Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 51205 |
| ensemblid | ENSG00000162836.12 |
| hgncid | 29609 |
| symbol | ACP6 |
| name | acid phosphatase 6, lysophosphatidic |
| refseq_nuc | NM_016361.5 |
| refseq_prot | NP_057445.4 |
| ensembl_nuc | ENST00000583509.7 |
| ensembl_prot | ENSP00000463574.1 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 147642230 |
| end | 147670524 |
| strand | - |
| ver | v1.2 |
| region | chr1:147642230-147670524 |
| region5000 | chr1:147637230-147675524 |
| regionname0 | ACP6_chr1_147642230_147670524 |
| regionname5000 | ACP6_chr1_147637230_147675524 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 428 | 387 | 76 | 61 | 194 | 14 | 40 | 146 | ACP6_chr1_147637230_147675524 | ACP6 | MITGV others(423): Show |
chr1 | 147637230 | 147675524 |
| a0002 | 0/0 | 428 | 11 | 11 | 0 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | MITGV others(423): Show |
chr1 | 147637230 | 147675524 |
| a0003 | 0/0 | 428 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | MITGV others(423): Show |
chr1 | 147637230 | 147675524 |
| a0004 | 0/0 | 428 | 2 | 1 | 0 | 1 | 0 | 0 | 1 | ACP6_chr1_147637230_147675524 | ACP6 | MITGV others(423): Show |
chr1 | 147637230 | 147675524 |
| a0005 | 0/0 | 428 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | MITGV others(423): Show |
chr1 | 147637230 | 147675524 |
| a0006 | 0/0 | 428 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ACP6_chr1_147637230_147675524 | ACP6 | MITGV others(423): Show |
chr1 | 147637230 | 147675524 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1284 | 177 | 38 | 34 | 79 | 8 | 17 | ACP6_chr1_147637230_147675524 | ACP6 | ATGAT others(1279): Show |
chr1 | 147637230 | 147675524 | ||
| a0001c0002 | 1/0 | 1284 | 101 | 11 | 17 | 54 | 4 | 14 | ACP6_chr1_147637230_147675524 | ACP6 | ATGAT others(1279): Show |
chr1 | 147637230 | 147675524 | ||
| a0001c0003 | 0/0 | 1284 | 101 | 22 | 7 | 61 | 2 | 9 | ACP6_chr1_147637230_147675524 | ACP6 | ATGAT others(1279): Show |
chr1 | 147637230 | 147675524 | ||
| a0001c0005 | 0/0 | 1284 | 2 | 1 | 1 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | ATGAT others(1279): Show |
chr1 | 147637230 | 147675524 | ||
| a0001c0007 | 0/0 | 1284 | 2 | 2 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | ATGAT others(1279): Show |
chr1 | 147637230 | 147675524 | ||
| a0001c0008 | 0/0 | 1284 | 2 | 0 | 2 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | ATGAT others(1279): Show |
chr1 | 147637230 | 147675524 | ||
| a0001c0009 | 0/0 | 1284 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | ATGAT others(1279): Show |
chr1 | 147637230 | 147675524 | ||
| a0001c0011 | 0/0 | 1284 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | ATGAT others(1279): Show |
chr1 | 147637230 | 147675524 | ||
| a0002c0004 | 0/0 | 1284 | 11 | 11 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | ATGAT others(1279): Show |
chr1 | 147637230 | 147675524 | ||
| a0003c0006 | 0/0 | 1284 | 2 | 2 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | ATGAT others(1279): Show |
chr1 | 147637230 | 147675524 | ||
| a0004c0013 | 0/0 | 1284 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | ATGAT others(1279): Show |
chr1 | 147637230 | 147675524 | ||
| a0004c0014 | 0/0 | 1284 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | ATGAT others(1279): Show |
chr1 | 147637230 | 147675524 | ||
| a0005c0012 | 0/0 | 1284 | 1 | 0 | 1 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | ATGAT others(1279): Show |
chr1 | 147637230 | 147675524 | ||
| a0006c0010 | 0/0 | 1284 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | ATGAT others(1279): Show |
chr1 | 147637230 | 147675524 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 6957 | 72 | 19 | 12 | 34 | 2 | 5 | ACP6_chr1_147637230_147675524 | ACP6 | CACTT others(6952): Show |
chr1 | 147637230 | 147675524 |
| a0001c0001t0004 | 0/0 | 6957 | 48 | 6 | 13 | 15 | 6 | 8 | ACP6_chr1_147637230_147675524 | ACP6 | CACTT others(6952): Show |
chr1 | 147637230 | 147675524 |
| a0001c0001t0008 | 0/0 | 6957 | 9 | 0 | 7 | 1 | 0 | 1 | ACP6_chr1_147637230_147675524 | ACP6 | CACTT others(6952): Show |
chr1 | 147637230 | 147675524 |
| a0001c0001t0009 | 0/0 | 6957 | 8 | 0 | 0 | 8 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | CACTT others(6952): Show |
chr1 | 147637230 | 147675524 |
| a0001c0001t0010 | 0/0 | 6957 | 5 | 0 | 1 | 2 | 0 | 2 | ACP6_chr1_147637230_147675524 | ACP6 | CACTT others(6952): Show |
chr1 | 147637230 | 147675524 |
| a0001c0001t0011 | 0/0 | 6957 | 6 | 6 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | CACTT others(6952): Show |
chr1 | 147637230 | 147675524 |
| a0001c0001t0012 | 0/0 | 6957 | 6 | 0 | 0 | 6 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | CACTT others(6952): Show |
chr1 | 147637230 | 147675524 |
| a0001c0001t0013 | 0/0 | 6957 | 4 | 4 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | CACTT others(6952): Show |
chr1 | 147637230 | 147675524 |
| a0001c0001t0016 | 0/0 | 6957 | 4 | 0 | 0 | 4 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | CACTT others(6952): Show |
chr1 | 147637230 | 147675524 |
| a0001c0001t0023 | 0/0 | 6957 | 2 | 0 | 1 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | CACTT others(6952): Show |
chr1 | 147637230 | 147675524 |
| a0001c0001t0027 | 0/0 | 6957 | 2 | 0 | 0 | 2 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | CACTT others(6952): Show |
chr1 | 147637230 | 147675524 |
| a0001c0001t0028 | 0/0 | 6957 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | CACTT others(6952): Show |
chr1 | 147637230 | 147675524 |
| a0001c0001t0034 | 0/0 | 6958 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | CACTT others(6953): Show |
chr1 | 147637230 | 147675524 |
| a0001c0001t0035 | 0/0 | 6958 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | CACTT others(6953): Show |
chr1 | 147637230 | 147675524 |
| a0001c0001t0036 | 0/0 | 6957 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | CACTT others(6952): Show |
chr1 | 147637230 | 147675524 |
| a0001c0001t0047 | 0/1 | 6959 | 1 | 0 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | CACTT others(6954): Show |
chr1 | 147637230 | 147675524 |
| a0001c0001t0049 | 0/0 | 6957 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | CACTT others(6952): Show |
chr1 | 147637230 | 147675524 |
| a0001c0001t0050 | 0/0 | 6957 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | CACTT others(6952): Show |
chr1 | 147637230 | 147675524 |
| a0001c0001t0053 | 0/0 | 6957 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | CACTT others(6952): Show |
chr1 | 147637230 | 147675524 |
| a0001c0001t0057 | 0/0 | 6956 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | CACTT others(6951): Show |
chr1 | 147637230 | 147675524 |
| a0001c0001t0058 | 0/0 | 6957 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | CACTT others(6952): Show |
chr1 | 147637230 | 147675524 |
| a0001c0001t0059 | 0/0 | 6957 | 1 | 0 | 0 | 0 | 0 | 1 | ACP6_chr1_147637230_147675524 | ACP6 | CACTT others(6952): Show |
chr1 | 147637230 | 147675524 |
| a0001c0002t0002 | 0/0 | 6957 | 60 | 4 | 10 | 32 | 3 | 11 | ACP6_chr1_147637230_147675524 | ACP6 | CACTT others(6952): Show |
chr1 | 147637230 | 147675524 |
| a0001c0002t0005 | 0/0 | 6957 | 22 | 3 | 2 | 15 | 1 | 1 | ACP6_chr1_147637230_147675524 | ACP6 | CACTT others(6952): Show |
chr1 | 147637230 | 147675524 |
| a0001c0002t0015 | 0/0 | 6957 | 4 | 0 | 0 | 4 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | CACTT others(6952): Show |
chr1 | 147637230 | 147675524 |
| a0001c0002t0017 | 0/0 | 6957 | 3 | 0 | 3 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | CACTT others(6952): Show |
chr1 | 147637230 | 147675524 |
| a0001c0002t0020 | 0/0 | 6958 | 2 | 0 | 0 | 1 | 0 | 1 | ACP6_chr1_147637230_147675524 | ACP6 | CACTT others(6953): Show |
chr1 | 147637230 | 147675524 |
| a0001c0002t0021 | 0/0 | 6957 | 2 | 2 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | CACTT others(6952): Show |
chr1 | 147637230 | 147675524 |
| a0001c0002t0025 | 0/0 | 6957 | 2 | 0 | 2 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | CACTT others(6952): Show |
chr1 | 147637230 | 147675524 |
| a0001c0002t0029 | 0/0 | 6957 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | CACTT others(6952): Show |
chr1 | 147637230 | 147675524 |
| a0001c0002t0033 | 0/0 | 6957 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | CACTT others(6952): Show |
chr1 | 147637230 | 147675524 |
| a0001c0002t0040 | 0/0 | 6957 | 1 | 0 | 0 | 0 | 0 | 1 | ACP6_chr1_147637230_147675524 | ACP6 | CACTT others(6952): Show |
chr1 | 147637230 | 147675524 |
| a0001c0002t0041 | 0/0 | 7016 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | CACTT others(7011): Show |
chr1 | 147637230 | 147675524 |
| a0001c0002t0042 | 1/0 | 6956 | 1 | 0 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | CACTT others(6951): Show |
chr1 | 147637230 | 147675524 |
| a0001c0002t0043 | 0/0 | 6957 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | CACTT others(6952): Show |
chr1 | 147637230 | 147675524 |
| a0001c0003t0001 | 0/0 | 6957 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | CACTT others(6952): Show |
chr1 | 147637230 | 147675524 |
| a0001c0003t0003 | 0/0 | 6957 | 63 | 0 | 5 | 52 | 2 | 4 | ACP6_chr1_147637230_147675524 | ACP6 | CACTT others(6952): Show |
chr1 | 147637230 | 147675524 |
| a0001c0003t0006 | 0/0 | 6957 | 10 | 7 | 0 | 0 | 0 | 3 | ACP6_chr1_147637230_147675524 | ACP6 | CACTT others(6952): Show |
chr1 | 147637230 | 147675524 |
| a0001c0003t0014 | 0/0 | 6958 | 4 | 0 | 1 | 3 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | CACTT others(6953): Show |
chr1 | 147637230 | 147675524 |
| a0001c0003t0018 | 0/0 | 6954 | 3 | 3 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | CACTT others(6949): Show |
chr1 | 147637230 | 147675524 |
| a0001c0003t0019 | 0/0 | 6957 | 2 | 0 | 0 | 0 | 0 | 2 | ACP6_chr1_147637230_147675524 | ACP6 | CACTT others(6952): Show |
chr1 | 147637230 | 147675524 |
| a0001c0003t0024 | 0/0 | 6957 | 2 | 0 | 0 | 2 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | CACTT others(6952): Show |
chr1 | 147637230 | 147675524 |
| a0001c0003t0026 | 0/0 | 6957 | 2 | 2 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | CACTT others(6952): Show |
chr1 | 147637230 | 147675524 |
| a0001c0003t0030 | 0/0 | 6957 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | CACTT others(6952): Show |
chr1 | 147637230 | 147675524 |
| a0001c0003t0031 | 0/0 | 6938 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | CACTT others(6933): Show |
chr1 | 147637230 | 147675524 |
| a0001c0003t0032 | 0/0 | 6957 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | CACTT others(6952): Show |
chr1 | 147637230 | 147675524 |
| a0001c0003t0037 | 0/0 | 6957 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | CACTT others(6952): Show |
chr1 | 147637230 | 147675524 |
| a0001c0003t0038 | 0/0 | 6954 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | CACTT others(6949): Show |
chr1 | 147637230 | 147675524 |
| a0001c0003t0039 | 0/0 | 6954 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | CACTT others(6949): Show |
chr1 | 147637230 | 147675524 |
| a0001c0003t0044 | 0/0 | 6957 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | CACTT others(6952): Show |
chr1 | 147637230 | 147675524 |
| a0001c0003t0045 | 0/0 | 6957 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | CACTT others(6952): Show |
chr1 | 147637230 | 147675524 |
| a0001c0003t0046 | 0/0 | 6957 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | CACTT others(6952): Show |
chr1 | 147637230 | 147675524 |
| a0001c0003t0051 | 0/0 | 6957 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | CACTT others(6952): Show |
chr1 | 147637230 | 147675524 |
| a0001c0003t0052 | 0/0 | 6956 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | CACTT others(6951): Show |
chr1 | 147637230 | 147675524 |
| a0001c0003t0054 | 0/0 | 6957 | 1 | 0 | 1 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | CACTT others(6952): Show |
chr1 | 147637230 | 147675524 |
| a0001c0003t0055 | 0/0 | 6957 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | CACTT others(6952): Show |
chr1 | 147637230 | 147675524 |
| a0001c0003t0056 | 0/0 | 6957 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | CACTT others(6952): Show |
chr1 | 147637230 | 147675524 |
| a0001c0005t0002 | 0/0 | 6957 | 2 | 1 | 1 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | CACTT others(6952): Show |
chr1 | 147637230 | 147675524 |
| a0001c0007t0006 | 0/0 | 6957 | 2 | 2 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | CACTT others(6952): Show |
chr1 | 147637230 | 147675524 |
| a0001c0008t0010 | 0/0 | 6957 | 2 | 0 | 2 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | CACTT others(6952): Show |
chr1 | 147637230 | 147675524 |
| a0001c0009t0001 | 0/0 | 6957 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | CACTT others(6952): Show |
chr1 | 147637230 | 147675524 |
| a0001c0011t0006 | 0/0 | 6957 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | CACTT others(6952): Show |
chr1 | 147637230 | 147675524 |
| a0002c0004t0007 | 0/0 | 6957 | 10 | 10 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | CACTT others(6952): Show |
chr1 | 147637230 | 147675524 |
| a0002c0004t0048 | 0/0 | 6957 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | CACTT others(6952): Show |
chr1 | 147637230 | 147675524 |
| a0003c0006t0022 | 0/0 | 6957 | 2 | 2 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | CACTT others(6952): Show |
chr1 | 147637230 | 147675524 |
| a0004c0013t0002 | 0/0 | 6957 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | CACTT others(6952): Show |
chr1 | 147637230 | 147675524 |
| a0004c0014t0001 | 0/0 | 6957 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | CACTT others(6952): Show |
chr1 | 147637230 | 147675524 |
| a0005c0012t0002 | 0/0 | 6957 | 1 | 0 | 1 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | CACTT others(6952): Show |
chr1 | 147637230 | 147675524 |
| a0006c0010t0001 | 0/0 | 6957 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | CACTT others(6952): Show |
chr1 | 147637230 | 147675524 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 38 | 2 | 10 | 21 | 2 | 3 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0001t0001g0011 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0001t0001g0017 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0001t0001g0029 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0001t0004g0002 | 0/0 | 24 | 3 | 11 | 2 | 6 | 2 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0001t0004g0014 | 0/0 | 5 | 0 | 0 | 3 | 0 | 2 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0001t0004g0016 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0001t0004g0035 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0001t0004g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0001t0004g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0001t0004g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0001t0004g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0001t0004g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0001t0004g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0001t0004g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0001t0004g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0001t0004g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0001t0004g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0001t0004g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0001t0004g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0001t0008g0015 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0001t0008g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0001t0008g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0001t0008g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0001t0008g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0001t0009g0009 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0001t0009g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0001t0010g0036 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0001t0010g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0001t0010g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0001t0010g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0001t0011g0018 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0001t0011g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0001t0011g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0001t0012g0012 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0001t0013g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0001t0013g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0001t0016g0028 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0001t0016g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0001t0023g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0001t0023g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0001t0027g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0001t0027g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0001t0028g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0001t0034g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0001t0035g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0001t0036g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0001t0047g0122 