Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 55364 |
| ensemblid | ENSG00000154059.11 |
| hgncid | 20387 |
| symbol | IMPACT |
| name | impact RWD domain protein |
| refseq_nuc | NM_018439.4 |
| refseq_prot | NP_060909.2 |
| ensembl_nuc | ENST00000284202.9 |
| ensembl_prot | ENSP00000284202.4 |
| mane_status | MANE Select |
| chr | chr18 |
| start | 24426670 |
| end | 24453531 |
| strand | + |
| ver | v1.2 |
| region | chr18:24426670-24453531 |
| region5000 | chr18:24421670-24458531 |
| regionname0 | IMPACT_chr18_24426670_24453531 |
| regionname5000 | IMPACT_chr18_24421670_24458531 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 320 | 308 | 88 | 61 | 120 | 12 | 27 | 92 | IMPACT_chr18_24421670_24458531 | IMPACT | MAEGD others(315): Show |
chr18 | 24421670 | 24458531 |
| a0002 | 1/1 | 320 | 69 | 3 | 1 | 58 | 0 | 5 | 42 | IMPACT_chr18_24421670_24458531 | IMPACT | MAEGD others(315): Show |
chr18 | 24421670 | 24458531 |
| a0003 | 0/0 | 320 | 21 | 3 | 9 | 1 | 2 | 6 | 1 | IMPACT_chr18_24421670_24458531 | IMPACT | MAEGD others(315): Show |
chr18 | 24421670 | 24458531 |
| a0004 | 0/0 | 320 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | MAEGD others(315): Show |
chr18 | 24421670 | 24458531 |
| a0005 | 0/0 | 320 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | MAEGD others(315): Show |
chr18 | 24421670 | 24458531 |
| a0006 | 0/0 | 320 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | MAEGD others(315): Show |
chr18 | 24421670 | 24458531 |
| a0007 | 0/0 | 268 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | IMPACT_chr18_24421670_24458531 | IMPACT | MAEGD others(263): Show |
chr18 | 24421670 | 24458531 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 960 | 307 | 87 | 61 | 120 | 12 | 27 | IMPACT_chr18_24421670_24458531 | IMPACT | ATGGC others(955): Show |
chr18 | 24421670 | 24458531 | ||
| a0001c0004 | 0/0 | 960 | 1 | 1 | 0 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | ATGGC others(955): Show |
chr18 | 24421670 | 24458531 | ||
| a0002c0002 | 1/1 | 960 | 69 | 3 | 1 | 58 | 0 | 5 | IMPACT_chr18_24421670_24458531 | IMPACT | ATGGC others(955): Show |
chr18 | 24421670 | 24458531 | ||
| a0003c0003 | 0/0 | 960 | 21 | 3 | 9 | 1 | 2 | 6 | IMPACT_chr18_24421670_24458531 | IMPACT | ATGGC others(955): Show |
chr18 | 24421670 | 24458531 | ||
| a0004c0008 | 0/0 | 960 | 1 | 0 | 1 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | ATGGC others(955): Show |
chr18 | 24421670 | 24458531 | ||
| a0005c0007 | 0/0 | 960 | 1 | 0 | 0 | 0 | 0 | 1 | IMPACT_chr18_24421670_24458531 | IMPACT | ATGGC others(955): Show |
chr18 | 24421670 | 24458531 | ||
| a0006c0005 | 0/0 | 960 | 1 | 0 | 0 | 0 | 0 | 1 | IMPACT_chr18_24421670_24458531 | IMPACT | ATGGC others(955): Show |
chr18 | 24421670 | 24458531 | ||
| a0007c0006 | 0/0 | 960 | 1 | 0 | 0 | 1 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | ATGGC others(955): Show |
chr18 | 24421670 | 24458531 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3734 | 210 | 23 | 46 | 110 | 9 | 22 | IMPACT_chr18_24421670_24458531 | IMPACT | AGCCA others(3729): Show |
chr18 | 24421670 | 24458531 |
| a0001c0001t0002 | 0/0 | 3734 | 33 | 22 | 8 | 0 | 3 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | AGCCA others(3729): Show |
chr18 | 24421670 | 24458531 |
| a0001c0001t0004 | 0/0 | 3734 | 12 | 11 | 1 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | AGCCA others(3729): Show |
chr18 | 24421670 | 24458531 |
| a0001c0001t0005 | 0/0 | 3734 | 11 | 8 | 2 | 0 | 0 | 1 | IMPACT_chr18_24421670_24458531 | IMPACT | AGCCA others(3729): Show |
chr18 | 24421670 | 24458531 |
| a0001c0001t0006 | 0/0 | 3734 | 7 | 7 | 0 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | AGCCA others(3729): Show |
chr18 | 24421670 | 24458531 |
| a0001c0001t0007 | 0/0 | 3734 | 4 | 4 | 0 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | AGCCA others(3729): Show |
chr18 | 24421670 | 24458531 |
| a0001c0001t0008 | 0/0 | 3734 | 4 | 0 | 0 | 4 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | AGCCA others(3729): Show |
chr18 | 24421670 | 24458531 |
| a0001c0001t0009 | 0/0 | 3734 | 3 | 3 | 0 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | AGCCA others(3729): Show |
chr18 | 24421670 | 24458531 |
| a0001c0001t0010 | 0/0 | 3734 | 3 | 3 | 0 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | AGCCA others(3729): Show |
chr18 | 24421670 | 24458531 |
| a0001c0001t0011 | 0/0 | 3734 | 3 | 0 | 0 | 3 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | AGCCA others(3729): Show |
chr18 | 24421670 | 24458531 |
| a0001c0001t0013 | 0/0 | 3734 | 3 | 1 | 2 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | AGCCA others(3729): Show |
chr18 | 24421670 | 24458531 |
| a0001c0001t0015 | 0/0 | 3734 | 2 | 2 | 0 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | AGCCA others(3729): Show |
chr18 | 24421670 | 24458531 |
| a0001c0001t0016 | 0/0 | 3734 | 1 | 1 | 0 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | AGCCA others(3729): Show |
chr18 | 24421670 | 24458531 |
| a0001c0001t0017 | 0/0 | 3734 | 1 | 0 | 0 | 0 | 0 | 1 | IMPACT_chr18_24421670_24458531 | IMPACT | AGCCA others(3729): Show |
chr18 | 24421670 | 24458531 |
| a0001c0001t0018 | 0/0 | 3734 | 1 | 0 | 0 | 1 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | AGCCA others(3729): Show |
chr18 | 24421670 | 24458531 |
| a0001c0001t0020 | 0/0 | 3734 | 1 | 0 | 0 | 1 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | AGCCA others(3729): Show |
chr18 | 24421670 | 24458531 |
| a0001c0001t0021 | 0/0 | 3734 | 1 | 0 | 0 | 0 | 0 | 1 | IMPACT_chr18_24421670_24458531 | IMPACT | AGCCA others(3729): Show |
chr18 | 24421670 | 24458531 |
| a0001c0001t0022 | 0/0 | 3734 | 1 | 0 | 1 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | AGCCA others(3729): Show |
chr18 | 24421670 | 24458531 |
| a0001c0001t0023 | 0/0 | 3734 | 1 | 0 | 0 | 0 | 0 | 1 | IMPACT_chr18_24421670_24458531 | IMPACT | AGCCA others(3729): Show |
