Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 51666 |
| ensemblid | ENSG00000005981.13 |
| hgncid | 16009 |
| symbol | ASB4 |
| name | ankyrin repeat and SOCS box containing 4 |
| refseq_nuc | NM_016116.3 |
| refseq_prot | NP_057200.1 |
| ensembl_nuc | ENST00000325885.6 |
| ensembl_prot | ENSP00000321388.5 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 95485943 |
| end | 95540233 |
| strand | + |
| ver | v1.2 |
| region | chr7:95485943-95540233 |
| region5000 | chr7:95480943-95545233 |
| regionname0 | ASB4_chr7_95485943_95540233 |
| regionname5000 | ASB4_chr7_95480943_95545233 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 426 | 371 | 84 | 76 | 149 | 14 | 46 | 109 | ASB4_chr7_95480943_95545233 | ASB4 | MDGTT others(421): Show |
chr7 | 95480943 | 95545233 |
| a0002 | 0/0 | 426 | 14 | 13 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | MDGTT others(421): Show |
chr7 | 95480943 | 95545233 |
| a0003 | 0/0 | 426 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | MDGTT others(421): Show |
chr7 | 95480943 | 95545233 |
| a0004 | 0/0 | 426 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | MDGTT others(421): Show |
chr7 | 95480943 | 95545233 |
| a0005 | 0/0 | 426 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | MDGTT others(421): Show |
chr7 | 95480943 | 95545233 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1278 | 370 | 83 | 76 | 149 | 14 | 46 | ASB4_chr7_95480943_95545233 | ASB4 | ATGGA others(1273): Show |
chr7 | 95480943 | 95545233 | ||
| a0001c0006 | 0/0 | 1278 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | ATGGA others(1273): Show |
chr7 | 95480943 | 95545233 | ||
| a0002c0002 | 0/0 | 1278 | 14 | 13 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | ATGGA others(1273): Show |
chr7 | 95480943 | 95545233 | ||
| a0003c0005 | 0/0 | 1278 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | ATGGA others(1273): Show |
chr7 | 95480943 | 95545233 | ||
| a0004c0003 | 0/0 | 1278 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | ATGGA others(1273): Show |
chr7 | 95480943 | 95545233 | ||
| a0005c0004 | 0/0 | 1278 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | ATGGA others(1273): Show |
chr7 | 95480943 | 95545233 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3784 | 194 | 9 | 34 | 115 | 7 | 29 | ASB4_chr7_95480943_95545233 | ASB4 | ACAAC others(3779): Show |
chr7 | 95480943 | 95545233 |
| a0001c0001t0002 | 0/0 | 3784 | 47 | 14 | 8 | 19 | 0 | 6 | ASB4_chr7_95480943_95545233 | ASB4 | ACAAC others(3779): Show |
chr7 | 95480943 | 95545233 |
| a0001c0001t0003 | 0/0 | 3784 | 38 | 9 | 16 | 6 | 3 | 4 | ASB4_chr7_95480943_95545233 | ASB4 | ACAAC others(3779): Show |
chr7 | 95480943 | 95545233 |
| a0001c0001t0004 | 1/0 | 3784 | 33 | 12 | 8 | 5 | 2 | 5 | ASB4_chr7_95480943_95545233 | ASB4 | ACAAC others(3779): Show |
chr7 | 95480943 | 95545233 |
| a0001c0001t0005 | 0/0 | 3782 | 13 | 13 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | ACAAC others(3777): Show |
chr7 | 95480943 | 95545233 |
| a0001c0001t0006 | 0/0 | 3784 | 3 | 3 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | ACAAC others(3779): Show |
chr7 | 95480943 | 95545233 |
| a0001c0001t0007 | 0/0 | 3783 | 6 | 6 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | ACAAC others(3778): Show |
chr7 | 95480943 | 95545233 |
| a0001c0001t0008 | 0/0 | 3784 | 5 | 5 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | ACAAC others(3779): Show |
chr7 | 95480943 | 95545233 |
| a0001c0001t0009 | 0/0 | 3784 | 5 | 0 | 5 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | ACAAC others(3779): Show |
chr7 | 95480943 | 95545233 |
| a0001c0001t0010 | 0/0 | 3785 | 4 | 4 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | ACAAC others(3780): Show |
chr7 | 95480943 | 95545233 |
| a0001c0001t0011 | 0/0 | 3785 | 2 | 2 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | ACAAC others(3780): Show |
chr7 | 95480943 | 95545233 |
| a0001c0001t0012 | 0/0 | 3784 | 3 | 0 | 3 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | ACAAC others(3779): Show |
chr7 | 95480943 | 95545233 |
| a0001c0001t0013 | 0/0 | 3784 | 2 | 0 | 1 | 0 | 1 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | ACAAC others(3779): Show |
chr7 | 95480943 | 95545233 |
| a0001c0001t0014 | 0/0 | 3784 | 2 | 2 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | ACAAC others(3779): Show |
chr7 | 95480943 | 95545233 |
| a0001c0001t0015 | 0/0 | 3784 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | ACAAC others(3779): Show |
chr7 | 95480943 | 95545233 |
| a0001c0001t0016 | 0/0 | 3784 | 2 | 0 | 0 | 0 | 0 | 2 | ASB4_chr7_95480943_95545233 | ASB4 | ACAAC others(3779): Show |
chr7 | 95480943 | 95545233 |
| a0001c0001t0017 | 0/0 | 3784 | 2 | 2 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | ACAAC others(3779): Show |
chr7 | 95480943 | 95545233 |
| a0001c0001t0018 | 0/0 | 3784 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | ACAAC others(3779): Show |
chr7 | 95480943 | 95545233 |
| a0001c0001t0019 | 0/0 | 3784 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | ACAAC others(3779): Show |
chr7 | 95480943 | 95545233 |
| a0001c0001t0020 | 0/0 | 3785 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | ACAAC others(3780): Show |
chr7 | 95480943 | 95545233 |
| a0001c0001t0021 | 0/0 | 3784 | 1 | 0 | 0 | 0 | 1 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | ACAAC others(3779): Show |
chr7 | 95480943 | 95545233 |
| a0001c0001t0022 | 0/1 | 3782 | 1 | 0 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | ACAAC others(3777): Show |
chr7 | 95480943 | 95545233 |
| a0001c0001t0023 | 0/0 | 3784 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | ACAAC others(3779): Show |
chr7 | 95480943 | 95545233 |
| a0001c0001t0024 | 0/0 | 3784 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | ACAAC others(3779): Show |
chr7 | 95480943 | 95545233 |
| a0001c0001t0025 | 0/0 | 3784 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | ACAAC others(3779): Show |
chr7 | 95480943 | 95545233 |
| a0001c0006t0003 | 0/0 | 3784 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | ACAAC others(3779): Show |
chr7 | 95480943 | 95545233 |
| a0002c0002t0001 | 0/0 | 3784 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | ACAAC others(3779): Show |
chr7 | 95480943 | 95545233 |
| a0002c0002t0003 | 0/0 | 3784 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | ACAAC others(3779): Show |
chr7 | 95480943 | 95545233 |
| a0002c0002t0004 | 0/0 | 3784 | 3 | 3 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | ACAAC others(3779): Show |
chr7 | 95480943 | 95545233 |
| a0002c0002t0006 | 0/0 | 3784 | 8 | 7 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | ACAAC others(3779): Show |
chr7 | 95480943 | 95545233 |
| a0002c0002t0011 | 0/0 | 3785 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | ACAAC others(3780): Show |
chr7 | 95480943 | 95545233 |
| a0003c0005t0001 | 0/0 | 3784 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | ACAAC others(3779): Show |
chr7 | 95480943 | 95545233 |
| a0004c0003t0015 | 0/0 | 3784 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | ACAAC others(3779): Show |
chr7 | 95480943 | 95545233 |
| a0005c0004t0004 | 0/0 | 3784 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | ACAAC others(3779): Show |
chr7 | 95480943 | 95545233 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0346 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0348 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0001g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0002g0002 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0002g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0002g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0002g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0002g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0002g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0003g0006 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0003g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0003g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0003g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0003g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0003g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0003g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0003g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0003g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0003g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0003g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0003g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0003g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0003g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0003g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0003g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0003g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0003g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0003g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0003g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0003g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0003g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0003g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0003g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0003g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0003g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0003g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0003g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0003g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0004g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0004g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0004g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0004g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0004g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0004g0086 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0004g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0004g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0004g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0004g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0004g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0004g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0004g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0004g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0004g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0004g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0004g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0004g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0004g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0004g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0004g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0004g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0004g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0004g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0004g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0004g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0004g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0004g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0004g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0004g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0004g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0004g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0004g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0005g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0005g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0005g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0005g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0005g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0005g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0005g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0005g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0005g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0005g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0005g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0005g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0006g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0006g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0006g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0007g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0007g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0007g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0007g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0007g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0007g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0008g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0008g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0008g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0008g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0008g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0009g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0009g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0009g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0009g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0009g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0010g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0010g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0010g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0010g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0011g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0011g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0012g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0012g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0012g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0013g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0013g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0014g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0014g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0015g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0016g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0016g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0017g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0017g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0018g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0019g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0020g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0021g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0022g0360 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0023g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0024g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0001t0025g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0001c0006t0003g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0002c0002t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0002c0002t0003g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0002c0002t0004g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0002c0002t0004g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0002c0002t0004g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0002c0002t0006g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0002c0002t0006g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0002c0002t0006g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0002c0002t0006g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0002c0002t0006g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0002c0002t0006g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0002c0002t0006g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0002c0002t0011g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0003c0005t0001g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0004c0003t0015g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| a0005c0004t0004g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0293 | EUR | GBR | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0262 | EUR | GBR | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0249 | EUR | FIN | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0344 | EUR | FIN | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG00323 | hp1 | a0001 | c0001 | t0003 | g0083 | EUR | FIN | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0330 | EUR | FIN | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | CHS | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | CHS | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0153 | EAS | CHS | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | CHS | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | CHS | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | CHS | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | CHS | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | CHS | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | CHS | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0358 | EAS | CHS | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | CHS | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG00621 | hp1 | a0001 | c0001 | t0004 | g0102 | EAS | CHS | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | CHS | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG00639 | hp1 | a0001 | c0001 | t0004 | g0031 | AMR | PUR | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0265 | AMR | PUR | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0328 | EAS | CHS | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG00735 | hp2 | a0001 | c0001 | t0004 | g0092 | AMR | PUR | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0300 | AMR | PUR | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG00738 | hp2 | a0002 | c0002 | t0006 | g0361 | AMR | PUR | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG00741 | hp1 | a0003 | c0005 | t0001 | g0345 | AMR | PUR | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0295 | AMR | PUR | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG01070 | hp1 | a0001 | c0001 | t0003 | g0098 | AMR | PUR | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | PUR | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0050 | AMR | PUR | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG01099 | hp2 | a0001 | c0001 | t0004 | g0143 | AMR | PUR | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0316 | AMR | PUR | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0266 | AMR | PUR | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG01109 | hp1 | a0001 | c0001 | t0003 | g0099 | AMR | PUR | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0331 | AMR | PUR | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG01167 | hp1 | a0001 | c0001 | t0004 | g0128 | AMR | PUR | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0292 | AMR | PUR | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0324 | AMR | PUR | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0247 | AMR | PUR | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0235 | AMR | PUR | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG01175 | hp1 | a0001 | c0001 | t0003 | g0351 | AMR | PUR | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG01175 | hp2 | a0001 | c0001 | t0003 | g0061 | AMR | PUR | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG01192 | hp1 | a0001 | c0001 | t0009 | g0186 | AMR | PUR | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG01192 | hp2 | a0001 | c0001 | t0003 | g0304 | AMR | PUR | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG01243 | hp1 | a0001 | c0001 | t0003 | g0071 | AMR | PUR | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG01243 | hp2 | a0001 | c0001 | t0004 | g0323 | AMR | PUR | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG01255 | hp1 | a0001 | c0001 | t0003 | g0084 | AMR | CLM | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG01255 | hp2 | a0001 | c0001 | t0003 | g0022 | AMR | CLM | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG01256 | hp1 | a0001 | c0001 | t0003 | g0096 | AMR | CLM | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG01256 | hp2 | a0001 | c0001 | t0003 | g0060 | AMR | CLM | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG01257 | hp1 | a0001 | c0001 | t0012 | g0199 | AMR | CLM | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0242 | AMR | CLM | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG01258 | hp1 | a0001 | c0001 | t0012 | g0197 | AMR | CLM | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG01258 | hp2 | a0001 | c0001 | t0003 | g0006 | AMR | CLM | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG01261 | hp1 | a0001 | c0001 | t0013 | g0101 | AMR | CLM | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0307 | AMR | CLM | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | CLM | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG01346 | hp2 | a0001 | c0001 | t0004 | g0094 | AMR | CLM | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG01358 | hp1 | a0001 | c0001 | t0009 | g0184 | AMR | CLM | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | CLM | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG01361 | hp1 | a0001 | c0001 | t0003 | g0063 | AMR | CLM | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG01361 | hp2 | a0001 | c0001 | t0012 | g0198 | AMR | CLM | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG01433 | hp1 | a0001 | c0001 | t0009 | g0188 | AMR | CLM | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | CLM | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | CLM | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG01496 | hp2 | a0001 | c0001 | t0004 | g0105 | AMR | CLM | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0346 | EUR | IBS | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG01515 | hp2 | a0001 | c0001 | t0003 | g0006 | EUR | IBS | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG01516 | hp1 | a0001 | c0001 | t0013 | g0107 | EUR | IBS | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG01516 | hp2 | a0001 | c0001 | t0004 | g0264 | EUR | IBS | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG01884 | hp1 | a0001 | c0001 | t0006 | g0136 | AFR | ACB | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG01884 | hp2 | a0001 | c0001 | t0014 | g0311 | AFR | ACB | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG01891 | hp1 | a0001 | c0001 | t0005 | g0276 | AFR | ACB | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG01891 | hp2 | a0001 | c0001 | t0004 | g0114 | AFR | ACB | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0236 | AMR | PEL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG01928 | hp2 | a0001 | c0001 | t0003 | g0088 | AMR | PEL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG01934 | hp2 | a0001 | c0001 | t0004 | g0085 | AMR | PEL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG01943 | hp1 | a0001 | c0001 | t0003 | g0073 | AMR | PEL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0298 | AMR | PEL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0299 | AMR | PEL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0174 | AMR | PEL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0156 | AMR | PEL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG01975 | hp2 | a0001 | c0001 | t0009 | g0187 | AMR | PEL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | PEL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0306 | AMR | PEL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0332 | AMR | PEL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0301 | AMR | PEL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0175 | AMR | PEL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0233 | AMR | PEL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0308 | AMR | PEL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0237 | AMR | PEL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | KHV | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | KHV | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0325 | EAS | KHV | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | KHV | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | KHV | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | KHV | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG02055 | hp1 | a0001 | c0001 | t0005 | g0032 | AFR | ACB | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG02055 | hp2 | a0001 | c0001 | t0006 | g0158 | AFR | ACB | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | KHV | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | KHV | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0334 | EAS | KHV | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | KHV | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | KHV | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0142 | EAS | KHV | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0349 | EAS | KHV | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG02129 | hp2 | a0001 | c0001 | t0003 | g0283 | EAS | KHV | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0342 | EAS | KHV | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | KHV | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0219 | AMR | PEL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG02148 | hp2 | a0001 | c0001 | t0003 | g0087 | AMR | PEL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | CDX | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | CDX | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG02257 | hp1 | a0001 | c0001 | t0005 | g0034 | AFR | ACB | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0076 | AFR | ACB | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0025 | AFR | ACB | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG02258 | hp2 | a0001 | c0006 | t0003 | g0275 | AFR | ACB | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | PEL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | ACB | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG02280 | hp2 | a0001 | c0001 | t0008 | g0212 | AFR | ACB | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG02293 | hp1 | a0001 | c0001 | t0019 | g0103 | AMR | PEL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0138 | AMR | PEL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG02300 | hp1 | a0001 | c0001 | t0009 | g0183 | AMR | PEL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0302 | AMR | PEL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG02451 | hp1 | a0001 | c0001 | t0004 | g0030 | AFR | ACB | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG02451 | hp2 | a0002 | c0002 | t0004 | g0044 | AFR | ACB | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0362 | EAS | KHV | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | KHV | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG02572 | hp1 | a0002 | c0002 | t0003 | g0317 | AFR | GWD | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG02572 | hp2 | a0001 | c0001 | t0004 | g0318 | AFR | GWD | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0234 | SAS | PJL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG02602 | hp2 | a0001 | c0001 | t0004 | g0167 | SAS | PJL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG02615 | hp1 | a0001 | c0001 | t0007 | g0273 | AFR | GWD | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | GWD | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0314 | AFR | GWD | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0123 | AFR | GWD | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG02630 | hp1 | a0001 | c0001 | t0003 | g0364 | AFR | GWD | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG02630 | hp2 | a0001 | c0001 | t0005 | g0012 | AFR | GWD | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0072 | AFR | GWD | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG02647 | hp2 | a0001 | c0001 | t0010 | g0017 | AFR | GWD | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG02717 | hp1 | a0004 | c0003 | t0015 | g0059 | AFR | GWD | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0215 | AFR | GWD | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG02723 | hp1 | a0001 | c0001 | t0004 | g0090 | AFR | GWD | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0016 | AFR | GWD | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0290 | SAS | PJL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0067 | SAS | PJL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0185 | SAS | PJL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG02809 | hp1 | a0002 | c0002 | t0006 | g0004 | AFR | GWD | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG02809 | hp2 | a0002 | c0002 | t0001 | g0045 | AFR | GWD | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG02818 | hp1 | a0001 | c0001 | t0011 | g0367 | AFR | GWD | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG02818 | hp2 | a0001 | c0001 | t0007 | g0319 | AFR | GWD | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG02886 | hp1 | a0001 | c0001 | t0004 | g0214 | AFR | GWD | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG02886 | hp2 | a0002 | c0002 | t0011 | g0038 | AFR | GWD | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG02895 | hp1 | a0002 | c0002 | t0006 | g0039 | AFR | GWD | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG02895 | hp2 | a0001 | c0001 | t0007 | g0208 | AFR | GWD | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG02896 | hp1 | a0001 | c0001 | t0010 | g0029 | AFR | GWD | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0058 | AFR | GWD | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG02897 | hp1 | a0002 | c0002 | t0006 | g0040 | AFR | GWD | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG02897 | hp2 | a0001 | c0001 | t0010 | g0028 | AFR | GWD | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG02922 | hp1 | a0001 | c0001 | t0008 | g0291 | AFR | ESN | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG02922 | hp2 | a0001 | c0001 | t0015 | g0315 | AFR | ESN | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG02965 | hp1 | a0001 | c0001 | t0005 | g0294 | AFR | ESN | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG02965 | hp2 | a0001 | c0001 | t0004 | g0312 | AFR | ESN | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG02970 | hp1 | a0001 | c0001 | t0017 | g0305 | AFR | ESN | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG02970 | hp2 | a0001 | c0001 | t0005 | g0012 | AFR | ESN | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG02976 | hp1 | a0001 | c0001 | t0017 | g0274 | AFR | ESN | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG02976 | hp2 | a0002 | c0002 | t0006 | g0043 | AFR | ESN | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0347 | SAS | PJL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0164 | SAS | PJL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | GWD | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG03098 | hp1 | a0001 | c0001 | t0004 | g0313 | AFR | MSL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG03098 | hp2 | a0001 | c0001 | t0006 | g0268 | AFR | MSL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG03130 | hp1 | a0001 | c0001 | t0011 | g0368 | AFR | ESN | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG03130 | hp2 | a0002 | c0002 | t0006 | g0004 | AFR | ESN | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG03139 | hp1 | a0001 | c0001 | t0007 | g0269 | AFR | ESN | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG03139 | hp2 | a0001 | c0001 | t0020 | g0026 | AFR | ESN | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG03195 | hp1 | a0001 | c0001 | t0008 | g0206 | AFR | ESN | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG03195 | hp2 | a0001 | c0001 | t0005 | g0195 | AFR | ESN | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG03209 | hp1 | a0001 | c0001 | t0005 | g0320 | AFR | MSL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0309 | AFR | MSL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0049 | AFR | MSL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG03225 | hp2 | a0001 | c0001 | t0004 | g0111 | AFR | MSL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0231 | SAS | PJL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG03453 | hp1 | a0001 | c0001 | t0004 | g0365 | AFR | MSL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | MSL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG03486 | hp1 | a0001 | c0001 | t0010 | g0047 | AFR | MSL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG03486 | hp2 | a0001 | c0001 | t0004 | g0213 | AFR | MSL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG03490 | hp1 | a0001 | c0001 | t0016 | g0267 | SAS | PJL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0182 | SAS | PJL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG03516 | hp1 | a0001 | c0001 | t0004 | g0104 | AFR | ESN | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG03516 | hp2 | a0001 | c0001 | t0008 | g0027 | AFR | ESN | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG03540 | hp1 | a0001 | c0001 | t0005 | g0033 | AFR | GWD | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0051 | AFR | GWD | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0152 | AFR | MSL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG03579 | hp2 | a0002 | c0002 | t0006 | g0041 | AFR | MSL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0221 | SAS | PJL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG03669 | hp1 | a0001 | c0001 | t0003 | g0303 | SAS | PJL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG03669 | hp2 | a0001 | c0001 | t0004 | g0091 | SAS | PJL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0068 | SAS | STU | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | STU | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG03704 | hp1 | a0001 | c0001 | t0004 | g0021 | SAS | PJL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0310 | SAS | PJL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG03710 | hp2 | a0001 | c0001 | t0003 | g0220 | SAS | PJL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0159 | SAS | BEB | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG03831 | hp2 | a0001 | c0001 | t0004 | g0097 | SAS | BEB | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | BEB | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0289 | SAS | BEB | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0069 | SAS | BEB | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0218 | SAS | BEB | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0070 | SAS | BEB | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0181 | SAS | BEB | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG04115 | hp1 | a0001 | c0001 | t0016 | g0281 | SAS | STU | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG04115 | hp2 | a0001 | c0001 | t0003 | g0074 | SAS | STU | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | BEB | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0227 | SAS | BEB | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG04199 | hp1 | a0001 | c0001 | t0004 | g0113 | SAS | STU | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0348 | SAS | STU | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0285 | SAS | STU | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0066 | SAS | STU | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0340 | SAS | STU | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0150 | SAS | STU | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA18522 | hp1 | a0001 | c0001 | t0005 | g0194 | AFR | YRI | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0082 | AFR | YRI | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | CHB | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | CHB | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA18906 | hp1 | a0001 | c0001 | t0008 | g0297 | AFR | YRI | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0048 | AFR | YRI | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA18945 | hp1 | a0001 | c0001 | t0004 | g0132 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0354 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0350 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0355 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA18953 | hp2 | a0001 | c0001 | t0018 | g0173 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA18959 | hp2 | a0005 | c0004 | t0004 | g0109 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0337 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA18966 | hp1 | a0001 | c0001 | t0024 | g0224 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA18968 | hp1 | a0001 | c0001 | t0004 | g0108 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA18968 | hp2 | a0001 | c0001 | t0003 | g0095 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0352 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA18972 | hp2 | a0001 | c0001 | t0025 | g0228 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0343 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0336 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0353 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0338 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA18995 | hp2 | a0001 | c0001 | t0003 | g0177 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0356 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA18999 | hp2 | a0001 | c0001 | t0003 | g0127 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA19001 | hp2 | a0001 | c0001 | t0004 | g0163 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA19002 | hp1 | a0001 | c0001 | t0023 | g0241 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0335 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0339 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA19011 | hp1 | a0001 | c0001 | t0004 | g0149 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA19011 | hp2 | a0001 | c0001 | t0003 | g0126 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0160 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0366 | AFR | LWK | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA19030 | hp2 | a0001 | c0001 | t0007 | g0363 | AFR | LWK | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA19043 | hp1 | a0002 | c0002 | t0004 | g0037 | AFR | LWK | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA19043 | hp2 | a0001 | c0001 | t0007 | g0211 | AFR | LWK | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0357 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA19059 | hp1 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA19059 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0329 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0333 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA19075 | hp1 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0359 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA19090 | hp2 | a0001 | c0001 | t0003 | g0078 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA19240 | hp1 | a0001 | c0001 | t0004 | g0210 | AFR | YRI | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA19240 | hp2 | a0001 | c0001 | t0014 | g0117 | AFR | YRI | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0075 | AFR | ASW | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0052 | AFR | ASW | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA20752 | hp1 | a0001 | c0001 | t0021 | g0077 | EUR | TSI | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0282 | EUR | TSI | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA20805 | hp1 | a0001 | c0001 | t0004 | g0020 | EUR | TSI | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA20805 | hp2 | a0001 | c0001 | t0003 | g0089 | EUR | TSI | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0341 | SAS | GIH | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA20905 | hp2 | a0001 | c0001 | t0003 | g0121 | SAS | GIH | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0053 | AFR | ACB | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG02109 | hp2 | a0001 | c0001 | t0005 | g0271 | AFR | ACB | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0134 | AFR | ACB | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG02486 | hp2 | a0002 | c0002 | t0004 | g0036 | AFR | ACB | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG02559 | hp1 | a0001 | c0001 | t0005 | g0272 | AFR | ACB | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG02559 | hp2 | a0001 | c0001 | t0003 | g0296 | AFR | ACB | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG03471 | hp1 | a0002 | c0002 | t0006 | g0042 | AFR | MSL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0116 | AFR | MSL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0062 | AFR | USA | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | USA | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0169 | AFR | USA | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | USA | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0115 | AFR | LWK | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| NA21309 | hp2 | a0001 | c0001 | t0005 | g0369 | AFR | LWK | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0022 | g0360 | REF | REF | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0004 | g0086 | REF | REF | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:95486020 | G | C | 1 | a0002 | 14 | HG00738.hp2 HG02451.hp2 HG02486.hp2 others(11): Show |
missense_variant | MODERATE | c.49G>C | p.Val17Leu | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/5 | 78/3784 | 49/1281 | 17/426 | chr7 | 95486020 | |||
| chr7:95486062 | G | A | 1 | a0004 | 1 | HG02717.hp1 | missense_variant | MODERATE | c.91G>A | p.Gly31Arg | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/5 | 120/3784 | 91/1281 | 31/426 | chr7 | 95486062 | |||
| chr7:95528113 | G | C | 1 | a0005 | 1 | NA18959.hp2 | missense_variant | MODERATE | c.788G>C | p.Cys263Ser | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/5 | 817/3784 | 788/1281 | 263/426 | chr7 | 95528113 | |||
| chr7:95536518 | T | C | 1 | a0003 | 1 | HG00741.hp1 | missense_variant | MODERATE | c.1060T>C | p.Trp354Arg | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 4/5 | 1089/3784 | 1060/1281 | 354/426 | chr7 | 95536518 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:95536448 | C | T | 1 | a0001c0006 | 1 | HG02258.hp2 | synonymous_variant | LOW | c.990C>T | p.Ala330Ala | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 4/5 | 1019/3784 | 990/1281 | 330/426 | chr7 | 95536448 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:95537892 | C | T | 9 | a0001c0001t0001 a0001c0001t0009 a0001c0001t0016 others(6): Show |
208 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(205): Show |
3_prime_UTR_variant | MODIFIER | c.*133C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 5/5 | 133 | chr7 | 95537892 | ||||||
| chr7:95538122 | T | C | 3 | a0001c0001t0002 a0001c0001t0013 a0001c0001t0018 |
50 | HG00423.hp1 HG00741.hp2 HG01081.hp2 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*363T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 5/5 | 363 | chr7 | 95538122 | ||||||
| chr7:95538191 | C | A | 1 | a0001c0001t0009 | 5 | HG01192.hp1 HG01358.hp1 HG01433.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*432C>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 5/5 | 432 | chr7 | 95538191 | ||||||
| chr7:95538231 | G | A | 8 | a0001c0001t0001 a0001c0001t0009 a0001c0001t0016 others(5): Show |
206 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(203): Show |
3_prime_UTR_variant | MODIFIER | c.*472G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 5/5 | 472 | chr7 | 95538231 | ||||||
| chr7:95538256 | C | T | 1 | a0001c0001t0012 | 3 | HG01257.hp1 HG01258.hp1 HG01361.hp2 |
3_prime_UTR_variant | MODIFIER | c.*497C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 5/5 | 497 | chr7 | 95538256 | ||||||
| chr7:95538669 | A | C | 1 | a0001c0001t0008 | 5 | HG02280.hp2 HG02922.hp1 HG03195.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*910A>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 5/5 | 910 | chr7 | 95538669 | ||||||
| chr7:95538818 | T | C | 1 | a0001c0001t0016 | 2 | HG03490.hp1 HG04115.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1059T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 5/5 | 1059 | chr7 | 95538818 | ||||||
| chr7:95538828 | C | T | 1 | a0001c0001t0021 | 1 | NA20752.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1069C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 5/5 | 1069 | chr7 | 95538828 | ||||||
| chr7:95538909 | C | T | 2 | a0001c0001t0011 a0002c0002t0011 |
3 | HG02818.hp1 HG02886.hp2 HG03130.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1150C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 5/5 | 1150 | chr7 | 95538909 | ||||||
| chr7:95538910 | G | A | 1 | a0001c0001t0014 | 2 | HG01884.hp2 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1151G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 5/5 | 1151 | chr7 | 95538910 | ||||||
| chr7:95539067 | C | CT | 4 | a0001c0001t0010 a0001c0001t0011 a0001c0001t0020 others(1): Show |
8 | HG02647.hp2 HG02818.hp1 HG02886.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1318dupT | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 5/5 | 1319 | INFO_REALIGN_3_PRIME | chr7 | 95539067 | |||||
| chr7:95539084 | GCT | G | 1 | a0001c0001t0005 | 13 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1326_*1327delCT | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 5/5 | 1326 | chr7 | 95539084 | ||||||
| chr7:95539085 | CTA | C | 25 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(22): Show |
323 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(320): Show |
3_prime_UTR_variant | MODIFIER | c.*1329_*1330delTA | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 5/5 | 1329 | INFO_REALIGN_3_PRIME | chr7 | 95539085 | |||||
| chr7:95539087 | A | T | 1 | a0001c0001t0005 | 13 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1328A>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 5/5 | 1328 | chr7 | 95539087 | ||||||
| chr7:95539144 | G | A | 1 | a0001c0001t0018 | 1 | NA18953.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1385G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 5/5 | 1385 | chr7 | 95539144 | ||||||
| chr7:95539249 | G | A | 1 | a0001c0001t0023 | 1 | NA19002.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1490G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 5/5 | 1490 | chr7 | 95539249 | ||||||
| chr7:95539523 | G | T | 1 | a0001c0001t0008 | 5 | HG02280.hp2 HG02922.hp1 HG03195.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1764G>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 5/5 | 1764 | chr7 | 95539523 | ||||||
| chr7:95539664 | T | C | 1 | a0001c0001t0020 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1905T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 5/5 | 1905 | chr7 | 95539664 | ||||||
| chr7:95539815 | A | T | 2 | a0001c0001t0006 a0002c0002t0006 |
11 | HG00738.hp2 HG01884.hp1 HG02055.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2056A>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 5/5 | 2056 | chr7 | 95539815 | ||||||
| chr7:95539959 | T | C | 2 | a0001c0001t0015 a0004c0003t0015 |
2 | HG02717.hp1 HG02922.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2200T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 5/5 | 2200 | chr7 | 95539959 | ||||||
| chr7:95540053 | C | T | 1 | a0001c0001t0025 | 1 | NA18972.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2294C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 5/5 | 2294 | chr7 | 95540053 | ||||||
| chr7:95540070 | AC | A | 1 | a0001c0001t0007 | 6 | HG02615.hp1 HG02818.hp2 HG02895.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2312delC | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 5/5 | 2312 | chr7 | 95540070 | ||||||
| chr7:95540078 | T | A | 1 | a0001c0001t0019 | 1 | HG02293.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2319T>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 5/5 | 2319 | chr7 | 95540078 | ||||||
| chr7:95540102 | A | T | 1 | a0001c0001t0024 | 1 | NA18966.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2343A>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 5/5 | 2343 | chr7 | 95540102 | ||||||
| chr7:95540202 | G | T | 7 | a0001c0001t0003 a0001c0001t0013 a0001c0001t0015 others(4): Show |
45 | HG00323.hp1 HG01070.hp1 HG01109.hp1 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*2443G>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 5/5 | 2443 | chr7 | 95540202 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:95486187 | CT | C | 9 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0023 others(6): Show |
9 | HG01255.hp2 HG02647.hp2 HG02698.hp2 others(6): Show |
intron_variant | MODIFIER | c.187+30delT | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95486187 | |||||||
| chr7:95486204 | A | T | 7 | a0001c0001t0003g0364 a0001c0001t0003g0366 a0001c0001t0004g0365 others(4): Show |
7 | HG02630.hp1 HG02818.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.187+46A>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95486204 | |||||||
| chr7:95486267 | C | T | 1 | a0001c0001t0001g0362 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.187+109C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95486267 | |||||||
| chr7:95486334 | T | C | 1 | a0001c0001t0002g0025 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.187+176T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95486334 | |||||||
| chr7:95486336 | T | C | 12 | a0001c0001t0003g0364 a0001c0001t0003g0366 a0001c0001t0004g0030 others(9): Show |
12 | HG02451.hp1 HG02630.hp1 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.187+178T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95486336 | |||||||
| chr7:95486348 | G | A | 5 | a0001c0001t0001g0035 a0001c0001t0004g0031 a0001c0001t0005g0032 others(2): Show |
5 | HG00639.hp1 HG02055.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.187+190G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95486348 | |||||||
| chr7:95486375 | TG | T | 9 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0023 others(6): Show |
9 | HG01255.hp2 HG02647.hp2 HG02698.hp2 others(6): Show |
intron_variant | MODIFIER | c.187+220delG | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr7 | 95486375 | ||||||
| chr7:95486650 | C | T | 51 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(48): Show |
56 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.187+492C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95486650 | |||||||
| chr7:95486661 | G | T | 3 | a0001c0001t0004g0312 a0001c0001t0004g0313 a0001c0001t0014g0311 |
3 | HG01884.hp2 HG02965.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.187+503G>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95486661 | |||||||
| chr7:95486673 | T | C | 1 | a0001c0001t0007g0363 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.187+515T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95486673 | |||||||
| chr7:95486756 | C | A | 11 | a0002c0002t0001g0045 a0002c0002t0004g0036 a0002c0002t0004g0037 others(8): Show |
12 | HG02451.hp2 HG02486.hp2 HG02809.hp1 others(9): Show |
intron_variant | MODIFIER | c.187+598C>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95486756 | |||||||
| chr7:95486832 | G | A | 2 | a0002c0002t0004g0036 a0002c0002t0004g0037 |
2 | HG02486.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.187+674G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95486832 | |||||||
| chr7:95486865 | A | G | 1 | a0001c0001t0001g0310 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.187+707A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95486865 | |||||||
| chr7:95487053 | C | A | 1 | a0001c0001t0001g0046 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.187+895C>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95487053 | |||||||
| chr7:95487192 | A | G | 1 | a0001c0001t0001g0309 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.187+1034A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95487192 | |||||||
| chr7:95487342 | A | G | 1 | a0002c0002t0001g0045 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.187+1184A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95487342 | |||||||
| chr7:95487403 | AAACT | A | 4 | a0001c0001t0001g0013 a0001c0001t0001g0306 a0001c0001t0001g0307 others(1): Show |
5 | HG01261.hp2 HG01934.hp1 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.187+1248_187+1251d others(6): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr7 | 95487403 | ||||||
| chr7:95487520 | T | G | 7 | a0001c0001t0002g0048 a0001c0001t0002g0050 a0001c0001t0002g0051 others(4): Show |
7 | HG01081.hp2 HG02109.hp1 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.187+1362T>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95487520 | |||||||
| chr7:95487565 | A | T | 10 | a0002c0002t0004g0036 a0002c0002t0004g0037 a0002c0002t0004g0044 others(7): Show |
11 | HG02451.hp2 HG02486.hp2 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.187+1407A>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95487565 | |||||||
| chr7:95487709 | T | C | 5 | a0001c0001t0003g0364 a0001c0001t0003g0366 a0001c0001t0004g0365 others(2): Show |
5 | HG02630.hp1 HG02818.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.187+1551T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95487709 | |||||||
| chr7:95487794 | G | A | 4 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0056 others(1): Show |
4 | HG02040.hp2 NA18954.hp2 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.187+1636G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95487794 | |||||||
| chr7:95487829 | A | C | 2 | a0001c0001t0003g0304 a0001c0001t0017g0305 |
2 | HG01192.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.187+1671A>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95487829 | |||||||
| chr7:95488157 | C | T | 5 | a0001c0001t0003g0364 a0001c0001t0003g0366 a0001c0001t0004g0365 others(2): Show |
5 | HG02630.hp1 HG02818.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.187+1999C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95488157 | |||||||
| chr7:95488191 | A | G | 1 | a0001c0001t0003g0303 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.187+2033A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95488191 | |||||||
| chr7:95488251 | G | T | 113 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(110): Show |
118 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.187+2093G>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95488251 | |||||||
| chr7:95488254 | T | C | 13 | a0001c0001t0002g0048 a0001c0001t0002g0050 a0001c0001t0002g0051 others(10): Show |
13 | HG00639.hp1 HG01081.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.187+2096T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95488254 | |||||||
| chr7:95488294 | T | C | 1 | a0001c0001t0020g0026 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.187+2136T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95488294 | |||||||
| chr7:95488346 | GA | G | 303 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(300): Show |
320 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.187+2199delA | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr7 | 95488346 | ||||||
| chr7:95488391 | A | G | 337 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(334): Show |
355 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(352): Show |
intron_variant | MODIFIER | c.187+2233A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95488391 | |||||||
| chr7:95488506 | T | G | 1 | a0001c0001t0001g0196 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.187+2348T>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95488506 | |||||||
| chr7:95488531 | T | C | 3 | a0001c0001t0002g0115 a0001c0001t0003g0116 a0001c0001t0014g0117 |
3 | HG03471.hp2 NA19240.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.187+2373T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95488531 | |||||||
| chr7:95488675 | G | C | 194 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(191): Show |
205 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.187+2517G>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95488675 | |||||||
| chr7:95488754 | T | C | 1 | a0001c0001t0001g0314 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.187+2596T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95488754 | |||||||
| chr7:95488774 | C | G | 5 | a0001c0001t0001g0298 a0001c0001t0001g0299 a0001c0001t0001g0300 others(2): Show |
5 | HG00738.hp1 HG01943.hp2 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.187+2616C>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95488774 | |||||||
| chr7:95488804 | C | G | 113 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(110): Show |
118 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.187+2646C>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95488804 | |||||||
| chr7:95488885 | A | C | 4 | a0001c0001t0001g0013 a0001c0001t0001g0306 a0001c0001t0001g0307 others(1): Show |
5 | HG01261.hp2 HG01934.hp1 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.187+2727A>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95488885 | |||||||
| chr7:95488904 | A | G | 1 | a0002c0002t0006g0361 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.187+2746A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95488904 | |||||||
| chr7:95489052 | G | C | 1 | a0001c0001t0007g0363 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.187+2894G>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95489052 | |||||||
| chr7:95489279 | G | A | 5 | a0001c0001t0003g0058 a0001c0001t0004g0031 a0001c0001t0005g0032 others(2): Show |
5 | HG00639.hp1 HG02055.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.187+3121G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95489279 | |||||||
| chr7:95489283 | T | C | 68 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(65): Show |
73 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.187+3125T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95489283 | |||||||
| chr7:95489375 | A | C | 1 | a0001c0001t0008g0297 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.187+3217A>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95489375 | |||||||
| chr7:95489407 | A | G | 10 | a0002c0002t0004g0036 a0002c0002t0004g0037 a0002c0002t0004g0044 others(7): Show |