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0001t0049g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0001t0050g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0001t0053g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0001t0057g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0001t0058g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0001t0059g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0002t0002g0005 | 0/0 | 12 | 0 | 3 | 5 | 0 | 4 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0002t0002g0006 | 0/0 | 10 | 0 | 2 | 5 | 1 | 2 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0002t0002g0019 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0002t0002g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0002t0002g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0002t0002g0025 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0002t0002g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0002t0002g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0002t0002g0040 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0002t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0002t0002g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0002t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0002t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0002t0002g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0002t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0002t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0002t0002g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0002t0005g0007 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0002t0005g0013 | 0/0 | 6 | 3 | 2 | 0 | 1 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0002t0005g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0002t0005g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0002t0005g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0002t0005g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0002t0005g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0002t0005g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0002t0005g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0002t0015g0030 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0002t0015g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0002t0017g0026 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0002t0020g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0002t0020g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0002t0021g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0002t0025g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0002t0029g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0002t0033g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0002t0040g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0002t0041g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0002t0042g0110 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0002t0043g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0003t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0003t0003g0003 | 0/0 | 23 | 0 | 0 | 23 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0003t0003g0004 | 0/0 | 16 | 0 | 1 | 11 | 1 | 3 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0003t0003g0010 | 0/0 | 7 | 0 | 1 | 6 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0003t0003g0027 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0003t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0003t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0003t0003g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0003t0003g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0003t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0003t0003g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0003t0003g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0003t0003g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0003t0003g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0003t0003g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0003t0003g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0003t0003g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0003t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0003t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0003t0006g0020 | 0/0 | 3 | 1 | 0 | 0 | 0 | 2 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0003t0006g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0003t0006g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0003t0006g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0003t0006g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0003t0006g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0003t0014g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0003t0014g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0003t0014g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0003t0014g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0003t0018g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0003t0018g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0003t0019g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0003t0024g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0003t0024g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0003t0026g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0003t0030g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0003t0031g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0003t0032g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0003t0037g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0003t0038g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0003t0039g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0003t0044g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0003t0045g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0003t0046g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0003t0051g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0003t0052g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0003t0054g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0003t0055g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0003t0056g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0005t0002g0038 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0007t0006g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0008t0010g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0008t0010g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0009t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0001c0011t0006g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0002c0004t0007g0008 | 0/0 | 8 | 8 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0002c0004t0007g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0002c0004t0007g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0002c0004t0048g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0003c0006t0022g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0004c0013t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0004c0014t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0005c0012t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| a0006c0010t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0004 | g0002 | EUR | GBR | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG00099 | hp2 | a0001 | c0003 | t0003 | g0143 | EUR | GBR | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG00140 | hp1 | a0001 | c0002 | t0005 | g0013 | EUR | GBR | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG00140 | hp2 | a0001 | c0001 | t0004 | g0002 | EUR | GBR | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG00323 | hp1 | a0001 | c0003 | t0003 | g0004 | EUR | FIN | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG00408 | hp1 | a0001 | c0003 | t0056 | g0137 | EAS | CHS | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG00408 | hp2 | a0001 | c0002 | t0002 | g0071 | EAS | CHS | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG00423 | hp1 | a0001 | c0002 | t0002 | g0006 | EAS | CHS | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG00438 | hp1 | a0001 | c0002 | t0005 | g0007 | EAS | CHS | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG00438 | hp2 | a0001 | c0001 | t0009 | g0009 | EAS | CHS | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG00544 | hp2 | a0001 | c0003 | t0003 | g0004 | EAS | CHS | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG00558 | hp1 | a0001 | c0003 | t0003 | g0003 | EAS | CHS | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG00558 | hp2 | a0001 | c0001 | t0016 | g0181 | EAS | CHS | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG00597 | hp1 | a0001 | c0003 | t0024 | g0127 | EAS | CHS | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG00597 | hp2 | a0001 | c0002 | t0002 | g0005 | EAS | CHS | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG00609 | hp1 | a0001 | c0002 | t0002 | g0111 | EAS | CHS | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG00609 | hp2 | a0001 | c0003 | t0003 | g0004 | EAS | CHS | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | CHS | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG00621 | hp2 | a0001 | c0003 | t0003 | g0125 | EAS | CHS | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG00639 | hp1 | a0001 | c0001 | t0004 | g0035 | AMR | PUR | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG00639 | hp2 | a0001 | c0002 | t0002 | g0040 | AMR | PUR | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG00673 | hp1 | a0001 | c0001 | t0058 | g0185 | EAS | CHS | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG00673 | hp2 | a0001 | c0001 | t0008 | g0096 | EAS | CHS | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG00735 | hp1 | a0001 | c0002 | t0002 | g0005 | AMR | PUR | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG00735 | hp2 | a0001 | c0001 | t0004 | g0067 | AMR | PUR | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG00738 | hp1 | a0001 | c0001 | t0023 | g0145 | AMR | PUR | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG00738 | hp2 | a0001 | c0002 | t0002 | g0006 | AMR | PUR | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG00741 | hp1 | a0001 | c0002 | t0002 | g0005 | AMR | PUR | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG00741 | hp2 | a0001 | c0001 | t0004 | g0002 | AMR | PUR | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG01069 | hp1 | a0001 | c0002 | t0017 | g0026 | AMR | PUR | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG01069 | hp2 | a0001 | c0008 | t0010 | g0097 | AMR | PUR | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG01071 | hp1 | a0001 | c0002 | t0017 | g0026 | AMR | PUR | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG01071 | hp2 | a0001 | c0008 | t0010 | g0119 | AMR | PUR | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG01081 | hp1 | a0001 | c0001 | t0010 | g0036 | AMR | PUR | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG01081 | hp2 | a0001 | c0002 | t0005 | g0013 | AMR | PUR | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG01106 | hp1 | a0001 | c0002 | t0017 | g0026 | AMR | PUR | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG01106 | hp2 | a0001 | c0001 | t0004 | g0002 | AMR | PUR | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG01109 | hp1 | a0001 | c0005 | t0002 | g0038 | AMR | PUR | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG01109 | hp2 | a0001 | c0001 | t0004 | g0002 | AMR | PUR | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG01167 | hp1 | a0001 | c0001 | t0004 | g0002 | AMR | PUR | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG01168 | hp1 | a0001 | c0003 | t0014 | g0142 | AMR | PUR | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG01168 | hp2 | a0001 | c0002 | t0025 | g0041 | AMR | PUR | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG01169 | hp1 | a0001 | c0002 | t0025 | g0041 | AMR | PUR | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG01175 | hp2 | a0005 | c0012 | t0002 | g0116 | AMR | PUR | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG01192 | hp1 | a0001 | c0003 | t0003 | g0141 | AMR | PUR | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG01192 | hp2 | a0001 | c0002 | t0002 | g0006 | AMR | PUR | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG01243 | hp1 | a0001 | c0003 | t0003 | g0004 | AMR | PUR | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG01243 | hp2 | a0001 | c0002 | t0002 | g0025 | AMR | PUR | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG01255 | hp1 | a0001 | c0001 | t0004 | g0002 | AMR | CLM | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG01255 | hp2 | a0001 | c0001 | t0008 | g0088 | AMR | CLM | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG01256 | hp1 | a0001 | c0001 | t0008 | g0015 | AMR | CLM | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG01257 | hp1 | a0001 | c0002 | t0002 | g0025 | AMR | CLM | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG01257 | hp2 | a0001 | c0001 | t0004 | g0002 | AMR | CLM | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG01258 | hp1 | a0001 | c0002 | t0002 | g0025 | AMR | CLM | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG01258 | hp2 | a0001 | c0001 | t0008 | g0015 | AMR | CLM | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG01346 | hp1 | a0001 | c0003 | t0003 | g0010 | AMR | CLM | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG01346 | hp2 | a0001 | c0001 | t0008 | g0015 | AMR | CLM | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG01358 | hp2 | a0001 | c0001 | t0004 | g0002 | AMR | CLM | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG01433 | hp1 | a0001 | c0002 | t0002 | g0107 | AMR | CLM | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG01433 | hp2 | a0001 | c0001 | t0004 | g0002 | AMR | CLM | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG01496 | hp1 | a0001 | c0001 | t0004 | g0002 | AMR | CLM | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG01496 | hp2 | a0001 | c0001 | t0008 | g0087 | AMR | CLM | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG01515 | hp1 | a0001 | c0001 | t0004 | g0002 | EUR | IBS | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG01515 | hp2 | a0001 | c0002 | t0002 | g0114 | EUR | IBS | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG01516 | hp1 | a0001 | c0001 | t0004 | g0002 | EUR | IBS | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG01516 | hp2 | a0001 | c0002 | t0002 | g0006 | EUR | IBS | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG01884 | hp1 | a0001 | c0001 | t0004 | g0089 | AFR | ACB | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG01884 | hp2 | a0001 | c0003 | t0006 | g0021 | AFR | ACB | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG01891 | hp1 | a0001 | c0007 | t0006 | g0032 | AFR | ACB | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG01891 | hp2 | a0001 | c0003 | t0032 | g0047 | AFR | ACB | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG01934 | hp1 | a0001 | c0001 | t0004 | g0002 | AMR | PEL | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG01943 | hp2 | a0001 | c0001 | t0008 | g0015 | AMR | PEL | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PEL | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG01952 | hp2 | a0001 | c0003 | t0003 | g0134 | AMR | PEL | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG01975 | hp1 | a0001 | c0002 | t0002 | g0005 | AMR | PEL | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG01978 | hp1 | a0001 | c0002 | t0005 | g0013 | AMR | PEL | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG01978 | hp2 | a0001 | c0003 | t0054 | g0140 | AMR | PEL | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG01981 | hp2 | a0001 | c0003 | t0003 | g0138 | AMR | PEL | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG02015 | hp1 | a0001 | c0001 | t0009 | g0070 | EAS | KHV | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG02015 | hp2 | a0001 | c0002 | t0002 | g0022 | EAS | KHV | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG02027 | hp2 | a0001 | c0002 | t0002 | g0037 | EAS | KHV | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG02040 | hp1 | a0001 | c0002 | t0043 | g0113 | EAS | KHV | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG02040 | hp2 | a0001 | c0003 | t0003 | g0003 | EAS | KHV | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG02056 | hp1 | a0001 | c0003 | t0003 | g0004 | EAS | KHV | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG02056 | hp2 | a0001 | c0001 | t0028 | g0046 | EAS | KHV | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG02074 | hp1 | a0001 | c0001 | t0009 | g0009 | EAS | KHV | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | KHV | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG02080 | hp1 | a0001 | c0002 | t0002 | g0006 | EAS | KHV | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | KHV | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG02083 | hp1 | a0001 | c0003 | t0003 | g0003 | EAS | KHV | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG02083 | hp2 | a0001 | c0001 | t0004 | g0093 | EAS | KHV | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG02129 | hp1 | a0001 | c0003 | t0003 | g0004 | EAS | KHV | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG02129 | hp2 | a0001 | c0002 | t0005 | g0007 | EAS | KHV | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | KHV | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG02132 | hp2 | a0001 | c0003 | t0003 | g0124 | EAS | KHV | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG02135 | hp1 | a0001 | c0001 | t0036 | g0091 | EAS | KHV | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG02135 | hp2 | a0001 | c0002 | t0005 | g0177 | EAS | KHV | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG02145 | hp1 | a0001 | c0002 | t0002 | g0019 | AFR | ACB | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG02145 | hp2 | a0003 | c0006 | t0022 | g0033 | AFR | ACB | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG02155 | hp1 | a0001 | c0002 | t0002 | g0005 | EAS | CDX | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG02155 | hp2 | a0001 | c0003 | t0003 | g0003 | EAS | CDX | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG02165 | hp1 | a0001 | c0002 | t0002 | g0115 | EAS | CDX | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG02165 | hp2 | a0001 | c0003 | t0003 | g0004 | EAS | CDX | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG02257 | hp1 | a0002 | c0004 | t0007 | g0008 | AFR | ACB | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG02258 | hp1 | a0001 | c0003 | t0006 | g0021 | AFR | ACB | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG02273 | hp1 | a0001 | c0001 | t0008 | g0015 | AMR | PEL | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG02280 | hp1 | a0001 | c0003 | t0006 | g0052 | AFR | ACB | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG02280 | hp2 | a0001 | c0003 | t0030 | g0049 | AFR | ACB | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG02523 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | KHV | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | KHV | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG02572 | hp1 | a0001 | c0002 | t0002 | g0019 | AFR | GWD | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG02572 | hp2 | a0002 | c0004 | t0007 | g0104 | AFR | GWD | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG02615 | hp2 | a0001 | c0002 | t0021 | g0039 | AFR | GWD | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | GWD | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG02630 | hp1 | a0001 | c0003 | t0018 | g0045 | AFR | GWD | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG02630 | hp2 | a0001 | c0003 | t0006 | g0059 | AFR | GWD | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG02647 | hp2 | a0001 | c0003 | t0045 | g0101 | AFR | GWD | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG02683 | hp1 | a0001 | c0001 | t0004 | g0014 | SAS | PJL | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0174 | SAS | PJL | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG02698 | hp1 | a0001 | c0002 | t0002 | g0121 | SAS | PJL | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG02698 | hp2 | a0001 | c0002 | t0002 | g0005 | SAS | PJL | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG02717 | hp1 | a0001 | c0003 | t0006 | g0058 | AFR | GWD | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG02717 | hp2 | a0002 | c0004 | t0007 | g0008 | AFR | GWD | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG02723 | hp1 | a0001 | c0003 | t0018 | g0045 | AFR | GWD | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG02723 | hp2 | a0001 | c0001 | t0049 | g0063 | AFR | GWD | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG02735 | hp1 | a0001 | c0001 | t0004 | g0002 | SAS | PJL | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG02738 | hp1 | a0001 | c0001 | t0059 | g0186 | SAS | PJL | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG02738 | hp2 | a0001 | c0001 | t0010 | g0098 | SAS | PJL | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG02809 | hp1 | a0001 | c0003 | t0006 | g0021 | AFR | GWD | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | GWD | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG02818 | hp1 | a0003 | c0006 | t0022 | g0033 | AFR | GWD | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG02818 | hp2 | a0001 | c0001 | t0004 | g0002 | AFR | GWD | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG02886 | hp1 | a0001 | c0001 | t0011 | g0018 | AFR | GWD | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | GWD | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG02895 | hp1 | a0001 | c0003 | t0026 | g0044 | AFR | GWD | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG02896 | hp1 | a0001 | c0001 | t0011 | g0018 | AFR | GWD | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG02896 | hp2 | a0001 | c0002 | t0002 | g0019 | AFR | GWD | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG02897 | hp1 | a0001 | c0001 | t0011 | g0018 | AFR | GWD | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG02922 | hp2 | a0002 | c0004 | t0007 | g0008 | AFR | ESN | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG02965 | hp1 | a0001 | c0001 | t0004 | g0002 | AFR | ESN | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG02965 | hp2 | a0001 | c0001 | t0050 | g0175 | AFR | ESN | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG02970 | hp1 | a0001 | c0002 | t0033 | g0057 | AFR | ESN | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG02970 | hp2 | a0001 | c0001 | t0011 | g0056 | AFR | ESN | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG02976 | hp1 | a0001 | c0001 | t0034 | g0048 | AFR | ESN | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG02976 | hp2 | a0001 | c0003 | t0038 | g0095 | AFR | ESN | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG03017 | hp1 | a0001 | c0003 | t0003 | g0004 | SAS | PJL | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG03017 | hp2 | a0001 | c0002 | t0002 | g0064 | SAS | PJL | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG03041 | hp1 | a0001 | c0001 | t0011 | g0055 | AFR | GWD | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG03041 | hp2 | a0001 | c0002 | t0002 | g0019 | AFR | GWD | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG03098 | hp1 | a0001 | c0003 | t0046 | g0062 | AFR | MSL | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG03130 | hp1 | a0001 | c0009 | t0001 | g0123 | AFR | ESN | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG03130 | hp2 | a0001 | c0002 | t0005 | g0013 | AFR | ESN | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG03139 | hp1 | a0002 | c0004 | t0007 | g0008 | AFR | ESN | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG03139 | hp2 | a0001 | c0003 | t0006 | g0020 | AFR | ESN | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG03195 | hp2 | a0001 | c0001 | t0013 | g0024 | AFR | ESN | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG03209 | hp1 | a0001 | c0001 | t0013 | g0105 | AFR | MSL | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG03209 | hp2 | a0002 | c0004 | t0007 | g0008 | AFR | MSL | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG03225 | hp1 | a0004 | c0014 | t0001 | g0163 | AFR | MSL | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG03225 | hp2 | a0001 | c0002 | t0029 | g0051 | AFR | MSL | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG03239 | hp1 | a0001 | c0002 | t0002 | g0006 | SAS | PJL | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG03239 | hp2 | a0001 | c0001 | t0010 | g0083 | SAS | PJL | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG03453 | hp1 | a0001 | c0003 | t0051 | g0149 | AFR | MSL | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | MSL | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG03486 | hp1 | a0001 | c0003 | t0018 | g0182 | AFR | MSL | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG03491 | hp1 | a0001 | c0002 | t0020 | g0076 | SAS | PJL | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG03491 | hp2 | a0001 | c0001 | t0004 | g0068 | SAS | PJL | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG03492 | hp2 | a0001 | c0002 | t0002 | g0005 | SAS | PJL | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | GWD | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG03540 | hp2 | a0001 | c0001 | t0004 | g0002 | AFR | GWD | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG03579 | hp1 | a0002 | c0004 | t0007 | g0008 | AFR | MSL | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG03654 | hp1 | a0001 | c0002 | t0002 | g0005 | SAS | PJL | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG03654 | hp2 | a0001 | c0002 | t0002 | g0108 | SAS | PJL | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG03669 | hp1 | a0001 | c0001 | t0004 | g0078 | SAS | PJL | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG03669 | hp2 | a0001 | c0003 | t0003 | g0004 | SAS | PJL | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG03710 | hp1 | a0001 | c0001 | t0008 | g0100 | SAS | PJL | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG03710 | hp2 | a0001 | c0002 | t0040 | g0077 | SAS | PJL | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG03831 | hp1 | a0001 | c0002 | t0002 | g0074 | SAS | BEB | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG03831 | hp2 | a0001 | c0003 | t0006 | g0020 | SAS | BEB | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG03834 | hp1 | a0001 | c0003 | t0006 | g0020 | SAS | BEB | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0169 | SAS | BEB | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG03927 | hp1 | a0001 | c0001 | t0004 | g0002 | SAS | BEB | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG03927 | hp2 | a0001 | c0003 | t0006 | g0050 | SAS | BEB | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG03942 | hp1 | a0001 | c0001 | t0004 | g0066 | SAS | BEB | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG03942 | hp2 | a0001 | c0003 | t0003 | g0004 | SAS | BEB | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG04115 | hp2 | a0001 | c0002 | t0002 | g0006 | SAS | STU | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG04184 | hp1 | a0001 | c0003 | t0019 | g0031 | SAS | BEB | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG04184 | hp2 | a0001 | c0002 | t0002 | g0005 | SAS | BEB | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG04199 | hp1 | a0001 | c0002 | t0002 | g0106 | SAS | STU | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG04199 | hp2 | a0001 | c0001 | t0004 | g0084 | SAS | STU | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG04204 | hp1 | a0001 | c0001 | t0004 | g0014 | SAS | STU | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG04204 | hp2 | a0001 | c0003 | t0003 | g0144 | SAS | STU | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA18522 | hp1 | a0002 | c0004 | t0007 | g0008 | AFR | YRI | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | YRI | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA18612 | hp1 | a0001 | c0001 | t0004 | g0014 | EAS | CHB | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA18612 | hp2 | a0001 | c0002 | t0002 | g0080 | EAS | CHB | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA18747 | hp1 | a0001 | c0002 | t0002 | g0079 | EAS | CHB | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA18747 | hp2 | a0001 | c0002 | t0002 | g0037 | EAS | CHB | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA18906 | hp1 | a0001 | c0001 | t0013 | g0024 | AFR | YRI | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA18906 | hp2 | a0001 | c0003 | t0031 | g0053 | AFR | YRI | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA18940 | hp1 | a0001 | c0003 | t0003 | g0010 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA18940 | hp2 | a0001 | c0001 | t0012 | g0012 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA18942 | hp1 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA18942 | hp2 | a0001 | c0001 | t0009 | g0009 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA18943 | hp1 | a0001 | c0001 | t0009 | g0009 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA18944 | hp2 | a0001 | c0003 | t0003 | g0010 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA18945 | hp1 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA18946 | hp1 | a0001 | c0002 | t0015 | g0184 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA18948 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA18948 | hp2 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA18949 | hp1 | a0001 | c0003 | t0003 | g0004 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA18949 | hp2 | a0001 | c0002 | t0002 | g0112 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA18950 | hp1 | a0001 | c0001 | t0004 | g0086 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA18950 | hp2 | a0001 | c0003 | t0003 | g0183 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA18951 | hp1 | a0001 | c0001 | t0035 | g0060 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA18951 | hp2 | a0001 | c0003 | t0003 | g0130 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA18952 | hp1 | a0001 | c0003 | t0003 | g0004 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA18953 | hp2 | a0001 | c0002 | t0002 | g0034 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA18954 | hp2 | a0001 | c0002 | t0002 | g0120 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA18956 | hp1 | a0001 | c0001 | t0010 | g0092 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA18956 | hp2 | a0001 | c0003 | t0003 | g0004 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA18957 | hp1 | a0001 | c0003 | t0014 | g0135 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA18957 | hp2 | a0001 | c0001 | t0057 | g0157 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA18959 | hp1 | a0001 | c0002 | t0002 | g0022 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA18959 | hp2 | a0001 | c0003 | t0014 | g0136 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA18960 | hp1 | a0001 | c0002 | t0002 | g0075 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA18960 | hp2 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA18962 | hp2 | a0006 | c0010 | t0001 | g0168 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA18963 | hp1 | a0001 | c0002 | t0015 | g0030 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA18963 | hp2 | a0001 | c0003 | t0003 | g0131 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA18966 | hp1 | a0001 | c0003 | t0024 | g0129 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA18966 | hp2 | a0001 | c0001 | t0004 | g0014 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA18968 | hp1 | a0001 | c0001 | t0009 | g0009 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA18968 | hp2 | a0001 | c0002 | t0015 | g0030 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA18969 | hp1 | a0001 | c0002 | t0002 | g0073 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA18971 | hp1 | a0001 | c0002 | t0002 | g0022 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA18971 | hp2 | a0001 | c0001 | t0012 | g0012 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA18973 | hp1 | a0001 | c0001 | t0004 | g0016 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA18974 | hp1 | a0001 | c0001 | t0012 | g0012 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA18974 | hp2 | a0001 | c0002 | t0005 | g0007 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA18975 | hp1 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA18975 | hp2 | a0001 | c0002 | t0002 | g0117 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA18977 | hp1 | a0001 | c0003 | t0055 | g0128 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA18977 | hp2 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA18978 | hp1 | a0001 | c0002 | t0015 | g0030 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA18979 | hp1 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA18980 | hp1 | a0001 | c0001 | t0016 | g0028 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA18980 | hp2 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA18981 | hp1 | a0001 | c0002 | t0005 | g0007 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA18981 | hp2 | a0001 | c0001 | t0004 | g0016 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA18982 | hp1 | a0001 | c0003 | t0003 | g0027 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA18982 | hp2 | a0001 | c0002 | t0005 | g0007 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA18983 | hp2 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA18984 | hp1 | a0001 | c0002 | t0005 | g0007 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA18985 | hp1 | a0001 | c0002 | t0005 | g0152 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA18986 | hp2 | a0001 | c0003 | t0003 | g0027 