Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 10095 |
| ensemblid | ENSG00000130429.16 |
| hgncid | 704 |
| symbol | ARPC1B |
| name | actin related protein 2/3 complex subunit 1B |
| refseq_nuc | NM_005720.4 |
| refseq_prot | NP_005711.1 |
| ensembl_nuc | ENST00000646101.2 |
| ensembl_prot | ENSP00000496599.1 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 99374730 |
| end | 99394816 |
| strand | + |
| ver | v1.2 |
| region | chr7:99374730-99394816 |
| region5000 | chr7:99369730-99399816 |
| regionname0 | ARPC1B_chr7_99374730_99394816 |
| regionname5000 | ARPC1B_chr7_99369730_99399816 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 372 | 314 | 71 | 39 | 144 | 15 | 43 | 105 | ARPC1B_chr7_99369730_99399816 | ARPC1B | MAYHS others(367): Show |
chr7 | 99369730 | 99399816 |
| a0002 | 0/0 | 372 | 25 | 15 | 1 | 7 | 1 | 1 | 6 | ARPC1B_chr7_99369730_99399816 | ARPC1B | MAYHS others(367): Show |
chr7 | 99369730 | 99399816 |
| a0003 | 0/0 | 372 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ARPC1B_chr7_99369730_99399816 | ARPC1B | MAYHS others(367): Show |
chr7 | 99369730 | 99399816 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1116 | 234 | 11 | 34 | 136 | 12 | 39 | ARPC1B_chr7_99369730_99399816 | ARPC1B | ATGGC others(1111): Show |
chr7 | 99369730 | 99399816 | ||
| a0001c0002 | 0/0 | 1116 | 73 | 60 | 5 | 1 | 3 | 4 | ARPC1B_chr7_99369730_99399816 | ARPC1B | ATGGC others(1111): Show |
chr7 | 99369730 | 99399816 | ||
| a0001c0004 | 0/0 | 1116 | 4 | 0 | 0 | 4 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | ATGGC others(1111): Show |
chr7 | 99369730 | 99399816 | ||
| a0001c0005 | 0/0 | 1116 | 3 | 0 | 0 | 3 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | ATGGC others(1111): Show |
chr7 | 99369730 | 99399816 | ||
| a0002c0003 | 0/0 | 1116 | 25 | 15 | 1 | 7 | 1 | 1 | ARPC1B_chr7_99369730_99399816 | ARPC1B | ATGGC others(1111): Show |
chr7 | 99369730 | 99399816 | ||
| a0003c0006 | 0/0 | 1116 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | ATGGC others(1111): Show |
chr7 | 99369730 | 99399816 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1511 | 124 | 5 | 22 | 67 | 9 | 19 | ARPC1B_chr7_99369730_99399816 | ARPC1B | AGAGC others(1506): Show |
chr7 | 99369730 | 99399816 |
| a0001c0001t0002 | 0/0 | 1513 | 76 | 4 | 4 | 52 | 1 | 15 | ARPC1B_chr7_99369730_99399816 | ARPC1B | AGAGC others(1508): Show |
chr7 | 99369730 | 99399816 |
| a0001c0001t0003 | 0/0 | 1518 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | AGAGC others(1513): Show |
chr7 | 99369730 | 99399816 |
| a0001c0001t0005 | 0/0 | 1512 | 9 | 0 | 2 | 5 | 2 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | AGAGC others(1507): Show |
chr7 | 99369730 | 99399816 |
| a0001c0001t0007 | 0/0 | 1512 | 10 | 0 | 3 | 4 | 0 | 3 | ARPC1B_chr7_99369730_99399816 | ARPC1B | AGAGC others(1507): Show |
chr7 | 99369730 | 99399816 |
| a0001c0001t0008 | 0/0 | 1514 | 7 | 2 | 1 | 3 | 0 | 1 | ARPC1B_chr7_99369730_99399816 | ARPC1B | AGAGC others(1509): Show |
chr7 | 99369730 | 99399816 |
| a0001c0001t0015 | 0/0 | 1510 | 2 | 0 | 0 | 2 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | AGAGC others(1505): Show |
chr7 | 99369730 | 99399816 |
| a0001c0001t0017 | 0/0 | 1513 | 2 | 0 | 1 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | AGAGC others(1508): Show |
chr7 | 99369730 | 99399816 |
| a0001c0001t0020 | 0/0 | 1513 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC1B_chr7_99369730_99399816 | ARPC1B | AGAGC others(1508): Show |
chr7 | 99369730 | 99399816 |
| a0001c0001t0021 | 0/0 | 1514 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | AGAGC others(1509): Show |
chr7 | 99369730 | 99399816 |
| a0001c0001t0022 | 0/0 | 1514 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | AGAGC others(1509): Show |
chr7 | 99369730 | 99399816 |
| a0001c0002t0003 | 0/0 | 1518 | 22 | 14 | 0 | 1 | 3 | 4 | ARPC1B_chr7_99369730_99399816 | ARPC1B | AGAGC others(1513): Show |
chr7 | 99369730 | 99399816 |
| a0001c0002t0004 | 0/0 | 1513 | 21 | 16 | 5 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | AGAGC others(1508): Show |
chr7 | 99369730 | 99399816 |
| a0001c0002t0009 | 0/0 | 1519 | 6 | 6 | 0 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | AGAGC others(1514): Show |
chr7 | 99369730 | 99399816 |
| a0001c0002t0010 | 0/0 | 1515 | 6 | 6 | 0 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | AGAGC others(1510): Show |
chr7 | 99369730 | 99399816 |
| a0001c0002t0012 | 0/0 | 1514 | 4 | 4 | 0 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | AGAGC others(1509): Show |
chr7 | 99369730 | 99399816 |
| a0001c0002t0013 | 0/0 | 1513 | 4 | 4 | 0 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | AGAGC others(1508): Show |
chr7 | 99369730 | 99399816 |
| a0001c0002t0014 | 0/0 | 1512 | 4 | 4 | 0 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | AGAGC others(1507): Show |
chr7 | 99369730 | 99399816 |
| a0001c0002t0016 | 0/0 | 1516 | 3 | 3 | 0 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | AGAGC others(1511): Show |
chr7 | 99369730 | 99399816 |
| a0001c0002t0019 | 0/0 | 1514 | 2 | 2 | 0 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | AGAGC others(1509): Show |
chr7 | 99369730 | 99399816 |
| a0001c0002t0025 | 0/0 | 1517 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | AGAGC others(1512): Show |
chr7 | 99369730 | 99399816 |
| a0001c0004t0001 | 0/0 | 1511 | 4 | 0 | 0 | 4 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | AGAGC others(1506): Show |
chr7 | 99369730 | 99399816 |
| a0001c0005t0001 | 0/0 | 1511 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | AGAGC others(1506): Show |
chr7 | 99369730 | 99399816 |
| a0001c0005t0007 | 0/0 | 1512 | 2 | 0 | 0 | 2 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | AGAGC others(1507): Show |
chr7 | 99369730 | 99399816 |
| a0002c0003t0005 | 0/0 | 1512 | 3 | 3 | 0 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | AGAGC others(1507): Show |
chr7 | 99369730 | 99399816 |
| a0002c0003t0006 | 0/0 | 1510 | 12 | 6 | 1 | 4 | 1 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | AGAGC others(1505): Show |
chr7 | 99369730 | 99399816 |
| a0002c0003t0011 | 0/0 | 1511 | 5 | 5 | 0 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | AGAGC others(1506): Show |
chr7 | 99369730 | 99399816 |
| a0002c0003t0015 | 0/0 | 1510 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | AGAGC others(1505): Show |
chr7 | 99369730 | 99399816 |
| a0002c0003t0018 | 0/0 | 1509 | 2 | 0 | 0 | 2 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | AGAGC others(1504): Show |
chr7 | 99369730 | 99399816 |
| a0002c0003t0023 | 0/0 | 1513 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | AGAGC others(1508): Show |
chr7 | 99369730 | 99399816 |
| a0002c0003t0024 | 0/0 | 1511 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC1B_chr7_99369730_99399816 | ARPC1B | AGAGC others(1506): Show |
chr7 | 99369730 | 99399816 |
| a0003c0006t0001 | 0/0 | 1511 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | AGAGC others(1506): Show |
chr7 | 99369730 | 99399816 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 1/0 | 4 | 0 | 0 | 2 | 1 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0001g0003 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0001g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0001g0008 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0001g0014 | 0/0 | 3 | 1 | 1 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0001g0244 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0002g0001 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0002g0006 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0002g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0002g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0002g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0002g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0002g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0002g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0003g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0005g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0005g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0005g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0005g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0005g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0005g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0005g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0005g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0007g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0007g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0007g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0007g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0007g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0007g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0007g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0007g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0007g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0007g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0008g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0008g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0008g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0008g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0008g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0008g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0008g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0015g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0015g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0017g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0017g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0020g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0021g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0001t0022g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0002t0003g0004 | 0/0 | 4 | 3 | 0 | 0 | 0 | 1 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0002t0003g0019 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0002t0003g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0002t0003g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0002t0003g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0002t0003g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0002t0003g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0002t0003g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0002t0003g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0002t0003g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0002t0003g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0002t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0002t0003g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0002t0003g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0002t0003g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0002t0003g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0002t0003g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0002t0003g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0002t0004g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0002t0004g0011 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0002t0004g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0002t0004g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0002t0004g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0002t0004g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0002t0004g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0002t0004g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0002t0004g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0002t0004g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0002t0004g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0002t0004g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0002t0004g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0002t0004g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0002t0004g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0002t0004g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0002t0009g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0002t0009g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0002t0009g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0002t0009g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0002t0009g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0002t0010g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0002t0010g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0002t0010g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0002t0010g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0002t0010g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0002t0010g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0002t0012g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0002t0012g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0002t0012g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0002t0012g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0002t0013g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0002t0013g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