11 | HG02451.hp2 HG02486.hp2 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.187+3249A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95489407 | |||||||
| chr7:95489433 | C | G | 1 | a0001c0001t0003g0296 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.187+3275C>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95489433 | |||||||
| chr7:95489516 | G | A | 85 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0013 others(82): Show |
91 | HG00423.hp1 HG00609.hp2 HG01081.hp2 others(88): Show |
intron_variant | MODIFIER | c.187+3358G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95489516 | |||||||
| chr7:95489698 | C | T | 51 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(48): Show |
56 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.187+3540C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95489698 | |||||||
| chr7:95489760 | C | T | 1 | a0001c0001t0001g0182 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.187+3602C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95489760 | |||||||
| chr7:95489831 | A | G | 2 | a0001c0001t0004g0312 a0001c0001t0004g0313 |
2 | HG02965.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.187+3673A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95489831 | |||||||
| chr7:95489898 | G | C | 302 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(299): Show |
319 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(316): Show |
intron_variant | MODIFIER | c.187+3740G>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95489898 | |||||||
| chr7:95489931 | G | C | 1 | a0002c0002t0011g0038 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.187+3773G>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95489931 | |||||||
| chr7:95489949 | T | C | 194 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(191): Show |
205 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.187+3791T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95489949 | |||||||
| chr7:95490066 | T | G | 1 | a0001c0001t0005g0369 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.187+3908T>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95490066 | |||||||
| chr7:95490283 | T | C | 1 | a0001c0001t0005g0369 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.187+4125T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95490283 | |||||||
| chr7:95490343 | C | T | 78 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0013 others(75): Show |
84 | HG00423.hp1 HG00609.hp2 HG01099.hp2 others(81): Show |
intron_variant | MODIFIER | c.187+4185C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95490343 | |||||||
| chr7:95490366 | A | C | 1 | a0001c0001t0002g0295 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.187+4208A>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95490366 | |||||||
| chr7:95490719 | C | T | 1 | a0001c0001t0005g0294 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.187+4561C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95490719 | |||||||
| chr7:95490815 | C | T | 8 | a0001c0001t0001g0185 a0001c0001t0001g0189 a0001c0001t0001g0190 others(5): Show |
8 | HG01192.hp1 HG01358.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.187+4657C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95490815 | |||||||
| chr7:95490818 | A | T | 1 | a0001c0001t0005g0369 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.187+4660A>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95490818 | |||||||
| chr7:95490835 | C | T | 104 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0013 others(101): Show |
111 | HG00423.hp1 HG00609.hp2 HG01099.hp2 others(108): Show |
intron_variant | MODIFIER | c.187+4677C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95490835 | |||||||
| chr7:95490939 | C | T | 20 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0023 others(17): Show |
21 | HG01255.hp2 HG02451.hp2 HG02486.hp2 others(18): Show |
intron_variant | MODIFIER | c.187+4781C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95490939 | |||||||
| chr7:95490950 | C | A | 7 | a0001c0001t0002g0048 a0001c0001t0002g0050 a0001c0001t0002g0051 others(4): Show |
7 | HG01081.hp2 HG02109.hp1 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.187+4792C>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95490950 | |||||||
| chr7:95490950 | C | T | 10 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0023 others(7): Show |
10 | HG01255.hp2 HG02647.hp2 HG02698.hp2 others(7): Show |
intron_variant | MODIFIER | c.187+4792C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95490950 | |||||||
| chr7:95491112 | T | A | 5 | a0001c0001t0003g0058 a0001c0001t0004g0031 a0001c0001t0005g0032 others(2): Show |
5 | HG00639.hp1 HG02055.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.188-4646T>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95491112 | |||||||
| chr7:95491242 | ATC | A | 4 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0056 others(1): Show |
4 | HG02040.hp2 NA18954.hp2 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.188-4512_188-4511d others(4): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr7 | 95491242 | ||||||
| chr7:95491324 | C | G | 88 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0013 others(85): Show |
95 | HG00423.hp1 HG00609.hp2 HG01099.hp2 others(92): Show |
intron_variant | MODIFIER | c.188-4434C>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95491324 | |||||||
| chr7:95491334 | G | T | 1 | a0004c0003t0015g0059 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.188-4424G>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95491334 | |||||||
| chr7:95491412 | C | T | 117 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(114): Show |
122 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.188-4346C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95491412 | |||||||
| chr7:95491707 | T | C | 300 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(297): Show |
317 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(314): Show |
intron_variant | MODIFIER | c.188-4051T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95491707 | |||||||
| chr7:95491900 | C | T | 59 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(56): Show |
64 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.188-3858C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95491900 | |||||||
| chr7:95491933 | C | A | 3 | a0001c0001t0004g0312 a0001c0001t0004g0313 a0001c0001t0014g0311 |
3 | HG01884.hp2 HG02965.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.188-3825C>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95491933 | |||||||
| chr7:95492248 | C | T | 3 | a0001c0001t0004g0312 a0001c0001t0004g0313 a0001c0001t0014g0311 |
3 | HG01884.hp2 HG02965.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.188-3510C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95492248 | |||||||
| chr7:95492260 | G | A | 2 | a0001c0001t0002g0118 a0001c0001t0002g0119 |
2 | NA18970.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.188-3498G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95492260 | |||||||
| chr7:95492299 | A | C | 5 | a0001c0001t0003g0364 a0001c0001t0003g0366 a0001c0001t0004g0365 others(2): Show |
5 | HG02630.hp1 HG02818.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.188-3459A>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95492299 | |||||||
| chr7:95492334 | A | G | 5 | a0001c0001t0003g0058 a0001c0001t0004g0031 a0001c0001t0005g0032 others(2): Show |
5 | HG00639.hp1 HG02055.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.188-3424A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95492334 | |||||||
| chr7:95492454 | T | C | 20 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0023 others(17): Show |
21 | HG01255.hp2 HG02451.hp2 HG02486.hp2 others(18): Show |
intron_variant | MODIFIER | c.188-3304T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95492454 | |||||||
| chr7:95492596 | T | C | 3 | a0001c0001t0012g0197 a0001c0001t0012g0198 a0001c0001t0012g0199 |
3 | HG01257.hp1 HG01258.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.188-3162T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95492596 | |||||||
| chr7:95492675 | C | T | 1 | a0001c0001t0002g0295 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.188-3083C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95492675 | |||||||
| chr7:95492690 | C | T | 1 | a0001c0001t0001g0293 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.188-3068C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95492690 | |||||||
| chr7:95493328 | C | G | 1 | a0001c0001t0001g0180 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.188-2430C>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95493328 | |||||||
| chr7:95493361 | A | AGT | 6 | a0001c0001t0003g0087 a0001c0001t0003g0088 a0001c0001t0003g0089 others(3): Show |
6 | HG00639.hp1 HG01928.hp2 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.188-2368_188-2367d others(4): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr7 | 95493361 | ||||||
| chr7:95493361 | A | AGTGTGT | 3 | a0001c0001t0005g0032 a0001c0001t0005g0033 a0001c0001t0005g0034 |
3 | HG02055.hp1 HG02257.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.188-2372_188-2367d others(8): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr7 | 95493361 | ||||||
| chr7:95493361 | AGT | A | 10 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0023 others(7): Show |
10 | HG01255.hp2 HG02647.hp2 HG02698.hp2 others(7): Show |
intron_variant | MODIFIER | c.188-2368_188-2367d others(4): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr7 | 95493361 | ||||||
| chr7:95493361 | AGTGT | A | 7 | a0001c0001t0001g0093 a0001c0001t0002g0179 a0001c0001t0004g0091 others(4): Show |
7 | HG00735.hp2 HG01346.hp2 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.188-2370_188-2367d others(6): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr7 | 95493361 | ||||||
| chr7:95493361 | AGTGTGT | A | 87 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0124 others(84): Show |
93 | HG00423.hp1 HG00609.hp2 HG01099.hp2 others(90): Show |
intron_variant | MODIFIER | c.188-2372_188-2367d others(8): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr7 | 95493361 | ||||||
| chr7:95493361 | AGTGTGTG others(1): Show |
A | 7 | a0001c0001t0001g0013 a0001c0001t0001g0120 a0001c0001t0001g0180 others(4): Show |
8 | HG01261.hp2 HG01934.hp1 HG01978.hp2 others(5): Show |
intron_variant | MODIFIER | c.188-2374_188-2367d others(10): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr7 | 95493361 | ||||||
| chr7:95493374 | GTGTGTGT others(11): Show |
G | 3 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 |
3 | HG02083.hp1 NA18977.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.188-2368_188-2351d others(20): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr7 | 95493374 | ||||||
| chr7:95493378 | GTGTGTGT others(7): Show |
G | 2 | a0001c0001t0001g0003 a0001c0001t0001g0253 |
2 | NA18959.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.188-2366_188-2353d others(16): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr7 | 95493378 | ||||||
| chr7:95493380 | GTGTGTGT others(5): Show |
G | 50 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(47): Show |
53 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.188-2366_188-2355d others(14): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr7 | 95493380 | ||||||
| chr7:95493382 | GTGTGTGT others(3): Show |
G | 21 | a0001c0001t0001g0001 a0001c0001t0001g0205 a0001c0001t0001g0232 others(18): Show |
24 | HG00408.hp1 HG00408.hp2 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.188-2366_188-2357d others(12): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr7 | 95493382 | ||||||
| chr7:95493384 | GTGTGTGT others(1): Show |
G | 87 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0209 others(84): Show |
90 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.188-2366_188-2359d others(10): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr7 | 95493384 | ||||||
| chr7:95493386 | GTGTGTA | G | 3 | a0001c0001t0015g0315 a0002c0002t0003g0317 a0002c0002t0006g0361 |
3 | HG00738.hp2 HG02572.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.188-2366_188-2361d others(8): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr7 | 95493386 | ||||||
| chr7:95493388 | G | A | 5 | a0001c0001t0003g0364 a0001c0001t0003g0366 a0001c0001t0004g0365 others(2): Show |
5 | HG02630.hp1 HG02818.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.188-2370G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95493388 | |||||||
| chr7:95493390 | GTA | G | 17 | a0001c0001t0001g0185 a0001c0001t0001g0189 a0001c0001t0001g0190 others(14): Show |
17 | HG01081.hp2 HG01192.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.188-2366_188-2365d others(4): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr7 | 95493390 | ||||||
| chr7:95493392 | A | G | 9 | a0001c0001t0003g0058 a0001c0001t0004g0031 a0001c0001t0005g0032 others(6): Show |
9 | HG00639.hp1 HG01358.hp1 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.188-2366A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95493392 | |||||||
| chr7:95493595 | A | G | 2 | a0001c0001t0001g0358 a0001c0001t0001g0359 |
2 | HG00609.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.188-2163A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95493595 | |||||||
| chr7:95493670 | C | T | 5 | a0001c0001t0003g0058 a0001c0001t0004g0031 a0001c0001t0005g0032 others(2): Show |
5 | HG00639.hp1 HG02055.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.188-2088C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95493670 | |||||||
| chr7:95493876 | A | G | 29 | a0001c0001t0001g0035 a0001c0001t0001g0054 a0001c0001t0001g0055 others(26): Show |
30 | HG00438.hp2 HG00621.hp1 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.188-1882A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95493876 | |||||||
| chr7:95493891 | C | T | 120 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(117): Show |
125 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.188-1867C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95493891 | |||||||
| chr7:95493892 | G | A | 2 | a0002c0002t0006g0039 a0002c0002t0006g0040 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.188-1866G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95493892 | |||||||
| chr7:95493928 | A | G | 5 | a0001c0001t0003g0058 a0001c0001t0004g0031 a0001c0001t0005g0032 others(2): Show |
5 | HG00639.hp1 HG02055.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.188-1830A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95493928 | |||||||
| chr7:95493981 | T | A | 2 | a0001c0001t0001g0203 a0001c0001t0002g0204 |
2 | HG02132.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.188-1777T>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95493981 | |||||||
| chr7:95494028 | T | A | 1 | a0001c0001t0015g0315 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.188-1730T>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95494028 | |||||||
| chr7:95494158 | A | G | 183 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(180): Show |
193 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.188-1600A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95494158 | |||||||
| chr7:95494161 | T | G | 3 | a0001c0001t0004g0312 a0001c0001t0004g0313 a0001c0001t0014g0311 |
3 | HG01884.hp2 HG02965.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.188-1597T>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95494161 | |||||||
| chr7:95494287 | A | G | 51 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(48): Show |
56 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.188-1471A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95494287 | |||||||
| chr7:95494598 | T | G | 1 | a0001c0001t0001g0316 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.188-1160T>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95494598 | |||||||
| chr7:95494677 | T | A | 8 | a0001c0001t0001g0185 a0001c0001t0001g0189 a0001c0001t0001g0190 others(5): Show |
8 | HG01192.hp1 HG01358.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.188-1081T>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95494677 | |||||||
| chr7:95494701 | G | C | 1 | a0001c0001t0003g0060 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.188-1057G>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95494701 | |||||||
| chr7:95494876 | A | C | 1 | a0001c0001t0010g0047 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.188-882A>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95494876 | |||||||
| chr7:95495069 | T | C | 124 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(121): Show |
129 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.188-689T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95495069 | |||||||
| chr7:95495098 | T | C | 1 | a0001c0001t0002g0016 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.188-660T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95495098 | |||||||
| chr7:95495174 | C | A | 1 | a0001c0001t0005g0369 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.188-584C>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95495174 | |||||||
| chr7:95495174 | C | T | 1 | a0001c0001t0001g0357 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.188-584C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95495174 | |||||||
| chr7:95495187 | C | A | 1 | a0001c0001t0001g0205 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.188-571C>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95495187 | |||||||
| chr7:95495207 | G | A | 98 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0013 others(95): Show |
105 | HG00423.hp1 HG00609.hp2 HG01099.hp2 others(102): Show |
intron_variant | MODIFIER | c.188-551G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95495207 | |||||||
| chr7:95495242 | T | A | 1 | a0002c0002t0003g0317 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.188-516T>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95495242 | |||||||
| chr7:95495380 | T | A | 1 | a0001c0001t0003g0061 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.188-378T>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95495380 | |||||||
| chr7:95495539 | C | T | 5 | a0001c0001t0003g0364 a0001c0001t0003g0366 a0001c0001t0004g0365 others(2): Show |
5 | HG02630.hp1 HG02818.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.188-219C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95495539 | |||||||
| chr7:95495591 | C | T | 69 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(66): Show |
74 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(71): Show |
intron_variant | MODIFIER | c.188-167C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95495591 | |||||||
| chr7:95495643 | C | T | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02698.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.188-115C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95495643 | |||||||
| chr7:95495658 | T | C | 2 | a0001c0001t0002g0122 a0001c0001t0002g0179 |
2 | NA19059.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.188-100T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95495658 | |||||||
| chr7:95495738 | C | CT | 31 | a0001c0001t0001g0035 a0001c0001t0001g0054 a0001c0001t0001g0055 others(28): Show |
32 | HG00438.hp2 HG00621.hp1 HG00735.hp2 others(29): Show |
splice_region_variant&intron_variant | LOW | c.188-4dupT | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr7 | 95495738 | ||||||
| chr7:95495738 | CT | C | 38 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0023 others(35): Show |
39 | HG01255.hp2 HG01884.hp2 HG02451.hp1 others(36): Show |
splice_region_variant&intron_variant | LOW | c.188-4delT | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr7 | 95495738 | ||||||
| chr7:95495738 | CTT | C | 254 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(251): Show |
270 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(267): Show |
splice_region_variant&intron_variant | LOW | c.188-5_188-4delTT | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr7 | 95495738 | ||||||
| chr7:95496150 | A | G | 5 | a0001c0001t0003g0058 a0001c0001t0004g0031 a0001c0001t0005g0032 others(2): Show |
5 | HG00639.hp1 HG02055.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.487+93A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95496150 | |||||||
| chr7:95496388 | G | A | 5 | a0001c0001t0003g0058 a0001c0001t0004g0031 a0001c0001t0005g0032 others(2): Show |
5 | HG00639.hp1 HG02055.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.487+331G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95496388 | |||||||
| chr7:95496420 | A | G | 1 | a0001c0001t0003g0177 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.487+363A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95496420 | |||||||
| chr7:95496477 | A | C | 78 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0013 others(75): Show |
84 | HG00423.hp1 HG00609.hp2 HG01099.hp2 others(81): Show |
intron_variant | MODIFIER | c.487+420A>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95496477 | |||||||
| chr7:95496515 | C | A | 5 | a0001c0001t0003g0058 a0001c0001t0004g0031 a0001c0001t0005g0032 others(2): Show |
5 | HG00639.hp1 HG02055.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.487+458C>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95496515 | |||||||
| chr7:95496619 | A | G | 5 | a0001c0001t0003g0058 a0001c0001t0004g0031 a0001c0001t0005g0032 others(2): Show |
5 | HG00639.hp1 HG02055.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.487+562A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95496619 | |||||||
| chr7:95496631 | G | A | 1 | a0001c0001t0007g0363 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.487+574G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95496631 | |||||||
| chr7:95496644 | C | T | 3 | a0002c0002t0004g0044 a0002c0002t0006g0042 a0002c0002t0006g0043 |
3 | HG02451.hp2 HG02976.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.487+587C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95496644 | |||||||
| chr7:95496697 | A | C | 5 | a0001c0001t0003g0058 a0001c0001t0004g0031 a0001c0001t0005g0032 others(2): Show |
5 | HG00639.hp1 HG02055.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.487+640A>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95496697 | |||||||
| chr7:95496705 | G | A | 2 | a0001c0001t0008g0206 a0001c0001t0008g0297 |
2 | HG03195.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.487+648G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95496705 | |||||||
| chr7:95496864 | A | G | 51 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(48): Show |
56 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.487+807A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95496864 | |||||||
| chr7:95497031 | G | A | 1 | a0001c0001t0005g0369 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.487+974G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95497031 | |||||||
| chr7:95497072 | G | A | 1 | a0001c0001t0002g0207 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.487+1015G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95497072 | |||||||
| chr7:95497094 | G | A | 1 | a0001c0001t0005g0369 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.487+1037G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95497094 | |||||||
| chr7:95497111 | GC | G | 5 | a0001c0001t0003g0058 a0001c0001t0004g0031 a0001c0001t0005g0032 others(2): Show |
5 | HG00639.hp1 HG02055.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.487+1056delC | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95497111 | ||||||
| chr7:95497209 | T | C | 2 | a0001c0001t0003g0006 a0001c0001t0003g0096 |
3 | HG01256.hp1 HG01258.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.487+1152T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95497209 | |||||||
| chr7:95497401 | T | G | 1 | a0001c0001t0004g0313 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.487+1344T>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95497401 | |||||||
| chr7:95497492 | G | T | 1 | a0001c0001t0005g0369 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.487+1435G>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95497492 | |||||||
| chr7:95497523 | T | C | 1 | a0001c0001t0003g0058 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.487+1466T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95497523 | |||||||
| chr7:95497523 | T | G | 120 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(117): Show |
125 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.487+1466T>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95497523 | |||||||
| chr7:95497625 | T | G | 7 | a0001c0001t0004g0030 a0001c0001t0004g0090 a0001c0001t0008g0027 others(4): Show |
7 | HG02451.hp1 HG02717.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.487+1568T>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95497625 | |||||||
| chr7:95497633 | T | C | 1 | a0001c0001t0009g0183 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.487+1576T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95497633 | |||||||
| chr7:95497658 | A | C | 1 | a0001c0001t0001g0290 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.487+1601A>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95497658 | |||||||
| chr7:95497766 | A | T | 111 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0013 others(108): Show |
118 | HG00423.hp1 HG00609.hp2 HG01099.hp2 others(115): Show |
intron_variant | MODIFIER | c.487+1709A>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95497766 | |||||||
| chr7:95497899 | T | C | 1 | a0001c0001t0002g0115 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.487+1842T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95497899 | |||||||
| chr7:95497922 | C | T | 111 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0013 others(108): Show |
118 | HG00423.hp1 HG00609.hp2 HG01099.hp2 others(115): Show |
intron_variant | MODIFIER | c.487+1865C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95497922 | |||||||
| chr7:95498043 | G | T | 1 | a0001c0001t0001g0355 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.487+1986G>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95498043 | |||||||
| chr7:95498199 | G | A | 1 | a0001c0001t0002g0295 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.487+2142G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95498199 | |||||||
| chr7:95498222 | G | C | 123 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(120): Show |
128 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.487+2165G>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95498222 | |||||||
| chr7:95498342 | C | T | 5 | a0001c0001t0003g0364 a0001c0001t0003g0366 a0001c0001t0004g0365 others(2): Show |
5 | HG02630.hp1 HG02818.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.487+2285C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95498342 | |||||||
| chr7:95498385 | C | G | 2 | a0002c0002t0004g0036 a0002c0002t0004g0037 |
2 | HG02486.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.487+2328C>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95498385 | |||||||
| chr7:95498487 | T | C | 1 | a0001c0001t0003g0063 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.487+2430T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95498487 | |||||||
| chr7:95498606 | A | T | 98 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0013 others(95): Show |
105 | HG00423.hp1 HG00609.hp2 HG01099.hp2 others(102): Show |
intron_variant | MODIFIER | c.487+2549A>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95498606 | |||||||
| chr7:95498607 | T | C | 1 | a0001c0001t0010g0047 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.487+2550T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95498607 | |||||||
| chr7:95498692 | G | A | 5 | a0001c0001t0003g0364 a0001c0001t0003g0366 a0001c0001t0004g0365 others(2): Show |
5 | HG02630.hp1 HG02818.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.487+2635G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95498692 | |||||||
| chr7:95498748 | A | G | 59 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(56): Show |
64 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.487+2691A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95498748 | |||||||
| chr7:95498750 | G | A | 1 | a0001c0001t0003g0058 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.487+2693G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95498750 | |||||||
| chr7:95498864 | G | T | 1 | a0001c0001t0001g0289 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.487+2807G>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95498864 | |||||||
| chr7:95498987 | A | G | 2 | a0001c0001t0001g0287 a0001c0001t0001g0288 |
2 | HG02027.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.487+2930A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95498987 | |||||||
| chr7:95499296 | A | G | 8 | a0001c0001t0001g0185 a0001c0001t0001g0189 a0001c0001t0001g0190 others(5): Show |
8 | HG01192.hp1 HG01358.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.487+3239A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95499296 | |||||||