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA18988 | hp1 | a0001 | c0002 | t0005 | g0154 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA18988 | hp2 | a0001 | c0003 | t0003 | g0132 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA18989 | hp1 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA18989 | hp2 | a0001 | c0001 | t0027 | g0172 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA18990 | hp2 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA18994 | hp2 | a0001 | c0002 | t0005 | g0153 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA18995 | hp1 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA18995 | hp2 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA18999 | hp2 | a0001 | c0002 | t0002 | g0023 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA19001 | hp1 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA19001 | hp2 | a0001 | c0001 | t0004 | g0014 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA19002 | hp1 | a0001 | c0003 | t0003 | g0004 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA19002 | hp2 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA19003 | hp2 | a0001 | c0001 | t0004 | g0016 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA19004 | hp2 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA19005 | hp1 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA19005 | hp2 | a0001 | c0001 | t0009 | g0009 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA19007 | hp1 | a0001 | c0001 | t0027 | g0171 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA19007 | hp2 | a0001 | c0003 | t0003 | g0004 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA19009 | hp1 | a0001 | c0002 | t0005 | g0007 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA19009 | hp2 | a0001 | c0001 | t0004 | g0016 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA19010 | hp1 | a0001 | c0003 | t0003 | g0010 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA19010 | hp2 | a0001 | c0001 | t0009 | g0009 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA19012 | hp1 | a0001 | c0001 | t0012 | g0012 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA19012 | hp2 | a0001 | c0003 | t0003 | g0027 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA19043 | hp1 | a0001 | c0002 | t0005 | g0013 | AFR | LWK | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA19043 | hp2 | a0001 | c0003 | t0052 | g0150 | AFR | LWK | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA19054 | hp2 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA19056 | hp1 | a0001 | c0003 | t0014 | g0139 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA19056 | hp2 | a0001 | c0001 | t0012 | g0012 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA19057 | hp1 | a0001 | c0001 | t0004 | g0118 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA19057 | hp2 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA19058 | hp1 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA19058 | hp2 | a0001 | c0002 | t0002 | g0023 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA19059 | hp1 | a0001 | c0002 | t0020 | g0109 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA19059 | hp2 | a0001 | c0003 | t0003 | g0133 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA19060 | hp1 | a0001 | c0001 | t0016 | g0028 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA19060 | hp2 | a0001 | c0002 | t0005 | g0156 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA19062 | hp1 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA19062 | hp2 | a0001 | c0003 | t0037 | g0099 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA19063 | hp1 | a0001 | c0003 | t0003 | g0148 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA19063 | hp2 | a0001 | c0002 | t0005 | g0155 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA19065 | hp1 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA19065 | hp2 | a0001 | c0001 | t0012 | g0012 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA19068 | hp1 | a0001 | c0002 | t0002 | g0069 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA19068 | hp2 | a0001 | c0001 | t0010 | g0036 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA19070 | hp1 | a0001 | c0001 | t0004 | g0065 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA19070 | hp2 | a0001 | c0003 | t0003 | g0010 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA19072 | hp1 | a0001 | c0002 | t0041 | g0082 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA19072 | hp2 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA19074 | hp1 | a0001 | c0001 | t0016 | g0028 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA19074 | hp2 | a0001 | c0003 | t0003 | g0004 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA19078 | hp1 | a0001 | c0001 | t0053 | g0159 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA19078 | hp2 | a0001 | c0003 | t0003 | g0126 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA19079 | hp1 | a0001 | c0002 | t0005 | g0007 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA19079 | hp2 | a0001 | c0001 | t0023 | g0180 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA19080 | hp1 | a0001 | c0002 | t0002 | g0034 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA19080 | hp2 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA19081 | hp2 | a0001 | c0003 | t0003 | g0010 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA19082 | hp1 | a0001 | c0002 | t0002 | g0023 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA19082 | hp2 | a0001 | c0001 | t0004 | g0085 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA19084 | hp1 | a0001 | c0003 | t0003 | g0010 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA19088 | hp1 | a0001 | c0001 | t0004 | g0016 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA19088 | hp2 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA19090 | hp1 | a0004 | c0013 | t0002 | g0081 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA19091 | hp2 | a0001 | c0002 | t0005 | g0007 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA19240 | hp1 | a0002 | c0004 | t0048 | g0102 | AFR | YRI | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA19240 | hp2 | a0001 | c0002 | t0005 | g0013 | AFR | YRI | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA20129 | hp1 | a0001 | c0005 | t0002 | g0038 | AFR | ASW | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA20129 | hp2 | a0001 | c0001 | t0011 | g0018 | AFR | ASW | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA20752 | hp1 | a0001 | c0001 | t0004 | g0002 | EUR | TSI | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA20805 | hp1 | a0001 | c0002 | t0002 | g0040 | EUR | TSI | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA20805 | hp2 | a0001 | c0001 | t0004 | g0002 | EUR | TSI | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA20905 | hp1 | a0001 | c0002 | t0005 | g0178 | SAS | GIH | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA20905 | hp2 | a0001 | c0003 | t0019 | g0031 | SAS | GIH | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG01123 | hp2 | a0001 | c0001 | t0004 | g0002 | AMR | CLM | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG02109 | hp1 | a0001 | c0001 | t0013 | g0024 | AFR | ACB | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG02109 | hp2 | a0002 | c0004 | t0007 | g0103 | AFR | ACB | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG02486 | hp1 | a0001 | c0007 | t0006 | g0032 | AFR | ACB | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG02486 | hp2 | a0001 | c0003 | t0044 | g0061 | AFR | ACB | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG02559 | hp1 | a0001 | c0001 | t0004 | g0090 | AFR | ACB | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG02559 | hp2 | a0002 | c0004 | t0007 | g0008 | AFR | ACB | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG03471 | hp1 | a0001 | c0003 | t0026 | g0044 | AFR | MSL | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | MSL | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG06807 | hp1 | a0001 | c0002 | t0021 | g0039 | AFR | USA | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| HG06807 | hp2 | a0001 | c0011 | t0006 | g0054 | AFR | USA | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA18955 | hp1 | a0001 | c0003 | t0001 | g0170 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA18955 | hp2 | a0001 | c0002 | t0002 | g0072 | EAS | JPT | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA21309 | hp1 | a0001 | c0003 | t0039 | g0094 | AFR | LWK | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| NA21309 | hp2 | a0001 | c0001 | t0004 | g0035 | AFR | LWK | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0047 | g0122 | REF | REF | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0042 | g0110 | REF | REF | ACP6_chr1_147637230_147675524 | ACP6 | chr1 | 147637230 | 147675524 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:147647506 | T | C | 1 | a0003 | 2 | HG02145.hp2 HG02818.hp1 |
missense_variant | MODERATE | c.1204A>G | p.Met402Val | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 1680/6956 | 1204/1287 | 402/428 | chr1 | 147647506 | |||
| chr1:147648394 | G | A | 1 | a0003 | 2 | HG02145.hp2 HG02818.hp1 |
missense_variant | MODERATE | c.995C>T | p.Ala332Val | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 9/10 | 1471/6956 | 995/1287 | 332/428 | chr1 | 147648394 | |||
| chr1:147650174 | T | C | 1 | a0002 | 11 | HG02109.hp2 HG02257.hp1 HG02559.hp2 others(8): Show |
missense_variant | MODERATE | c.946A>G | p.Met316Val | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 8/10 | 1422/6956 | 946/1287 | 316/428 | chr1 | 147650174 | |||
| chr1:147650194 | T | C | 1 | a0006 | 1 | NA18962.hp2 | missense_variant | MODERATE | c.926A>G | p.Glu309Gly | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 8/10 | 1402/6956 | 926/1287 | 309/428 | chr1 | 147650194 | |||
| chr1:147650195 | C | T | 1 | a0006 | 1 | NA18962.hp2 | missense_variant | MODERATE | c.925G>A | p.Glu309Lys | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 8/10 | 1401/6956 | 925/1287 | 309/428 | chr1 | 147650195 | |||
| chr1:147654322 | G | A | 1 | a0005 | 1 | HG01175.hp2 | missense_variant | MODERATE | c.652C>T | p.Arg218Trp | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 6/10 | 1128/6956 | 652/1287 | 218/428 | chr1 | 147654322 | |||
| chr1:147659696 | G | A | 1 | a0004 | 2 | HG03225.hp1 NA19090.hp1 |
missense_variant | MODERATE | c.299C>T | p.Pro100Leu | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 2/10 | 775/6956 | 299/1287 | 100/428 | chr1 | 147659696 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:147647471 | G | A | 5 | a0001c0001 a0001c0008 a0001c0009 others(2): Show |
181 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(178): Show |
synonymous_variant | LOW | c.1239C>T | p.His413His | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 1715/6956 | 1239/1287 | 413/428 | chr1 | 147647471 | |||
| chr1:147648369 | C | A | 1 | a0001c0011 | 1 | HG06807.hp2 | synonymous_variant | LOW | c.1020G>T | p.Pro340Pro | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 9/10 | 1496/6956 | 1020/1287 | 340/428 | chr1 | 147648369 | |||
| chr1:147652507 | T | G | 9 | a0001c0001 a0001c0003 a0001c0007 others(6): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(284): Show |
synonymous_variant | LOW | c.823A>C | p.Arg275Arg | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 7/10 | 1299/6956 | 823/1287 | 275/428 | chr1 | 147652507 | |||
| chr1:147654302 | T | C | 1 | a0001c0007 | 2 | HG01891.hp1 HG02486.hp1 |
synonymous_variant | LOW | c.672A>G | p.Leu224Leu | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 6/10 | 1148/6956 | 672/1287 | 224/428 | chr1 | 147654302 | |||
| chr1:147658988 | C | T | 1 | a0001c0005 | 2 | HG01109.hp1 NA20129.hp1 |
synonymous_variant | LOW | c.531G>A | p.Leu177Leu | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 4/10 | 1007/6956 | 531/1287 | 177/428 | chr1 | 147658988 | |||
| chr1:147659689 | T | C | 1 | a0001c0008 | 2 | HG01069.hp2 HG01071.hp2 |
synonymous_variant | LOW | c.306A>G | p.Pro102Pro | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 2/10 | 782/6956 | 306/1287 | 102/428 | chr1 | 147659689 | |||
| chr1:147669857 | A | G | 1 | a0001c0009 | 1 | HG03130.hp1 | synonymous_variant | LOW | c.192T>C | p.Pro64Pro | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/10 | 668/6956 | 192/1287 | 64/428 | chr1 | 147669857 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:147642386 | T | C | 1 | a0001c0003t0030 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5037A>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 5037 | chr1 | 147642386 | ||||||
| chr1:147642394 | C | G | 1 | a0001c0002t0025 | 2 | HG01168.hp2 HG01169.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5029G>C | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 5029 | chr1 | 147642394 | ||||||
| chr1:147642472 | T | G | 2 | a0001c0003t0038 a0001c0003t0039 |
2 | HG02976.hp2 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4951A>C | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 4951 | chr1 | 147642472 | ||||||
| chr1:147642474 | T | C | 1 | a0001c0001t0057 | 1 | NA18957.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4949A>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 4949 | chr1 | 147642474 | ||||||
| chr1:147642476 | C | CT | 15 | a0001c0001t0008 a0001c0001t0027 a0001c0002t0002 others(12): Show |
110 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(107): Show |
3_prime_UTR_variant | MODIFIER | c.*4946dupA | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 4946 | chr1 | 147642476 | ||||||
| chr1:147642476 | C | T | 1 | a0001c0001t0057 | 1 | NA18957.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4947G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 4947 | chr1 | 147642476 | ||||||
| chr1:147642485 | T | A | 1 | a0001c0001t0057 | 1 | NA18957.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4938A>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 4938 | chr1 | 147642485 | ||||||
| chr1:147642485 | T | TA | 50 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0009 others(47): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(287): Show |
3_prime_UTR_variant | MODIFIER | c.*4937dupT | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 4937 | chr1 | 147642485 | ||||||
| chr1:147642503 | G | A | 25 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0009 others(22): Show |
174 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(171): Show |
3_prime_UTR_variant | MODIFIER | c.*4920C>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 4920 | chr1 | 147642503 | ||||||
| chr1:147642814 | C | T | 1 | a0001c0001t0036 | 1 | HG02135.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4609G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 4609 | chr1 | 147642814 | ||||||
| chr1:147642918 | GAAA | G | 3 | a0001c0003t0018 a0001c0003t0038 a0001c0003t0039 |
5 | HG02630.hp1 HG02723.hp1 HG02976.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4502_*4504delTTT | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 4502 | chr1 | 147642918 | ||||||
| chr1:147642925 | A | G | 1 | a0002c0004t0048 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4498T>C | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 4498 | chr1 | 147642925 | ||||||
| chr1:147643010 | C | T | 2 | a0001c0003t0051 a0001c0003t0052 |
2 | HG03453.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4413G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 4413 | chr1 | 147643010 | ||||||
| chr1:147643320 | G | A | 2 | a0001c0003t0051 a0001c0003t0052 |
2 | HG03453.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4103C>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 4103 | chr1 | 147643320 | ||||||
| chr1:147643425 | A | C | 2 | a0001c0003t0051 a0001c0003t0052 |
2 | HG03453.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3998T>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 3998 | chr1 | 147643425 | ||||||
| chr1:147643601 | A | G | 2 | a0001c0003t0051 a0001c0003t0052 |
2 | HG03453.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3822T>C | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 3822 | chr1 | 147643601 | ||||||
| chr1:147643626 | C | T | 1 | a0001c0003t0054 | 1 | HG01978.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3797G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 3797 | chr1 | 147643626 | ||||||
| chr1:147643632 | T | G | 9 | a0001c0003t0006 a0001c0003t0026 a0001c0003t0031 others(6): Show |
20 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*3791A>C | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 3791 | chr1 | 147643632 | ||||||
| chr1:147643722 | T | C | 1 | a0001c0002t0043 | 1 | HG02040.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3701A>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 3701 | chr1 | 147643722 | ||||||
| chr1:147643819 | A | T | 10 | a0001c0003t0006 a0001c0003t0026 a0001c0003t0030 others(7): Show |