0002t0013g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0002t0013g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0002t0014g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0002t0014g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0002t0014g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0002t0014g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0002t0016g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0002t0016g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0002t0016g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0002t0019g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0002t0025g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0004t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0004t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0004t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0005t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0001c0005t0007g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0002c0003t0005g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0002c0003t0005g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0002c0003t0006g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0002c0003t0006g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0002c0003t0006g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0002c0003t0006g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0002c0003t0006g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0002c0003t0006g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0002c0003t0006g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0002c0003t0006g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0002c0003t0006g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0002c0003t0006g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0002c0003t0011g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0002c0003t0011g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0002c0003t0011g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0002c0003t0011g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0002c0003t0011g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0002c0003t0015g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0002c0003t0018g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0002c0003t0018g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0002c0003t0023g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0002c0003t0024g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| a0003c0006t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0003 | t0006 | g0087 | EUR | GBR | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0171 | EUR | GBR | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0207 | EUR | GBR | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG00140 | hp2 | a0001 | c0001 | t0005 | g0188 | EUR | GBR | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0141 | EUR | FIN | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG00280 | hp2 | a0001 | c0001 | t0005 | g0170 | EUR | FIN | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0178 | EUR | FIN | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0194 | EUR | FIN | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | CHS | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | CHS | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG00438 | hp1 | a0001 | c0004 | t0001 | g0251 | EAS | CHS | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0114 | EAS | CHS | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0106 | EAS | CHS | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | CHS | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0120 | EAS | CHS | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG00597 | hp1 | a0001 | c0001 | t0008 | g0275 | EAS | CHS | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | CHS | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | CHS | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | CHS | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | CHS | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | CHS | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | PUR | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0210 | AMR | PUR | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | CHS | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | CHS | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG01081 | hp1 | a0001 | c0002 | t0004 | g0269 | AMR | PUR | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG01081 | hp2 | a0001 | c0002 | t0004 | g0011 | AMR | PUR | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0134 | AMR | PUR | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0215 | AMR | PUR | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0238 | AMR | PUR | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0249 | AMR | PUR | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG01167 | hp1 | a0001 | c0001 | t0007 | g0002 | AMR | PUR | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG01167 | hp2 | a0001 | c0002 | t0004 | g0040 | AMR | PUR | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG01169 | hp1 | a0001 | c0001 | t0005 | g0186 | AMR | PUR | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG01169 | hp2 | a0001 | c0002 | t0004 | g0041 | AMR | PUR | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG01175 | hp1 | a0002 | c0003 | t0006 | g0088 | AMR | PUR | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG01175 | hp2 | a0001 | c0001 | t0007 | g0189 | AMR | PUR | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0234 | AMR | PUR | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0127 | AMR | PUR | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG01243 | hp1 | a0001 | c0002 | t0004 | g0044 | AMR | PUR | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG01243 | hp2 | a0001 | c0001 | t0007 | g0180 | AMR | PUR | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | CLM | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | CLM | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG01346 | hp1 | a0001 | c0001 | t0003 | g0054 | AMR | CLM | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | CLM | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0250 | AMR | CLM | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | CLM | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | CLM | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG01433 | hp2 | a0001 | c0001 | t0008 | g0131 | AMR | CLM | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0119 | AMR | CLM | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0200 | EUR | IBS | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0158 | EUR | IBS | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG01516 | hp1 | a0001 | c0002 | t0003 | g0053 | EUR | IBS | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0174 | EUR | IBS | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG01517 | hp1 | a0001 | c0002 | t0003 | g0019 | EUR | IBS | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0243 | EUR | IBS | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG01884 | hp1 | a0001 | c0002 | t0004 | g0034 | AFR | ACB | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG01884 | hp2 | a0001 | c0001 | t0008 | g0111 | AFR | ACB | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG01891 | hp1 | a0001 | c0002 | t0004 | g0268 | AFR | ACB | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG01891 | hp2 | a0001 | c0002 | t0003 | g0069 | AFR | ACB | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG01934 | hp2 | a0001 | c0001 | t0005 | g0236 | AMR | PEL | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0129 | AMR | PEL | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | PEL | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | PEL | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG01978 | hp2 | a0001 | c0001 | t0017 | g0209 | AMR | PEL | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | KHV | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | KHV | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | KHV | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | KHV | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG02055 | hp1 | a0001 | c0002 | t0014 | g0081 | AFR | ACB | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0237 | AFR | ACB | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0279 | EAS | KHV | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | KHV | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | KHV | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | KHV | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | KHV | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0135 | EAS | KHV | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG02080 | hp1 | a0001 | c0001 | t0008 | g0130 | EAS | KHV | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | KHV | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG02083 | hp1 | a0001 | c0002 | t0003 | g0058 | EAS | KHV | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | KHV | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | KHV | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG02135 | hp2 | a0001 | c0001 | t0007 | g0008 | EAS | KHV | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG02257 | hp1 | a0002 | c0003 | t0011 | g0258 | AFR | ACB | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG02257 | hp2 | a0001 | c0002 | t0003 | g0046 | AFR | ACB | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG02258 | hp1 | a0001 | c0002 | t0009 | g0051 | AFR | ACB | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG02258 | hp2 | a0002 | c0003 | t0006 | g0076 | AFR | ACB | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | ACB | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG02280 | hp2 | a0001 | c0002 | t0009 | g0018 | AFR | ACB | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG02451 | hp1 | a0001 | c0002 | t0012 | g0038 | AFR | ACB | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG02451 | hp2 | a0001 | c0002 | t0010 | g0264 | AFR | ACB | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0122 | EAS | KHV | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG02523 | hp2 | a0002 | c0003 | t0006 | g0085 | EAS | KHV | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG02602 | hp2 | a0001 | c0002 | t0003 | g0057 | SAS | PJL | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG02615 | hp1 | a0001 | c0002 | t0010 | g0265 | AFR | GWD | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG02615 | hp2 | a0002 | c0003 | t0006 | g0005 | AFR | GWD | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG02622 | hp1 | a0001 | c0002 | t0009 | g0066 | AFR | GWD | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG02622 | hp2 | a0001 | c0002 | t0009 | g0050 | AFR | GWD | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0138 | AFR | GWD | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG02630 | hp2 | a0001 | c0002 | t0004 | g0011 | AFR | GWD | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG02647 | hp1 | a0001 | c0002 | t0004 | g0033 | AFR | GWD | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG02647 | hp2 | a0001 | c0002 | t0019 | g0020 | AFR | GWD | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0219 | SAS | PJL | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0240 | SAS | PJL | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG02717 | hp1 | a0001 | c0002 | t0004 | g0017 | AFR | GWD | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG02717 | hp2 | a0001 | c0002 | t0014 | g0015 | AFR | GWD | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG02723 | hp1 | a0001 | c0002 | t0003 | g0055 | AFR | GWD | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG02723 | hp2 | a0001 | c0002 | t0003 | g0032 | AFR | GWD | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0105 | SAS | PJL | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0091 | SAS | PJL | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0277 | SAS | PJL | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG02738 | hp2 | a0001 | c0001 | t0007 | g0093 | SAS | PJL | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG02809 | hp1 | a0001 | c0002 | t0016 | g0280 | AFR | GWD | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG02809 | hp2 | a0002 | c0003 | t0015 | g0080 | AFR | GWD | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0110 | AFR | GWD | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG02818 | hp2 | a0001 | c0002 | t0004 | g0017 | AFR | GWD | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG02886 | hp1 | a0001 | c0002 | t0004 | g0016 | AFR | GWD | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG02886 | hp2 | a0001 | c0002 | t0004 | g0039 | AFR | GWD | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0026 | AFR | GWD | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG02895 | hp2 | a0001 | c0002 | t0003 | g0045 | AFR | GWD | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG02896 | hp1 | a0002 | c0003 | t0006 | g0077 | AFR | GWD | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG02896 | hp2 | a0001 | c0002 | t0013 | g0063 | AFR | GWD | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG02897 | hp1 | a0001 | c0002 | t0014 | g0270 | AFR | GWD | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0026 | AFR | GWD | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG02922 | hp1 | a0001 | c0002 | t0003 | g0004 | AFR | ESN | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG02922 | hp2 | a0001 | c0002 | t0004 | g0010 | AFR | ESN | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG02965 | hp1 | a0002 | c0003 | t0005 | g0078 | AFR | ESN | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG02965 | hp2 | a0001 | c0002 | t0003 | g0004 | AFR | ESN | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG02970 | hp1 | a0002 | c0003 | t0011 | g0255 | AFR | ESN | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG02970 | hp2 | a0001 | c0002 | t0004 | g0010 | AFR | ESN | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG03017 | hp1 | a0001 | c0001 | t0008 | g0022 | SAS | PJL | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG03041 | hp1 | a0001 | c0002 | t0004 | g0267 | AFR | GWD | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG03041 | hp2 | a0001 | c0002 | t0004 | g0011 | AFR | GWD | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG03130 | hp1 | a0001 | c0002 | t0019 | g0020 | AFR | ESN | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG03130 | hp2 | a0001 | c0002 | t0012 | g0037 | AFR | ESN | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG03139 | hp1 | a0001 | c0002 | t0003 | g0052 | AFR | ESN | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG03139 | hp2 | a0001 | c0002 | t0003 | g0059 | AFR | ESN | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG03209 | hp1 | a0002 | c0003 | t0005 | g0005 | AFR | MSL | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG03209 | hp2 | a0001 | c0002 | t0003 | g0068 | AFR | MSL | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG03225 | hp1 | a0002 | c0003 | t0006 | g0005 | AFR | MSL | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG03225 | hp2 | a0002 | c0003 | t0006 | g0079 | AFR | MSL | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0097 | SAS | PJL | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0208 | SAS | PJL | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG03453 | hp1 | a0001 | c0002 | t0004 | g0035 | AFR | MSL | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG03453 | hp2 | a0001 | c0002 | t0012 | g0042 | AFR | MSL | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG03486 | hp1 | a0002 | c0003 | t0005 | g0005 | AFR | MSL | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG03486 | hp2 | a0001 | c0002 | t0010 | g0073 | AFR | MSL | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0214 | SAS | PJL | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0089 | SAS | PJL | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0166 | SAS | PJL | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0167 | SAS | PJL | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0090 | SAS | PJL | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0165 | SAS | PJL | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG03516 | hp1 | a0001 | c0002 | t0010 | g0263 | AFR | ESN | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG03516 | hp2 | a0001 | c0002 | t0003 | g0067 | AFR | ESN | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG03540 | hp1 | a0001 | c0002 | t0016 | g0262 | AFR | GWD | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG03540 | hp2 | a0001 | c0002 | t0025 | g0065 | AFR | GWD | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG03579 | hp1 | a0002 | c0003 | t0006 | g0266 | AFR | MSL | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG03579 | hp2 | a0001 | c0002 | t0004 | g0036 | AFR | MSL | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG03654 | hp1 | a0001 | c0002 | t0003 | g0019 | SAS | PJL | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0169 | SAS | PJL | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG03669 | hp2 | a0001 | c0002 | t0003 | g0056 | SAS | PJL | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0221 | SAS | STU | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0104 | SAS | STU | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG03704 | hp1 | a0002 | c0003 | t0024 | g0084 | SAS | PJL | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0197 | SAS | PJL | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG03710 | hp1 | a0001 | c0001 | t0020 | g0100 | SAS | PJL | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0099 | SAS | PJL | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG03831 | hp1 | a0001 | c0002 | t0003 | g0004 | SAS | BEB | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG03831 | hp2 | a0001 | c0001 | t0007 | g0201 | SAS | BEB | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0022 | SAS | BEB | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG03927 | hp2 | a0001 | c0001 | t0007 | g0030 | SAS | BEB | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0112 | SAS | BEB | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0103 | SAS | BEB | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0155 | SAS | STU | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0136 | SAS | STU | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0205 | SAS | BEB | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0273 | SAS | BEB | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | STU | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0092 | SAS | STU | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0271 | SAS | STU | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0151 | SAS | STU | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA18522 | hp1 | a0001 | c0002 | t0003 | g0004 | AFR | YRI | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA18522 | hp2 | a0001 | c0002 | t0016 | g0261 | AFR | YRI | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA18612 | hp1 | a0001 | c0001 | t0015 | g0226 | EAS | CHB | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | CHB | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA18906 | hp1 | a0001 | c0002 | t0013 | g0015 | AFR | YRI | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA18906 | hp2 | a0001 | c0002 | t0004 | g0010 | AFR | YRI | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA18939 | hp1 | a0002 | c0003 | t0006 | g0012 | EAS | JPT | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA18945 | hp1 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA18946 | hp1 | a0001 | c0005 | t0001 | g0193 | EAS | JPT | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA18950 | hp1 | a0001 | c0005 | t0007 | g0028 | EAS | JPT | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA18959 | hp1 | a0001 | c0005 | t0007 | g0028 | EAS | JPT | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0272 | EAS | JPT | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA18962 | hp1 | a0001 | c0001 | t0007 | g0107 | EAS | JPT | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA18964 | hp2 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0274 | EAS | JPT | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA18966 | hp1 | a0003 | c0006 | t0001 | g0027 | EAS | JPT | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA18967 | hp2 | a0001 | c0001 | t0007 | g0144 | EAS | JPT | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA18968 | hp2 | a0001 | c0001 | t0005 | g0070 | EAS | JPT | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA18969 | hp1 | a0001 | c0001 | t0015 | g0222 | EAS | JPT | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA18971 | hp1 | a0002 | c0003 | t0018 | g0012 | EAS | JPT | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA18982 | hp1 | a0001 | c0001 | t0005 | g0013 | EAS | JPT | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA18989 | hp1 | a0002 | c0003 | t0006 | g0082 | EAS | JPT | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA18989 | hp2 | a0001 | c0001 | t0017 | g0190 | EAS | JPT | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA18997 | hp2 | a0001 | c0001 | t0002 | g0276 | EAS | JPT | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA19002 | hp1 | a0002 | c0003 | t0006 | g0012 | EAS | JPT | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA19005 | hp1 | a0001 | c0001 | t0008 | g0126 | EAS | JPT | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA19006 | hp2 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA19010 | hp2 | a0001 | c0004 | t0001 | g0031 | EAS | JPT | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA19030 | hp1 | a0001 | c0002 | t0013 | g0047 | AFR | LWK | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | LWK | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA19043 | hp1 | a0001 | c0002 | t0009 | g0049 | AFR | LWK | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA19043 | hp2 | a0001 | c0002 | t0012 | g0016 | AFR | LWK | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA19054 | hp1 | a0002 | c0003 | t0018 | g0086 | EAS | JPT | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA19063 | hp2 | a0001 | c0004 | t0001 | g0009 | EAS | JPT | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA19075 | hp1 | a0002 | c0003 | t0023 | g0083 | EAS | JPT | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA19078 | hp1 | a0001 | c0001 | t0007 | g0278 | EAS | JPT | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA19078 | hp2 | a0001 | c0001 | t0021 | g0117 | EAS | JPT | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA19080 | hp1 | a0001 | c0004 | t0001 | g0031 | EAS | JPT | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA19086 | hp1 | a0001 | c0001 | t0022 | g0118 | EAS | JPT | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA19088 | hp1 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA19240 | hp1 | a0001 | c0002 | t0003 | g0061 | AFR | YRI | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA19240 | hp2 | a0002 | c0003 | t0011 | g0256 | AFR | YRI | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA20129 | hp1 | a0001 | c0002 | t0003 | g0048 | AFR | ASW | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA20129 | hp2 | a0001 | c0002 | t0009 | g0018 | AFR | ASW | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA20752 | hp2 | a0001 | c0002 | t0003 | g0062 | EUR | TSI | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0006 | SAS | GIH | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0195 | SAS | GIH | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG02486 | hp1 | a0001 | c0002 | t0013 | g0060 | AFR | ACB | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG02486 | hp2 | a0001 | c0002 | t0010 | g0074 | AFR | ACB | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG02559 | hp1 | a0001 | c0002 | t0004 | g0043 | AFR | ACB | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG02559 | hp2 | a0001 | c0001 | t0008 | g0109 | AFR | ACB | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG03471 | hp1 | a0001 | c0002 | t0010 | g0075 | AFR | MSL | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG03471 | hp2 | a0002 | c0003 | t0011 | g0254 | AFR | MSL | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | USA | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| HG06807 | hp2 | a0002 | c0003 | t0011 | g0257 | AFR | USA | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | USA | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| NA20300 | hp2 | a0001 | c0002 | t0014 | g0064 | AFR | USA | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0244 | REF | REF | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0002 | REF | REF | ARPC1B_chr7_99369730_99399816 | ARPC1B | chr7 | 99369730 | 99399816 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:99386731 | G | C | 1 | a0002 | 25 | HG00099.hp1 HG01175.hp1 HG02257.hp1 others(22): Show |
missense_variant | MODERATE | c.111G>C | p.Lys37Asn | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 3/10 | 176/1511 | 111/1119 | 37/372 | chr7 | 99386731 | |||
| chr7:99392746 | G | T | 1 | a0003 | 1 | NA18966.hp1 | missense_variant | MODERATE | c.859G>T | p.Val287Phe | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 8/10 | 924/1511 | 859/1119 | 287/372 | chr7 | 99392746 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:99386776 | C | T | 1 | a0001c0002 | 73 | HG01081.hp1 HG01081.hp2 HG01167.hp2 others(70): Show |
synonymous_variant | LOW | c.156C>T | p.Asn52Asn | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 3/10 | 221/1511 | 156/1119 | 52/372 | chr7 | 99386776 | |||
| chr7:99391040 | C | T | 1 | a0001c0005 | 3 | NA18946.hp1 NA18950.hp1 NA18959.hp1 |
synonymous_variant | LOW | c.648C>T | p.Arg216Arg | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 6/10 | 713/1511 | 648/1119 | 216/372 | chr7 | 99391040 | |||
| chr7:99392796 | G | A | 1 | a0001c0004 | 4 | HG00438.hp1 NA19010.hp2 NA19063.hp2 others(1): Show |
synonymous_variant | LOW | c.909G>A | p.Gln303Gln | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 8/10 | 974/1511 | 909/1119 | 303/372 | chr7 | 99392796 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:99374741 | G | C | 1 | a0001c0001t0020 | 1 | HG03710.hp1 | 5_prime_UTR_variant | MODIFIER | c.-54G>C | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/10 | 10974 | chr7 | 99374741 | ||||||