| chr7:95499315 | A | G | 5 | a0001c0001t0003g0364 a0001c0001t0003g0366 a0001c0001t0004g0365 others(2): Show |
5 | HG02630.hp1 HG02818.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.487+3258A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95499315 | |||||||
| chr7:95499337 | T | C | 1 | a0002c0002t0001g0045 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.487+3280T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95499337 | |||||||
| chr7:95499364 | G | T | 123 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(120): Show |
128 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.487+3307G>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95499364 | |||||||
| chr7:95499384 | A | C | 5 | a0001c0001t0003g0058 a0001c0001t0004g0031 a0001c0001t0005g0032 others(2): Show |
5 | HG00639.hp1 HG02055.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.487+3327A>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95499384 | |||||||
| chr7:95499441 | G | A | 294 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(291): Show |
311 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(308): Show |
intron_variant | MODIFIER | c.487+3384G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95499441 | |||||||
| chr7:95499710 | A | G | 10 | a0002c0002t0004g0036 a0002c0002t0004g0037 a0002c0002t0004g0044 others(7): Show |
11 | HG02451.hp2 HG02486.hp2 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.487+3653A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95499710 | |||||||
| chr7:95499766 | T | A | 7 | a0001c0001t0001g0005 a0001c0001t0001g0064 a0001c0001t0001g0065 others(4): Show |
8 | HG00735.hp1 HG01358.hp2 HG02735.hp2 others(5): Show |
intron_variant | MODIFIER | c.487+3709T>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95499766 | |||||||
| chr7:95499794 | C | T | 1 | a0001c0001t0007g0363 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.487+3737C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95499794 | |||||||
| chr7:95499860 | A | G | 1 | a0001c0001t0002g0053 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.487+3803A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95499860 | |||||||
| chr7:95499865 | C | CT | 7 | a0001c0001t0001g0024 a0001c0001t0001g0350 a0001c0001t0001g0353 others(4): Show |
8 | HG01175.hp1 HG02630.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.487+3834dupT | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95499865 | ||||||
| chr7:95499865 | CT | C | 188 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(185): Show |
198 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.487+3834delT | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95499865 | ||||||
| chr7:95499865 | CTT | C | 70 | a0001c0001t0001g0005 a0001c0001t0001g0054 a0001c0001t0001g0055 others(67): Show |
73 | HG00323.hp1 HG00438.hp2 HG00621.hp1 others(70): Show |
intron_variant | MODIFIER | c.487+3833_487+3834d others(4): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95499865 | ||||||
| chr7:95499865 | CTTT | C | 17 | a0001c0001t0001g0035 a0001c0001t0001g0185 a0001c0001t0003g0098 others(14): Show |
17 | HG01070.hp1 HG01192.hp1 HG01358.hp1 others(14): Show |
intron_variant | MODIFIER | c.487+3832_487+3834d others(5): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95499865 | ||||||
| chr7:95499912 | C | T | 1 | a0002c0002t0003g0317 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.487+3855C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95499912 | |||||||
| chr7:95499913 | G | T | 8 | a0001c0001t0001g0185 a0001c0001t0001g0189 a0001c0001t0001g0190 others(5): Show |
8 | HG01192.hp1 HG01358.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.487+3856G>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95499913 | |||||||
| chr7:95499942 | C | T | 1 | a0001c0001t0001g0270 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.487+3885C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95499942 | |||||||
| chr7:95499974 | C | T | 2 | a0001c0001t0003g0121 a0002c0002t0006g0361 |
2 | HG00738.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.487+3917C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95499974 | |||||||
| chr7:95500011 | G | A | 120 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(117): Show |
125 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.487+3954G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95500011 | |||||||
| chr7:95500016 | C | T | 5 | a0001c0001t0003g0364 a0001c0001t0003g0366 a0001c0001t0004g0365 others(2): Show |
5 | HG02630.hp1 HG02818.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.487+3959C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95500016 | |||||||
| chr7:95500036 | C | G | 1 | a0001c0001t0001g0286 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.487+3979C>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95500036 | |||||||
| chr7:95500039 | A | G | 1 | a0001c0001t0007g0363 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.487+3982A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95500039 | |||||||
| chr7:95500103 | G | A | 5 | a0001c0001t0003g0364 a0001c0001t0003g0366 a0001c0001t0004g0365 others(2): Show |
5 | HG02630.hp1 HG02818.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.487+4046G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95500103 | |||||||
| chr7:95500209 | G | C | 1 | a0001c0001t0004g0312 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.487+4152G>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95500209 | |||||||
| chr7:95500270 | A | C | 2 | a0001c0001t0001g0165 a0001c0001t0001g0166 |
2 | NA19002.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.487+4213A>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95500270 | |||||||
| chr7:95500294 | C | T | 1 | a0004c0003t0015g0059 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.487+4237C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95500294 | |||||||
| chr7:95500295 | G | A | 10 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0193 others(7): Show |
10 | HG00639.hp1 HG02055.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.487+4238G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95500295 | |||||||
| chr7:95500471 | C | G | 5 | a0001c0001t0003g0058 a0001c0001t0004g0031 a0001c0001t0005g0032 others(2): Show |
5 | HG00639.hp1 HG02055.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.487+4414C>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95500471 | |||||||
| chr7:95500492 | C | T | 8 | a0001c0001t0001g0185 a0001c0001t0001g0189 a0001c0001t0001g0190 others(5): Show |
8 | HG01192.hp1 HG01358.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.487+4435C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95500492 | |||||||
| chr7:95500522 | A | G | 93 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(90): Show |
97 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.487+4465A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95500522 | |||||||
| chr7:95500568 | C | CA | 48 | a0001c0001t0001g0010 a0001c0001t0001g0064 a0001c0001t0001g0065 others(45): Show |
50 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.487+4539dupA | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95500568 | ||||||
| chr7:95500568 | C | CAA | 10 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0024 others(7): Show |
10 | HG01255.hp2 HG02647.hp2 HG02698.hp2 others(7): Show |
intron_variant | MODIFIER | c.487+4538_487+4539d others(4): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95500568 | ||||||
| chr7:95500568 | CA | C | 79 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0093 others(76): Show |
84 | HG00323.hp1 HG00423.hp1 HG00639.hp2 others(81): Show |
intron_variant | MODIFIER | c.487+4539delA | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95500568 | ||||||
| chr7:95500568 | CAA | C | 19 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0176 others(16): Show |
19 | HG00609.hp2 HG00639.hp1 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.487+4538_487+4539d others(4): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95500568 | ||||||
| chr7:95500568 | CAAA | C | 18 | a0001c0001t0001g0325 a0001c0001t0001g0326 a0001c0001t0001g0327 others(15): Show |
18 | HG00323.hp2 HG00609.hp1 HG00673.hp1 others(15): Show |
intron_variant | MODIFIER | c.487+4537_487+4539d others(5): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95500568 | ||||||
| chr7:95500568 | CAAAA | C | 35 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(32): Show |
40 | HG00280.hp2 HG00597.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.487+4536_487+4539d others(6): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95500568 | ||||||
| chr7:95500568 | CAAAAAA | C | 7 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0002g0119 others(4): Show |
7 | HG01192.hp1 HG01433.hp1 HG01975.hp2 others(4): Show |
intron_variant | MODIFIER | c.487+4534_487+4539d others(8): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95500568 | ||||||
| chr7:95500832 | A | G | 5 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0193 others(2): Show |
5 | HG02615.hp2 HG03041.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.487+4775A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95500832 | |||||||
| chr7:95501125 | C | G | 1 | a0001c0001t0002g0082 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.487+5068C>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95501125 | |||||||
| chr7:95501301 | G | T | 1 | a0001c0001t0003g0084 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.487+5244G>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95501301 | |||||||
| chr7:95501329 | C | T | 1 | a0001c0001t0003g0072 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.487+5272C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95501329 | |||||||
| chr7:95501332 | C | T | 5 | a0001c0001t0003g0058 a0001c0001t0004g0031 a0001c0001t0005g0032 others(2): Show |
5 | HG00639.hp1 HG02055.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.487+5275C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95501332 | |||||||
| chr7:95501460 | G | A | 98 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0013 others(95): Show |
105 | HG00423.hp1 HG00609.hp2 HG01099.hp2 others(102): Show |
intron_variant | MODIFIER | c.487+5403G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95501460 | |||||||
| chr7:95501512 | G | T | 5 | a0001c0001t0003g0364 a0001c0001t0003g0366 a0001c0001t0004g0365 others(2): Show |
5 | HG02630.hp1 HG02818.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.487+5455G>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95501512 | |||||||
| chr7:95501564 | T | C | 1 | a0001c0001t0001g0161 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.487+5507T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95501564 | |||||||
| chr7:95501646 | A | T | 1 | a0001c0001t0005g0369 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.487+5589A>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95501646 | |||||||
| chr7:95501700 | T | G | 1 | a0001c0001t0002g0123 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.487+5643T>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95501700 | |||||||
| chr7:95501724 | T | G | 1 | a0001c0001t0025g0228 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.487+5667T>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95501724 | |||||||
| chr7:95501866 | T | A | 6 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0325 others(3): Show |
8 | HG00597.hp2 HG02027.hp1 HG02071.hp2 others(5): Show |
intron_variant | MODIFIER | c.487+5809T>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95501866 | |||||||
| chr7:95501905 | C | T | 183 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(180): Show |
193 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.487+5848C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95501905 | |||||||
| chr7:95501932 | G | A | 8 | a0001c0001t0001g0185 a0001c0001t0001g0189 a0001c0001t0001g0190 others(5): Show |
8 | HG01192.hp1 HG01358.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.487+5875G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95501932 | |||||||
| chr7:95501998 | C | G | 124 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(121): Show |
129 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.487+5941C>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95501998 | |||||||
| chr7:95502014 | C | G | 5 | a0001c0001t0003g0364 a0001c0001t0003g0366 a0001c0001t0004g0365 others(2): Show |
5 | HG02630.hp1 HG02818.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.487+5957C>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95502014 | |||||||
| chr7:95502068 | C | A | 1 | a0001c0001t0003g0073 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.487+6011C>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95502068 | |||||||
| chr7:95502069 | G | A | 1 | a0001c0001t0007g0363 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.487+6012G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95502069 | |||||||
| chr7:95502106 | TA | T | 69 | a0001c0001t0001g0005 a0001c0001t0001g0035 a0001c0001t0001g0054 others(66): Show |
71 | HG00323.hp1 HG00438.hp2 HG00621.hp1 others(68): Show |
intron_variant | MODIFIER | c.487+6059delA | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95502106 | ||||||
| chr7:95502275 | C | A | 297 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(294): Show |
314 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(311): Show |
intron_variant | MODIFIER | c.487+6218C>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95502275 | |||||||
| chr7:95502276 | T | C | 1 | a0001c0001t0003g0084 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.487+6219T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95502276 | |||||||
| chr7:95502339 | T | C | 2 | a0001c0001t0002g0118 a0001c0001t0002g0119 |
2 | NA18970.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.487+6282T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95502339 | |||||||
| chr7:95502386 | G | GC | 3 | a0001c0001t0001g0124 a0001c0001t0001g0140 a0001c0001t0001g0307 |
3 | HG01261.hp2 HG02056.hp1 NA19059.hp2 |
intron_variant | MODIFIER | c.487+6331dupC | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95502386 | ||||||
| chr7:95502389 | T | C | 75 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0013 others(72): Show |
81 | HG00423.hp1 HG00609.hp2 HG01099.hp2 others(78): Show |
intron_variant | MODIFIER | c.487+6332T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95502389 | |||||||
| chr7:95502389 | T | TG | 6 | a0001c0001t0001g0024 a0001c0001t0004g0021 a0001c0001t0009g0183 others(3): Show |
6 | HG01192.hp1 HG01433.hp1 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.487+6333dupG | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95502389 | ||||||
| chr7:95502389 | TGC | T | 127 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(124): Show |
132 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.487+6334_487+6335d others(4): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95502389 | ||||||
| chr7:95502390 | G | T | 75 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0013 others(72): Show |
81 | HG00423.hp1 HG00609.hp2 HG01099.hp2 others(78): Show |
intron_variant | MODIFIER | c.487+6333G>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95502390 | |||||||
| chr7:95502390 | GC | G | 85 | a0001c0001t0001g0005 a0001c0001t0001g0035 a0001c0001t0001g0054 others(82): Show |
88 | HG00323.hp1 HG00438.hp2 HG00621.hp1 others(85): Show |
intron_variant | MODIFIER | c.487+6334delC | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95502390 | |||||||
| chr7:95502391 | C | G | 99 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0013 others(96): Show |
105 | HG00423.hp1 HG00609.hp2 HG01099.hp2 others(102): Show |
intron_variant | MODIFIER | c.487+6334C>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95502391 | |||||||
| chr7:95502391 | CG | C | 47 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(44): Show |
52 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.487+6344delG | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95502391 | ||||||
| chr7:95502399 | G | C | 1 | a0001c0001t0003g0058 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.487+6342G>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95502399 | |||||||
| chr7:95502400 | G | C | 1 | a0001c0001t0014g0117 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.487+6343G>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95502400 | |||||||
| chr7:95502493 | A | G | 6 | a0001c0001t0002g0295 a0001c0001t0003g0058 a0001c0001t0004g0031 others(3): Show |
6 | HG00639.hp1 HG00741.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.487+6436A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95502493 | |||||||
| chr7:95502655 | A | G | 97 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0013 others(94): Show |
104 | HG00423.hp1 HG00609.hp2 HG01099.hp2 others(101): Show |
intron_variant | MODIFIER | c.487+6598A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95502655 | |||||||
| chr7:95503044 | G | A | 1 | a0001c0001t0007g0363 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.487+6987G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95503044 | |||||||
| chr7:95503064 | A | G | 2 | a0001c0001t0001g0165 a0001c0001t0001g0166 |
2 | NA19002.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.487+7007A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95503064 | |||||||
| chr7:95503085 | A | G | 44 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(41): Show |
49 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.487+7028A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95503085 | |||||||
| chr7:95503091 | A | G | 1 | a0002c0002t0001g0045 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.487+7034A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95503091 | |||||||
| chr7:95503212 | G | A | 1 | a0002c0002t0006g0361 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.487+7155G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95503212 | |||||||
| chr7:95503717 | A | G | 1 | a0001c0001t0002g0160 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.487+7660A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95503717 | |||||||
| chr7:95503741 | C | T | 7 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0024 others(4): Show |
7 | HG02647.hp2 HG02698.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.487+7684C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95503741 | |||||||
| chr7:95503938 | T | C | 53 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(50): Show |
58 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.487+7881T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95503938 | |||||||
| chr7:95504131 | T | C | 26 | a0001c0001t0001g0185 a0001c0001t0001g0189 a0001c0001t0001g0190 others(23): Show |
26 | HG00639.hp2 HG00738.hp1 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.487+8074T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95504131 | |||||||
| chr7:95504135 | A | G | 1 | a0001c0001t0001g0332 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.487+8078A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95504135 | |||||||
| chr7:95504350 | A | C | 30 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0024 others(27): Show |
31 | HG00741.hp2 HG01192.hp1 HG01358.hp1 others(28): Show |
intron_variant | MODIFIER | c.487+8293A>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95504350 | |||||||
| chr7:95504354 | CAT | C | 30 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0024 others(27): Show |
31 | HG00741.hp2 HG01192.hp1 HG01358.hp1 others(28): Show |
intron_variant | MODIFIER | c.487+8298_487+8299d others(4): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95504354 | |||||||
| chr7:95504437 | T | G | 6 | a0001c0001t0001g0185 a0001c0001t0009g0183 a0001c0001t0009g0184 others(3): Show |
6 | HG01192.hp1 HG01358.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.487+8380T>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95504437 | |||||||
| chr7:95504478 | C | G | 2 | a0001c0001t0002g0122 a0001c0001t0002g0179 |
2 | NA19059.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.487+8421C>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95504478 | |||||||
| chr7:95504704 | C | T | 171 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(168): Show |
181 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(178): Show |
intron_variant | MODIFIER | c.487+8647C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95504704 | |||||||
| chr7:95504931 | C | T | 1 | a0001c0001t0003g0062 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.487+8874C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95504931 | |||||||
| chr7:95504947 | C | T | 1 | a0001c0001t0002g0204 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.487+8890C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95504947 | |||||||
| chr7:95505073 | G | A | 22 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0056 others(19): Show |
22 | HG00438.hp2 HG00621.hp1 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.487+9016G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95505073 | |||||||
| chr7:95505295 | TTGCATTT others(11): Show |
T | 2 | a0002c0002t0004g0036 a0002c0002t0004g0037 |
2 | HG02486.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.487+9239_487+9256d others(20): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95505295 | |||||||
| chr7:95505406 | G | A | 4 | a0001c0001t0001g0093 a0001c0001t0004g0091 a0001c0001t0004g0092 others(1): Show |
4 | HG00735.hp2 HG01346.hp2 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.487+9349G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95505406 | |||||||
| chr7:95505683 | G | A | 22 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0056 others(19): Show |
22 | HG00438.hp2 HG00621.hp1 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.487+9626G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95505683 | |||||||
| chr7:95505686 | T | TC | 15 | a0001c0001t0001g0348 a0001c0001t0002g0137 a0001c0001t0002g0138 others(12): Show |
15 | HG01175.hp1 HG02055.hp2 HG02293.hp2 others(12): Show |
intron_variant | MODIFIER | c.487+9641dupC | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95505686 | ||||||
| chr7:95505686 | TC | T | 185 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(182): Show |
194 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.487+9641delC | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95505686 | ||||||
| chr7:95505692 | C | G | 6 | a0001c0001t0003g0304 a0001c0001t0004g0030 a0001c0001t0004g0090 others(3): Show |
6 | HG01192.hp2 HG02451.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.487+9635C>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95505692 | |||||||
| chr7:95505694 | C | A | 1 | a0001c0001t0002g0150 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.487+9637C>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95505694 | |||||||
| chr7:95505696 | C | A | 3 | a0001c0001t0004g0318 a0001c0001t0004g0323 a0001c0001t0010g0047 |
3 | HG01243.hp2 HG02572.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.487+9639C>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95505696 | |||||||
| chr7:95505696 | C | CG | 5 | a0001c0001t0004g0031 a0001c0001t0005g0032 a0001c0001t0005g0033 others(2): Show |
5 | HG00639.hp1 HG02055.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.487+9639_487+9640i others(3): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95505696 | |||||||
| chr7:95505696 | C | G | 1 | a0001c0001t0005g0369 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.487+9639C>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95505696 | |||||||
| chr7:95505697 | C | A | 26 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0056 others(23): Show |
26 | HG00438.hp2 HG00621.hp1 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.487+9640C>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95505697 | |||||||
| chr7:95505697 | C | T | 3 | a0001c0001t0005g0012 a0001c0001t0005g0271 a0001c0001t0005g0276 |
4 | HG01891.hp1 HG02109.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.487+9640C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95505697 | |||||||
| chr7:95505848 | C | A | 2 | a0001c0001t0001g0125 a0001c0001t0001g0141 |
2 | NA18955.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.487+9791C>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95505848 | |||||||
| chr7:95505961 | A | G | 3 | a0001c0001t0004g0132 a0001c0001t0004g0149 a0001c0001t0004g0163 |
3 | NA18945.hp1 NA19001.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.487+9904A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95505961 | |||||||
| chr7:95505967 | C | T | 2 | a0001c0001t0002g0002 a0001c0001t0002g0159 |
4 | HG02738.hp1 HG03239.hp1 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.487+9910C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95505967 | |||||||
| chr7:95506049 | T | TGCCTGGC others(319): Show |
1 | a0001c0001t0001g0236 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.487+10007_487+1000 others(330): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95506049 | ||||||
| chr7:95506051 | C | A | 1 | a0001c0001t0003g0058 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.487+9994C>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95506051 | |||||||
| chr7:95506152 | G | A | 1 | a0001c0001t0001g0310 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.487+10095G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95506152 | |||||||
| chr7:95506243 | A | G | 6 | a0001c0001t0001g0185 a0001c0001t0009g0183 a0001c0001t0009g0184 others(3): Show |
6 | HG01192.hp1 HG01358.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.487+10186A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95506243 | |||||||
| chr7:95506302 | T | C | 166 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(163): Show |
176 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(173): Show |
intron_variant | MODIFIER | c.487+10245T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95506302 | |||||||
| chr7:95506305 | G | A | 1 | a0001c0001t0001g0237 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.487+10248G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95506305 | |||||||
| chr7:95506521 | C | T | 1 | a0001c0001t0010g0047 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.487+10464C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95506521 | |||||||
| chr7:95506657 | T | A | 166 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(163): Show |
176 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(173): Show |
intron_variant | MODIFIER | c.487+10600T>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95506657 | |||||||
| chr7:95506686 | C | CT | 20 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0148 others(17): Show |
20 | HG00323.hp1 HG01099.hp1 HG01167.hp2 others(17): Show |
intron_variant | MODIFIER | c.487+10647dupT | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95506686 | ||||||
| chr7:95506686 | CT | C | 152 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(149): Show |
162 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.487+10647delT | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95506686 | ||||||
| chr7:95506742 | T | G | 2 | a0001c0001t0004g0104 a0001c0001t0004g0111 |
2 | HG03225.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.487+10685T>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95506742 | |||||||
| chr7:95506825 | T | G | 14 | a0001c0001t0003g0364 a0001c0001t0003g0366 a0001c0001t0004g0031 others(11): Show |
14 | HG00639.hp1 HG02055.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.487+10768T>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95506825 | |||||||
| chr7:95507018 | C | G | 6 | a0001c0001t0001g0185 a0001c0001t0009g0183 a0001c0001t0009g0184 others(3): Show |
6 | HG01192.hp1 HG01358.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.487+10961C>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95507018 | |||||||
| chr7:95507105 | T | C | 1 | a0001c0001t0003g0058 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.487+11048T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95507105 | |||||||
| chr7:95507150 | G | T | 1 | a0001c0001t0001g0185 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.487+11093G>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95507150 | |||||||
| chr7:95507154 | T | G | 83 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(80): Show |
89 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.487+11097T>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95507154 | |||||||
| chr7:95507249 | C | T | 17 | a0001c0001t0002g0204 a0001c0001t0003g0364 a0001c0001t0003g0366 others(14): Show |
17 | HG00639.hp1 HG02055.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.487+11192C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95507249 | |||||||
| chr7:95507250 | G | A | 1 | a0001c0001t0010g0017 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.487+11193G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95507250 | |||||||