21 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*3604T>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 3604 | chr1 | 147643819 | ||||||
| chr1:147644356 | G | A | 1 | a0001c0002t0015 | 4 | NA18946.hp1 NA18963.hp1 NA18968.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3067C>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 3067 | chr1 | 147644356 | ||||||
| chr1:147644394 | G | A | 2 | a0001c0003t0051 a0001c0003t0052 |
2 | HG03453.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3029C>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 3029 | chr1 | 147644394 | ||||||
| chr1:147644466 | G | A | 1 | a0001c0003t0038 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2957C>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 2957 | chr1 | 147644466 | ||||||
| chr1:147644493 | T | C | 2 | a0001c0003t0051 a0001c0003t0052 |
2 | HG03453.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2930A>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 2930 | chr1 | 147644493 | ||||||
| chr1:147644548 | C | T | 1 | a0001c0003t0038 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2875G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 2875 | chr1 | 147644548 | ||||||
| chr1:147644569 | G | GGTAAAAG others(52): Show |
1 | a0001c0002t0041 | 1 | NA19072.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2795_*2853dupAATT others(55): Show |
ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 2853 | chr1 | 147644569 | ||||||
| chr1:147644592 | A | C | 1 | a0001c0002t0040 | 1 | HG03710.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2831T>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 2831 | chr1 | 147644592 | ||||||
| chr1:147644602 | A | G | 10 | a0001c0003t0006 a0001c0003t0026 a0001c0003t0031 others(7): Show |
21 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*2821T>C | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 2821 | chr1 | 147644602 | ||||||
| chr1:147644647 | G | A | 1 | a0001c0003t0056 | 1 | HG00408.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2776C>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 2776 | chr1 | 147644647 | ||||||
| chr1:147644677 | A | G | 1 | a0001c0003t0044 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2746T>C | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 2746 | chr1 | 147644677 | ||||||
| chr1:147644716 | C | T | 4 | a0001c0001t0009 a0001c0001t0016 a0001c0001t0028 others(1): Show |
14 | HG00438.hp2 HG00558.hp2 HG00673.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*2707G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 2707 | chr1 | 147644716 | ||||||
| chr1:147644792 | G | A | 3 | a0001c0003t0024 a0001c0003t0038 a0001c0003t0039 |
4 | HG00597.hp1 HG02976.hp2 NA18966.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2631C>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 2631 | chr1 | 147644792 | ||||||
| chr1:147644805 | C | T | 3 | a0001c0003t0018 a0001c0003t0038 a0001c0003t0039 |
5 | HG02630.hp1 HG02723.hp1 HG02976.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2618G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 2618 | chr1 | 147644805 | ||||||
| chr1:147644981 | C | CT | 4 | a0001c0001t0034 a0001c0001t0035 a0001c0002t0020 others(1): Show |
8 | HG01168.hp1 HG02976.hp1 HG03491.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2441dupA | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 2441 | chr1 | 147644981 | ||||||
| chr1:147645193 | A | C | 1 | a0003c0006t0022 | 2 | HG02145.hp2 HG02818.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2230T>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 2230 | chr1 | 147645193 | ||||||
| chr1:147645194 | ATATAATA others(12): Show |
A | 1 | a0001c0003t0031 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2210_*2228delATTT others(15): Show |
ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 2210 | chr1 | 147645194 | ||||||
| chr1:147645423 | G | A | 1 | a0001c0003t0032 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2000C>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 2000 | chr1 | 147645423 | ||||||
| chr1:147645486 | C | T | 2 | a0001c0003t0051 a0001c0003t0052 |
2 | HG03453.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1937G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 1937 | chr1 | 147645486 | ||||||
| chr1:147645738 | T | C | 13 | a0001c0003t0006 a0001c0003t0026 a0001c0003t0030 others(10): Show |
24 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*1685A>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 1685 | chr1 | 147645738 | ||||||
| chr1:147645935 | T | G | 1 | a0001c0001t0013 | 4 | HG02109.hp1 HG03195.hp2 HG03209.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1488A>C | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 1488 | chr1 | 147645935 | ||||||
| chr1:147646084 | G | A | 2 | a0001c0003t0051 a0001c0003t0052 |
2 | HG03453.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1339C>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 1339 | chr1 | 147646084 | ||||||
| chr1:147646147 | T | A | 1 | a0001c0001t0034 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1276A>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 1276 | chr1 | 147646147 | ||||||
| chr1:147646204 | T | C | 11 | a0001c0003t0006 a0001c0003t0026 a0001c0003t0030 others(8): Show |
22 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*1219A>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 1219 | chr1 | 147646204 | ||||||
| chr1:147646264 | G | A | 1 | a0001c0003t0019 | 2 | HG04184.hp1 NA20905.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1159C>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 1159 | chr1 | 147646264 | ||||||
| chr1:147646283 | A | G | 2 | a0001c0003t0051 a0001c0003t0052 |
2 | HG03453.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1140T>C | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 1140 | chr1 | 147646283 | ||||||
| chr1:147646326 | G | A | 2 | a0001c0003t0051 a0001c0003t0052 |
2 | HG03453.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1097C>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 1097 | chr1 | 147646326 | ||||||
| chr1:147646379 | T | C | 30 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0008 others(27): Show |
196 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(193): Show |
3_prime_UTR_variant | MODIFIER | c.*1044A>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 1044 | chr1 | 147646379 | ||||||
| chr1:147646668 | C | T | 8 | a0001c0003t0003 a0001c0003t0014 a0001c0003t0019 others(5): Show |
75 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*755G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 755 | chr1 | 147646668 | ||||||
| chr1:147646698 | A | G | 5 | a0001c0001t0004 a0001c0001t0008 a0001c0001t0023 others(2): Show |
61 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*725T>C | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 725 | chr1 | 147646698 | ||||||
| chr1:147646804 | C | T | 1 | a0001c0001t0012 | 6 | NA18940.hp2 NA18971.hp2 NA18974.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*619G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 619 | chr1 | 147646804 | ||||||
| chr1:147646818 | A | G | 2 | a0001c0003t0051 a0001c0003t0052 |
2 | HG03453.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*605T>C | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 605 | chr1 | 147646818 | ||||||
| chr1:147646899 | G | A | 2 | a0001c0003t0051 a0001c0003t0052 |
2 | HG03453.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*524C>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 524 | chr1 | 147646899 | ||||||
| chr1:147646988 | G | C | 2 | a0001c0003t0051 a0001c0003t0052 |
2 | HG03453.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*435C>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 435 | chr1 | 147646988 | ||||||
| chr1:147647125 | T | C | 1 | a0001c0001t0053 | 1 | NA19078.hp1 | 3_prime_UTR_variant | MODIFIER | c.*298A>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 298 | chr1 | 147647125 | ||||||
| chr1:147647126 | A | T | 1 | a0001c0001t0053 | 1 | NA19078.hp1 | 3_prime_UTR_variant | MODIFIER | c.*297T>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 297 | chr1 | 147647126 | ||||||
| chr1:147647308 | A | C | 2 | a0001c0003t0051 a0001c0003t0052 |
2 | HG03453.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*115T>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 115 | chr1 | 147647308 | ||||||
| chr1:147647321 | A | G | 1 | a0001c0001t0050 | 1 | HG02965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*102T>C | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 102 | chr1 | 147647321 | ||||||
| chr1:147647375 | T | A | 1 | a0001c0001t0049 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*48A>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 48 | chr1 | 147647375 | ||||||
| chr1:147670155 | G | C | 1 | a0001c0001t0058 | 1 | HG00673.hp1 | 5_prime_UTR_variant | MODIFIER | c.-107C>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/10 | 107 | chr1 | 147670155 | ||||||
| chr1:147670174 | T | C | 38 | a0001c0001t0001 a0001c0001t0011 a0001c0001t0012 others(35): Show |
229 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(226): Show |
5_prime_UTR_variant | MODIFIER | c.-126A>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/10 | 126 | chr1 | 147670174 | ||||||
| chr1:147670230 | C | G | 1 | a0001c0001t0035 | 1 | NA18951.hp1 | 5_prime_UTR_variant | MODIFIER | c.-182G>C | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/10 | 182 | chr1 | 147670230 | ||||||
| chr1:147670231 | G | A | 1 | a0001c0001t0059 | 1 | HG02738.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-183C>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/10 | chr1 | 147670231 | |||||||
| chr1:147670335 | C | T | 10 | a0001c0001t0011 a0001c0001t0034 a0001c0002t0029 others(7): Show |
25 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(22): Show |
5_prime_UTR_variant | MODIFIER | c.-287G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/10 | 287 | chr1 | 147670335 | ||||||
| chr1:147670473 | A | G | 1 | a0001c0003t0019 | 2 | HG04184.hp1 NA20905.hp2 |
5_prime_UTR_variant | MODIFIER | c.-425T>C | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/10 | 425 | chr1 | 147670473 | ||||||
| chr1:147670485 | C | T | 1 | a0001c0001t0028 | 1 | HG02056.hp2 | 5_prime_UTR_variant | MODIFIER | c.-437G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/10 | 437 | chr1 | 147670485 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:147647595 | C | T | 1 | a0001c0001t0001g0169 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1144-29G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 9/9 | chr1 | 147647595 | |||||||
| chr1:147647599 | G | A | 1 | a0001c0003t0003g0138 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1144-33C>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 9/9 | chr1 | 147647599 | |||||||
| chr1:147647835 | G | A | 3 | a0001c0003t0003g0010 a0001c0003t0014g0139 a0001c0003t0054g0140 |
9 | HG01346.hp1 HG01978.hp2 NA18940.hp1 others(6): Show |
intron_variant | MODIFIER | c.1144-269C>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 9/9 | chr1 | 147647835 | |||||||
| chr1:147647982 | C | T | 5 | a0001c0001t0001g0011 a0001c0001t0001g0160 a0001c0001t0001g0161 others(2): Show |
10 | HG02257.hp2 HG02258.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.1143+264G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 9/9 | chr1 | 147647982 | |||||||
| chr1:147648029 | G | C | 1 | a0006c0010t0001g0168 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1143+217C>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 9/9 | chr1 | 147648029 | |||||||
| chr1:147648126 | G | A | 2 | a0001c0003t0051g0149 a0001c0003t0052g0150 |
2 | HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1143+120C>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 9/9 | chr1 | 147648126 | |||||||
| chr1:147648446 | C | G | 1 | a0001c0002t0005g0154 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.978-35G>C | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 8/9 | chr1 | 147648446 | |||||||
| chr1:147648616 | C | T | 1 | a0001c0001t0004g0090 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.978-205G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 8/9 | chr1 | 147648616 | |||||||
| chr1:147649175 | C | T | 2 | a0001c0003t0051g0149 a0001c0003t0052g0150 |
2 | HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.978-764G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 8/9 | chr1 | 147649175 | |||||||
| chr1:147649198 | G | A | 2 | a0001c0003t0051g0149 a0001c0003t0052g0150 |
2 | HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.978-787C>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 8/9 | chr1 | 147649198 | |||||||
| chr1:147649213 | C | T | 2 | a0001c0002t0002g0069 a0001c0002t0002g0075 |
2 | NA18960.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.978-802G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 8/9 | chr1 | 147649213 | |||||||
| chr1:147649246 | G | A | 2 | a0001c0003t0051g0149 a0001c0003t0052g0150 |
2 | HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.978-835C>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 8/9 | chr1 | 147649246 | |||||||
| chr1:147649276 | T | C | 2 | a0001c0003t0051g0149 a0001c0003t0052g0150 |
2 | HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.978-865A>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 8/9 | chr1 | 147649276 | |||||||
| chr1:147649431 | G | C | 1 | a0001c0002t0041g0082 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.977+712C>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 8/9 | chr1 | 147649431 | |||||||
| chr1:147649432 | C | G | 1 | a0001c0002t0041g0082 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.977+711G>C | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 8/9 | chr1 | 147649432 | |||||||
| chr1:147649451 | A | ATT | 4 | a0001c0003t0006g0021 a0001c0003t0006g0058 a0001c0003t0051g0149 others(1): Show |
6 | HG01884.hp2 HG02258.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.977+690_977+691dup others(2): Show |
ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 8/9 | chr1 | 147649451 | |||||||
| chr1:147649828 | A | G | 2 | a0001c0003t0051g0149 a0001c0003t0052g0150 |
2 | HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.977+315T>C | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 8/9 | chr1 | 147649828 | |||||||
| chr1:147649941 | A | G | 2 | a0001c0003t0051g0149 a0001c0003t0052g0150 |
2 | HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.977+202T>C | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 8/9 | chr1 | 147649941 | |||||||
| chr1:147650007 | A | C | 1 | a0001c0002t0002g0074 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.977+136T>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 8/9 | chr1 | 147650007 | |||||||
| chr1:147650009 | T | C | 2 | a0001c0003t0018g0045 a0001c0003t0018g0182 |
3 | HG02630.hp1 HG02723.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.977+134A>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 8/9 | chr1 | 147650009 | |||||||
| chr1:147650422 | T | C | 2 | a0001c0003t0051g0149 a0001c0003t0052g0150 |
2 | HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.882-184A>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 7/9 | chr1 | 147650422 | |||||||
| chr1:147650667 | T | C | 2 | a0001c0003t0051g0149 a0001c0003t0052g0150 |
2 | HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.882-429A>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 7/9 | chr1 | 147650667 | |||||||
| chr1:147650704 | A | G | 2 | a0001c0003t0051g0149 a0001c0003t0052g0150 |
2 | HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.882-466T>C | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 7/9 | chr1 | 147650704 | |||||||
| chr1:147650813 | T | C | 29 | a0001c0001t0004g0002 a0001c0001t0004g0014 a0001c0001t0004g0016 others(26): Show |
65 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.882-575A>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 7/9 | chr1 | 147650813 | |||||||
| chr1:147650889 | G | T | 1 | a0001c0003t0006g0058 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.882-651C>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 7/9 | chr1 | 147650889 | |||||||
| chr1:147650973 | T | C | 1 | a0001c0003t0003g0141 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.882-735A>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 7/9 | chr1 | 147650973 | |||||||
| chr1:147651028 | C | T | 29 | a0001c0001t0004g0002 a0001c0001t0004g0014 a0001c0001t0004g0016 others(26): Show |
65 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.882-790G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 7/9 | chr1 | 147651028 | |||||||
| chr1:147651286 | T | C | 1 | a0001c0002t0002g0114 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.882-1048A>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 7/9 | chr1 | 147651286 | |||||||