chr18 | 24421670 | 24458531 |
| a0001c0001t0024 | 0/0 | 3734 | 1 | 0 | 0 | 1 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | AGCCA others(3729): Show |
chr18 | 24421670 | 24458531 |
| a0001c0001t0025 | 0/0 | 3734 | 1 | 0 | 1 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | AGCCA others(3729): Show |
chr18 | 24421670 | 24458531 |
| a0001c0001t0026 | 0/0 | 3734 | 1 | 1 | 0 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | AGCCA others(3729): Show |
chr18 | 24421670 | 24458531 |
| a0001c0001t0029 | 0/0 | 3734 | 1 | 1 | 0 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | AGCCA others(3729): Show |
chr18 | 24421670 | 24458531 |
| a0001c0001t0032 | 0/0 | 3734 | 1 | 0 | 0 | 0 | 0 | 1 | IMPACT_chr18_24421670_24458531 | IMPACT | AGGCA others(3729): Show |
chr18 | 24421670 | 24458531 |
| a0001c0004t0019 | 0/0 | 3734 | 1 | 1 | 0 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | AGCCA others(3729): Show |
chr18 | 24421670 | 24458531 |
| a0002c0002t0002 | 1/0 | 3734 | 61 | 1 | 1 | 53 | 0 | 5 | IMPACT_chr18_24421670_24458531 | IMPACT | AGCCA others(3729): Show |
chr18 | 24421670 | 24458531 |
| a0002c0002t0012 | 0/0 | 3734 | 3 | 0 | 0 | 3 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | AGCCA others(3729): Show |
chr18 | 24421670 | 24458531 |
| a0002c0002t0014 | 0/0 | 3734 | 2 | 2 | 0 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | AGCCA others(3729): Show |
chr18 | 24421670 | 24458531 |
| a0002c0002t0027 | 0/0 | 3734 | 1 | 0 | 0 | 1 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | AGCCA others(3729): Show |
chr18 | 24421670 | 24458531 |
| a0002c0002t0030 | 0/0 | 3734 | 1 | 0 | 0 | 1 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | AGCCA others(3729): Show |
chr18 | 24421670 | 24458531 |
| a0002c0002t0031 | 0/1 | 3734 | 1 | 0 | 0 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | AGCCA others(3729): Show |
chr18 | 24421670 | 24458531 |
| a0003c0003t0003 | 0/0 | 3731 | 20 | 2 | 9 | 1 | 2 | 6 | IMPACT_chr18_24421670_24458531 | IMPACT | AGCCA others(3726): Show |
chr18 | 24421670 | 24458531 |
| a0003c0003t0028 | 0/0 | 3731 | 1 | 1 | 0 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | AGCCA others(3726): Show |
chr18 | 24421670 | 24458531 |
| a0004c0008t0001 | 0/0 | 3734 | 1 | 0 | 1 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | AGCCA others(3729): Show |
chr18 | 24421670 | 24458531 |
| a0005c0007t0001 | 0/0 | 3734 | 1 | 0 | 0 | 0 | 0 | 1 | IMPACT_chr18_24421670_24458531 | IMPACT | AGCCA others(3729): Show |
chr18 | 24421670 | 24458531 |
| a0006c0005t0003 | 0/0 | 3731 | 1 | 0 | 0 | 0 | 0 | 1 | IMPACT_chr18_24421670_24458531 | IMPACT | AGCCA others(3726): Show |
chr18 | 24421670 | 24458531 |
| a0007c0006t0001 | 0/0 | 3734 | 1 | 0 | 0 | 1 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | AGCCA others(3729): Show |
chr18 | 24421670 | 24458531 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 20 | 0 | 4 | 14 | 1 | 1 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0003 | 0/0 | 18 | 1 | 1 | 16 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0005 | 0/0 | 8 | 0 | 1 | 7 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0006 | 0/0 | 6 | 0 | 1 | 3 | 1 | 1 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0012 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0013 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0014 | 0/0 | 4 | 0 | 1 | 2 | 0 | 1 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0020 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0021 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0022 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0023 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0026 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0027 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0028 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0047 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0002g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0002g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0002g0019 | 0/0 | 3 | 1 | 0 | 0 | 2 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0002g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0002g0040 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0002g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0002g0042 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0002g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0004g0008 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0004g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0004g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0004g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0004g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0004g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0005g0010 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0005g0039 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0005g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0005g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0005g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0005g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0005g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0006g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0006g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0006g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0006g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0006g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0006g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0007g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0007g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0007g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0007g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0008g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0008g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0008