| chr7:95507279 | G | A | 1 | a0001c0001t0005g0194 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.487+11222G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95507279 | |||||||
| chr7:95507407 | G | C | 1 | a0001c0001t0003g0084 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.487+11350G>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95507407 | |||||||
| chr7:95507424 | A | C | 1 | a0001c0001t0001g0362 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.487+11367A>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95507424 | |||||||
| chr7:95507664 | T | G | 1 | a0001c0001t0010g0047 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.487+11607T>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95507664 | |||||||
| chr7:95507669 | G | C | 14 | a0001c0001t0001g0001 a0001c0001t0001g0229 a0001c0001t0001g0321 others(11): Show |
17 | HG02165.hp2 NA18944.hp1 NA18947.hp1 others(14): Show |
intron_variant | MODIFIER | c.487+11612G>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95507669 | |||||||
| chr7:95507838 | C | T | 1 | a0001c0001t0003g0058 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.487+11781C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95507838 | |||||||
| chr7:95507913 | C | CAATGAGT others(4): Show |
1 | a0001c0001t0002g0137 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.487+11857_487+1186 others(15): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95507913 | ||||||
| chr7:95507955 | T | C | 5 | a0001c0001t0004g0031 a0001c0001t0005g0032 a0001c0001t0005g0033 others(2): Show |
5 | HG00639.hp1 HG02055.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.487+11898T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95507955 | |||||||
| chr7:95508250 | T | C | 3 | a0001c0001t0002g0115 a0001c0001t0003g0116 a0001c0001t0014g0117 |
3 | HG03471.hp2 NA19240.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.487+12193T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95508250 | |||||||
| chr7:95508452 | C | A | 1 | a0001c0001t0014g0311 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.487+12395C>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95508452 | |||||||
| chr7:95508638 | G | C | 1 | a0001c0001t0015g0315 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.487+12581G>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95508638 | |||||||
| chr7:95508729 | A | T | 6 | a0001c0001t0001g0185 a0001c0001t0009g0183 a0001c0001t0009g0184 others(3): Show |
6 | HG01192.hp1 HG01358.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.487+12672A>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95508729 | |||||||
| chr7:95508980 | A | T | 6 | a0001c0001t0003g0304 a0001c0001t0004g0030 a0001c0001t0004g0090 others(3): Show |
6 | HG01192.hp2 HG02451.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.487+12923A>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95508980 | |||||||
| chr7:95509365 | G | C | 3 | a0001c0001t0008g0027 a0001c0001t0008g0206 a0001c0001t0008g0297 |
3 | HG03195.hp1 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.487+13308G>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95509365 | |||||||
| chr7:95509443 | A | G | 336 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(333): Show |
354 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(351): Show |
intron_variant | MODIFIER | c.487+13386A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95509443 | |||||||
| chr7:95509690 | C | T | 8 | a0001c0001t0003g0364 a0001c0001t0003g0366 a0001c0001t0004g0365 others(5): Show |
8 | HG02630.hp1 HG02818.hp1 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.487+13633C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95509690 | |||||||
| chr7:95509884 | T | C | 8 | a0001c0001t0003g0364 a0001c0001t0003g0366 a0001c0001t0004g0365 others(5): Show |
8 | HG02630.hp1 HG02818.hp1 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.487+13827T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95509884 | |||||||
| chr7:95509903 | A | G | 1 | a0001c0001t0003g0078 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.487+13846A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95509903 | |||||||
| chr7:95509933 | C | G | 1 | a0001c0001t0001g0181 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.487+13876C>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95509933 | |||||||
| chr7:95510066 | A | G | 1 | a0001c0001t0004g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.487+14009A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95510066 | |||||||
| chr7:95510126 | T | TA | 39 | a0001c0001t0001g0310 a0001c0001t0002g0002 a0001c0001t0002g0009 others(36): Show |
42 | HG00423.hp1 HG00738.hp2 HG01496.hp1 others(39): Show |
intron_variant | MODIFIER | c.487+14079dupA | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95510126 | ||||||
| chr7:95510579 | A | G | 61 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(58): Show |
67 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(64): Show |
intron_variant | MODIFIER | c.487+14522A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95510579 | |||||||
| chr7:95510719 | C | T | 31 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0024 others(28): Show |
31 | HG00438.hp2 HG00621.hp1 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.487+14662C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95510719 | |||||||
| chr7:95510810 | C | T | 2 | a0001c0001t0015g0315 a0004c0003t0015g0059 |
2 | HG02717.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.487+14753C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95510810 | |||||||
| chr7:95510857 | A | T | 6 | a0001c0001t0001g0185 a0001c0001t0009g0183 a0001c0001t0009g0184 others(3): Show |
6 | HG01192.hp1 HG01358.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.487+14800A>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95510857 | |||||||
| chr7:95510858 | G | A | 167 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(164): Show |
177 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(174): Show |
intron_variant | MODIFIER | c.487+14801G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95510858 | |||||||
| chr7:95511264 | A | T | 39 | a0001c0001t0001g0310 a0001c0001t0002g0002 a0001c0001t0002g0009 others(36): Show |
42 | HG00423.hp1 HG00738.hp2 HG01496.hp1 others(39): Show |
intron_variant | MODIFIER | c.487+15207A>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95511264 | |||||||
| chr7:95511450 | C | T | 1 | a0001c0001t0003g0058 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.487+15393C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95511450 | |||||||
| chr7:95511558 | A | T | 1 | a0001c0001t0001g0263 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.487+15501A>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95511558 | |||||||
| chr7:95511603 | G | A | 6 | a0001c0001t0002g0295 a0001c0001t0005g0272 a0001c0001t0005g0320 others(3): Show |
6 | HG00741.hp2 HG02559.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.487+15546G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95511603 | |||||||
| chr7:95511662 | C | CA | 24 | a0001c0001t0001g0057 a0001c0001t0001g0172 a0001c0001t0001g0185 others(21): Show |
25 | HG00639.hp1 HG01192.hp1 HG01358.hp1 others(22): Show |
intron_variant | MODIFIER | c.487+15617dupA | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95511662 | ||||||
| chr7:95511670 | A | T | 1 | a0001c0001t0001g0056 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.487+15613A>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95511670 | |||||||
| chr7:95511671 | A | T | 8 | a0001c0001t0001g0339 a0001c0001t0002g0009 a0001c0001t0002g0138 others(5): Show |
9 | HG01496.hp1 HG01928.hp2 HG01952.hp2 others(6): Show |
intron_variant | MODIFIER | c.487+15614A>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95511671 | |||||||
| chr7:95511675 | T | A | 1 | a0001c0001t0012g0198 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.487+15618T>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95511675 | |||||||
| chr7:95511843 | G | C | 3 | a0001c0001t0002g0135 a0001c0001t0002g0139 a0001c0001t0002g0151 |
3 | NA18974.hp1 NA18993.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.487+15786G>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95511843 | |||||||
| chr7:95511856 | A | G | 2 | a0001c0001t0015g0315 a0004c0003t0015g0059 |
2 | HG02717.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.487+15799A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95511856 | |||||||
| chr7:95511881 | G | T | 1 | a0001c0001t0001g0262 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.487+15824G>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95511881 | |||||||
| chr7:95511885 | C | T | 2 | a0001c0001t0004g0312 a0001c0001t0004g0313 |
2 | HG02965.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.487+15828C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95511885 | |||||||
| chr7:95511906 | A | G | 9 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0024 others(6): Show |
9 | HG00741.hp2 HG02647.hp2 HG02698.hp2 others(6): Show |
intron_variant | MODIFIER | c.487+15849A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95511906 | |||||||
| chr7:95511960 | GT | G | 5 | a0001c0001t0005g0272 a0001c0001t0005g0320 a0001c0001t0007g0273 others(2): Show |
5 | HG02559.hp1 HG02615.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.488-15848delT | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95511960 | ||||||
| chr7:95511971 | A | C | 1 | a0001c0001t0001g0057 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.488-15842A>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95511971 | |||||||
| chr7:95512110 | T | TC | 5 | a0001c0001t0003g0364 a0001c0001t0003g0366 a0001c0001t0004g0365 others(2): Show |
5 | HG02630.hp1 HG02818.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.488-15701dupC | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95512110 | ||||||
| chr7:95512247 | C | G | 168 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(165): Show |
178 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(175): Show |
intron_variant | MODIFIER | c.488-15566C>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95512247 | |||||||
| chr7:95512396 | C | T | 5 | a0001c0001t0003g0364 a0001c0001t0003g0366 a0001c0001t0004g0365 others(2): Show |
5 | HG02630.hp1 HG02818.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.488-15417C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95512396 | |||||||
| chr7:95512424 | A | G | 35 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0013 others(32): Show |
38 | HG00408.hp2 HG00609.hp2 HG01261.hp2 others(35): Show |
intron_variant | MODIFIER | c.488-15389A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95512424 | |||||||
| chr7:95512451 | G | A | 6 | a0001c0001t0001g0185 a0001c0001t0009g0183 a0001c0001t0009g0184 others(3): Show |
6 | HG01192.hp1 HG01358.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.488-15362G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95512451 | |||||||
| chr7:95512748 | G | A | 7 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0024 others(4): Show |
7 | HG02647.hp2 HG02698.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.488-15065G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95512748 | |||||||
| chr7:95512753 | A | G | 36 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0024 others(33): Show |
37 | HG00438.hp2 HG00621.hp1 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.488-15060A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95512753 | |||||||
| chr7:95512968 | G | A | 36 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0024 others(33): Show |
37 | HG00438.hp2 HG00621.hp1 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.488-14845G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95512968 | |||||||
| chr7:95513029 | G | A | 5 | a0001c0001t0003g0364 a0001c0001t0003g0366 a0001c0001t0004g0365 others(2): Show |
5 | HG02630.hp1 HG02818.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.488-14784G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95513029 | |||||||
| chr7:95513075 | T | C | 3 | a0001c0001t0008g0027 a0001c0001t0008g0206 a0001c0001t0008g0297 |
3 | HG03195.hp1 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.488-14738T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95513075 | |||||||
| chr7:95513081 | G | A | 5 | a0001c0001t0004g0031 a0001c0001t0005g0032 a0001c0001t0005g0033 others(2): Show |
5 | HG00639.hp1 HG02055.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.488-14732G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95513081 | |||||||
| chr7:95513101 | C | A | 130 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(127): Show |
138 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.488-14712C>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95513101 | |||||||
| chr7:95513142 | G | A | 1 | a0001c0001t0001g0209 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.488-14671G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95513142 | |||||||
| chr7:95513233 | G | GT | 5 | a0001c0001t0001g0110 a0001c0001t0001g0270 a0001c0001t0001g0280 others(2): Show |
5 | HG02602.hp2 HG03688.hp2 NA18953.hp2 others(2): Show |
intron_variant | MODIFIER | c.488-14572dupT | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95513233 | ||||||
| chr7:95513242 | G | T | 1 | a0001c0001t0001g0057 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.488-14571G>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95513242 | |||||||
| chr7:95513252 | TG | T | 37 | a0001c0001t0001g0310 a0001c0001t0002g0002 a0001c0001t0002g0009 others(34): Show |
40 | HG00423.hp1 HG01496.hp1 HG01952.hp2 others(37): Show |
intron_variant | MODIFIER | c.488-14560delG | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95513252 | |||||||
| chr7:95513253 | G | GTT | 10 | a0001c0001t0006g0136 a0001c0001t0006g0158 a0002c0002t0004g0044 others(7): Show |
11 | HG01884.hp1 HG02055.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.488-14540_488-1453 others(6): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95513253 | ||||||
| chr7:95513253 | G | T | 5 | a0001c0001t0002g0134 a0001c0001t0002g0159 a0001c0001t0002g0352 others(2): Show |
5 | HG00738.hp2 HG02486.hp1 HG03831.hp1 others(2): Show |
intron_variant | MODIFIER | c.488-14560G>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95513253 | |||||||
| chr7:95513253 | GT | G | 149 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(146): Show |
154 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.488-14539delT | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95513253 | ||||||
| chr7:95513253 | GTT | G | 65 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0093 others(62): Show |
66 | HG00323.hp1 HG00438.hp2 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.488-14540_488-1453 others(6): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95513253 | ||||||
| chr7:95513253 | GTTTTTTT others(5): Show |
G | 3 | a0001c0001t0008g0027 a0001c0001t0008g0206 a0001c0001t0008g0297 |
3 | HG03195.hp1 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.488-14550_488-1453 others(16): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95513253 | ||||||
| chr7:95513256 | T | G | 5 | a0001c0001t0001g0054 a0001c0001t0001g0056 a0001c0001t0005g0012 others(2): Show |
6 | HG01891.hp1 HG02109.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.488-14557T>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95513256 | |||||||
| chr7:95513258 | T | G | 1 | a0001c0001t0001g0293 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.488-14555T>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95513258 | |||||||
| chr7:95513260 | T | G | 2 | a0001c0001t0002g0052 a0001c0001t0002g0152 |
2 | HG03579.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.488-14553T>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95513260 | |||||||
| chr7:95513293 | A | ATG | 9 | a0001c0001t0001g0068 a0001c0001t0001g0222 a0001c0001t0001g0259 others(6): Show |
9 | HG01081.hp2 HG02109.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.488-14482_488-1448 others(6): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95513293 | ||||||
| chr7:95513293 | A | ATGTG | 63 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0046 others(60): Show |
66 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.488-14484_488-1448 others(8): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95513293 | ||||||
| chr7:95513293 | A | ATGTGTG | 81 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(78): Show |
86 | HG00280.hp1 HG00408.hp2 HG00609.hp2 others(83): Show |
intron_variant | MODIFIER | c.488-14486_488-1448 others(10): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95513293 | ||||||
| chr7:95513293 | A | ATGTGTGT others(1): Show |
39 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0024 others(36): Show |
39 | HG00140.hp1 HG00140.hp2 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.488-14488_488-1448 others(12): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95513293 | ||||||
| chr7:95513293 | A | ATGTGTGT others(3): Show |
32 | a0001c0001t0001g0217 a0001c0001t0001g0226 a0001c0001t0001g0230 others(29): Show |
32 | HG00597.hp1 HG01099.hp2 HG01167.hp1 others(29): Show |
intron_variant | MODIFIER | c.488-14490_488-1448 others(14): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95513293 | ||||||
| chr7:95513293 | A | ATGTGTGT others(5): Show |
4 | a0001c0001t0001g0265 a0001c0001t0001g0266 a0001c0001t0003g0049 others(1): Show |
4 | HG00639.hp2 HG01106.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.488-14492_488-1448 others(16): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95513293 | ||||||
| chr7:95513293 | ATG | A | 13 | a0001c0001t0001g0225 a0001c0001t0001g0310 a0001c0001t0002g0135 others(10): Show |
13 | HG00423.hp1 HG01192.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.488-14482_488-1448 others(6): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95513293 | ||||||
| chr7:95513293 | ATGTG | A | 41 | a0001c0001t0001g0069 a0001c0001t0001g0216 a0001c0001t0001g0233 others(38): Show |
44 | HG00673.hp1 HG00738.hp2 HG01168.hp2 others(41): Show |
intron_variant | MODIFIER | c.488-14484_488-1448 others(8): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95513293 | ||||||
| chr7:95513293 | ATGTGTG | A | 19 | a0001c0001t0001g0001 a0001c0001t0001g0182 a0001c0001t0001g0229 others(16): Show |
22 | HG01243.hp2 HG01256.hp1 HG02165.hp2 others(19): Show |
intron_variant | MODIFIER | c.488-14486_488-1448 others(10): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95513293 | ||||||
| chr7:95513293 | ATGTGTGT others(1): Show |
A | 46 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0054 others(43): Show |
50 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.488-14488_488-1448 others(12): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95513293 | ||||||
| chr7:95513293 | ATGTGTGT others(3): Show |
A | 8 | a0001c0001t0004g0031 a0001c0001t0005g0012 a0001c0001t0005g0032 others(5): Show |
9 | HG00639.hp1 HG01891.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.488-14490_488-1448 others(14): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95513293 | ||||||
| chr7:95513293 | ATGTGTGT others(9): Show |
A | 6 | a0001c0001t0001g0185 a0001c0001t0009g0183 a0001c0001t0009g0184 others(3): Show |
6 | HG01192.hp1 HG01358.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.488-14496_488-1448 others(20): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95513293 | ||||||
| chr7:95513303 | G | C | 1 | a0001c0001t0015g0315 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.488-14510G>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95513303 | |||||||
| chr7:95513448 | G | A | 6 | a0001c0001t0001g0185 a0001c0001t0009g0183 a0001c0001t0009g0184 others(3): Show |
6 | HG01192.hp1 HG01358.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.488-14365G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95513448 | |||||||
| chr7:95513492 | G | A | 1 | a0001c0001t0007g0363 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.488-14321G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95513492 | |||||||
| chr7:95513569 | G | T | 39 | a0001c0001t0001g0310 a0001c0001t0002g0002 a0001c0001t0002g0009 others(36): Show |
42 | HG00423.hp1 HG00738.hp2 HG01496.hp1 others(39): Show |
intron_variant | MODIFIER | c.488-14244G>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95513569 | |||||||
| chr7:95513607 | C | T | 1 | a0001c0001t0001g0146 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.488-14206C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95513607 | |||||||
| chr7:95513831 | A | G | 1 | a0001c0001t0001g0270 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.488-13982A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95513831 | |||||||
| chr7:95513859 | G | A | 1 | a0001c0001t0001g0193 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.488-13954G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95513859 | |||||||
| chr7:95513927 | C | T | 18 | a0001c0001t0001g0093 a0001c0001t0001g0100 a0001c0001t0001g0106 others(15): Show |
18 | HG00438.hp2 HG00621.hp1 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.488-13886C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95513927 | |||||||
| chr7:95513929 | C | T | 6 | a0001c0001t0001g0185 a0001c0001t0009g0183 a0001c0001t0009g0184 others(3): Show |
6 | HG01192.hp1 HG01358.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.488-13884C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95513929 | |||||||
| chr7:95514021 | A | C | 6 | a0001c0001t0001g0185 a0001c0001t0009g0183 a0001c0001t0009g0184 others(3): Show |
6 | HG01192.hp1 HG01358.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.488-13792A>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95514021 | |||||||
| chr7:95514030 | G | C | 1 | a0001c0001t0001g0329 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.488-13783G>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95514030 | |||||||
| chr7:95514197 | A | T | 2 | a0001c0001t0001g0338 a0001c0001t0001g0350 |
2 | NA18949.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.488-13616A>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95514197 | |||||||
| chr7:95514231 | G | C | 1 | a0004c0003t0015g0059 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.488-13582G>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95514231 | |||||||
| chr7:95514447 | A | C | 1 | a0001c0001t0001g0244 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.488-13366A>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95514447 | |||||||
| chr7:95514631 | G | C | 1 | a0001c0001t0001g0250 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.488-13182G>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95514631 | |||||||
| chr7:95514688 | G | T | 1 | a0001c0001t0001g0339 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.488-13125G>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95514688 | |||||||
| chr7:95514830 | T | G | 3 | a0001c0001t0008g0027 a0001c0001t0008g0206 a0001c0001t0008g0297 |
3 | HG03195.hp1 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.488-12983T>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95514830 | |||||||
| chr7:95514937 | C | G | 1 | a0001c0001t0002g0207 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.488-12876C>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95514937 | |||||||
| chr7:95515090 | G | T | 1 | a0001c0001t0004g0092 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.488-12723G>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95515090 | |||||||
| chr7:95515145 | TTTTC | T | 47 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0055 others(44): Show |
51 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.488-12654_488-1265 others(8): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515145 | ||||||
| chr7:95515155 | T | TTC | 8 | a0001c0001t0001g0325 a0001c0001t0001g0333 a0001c0001t0001g0340 others(5): Show |
8 | HG00738.hp2 HG01516.hp2 HG02027.hp1 others(5): Show |
intron_variant | MODIFIER | c.488-12656_488-1265 others(6): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515155 | ||||||
| chr7:95515155 | TTCTTTC | T | 3 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0005c0004t0004g0109 |
3 | HG02698.hp2 HG03710.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.488-12644_488-1263 others(10): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515155 | ||||||
| chr7:95515157 | CTTTCTCT others(1): Show |
C | 10 | a0001c0001t0001g0182 a0001c0001t0001g0326 a0001c0001t0001g0336 others(7): Show |
11 | HG01496.hp1 HG01952.hp2 HG01993.hp1 others(8): Show |
intron_variant | MODIFIER | c.488-12654_488-1264 others(12): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515157 | ||||||
| chr7:95515159 | T | C | 56 | a0001c0001t0001g0015 a0001c0001t0001g0054 a0001c0001t0001g0056 others(53): Show |
60 | HG00280.hp1 HG00423.hp1 HG00673.hp1 others(57): Show |
intron_variant | MODIFIER | c.488-12654T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95515159 | |||||||
| chr7:95515161 | C | CTCTCTT | 5 | a0001c0001t0001g0310 a0001c0001t0001g0355 a0001c0001t0002g0151 others(2): Show |
5 | HG02572.hp2 HG03704.hp2 HG03831.hp1 others(2): Show |
intron_variant | MODIFIER | c.488-12649_488-1264 others(10): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515161 | ||||||
| chr7:95515161 | C | T | 1 | a0001c0001t0001g0249 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.488-12652C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95515161 | |||||||
| chr7:95515161 | CTCTT | C | 9 | a0001c0001t0004g0094 a0001c0001t0004g0104 a0001c0001t0004g0105 others(6): Show |
9 | HG01346.hp2 HG01433.hp1 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.488-12648_488-1264 others(8): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515161 | ||||||
| chr7:95515161 | CTCTTTCT others(3): Show |
C | 1 | a0001c0001t0001g0019 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.488-12644_488-1263 others(14): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515161 | ||||||
| chr7:95515163 | C | T | 1 | a0001c0001t0001g0327 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.488-12650C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95515163 | |||||||
| chr7:95515163 | CTT | C | 3 | a0001c0001t0003g0364 a0001c0001t0004g0102 a0001c0001t0011g0367 |
3 | HG00621.hp1 HG02630.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.488-12648_488-1264 others(6): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515163 | ||||||
| chr7:95515163 | CTTTCTCT others(1): Show |
C | 4 | a0001c0001t0001g0100 a0001c0001t0001g0106 a0001c0001t0005g0033 others(1): Show |
4 | HG00438.hp2 HG01192.hp1 HG02523.hp2 others(1): Show |
intron_variant | MODIFIER | c.488-12648_488-1264 others(12): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515163 | ||||||
| chr7:95515163 | CTTTCTCT others(5): Show |
C | 10 | a0001c0001t0001g0185 a0001c0001t0001g0332 a0001c0001t0002g0295 others(7): Show |
10 | HG00735.hp2 HG00741.hp2 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.488-12648_488-1263 others(16): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515163 | ||||||
| chr7:95515163 | CTTTCTCT others(9): Show |
C | 4 | a0001c0001t0001g0347 a0001c0001t0006g0158 a0002c0002t0006g0004 others(1): Show |
4 | HG02055.hp2 HG02886.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.488-12648_488-1263 others(20): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515163 | ||||||
| chr7:95515163 | CTTTCTCT others(21): Show |
C | 1 | a0001c0001t0002g0157 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.488-12648_488-1262 others(32): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515163 | ||||||
| chr7:95515163 | CTTTCTCT others(29): Show |
C | 2 | a0001c0001t0003g0304 a0001c0001t0010g0029 |
2 | HG01192.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.488-12648_488-1261 others(40): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515163 | ||||||
| chr7:95515165 | T | C | 105 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(102): Show |
113 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(110): Show |
intron_variant | MODIFIER | c.488-12648T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95515165 | |||||||
| chr7:95515165 | TTC | T | 4 | a0001c0001t0002g0016 a0001c0001t0002g0155 a0001c0001t0004g0020 others(1): Show |
4 | HG02723.hp2 HG03704.hp1 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.488-12644_488-1264 others(6): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515165 | ||||||
| chr7:95515167 | C | CTCTCTTT others(7): Show |
1 | a0001c0001t0001g0284 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.488-12643_488-1264 others(18): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515167 | ||||||
| chr7:95515167 | C | CTCTT | 23 | a0001c0001t0001g0093 a0001c0001t0001g0125 a0001c0001t0001g0145 others(20): Show |
23 | HG01099.hp2 HG01106.hp2 HG01167.hp2 others(20): Show |
intron_variant | MODIFIER | c.488-12584_488-1258 others(8): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515167 | ||||||