| chr7:99394517 | T | G | 1 | a0001c0001t0021 | 1 | NA19078.hp2 | 3_prime_UTR_variant | MODIFIER | c.*28T>G | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 10/10 | 28 | chr7 | 99394517 | ||||||
| chr7:99394630 | G | T | 11 | a0001c0001t0003 a0001c0002t0003 a0001c0002t0004 others(8): Show |
74 | HG01081.hp1 HG01081.hp2 HG01167.hp2 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*141G>T | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 10/10 | 141 | chr7 | 99394630 | ||||||
| chr7:99394698 | G | GA | 7 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0008 others(4): Show |
113 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(110): Show |
3_prime_UTR_variant | MODIFIER | c.*223dupA | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 10/10 | 224 | INFO_REALIGN_3_PRIME | chr7 | 99394698 | |||||
| chr7:99394698 | G | GAA | 6 | a0001c0001t0021 a0001c0001t0022 a0001c0002t0004 others(3): Show |
29 | HG01081.hp1 HG01081.hp2 HG01167.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*222_*223dupAA | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 10/10 | 224 | INFO_REALIGN_3_PRIME | chr7 | 99394698 | |||||
| chr7:99394698 | G | GAAA | 3 | a0001c0002t0010 a0001c0002t0016 a0001c0002t0019 |
11 | HG02451.hp2 HG02486.hp2 HG02615.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*221_*223dupAAA | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 10/10 | 224 | INFO_REALIGN_3_PRIME | chr7 | 99394698 | |||||
| chr7:99394698 | G | GAAAAA | 4 | a0001c0001t0003 a0001c0002t0003 a0001c0002t0009 others(1): Show |
30 | HG01346.hp1 HG01516.hp1 HG01517.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*219_*223dupAAAAA | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 10/10 | 224 | INFO_REALIGN_3_PRIME | chr7 | 99394698 | |||||
| chr7:99394779 | T | TA | 10 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0020 others(7): Show |
106 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(103): Show |
3_prime_UTR_variant | MODIFIER | c.*312dupA | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 10/10 | 313 | INFO_REALIGN_3_PRIME | chr7 | 99394779 | |||||
| chr7:99394779 | T | TAA | 6 | a0001c0001t0003 a0001c0001t0008 a0001c0001t0017 others(3): Show |
39 | HG00597.hp1 HG01346.hp1 HG01433.hp2 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*311_*312dupAA | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 10/10 | 313 | INFO_REALIGN_3_PRIME | chr7 | 99394779 | |||||
| chr7:99394779 | T | TAAA | 1 | a0001c0002t0009 | 6 | HG02258.hp1 HG02280.hp2 HG02622.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*310_*312dupAAA | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 10/10 | 313 | INFO_REALIGN_3_PRIME | chr7 | 99394779 | |||||
| chr7:99394779 | TA | T | 3 | a0001c0001t0015 a0002c0003t0011 a0002c0003t0015 |
8 | HG02257.hp1 HG02809.hp2 HG02970.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*312delA | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 10/10 | 312 | INFO_REALIGN_3_PRIME | chr7 | 99394779 | |||||
| chr7:99394779 | TAA | T | 3 | a0002c0003t0006 a0002c0003t0018 a0002c0003t0024 |
15 | HG00099.hp1 HG01175.hp1 HG02258.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*311_*312delAA | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 10/10 | 311 | INFO_REALIGN_3_PRIME | chr7 | 99394779 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:99374800 | C | T | 1 | a0001c0002t0016g0280 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-14+19C>T | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99374800 | |||||||
| chr7:99374834 | T | TG | 10 | a0001c0001t0001g0277 a0001c0001t0002g0271 a0001c0001t0002g0272 others(7): Show |
10 | HG00597.hp1 HG02056.hp1 HG02738.hp1 others(7): Show |
intron_variant | MODIFIER | c.-14+60dupG | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 99374834 | ||||||
| chr7:99374938 | A | T | 9 | a0001c0002t0004g0267 a0001c0002t0004g0268 a0001c0002t0004g0269 others(6): Show |
9 | HG01081.hp1 HG01891.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.-14+157A>T | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99374938 | |||||||
| chr7:99375061 | G | A | 1 | a0001c0002t0003g0032 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-14+280G>A | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99375061 | |||||||
| chr7:99375095 | TC | T | 49 | a0001c0001t0003g0054 a0001c0002t0003g0004 a0001c0002t0003g0019 others(46): Show |
59 | HG01081.hp2 HG01167.hp2 HG01169.hp2 others(56): Show |
intron_variant | MODIFIER | c.-14+317delC | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 99375095 | ||||||
| chr7:99375143 | GCTTCCGC others(7): Show |
G | 1 | a0001c0001t0005g0070 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-14+371_-14+384del others(14): Show |
ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 99375143 | ||||||
| chr7:99375178 | C | G | 1 | a0001c0001t0002g0279 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-14+397C>G | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99375178 | |||||||
| chr7:99375327 | C | T | 1 | a0001c0001t0001g0260 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-14+546C>T | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99375327 | |||||||
| chr7:99375365 | C | T | 1 | a0001c0001t0001g0259 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-14+584C>T | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99375365 | |||||||
| chr7:99375513 | C | T | 5 | a0002c0003t0011g0254 a0002c0003t0011g0255 a0002c0003t0011g0256 others(2): Show |
5 | HG02257.hp1 HG02970.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.-14+732C>T | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99375513 | |||||||
| chr7:99375573 | G | GC | 158 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0013 others(155): Show |
187 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(184): Show |
intron_variant | MODIFIER | c.-14+794dupC | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 99375573 | ||||||
| chr7:99375573 | GCCTGGGG others(12): Show |
G | 1 | a0001c0001t0002g0071 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.-14+795_-14+813del others(19): Show |
ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 99375573 | ||||||
| chr7:99375643 | C | G | 1 | a0001c0001t0002g0142 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.-14+862C>G | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99375643 | |||||||
| chr7:99375656 | C | G | 49 | a0001c0001t0003g0054 a0001c0002t0003g0004 a0001c0002t0003g0019 others(46): Show |
59 | HG01081.hp2 HG01167.hp2 HG01169.hp2 others(56): Show |
intron_variant | MODIFIER | c.-14+875C>G | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99375656 | |||||||
| chr7:99375661 | A | C | 1 | a0001c0001t0001g0253 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-14+880A>C | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99375661 | |||||||
| chr7:99375675 | C | T | 30 | a0001c0001t0003g0054 a0001c0002t0003g0004 a0001c0002t0003g0019 others(27): Show |
35 | HG01346.hp1 HG01516.hp1 HG01517.hp1 others(32): Show |
intron_variant | MODIFIER | c.-14+894C>T | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99375675 | |||||||
| chr7:99375788 | C | A | 2 | a0001c0002t0013g0015 a0001c0002t0014g0015 |
2 | HG02717.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-14+1007C>A | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99375788 | |||||||
| chr7:99375789 | G | C | 1 | a0001c0001t0002g0072 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-14+1008G>C | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99375789 | |||||||
| chr7:99375875 | G | A | 1 | a0001c0002t0004g0033 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-14+1094G>A | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99375875 | |||||||
| chr7:99375907 | C | T | 75 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0013 others(72): Show |
90 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.-14+1126C>T | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99375907 | |||||||
| chr7:99376061 | C | CA | 85 | a0001c0001t0001g0027 a0001c0001t0001g0143 a0001c0001t0001g0145 others(82): Show |
98 | HG00544.hp1 HG01081.hp2 HG01167.hp2 others(95): Show |
intron_variant | MODIFIER | c.-14+1296dupA | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 99376061 | ||||||
| chr7:99376061 | C | CAA | 8 | a0001c0001t0002g0089 a0001c0001t0002g0090 a0001c0001t0002g0091 others(5): Show |
10 | HG01884.hp1 HG02056.hp1 HG02735.hp2 others(7): Show |
intron_variant | MODIFIER | c.-14+1295_-14+1296d others(4): Show |
ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 99376061 | ||||||
| chr7:99376061 | CA | C | 24 | a0001c0001t0001g0252 a0001c0002t0014g0081 a0001c0002t0019g0020 others(21): Show |
28 | HG00099.hp1 HG01175.hp1 HG02055.hp1 others(25): Show |
intron_variant | MODIFIER | c.-14+1296delA | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 99376061 | ||||||
| chr7:99376082 | C | G | 4 | a0001c0002t0003g0067 a0001c0002t0003g0068 a0001c0002t0003g0069 others(1): Show |
4 | HG01891.hp2 HG02622.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-14+1301C>G | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99376082 | |||||||
| chr7:99376229 | T | C | 2 | a0001c0001t0001g0149 a0001c0001t0001g0150 |
2 | NA19004.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.-14+1448T>C | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99376229 | |||||||
| chr7:99376364 | GCAAGACA others(1): Show |
G | 3 | a0001c0002t0010g0073 a0001c0002t0010g0074 a0001c0002t0010g0075 |
3 | HG02486.hp2 HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-14+1585_-14+1592d others(10): Show |
ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 99376364 | ||||||
| chr7:99376415 | T | A | 23 | a0001c0002t0014g0081 a0001c0002t0019g0020 a0002c0003t0005g0005 others(20): Show |
27 | HG00099.hp1 HG01175.hp1 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.-14+1634T>A | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99376415 | |||||||
| chr7:99376425 | G | T | 2 | a0001c0001t0002g0112 a0001c0001t0002g0273 |
2 | HG03942.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.-14+1644G>T | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99376425 | |||||||
| chr7:99376596 | C | T | 9 | a0002c0003t0006g0012 a0002c0003t0006g0082 a0002c0003t0006g0085 others(6): Show |
10 | HG00099.hp1 HG01175.hp1 HG02523.hp2 others(7): Show |
intron_variant | MODIFIER | c.-14+1815C>T | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99376596 | |||||||
| chr7:99376633 | G | A | 1 | a0001c0002t0003g0045 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-14+1852G>A | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99376633 | |||||||
| chr7:99376669 | G | A | 1 | a0002c0003t0006g0076 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-14+1888G>A | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99376669 | |||||||
| chr7:99376801 | C | T | 1 | a0001c0001t0002g0141 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-14+2020C>T | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99376801 | |||||||
| chr7:99376871 | C | CA | 28 | a0001c0001t0001g0143 a0001c0001t0001g0149 a0001c0001t0001g0151 others(25): Show |
28 | HG00438.hp2 HG01515.hp2 HG02027.hp1 others(25): Show |
intron_variant | MODIFIER | c.-14+2106dupA | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 99376871 | ||||||
| chr7:99376965 | G | A | 85 | a0001c0001t0003g0054 a0001c0002t0003g0004 a0001c0002t0003g0019 others(82): Show |
99 | HG00099.hp1 HG01081.hp1 HG01081.hp2 others(96): Show |
intron_variant | MODIFIER | c.-14+2184G>A | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99376965 | |||||||
| chr7:99376984 | A | G | 2 | a0001c0004t0001g0031 a0001c0004t0001g0251 |
3 | HG00438.hp1 NA19010.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.-14+2203A>G | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99376984 | |||||||
| chr7:99377175 | GT | G | 4 | a0001c0002t0010g0263 a0001c0002t0010g0264 a0001c0002t0010g0265 others(1): Show |
4 | HG02451.hp2 HG02615.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.-14+2397delT | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 99377175 | ||||||
| chr7:99377254 | C | T | 2 | a0001c0001t0002g0139 a0001c0001t0002g0140 |
2 | NA19004.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.-14+2473C>T | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99377254 | |||||||
| chr7:99377311 | C | CT | 12 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 others(9): Show |
12 | HG01106.hp2 HG01361.hp1 HG01515.hp2 others(9): Show |
intron_variant | MODIFIER | c.-14+2549dupT | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 99377311 | ||||||
| chr7:99377316 | T | C | 157 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0013 others(154): Show |
186 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(183): Show |
intron_variant | MODIFIER | c.-14+2535T>C | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99377316 | |||||||