| chr1:147651311 | T | C | 1 | a0001c0002t0005g0155 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.882-1073A>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 7/9 | chr1 | 147651311 | |||||||
| chr1:147651339 | T | C | 2 | a0001c0003t0051g0149 a0001c0003t0052g0150 |
2 | HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.882-1101A>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 7/9 | chr1 | 147651339 | |||||||
| chr1:147651367 | C | T | 2 | a0001c0003t0051g0149 a0001c0003t0052g0150 |
2 | HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.881+1082G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 7/9 | chr1 | 147651367 | |||||||
| chr1:147651387 | C | A | 2 | a0001c0003t0051g0149 a0001c0003t0052g0150 |
2 | HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.881+1062G>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 7/9 | chr1 | 147651387 | |||||||
| chr1:147651435 | G | A | 15 | a0001c0003t0006g0020 a0001c0003t0006g0021 a0001c0003t0006g0050 others(12): Show |
21 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.881+1014C>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 7/9 | chr1 | 147651435 | |||||||
| chr1:147651537 | C | T | 3 | a0001c0001t0013g0024 a0001c0001t0013g0105 a0003c0006t0022g0033 |
6 | HG02109.hp1 HG02145.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.881+912G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 7/9 | chr1 | 147651537 | |||||||
| chr1:147651616 | G | T | 3 | a0001c0001t0013g0024 a0001c0001t0013g0105 a0003c0006t0022g0033 |
6 | HG02109.hp1 HG02145.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.881+833C>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 7/9 | chr1 | 147651616 | |||||||
| chr1:147651639 | C | T | 1 | a0001c0001t0013g0024 | 3 | HG02109.hp1 HG03195.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.881+810G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 7/9 | chr1 | 147651639 | |||||||
| chr1:147651671 | C | T | 1 | a0001c0003t0051g0149 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.881+778G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 7/9 | chr1 | 147651671 | |||||||
| chr1:147651733 | G | A | 1 | a0001c0001t0027g0172 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.881+716C>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 7/9 | chr1 | 147651733 | |||||||
| chr1:147651831 | C | T | 2 | a0001c0003t0051g0149 a0001c0003t0052g0150 |
2 | HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.881+618G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 7/9 | chr1 | 147651831 | |||||||
| chr1:147652080 | C | T | 1 | a0001c0001t0004g0089 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.881+369G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 7/9 | chr1 | 147652080 | |||||||
| chr1:147652223 | G | A | 1 | a0001c0003t0038g0095 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.881+226C>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 7/9 | chr1 | 147652223 | |||||||
| chr1:147652232 | T | C | 1 | a0002c0004t0007g0103 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.881+217A>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 7/9 | chr1 | 147652232 | |||||||
| chr1:147652589 | T | C | 2 | a0001c0003t0051g0149 a0001c0003t0052g0150 |
2 | HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.781-40A>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 6/9 | chr1 | 147652589 | |||||||
| chr1:147652753 | G | GAA | 29 | a0001c0003t0003g0003 a0001c0003t0003g0004 a0001c0003t0003g0010 others(26): Show |
75 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.781-206_781-205dup others(2): Show |
ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 6/9 | chr1 | 147652753 | |||||||
| chr1:147652753 | G | GAAAA | 7 | a0001c0001t0001g0151 a0001c0001t0001g0167 a0001c0001t0004g0084 others(4): Show |
8 | HG00673.hp2 HG01952.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.781-208_781-205dup others(4): Show |
ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 6/9 | chr1 | 147652753 | |||||||
| chr1:147652837 | G | GTT | 7 | a0001c0001t0001g0167 a0001c0001t0053g0159 a0001c0002t0002g0071 others(4): Show |
7 | HG00408.hp2 HG00597.hp1 HG02135.hp2 others(4): Show |
intron_variant | MODIFIER | c.781-290_781-289dup others(2): Show |
ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 6/9 | chr1 | 147652837 | |||||||
| chr1:147652837 | G | T | 3 | a0001c0001t0004g0067 a0001c0002t0002g0112 a0001c0002t0005g0153 |
3 | HG00735.hp2 NA18949.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.781-288C>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 6/9 | chr1 | 147652837 | |||||||
| chr1:147652858 | G | A | 1 | a0001c0002t0002g0025 | 3 | HG01243.hp2 HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.781-309C>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 6/9 | chr1 | 147652858 | |||||||
| chr1:147652889 | C | CGATCTCG others(299): Show |
2 | a0001c0003t0018g0045 a0001c0003t0018g0182 |
3 | HG02630.hp1 HG02723.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.781-341_781-340ins others(306): Show |
ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 6/9 | chr1 | 147652889 | |||||||
| chr1:147652889 | C | CGATCTCG others(299): Show |
1 | a0001c0001t0004g0068 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.781-341_781-340ins others(306): Show |
ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 6/9 | chr1 | 147652889 | |||||||
| chr1:147652889 | C | CGATCTCG others(299): Show |
6 | a0001c0001t0013g0024 a0001c0001t0013g0105 a0001c0001t0034g0048 others(3): Show |
9 | HG02109.hp1 HG02145.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.781-341_781-340ins others(306): Show |
ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 6/9 | chr1 | 147652889 | |||||||
| chr1:147652889 | C | CGATCTCG others(300): Show |
51 | a0001c0001t0004g0002 a0001c0001t0004g0014 a0001c0001t0004g0016 others(48): Show |
133 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.781-341_781-340ins others(307): Show |
ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 6/9 | chr1 | 147652889 | |||||||
| chr1:147652895 | C | CGGCTCAC others(299): Show |
1 | a0001c0001t0049g0063 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.781-347_781-346ins others(306): Show |
ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 6/9 | chr1 | 147652895 | |||||||
| chr1:147652896 | G | A | 1 | a0001c0002t0002g0107 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.781-347C>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 6/9 | chr1 | 147652896 | |||||||
| chr1:147652919 | T | C | 128 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0017 others(125): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(284): Show |
intron_variant | MODIFIER | c.781-370A>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 6/9 | chr1 | 147652919 | |||||||
| chr1:147652919 | T | TGGGTTCA others(299): Show |
1 | a0001c0002t0002g0079 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.781-371_781-370ins others(306): Show |
ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 6/9 | chr1 | 147652919 | |||||||
| chr1:147652919 | T | TGGGTTCA others(299): Show |
43 | a0001c0002t0002g0005 a0001c0002t0002g0006 a0001c0002t0002g0019 others(40): Show |
93 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.781-371_781-370ins others(306): Show |
ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 6/9 | chr1 | 147652919 | |||||||
| chr1:147652919 | T | TGGGTTCA others(300): Show |
1 | a0001c0002t0005g0156 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.781-371_781-370ins others(307): Show |
ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 6/9 | chr1 | 147652919 | |||||||
| chr1:147652922 | G | GTTCACGC others(300): Show |
1 | a0001c0002t0020g0109 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.781-374_781-373ins others(307): Show |
ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 6/9 | chr1 | 147652922 | |||||||
| chr1:147652922 | G | GTTCACGC others(299): Show |
5 | a0001c0002t0033g0057 a0002c0004t0007g0008 a0002c0004t0007g0103 others(2): Show |
12 | HG02109.hp2 HG02257.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.781-374_781-373ins others(306): Show |
ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 6/9 | chr1 | 147652922 | |||||||
| chr1:147652927 | C | CGCCATTT others(299): Show |
14 | a0001c0003t0006g0020 a0001c0003t0006g0021 a0001c0003t0006g0050 others(11): Show |
20 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.781-379_781-378ins others(306): Show |
ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 6/9 | chr1 | 147652927 | |||||||
| chr1:147652955 | T | A | 1 | a0001c0001t0001g0161 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.781-406A>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 6/9 | chr1 | 147652955 | |||||||
| chr1:147652970 | G | A | 4 | a0001c0001t0001g0011 a0001c0001t0001g0160 a0001c0001t0001g0161 others(1): Show |
9 | HG02257.hp2 HG02258.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.781-421C>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 6/9 | chr1 | 147652970 | |||||||
| chr1:147652987 | C | CGGCTAAT others(299): Show |
1 | a0001c0003t0006g0052 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.781-439_781-438ins others(306): Show |
ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 6/9 | chr1 | 147652987 | |||||||
| chr1:147652993 | A | ATTTTTTT others(300): Show |
1 | a0001c0001t0001g0173 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.781-445_781-444ins others(307): Show |
ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 6/9 | chr1 | 147652993 | |||||||
| chr1:147653018 | G | AGGGTTTC others(299): Show |
4 | a0001c0002t0002g0023 a0001c0002t0002g0072 a0001c0002t0041g0082 others(1): Show |
6 | NA18955.hp2 NA18999.hp2 NA19058.hp2 others(3): Show |
intron_variant | MODIFIER | c.781-469_781-468ins others(306): Show |
ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 6/9 | chr1 | 147653018 | |||||||
| chr1:147653083 | T | TCCCAAAT others(301): Show |
1 | a0001c0003t0003g0126 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.781-535_781-534ins others(308): Show |
ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 6/9 | chr1 | 147653083 | |||||||
| chr1:147653119 | G | A | 4 | a0001c0001t0001g0164 a0001c0001t0001g0173 a0001c0001t0001g0176 others(1): Show |
4 | HG02965.hp2 HG03540.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.781-570C>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 6/9 | chr1 | 147653119 | |||||||
| chr1:147653119 | G | GCCTGGCC others(299): Show |
42 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0017 others(39): Show |
109 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.781-571_781-570ins others(306): Show |
ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 6/9 | chr1 | 147653119 | |||||||
| chr1:147653119 | G | GCCTGGCC others(300): Show |
1 | a0001c0001t0001g0166 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.781-571_781-570ins others(307): Show |
ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 6/9 | chr1 | 147653119 | |||||||
| chr1:147653122 | C | T | 129 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0017 others(126): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(285): Show |
intron_variant | MODIFIER | c.781-573G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 6/9 | chr1 | 147653122 | |||||||
| chr1:147653135 | T | TGTTTTTT others(300): Show |
2 | a0001c0003t0051g0149 a0001c0003t0052g0150 |
2 | HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.781-587_781-586ins others(307): Show |
ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 6/9 | chr1 | 147653135 | |||||||
| chr1:147653137 | G | GTTTTTTT others(300): Show |
1 | a0001c0002t0002g0073 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.781-589_781-588ins others(307): Show |
ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 6/9 | chr1 | 147653137 | |||||||
| chr1:147653137 | G | GTTTTTTT others(300): Show |
1 | a0001c0001t0053g0159 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.781-589_781-588ins others(307): Show |
ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 6/9 | chr1 | 147653137 | |||||||
| chr1:147653137 | G | T | 2 | a0001c0003t0051g0149 a0001c0003t0052g0150 |
2 | HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.781-588C>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 6/9 | chr1 | 147653137 | |||||||
| chr1:147653200 | G | A | 1 | a0001c0003t0030g0049 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.781-651C>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 6/9 | chr1 | 147653200 | |||||||
| chr1:147653209 | C | G | 1 | a0004c0014t0001g0163 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.781-660G>C | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 6/9 | chr1 | 147653209 | |||||||
| chr1:147653290 | C | A | 5 | a0001c0002t0033g0057 a0002c0004t0007g0008 a0002c0004t0007g0103 others(2): Show |
12 | HG02109.hp2 HG02257.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.781-741G>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 6/9 | chr1 | 147653290 | |||||||
| chr1:147653385 | T | C | 42 | a0001c0001t0004g0002 a0001c0001t0004g0014 a0001c0001t0004g0016 others(39): Show |
84 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(81): Show |
intron_variant | MODIFIER | c.780+809A>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 6/9 | chr1 | 147653385 | |||||||
| chr1:147653415 | C | T | 1 | a0001c0001t0008g0088 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.780+779G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 6/9 | chr1 | 147653415 | |||||||
| chr1:147653535 | A | G | 2 | a0001c0003t0051g0149 a0001c0003t0052g0150 |
2 | HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.780+659T>C | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 6/9 | chr1 | 147653535 | |||||||
| chr1:147654126 | A | C | 1 | a0001c0003t0003g0126 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.780+68T>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 6/9 | chr1 | 147654126 | |||||||
| chr1:147654437 | AT | A | 3 | a0001c0001t0013g0024 a0001c0001t0013g0105 a0003c0006t0022g0033 |
6 | HG02109.hp1 HG02145.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.648-112delA | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 5/9 | chr1 | 147654437 | |||||||
| chr1:147654531 | G | A | 1 | a0001c0001t0016g0181 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.648-205C>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 5/9 | chr1 | 147654531 | |||||||
| chr1:147654600 | G | C | 1 | a0001c0002t0005g0156 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.648-274C>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 5/9 | chr1 | 147654600 | |||||||
| chr1:147654827 | T | A | 1 | a0001c0001t0001g0173 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.647+334A>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 5/9 | chr1 | 147654827 | |||||||
| chr1:147654907 | G | A | 1 | a0001c0001t0008g0087 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.647+254C>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 5/9 | chr1 | 147654907 | |||||||
| chr1:147654954 | T | C | 1 | a0001c0003t0003g0130 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.647+207A>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 5/9 | chr1 | 147654954 | |||||||
| chr1:147655014 | G | A | 17 | a0001c0001t0034g0048 a0001c0002t0029g0051 a0001c0002t0033g0057 others(14): Show |
23 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.647+147C>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 5/9 | chr1 | 147655014 | |||||||
| chr1:147655487 | G | A | 47 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0017 others(44): Show |
114 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.560-239C>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 4/9 | chr1 | 147655487 | |||||||
| chr1:147655616 | T | G | 37 | a0001c0001t0013g0024 a0001c0001t0013g0105 a0001c0001t0049g0063 others(34): Show |
87 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.560-368A>C | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 4/9 | chr1 | 147655616 | |||||||
| chr1:147655622 | T | C | 31 | a0001c0003t0003g0003 a0001c0003t0003g0004 a0001c0003t0003g0010 others(28): Show |
77 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.560-374A>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 4/9 | chr1 | 147655622 | |||||||
| chr1:147655689 | C | G | 2 | a0001c0003t0051g0149 a0001c0003t0052g0150 |
2 | HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.560-441G>C | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 4/9 | chr1 | 147655689 | |||||||
| chr1:147655844 | T | A | 1 | a0001c0002t0020g0109 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.560-596A>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 4/9 | chr1 | 147655844 | |||||||
| chr1:147655882 | G | A | 2 | a0001c0003t0018g0045 a0001c0003t0018g0182 |
3 | HG02630.hp1 HG02723.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.560-634C>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 4/9 | chr1 | 147655882 | |||||||