| chr7:95515167 | C | CTCTTCTT others(4): Show |
1 | a0001c0001t0003g0366 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.488-12642_488-1264 others(15): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515167 | ||||||
| chr7:95515167 | C | CTCTTTCT others(1): Show |
16 | a0001c0001t0001g0046 a0001c0001t0001g0068 a0001c0001t0001g0144 others(13): Show |
16 | HG00639.hp1 HG01261.hp2 HG01943.hp1 others(13): Show |
intron_variant | MODIFIER | c.488-12588_488-1258 others(12): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515167 | ||||||
| chr7:95515167 | C | CTCTTTCT others(5): Show |
10 | a0001c0001t0001g0225 a0001c0001t0001g0230 a0001c0001t0001g0244 others(7): Show |
10 | HG00639.hp2 HG01952.hp1 HG02004.hp1 others(7): Show |
intron_variant | MODIFIER | c.488-12592_488-1258 others(16): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515167 | ||||||
| chr7:95515167 | C | CTCTTTCT others(9): Show |
3 | a0001c0001t0001g0170 a0001c0001t0001g0223 a0001c0001t0001g0287 |
3 | HG00621.hp2 HG02027.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.488-12596_488-1258 others(20): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515167 | ||||||
| chr7:95515167 | C | CTT | 16 | a0001c0001t0001g0018 a0001c0001t0001g0310 a0001c0001t0001g0325 others(13): Show |
16 | HG00738.hp2 HG01516.hp2 HG02027.hp1 others(13): Show |
intron_variant | MODIFIER | c.488-12645_488-1264 others(6): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515167 | ||||||
| chr7:95515167 | C | T | 30 | a0001c0001t0001g0015 a0001c0001t0001g0054 a0001c0001t0001g0056 others(27): Show |
33 | HG00280.hp1 HG00423.hp1 HG00673.hp1 others(30): Show |
intron_variant | MODIFIER | c.488-12646C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95515167 | |||||||
| chr7:95515167 | CTCTT | C | 42 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(39): Show |
47 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(44): Show |
intron_variant | MODIFIER | c.488-12584_488-1258 others(8): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515167 | ||||||
| chr7:95515167 | CTCTTTCT others(1): Show |
C | 13 | a0001c0001t0001g0035 a0001c0001t0001g0079 a0001c0001t0001g0131 others(10): Show |
13 | HG01346.hp1 HG02132.hp2 HG02698.hp1 others(10): Show |
intron_variant | MODIFIER | c.488-12588_488-1258 others(12): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515167 | ||||||
| chr7:95515167 | CTCTTTCT others(5): Show |
C | 5 | a0001c0001t0001g0070 a0001c0001t0001g0080 a0001c0001t0001g0161 others(2): Show |
5 | HG01099.hp1 HG02257.hp2 HG03942.hp1 others(2): Show |
intron_variant | MODIFIER | c.488-12592_488-1258 others(16): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515167 | ||||||
| chr7:95515167 | CTCTTTCT others(9): Show |
C | 4 | a0001c0001t0003g0303 a0001c0001t0012g0197 a0001c0001t0012g0198 others(1): Show |
4 | HG01257.hp1 HG01258.hp1 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.488-12596_488-1258 others(20): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515167 | ||||||
| chr7:95515171 | T | C | 21 | a0001c0001t0001g0112 a0001c0001t0001g0182 a0001c0001t0001g0326 others(18): Show |
22 | HG01346.hp2 HG01433.hp1 HG01496.hp1 others(19): Show |
intron_variant | MODIFIER | c.488-12642T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95515171 | |||||||
| chr7:95515175 | T | C | 4 | a0001c0001t0001g0100 a0001c0001t0001g0106 a0001c0001t0005g0033 others(1): Show |
4 | HG00438.hp2 HG01192.hp1 HG02523.hp2 others(1): Show |
intron_variant | MODIFIER | c.488-12638T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95515175 | |||||||
| chr7:95515179 | T | C | 5 | a0001c0001t0001g0185 a0001c0001t0004g0092 a0001c0001t0005g0195 others(2): Show |
5 | HG00735.hp2 HG01261.hp1 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.488-12634T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95515179 | |||||||
| chr7:95515190 | TTTCTTTC others(12): Show |
T | 2 | a0001c0001t0004g0312 a0001c0001t0004g0313 |
2 | HG02965.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.488-12620_488-1260 others(23): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515190 | ||||||
| chr7:95515195 | TTC | T | 4 | a0001c0001t0004g0030 a0001c0001t0004g0090 a0001c0001t0010g0028 others(1): Show |
4 | HG02451.hp1 HG02723.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.488-12616_488-1261 others(6): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515195 | ||||||
| chr7:95515203 | T | C | 2 | a0001c0001t0003g0304 a0001c0001t0010g0029 |
2 | HG01192.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.488-12610T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95515203 | |||||||
| chr7:95515215 | TTC | T | 3 | a0001c0001t0003g0061 a0001c0001t0014g0311 a0002c0002t0003g0317 |
3 | HG01175.hp2 HG01884.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.488-12596_488-1259 others(6): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515215 | ||||||
| chr7:95515215 | TTCTTTCT others(3): Show |
T | 1 | a0001c0001t0003g0296 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.488-12596_488-1258 others(14): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515215 | ||||||
| chr7:95515217 | C | CTT | 5 | a0001c0001t0001g0222 a0001c0001t0001g0238 a0001c0001t0001g0259 others(2): Show |
5 | HG01256.hp2 HG04115.hp1 NA19012.hp1 others(2): Show |
intron_variant | MODIFIER | c.488-12594_488-1259 others(6): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515217 | ||||||
| chr7:95515218 | T | C | 5 | a0001c0001t0004g0030 a0001c0001t0004g0090 a0001c0001t0010g0028 others(2): Show |
5 | HG02451.hp1 HG02723.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.488-12595T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95515218 | |||||||
| chr7:95515219 | T | TTCTTTCT others(7): Show |
1 | a0001c0001t0007g0211 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.488-12581_488-1258 others(18): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515219 | ||||||
| chr7:95515219 | T | TTCTTTCT others(15): Show |
1 | a0001c0001t0004g0210 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.488-12581_488-1258 others(26): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515219 | ||||||
| chr7:95515219 | TTC | T | 6 | a0001c0001t0001g0081 a0001c0001t0001g0172 a0001c0001t0001g0258 others(3): Show |
6 | HG00408.hp1 HG01243.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.488-12592_488-1259 others(6): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515219 | ||||||
| chr7:95515222 | T | TTTCTTTC others(13): Show |
1 | a0001c0001t0007g0208 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.488-12581_488-1258 others(24): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515222 | ||||||
| chr7:95515223 | TTC | T | 3 | a0001c0001t0001g0240 a0001c0001t0003g0098 a0001c0001t0017g0274 |
3 | HG01070.hp1 HG02071.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.488-12588_488-1258 others(6): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515223 | ||||||
| chr7:95515229 | C | T | 9 | a0001c0001t0001g0162 a0001c0001t0002g0002 a0001c0001t0002g0082 others(6): Show |
11 | HG00609.hp2 HG01109.hp1 HG02129.hp1 others(8): Show |
intron_variant | MODIFIER | c.488-12584C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95515229 | |||||||
| chr7:95515229 | CTT | C | 15 | a0001c0001t0001g0015 a0001c0001t0001g0081 a0001c0001t0001g0172 others(12): Show |
15 | HG00408.hp1 HG01070.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.488-12580_488-1257 others(6): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515229 | ||||||
| chr7:95515230 | T | TTTCTTTC others(4): Show |
1 | a0001c0001t0001g0140 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.488-12581_488-1258 others(15): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515230 | ||||||
| chr7:95515231 | T | C | 13 | a0001c0001t0001g0162 a0001c0001t0002g0002 a0001c0001t0002g0050 others(10): Show |
15 | HG00609.hp2 HG01081.hp2 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.488-12582T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95515231 | |||||||
| chr7:95515231 | T | TTC | 10 | a0001c0001t0001g0222 a0001c0001t0001g0238 a0001c0001t0001g0251 others(7): Show |
10 | HG00621.hp1 HG01256.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.488-12581_488-1258 others(6): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515231 | ||||||
| chr7:95515231 | T | TTCTTTCT others(5): Show |
1 | a0001c0001t0008g0212 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.488-12581_488-1258 others(16): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515231 | ||||||
| chr7:95515231 | TTTTC | T | 34 | a0001c0001t0001g0014 a0001c0001t0001g0057 a0001c0001t0001g0182 others(31): Show |
36 | HG00323.hp2 HG00597.hp2 HG01106.hp1 others(33): Show |
intron_variant | MODIFIER | c.488-12565_488-1256 others(8): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515231 | ||||||
| chr7:95515231 | TTTTCTTT others(39): Show |
T | 1 | a0001c0001t0010g0028 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.488-12561_488-1251 others(50): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515231 | ||||||
| chr7:95515233 | T | C | 54 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0069 others(51): Show |
54 | HG00280.hp2 HG00609.hp1 HG00673.hp1 others(51): Show |
intron_variant | MODIFIER | c.488-12580T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95515233 | |||||||
| chr7:95515235 | C | CTTTCTTT others(7): Show |
1 | a0001c0001t0002g0159 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.488-12576_488-1256 others(18): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515235 | ||||||
| chr7:95515235 | C | T | 50 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0069 others(47): Show |
50 | HG00280.hp2 HG00609.hp1 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.488-12578C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95515235 | |||||||
| chr7:95515236 | T | C | 7 | a0001c0001t0001g0222 a0001c0001t0001g0238 a0001c0001t0001g0259 others(4): Show |
7 | HG01256.hp2 HG01884.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.488-12577T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95515236 | |||||||
| chr7:95515237 | TTCTTTCT others(23): Show |
T | 1 | a0001c0001t0004g0090 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.488-12561_488-1253 others(34): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515237 | ||||||
| chr7:95515240 | T | C | 4 | a0001c0001t0001g0251 a0001c0001t0001g0261 a0001c0001t0002g0115 others(1): Show |
4 | HG01175.hp2 NA18974.hp2 NA19091.hp2 others(1): Show |
intron_variant | MODIFIER | c.488-12573T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95515240 | |||||||
| chr7:95515241 | TTC | T | 3 | a0001c0001t0002g0050 a0001c0001t0002g0053 a0001c0001t0008g0291 |
3 | HG01081.hp2 HG02109.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.488-12570_488-1256 others(6): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515241 | ||||||
| chr7:95515241 | TTCTTTCT others(19): Show |
T | 2 | a0001c0001t0004g0030 a0001c0001t0020g0026 |
2 | HG02451.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.488-12561_488-1253 others(30): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515241 | ||||||
| chr7:95515243 | C | CTT | 1 | a0001c0001t0002g0002 | 3 | HG02738.hp1 HG03239.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.488-12568_488-1256 others(6): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515243 | ||||||
| chr7:95515244 | T | C | 8 | a0001c0001t0001g0081 a0001c0001t0001g0172 a0001c0001t0001g0258 others(5): Show |
8 | HG00408.hp1 HG01243.hp1 HG02129.hp1 others(5): Show |
intron_variant | MODIFIER | c.488-12569T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95515244 | |||||||
| chr7:95515248 | T | C | 33 | a0001c0001t0001g0001 a0001c0001t0001g0054 a0001c0001t0001g0055 others(30): Show |
36 | HG00423.hp1 HG00609.hp2 HG01070.hp1 others(33): Show |
intron_variant | MODIFIER | c.488-12565T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95515248 | |||||||
| chr7:95515249 | TTCCTTCT others(11): Show |
T | 1 | a0001c0001t0010g0047 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.488-12561_488-1254 others(22): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515249 | ||||||
| chr7:95515251 | CCT | C | 6 | a0001c0001t0001g0222 a0001c0001t0001g0238 a0001c0001t0001g0259 others(3): Show |
6 | HG01256.hp2 HG01884.hp2 HG04115.hp1 others(3): Show |
intron_variant | MODIFIER | c.488-12561_488-1256 others(6): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95515251 | |||||||
| chr7:95515252 | C | T | 62 | a0001c0001t0001g0001 a0001c0001t0001g0054 a0001c0001t0001g0055 others(59): Show |
67 | HG00408.hp1 HG00423.hp1 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.488-12561C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95515252 | |||||||
| chr7:95515255 | CTT | C | 3 | a0001c0001t0001g0261 a0001c0001t0002g0115 a0001c0001t0003g0061 |
3 | HG01175.hp2 NA19091.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.488-12556_488-1255 others(6): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515255 | ||||||
| chr7:95515256 | T | C | 8 | a0001c0001t0001g0246 a0001c0001t0001g0247 a0001c0001t0003g0177 others(5): Show |
8 | HG01169.hp1 HG01358.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.488-12557T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95515256 | |||||||
| chr7:95515257 | T | TTC | 3 | a0001c0001t0002g0122 a0001c0001t0002g0164 a0002c0002t0004g0036 |
3 | HG02486.hp2 HG03017.hp2 NA19059.hp1 |
intron_variant | MODIFIER | c.488-12554_488-1255 others(6): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515257 | ||||||
| chr7:95515260 | T | C | 3 | a0001c0001t0002g0002 a0001c0001t0004g0213 a0001c0001t0005g0369 |
5 | HG02738.hp1 HG03239.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.488-12553T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95515260 | |||||||
| chr7:95515261 | T | C | 5 | a0001c0001t0001g0081 a0001c0001t0001g0172 a0001c0001t0001g0258 others(2): Show |
5 | HG00408.hp1 HG01243.hp1 HG02129.hp1 others(2): Show |
intron_variant | MODIFIER | c.488-12552T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95515261 | |||||||
| chr7:95515261 | T | TTC | 8 | a0001c0001t0001g0001 a0001c0001t0001g0054 a0001c0001t0001g0055 others(5): Show |
8 | HG01243.hp2 HG02040.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.488-12550_488-1254 others(6): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515261 | ||||||
| chr7:95515261 | TTCTTTC | T | 3 | a0001c0001t0001g0246 a0001c0001t0003g0177 a0001c0001t0007g0363 |
3 | NA18747.hp2 NA18995.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.488-12544_488-1253 others(10): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515261 | ||||||
| chr7:95515263 | C | T | 5 | a0001c0001t0001g0081 a0001c0001t0001g0172 a0001c0001t0001g0258 others(2): Show |
5 | HG00408.hp1 HG01243.hp1 HG02129.hp1 others(2): Show |
intron_variant | MODIFIER | c.488-12550C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95515263 | |||||||
| chr7:95515264 | T | C | 3 | a0001c0001t0002g0050 a0001c0001t0002g0053 a0001c0001t0008g0291 |
3 | HG01081.hp2 HG02109.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.488-12549T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95515264 | |||||||
| chr7:95515265 | T | C | 31 | a0001c0001t0001g0001 a0001c0001t0001g0081 a0001c0001t0001g0162 others(28): Show |
33 | HG00408.hp1 HG00423.hp1 HG00609.hp2 others(30): Show |
intron_variant | MODIFIER | c.488-12548T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95515265 | |||||||
| chr7:95515265 | TTC | T | 14 | a0001c0001t0001g0222 a0001c0001t0001g0259 a0001c0001t0001g0261 others(11): Show |
14 | HG01081.hp2 HG01175.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.488-12544_488-1254 others(6): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515265 | ||||||
| chr7:95515267 | C | CTCTT | 13 | a0001c0001t0001g0229 a0001c0001t0001g0328 a0001c0001t0001g0355 others(10): Show |
13 | HG00673.hp1 HG01099.hp2 HG01516.hp2 others(10): Show |
intron_variant | MODIFIER | c.488-12497_488-1249 others(8): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515267 | ||||||
| chr7:95515267 | C | CTCTTTCT others(5): Show |
3 | a0001c0001t0001g0357 a0001c0001t0004g0128 a0001c0001t0004g0167 |
3 | HG01167.hp1 HG02602.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.488-12505_488-1249 others(16): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515267 | ||||||
| chr7:95515267 | C | CTT | 16 | a0001c0001t0001g0001 a0001c0001t0001g0054 a0001c0001t0001g0055 others(13): Show |
18 | HG01243.hp2 HG01256.hp2 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.488-12545_488-1254 others(6): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515267 | ||||||
| chr7:95515267 | C | T | 31 | a0001c0001t0001g0001 a0001c0001t0001g0081 a0001c0001t0001g0162 others(28): Show |
33 | HG00408.hp1 HG00423.hp1 HG00609.hp2 others(30): Show |
intron_variant | MODIFIER | c.488-12546C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95515267 | |||||||
| chr7:95515267 | CTCTT | C | 37 | a0001c0001t0001g0011 a0001c0001t0001g0112 a0001c0001t0001g0192 others(34): Show |
39 | HG00323.hp1 HG00323.hp2 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.488-12497_488-1249 others(8): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515267 | ||||||
| chr7:95515267 | CTCTTTCT others(1): Show |
C | 16 | a0001c0001t0001g0182 a0001c0001t0001g0196 a0001c0001t0001g0332 others(13): Show |
16 | HG00738.hp2 HG01257.hp1 HG01258.hp1 others(13): Show |
intron_variant | MODIFIER | c.488-12501_488-1249 others(12): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515267 | ||||||
| chr7:95515267 | CTCTTTCT others(5): Show |
C | 8 | a0001c0001t0001g0243 a0001c0001t0002g0052 a0001c0001t0002g0133 others(5): Show |
8 | HG01891.hp2 HG03209.hp1 HG03579.hp1 others(5): Show |
intron_variant | MODIFIER | c.488-12505_488-1249 others(16): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515267 | ||||||
| chr7:95515267 | CTCTTTCT others(9): Show |
C | 2 | a0001c0001t0002g0048 a0001c0001t0002g0051 |
2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.488-12509_488-1249 others(20): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515267 | ||||||
| chr7:95515267 | CTCTTTCT others(13): Show |
C | 3 | a0001c0001t0001g0329 a0001c0001t0001g0335 a0001c0001t0001g0343 |
3 | NA18975.hp2 NA19009.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.488-12513_488-1249 others(24): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515267 | ||||||
| chr7:95515268 | T | C | 2 | a0001c0001t0008g0027 a0001c0001t0008g0206 |
2 | HG03195.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.488-12545T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95515268 | |||||||
| chr7:95515269 | C | T | 6 | a0001c0001t0001g0247 a0001c0001t0005g0369 a0001c0001t0007g0273 others(3): Show |
6 | HG01169.hp1 HG01358.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.488-12544C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95515269 | |||||||
| chr7:95515271 | T | C | 6 | a0001c0001t0001g0247 a0001c0001t0005g0369 a0001c0001t0007g0273 others(3): Show |
6 | HG01169.hp1 HG01358.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.488-12542T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95515271 | |||||||
| chr7:95515273 | C | T | 1 | a0001c0001t0005g0369 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.488-12540C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95515273 | |||||||
| chr7:95515275 | T | C | 1 | a0001c0001t0005g0369 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.488-12538T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95515275 | |||||||
| chr7:95515277 | CTT | C | 3 | a0001c0001t0001g0246 a0001c0001t0003g0177 a0001c0001t0004g0213 |
3 | HG03486.hp2 NA18747.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.488-12534_488-1253 others(6): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515277 | ||||||
| chr7:95515279 | T | C | 1 | a0001c0001t0010g0028 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.488-12534T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95515279 | |||||||
| chr7:95515281 | CTT | C | 3 | a0001c0001t0002g0050 a0001c0001t0002g0053 a0001c0001t0008g0291 |
3 | HG01081.hp2 HG02109.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.488-12530_488-1252 others(6): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515281 | ||||||
| chr7:95515304 | T | C | 1 | a0001c0001t0001g0286 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.488-12509T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95515304 | |||||||
| chr7:95515304 | TCTTTCTT others(13): Show |
T | 1 | a0001c0001t0008g0027 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.488-12505_488-1248 others(24): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515304 | ||||||
| chr7:95515308 | T | C | 18 | a0001c0001t0001g0100 a0001c0001t0001g0112 a0001c0001t0001g0222 others(15): Show |
18 | HG00408.hp1 HG00438.hp2 HG01261.hp1 others(15): Show |
intron_variant | MODIFIER | c.488-12505T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95515308 | |||||||
| chr7:95515308 | TCTTTCTT others(5): Show |
T | 1 | a0001c0001t0015g0315 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.488-12501_488-1249 others(16): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515308 | ||||||
| chr7:95515312 | T | C | 37 | a0001c0001t0001g0011 a0001c0001t0001g0023 a0001c0001t0001g0024 others(34): Show |
38 | HG00408.hp1 HG00438.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.488-12501T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95515312 | |||||||
| chr7:95515312 | T | TCTTC | 3 | a0001c0001t0001g0129 a0001c0001t0001g0290 a0001c0001t0002g0295 |
3 | HG00741.hp2 HG02735.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.488-12498_488-1249 others(8): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515312 | ||||||
| chr7:95515312 | T | TCTTCCTT others(1): Show |
4 | a0001c0001t0001g0249 a0001c0001t0001g0280 a0001c0001t0004g0163 others(1): Show |
4 | HG00280.hp1 NA18966.hp1 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.488-12498_488-1249 others(12): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515312 | ||||||
| chr7:95515316 | T | C | 114 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0019 others(111): Show |
118 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.488-12497T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95515316 | |||||||
| chr7:95515316 | T | TCTTC | 50 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(47): Show |
51 | HG00408.hp2 HG00597.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.488-12481_488-1247 others(8): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515316 | ||||||
| chr7:95515316 | T | TCTTCCTT others(1): Show |
4 | a0001c0001t0001g0008 a0001c0001t0001g0146 a0001c0001t0002g0150 others(1): Show |
5 | HG02165.hp1 HG03540.hp1 HG04228.hp2 others(2): Show |
intron_variant | MODIFIER | c.488-12485_488-1247 others(12): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515316 | ||||||
| chr7:95515316 | T | TCTTCCTT others(5): Show |
11 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0225 others(8): Show |
12 | HG00140.hp1 HG00423.hp2 HG00558.hp1 others(9): Show |
intron_variant | MODIFIER | c.488-12489_488-1247 others(16): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515316 | ||||||
| chr7:95515316 | T | TCTTCCTT others(9): Show |
3 | a0001c0001t0001g0003 a0001c0001t0001g0124 a0001c0001t0001g0270 |
3 | HG02056.hp1 HG02056.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.488-12493_488-1247 others(20): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515316 | ||||||
| chr7:95515316 | T | TCTTTCTT others(1): Show |
32 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0125 others(29): Show |
32 | HG00140.hp2 HG00639.hp1 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.488-12494_488-1249 others(12): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515316 | ||||||
| chr7:95515316 | T | TCTTTCTT others(5): Show |
1 | a0001c0001t0001g0277 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.488-12494_488-1249 others(16): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515316 | ||||||
| chr7:95515316 | T | TCTTTCTT others(9): Show |
7 | a0001c0001t0001g0003 a0001c0001t0001g0046 a0001c0001t0001g0252 others(4): Show |
7 | HG00438.hp1 HG00558.hp2 HG02027.hp2 others(4): Show |
intron_variant | MODIFIER | c.488-12494_488-1249 others(20): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515316 | ||||||
| chr7:95515316 | T | TCTTTCTT others(5): Show |
12 | a0001c0001t0001g0013 a0001c0001t0001g0110 a0001c0001t0001g0120 others(9): Show |
12 | HG01070.hp2 HG01361.hp1 HG01934.hp1 others(9): Show |
intron_variant | MODIFIER | c.488-12494_488-1249 others(16): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515316 | ||||||
| chr7:95515316 | T | TCTTTCTT others(13): Show |
2 | a0001c0001t0001g0250 a0001c0001t0001g0256 |
2 | HG02015.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.488-12494_488-1249 others(24): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515316 | ||||||
| chr7:95515316 | T | TCTTTCTT others(9): Show |
3 | a0001c0001t0001g0166 a0001c0001t0002g0137 a0001c0001t0003g0078 |
3 | NA19002.hp2 NA19009.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.488-12494_488-1249 others(20): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515316 | ||||||
| chr7:95515316 | T | TCTTTCTT others(13): Show |
1 | a0001c0001t0002g0154 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.488-12494_488-1249 others(24): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515316 | ||||||
| chr7:95515320 | C | T | 1 | a0001c0001t0008g0297 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.488-12493C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95515320 | |||||||
| chr7:95515324 | C | T | 1 | a0001c0001t0008g0297 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.488-12489C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95515324 | |||||||
| chr7:95515328 | C | T | 1 | a0001c0001t0020g0026 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.488-12485C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95515328 | |||||||
| chr7:95515332 | C | T | 4 | a0001c0001t0003g0304 a0001c0001t0004g0030 a0001c0001t0010g0047 others(1): Show |
4 | HG01192.hp2 HG02451.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.488-12481C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95515332 | |||||||
| chr7:95515336 | T | C | 79 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0024 others(76): Show |
83 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(80): Show |
intron_variant | MODIFIER | c.488-12477T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95515336 | |||||||
| chr7:95515340 | T | C | 41 | a0001c0001t0001g0019 a0001c0001t0001g0310 a0001c0001t0002g0002 others(38): Show |
44 | HG00423.hp1 HG00738.hp2 HG00741.hp2 others(41): Show |
intron_variant | MODIFIER | c.488-12473T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95515340 | |||||||
| chr7:95515350 | TTTTTCTT others(6): Show |
T | 1 | a0001c0001t0007g0363 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.488-12441_488-1242 others(17): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515350 | ||||||
| chr7:95515353 | T | C | 17 | a0001c0001t0001g0019 a0001c0001t0001g0093 a0001c0001t0002g0295 others(14): Show |
18 | HG00621.hp1 HG00639.hp1 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.488-12460T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95515353 | |||||||
| chr7:95515355 | C | T | 17 | a0001c0001t0001g0019 a0001c0001t0001g0093 a0001c0001t0002g0295 others(14): Show |
18 | HG00621.hp1 HG00639.hp1 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.488-12458C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95515355 | |||||||
| chr7:95515364 | TTTTC | T | 22 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0100 others(19): Show |
22 | HG00438.hp2 HG01106.hp1 HG01168.hp2 others(19): Show |
intron_variant | MODIFIER | c.488-12437_488-1243 others(8): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515364 | ||||||
| chr7:95515367 | T | C | 17 | a0001c0001t0001g0019 a0001c0001t0001g0093 a0001c0001t0002g0295 others(14): Show |
18 | HG00621.hp1 HG00639.hp1 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.488-12446T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95515367 | |||||||
| chr7:95515368 | C | T | 17 | a0001c0001t0001g0019 a0001c0001t0001g0093 a0001c0001t0002g0295 others(14): Show |
18 | HG00621.hp1 HG00639.hp1 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.488-12445C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95515368 | |||||||
| chr7:95515370 | T | C | 1 | a0001c0001t0007g0363 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.488-12443T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95515370 | |||||||
| chr7:95515386 | C | CT | 14 | a0001c0001t0001g0081 a0001c0001t0001g0180 a0001c0001t0001g0200 others(11): Show |
14 | HG00140.hp2 HG01884.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.488-12419dupT | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515386 | ||||||