| chr7:99377317 | T | C | 1 | a0001c0002t0013g0063 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-14+2536T>C | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99377317 | |||||||
| chr7:99377456 | G | A | 1 | a0001c0001t0002g0119 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-14+2675G>A | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99377456 | |||||||
| chr7:99377475 | G | A | 1 | a0001c0002t0009g0066 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-14+2694G>A | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99377475 | |||||||
| chr7:99377603 | G | A | 1 | a0002c0003t0011g0254 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-14+2822G>A | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99377603 | |||||||
| chr7:99377610 | G | GCTT | 3 | a0002c0003t0011g0255 a0002c0003t0011g0256 a0002c0003t0011g0257 |
3 | HG02970.hp1 HG06807.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-14+2851_-14+2853d others(5): Show |
ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 99377610 | ||||||
| chr7:99377632 | CT | C | 68 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0013 others(65): Show |
82 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.-14+2863delT | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 99377632 | ||||||
| chr7:99377635 | T | C | 22 | a0001c0002t0014g0081 a0002c0003t0005g0005 a0002c0003t0005g0078 others(19): Show |
25 | HG00099.hp1 HG01175.hp1 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.-14+2854T>C | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99377635 | |||||||
| chr7:99377636 | T | C | 2 | a0001c0001t0002g0120 a0001c0001t0002g0121 |
2 | HG00558.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.-14+2855T>C | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99377636 | |||||||
| chr7:99377673 | C | T | 1 | a0001c0001t0002g0272 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-14+2892C>T | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99377673 | |||||||
| chr7:99377927 | C | T | 1 | a0001c0002t0016g0280 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-14+3146C>T | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99377927 | |||||||
| chr7:99377938 | A | AG | 5 | a0002c0003t0005g0005 a0002c0003t0005g0078 a0002c0003t0006g0005 others(2): Show |
7 | HG02615.hp2 HG02896.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.-14+3159dupG | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 99377938 | ||||||
| chr7:99377982 | AATGTCAT others(7): Show |
A | 1 | a0001c0001t0002g0276 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-14+3202_-14+3215d others(16): Show |
ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99377982 | |||||||
| chr7:99377996 | C | T | 4 | a0001c0002t0009g0018 a0001c0002t0009g0049 a0001c0002t0009g0050 others(1): Show |
5 | HG02258.hp1 HG02280.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.-14+3215C>T | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99377996 | |||||||
| chr7:99378036 | C | A | 1 | a0001c0001t0002g0276 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-14+3255C>A | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99378036 | |||||||
| chr7:99378152 | C | T | 3 | a0001c0002t0004g0267 a0001c0002t0004g0268 a0001c0002t0004g0269 |
3 | HG01081.hp1 HG01891.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-14+3371C>T | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99378152 | |||||||
| chr7:99378192 | C | T | 3 | a0001c0002t0010g0073 a0001c0002t0010g0074 a0001c0002t0010g0075 |
3 | HG02486.hp2 HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-14+3411C>T | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99378192 | |||||||
| chr7:99378226 | A | AT | 22 | a0001c0001t0001g0160 a0001c0001t0001g0240 a0001c0001t0001g0241 others(19): Show |
26 | HG00099.hp1 HG01175.hp1 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.-14+3461dupT | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 99378226 | ||||||
| chr7:99378226 | AT | A | 11 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0163 others(8): Show |
11 | HG00609.hp2 HG01081.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.-14+3461delT | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 99378226 | ||||||
| chr7:99378318 | C | G | 1 | a0001c0002t0010g0075 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-14+3537C>G | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99378318 | |||||||
| chr7:99378491 | C | G | 1 | a0001c0002t0016g0280 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-14+3710C>G | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99378491 | |||||||
| chr7:99378543 | C | T | 2 | a0001c0002t0003g0061 a0001c0002t0013g0060 |
2 | HG02486.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-14+3762C>T | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99378543 | |||||||
| chr7:99378619 | G | T | 75 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0013 others(72): Show |
90 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.-14+3838G>T | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99378619 | |||||||
| chr7:99378661 | C | T | 3 | a0001c0002t0003g0059 a0001c0002t0013g0063 a0001c0002t0014g0270 |
3 | HG02896.hp2 HG02897.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-14+3880C>T | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99378661 | |||||||
| chr7:99378770 | T | G | 4 | a0001c0002t0003g0059 a0001c0002t0013g0047 a0001c0002t0013g0063 others(1): Show |
4 | HG02896.hp2 HG02897.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.-14+3989T>G | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99378770 | |||||||
| chr7:99378774 | C | CT | 19 | a0001c0001t0001g0009 a0001c0001t0001g0164 a0001c0001t0001g0234 others(16): Show |
21 | HG00558.hp2 HG01106.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.-14+4013dupT | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 99378774 | ||||||
| chr7:99378774 | C | CTT | 84 | a0001c0001t0001g0160 a0001c0001t0002g0001 a0001c0001t0002g0006 others(81): Show |
103 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.-14+4012_-14+4013d others(4): Show |
ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 99378774 | ||||||
| chr7:99378774 | C | CTTT | 64 | a0001c0001t0002g0095 a0001c0001t0002g0108 a0001c0001t0002g0116 others(61): Show |
74 | HG00099.hp1 HG01081.hp1 HG01081.hp2 others(71): Show |
intron_variant | MODIFIER | c.-14+4011_-14+4013d others(5): Show |
ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 99378774 | ||||||
| chr7:99378774 | C | CTTTT | 7 | a0001c0001t0002g0136 a0001c0002t0004g0036 a0001c0002t0010g0075 others(4): Show |
7 | HG02615.hp1 HG02809.hp1 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.-14+4010_-14+4013d others(6): Show |
ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 99378774 | ||||||
| chr7:99378807 | T | C | 85 | a0001c0001t0003g0054 a0001c0002t0003g0004 a0001c0002t0003g0019 others(82): Show |
99 | HG00099.hp1 HG01081.hp1 HG01081.hp2 others(96): Show |
intron_variant | MODIFIER | c.-14+4026T>C | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99378807 | |||||||
| chr7:99378863 | G | A | 59 | a0001c0001t0003g0054 a0001c0002t0003g0004 a0001c0002t0003g0019 others(56): Show |
69 | HG01081.hp1 HG01081.hp2 HG01167.hp2 others(66): Show |
intron_variant | MODIFIER | c.-14+4082G>A | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99378863 | |||||||
| chr7:99378869 | C | T | 1 | a0001c0001t0002g0091 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-14+4088C>T | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99378869 | |||||||
| chr7:99378887 | T | C | 1 | a0001c0001t0001g0151 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-14+4106T>C | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99378887 | |||||||
| chr7:99378930 | C | G | 3 | a0001c0002t0010g0073 a0001c0002t0010g0074 a0001c0002t0010g0075 |
3 | HG02486.hp2 HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-14+4149C>G | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99378930 | |||||||
| chr7:99379056 | C | T | 1 | a0002c0003t0006g0079 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-14+4275C>T | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99379056 | |||||||
| chr7:99379327 | C | G | 1 | a0002c0003t0006g0076 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-14+4546C>G | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99379327 | |||||||
| chr7:99379423 | C | T | 16 | a0001c0002t0014g0081 a0001c0002t0019g0020 a0002c0003t0005g0005 others(13): Show |
20 | HG00099.hp1 HG01175.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.-14+4642C>T | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99379423 | |||||||
| chr7:99379444 | A | G | 23 | a0001c0002t0014g0081 a0001c0002t0019g0020 a0002c0003t0005g0005 others(20): Show |
27 | HG00099.hp1 HG01175.hp1 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.-14+4663A>G | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99379444 | |||||||
| chr7:99379509 | C | T | 3 | a0001c0002t0010g0073 a0001c0002t0010g0074 a0001c0002t0010g0075 |
3 | HG02486.hp2 HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-14+4728C>T | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99379509 | |||||||
| chr7:99379564 | A | G | 160 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0013 others(157): Show |
189 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(186): Show |
intron_variant | MODIFIER | c.-14+4783A>G | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99379564 | |||||||
| chr7:99379589 | C | T | 1 | a0001c0001t0001g0233 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.-14+4808C>T | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99379589 | |||||||
| chr7:99379753 | C | T | 1 | a0001c0001t0008g0111 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-14+4972C>T | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99379753 | |||||||
| chr7:99379805 | A | AT | 55 | a0001c0001t0001g0240 a0001c0001t0002g0276 a0001c0001t0003g0054 others(52): Show |
65 | HG01081.hp1 HG01081.hp2 HG01167.hp2 others(62): Show |
intron_variant | MODIFIER | c.-14+5040dupT | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 99379805 | ||||||
| chr7:99379805 | A | ATT | 23 | a0001c0002t0003g0058 a0001c0002t0014g0081 a0001c0002t0019g0020 others(20): Show |
27 | HG00099.hp1 HG01175.hp1 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.-14+5039_-14+5040d others(4): Show |
ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 99379805 | ||||||
| chr7:99379805 | AT | A | 75 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0002g0001 others(72): Show |
90 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.-14+5040delT | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 99379805 | ||||||
| chr7:99379892 | A | G | 160 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0013 others(157): Show |
189 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(186): Show |
intron_variant | MODIFIER | c.-14+5111A>G | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99379892 | |||||||
| chr7:99379897 | G | A | 1 | a0001c0002t0019g0020 | 2 | HG02647.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-14+5116G>A | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99379897 | |||||||
| chr7:99379905 | A | G | 59 | a0001c0001t0003g0054 a0001c0002t0003g0004 a0001c0002t0003g0019 others(56): Show |
69 | HG01081.hp1 HG01081.hp2 HG01167.hp2 others(66): Show |
intron_variant | MODIFIER | c.-14+5124A>G | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99379905 | |||||||
| chr7:99379927 | G | A | 4 | a0001c0002t0009g0018 a0001c0002t0009g0049 a0001c0002t0009g0050 others(1): Show |
5 | HG02258.hp1 HG02280.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.-14+5146G>A | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99379927 | |||||||
| chr7:99380020 | T | C | 3 | a0001c0002t0010g0073 a0001c0002t0010g0074 a0001c0002t0010g0075 |
3 | HG02486.hp2 HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-14+5239T>C | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99380020 | |||||||
| chr7:99380331 | T | TTGGTAAG others(22): Show |
3 | a0001c0001t0002g0110 a0001c0001t0008g0109 a0001c0001t0008g0111 |
3 | HG01884.hp2 HG02559.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.-13-5371_-13-5370i others(31): Show |
ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99380331 | |||||||
| chr7:99380332 | A | G | 3 | a0001c0001t0002g0110 a0001c0001t0008g0109 a0001c0001t0008g0111 |
3 | HG01884.hp2 HG02559.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.-13-5370A>G | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99380332 | |||||||
| chr7:99380334 | C | T | 3 | a0001c0001t0002g0110 a0001c0001t0008g0109 a0001c0001t0008g0111 |
3 | HG01884.hp2 HG02559.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.-13-5368C>T | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99380334 | |||||||
| chr7:99380342 | C | T | 1 | a0001c0001t0001g0163 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-13-5360C>T | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99380342 | |||||||
| chr7:99380384 | G | C | 1 | a0001c0002t0013g0047 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-13-5318G>C | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99380384 | |||||||