g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0009g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0009g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0010g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0010g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0011g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0011g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0011g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0013g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0013g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0013g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0015g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0015g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0016g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0017g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0018g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0020g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0021g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0022g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0023g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0024g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0025g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0026g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0029g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0001t0032g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0001c0004t0019g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0002c0002t0002g0001 | 0/0 | 20 | 0 | 0 | 19 | 0 | 1 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0002c0002t0002g0007 | 0/0 | 5 | 0 | 0 | 3 | 0 | 2 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0002c0002t0002g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0002c0002t0002g0018 | 1/0 | 3 | 0 | 0 | 0 | 0 | 2 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0002c0002t0002g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0002c0002t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0002c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0002c0002t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0002c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0002c0002t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0002c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0002c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0002c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0002c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0002c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0002c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0002c0002t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0002c0002t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0002c0002t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0002c0002t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0002c0002t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0002c0002t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0002c0002t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0002c0002t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0002c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0002c0002t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0002c0002t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0002c0002t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0002c0002t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0002c0002t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0002c0002t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0002c0002t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0002c0002t0012g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0002c0002t0012g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0002c0002t0014g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0002c0002t0014g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0002c0002t0027g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0002c0002t0030g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0002c0002t0031g0115 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0003c0003t0003g0004 | 0/0 | 11 | 0 | 5 | 0 | 0 | 6 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0003c0003t0003g0029 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0003c0003t0003g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0003c0003t0003g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0003c0003t0003g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0003c0003t0003g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0003c0003t0003g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0003c0003t0003g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0003c0003t0028g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0004c0008t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0005c0007t0001g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0006c0005t0003g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| a0007c0006t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0003 | c0003 | t0003 | g0029 | EUR | GBR | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0089 | EUR | GBR | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | FIN | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0193 | EUR | FIN | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG00408 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | CHS | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | CHS | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG00423 | hp2 | a0002 | c0002 | t0002 | g0120 | EAS | CHS | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | CHS | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG00438 | hp2 | a0002 | c0002 | t0002 | g0007 | EAS | CHS | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG00544 | hp2 | a0001 | c0001 | t0011 | g0127 | EAS | CHS | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | CHS | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG00558 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | CHS | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | CHS | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG00597 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | CHS | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG00642 | hp2 | a0004 | c0008 | t0001 | g0092 | AMR | PUR | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0041 | AMR | PUR | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG00735 | hp1 | a0001 | c0001 | t0005 | g0039 | AMR | PUR | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0173 | AMR | PUR | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0174 | AMR | PUR | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG01106 | hp1 | a0003 | c0003 | t0003 | g0228 | AMR | PUR | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG01109 | hp1 | a0001 | c0001 | t0004 | g0054 | AMR | PUR | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0142 | AMR | PUR | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG01167 | hp1 | a0001 | c0001 | t0013 | g0053 | AMR | PUR | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0140 | AMR | PUR | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0135 | AMR | PUR | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG01168 | hp2 | a0003 | c0003 | t0003 | g0004 | AMR | PUR | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG01169 | hp1 | a0003 | c0003 | t0003 | g0004 | AMR | PUR | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG01169 | hp2 | a0001 | c0001 | t0013 | g0051 | AMR | PUR | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG01175 | hp1 | a0002 | c0002 | t0002 | g0112 | AMR | PUR | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG01175 | hp2 | a0001 | c0001 | t0005 | g0134 | AMR | PUR | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | CLM | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG01257 | hp1 | a0003 | c0003 | t0003 | g0004 | AMR | CLM | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | CLM | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | CLM | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0042 | AMR | CLM | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0205 | AMR | CLM | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | CLM | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0041 | AMR | CLM | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | CLM | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | CLM | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG01496 | hp1 | a0003 | c0003 | t0003 | g0231 | AMR | CLM | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG01496 | hp2 | a0001 | c0001 | t0022 | g0006 | AMR | CLM | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0035 | EUR | IBS | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0149 | EUR | IBS | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0019 | EUR | IBS | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0206 | EUR | IBS | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0019 | EUR | IBS | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0035 | EUR | IBS | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0136 | AFR | ACB | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | ACB | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG01891 | hp1 | a0001 | c0001 | t0004 | g0008 | AFR | ACB | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG01891 | hp2 | a0001 | c0001 | t0005 | g0132 | AFR | ACB | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | PEL | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG01943 | hp1 | a0003 | c0003 | t0003 | g0230 | AMR | PEL | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | PEL | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PEL | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG01975 | hp1 | a0003 | c0003 | t0003 | g0029 | AMR | PEL | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | PEL | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PEL | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | PEL | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PEL | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG02015 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | KHV | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG02015 | hp2 | a0002 | c0002 | t0002 | g0122 | EAS | KHV | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG02027 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | KHV | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG02040 | hp1 | a0001 | c0001 | t0020 | g0003 | EAS | KHV | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG02040 | hp2 | a0002 | c0002 | t0030 | g0001 | EAS | KHV | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG02055 | hp1 | a0001 | c0001 | t0006 | g0056 | AFR | ACB | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG02056 | hp1 | a0002 | c0002 | t0002 | g0111 | EAS | KHV | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | KHV | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG02071 | hp2 | a0002 | c0002 | t0002 | g0038 | EAS | KHV | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | KHV | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG02074 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | KHV | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG02080 | hp2 | a0002 | c0002 | t0002 | g0105 | EAS | KHV | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | KHV | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | KHV | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | KHV | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | KHV | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | ACB | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG02145 | hp2 | a0001 | c0001 | t0006 | g0062 | AFR | ACB | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CDX | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG02165 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | CDX | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | CDX | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG02257 | hp1 | a0001 | c0001 | t0005 | g0010 | AFR | ACB | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG02257 | hp2 | a0003 | c0003 | t0028 | g0232 | AFR | ACB | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG02258 | hp1 | a0001 | c0001 | t0005 | g0010 | AFR | ACB | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | ACB | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG02273 | hp1 | a0003 | c0003 | t0003 | g0004 | AMR | PEL | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG02280 | hp1 | a0003 | c0003 | t0003 | g0227 | AFR | ACB | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG02280 | hp2 | a0001 | c0001 | t0004 | g0238 | AFR | ACB | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | PEL | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG02293 | hp2 | a0001 | c0001 | t0025 | g0045 | AMR | PEL | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG02451 | hp1 | a0001 | c0001 | t0004 | g0008 | AFR | ACB | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG02451 | hp2 | a0001 | c0001 | t0006 | g0060 | AFR | ACB | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | KHV | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | PJL | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG02615 | hp1 | a0001 | c0001 | t0004 | g0008 | AFR | GWD | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG02622 | hp2 | a0001 | c0001 | t0029 | g0217 | AFR | GWD | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG02630 | hp2 | a0001 | c0001 | t0015 | g0156 | AFR | GWD | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0179 | AFR | GWD | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0139 | AFR | GWD | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG02683 | hp1 | a0003 | c0003 | t0003 | g0004 | SAS | PJL | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG02683 | hp2 | a0002 | c0002 | t0002 | g0001 | SAS | PJL | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0215 | SAS | PJL | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG02698 | hp2 | a0001 | c0001 | t0032 | g0002 | SAS | PJL | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG02723 | hp1 | a0001 | c0001 | t0004 | g0008 | AFR | GWD | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0137 | AFR | GWD | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0072 | SAS | PJL | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0044 | SAS | PJL | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0090 | SAS | PJL | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0178 | SAS | PJL | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG02809 | hp2 | a0001 | c0001 | t0007 | g0048 | AFR | GWD | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | GWD | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG02818 | hp2 | a0001 | c0001 | t0015 | g0005 | AFR | GWD | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG02886 | hp1 | a0001 | c0001 | t0006 | g0058 | AFR | GWD | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0233 | AFR | GWD | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG02895 | hp2 | a0001 | c0001 | t0010 | g0037 | AFR | GWD | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0033 | AFR | GWD | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG02896 | hp2 | a0001 | c0001 | t0004 | g0030 | AFR | GWD | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG02897 | hp1 | a0001 | c0001 | t0004 | g0030 | AFR | GWD | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG02897 | hp2 | a0001 | c0001 | t0010 | g0093 | AFR | GWD | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | ESN | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | ESN | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG02970 | hp1 | a0001 | c0001 | t0006 | g0031 | AFR | ESN | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG02970 | hp2 | a0001 | c0001 | t0004 | g0015 | AFR | ESN | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0011 | AFR | ESN | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG02976 | hp2 | a0001 | c0001 | t0006 | g0059 | AFR | ESN | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG03041 | hp1 | a0001 | c0001 | t0006 | g0031 | AFR | GWD | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0011 | AFR | GWD | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG03098 | hp1 | a0002 | c0002 | t0014 | g0095 | AFR | MSL | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0040 | AFR | MSL | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | ESN | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0011 | AFR | ESN | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG03139 | hp1 | a0002 | c0002 | t0014 | g0096 | AFR | ESN | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0016 | AFR | ESN | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG03195 | hp1 | a0001 | c0001 | t0010 | g0037 | AFR | ESN | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0033 | AFR | ESN | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | MSL | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG03209 | hp2 | a0001 | c0004 | t0019 | g0237 | AFR | MSL | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG03225 | hp1 | a0001 | c0001 | t0009 | g0061 | AFR | MSL | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG03225 | hp2 | a0001 | c0001 | t0009 | g0032 | AFR | MSL | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0195 | SAS | PJL | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0069 | SAS | PJL | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG03453 | hp1 | a0001 | c0001 | t0007 | g0241 | AFR | MSL | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG03453 | hp2 | a0001 | c0001 | t0009 | g0032 | AFR | MSL | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0235 | AFR | MSL | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | MSL | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG03490 | hp1 | a0002 | c0002 | t0002 | g0018 | SAS | PJL | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0077 | SAS | PJL | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG03491 | hp2 | a0003 | c0003 | t0003 | g0004 | SAS | PJL | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG03492 | hp1 | a0003 | c0003 | t0003 | g0004 | SAS | PJL | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG03492 | hp2 | a0002 | c0002 | t0002 | g0018 | SAS | PJL | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0064 | AFR | ESN | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG03516 | hp2 | a0001 | c0001 | t0013 | g0052 | AFR | ESN | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0138 | AFR | GWD | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | GWD | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | MSL | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG03579 | hp2 | a0001 | c0001 | t0026 | g0130 | AFR | MSL | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG03669 | hp2 | a0003 | c0003 | t0003 | g0004 | SAS | PJL | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG03704 | hp1 | a0001 | c0001 | t0021 | g0082 | SAS | PJL | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG03704 | hp2 | a0005 | c0007 | t0001 | g0002 | SAS | PJL | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0168 | SAS | PJL | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG03834 | hp1 | a0006 | c0005 | t0003 | g0004 | SAS | BEB | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG03834 | hp2 | a0001 | c0001 | t0005 | g0039 | SAS | BEB | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | BEB | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0147 | SAS | BEB | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0175 | SAS | STU | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG04115 | hp2 | a0002 | c0002 | t0002 | g0007 | SAS | STU | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG04184 | hp1 | a0003 | c0003 | t0003 | g0004 | SAS | BEB | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG04184 | hp2 | a0001 | c0001 | t0017 | g0084 | SAS | BEB | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0167 | SAS | STU | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG04199 | hp2 | a0003 | c0003 | t0003 | g0004 | SAS | STU | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG04204 | hp1 | a0002 | c0002 | t0002 | g0007 | SAS | STU | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG04204 | hp2 | a0001 | c0001 | t0023 | g0200 | SAS | STU | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0226 | SAS | STU | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0128 | SAS | STU | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA18522 | hp1 | a0001 | c0001 | t0004 | g0055 | AFR | YRI | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0016 | AFR | YRI | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA18612 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | CHB | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | CHB | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA18747 | hp1 | a0002 | c0002 | t0002 | g0121 | EAS | CHB | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHB | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0141 | AFR | YRI | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA18906 | hp2 | a0001 | c0001 | t0005 | g0131 | AFR | YRI | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA18940 | hp1 | a0002 | c0002 | t0002 | g0107 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA18942 | hp1 | a0003 | c0003 | t0003 | g0234 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA18942 | hp2 | a0002 | c0002 | t0002 | g0097 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA18944 | hp1 | a0001 | c0001 | t0024 | g0081 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA18944 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA18945 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA18946 | hp1 | a0002 | c0002 | t0012 | g0098 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA18947 | hp2 | a0002 | c0002 | t0002 | g0009 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA18953 | hp1 | a0002 | c0002 | t0002 | g0104 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA18954 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA18956 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA18957 | hp2 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA18959 | hp1 | a0002 | c0002 | t0002 | g0100 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA18963 | hp1 | a0002 | c0002 | t0002 | g0099 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA18966 | hp1 | a0001 | c0001 | t0008 | g0024 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA18967 | hp1 | a0002 | c0002 | t0002 | g0110 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA18968 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA18971 | hp2 | a0002 | c0002 | t0002 | g0009 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA18975 | hp1 | a0001 | c0001 | t0008 | g0181 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA18981 | hp1 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA18983 | hp1 | a0002 | c0002 | t0002 | g0119 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA18985 | hp2 | a0002 | c0002 | t0002 | g0114 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA18988 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA18990 | hp2 | a0002 | c0002 | t0002 | g0009 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA18991 | hp2 | a0002 | c0002 | t0027 | g0094 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA18992 | hp2 | a0001 | c0001 | t0018 | g0005 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA18994 | hp1 | a0002 | c0002 | t0002 | g0109 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA18998 | hp1 | a0001 | c0001 | t0008 | g0024 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA18998 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA19000 | hp1 | a0001 | c0001 | t0008 | g0180 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA19000 | hp2 | a0002 | c0002 | t0002 | g0116 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA19003 | hp1 | a0002 | c0002 | t0012 | g0001 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA19005 | hp2 | a0002 | c0002 | t0002 | g0123 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA19007 | hp2 | a0002 | c0002 | t0002 | g0101 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA19009 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA19010 | hp1 | a0002 | c0002 | t0002 | g0106 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | LWK | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | LWK | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0065 | AFR | LWK | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA19043 | hp2 | a0001 | c0001 | t0005 | g0129 | AFR | LWK | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA19055 | hp1 | a0002 | c0002 | t0002 | g0108 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA19056 | hp2 | a0001 | c0001 | t0011 | g0126 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA19058 | hp2 | a0001 | c0001 | t0011 | g0125 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA19059 | hp1 | a0002 | c0002 | t0002 | g0103 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA19059 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA19063 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA19064 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA19066 | hp1 | a0002 | c0002 | t0012 | g0001 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA19074 | hp1 | a0002 | c0002 | t0002 | g0118 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA19078 | hp1 | a0002 | c0002 | t0002 | g0124 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA19080 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA19082 | hp1 | a0002 | c0002 | t0002 | g0009 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA19083 | hp2 | a0002 | c0002 | t0002 | g0038 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA19089 | hp1 | a0002 | c0002 | t0002 | g0117 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA19089 | hp2 | a0007 | c0006 | t0001 | g0157 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA19090 | hp1 | a0002 | c0002 | t0002 | g0113 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA19091 | hp2 | a0002 | c0002 | t0002 | g0102 | EAS | JPT | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA19240 | hp1 | a0001 | c0001 | t0005 | g0010 | AFR | YRI | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA19240 | hp2 | a0001 | c0001 | t0007 | g0239 | AFR | YRI | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA20129 | hp1 | a0001 | c0001 | t0004 | g0015 | AFR | ASW | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0019 | AFR | ASW | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0087 | EUR | TSI | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0040 | EUR | TSI | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA20805 | hp1 | a0003 | c0003 | t0003 | g0029 | EUR | TSI | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0073 | SAS | GIH | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0214 | SAS | GIH | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG01123 | hp1 | a0003 | c0003 | t0003 | g0004 | AMR | CLM | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | CLM | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG02109 | hp1 | a0003 | c0003 | t0003 | g0229 | AFR | ACB | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG02109 | hp2 | a0001 | c0001 | t0004 | g0015 | AFR | ACB | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG02486 | hp1 | a0001 | c0001 | t0005 | g0010 | AFR | ACB | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | ACB | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0042 | AFR | ACB | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG02559 | hp2 | a0001 | c0001 | t0007 | g0240 | AFR | ACB | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | MSL | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG03471 | hp2 | a0001 | c0001 | t0005 | g0133 | AFR | MSL | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0057 | AFR | USA | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| HG06807 | hp2 | a0001 | c0001 | t0016 | g0048 | AFR | USA | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | USA | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0016 | AFR | USA | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA21309 | hp1 | a0002 | c0002 | t0002 | g0049 | AFR | LWK | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0011 | AFR | LWK | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0031 | g0115 | REF | REF | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0002 | g0018 | REF | REF | IMPACT_chr18_24421670_24458531 | IMPACT | chr18 | 24421670 | 24458531 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:24428878 | C | T | 1 | a0004 | 1 | HG00642.hp2 | missense_variant | MODERATE | c.175C>T | p.Pro59Ser | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 3/11 | 262/3734 | 175/963 | 59/320 | chr18 | 24428878 | |||
| chr18:24440503 | T | A | 2 | a0003 a0006 |
22 | HG00099.hp1 HG01106.hp1 HG01123.hp1 others(19): Show |
missense_variant | MODERATE | c.375T>A | p.Asp125Glu | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 6/11 | 462/3734 | 375/963 | 125/320 | chr18 | 24440503 | |||
| chr18:24440579 | C | G | 6 | a0001 a0003 a0004 others(3): Show |
333 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(330): Show |
