 | a0001c0001t0003g0056 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.859+1236T>C | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 7/7 | chr14 | 67649419 | |||||||
| chr14:67649607 | A | G | 18 | a0001c0001t0001g0006 a0001c0001t0001g0051 a0001c0001t0001g0053 others(15): Show |
21 | HG00639.hp1 HG00735.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.860-1108A>G | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 7/7 | chr14 | 67649607 | |||||||
| chr14:67649747 | A | G | 1 | a0001c0001t0001g0238 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.860-968A>G | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 7/7 | chr14 | 67649747 | |||||||
| chr14:67650164 | T | G | 82 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(79): Show |
104 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.860-551T>G | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 7/7 | chr14 | 67650164 | |||||||
| chr14:67650289 | C | A | 147 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0012 others(144): Show |
176 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.860-426C>A | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 7/7 | chr14 | 67650289 | |||||||
| chr14:67650367 | G | A | 1 | a0003c0004t0001g0107 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.860-348G>A | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 7/7 | chr14 | 67650367 | |||||||
| chr14:67650440 | C | T | 2 | a0001c0001t0001g0309 a0001c0001t0001g0310 |
2 | NA18986.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.860-275C>T | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 7/7 | chr14 | 67650440 | |||||||
| chr14:67650556 | AGAG | A | 67 | a0001c0001t0003g0003 a0001c0001t0003g0011 a0001c0001t0003g0020 others(64): Show |
79 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.860-156_860-154del others(3): Show |
ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr14 | 67650556 | ||||||
| chr14:67650704 | T | C | 67 | a0001c0001t0003g0003 a0001c0001t0003g0011 a0001c0001t0003g0020 others(64): Show |
79 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.860-11T>C | ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 7/7 | chr14 | 67650704 |