| chr7:99380715 | G | A | 2 | a0001c0001t0001g0199 a0001c0001t0001g0200 |
2 | HG01070.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.-13-4987G>A | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99380715 | |||||||
| chr7:99380755 | T | A | 1 | a0001c0001t0002g0276 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-13-4947T>A | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99380755 | |||||||
| chr7:99380758 | C | T | 3 | a0001c0002t0013g0015 a0001c0002t0014g0015 a0001c0002t0014g0081 |
3 | HG02055.hp1 HG02717.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-13-4944C>T | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99380758 | |||||||
| chr7:99380766 | G | T | 1 | a0001c0001t0002g0276 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-13-4936G>T | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99380766 | |||||||
| chr7:99380814 | G | T | 1 | a0001c0001t0002g0276 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-13-4888G>T | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99380814 | |||||||
| chr7:99380941 | T | A | 1 | a0001c0001t0002g0276 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-13-4761T>A | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99380941 | |||||||
| chr7:99380976 | G | A | 1 | a0001c0002t0016g0261 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-13-4726G>A | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99380976 | |||||||
| chr7:99381100 | T | G | 6 | a0001c0001t0001g0158 a0001c0001t0001g0167 a0001c0001t0001g0168 others(3): Show |
6 | HG00642.hp1 HG01515.hp2 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.-13-4602T>G | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99381100 | |||||||
| chr7:99381132 | A | G | 108 | a0001c0001t0001g0008 a0001c0001t0001g0027 a0001c0001t0001g0149 others(105): Show |
124 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.-13-4570A>G | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99381132 | |||||||
| chr7:99381143 | G | A | 70 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0013 others(67): Show |
84 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.-13-4559G>A | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99381143 | |||||||
| chr7:99381243 | C | T | 1 | a0001c0001t0002g0135 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-13-4459C>T | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99381243 | |||||||
| chr7:99381278 | G | A | 2 | a0001c0001t0002g0112 a0001c0001t0002g0273 |
2 | HG03942.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.-13-4424G>A | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99381278 | |||||||
| chr7:99381337 | C | G | 160 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0013 others(157): Show |
189 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(186): Show |
intron_variant | MODIFIER | c.-13-4365C>G | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99381337 | |||||||
| chr7:99381342 | C | T | 2 | a0001c0001t0001g0220 a0001c0001t0001g0221 |
2 | HG01361.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.-13-4360C>T | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99381342 | |||||||
| chr7:99381486 | C | T | 1 | a0001c0002t0019g0020 | 2 | HG02647.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-13-4216C>T | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99381486 | |||||||
| chr7:99381493 | T | A | 2 | a0001c0002t0009g0049 a0001c0002t0009g0050 |
2 | HG02622.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-13-4209T>A | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99381493 | |||||||
| chr7:99381498 | C | G | 1 | a0001c0001t0001g0219 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-13-4204C>G | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99381498 | |||||||
| chr7:99381630 | G | A | 5 | a0001c0002t0010g0073 a0001c0002t0010g0074 a0001c0002t0010g0075 others(2): Show |
6 | HG02486.hp2 HG02647.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.-13-4072G>A | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99381630 | |||||||
| chr7:99381703 | G | A | 1 | a0001c0001t0005g0170 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-13-3999G>A | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99381703 | |||||||
| chr7:99381828 | T | C | 5 | a0001c0002t0010g0073 a0001c0002t0010g0074 a0001c0002t0010g0075 others(2): Show |
6 | HG02486.hp2 HG02647.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.-13-3874T>C | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99381828 | |||||||
| chr7:99382090 | G | C | 1 | a0001c0002t0003g0052 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-13-3612G>C | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99382090 | |||||||
| chr7:99382164 | G | A | 3 | a0001c0002t0010g0263 a0001c0002t0010g0264 a0001c0002t0010g0265 |
3 | HG02451.hp2 HG02615.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-13-3538G>A | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99382164 | |||||||
| chr7:99382358 | C | T | 1 | a0001c0001t0001g0238 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-13-3344C>T | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99382358 | |||||||
| chr7:99382402 | G | GA | 16 | a0001c0001t0001g0152 a0001c0001t0001g0171 a0001c0001t0001g0241 others(13): Show |
16 | HG00099.hp2 HG02257.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.-13-3283dupA | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 99382402 | ||||||
| chr7:99382402 | G | GAA | 14 | a0002c0003t0005g0005 a0002c0003t0005g0078 a0002c0003t0006g0005 others(11): Show |
17 | HG00099.hp1 HG02523.hp2 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.-13-3284_-13-3283d others(4): Show |
ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 99382402 | ||||||
| chr7:99382419 | AG | A | 4 | a0001c0002t0010g0073 a0001c0002t0010g0074 a0001c0002t0010g0075 others(1): Show |
4 | HG02486.hp2 HG02809.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-13-3281delG | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 99382419 | ||||||
| chr7:99382622 | C | T | 1 | a0001c0001t0001g0238 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-13-3080C>T | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99382622 | |||||||
| chr7:99382625 | C | T | 1 | a0001c0001t0001g0218 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.-13-3077C>T | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99382625 | |||||||
| chr7:99382755 | T | G | 1 | a0001c0002t0012g0037 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-13-2947T>G | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99382755 | |||||||
| chr7:99382837 | C | T | 1 | a0001c0001t0002g0134 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-13-2865C>T | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99382837 | |||||||
| chr7:99382842 | C | CT | 36 | a0001c0001t0001g0152 a0001c0001t0001g0164 a0001c0001t0001g0210 others(33): Show |
41 | HG00621.hp1 HG00642.hp2 HG01081.hp2 others(38): Show |
intron_variant | MODIFIER | c.-13-2840dupT | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 99382842 | ||||||
| chr7:99382842 | CT | C | 15 | a0001c0001t0001g0145 a0001c0001t0001g0150 a0001c0001t0002g0026 others(12): Show |
16 | HG00438.hp2 HG02486.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.-13-2840delT | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 99382842 | ||||||
| chr7:99382842 | CTT | C | 67 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0013 others(64): Show |
82 | HG00280.hp1 HG00408.hp2 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.-13-2841_-13-2840d others(4): Show |
ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 99382842 | ||||||
| chr7:99382940 | G | A | 1 | a0001c0001t0001g0237 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-13-2762G>A | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99382940 | |||||||
| chr7:99382993 | C | T | 1 | a0001c0002t0019g0020 | 2 | HG02647.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-13-2709C>T | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99382993 | |||||||
| chr7:99382994 | G | A | 1 | a0001c0001t0001g0152 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.-13-2708G>A | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99382994 | |||||||
| chr7:99383036 | T | G | 160 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0013 others(157): Show |
189 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(186): Show |
intron_variant | MODIFIER | c.-13-2666T>G | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99383036 | |||||||
| chr7:99383091 | C | T | 3 | a0001c0002t0004g0267 a0001c0002t0004g0268 a0001c0002t0004g0269 |
3 | HG01081.hp1 HG01891.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-13-2611C>T | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99383091 | |||||||
| chr7:99383134 | C | T | 30 | a0001c0001t0003g0054 a0001c0002t0003g0004 a0001c0002t0003g0019 others(27): Show |
35 | HG01346.hp1 HG01516.hp1 HG01517.hp1 others(32): Show |
intron_variant | MODIFIER | c.-13-2568C>T | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99383134 | |||||||
| chr7:99383256 | A | G | 160 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0013 others(157): Show |
189 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(186): Show |
intron_variant | MODIFIER | c.-13-2446A>G | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99383256 | |||||||
| chr7:99383523 | G | A | 5 | a0001c0002t0010g0073 a0001c0002t0010g0074 a0001c0002t0010g0075 others(2): Show |
6 | HG02486.hp2 HG02647.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.-13-2179G>A | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99383523 | |||||||
| chr7:99383584 | G | A | 2 | a0001c0001t0001g0165 a0001c0001t0001g0166 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-13-2118G>A | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99383584 | |||||||
| chr7:99383600 | C | T | 3 | a0001c0002t0013g0015 a0001c0002t0014g0015 a0001c0002t0014g0081 |
3 | HG02055.hp1 HG02717.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-13-2102C>T | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99383600 | |||||||
| chr7:99383601 | G | A | 2 | a0001c0002t0016g0261 a0001c0002t0016g0262 |
2 | HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-13-2101G>A | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99383601 | |||||||
| chr7:99383610 | A | G | 160 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0013 others(157): Show |
189 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(186): Show |
intron_variant | MODIFIER | c.-13-2092A>G | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99383610 | |||||||
| chr7:99383736 | A | C | 1 | a0001c0001t0001g0208 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-13-1966A>C | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99383736 | |||||||
| chr7:99383843 | C | T | 3 | a0001c0001t0002g0110 a0001c0001t0008g0109 a0001c0001t0008g0111 |
3 | HG01884.hp2 HG02559.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.-13-1859C>T | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99383843 | |||||||
| chr7:99383927 | T | A | 1 | a0002c0003t0006g0266 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-13-1775T>A | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99383927 | |||||||
| chr7:99384134 | C | T | 1 | a0002c0003t0011g0254 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-13-1568C>T | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99384134 | |||||||
| chr7:99384301 | G | C | 1 | a0001c0002t0003g0058 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-13-1401G>C | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99384301 | |||||||
| chr7:99384417 | CT | C | 22 | a0002c0003t0005g0005 a0002c0003t0005g0078 a0002c0003t0006g0005 others(19): Show |
25 | HG00099.hp1 HG01175.hp1 HG02257.hp1 others(22): Show |
intron_variant | MODIFIER | c.-13-1284delT | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99384417 | |||||||
| chr7:99384729 | G | C | 1 | a0002c0003t0024g0084 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-13-973G>C | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99384729 | |||||||
| chr7:99384798 | C | T | 1 | a0001c0001t0001g0207 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-13-904C>T | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99384798 | |||||||
| chr7:99384843 | A | T | 1 | a0001c0001t0002g0133 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-13-859A>T | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99384843 | |||||||
| chr7:99384860 | C | CT | 19 | a0001c0001t0001g0162 a0001c0001t0001g0206 a0001c0001t0001g0217 others(16): Show |
22 | HG00438.hp1 HG00544.hp1 HG00621.hp1 others(19): Show |
intron_variant | MODIFIER | c.-13-824dupT | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 99384860 | ||||||
| chr7:99384860 | CT | C | 23 | a0001c0001t0001g0145 a0001c0001t0001g0172 a0001c0001t0001g0173 others(20): Show |
27 | HG00423.hp1 HG01074.hp2 HG01081.hp2 others(24): Show |
intron_variant | MODIFIER | c.-13-824delT | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 99384860 | ||||||