| chr7:95515407 | T | C | 1 | a0001c0001t0003g0078 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.488-12406T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95515407 | |||||||
| chr7:95515414 | TTCTC | T | 18 | a0001c0001t0001g0093 a0001c0001t0001g0100 a0001c0001t0001g0106 others(15): Show |
18 | HG00438.hp2 HG00621.hp1 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.488-12391_488-1238 others(8): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515414 | ||||||
| chr7:95515424 | C | CT | 109 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(106): Show |
118 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.488-12379dupT | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515424 | ||||||
| chr7:95515425 | T | TC | 6 | a0001c0001t0003g0304 a0001c0001t0004g0030 a0001c0001t0004g0090 others(3): Show |
6 | HG01192.hp2 HG02451.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.488-12388_488-1238 others(5): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95515425 | |||||||
| chr7:95515509 | G | A | 15 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0024 others(12): Show |
15 | HG00741.hp2 HG01192.hp1 HG01358.hp1 others(12): Show |
intron_variant | MODIFIER | c.488-12304G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95515509 | |||||||
| chr7:95515605 | G | A | 1 | a0001c0001t0013g0101 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.488-12208G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95515605 | |||||||
| chr7:95515827 | C | T | 1 | a0001c0001t0001g0262 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.488-11986C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95515827 | |||||||
| chr7:95515982 | C | A | 1 | a0001c0001t0002g0295 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.488-11831C>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95515982 | |||||||
| chr7:95516116 | G | T | 18 | a0001c0001t0001g0093 a0001c0001t0001g0100 a0001c0001t0001g0106 others(15): Show |
18 | HG00438.hp2 HG00621.hp1 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.488-11697G>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95516116 | |||||||
| chr7:95516306 | T | C | 1 | a0001c0001t0001g0341 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.488-11507T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95516306 | |||||||
| chr7:95516357 | A | G | 5 | a0001c0001t0005g0272 a0001c0001t0005g0320 a0001c0001t0007g0273 others(2): Show |
5 | HG02559.hp1 HG02615.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.488-11456A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95516357 | |||||||
| chr7:95516495 | G | A | 9 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0024 others(6): Show |
9 | HG00741.hp2 HG02647.hp2 HG02698.hp2 others(6): Show |
intron_variant | MODIFIER | c.488-11318G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95516495 | |||||||
| chr7:95516548 | T | C | 1 | a0001c0001t0003g0364 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.488-11265T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95516548 | |||||||
| chr7:95516595 | G | A | 1 | a0001c0001t0001g0120 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.488-11218G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95516595 | |||||||
| chr7:95516695 | T | C | 18 | a0001c0001t0001g0093 a0001c0001t0001g0100 a0001c0001t0001g0106 others(15): Show |
18 | HG00438.hp2 HG00621.hp1 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.488-11118T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95516695 | |||||||
| chr7:95517077 | G | A | 4 | a0001c0001t0001g0005 a0001c0001t0001g0064 a0001c0001t0001g0065 others(1): Show |
5 | HG00735.hp1 HG01358.hp2 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.488-10736G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95517077 | |||||||
| chr7:95517141 | T | C | 1 | a0001c0001t0001g0233 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.488-10672T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95517141 | |||||||
| chr7:95517143 | T | C | 3 | a0002c0002t0004g0044 a0002c0002t0006g0042 a0002c0002t0006g0043 |
3 | HG02451.hp2 HG02976.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.488-10670T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95517143 | |||||||
| chr7:95517147 | T | C | 1 | a0001c0001t0001g0255 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.488-10666T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95517147 | |||||||
| chr7:95517215 | C | A | 6 | a0001c0001t0001g0185 a0001c0001t0009g0183 a0001c0001t0009g0184 others(3): Show |
6 | HG01192.hp1 HG01358.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.488-10598C>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95517215 | |||||||
| chr7:95517313 | C | T | 41 | a0001c0001t0001g0310 a0001c0001t0002g0002 a0001c0001t0002g0009 others(38): Show |
44 | HG00423.hp1 HG00738.hp2 HG01496.hp1 others(41): Show |
intron_variant | MODIFIER | c.488-10500C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95517313 | |||||||
| chr7:95517369 | G | A | 18 | a0001c0001t0001g0093 a0001c0001t0001g0100 a0001c0001t0001g0106 others(15): Show |
18 | HG00438.hp2 HG00621.hp1 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.488-10444G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95517369 | |||||||
| chr7:95517446 | T | G | 42 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0024 others(39): Show |
43 | HG00438.hp2 HG00621.hp1 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.488-10367T>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95517446 | |||||||
| chr7:95517601 | G | GA | 28 | a0001c0001t0003g0364 a0001c0001t0003g0366 a0001c0001t0004g0031 others(25): Show |
30 | HG00639.hp1 HG01884.hp1 HG01884.hp2 others(27): Show |
intron_variant | MODIFIER | c.488-10201dupA | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95517601 | ||||||
| chr7:95517614 | A | G | 3 | a0001c0001t0008g0027 a0001c0001t0008g0206 a0001c0001t0008g0297 |
3 | HG03195.hp1 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.488-10199A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95517614 | |||||||
| chr7:95517782 | G | A | 11 | a0001c0001t0002g0009 a0001c0001t0002g0137 a0001c0001t0002g0138 others(8): Show |
12 | HG00423.hp1 HG01496.hp1 HG01952.hp2 others(9): Show |
intron_variant | MODIFIER | c.488-10031G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95517782 | |||||||
| chr7:95517800 | G | A | 1 | a0001c0001t0009g0187 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.488-10013G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95517800 | |||||||
| chr7:95517842 | G | A | 2 | a0001c0001t0010g0028 a0001c0001t0010g0029 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.488-9971G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95517842 | |||||||
| chr7:95518041 | G | A | 1 | a0001c0001t0014g0311 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.488-9772G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95518041 | |||||||
| chr7:95518064 | G | A | 7 | a0001c0001t0002g0075 a0001c0001t0002g0076 a0001c0001t0002g0082 others(4): Show |
7 | HG01175.hp2 HG01257.hp1 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.488-9749G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95518064 | |||||||
| chr7:95518682 | A | T | 10 | a0001c0001t0006g0136 a0001c0001t0006g0158 a0002c0002t0004g0044 others(7): Show |
11 | HG01884.hp1 HG02055.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.488-9131A>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95518682 | |||||||
| chr7:95518736 | C | T | 39 | a0001c0001t0001g0310 a0001c0001t0002g0002 a0001c0001t0002g0009 others(36): Show |
42 | HG00423.hp1 HG00738.hp2 HG01496.hp1 others(39): Show |
intron_variant | MODIFIER | c.488-9077C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95518736 | |||||||
| chr7:95518762 | C | T | 1 | a0001c0001t0005g0320 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.488-9051C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95518762 | |||||||
| chr7:95518852 | GAGATAAA others(5): Show |
G | 2 | a0001c0001t0001g0358 a0001c0001t0001g0359 |
2 | HG00609.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.488-8960_488-8949d others(14): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95518852 | |||||||
| chr7:95518922 | A | G | 9 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0024 others(6): Show |
9 | HG00741.hp2 HG02647.hp2 HG02698.hp2 others(6): Show |
intron_variant | MODIFIER | c.488-8891A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95518922 | |||||||
| chr7:95519229 | T | C | 2 | a0001c0001t0004g0020 a0001c0001t0004g0021 |
2 | HG03704.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.488-8584T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95519229 | |||||||
| chr7:95519653 | C | T | 5 | a0001c0001t0004g0030 a0001c0001t0004g0090 a0001c0001t0010g0028 others(2): Show |
5 | HG02451.hp1 HG02723.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.488-8160C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95519653 | |||||||
| chr7:95519703 | T | C | 1 | a0001c0001t0002g0157 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.488-8110T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95519703 | |||||||
| chr7:95519748 | T | C | 43 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0024 others(40): Show |
44 | HG00438.hp2 HG00621.hp1 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.488-8065T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95519748 | |||||||
| chr7:95519792 | T | C | 10 | a0001c0001t0006g0136 a0001c0001t0006g0158 a0002c0002t0004g0044 others(7): Show |
11 | HG01884.hp1 HG02055.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.488-8021T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95519792 | |||||||
| chr7:95520163 | G | T | 70 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(67): Show |
76 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.488-7650G>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95520163 | |||||||
| chr7:95520362 | A | G | 5 | a0001c0001t0003g0364 a0001c0001t0003g0366 a0001c0001t0004g0365 others(2): Show |
5 | HG02630.hp1 HG02818.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.488-7451A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95520362 | |||||||
| chr7:95520482 | A | G | 5 | a0001c0001t0003g0364 a0001c0001t0003g0366 a0001c0001t0004g0365 others(2): Show |
5 | HG02630.hp1 HG02818.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.488-7331A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95520482 | |||||||
| chr7:95520642 | AC | A | 43 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0024 others(40): Show |
44 | HG00438.hp2 HG00621.hp1 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.488-7165delC | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95520642 | ||||||
| chr7:95520776 | T | C | 43 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0024 others(40): Show |
44 | HG00438.hp2 HG00621.hp1 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.488-7037T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95520776 | |||||||
| chr7:95520881 | G | T | 9 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0024 others(6): Show |
9 | HG00741.hp2 HG02647.hp2 HG02698.hp2 others(6): Show |
intron_variant | MODIFIER | c.488-6932G>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95520881 | |||||||
| chr7:95520891 | C | T | 1 | a0001c0001t0001g0339 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.488-6922C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95520891 | |||||||
| chr7:95520919 | T | C | 1 | a0001c0001t0001g0223 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.488-6894T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95520919 | |||||||
| chr7:95521064 | A | G | 71 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(68): Show |
77 | HG00280.hp2 HG00323.hp2 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.488-6749A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95521064 | |||||||
| chr7:95521145 | A | C | 41 | a0001c0001t0001g0310 a0001c0001t0002g0002 a0001c0001t0002g0009 others(38): Show |
44 | HG00423.hp1 HG00738.hp2 HG01496.hp1 others(41): Show |
intron_variant | MODIFIER | c.488-6668A>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95521145 | |||||||
| chr7:95521152 | T | C | 9 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0024 others(6): Show |
9 | HG00741.hp2 HG02647.hp2 HG02698.hp2 others(6): Show |
intron_variant | MODIFIER | c.488-6661T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95521152 | |||||||
| chr7:95521274 | A | C | 1 | a0001c0001t0001g0192 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.488-6539A>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95521274 | |||||||
| chr7:95521493 | T | C | 1 | a0001c0001t0010g0017 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.488-6320T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95521493 | |||||||
| chr7:95521501 | A | G | 3 | a0001c0001t0003g0006 a0001c0001t0003g0022 a0001c0001t0003g0096 |
4 | HG01255.hp2 HG01256.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.488-6312A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95521501 | |||||||
| chr7:95521686 | T | TA | 48 | a0001c0001t0001g0093 a0001c0001t0001g0100 a0001c0001t0001g0106 others(45): Show |
51 | HG00438.hp2 HG00639.hp1 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.488-6114dupA | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95521686 | ||||||
| chr7:95521686 | TA | T | 192 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(189): Show |
201 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.488-6114delA | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95521686 | ||||||
| chr7:95521686 | TAA | T | 8 | a0001c0001t0001g0201 a0001c0001t0001g0240 a0001c0001t0003g0126 others(5): Show |
8 | HG01099.hp2 HG01167.hp1 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.488-6115_488-6114d others(4): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95521686 | ||||||
| chr7:95521796 | A | AT | 43 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0024 others(40): Show |
44 | HG00438.hp2 HG00621.hp1 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.488-6011dupT | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95521796 | ||||||
| chr7:95521818 | T | C | 9 | a0001c0001t0004g0031 a0001c0001t0005g0012 a0001c0001t0005g0032 others(6): Show |
10 | HG00639.hp1 HG01891.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.488-5995T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95521818 | |||||||
| chr7:95521857 | A | C | 1 | a0001c0001t0005g0369 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.488-5956A>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95521857 | |||||||
| chr7:95521899 | A | G | 1 | a0001c0001t0010g0047 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.488-5914A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95521899 | |||||||
| chr7:95521979 | T | C | 3 | a0001c0001t0002g0075 a0001c0001t0002g0076 a0001c0001t0002g0082 |
3 | HG02257.hp2 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.488-5834T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95521979 | |||||||
| chr7:95522064 | T | C | 2 | a0001c0001t0015g0315 a0004c0003t0015g0059 |
2 | HG02717.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.488-5749T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95522064 | |||||||
| chr7:95522275 | T | C | 1 | a0001c0001t0001g0106 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.488-5538T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95522275 | |||||||
| chr7:95522314 | G | T | 1 | a0001c0001t0001g0203 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.488-5499G>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95522314 | |||||||
| chr7:95522321 | G | A | 6 | a0001c0001t0001g0185 a0001c0001t0009g0183 a0001c0001t0009g0184 others(3): Show |
6 | HG01192.hp1 HG01358.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.488-5492G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95522321 | |||||||
| chr7:95522326 | G | A | 1 | a0001c0001t0002g0154 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.488-5487G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95522326 | |||||||
| chr7:95522345 | A | G | 9 | a0001c0001t0004g0031 a0001c0001t0005g0012 a0001c0001t0005g0032 others(6): Show |
10 | HG00639.hp1 HG01891.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.488-5468A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95522345 | |||||||
| chr7:95522400 | AAAT | A | 70 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(67): Show |
76 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.488-5408_488-5406d others(5): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95522400 | ||||||
| chr7:95522611 | G | C | 9 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0024 others(6): Show |
9 | HG00741.hp2 HG02647.hp2 HG02698.hp2 others(6): Show |
intron_variant | MODIFIER | c.488-5202G>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95522611 | |||||||
| chr7:95522625 | T | C | 6 | a0001c0001t0003g0304 a0001c0001t0004g0030 a0001c0001t0004g0090 others(3): Show |
6 | HG01192.hp2 HG02451.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.488-5188T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95522625 | |||||||
| chr7:95522627 | T | C | 38 | a0001c0001t0001g0209 a0001c0001t0001g0217 a0001c0001t0001g0218 others(35): Show |
38 | HG00140.hp2 HG00597.hp1 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.488-5186T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95522627 | |||||||
| chr7:95522638 | C | G | 1 | a0001c0001t0008g0206 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.488-5175C>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95522638 | |||||||
| chr7:95522885 | T | C | 6 | a0001c0001t0003g0304 a0001c0001t0004g0030 a0001c0001t0004g0090 others(3): Show |
6 | HG01192.hp2 HG02451.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.488-4928T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95522885 | |||||||
| chr7:95523068 | A | G | 1 | a0001c0001t0001g0240 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.488-4745A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95523068 | |||||||
| chr7:95523631 | T | C | 1 | a0001c0001t0003g0095 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.488-4182T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95523631 | |||||||
| chr7:95523725 | T | A | 39 | a0001c0001t0001g0310 a0001c0001t0002g0002 a0001c0001t0002g0009 others(36): Show |
42 | HG00423.hp1 HG00738.hp2 HG01496.hp1 others(39): Show |
intron_variant | MODIFIER | c.488-4088T>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95523725 | |||||||
| chr7:95523748 | A | C | 3 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0024 |
3 | HG02698.hp2 HG03710.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.488-4065A>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95523748 | |||||||
| chr7:95523866 | A | G | 1 | a0001c0001t0003g0351 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.488-3947A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95523866 | |||||||
| chr7:95523870 | T | C | 6 | a0001c0001t0001g0185 a0001c0001t0009g0183 a0001c0001t0009g0184 others(3): Show |
6 | HG01192.hp1 HG01358.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.488-3943T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95523870 | |||||||
| chr7:95523947 | C | T | 1 | a0001c0001t0010g0047 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.488-3866C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95523947 | |||||||
| chr7:95523959 | G | C | 169 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(166): Show |
179 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(176): Show |
intron_variant | MODIFIER | c.488-3854G>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95523959 | |||||||
| chr7:95523983 | G | A | 2 | a0001c0001t0015g0315 a0004c0003t0015g0059 |
2 | HG02717.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.488-3830G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95523983 | |||||||
| chr7:95524006 | A | G | 5 | a0001c0001t0002g0122 a0001c0001t0002g0135 a0001c0001t0002g0139 others(2): Show |
5 | NA18974.hp1 NA18993.hp1 NA19059.hp1 others(2): Show |
intron_variant | MODIFIER | c.488-3807A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95524006 | |||||||
| chr7:95524015 | A | G | 6 | a0001c0001t0001g0185 a0001c0001t0009g0183 a0001c0001t0009g0184 others(3): Show |
6 | HG01192.hp1 HG01358.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.488-3798A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95524015 | |||||||
| chr7:95524062 | C | T | 1 | a0001c0001t0002g0156 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.488-3751C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95524062 | |||||||
| chr7:95524137 | G | A | 1 | a0001c0001t0010g0047 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.488-3676G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95524137 | |||||||
| chr7:95524150 | T | C | 167 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(164): Show |
177 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(174): Show |
intron_variant | MODIFIER | c.488-3663T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95524150 | |||||||
| chr7:95524168 | A | G | 1 | a0003c0005t0001g0345 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.488-3645A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95524168 | |||||||
| chr7:95524240 | A | G | 161 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(158): Show |
171 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(168): Show |
intron_variant | MODIFIER | c.488-3573A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95524240 | |||||||
| chr7:95524327 | A | G | 1 | a0001c0001t0005g0369 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.488-3486A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95524327 | |||||||
| chr7:95524373 | A | G | 1 | a0001c0001t0001g0146 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.488-3440A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95524373 | |||||||
| chr7:95524498 | TA | T | 166 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(163): Show |
176 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(173): Show |
intron_variant | MODIFIER | c.488-3307delA | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95524498 | ||||||
| chr7:95524513 | A | G | 6 | a0001c0001t0003g0304 a0001c0001t0004g0030 a0001c0001t0004g0090 others(3): Show |
6 | HG01192.hp2 HG02451.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.488-3300A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95524513 | |||||||
| chr7:95524537 | C | G | 1 | a0001c0001t0003g0058 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.488-3276C>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95524537 | |||||||
| chr7:95524551 | T | C | 3 | a0001c0001t0008g0027 a0001c0001t0008g0206 a0001c0001t0008g0297 |
3 | HG03195.hp1 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.488-3262T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95524551 | |||||||
| chr7:95524562 | T | C | 5 | a0001c0001t0004g0030 a0001c0001t0004g0090 a0001c0001t0010g0028 others(2): Show |
5 | HG02451.hp1 HG02723.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.488-3251T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95524562 | |||||||
| chr7:95524697 | G | A | 1 | a0001c0001t0002g0142 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.488-3116G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95524697 | |||||||
| chr7:95524843 | G | T | 3 | a0001c0001t0008g0027 a0001c0001t0008g0206 a0001c0001t0008g0297 |
3 | HG03195.hp1 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.488-2970G>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95524843 | |||||||
| chr7:95524906 | C | T | 6 | a0001c0001t0001g0185 a0001c0001t0009g0183 a0001c0001t0009g0184 others(3): Show |
6 | HG01192.hp1 HG01358.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.488-2907C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95524906 | |||||||
| chr7:95525015 | C | T | 41 | a0001c0001t0001g0310 a0001c0001t0002g0002 a0001c0001t0002g0009 others(38): Show |
44 | HG00423.hp1 HG00738.hp2 HG01496.hp1 others(41): Show |
intron_variant | MODIFIER | c.488-2798C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95525015 | |||||||
| chr7:95525139 | T | G | 42 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0024 others(39): Show |
43 | HG00438.hp2 HG00621.hp1 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.488-2674T>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95525139 | |||||||
| chr7:95525217 | C | T | 1 | a0001c0001t0015g0315 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.488-2596C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95525217 | |||||||
| chr7:95525218 | A | G | 39 | a0001c0001t0001g0310 a0001c0001t0002g0002 a0001c0001t0002g0009 others(36): Show |
42 | HG00423.hp1 HG00738.hp2 HG01496.hp1 others(39): Show |
intron_variant | MODIFIER | c.488-2595A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95525218 | |||||||
| chr7:95525369 | G | A | 1 | a0001c0001t0005g0033 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.488-2444G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95525369 | |||||||
| chr7:95525370 | T | C | 3 | a0001c0001t0004g0114 a0001c0001t0004g0213 a0001c0001t0004g0214 |
3 | HG01891.hp2 HG02886.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.488-2443T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95525370 | |||||||
| chr7:95525383 | T | C | 9 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0024 others(6): Show |
9 | HG00741.hp2 HG02647.hp2 HG02698.hp2 others(6): Show |
intron_variant | MODIFIER | c.488-2430T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95525383 | |||||||
| chr7:95525474 | G | A | 1 | a0001c0001t0020g0026 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.488-2339G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95525474 | |||||||
| chr7:95525515 | A | C | 1 | a0002c0002t0011g0038 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.488-2298A>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95525515 | |||||||
| chr7:95525649 | C | G | 9 | a0001c0001t0004g0031 a0001c0001t0005g0012 a0001c0001t0005g0032 others(6): Show |
10 | HG00639.hp1 HG01891.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.488-2164C>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95525649 | |||||||
| chr7:95525733 | A | G | 1 | a0001c0001t0002g0207 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.488-2080A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95525733 | |||||||
| chr7:95525812 | A | G | 142 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(139): Show |
151 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.488-2001A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95525812 | |||||||
| chr7:95525882 | A | T | 1 | a0001c0001t0001g0067 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.488-1931A>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95525882 | |||||||
| chr7:95525894 | G | A | 1 | a0001c0001t0001g0337 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.488-1919G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95525894 | |||||||
| chr7:95525944 | G | A | 1 | a0001c0001t0001g0229 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.488-1869G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95525944 | |||||||
| chr7:95526025 | C | T | 1 | a0001c0001t0005g0369 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.488-1788C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95526025 | |||||||
| chr7:95526026 | G | A | 36 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0013 others(33): Show |
39 | HG00408.hp2 HG00609.hp2 HG01261.hp2 others(36): Show |
intron_variant | MODIFIER | c.488-1787G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95526026 | |||||||
| chr7:95526154 | T | A | 6 | a0001c0001t0003g0304 a0001c0001t0004g0030 a0001c0001t0004g0090 others(3): Show |
6 | HG01192.hp2 HG02451.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.488-1659T>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95526154 | |||||||
| chr7:95526218 | C | T | 9 | a0001c0001t0004g0031 a0001c0001t0005g0012 a0001c0001t0005g0032 others(6): Show |
10 | HG00639.hp1 HG01891.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.488-1595C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95526218 | |||||||
| chr7:95526447 | C | T | 2 | a0001c0001t0015g0315 a0004c0003t0015g0059 |
2 | HG02717.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.488-1366C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95526447 | |||||||
| chr7:95526454 | TCATA | T | 55 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0024 others(52): Show |
56 | HG00438.hp2 HG00621.hp1 HG00639.hp1 others(53): Show |
intron_variant | MODIFIER | c.488-1353_488-1350d others(6): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95526454 | ||||||
| chr7:95526466 | T | G | 112 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(109): Show |
121 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.488-1347T>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95526466 | |||||||