| chr1:147656034 | T | C | 1 | a0001c0002t0017g0026 | 3 | HG01069.hp1 HG01071.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.560-786A>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 4/9 | chr1 | 147656034 | |||||||
| chr1:147656493 | A | C | 29 | a0001c0003t0003g0003 a0001c0003t0003g0004 a0001c0003t0003g0010 others(26): Show |
75 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.560-1245T>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 4/9 | chr1 | 147656493 | |||||||
| chr1:147656613 | T | C | 2 | a0001c0003t0003g0143 a0001c0003t0014g0142 |
2 | HG00099.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.560-1365A>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 4/9 | chr1 | 147656613 | |||||||
| chr1:147656893 | T | C | 1 | a0001c0001t0004g0084 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.560-1645A>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 4/9 | chr1 | 147656893 | |||||||
| chr1:147656896 | A | G | 1 | a0004c0014t0001g0163 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.560-1648T>C | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 4/9 | chr1 | 147656896 | |||||||
| chr1:147656899 | G | A | 134 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0017 others(131): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(297): Show |
intron_variant | MODIFIER | c.560-1651C>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 4/9 | chr1 | 147656899 | |||||||
| chr1:147656921 | T | C | 1 | a0001c0001t0049g0063 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.560-1673A>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 4/9 | chr1 | 147656921 | |||||||
| chr1:147657037 | C | A | 1 | a0001c0001t0010g0092 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.560-1789G>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 4/9 | chr1 | 147657037 | |||||||
| chr1:147657040 | C | G | 1 | a0001c0002t0002g0108 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.560-1792G>C | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 4/9 | chr1 | 147657040 | |||||||
| chr1:147657148 | A | C | 1 | a0001c0001t0001g0165 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.559+1812T>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 4/9 | chr1 | 147657148 | |||||||
| chr1:147657208 | C | CCA | 29 | a0001c0003t0003g0003 a0001c0003t0003g0004 a0001c0003t0003g0010 others(26): Show |
75 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.559+1750_559+1751d others(4): Show |
ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 4/9 | chr1 | 147657208 | |||||||
| chr1:147657274 | G | A | 4 | a0001c0002t0033g0057 a0001c0003t0006g0021 a0001c0003t0006g0058 others(1): Show |
6 | HG01884.hp2 HG02258.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.559+1686C>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 4/9 | chr1 | 147657274 | |||||||
| chr1:147657461 | C | T | 3 | a0001c0001t0001g0017 a0001c0001t0001g0164 a0001c0009t0001g0123 |
7 | HG01175.hp1 HG02615.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.559+1499G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 4/9 | chr1 | 147657461 | |||||||
| chr1:147657466 | G | C | 48 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0017 others(45): Show |
115 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.559+1494C>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 4/9 | chr1 | 147657466 | |||||||
| chr1:147657506 | C | T | 1 | a0001c0001t0008g0087 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.559+1454G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 4/9 | chr1 | 147657506 | |||||||
| chr1:147657514 | G | A | 1 | a0001c0002t0002g0108 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.559+1446C>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 4/9 | chr1 | 147657514 | |||||||
| chr1:147657605 | C | G | 31 | a0001c0001t0013g0024 a0001c0001t0013g0105 a0001c0003t0003g0003 others(28): Show |
79 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.559+1355G>C | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 4/9 | chr1 | 147657605 | |||||||
| chr1:147657612 | G | T | 31 | a0001c0001t0013g0024 a0001c0001t0013g0105 a0001c0003t0003g0003 others(28): Show |
79 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.559+1348C>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 4/9 | chr1 | 147657612 | |||||||
| chr1:147657671 | A | G | 133 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0017 others(130): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(296): Show |
intron_variant | MODIFIER | c.559+1289T>C | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 4/9 | chr1 | 147657671 | |||||||
| chr1:147657885 | T | C | 68 | a0001c0001t0004g0002 a0001c0001t0004g0014 a0001c0001t0004g0016 others(65): Show |
164 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.559+1075A>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 4/9 | chr1 | 147657885 | |||||||
| chr1:147657893 | G | A | 1 | a0001c0002t0002g0040 | 2 | HG00639.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.559+1067C>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 4/9 | chr1 | 147657893 | |||||||
| chr1:147657928 | T | C | 28 | a0001c0001t0004g0002 a0001c0001t0004g0014 a0001c0001t0004g0016 others(25): Show |
65 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.559+1032A>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 4/9 | chr1 | 147657928 | |||||||
| chr1:147658107 | T | C | 30 | a0001c0001t0013g0024 a0001c0001t0013g0105 a0001c0003t0003g0003 others(27): Show |
78 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(75): Show |
intron_variant | MODIFIER | c.559+853A>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 4/9 | chr1 | 147658107 | |||||||
| chr1:147658160 | A | G | 67 | a0001c0001t0004g0002 a0001c0001t0004g0014 a0001c0001t0004g0016 others(64): Show |
160 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(157): Show |
intron_variant | MODIFIER | c.559+800T>C | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 4/9 | chr1 | 147658160 | |||||||
| chr1:147658170 | C | T | 6 | a0001c0002t0002g0022 a0001c0002t0002g0023 a0001c0002t0002g0071 others(3): Show |
10 | HG00408.hp2 HG02015.hp2 NA18955.hp2 others(7): Show |
intron_variant | MODIFIER | c.559+790G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 4/9 | chr1 | 147658170 | |||||||
| chr1:147658240 | T | C | 37 | a0001c0001t0004g0002 a0001c0001t0004g0014 a0001c0001t0004g0016 others(34): Show |
82 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(79): Show |
intron_variant | MODIFIER | c.559+720A>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 4/9 | chr1 | 147658240 | |||||||
| chr1:147658410 | C | T | 1 | a0001c0003t0014g0135 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.559+550G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 4/9 | chr1 | 147658410 | |||||||
| chr1:147658461 | T | A | 1 | a0001c0002t0020g0109 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.559+499A>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 4/9 | chr1 | 147658461 | |||||||
| chr1:147658465 | G | A | 1 | a0001c0002t0020g0109 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.559+495C>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 4/9 | chr1 | 147658465 | |||||||
| chr1:147658477 | G | A | 2 | a0001c0003t0051g0149 a0001c0003t0052g0150 |
2 | HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.559+483C>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 4/9 | chr1 | 147658477 | |||||||
| chr1:147658546 | C | T | 22 | a0001c0001t0004g0002 a0001c0001t0004g0014 a0001c0001t0004g0016 others(19): Show |
58 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.559+414G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 4/9 | chr1 | 147658546 | |||||||
| chr1:147658650 | G | A | 1 | a0001c0002t0002g0079 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.559+310C>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 4/9 | chr1 | 147658650 | |||||||
| chr1:147658655 | C | T | 2 | a0001c0003t0051g0149 a0001c0003t0052g0150 |
2 | HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.559+305G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 4/9 | chr1 | 147658655 | |||||||
| chr1:147658660 | T | C | 1 | a0001c0002t0002g0080 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.559+300A>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 4/9 | chr1 | 147658660 | |||||||
| chr1:147659207 | G | T | 28 | a0001c0003t0003g0003 a0001c0003t0003g0004 a0001c0003t0003g0010 others(25): Show |
74 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.480-168C>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 3/9 | chr1 | 147659207 | |||||||
| chr1:147659208 | A | T | 28 | a0001c0003t0003g0003 a0001c0003t0003g0004 a0001c0003t0003g0010 others(25): Show |
74 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.480-169T>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 3/9 | chr1 | 147659208 | |||||||
| chr1:147659214 | A | G | 1 | a0001c0003t0003g0134 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.480-175T>C | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 3/9 | chr1 | 147659214 | |||||||
| chr1:147659235 | C | T | 2 | a0001c0001t0013g0024 a0001c0001t0013g0105 |
4 | HG02109.hp1 HG03195.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.479+161G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 3/9 | chr1 | 147659235 | |||||||
| chr1:147659350 | T | C | 125 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0017 others(122): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(279): Show |
intron_variant | MODIFIER | c.479+46A>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 3/9 | chr1 | 147659350 | |||||||
| chr1:147659386 | A | T | 36 | a0001c0001t0004g0002 a0001c0001t0004g0014 a0001c0001t0004g0016 others(33): Show |
75 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.479+10T>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 3/9 | chr1 | 147659386 | |||||||
| chr1:147659547 | AAAG | A | 17 | a0001c0001t0011g0018 a0001c0001t0011g0055 a0001c0001t0034g0048 others(14): Show |
26 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.349-24_349-22delCT others(1): Show |
ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 2/9 | chr1 | 147659547 | |||||||
| chr1:147659595 | A | C | 28 | a0001c0003t0003g0003 a0001c0003t0003g0004 a0001c0003t0003g0010 others(25): Show |
74 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.348+52T>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 2/9 | chr1 | 147659595 | |||||||
| chr1:147659605 | C | A | 1 | a0001c0001t0008g0100 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.348+42G>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 2/9 | chr1 | 147659605 | |||||||
| chr1:147659642 | C | T | 1 | a0001c0001t0001g0043 | 2 | NA18945.hp2 NA18953.hp1 |
splice_region_variant&intron_variant | LOW | c.348+5G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 2/9 | chr1 | 147659642 | |||||||
| chr1:147659830 | T | C | 125 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0017 others(122): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(279): Show |
intron_variant | MODIFIER | c.220-55A>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147659830 | |||||||
| chr1:147659890 | A | T | 1 | a0001c0001t0001g0160 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.220-115T>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147659890 | |||||||
| chr1:147660017 | G | A | 1 | a0001c0001t0001g0174 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.220-242C>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147660017 | |||||||
| chr1:147660086 | G | A | 2 | a0001c0003t0018g0045 a0001c0003t0018g0182 |
3 | HG02630.hp1 HG02723.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.220-311C>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147660086 | |||||||
| chr1:147660169 | T | C | 1 | a0001c0001t0001g0162 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.220-394A>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147660169 | |||||||
| chr1:147660176 | G | A | 1 | a0001c0001t0004g0068 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.220-401C>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147660176 | |||||||
| chr1:147660250 | C | T | 1 | a0001c0003t0006g0050 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.220-475G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147660250 | |||||||
| chr1:147660300 | C | A | 1 | a0001c0002t0002g0117 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.220-525G>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147660300 | |||||||
| chr1:147660620 | A | G | 3 | a0001c0001t0049g0063 a0001c0003t0044g0061 a0001c0003t0046g0062 |
3 | HG02486.hp2 HG02723.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.220-845T>C | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147660620 | |||||||
| chr1:147660625 | C | T | 28 | a0001c0003t0003g0003 a0001c0003t0003g0004 a0001c0003t0003g0010 others(25): Show |
74 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.220-850G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147660625 | |||||||
| chr1:147660710 | T | C | 4 | a0001c0001t0001g0011 a0001c0001t0001g0160 a0001c0001t0001g0161 others(1): Show |
9 | HG02257.hp2 HG02258.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.220-935A>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147660710 | |||||||
| chr1:147660963 | T | C | 2 | a0001c0003t0018g0045 a0001c0003t0018g0182 |
3 | HG02630.hp1 HG02723.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.220-1188A>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147660963 | |||||||
| chr1:147661127 | T | C | 1 | a0001c0002t0005g0178 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.220-1352A>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147661127 | |||||||
| chr1:147661164 | G | A | 41 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0017 others(38): Show |
104 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.220-1389C>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147661164 | |||||||
| chr1:147661273 | C | T | 1 | a0001c0003t0051g0149 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.220-1498G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147661273 | |||||||
| chr1:147661315 | A | AT | 115 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0042 others(112): Show |
241 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(238): Show |
intron_variant | MODIFIER | c.220-1541dupA | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147661315 | |||||||
| chr1:147661315 | A | ATT | 33 | a0001c0001t0001g0011 a0001c0001t0001g0160 a0001c0001t0001g0161 others(30): Show |
84 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.220-1542_220-1541d others(4): Show |
ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147661315 | |||||||
| chr1:147661337 | G | A | 44 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0017 others(41): Show |
107 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.220-1562C>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147661337 | |||||||
| chr1:147661474 | C | T | 1 | a0001c0002t0002g0111 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.220-1699G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147661474 | |||||||
| chr1:147661492 | C | T | 28 | a0001c0003t0003g0003 a0001c0003t0003g0004 a0001c0003t0003g0010 others(25): Show |
74 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.220-1717G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147661492 | |||||||
| chr1:147661513 | T | C | 17 | a0001c0001t0011g0018 a0001c0001t0011g0055 a0001c0001t0034g0048 others(14): Show |
26 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.220-1738A>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147661513 | |||||||
| chr1:147661589 | T | A | 1 | a0001c0002t0020g0109 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.220-1814A>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147661589 | |||||||
| chr1:147661591 | A | T | 1 | a0001c0002t0020g0109 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.220-1816T>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147661591 | |||||||
| chr1:147661668 | A | G | 28 | a0001c0003t0003g0003 a0001c0003t0003g0004 a0001c0003t0003g0010 others(25): Show |
74 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.220-1893T>C | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147661668 | |||||||
| chr1:147661678 | G | A | 1 | a0002c0004t0007g0104 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.220-1903C>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147661678 | |||||||
| chr1:147661788 | A | C | 1 | a0001c0001t0004g0086 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.220-2013T>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147661788 | |||||||
| chr1:147661981 | T | C | 1 | a0001c0001t0001g0179 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.220-2206A>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147661981 | |||||||
| chr1:147662044 | T | C | 2 | a0001c0003t0051g0149 a0001c0003t0052g0150 |