| chr7:99384954 | A | AT | 58 | a0001c0001t0001g0003 a0001c0001t0001g0030 a0001c0001t0001g0143 others(55): Show |
64 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.-13-719dupT | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 99384954 | ||||||
| chr7:99384954 | A | ATT | 12 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0250 others(9): Show |
15 | HG00639.hp1 HG01243.hp1 HG01361.hp1 others(12): Show |
intron_variant | MODIFIER | c.-13-720_-13-719dup others(2): Show |
ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 99384954 | ||||||
| chr7:99384954 | AT | A | 81 | a0001c0001t0001g0145 a0001c0001t0001g0171 a0001c0001t0001g0172 others(78): Show |
97 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.-13-719delT | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 99384954 | ||||||
| chr7:99384954 | ATTTTTTT others(6): Show |
A | 3 | a0001c0001t0002g0110 a0001c0001t0008g0109 a0001c0001t0008g0111 |
3 | HG01884.hp2 HG02559.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.-13-731_-13-719del others(13): Show |
ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 99384954 | ||||||
| chr7:99385029 | G | A | 1 | a0001c0002t0004g0267 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-13-673G>A | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99385029 | |||||||
| chr7:99385305 | T | TG | 129 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(126): Show |
154 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.-13-384dupG | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 99385305 | ||||||
| chr7:99385305 | T | TGG | 22 | a0001c0001t0001g0153 a0001c0001t0001g0156 a0001c0001t0001g0179 others(19): Show |
23 | HG01243.hp2 HG01261.hp1 HG01261.hp2 others(20): Show |
intron_variant | MODIFIER | c.-13-385_-13-384dup others(2): Show |
ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 99385305 | ||||||
| chr7:99385305 | TGGG | T | 42 | a0001c0002t0003g0004 a0001c0002t0003g0019 a0001c0002t0003g0032 others(39): Show |
52 | HG01081.hp2 HG01167.hp2 HG01169.hp2 others(49): Show |
intron_variant | MODIFIER | c.-13-386_-13-384del others(3): Show |
ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 99385305 | ||||||
| chr7:99385308 | G | C | 1 | a0001c0001t0002g0124 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-13-394G>C | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 1/9 | chr7 | 99385308 | |||||||
| chr7:99385798 | C | T | 1 | a0001c0002t0016g0262 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.64+20C>T | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 2/9 | chr7 | 99385798 | |||||||
| chr7:99385974 | G | C | 1 | a0001c0001t0001g0192 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.64+196G>C | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 2/9 | chr7 | 99385974 | |||||||
| chr7:99385989 | G | T | 1 | a0001c0001t0001g0191 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.64+211G>T | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 2/9 | chr7 | 99385989 | |||||||
| chr7:99386001 | G | A | 2 | a0001c0001t0002g0091 a0001c0001t0002g0271 |
2 | HG02735.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.64+223G>A | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 2/9 | chr7 | 99386001 | |||||||
| chr7:99386080 | G | A | 4 | a0001c0001t0001g0176 a0001c0001t0001g0178 a0001c0001t0001g0182 others(1): Show |
4 | HG00323.hp1 HG00639.hp2 HG01070.hp1 others(1): Show |
intron_variant | MODIFIER | c.64+302G>A | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 2/9 | chr7 | 99386080 | |||||||
| chr7:99386241 | ACT | A | 4 | a0001c0001t0001g0027 a0001c0001t0001g0227 a0001c0001t0015g0226 others(1): Show |
4 | HG00673.hp1 HG02083.hp2 NA18612.hp1 others(1): Show |
intron_variant | MODIFIER | c.65-441_65-440delCT | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr7 | 99386241 | ||||||
| chr7:99386250 | CA | C | 7 | a0001c0001t0001g0158 a0001c0001t0001g0198 a0001c0001t0001g0199 others(4): Show |
7 | HG01070.hp2 HG01167.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.65-422delA | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr7 | 99386250 | ||||||
| chr7:99386262 | A | G | 1 | a0001c0001t0002g0103 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.65-423A>G | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 2/9 | chr7 | 99386262 | |||||||
| chr7:99386332 | C | G | 1 | a0001c0002t0016g0261 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.65-353C>G | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 2/9 | chr7 | 99386332 | |||||||
| chr7:99386478 | T | C | 1 | a0001c0002t0016g0262 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.65-207T>C | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 2/9 | chr7 | 99386478 | |||||||
| chr7:99386485 | G | A | 1 | a0001c0001t0020g0100 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.65-200G>A | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 2/9 | chr7 | 99386485 | |||||||
| chr7:99386590 | G | A | 15 | a0002c0003t0005g0005 a0002c0003t0005g0078 a0002c0003t0006g0005 others(12): Show |
18 | HG00099.hp1 HG01175.hp1 HG02523.hp2 others(15): Show |
intron_variant | MODIFIER | c.65-95G>A | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 2/9 | chr7 | 99386590 | |||||||
| chr7:99386905 | G | A | 1 | a0001c0002t0016g0262 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.169+116G>A | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 3/9 | chr7 | 99386905 | |||||||
| chr7:99386982 | G | C | 2 | a0001c0001t0002g0099 a0001c0001t0002g0105 |
2 | HG02735.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.169+193G>C | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 3/9 | chr7 | 99386982 | |||||||
| chr7:99387256 | A | T | 75 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0013 others(72): Show |
90 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.169+467A>T | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 3/9 | chr7 | 99387256 | |||||||
| chr7:99387349 | G | A | 2 | a0001c0001t0001g0234 a0001c0001t0007g0201 |
2 | HG01192.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.169+560G>A | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 3/9 | chr7 | 99387349 | |||||||
| chr7:99387512 | C | T | 75 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0013 others(72): Show |
90 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.170-527C>T | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 3/9 | chr7 | 99387512 | |||||||
| chr7:99387524 | G | A | 1 | a0002c0003t0006g0076 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.170-515G>A | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 3/9 | chr7 | 99387524 | |||||||
| chr7:99387536 | A | G | 2 | a0001c0001t0002g0096 a0001c0001t0002g0102 |
2 | NA18956.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.170-503A>G | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 3/9 | chr7 | 99387536 | |||||||
| chr7:99387691 | C | T | 2 | a0001c0001t0001g0234 a0001c0001t0007g0201 |
2 | HG01192.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.170-348C>T | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 3/9 | chr7 | 99387691 | |||||||
| chr7:99387716 | G | A | 2 | a0001c0001t0002g0026 a0001c0001t0002g0138 |
3 | HG02630.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.170-323G>A | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 3/9 | chr7 | 99387716 | |||||||
| chr7:99387717 | G | A | 2 | a0001c0001t0002g0026 a0001c0001t0002g0138 |
3 | HG02630.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.170-322G>A | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 3/9 | chr7 | 99387717 | |||||||
| chr7:99387736 | C | CA | 21 | a0001c0001t0001g0146 a0001c0001t0001g0148 a0001c0001t0001g0152 others(18): Show |
22 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(19): Show |
intron_variant | MODIFIER | c.170-281dupA | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr7 | 99387736 | ||||||
| chr7:99387736 | CA | C | 72 | a0001c0001t0001g0197 a0001c0001t0001g0248 a0001c0001t0002g0001 others(69): Show |
86 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.170-281delA | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr7 | 99387736 | ||||||
| chr7:99387736 | CAA | C | 82 | a0001c0001t0002g0024 a0001c0001t0002g0116 a0001c0001t0002g0129 others(79): Show |
97 | HG00099.hp1 HG01081.hp1 HG01081.hp2 others(94): Show |
intron_variant | MODIFIER | c.170-282_170-281del others(2): Show |
ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr7 | 99387736 | ||||||
| chr7:99387749 | A | C | 1 | a0001c0001t0017g0190 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.170-290A>C | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 3/9 | chr7 | 99387749 | |||||||
| chr7:99387758 | A | T | 75 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0013 others(72): Show |
90 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.170-281A>T | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 3/9 | chr7 | 99387758 | |||||||
| chr7:99387773 | A | G | 161 | a0001c0001t0001g0160 a0001c0001t0001g0237 a0001c0001t0002g0001 others(158): Show |
190 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(187): Show |
intron_variant | MODIFIER | c.170-266A>G | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 3/9 | chr7 | 99387773 | |||||||
| chr7:99387785 | G | A | 29 | a0001c0002t0003g0004 a0001c0002t0003g0019 a0001c0002t0003g0032 others(26): Show |
34 | HG01516.hp1 HG01517.hp1 HG01891.hp2 others(31): Show |
intron_variant | MODIFIER | c.170-254G>A | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 3/9 | chr7 | 99387785 | |||||||
| chr7:99387807 | C | T | 1 | a0001c0001t0001g0227 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.170-232C>T | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 3/9 | chr7 | 99387807 | |||||||
| chr7:99387854 | C | T | 1 | a0001c0001t0001g0214 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.170-185C>T | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 3/9 | chr7 | 99387854 | |||||||
| chr7:99387855 | A | G | 1 | a0001c0001t0001g0214 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.170-184A>G | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 3/9 | chr7 | 99387855 | |||||||
| chr7:99387883 | G | C | 5 | a0001c0001t0001g0184 a0001c0001t0001g0204 a0001c0001t0001g0207 others(2): Show |
5 | HG00140.hp1 HG00639.hp1 HG01346.hp2 others(2): Show |
intron_variant | MODIFIER | c.170-156G>C | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 3/9 | chr7 | 99387883 | |||||||
| chr7:99387899 | C | CA | 10 | a0001c0001t0001g0029 a0001c0001t0001g0143 a0001c0001t0001g0145 others(7): Show |
11 | HG01192.hp2 HG02257.hp1 HG02602.hp2 others(8): Show |
intron_variant | MODIFIER | c.170-126dupA | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr7 | 99387899 | ||||||
| chr7:99387957 | T | C | 5 | a0001c0002t0010g0073 a0001c0002t0010g0074 a0001c0002t0010g0075 others(2): Show |
6 | HG02486.hp2 HG02647.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.170-82T>C | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 3/9 | chr7 | 99387957 | |||||||
| chr7:99388013 | C | T | 1 | a0001c0002t0004g0039 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.170-26C>T | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 3/9 | chr7 | 99388013 | |||||||
| chr7:99388480 | G | C | 1 | a0001c0001t0001g0185 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.392+219G>C | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 4/9 | chr7 | 99388480 | |||||||
| chr7:99388657 | G | A | 3 | a0001c0002t0010g0263 a0001c0002t0010g0264 a0001c0002t0010g0265 |
3 | HG02451.hp2 HG02615.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.392+396G>A | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 4/9 | chr7 | 99388657 | |||||||
| chr7:99388771 | T | G | 3 | a0001c0001t0002g0022 a0001c0001t0002g0104 a0001c0001t0008g0022 |
3 | HG03017.hp1 HG03688.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.392+510T>G | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 4/9 | chr7 | 99388771 | |||||||
| chr7:99388786 | C | T | 1 | a0001c0001t0002g0115 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.392+525C>T | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 4/9 | chr7 | 99388786 | |||||||
| chr7:99388932 | A | AT | 80 | a0001c0001t0001g0030 a0001c0001t0001g0154 a0001c0001t0001g0164 others(77): Show |
91 | HG00597.hp1 HG00621.hp2 HG01081.hp2 others(88): Show |
intron_variant | MODIFIER | c.392+693dupT | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr7 | 99388932 | ||||||
| chr7:99388932 | A | ATT | 7 | a0001c0002t0003g0067 a0001c0002t0004g0035 a0001c0002t0009g0051 others(4): Show |
7 | HG02257.hp1 HG02258.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.392+692_392+693dup others(2): Show |
ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr7 | 99388932 | ||||||
| chr7:99389084 | G | A | 1 | a0001c0002t0025g0065 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.393-821G>A | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 4/9 | chr7 | 99389084 | |||||||
| chr7:99389093 | C | T | 1 | a0002c0003t0015g0080 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.393-812C>T | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 4/9 | chr7 | 99389093 | |||||||