| chr7:95526598 | G | A | 1 | a0001c0001t0002g0052 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.488-1215G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95526598 | |||||||
| chr7:95526950 | C | A | 3 | a0001c0001t0005g0012 a0001c0001t0005g0271 a0001c0001t0005g0276 |
4 | HG01891.hp1 HG02109.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.488-863C>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95526950 | |||||||
| chr7:95527022 | T | A | 3 | a0001c0001t0005g0012 a0001c0001t0005g0271 a0001c0001t0005g0276 |
4 | HG01891.hp1 HG02109.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.488-791T>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95527022 | |||||||
| chr7:95527064 | T | A | 2 | a0001c0001t0004g0030 a0001c0001t0004g0090 |
2 | HG02451.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.488-749T>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95527064 | |||||||
| chr7:95527111 | T | C | 6 | a0001c0001t0003g0304 a0001c0001t0004g0030 a0001c0001t0004g0090 others(3): Show |
6 | HG01192.hp2 HG02451.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.488-702T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95527111 | |||||||
| chr7:95527233 | G | C | 8 | a0001c0001t0004g0031 a0001c0001t0005g0012 a0001c0001t0005g0032 others(5): Show |
9 | HG00639.hp1 HG01891.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.488-580G>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95527233 | |||||||
| chr7:95527433 | C | T | 9 | a0001c0001t0004g0031 a0001c0001t0005g0012 a0001c0001t0005g0032 others(6): Show |
10 | HG00639.hp1 HG01891.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.488-380C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95527433 | |||||||
| chr7:95527472 | T | C | 5 | a0001c0001t0004g0031 a0001c0001t0005g0032 a0001c0001t0005g0033 others(2): Show |
5 | HG00639.hp1 HG02055.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.488-341T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95527472 | |||||||
| chr7:95527557 | C | CT | 6 | a0001c0001t0007g0363 a0001c0001t0008g0027 a0001c0001t0008g0206 others(3): Show |
6 | HG02717.hp1 HG02922.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.488-256_488-255ins others(1): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95527557 | |||||||
| chr7:95528353 | C | T | 3 | a0001c0001t0002g0135 a0001c0001t0002g0139 a0001c0001t0002g0151 |
3 | NA18974.hp1 NA18993.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.978+50C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95528353 | |||||||
| chr7:95528406 | C | T | 7 | a0001c0001t0001g0035 a0001c0001t0004g0031 a0001c0001t0005g0032 others(4): Show |
7 | HG00639.hp1 HG02055.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.978+103C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95528406 | |||||||
| chr7:95528558 | C | A | 39 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0025 others(36): Show |
42 | HG00423.hp1 HG01081.hp2 HG01496.hp1 others(39): Show |
intron_variant | MODIFIER | c.978+255C>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95528558 | |||||||
| chr7:95528623 | G | A | 22 | a0001c0001t0001g0285 a0001c0001t0004g0091 a0001c0001t0004g0092 others(19): Show |
22 | HG00621.hp1 HG00735.hp2 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.978+320G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95528623 | |||||||
| chr7:95528659 | T | C | 1 | a0001c0001t0001g0334 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.978+356T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95528659 | |||||||
| chr7:95528670 | C | T | 4 | a0001c0001t0010g0028 a0001c0001t0010g0029 a0001c0001t0010g0047 others(1): Show |
4 | HG02896.hp1 HG02897.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.978+367C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95528670 | |||||||
| chr7:95528693 | T | C | 3 | a0001c0001t0012g0197 a0001c0001t0012g0198 a0001c0001t0012g0199 |
3 | HG01257.hp1 HG01258.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.978+390T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95528693 | |||||||
| chr7:95528988 | G | A | 7 | a0001c0001t0001g0035 a0001c0001t0004g0031 a0001c0001t0005g0032 others(4): Show |
7 | HG00639.hp1 HG02055.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.978+685G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95528988 | |||||||
| chr7:95529071 | C | T | 1 | a0001c0001t0002g0175 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.978+768C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95529071 | |||||||
| chr7:95529142 | T | C | 3 | a0001c0001t0008g0027 a0001c0001t0008g0206 a0001c0001t0008g0297 |
3 | HG03195.hp1 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.978+839T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95529142 | |||||||
| chr7:95529221 | T | A | 4 | a0001c0001t0003g0366 a0001c0001t0011g0367 a0001c0001t0011g0368 others(1): Show |
4 | HG02818.hp1 HG02886.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.978+918T>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95529221 | |||||||
| chr7:95529258 | A | C | 1 | a0001c0001t0012g0198 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.978+955A>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95529258 | |||||||
| chr7:95529398 | G | A | 22 | a0001c0001t0001g0285 a0001c0001t0004g0091 a0001c0001t0004g0092 others(19): Show |
22 | HG00621.hp1 HG00735.hp2 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.978+1095G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95529398 | |||||||
| chr7:95529423 | G | A | 1 | a0001c0001t0025g0228 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.978+1120G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95529423 | |||||||
| chr7:95529542 | T | C | 22 | a0001c0001t0001g0285 a0001c0001t0004g0091 a0001c0001t0004g0092 others(19): Show |
22 | HG00621.hp1 HG00735.hp2 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.978+1239T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95529542 | |||||||
| chr7:95529554 | T | A | 1 | a0001c0001t0002g0153 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.978+1251T>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95529554 | |||||||
| chr7:95529641 | A | T | 30 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0035 others(27): Show |
31 | HG00639.hp1 HG00741.hp2 HG01192.hp1 others(28): Show |
intron_variant | MODIFIER | c.978+1338A>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95529641 | |||||||
| chr7:95529651 | A | G | 4 | a0001c0001t0010g0028 a0001c0001t0010g0029 a0001c0001t0010g0047 others(1): Show |
4 | HG02896.hp1 HG02897.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.978+1348A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95529651 | |||||||
| chr7:95529706 | G | T | 57 | a0001c0001t0001g0001 a0001c0001t0001g0054 a0001c0001t0001g0055 others(54): Show |
61 | HG00280.hp2 HG00323.hp2 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.978+1403G>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95529706 | |||||||
| chr7:95529806 | G | A | 320 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(317): Show |
338 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(335): Show |
intron_variant | MODIFIER | c.978+1503G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95529806 | |||||||
| chr7:95529869 | G | A | 11 | a0001c0001t0001g0035 a0001c0001t0004g0031 a0001c0001t0005g0012 others(8): Show |
12 | HG00639.hp1 HG01891.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.978+1566G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95529869 | |||||||
| chr7:95529998 | C | A | 3 | a0001c0001t0003g0366 a0001c0001t0011g0367 a0002c0002t0011g0038 |
3 | HG02818.hp1 HG02886.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.978+1695C>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95529998 | |||||||
| chr7:95530009 | A | G | 3 | a0001c0001t0012g0197 a0001c0001t0012g0198 a0001c0001t0012g0199 |
3 | HG01257.hp1 HG01258.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.978+1706A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95530009 | |||||||
| chr7:95530038 | A | C | 1 | a0001c0001t0003g0364 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.978+1735A>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95530038 | |||||||
| chr7:95530062 | A | G | 5 | a0001c0001t0009g0183 a0001c0001t0009g0184 a0001c0001t0009g0186 others(2): Show |
5 | HG01192.hp1 HG01358.hp1 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.978+1759A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95530062 | |||||||
| chr7:95530105 | C | CA | 12 | a0001c0001t0001g0093 a0001c0001t0001g0129 a0001c0001t0001g0321 others(9): Show |
12 | HG01433.hp2 HG01884.hp2 HG01928.hp2 others(9): Show |
intron_variant | MODIFIER | c.978+1817dupA | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr7 | 95530105 | ||||||
| chr7:95530105 | C | CAAAAA | 7 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0002g0295 others(4): Show |
7 | HG00741.hp2 HG02647.hp2 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.978+1813_978+1817d others(7): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr7 | 95530105 | ||||||
| chr7:95530105 | C | CAAAAAA | 20 | a0001c0001t0001g0035 a0001c0001t0001g0189 a0001c0001t0001g0190 others(17): Show |
21 | HG00639.hp1 HG01257.hp1 HG01258.hp1 others(18): Show |
intron_variant | MODIFIER | c.978+1812_978+1817d others(8): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr7 | 95530105 | ||||||
| chr7:95530105 | C | CAAAAAAA | 26 | a0001c0001t0001g0100 a0001c0001t0001g0106 a0001c0001t0001g0166 others(23): Show |
26 | HG00438.hp2 HG01192.hp1 HG01358.hp1 others(23): Show |
intron_variant | MODIFIER | c.978+1811_978+1817d others(9): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr7 | 95530105 | ||||||
| chr7:95530105 | C | CAAAAAAA others(1): Show |
146 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(143): Show |
156 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.978+1810_978+1817d others(10): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr7 | 95530105 | ||||||
| chr7:95530105 | C | CAAAAAAA others(2): Show |
6 | a0001c0001t0001g0185 a0001c0001t0001g0223 a0001c0001t0001g0245 others(3): Show |
6 | HG00621.hp2 HG01261.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.978+1809_978+1817d others(11): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr7 | 95530105 | ||||||
| chr7:95530372 | G | C | 11 | a0001c0001t0001g0035 a0001c0001t0004g0031 a0001c0001t0005g0012 others(8): Show |
12 | HG00639.hp1 HG01891.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.978+2069G>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95530372 | |||||||
| chr7:95530451 | C | A | 16 | a0001c0001t0004g0114 a0001c0001t0004g0210 a0001c0001t0004g0213 others(13): Show |
16 | HG01891.hp2 HG02280.hp2 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.978+2148C>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95530451 | |||||||
| chr7:95530479 | A | G | 21 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0035 others(18): Show |
22 | HG00639.hp1 HG00741.hp2 HG01257.hp1 others(19): Show |
intron_variant | MODIFIER | c.978+2176A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95530479 | |||||||
| chr7:95530555 | T | C | 1 | a0001c0001t0004g0030 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.978+2252T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95530555 | |||||||
| chr7:95530561 | G | A | 1 | a0001c0001t0001g0310 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.978+2258G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95530561 | |||||||
| chr7:95530940 | T | C | 4 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0056 others(1): Show |
4 | HG02040.hp2 NA18954.hp2 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.978+2637T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95530940 | |||||||
| chr7:95530995 | G | A | 57 | a0001c0001t0001g0001 a0001c0001t0001g0054 a0001c0001t0001g0055 others(54): Show |
61 | HG00280.hp2 HG00323.hp2 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.978+2692G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95530995 | |||||||
| chr7:95531284 | G | C | 1 | a0001c0001t0014g0311 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.978+2981G>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95531284 | |||||||
| chr7:95531334 | C | G | 148 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(145): Show |
158 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.978+3031C>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95531334 | |||||||
| chr7:95531541 | C | T | 56 | a0001c0001t0001g0001 a0001c0001t0001g0054 a0001c0001t0001g0055 others(53): Show |
60 | HG00280.hp2 HG00323.hp2 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.978+3238C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95531541 | |||||||
| chr7:95531693 | C | T | 1 | a0001c0001t0003g0095 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.978+3390C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95531693 | |||||||
| chr7:95531893 | T | C | 1 | a0001c0001t0001g0332 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.978+3590T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95531893 | |||||||
| chr7:95531990 | T | C | 2 | a0002c0002t0004g0036 a0002c0002t0004g0037 |
2 | HG02486.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.978+3687T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95531990 | |||||||
| chr7:95532013 | G | A | 3 | a0001c0001t0003g0006 a0001c0001t0003g0022 a0001c0001t0003g0096 |
4 | HG01255.hp2 HG01256.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.978+3710G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95532013 | |||||||
| chr7:95532039 | G | A | 5 | a0001c0001t0004g0020 a0001c0001t0004g0021 a0001c0001t0012g0197 others(2): Show |
5 | HG01257.hp1 HG01258.hp1 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.978+3736G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95532039 | |||||||
| chr7:95532108 | A | G | 1 | a0001c0001t0001g0178 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.978+3805A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95532108 | |||||||
| chr7:95532133 | G | A | 2 | a0001c0001t0003g0126 a0001c0001t0003g0127 |
2 | NA18999.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.978+3830G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95532133 | |||||||
| chr7:95532160 | C | T | 3 | a0001c0001t0001g0332 a0002c0002t0006g0039 a0002c0002t0006g0040 |
3 | HG01981.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.978+3857C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95532160 | |||||||
| chr7:95532341 | C | T | 90 | a0001c0001t0001g0001 a0001c0001t0001g0054 a0001c0001t0001g0055 others(87): Show |
96 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.978+4038C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95532341 | |||||||
| chr7:95532348 | A | G | 22 | a0001c0001t0001g0285 a0001c0001t0004g0091 a0001c0001t0004g0092 others(19): Show |
22 | HG00621.hp1 HG00735.hp2 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.978+4045A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95532348 | |||||||
| chr7:95532417 | C | T | 1 | a0001c0001t0007g0363 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.979-4020C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95532417 | |||||||
| chr7:95532418 | G | A | 2 | a0001c0001t0001g0259 a0001c0001t0005g0276 |
2 | HG01891.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.979-4019G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95532418 | |||||||
| chr7:95532510 | C | T | 3 | a0001c0001t0012g0197 a0001c0001t0012g0198 a0001c0001t0012g0199 |
3 | HG01257.hp1 HG01258.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.979-3927C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95532510 | |||||||
| chr7:95532511 | G | A | 13 | a0001c0001t0004g0031 a0001c0001t0004g0312 a0001c0001t0004g0313 others(10): Show |
13 | HG00639.hp1 HG01884.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.979-3926G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95532511 | |||||||
| chr7:95532517 | C | T | 325 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(322): Show |
343 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(340): Show |
intron_variant | MODIFIER | c.979-3920C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95532517 | |||||||
| chr7:95532698 | A | G | 324 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(321): Show |
342 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(339): Show |
intron_variant | MODIFIER | c.979-3739A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95532698 | |||||||
| chr7:95532725 | G | T | 154 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(151): Show |
164 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.979-3712G>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95532725 | |||||||
| chr7:95532951 | C | T | 5 | a0001c0001t0008g0027 a0001c0001t0008g0206 a0001c0001t0008g0212 others(2): Show |
5 | HG02280.hp2 HG02922.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.979-3486C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95532951 | |||||||
| chr7:95533175 | A | G | 3 | a0001c0001t0001g0069 a0001c0001t0001g0340 a0001c0001t0001g0344 |
3 | HG00280.hp2 HG03927.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.979-3262A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95533175 | |||||||
| chr7:95533345 | A | T | 1 | a0003c0005t0001g0345 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.979-3092A>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95533345 | |||||||
| chr7:95533347 | G | A | 1 | a0001c0001t0007g0319 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.979-3090G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95533347 | |||||||
| chr7:95533366 | C | T | 1 | a0001c0001t0005g0369 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.979-3071C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95533366 | |||||||
| chr7:95533400 | C | G | 1 | a0001c0001t0001g0182 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.979-3037C>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95533400 | |||||||
| chr7:95533505 | A | G | 1 | a0001c0001t0002g0016 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.979-2932A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95533505 | |||||||
| chr7:95533557 | T | A | 2 | a0001c0001t0001g0125 a0001c0001t0001g0141 |
2 | NA18955.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.979-2880T>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95533557 | |||||||
| chr7:95533562 | A | G | 2 | a0001c0001t0008g0212 a0001c0001t0008g0291 |
2 | HG02280.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.979-2875A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95533562 | |||||||
| chr7:95533566 | C | T | 3 | a0001c0001t0011g0367 a0001c0001t0011g0368 a0002c0002t0011g0038 |
3 | HG02818.hp1 HG02886.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.979-2871C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95533566 | |||||||
| chr7:95533601 | T | C | 154 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(151): Show |
164 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.979-2836T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95533601 | |||||||
| chr7:95533696 | A | G | 1 | a0001c0001t0001g0280 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.979-2741A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95533696 | |||||||
| chr7:95533883 | G | A | 27 | a0001c0001t0001g0285 a0001c0001t0004g0020 a0001c0001t0004g0021 others(24): Show |
27 | HG00621.hp1 HG00735.hp2 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.979-2554G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95533883 | |||||||
| chr7:95533889 | A | G | 1 | a0001c0001t0004g0090 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.979-2548A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95533889 | |||||||
| chr7:95533921 | T | C | 1 | a0001c0001t0004g0318 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.979-2516T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95533921 | |||||||
| chr7:95534029 | G | A | 3 | a0001c0001t0005g0194 a0001c0001t0005g0272 a0001c0001t0005g0294 |
3 | HG02559.hp1 HG02965.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.979-2408G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95534029 | |||||||
| chr7:95534070 | C | T | 1 | a0001c0001t0001g0286 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.979-2367C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95534070 | |||||||
| chr7:95534071 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.979-2366G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95534071 | |||||||
| chr7:95534072 | C | CGGTGGCC others(1): Show |
22 | a0001c0001t0001g0285 a0001c0001t0004g0091 a0001c0001t0004g0092 others(19): Show |
22 | HG00621.hp1 HG00735.hp2 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.979-2359_979-2358i others(10): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr7 | 95534072 | ||||||
| chr7:95534073 | G | A | 6 | a0001c0001t0007g0208 a0001c0001t0007g0211 a0001c0001t0007g0269 others(3): Show |
6 | HG02615.hp1 HG02818.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.979-2364G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95534073 | |||||||
| chr7:95534174 | G | A | 7 | a0001c0001t0010g0028 a0001c0001t0010g0029 a0001c0001t0010g0047 others(4): Show |
7 | HG02818.hp1 HG02886.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.979-2263G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95534174 | |||||||
| chr7:95534206 | G | A | 107 | a0001c0001t0001g0001 a0001c0001t0001g0054 a0001c0001t0001g0055 others(104): Show |
114 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.979-2231G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95534206 | |||||||
| chr7:95534304 | T | C | 3 | a0001c0001t0002g0075 a0001c0001t0002g0076 a0001c0001t0002g0082 |
3 | HG02257.hp2 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.979-2133T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95534304 | |||||||
| chr7:95534328 | C | T | 2 | a0001c0001t0001g0243 a0001c0001t0001g0246 |
2 | NA18747.hp2 NA18945.hp2 |
intron_variant | MODIFIER | c.979-2109C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95534328 | |||||||
| chr7:95534341 | T | TA | 7 | a0001c0001t0001g0336 a0001c0001t0003g0049 a0001c0001t0003g0058 others(4): Show |
7 | HG02258.hp2 HG02559.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.979-2084dupA | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr7 | 95534341 | ||||||
| chr7:95534341 | TA | T | 159 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(156): Show |
169 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.979-2084delA | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr7 | 95534341 | ||||||
| chr7:95534571 | C | T | 7 | a0001c0001t0010g0028 a0001c0001t0010g0029 a0001c0001t0010g0047 others(4): Show |
7 | HG02818.hp1 HG02886.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.979-1866C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95534571 | |||||||
| chr7:95534699 | C | T | 1 | a0001c0001t0025g0228 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.979-1738C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95534699 | |||||||
| chr7:95534753 | C | T | 1 | a0001c0001t0005g0272 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.979-1684C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95534753 | |||||||
| chr7:95534767 | G | C | 152 | a0001c0001t0001g0001 a0001c0001t0001g0054 a0001c0001t0001g0055 others(149): Show |
160 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(157): Show |
intron_variant | MODIFIER | c.979-1670G>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95534767 | |||||||
| chr7:95534894 | A | T | 3 | a0001c0001t0004g0030 a0001c0001t0004g0090 a0002c0002t0003g0317 |
3 | HG02451.hp1 HG02572.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.979-1543A>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95534894 | |||||||
| chr7:95534965 | C | T | 39 | a0001c0001t0001g0285 a0001c0001t0004g0020 a0001c0001t0004g0021 others(36): Show |
40 | HG00621.hp1 HG00735.hp2 HG01243.hp2 others(37): Show |
intron_variant | MODIFIER | c.979-1472C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95534965 | |||||||
| chr7:95535021 | C | T | 1 | a0001c0001t0004g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.979-1416C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95535021 | |||||||
| chr7:95535067 | T | C | 1 | a0001c0001t0003g0351 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.979-1370T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95535067 | |||||||
| chr7:95535084 | G | C | 2 | a0001c0001t0016g0267 a0001c0001t0016g0281 |
2 | HG03490.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.979-1353G>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95535084 | |||||||
| chr7:95535101 | G | T | 1 | a0001c0001t0001g0322 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.979-1336G>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95535101 | |||||||
| chr7:95535132 | C | G | 2 | a0001c0001t0004g0020 a0001c0001t0004g0021 |
2 | HG03704.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.979-1305C>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95535132 | |||||||
| chr7:95535145 | G | T | 2 | a0001c0001t0013g0101 a0001c0001t0013g0107 |
2 | HG01261.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.979-1292G>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95535145 | |||||||
| chr7:95535327 | G | A | 1 | a0001c0001t0004g0085 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.979-1110G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95535327 | |||||||
| chr7:95535360 | T | C | 2 | a0001c0001t0014g0117 a0001c0001t0014g0311 |
2 | HG01884.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.979-1077T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95535360 | |||||||
| chr7:95535419 | TGATTTAT others(7): Show |
T | 30 | a0001c0001t0004g0020 a0001c0001t0004g0021 a0001c0001t0004g0091 others(27): Show |
30 | HG00621.hp1 HG00735.hp2 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.979-1015_979-1002d others(16): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr7 | 95535419 | ||||||
| chr7:95535435 | A | T | 1 | a0001c0001t0001g0226 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.979-1002A>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95535435 | |||||||
| chr7:95535595 | G | A | 149 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(146): Show |
159 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.979-842G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95535595 | |||||||
| chr7:95535659 | G | T | 149 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(146): Show |
159 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.979-778G>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95535659 | |||||||
| chr7:95535962 | C | T | 101 | a0001c0001t0001g0001 a0001c0001t0001g0054 a0001c0001t0001g0055 others(98): Show |
107 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.979-475C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95535962 | |||||||
| chr7:95536258 | C | A | 1 | a0001c0001t0004g0097 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.979-179C>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95536258 | |||||||
| chr7:95536585 | A | G | 1 | a0001c0001t0007g0211 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1092+35A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 4/4 | chr7 | 95536585 | |||||||
| chr7:95536661 | G | A | 10 | a0001c0001t0006g0136 a0001c0001t0006g0158 a0001c0001t0006g0268 others(7): Show |
11 | HG00738.hp2 HG01884.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.1092+111G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 4/4 | chr7 | 95536661 | |||||||
| chr7:95536842 | C | G | 1 | a0001c0001t0001g0289 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1092+292C>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 4/4 | chr7 | 95536842 | |||||||
| chr7:95536910 | C | T | 1 | a0001c0001t0002g0082 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1092+360C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 4/4 | chr7 | 95536910 | |||||||
| chr7:95537038 | A | G | 1 | a0001c0001t0001g0277 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1092+488A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 4/4 | chr7 | 95537038 | |||||||
| chr7:95537123 | G | A | 1 | a0002c0002t0006g0361 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1093-448G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 4/4 | chr7 | 95537123 | |||||||
| chr7:95537124 | G | A | 12 | a0001c0001t0005g0012 a0001c0001t0005g0032 a0001c0001t0005g0033 others(9): Show |
13 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1093-447G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 4/4 | chr7 | 95537124 | |||||||
| chr7:95537254 | C | A | 28 | a0001c0001t0004g0020 a0001c0001t0004g0021 a0001c0001t0004g0091 others(25): Show |
28 | HG00621.hp1 HG00735.hp2 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.1093-317C>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 4/4 | chr7 | 95537254 |