2 | HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.220-2269A>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147662044 | |||||||
| chr1:147662283 | A | AT | 28 | a0001c0003t0003g0003 a0001c0003t0003g0004 a0001c0003t0003g0010 others(25): Show |
74 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.220-2509dupA | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147662283 | |||||||
| chr1:147662672 | T | C | 2 | a0001c0001t0001g0176 a0001c0001t0050g0175 |
2 | HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.220-2897A>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147662672 | |||||||
| chr1:147662687 | T | C | 18 | a0001c0001t0010g0083 a0001c0001t0011g0018 a0001c0001t0011g0055 others(15): Show |
27 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.220-2912A>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147662687 | |||||||
| chr1:147662710 | C | T | 28 | a0001c0003t0003g0003 a0001c0003t0003g0004 a0001c0003t0003g0010 others(25): Show |
74 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.220-2935G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147662710 | |||||||
| chr1:147662944 | A | T | 1 | a0001c0002t0020g0109 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.220-3169T>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147662944 | |||||||
| chr1:147662956 | T | A | 2 | a0001c0003t0018g0045 a0001c0003t0018g0182 |
3 | HG02630.hp1 HG02723.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.220-3181A>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147662956 | |||||||
| chr1:147663121 | A | G | 1 | a0001c0001t0004g0085 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.220-3346T>C | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147663121 | |||||||
| chr1:147663195 | C | T | 2 | a0001c0003t0018g0045 a0001c0003t0018g0182 |
3 | HG02630.hp1 HG02723.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.220-3420G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147663195 | |||||||
| chr1:147663226 | G | C | 28 | a0001c0003t0003g0003 a0001c0003t0003g0004 a0001c0003t0003g0010 others(25): Show |
74 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.220-3451C>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147663226 | |||||||
| chr1:147663290 | G | GC | 129 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0017 others(126): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(290): Show |
intron_variant | MODIFIER | c.220-3516_220-3515i others(3): Show |
ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147663290 | |||||||
| chr1:147663291 | T | C | 1 | a0001c0003t0003g0133 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.220-3516A>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147663291 | |||||||
| chr1:147663292 | G | T | 1 | a0001c0003t0003g0133 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.220-3517C>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147663292 | |||||||
| chr1:147663355 | A | G | 2 | a0001c0003t0051g0149 a0001c0003t0052g0150 |
2 | HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.220-3580T>C | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147663355 | |||||||
| chr1:147663473 | A | G | 28 | a0001c0003t0003g0003 a0001c0003t0003g0004 a0001c0003t0003g0010 others(25): Show |
74 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.220-3698T>C | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147663473 | |||||||
| chr1:147663515 | A | G | 28 | a0001c0003t0003g0003 a0001c0003t0003g0004 a0001c0003t0003g0010 others(25): Show |
74 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.220-3740T>C | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147663515 | |||||||
| chr1:147663587 | C | T | 41 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0017 others(38): Show |
102 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.220-3812G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147663587 | |||||||
| chr1:147663649 | A | G | 1 | a0001c0003t0046g0062 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.220-3874T>C | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147663649 | |||||||
| chr1:147663658 | A | T | 1 | a0001c0002t0002g0121 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.220-3883T>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147663658 | |||||||
| chr1:147663733 | A | C | 28 | a0001c0003t0003g0003 a0001c0003t0003g0004 a0001c0003t0003g0010 others(25): Show |
74 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.220-3958T>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147663733 | |||||||
| chr1:147663749 | T | C | 1 | a0001c0003t0003g0144 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.220-3974A>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147663749 | |||||||
| chr1:147664166 | G | A | 32 | a0001c0001t0004g0002 a0001c0001t0004g0035 a0001c0001t0004g0065 others(29): Show |
68 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.220-4391C>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147664166 | |||||||
| chr1:147664206 | C | T | 1 | a0001c0001t0011g0056 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.220-4431G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147664206 | |||||||
| chr1:147664277 | C | T | 1 | a0001c0003t0032g0047 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.220-4502G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147664277 | |||||||
| chr1:147664384 | A | G | 16 | a0001c0001t0011g0018 a0001c0001t0011g0055 a0001c0001t0034g0048 others(13): Show |
24 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.220-4609T>C | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147664384 | |||||||
| chr1:147664455 | T | C | 46 | a0001c0001t0011g0018 a0001c0001t0011g0055 a0001c0001t0016g0181 others(43): Show |
100 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.220-4680A>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147664455 | |||||||
| chr1:147664515 | G | C | 1 | a0001c0003t0037g0099 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.220-4740C>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147664515 | |||||||
| chr1:147664654 | A | G | 16 | a0001c0001t0011g0018 a0001c0001t0011g0055 a0001c0001t0034g0048 others(13): Show |
24 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.220-4879T>C | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147664654 | |||||||
| chr1:147664733 | G | A | 2 | a0001c0003t0018g0045 a0001c0003t0018g0182 |
3 | HG02630.hp1 HG02723.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.220-4958C>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147664733 | |||||||
| chr1:147664806 | A | G | 1 | a0001c0003t0030g0049 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.219+5024T>C | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147664806 | |||||||
| chr1:147664983 | C | T | 1 | a0001c0001t0001g0158 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.219+4847G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147664983 | |||||||
| chr1:147665106 | T | C | 45 | a0001c0001t0011g0018 a0001c0001t0011g0055 a0001c0001t0011g0056 others(42): Show |
99 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.219+4724A>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147665106 | |||||||
| chr1:147665250 | T | C | 45 | a0001c0001t0011g0018 a0001c0001t0011g0055 a0001c0001t0011g0056 others(42): Show |
99 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.219+4580A>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147665250 | |||||||
| chr1:147665557 | C | T | 2 | a0001c0003t0018g0045 a0001c0003t0018g0182 |
3 | HG02630.hp1 HG02723.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.219+4273G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147665557 | |||||||
| chr1:147665695 | G | A | 1 | a0001c0002t0002g0019 | 4 | HG02145.hp1 HG02572.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.219+4135C>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147665695 | |||||||
| chr1:147665765 | A | G | 2 | a0001c0001t0001g0042 a0001c0001t0057g0157 |
3 | HG02074.hp2 HG02132.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.219+4065T>C | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147665765 | |||||||
| chr1:147665784 | G | A | 5 | a0001c0003t0045g0101 a0002c0004t0007g0008 a0002c0004t0007g0103 others(2): Show |
12 | HG02109.hp2 HG02257.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.219+4046C>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147665784 | |||||||
| chr1:147665846 | A | G | 1 | a0001c0001t0057g0157 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.219+3984T>C | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147665846 | |||||||
| chr1:147665867 | C | T | 28 | a0001c0001t0023g0145 a0001c0003t0003g0003 a0001c0003t0003g0004 others(25): Show |
74 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.219+3963G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147665867 | |||||||
| chr1:147665916 | A | C | 7 | a0001c0002t0002g0069 a0001c0002t0005g0007 a0001c0002t0005g0152 others(4): Show |
15 | HG00438.hp1 HG02129.hp2 NA18974.hp2 others(12): Show |
intron_variant | MODIFIER | c.219+3914T>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147665916 | |||||||
| chr1:147665926 | T | A | 1 | a0001c0001t0008g0100 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.219+3904A>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147665926 | |||||||
| chr1:147666072 | G | A | 1 | a0001c0002t0002g0037 | 2 | HG02027.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.219+3758C>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147666072 | |||||||
| chr1:147666206 | C | T | 1 | a0001c0003t0018g0182 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.219+3624G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147666206 | |||||||
| chr1:147666331 | G | T | 1 | a0001c0003t0044g0061 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.219+3499C>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147666331 | |||||||
| chr1:147666481 | G | T | 1 | a0001c0001t0001g0151 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.219+3349C>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147666481 | |||||||
| chr1:147666583 | G | A | 1 | a0001c0003t0003g0131 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.219+3247C>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147666583 | |||||||
| chr1:147666691 | C | T | 100 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0017 others(97): Show |
226 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(223): Show |
intron_variant | MODIFIER | c.219+3139G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147666691 | |||||||
| chr1:147666696 | CAATTA | C | 3 | a0001c0003t0003g0027 a0001c0003t0003g0132 a0001c0003t0003g0133 |
5 | NA18982.hp1 NA18986.hp2 NA18988.hp2 others(2): Show |
intron_variant | MODIFIER | c.219+3129_219+3133d others(7): Show |
ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147666696 | |||||||
| chr1:147666712 | C | T | 1 | a0001c0001t0034g0048 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.219+3118G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147666712 | |||||||
| chr1:147666777 | G | A | 48 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0017 others(45): Show |
119 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.219+3053C>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147666777 | |||||||
| chr1:147667102 | GA | G | 3 | a0001c0001t0004g0035 a0001c0001t0004g0067 a0001c0001t0004g0068 |
4 | HG00639.hp1 HG00735.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.219+2727delT | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147667102 | |||||||
| chr1:147667377 | C | T | 1 | a0001c0003t0003g0125 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.219+2453G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147667377 | |||||||
| chr1:147667437 | C | T | 1 | a0001c0003t0003g0148 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.219+2393G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147667437 | |||||||
| chr1:147667786 | T | G | 100 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0017 others(97): Show |
226 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(223): Show |
intron_variant | MODIFIER | c.219+2044A>C | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147667786 | |||||||
| chr1:147667882 | C | T | 1 | a0001c0002t0002g0034 | 2 | NA18953.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.219+1948G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147667882 | |||||||
| chr1:147667931 | G | A | 106 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0017 others(103): Show |
240 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(237): Show |
intron_variant | MODIFIER | c.219+1899C>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147667931 | |||||||
| chr1:147667988 | C | CA | 180 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0017 others(177): Show |
398 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(395): Show |
intron_variant | MODIFIER | c.219+1841dupT | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147667988 | |||||||
| chr1:147668073 | A | G | 1 | a0003c0006t0022g0033 | 2 | HG02145.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.219+1757T>C | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147668073 | |||||||
| chr1:147668334 | G | C | 55 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0017 others(52): Show |
127 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.219+1496C>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147668334 | |||||||
| chr1:147668399 | T | G | 9 | a0001c0001t0013g0024 a0001c0001t0013g0105 a0001c0002t0002g0019 others(6): Show |
17 | HG00639.hp2 HG01109.hp1 HG01433.hp1 others(14): Show |
intron_variant | MODIFIER | c.219+1431A>C | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147668399 | |||||||
| chr1:147668408 | C | A | 2 | a0001c0003t0018g0045 a0001c0003t0018g0182 |
3 | HG02630.hp1 HG02723.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.219+1422G>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147668408 | |||||||
| chr1:147668415 | G | GAT | 29 | a0001c0001t0004g0065 a0001c0001t0011g0018 a0001c0001t0011g0055 others(26): Show |
59 | HG00558.hp1 HG00597.hp1 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.219+1413_219+1414d others(4): Show |
ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147668415 | |||||||
| chr1:147668415 | GAT | G | 52 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0017 others(49): Show |
124 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.219+1413_219+1414d others(4): Show |
ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147668415 | |||||||
| chr1:147668828 | C | T | 1 | a0001c0001t0001g0146 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.219+1002G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147668828 | |||||||
| chr1:147668829 | G | A | 4 | a0001c0002t0033g0057 a0001c0003t0006g0021 a0001c0003t0006g0058 others(1): Show |
6 | HG01884.hp2 HG02258.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.219+1001C>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147668829 | |||||||
| chr1:147669040 | C | T | 3 | a0001c0001t0049g0063 a0001c0003t0044g0061 a0001c0003t0046g0062 |
3 | HG02486.hp2 HG02723.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.219+790G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147669040 | |||||||
| chr1:147669073 | A | T | 1 | a0001c0003t0003g0124 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.219+757T>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147669073 | |||||||
| chr1:147669081 | G | T | 1 | a0001c0003t0019g0031 | 2 | HG04184.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.219+749C>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147669081 | |||||||
| chr1:147669092 | A | AT | 111 | a0001c0001t0004g0002 a0001c0001t0004g0014 a0001c0001t0004g0016 others(108): Show |
241 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(238): Show |
intron_variant | MODIFIER | c.219+737dupA | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147669092 | |||||||
| chr1:147669340 | T | C | 1 | a0001c0001t0004g0016 | 5 | NA18973.hp1 NA18981.hp2 NA19003.hp2 others(2): Show |
intron_variant | MODIFIER | c.219+490A>G | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147669340 | |||||||
| chr1:147669579 | C | A | 1 | a0001c0003t0003g0183 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.219+251G>T | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147669579 | |||||||
| chr1:147669688 | C | T | 101 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0017 others(98): Show |
228 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(225): Show |
intron_variant | MODIFIER | c.219+142G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147669688 | |||||||
| chr1:147669798 | C | T | 3 | a0001c0001t0049g0063 a0001c0003t0044g0061 a0001c0003t0046g0062 |
3 | HG02486.hp2 HG02723.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.219+32G>A | ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 1/9 | chr1 | 147669798 |