| chr7:99389094 | G | A | 3 | a0001c0002t0004g0267 a0001c0002t0004g0268 a0001c0002t0004g0269 |
3 | HG01081.hp1 HG01891.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.393-811G>A | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 4/9 | chr7 | 99389094 | |||||||
| chr7:99389232 | C | G | 3 | a0001c0001t0005g0170 a0001c0001t0005g0188 a0001c0001t0005g0236 |
3 | HG00140.hp2 HG00280.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.393-673C>G | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 4/9 | chr7 | 99389232 | |||||||
| chr7:99389233 | G | A | 1 | a0002c0003t0015g0080 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.393-672G>A | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 4/9 | chr7 | 99389233 | |||||||
| chr7:99389379 | C | G | 1 | a0001c0002t0013g0060 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.393-526C>G | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 4/9 | chr7 | 99389379 | |||||||
| chr7:99389456 | A | G | 1 | a0001c0001t0001g0183 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.393-449A>G | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 4/9 | chr7 | 99389456 | |||||||
| chr7:99389524 | G | A | 5 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0001g0179 others(2): Show |
5 | HG01074.hp2 HG01099.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.393-381G>A | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 4/9 | chr7 | 99389524 | |||||||
| chr7:99389684 | A | G | 1 | a0002c0003t0015g0080 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.393-221A>G | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 4/9 | chr7 | 99389684 | |||||||
| chr7:99389752 | G | A | 1 | a0001c0001t0002g0132 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.393-153G>A | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 4/9 | chr7 | 99389752 | |||||||
| chr7:99389842 | C | T | 5 | a0001c0002t0010g0073 a0001c0002t0010g0074 a0001c0002t0010g0075 others(2): Show |
6 | HG02486.hp2 HG02647.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.393-63C>T | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 4/9 | chr7 | 99389842 | |||||||
| chr7:99389878 | C | G | 1 | a0001c0001t0001g0206 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.393-27C>G | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 4/9 | chr7 | 99389878 | |||||||
| chr7:99390261 | G | C | 8 | a0001c0002t0004g0267 a0001c0002t0004g0268 a0001c0002t0004g0269 others(5): Show |
8 | HG01081.hp1 HG01891.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.500+249G>C | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 5/9 | chr7 | 99390261 | |||||||
| chr7:99390369 | A | AT | 25 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0143 others(22): Show |
29 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.500+373dupT | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr7 | 99390369 | ||||||
| chr7:99390430 | G | A | 62 | a0001c0002t0003g0004 a0001c0002t0003g0019 a0001c0002t0003g0032 others(59): Show |
73 | HG01081.hp1 HG01081.hp2 HG01167.hp2 others(70): Show |
intron_variant | MODIFIER | c.500+418G>A | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 5/9 | chr7 | 99390430 | |||||||
| chr7:99390567 | A | G | 1 | a0001c0002t0019g0020 | 2 | HG02647.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.501-326A>G | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 5/9 | chr7 | 99390567 | |||||||
| chr7:99390569 | G | A | 3 | a0001c0002t0010g0263 a0001c0002t0010g0264 a0001c0002t0010g0265 |
3 | HG02451.hp2 HG02615.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.501-324G>A | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 5/9 | chr7 | 99390569 | |||||||
| chr7:99390702 | A | T | 1 | a0001c0001t0001g0260 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.501-191A>T | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 5/9 | chr7 | 99390702 | |||||||
| chr7:99390702 | AT | A | 9 | a0001c0005t0001g0193 a0002c0003t0006g0012 a0002c0003t0006g0082 others(6): Show |
10 | HG00099.hp1 HG01175.hp1 HG02523.hp2 others(7): Show |
intron_variant | MODIFIER | c.501-176delT | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr7 | 99390702 | ||||||
| chr7:99390703 | T | A | 14 | a0002c0003t0005g0005 a0002c0003t0005g0078 a0002c0003t0006g0005 others(11): Show |
16 | HG02257.hp1 HG02258.hp2 HG02615.hp2 others(13): Show |
intron_variant | MODIFIER | c.501-190T>A | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 5/9 | chr7 | 99390703 | |||||||
| chr7:99390704 | T | A | 8 | a0002c0003t0006g0012 a0002c0003t0006g0082 a0002c0003t0006g0085 others(5): Show |
9 | HG00099.hp1 HG01175.hp1 HG02523.hp2 others(6): Show |
intron_variant | MODIFIER | c.501-189T>A | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 5/9 | chr7 | 99390704 | |||||||
| chr7:99390810 | G | A | 1 | a0001c0001t0001g0213 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.501-83G>A | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 5/9 | chr7 | 99390810 | |||||||
| chr7:99391477 | G | A | 2 | a0001c0001t0001g0195 a0001c0001t0001g0197 |
2 | HG03704.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.783+224G>A | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 7/9 | chr7 | 99391477 | |||||||
| chr7:99391525 | A | T | 1 | a0001c0001t0001g0206 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.783+272A>T | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 7/9 | chr7 | 99391525 | |||||||
| chr7:99391539 | G | A | 1 | a0001c0002t0004g0044 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.783+286G>A | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 7/9 | chr7 | 99391539 | |||||||
| chr7:99391752 | C | CA | 7 | a0001c0001t0001g0143 a0001c0001t0001g0145 a0001c0001t0002g0273 others(4): Show |
7 | HG01433.hp2 HG04184.hp2 NA19000.hp1 others(4): Show |
intron_variant | MODIFIER | c.783+515dupA | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr7 | 99391752 | ||||||
| chr7:99391752 | CA | C | 74 | a0001c0001t0001g0208 a0001c0001t0002g0098 a0001c0001t0002g0136 others(71): Show |
87 | HG01081.hp1 HG01081.hp2 HG01169.hp2 others(84): Show |
intron_variant | MODIFIER | c.783+515delA | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr7 | 99391752 | ||||||
| chr7:99391759 | A | T | 5 | a0001c0002t0010g0073 a0001c0002t0010g0074 a0001c0002t0010g0075 others(2): Show |
6 | HG02486.hp2 HG02647.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.783+506A>T | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 7/9 | chr7 | 99391759 | |||||||
| chr7:99391760 | A | T | 5 | a0001c0002t0010g0073 a0001c0002t0010g0074 a0001c0002t0010g0075 others(2): Show |
6 | HG02486.hp2 HG02647.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.783+507A>T | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 7/9 | chr7 | 99391760 | |||||||
| chr7:99391991 | C | A | 1 | a0001c0001t0002g0272 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.784-680C>A | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 7/9 | chr7 | 99391991 | |||||||
| chr7:99391993 | G | A | 1 | a0001c0001t0002g0094 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.784-678G>A | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 7/9 | chr7 | 99391993 | |||||||
| chr7:99392003 | G | A | 50 | a0001c0001t0003g0054 a0001c0002t0003g0004 a0001c0002t0003g0019 others(47): Show |
60 | HG01081.hp2 HG01167.hp2 HG01169.hp2 others(57): Show |
intron_variant | MODIFIER | c.784-668G>A | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 7/9 | chr7 | 99392003 | |||||||
| chr7:99392125 | C | T | 1 | a0001c0001t0007g0278 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.784-546C>T | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 7/9 | chr7 | 99392125 | |||||||
| chr7:99392211 | G | C | 1 | a0001c0001t0002g0098 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.784-460G>C | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 7/9 | chr7 | 99392211 | |||||||
| chr7:99392613 | T | C | 22 | a0002c0003t0005g0005 a0002c0003t0005g0078 a0002c0003t0006g0005 others(19): Show |
25 | HG00099.hp1 HG01175.hp1 HG02257.hp1 others(22): Show |
intron_variant | MODIFIER | c.784-58T>C | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 7/9 | chr7 | 99392613 | |||||||
| chr7:99392916 | G | A | 1 | a0001c0001t0001g0224 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.989+40G>A | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 8/9 | chr7 | 99392916 | |||||||
| chr7:99393140 | G | A | 1 | a0001c0001t0002g0128 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.989+264G>A | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 8/9 | chr7 | 99393140 | |||||||
| chr7:99393213 | G | C | 1 | a0001c0005t0001g0193 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.989+337G>C | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 8/9 | chr7 | 99393213 | |||||||
| chr7:99393214 | C | G | 1 | a0001c0005t0001g0193 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.989+338C>G | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 8/9 | chr7 | 99393214 | |||||||
| chr7:99393218 | G | C | 1 | a0001c0005t0001g0193 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.989+342G>C | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 8/9 | chr7 | 99393218 | |||||||
| chr7:99393286 | A | G | 1 | a0001c0001t0002g0271 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.989+410A>G | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 8/9 | chr7 | 99393286 | |||||||
| chr7:99393398 | C | T | 3 | a0002c0003t0011g0255 a0002c0003t0011g0256 a0002c0003t0011g0257 |
3 | HG02970.hp1 HG06807.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.989+522C>T | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 8/9 | chr7 | 99393398 | |||||||
| chr7:99393465 | G | A | 1 | a0001c0001t0001g0198 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.990-564G>A | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 8/9 | chr7 | 99393465 | |||||||
| chr7:99393515 | C | T | 1 | a0001c0002t0019g0020 | 2 | HG02647.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.990-514C>T | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 8/9 | chr7 | 99393515 | |||||||
| chr7:99393544 | G | A | 2 | a0001c0002t0003g0061 a0001c0002t0013g0060 |
2 | HG02486.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.990-485G>A | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 8/9 | chr7 | 99393544 | |||||||
| chr7:99393558 | T | C | 85 | a0001c0001t0003g0054 a0001c0002t0003g0004 a0001c0002t0003g0019 others(82): Show |
99 | HG00099.hp1 HG01081.hp1 HG01081.hp2 others(96): Show |
intron_variant | MODIFIER | c.990-471T>C | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 8/9 | chr7 | 99393558 | |||||||
| chr7:99393574 | G | T | 58 | a0001c0001t0003g0054 a0001c0002t0003g0004 a0001c0002t0003g0019 others(55): Show |
68 | HG01081.hp1 HG01081.hp2 HG01167.hp2 others(65): Show |
intron_variant | MODIFIER | c.990-455G>T | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 8/9 | chr7 | 99393574 | |||||||
| chr7:99393614 | C | T | 7 | a0002c0003t0006g0076 a0002c0003t0011g0254 a0002c0003t0011g0255 others(4): Show |
7 | HG02257.hp1 HG02258.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.990-415C>T | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 8/9 | chr7 | 99393614 | |||||||
| chr7:99393733 | T | C | 1 | a0002c0003t0015g0080 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.990-296T>C | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 8/9 | chr7 | 99393733 | |||||||
| chr7:99393840 | G | C | 2 | a0001c0002t0016g0261 a0001c0002t0016g0262 |
2 | HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.990-189G>C | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 8/9 | chr7 | 99393840 | |||||||
| chr7:99393929 | G | C | 4 | a0001c0002t0004g0010 a0001c0002t0004g0034 a0001c0002t0004g0035 others(1): Show |
6 | HG01884.hp1 HG02922.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.990-100G>C | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 8/9 | chr7 | 99393929 | |||||||
| chr7:99393953 | G | T | 1 | a0001c0001t0001g0187 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.990-76G>T | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 8/9 | chr7 | 99393953 | |||||||
| chr7:99394170 | T | C | 1 | a0001c0002t0003g0032 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1080+51T>C | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 9/9 | chr7 | 99394170 | |||||||
| chr7:99394316 | C | T | 1 | a0001c0001t0005g0188 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1081-135C>T | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 9/9 | chr7 | 99394316 | |||||||
| chr7:99394321 | C | T | 160 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0013 others(157): Show |
189 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(186): Show |
intron_variant | MODIFIER | c.1081-130C>T | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 9/9 | chr7 | 99394321 | |||||||
| chr7:99394326 | A | G | 1 | a0001c0002t0003g0055 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1081-125A>G | ARPC1B | ENSG00000130429.16 | transcript | ENST00000646101.2 | protein_coding | 9/9 | chr7 | 99394326 |