missense_variant | MODERATE | c.451C>G | p.Leu151Val | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 6/11 | 538/3734 | 451/963 | 151/320 | chr18 | 24440579 | |||
| chr18:24445453 | A | G | 1 | a0005 | 1 | HG03704.hp2 | missense_variant | MODERATE | c.655A>G | p.Ile219Val | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 8/11 | 742/3734 | 655/963 | 219/320 | chr18 | 24445453 | |||
| chr18:24449835 | A | G | 1 | a0006 | 1 | HG03834.hp1 | missense_variant | MODERATE | c.776A>G | p.Asn259Ser | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 10/11 | 863/3734 | 776/963 | 259/320 | chr18 | 24449835 | |||
| chr18:24449864 | G | T | 1 | a0007 | 1 | NA19089.hp2 | stop_gained | HIGH | c.805G>T | p.Gly269* | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 10/11 | 892/3734 | 805/963 | 269/320 | chr18 | 24449864 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:24430352 | G | A | 1 | a0001c0004 | 1 | HG03209.hp2 | synonymous_variant | LOW | c.249G>A | p.Ala83Ala | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/11 | 336/3734 | 249/963 | 83/320 | chr18 | 24430352 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:24426672 | C | G | 1 | a0001c0001t0032 | 1 | HG02698.hp2 | 5_prime_UTR_variant | MODIFIER | c.-85C>G | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 1/11 | 85 | chr18 | 24426672 | ||||||
| chr18:24426730 | C | T | 1 | a0001c0001t0006 | 7 | HG02055.hp1 HG02145.hp2 HG02451.hp2 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-27C>T | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 1/11 | 27 | chr18 | 24426730 | ||||||
| chr18:24426747 | C | T | 1 | a0002c0002t0030 | 1 | HG02040.hp2 | 5_prime_UTR_variant | MODIFIER | c.-10C>T | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 1/11 | 10 | chr18 | 24426747 | ||||||
| chr18:24450933 | A | G | 1 | a0001c0001t0029 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*86A>G | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 11/11 | 86 | chr18 | 24450933 | ||||||
| chr18:24451000 | C | T | 2 | a0001c0001t0004 a0001c0001t0013 |
15 | HG01109.hp1 HG01167.hp1 HG01169.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*153C>T | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 11/11 | 153 | chr18 | 24451000 | ||||||
| chr18:24451024 | T | C | 1 | a0001c0001t0016 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*177T>C | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 11/11 | 177 | chr18 | 24451024 | ||||||
| chr18:24451057 | G | T | 1 | a0003c0003t0028 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*210G>T | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 11/11 | 210 | chr18 | 24451057 | ||||||
| chr18:24451245 | A | G | 1 | a0001c0001t0015 | 2 | HG02630.hp2 HG02818.hp2 |
3_prime_UTR_variant | MODIFIER | c.*398A>G | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 11/11 | 398 | chr18 | 24451245 | ||||||
| chr18:24451292 | T | A | 1 | a0001c0001t0017 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*445T>A | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 11/11 | 445 | chr18 | 24451292 | ||||||
| chr18:24451408 | C | T | 1 | a0002c0002t0012 | 3 | NA18946.hp1 NA19003.hp1 NA19066.hp1 |
3_prime_UTR_variant | MODIFIER | c.*561C>T | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 11/11 | 561 | chr18 | 24451408 | ||||||
| chr18:24451507 | A | G | 2 | a0001c0001t0011 a0002c0002t0027 |
4 | HG00544.hp2 NA18991.hp2 NA19056.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*660A>G | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 11/11 | 660 | chr18 | 24451507 | ||||||
| chr18:24451608 | A | G | 1 | a0001c0001t0010 | 3 | HG02895.hp2 HG02897.hp2 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*761A>G | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 11/11 | 761 | chr18 | 24451608 | ||||||
| chr18:24451619 | T | G | 1 | a0001c0001t0010 | 3 | HG02895.hp2 HG02897.hp2 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*772T>G | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 11/11 | 772 | chr18 | 24451619 | ||||||
| chr18:24451655 | T | C | 1 | a0001c0001t0018 | 1 | NA18992.hp2 | 3_prime_UTR_variant | MODIFIER | c.*808T>C | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 11/11 | 808 | chr18 | 24451655 | ||||||
| chr18:24451674 | T | C | 1 | a0002c0002t0014 | 2 | HG03098.hp1 HG03139.hp1 |
3_prime_UTR_variant | MODIFIER | c.*827T>C | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 11/11 | 827 | chr18 | 24451674 | ||||||
| chr18:24451675 | A | G | 2 | a0001c0001t0011 a0002c0002t0027 |
4 | HG00544.hp2 NA18991.hp2 NA19056.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*828A>G | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 11/11 | 828 | chr18 | 24451675 | ||||||
| chr18:24451805 | C | T | 1 | a0001c0001t0026 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*958C>T | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 11/11 | 958 | chr18 | 24451805 | ||||||
| chr18:24451889 | T | C | 1 | a0001c0004t0019 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1042T>C | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 11/11 | 1042 | chr18 | 24451889 | ||||||
| chr18:24451902 | A | G | 1 | a0001c0001t0025 | 1 | HG02293.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1055A>G | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 11/11 | 1055 | chr18 | 24451902 | ||||||
| chr18:24451921 | A | G | 1 | a0001c0001t0024 | 1 | NA18944.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1074A>G | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 11/11 | 1074 | chr18 | 24451921 | ||||||
| chr18:24452025 | A | G | 1 | a0001c0001t0004 | 12 | HG01109.hp1 HG01891.hp1 HG02109.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1178A>G | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 11/11 | 1178 | chr18 | 24452025 | ||||||
| chr18:24452047 | T | C | 3 | a0001c0001t0007 a0001c0001t0016 a0001c0001t0026 |
6 | HG02559.hp2 HG02809.hp2 HG03453.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1200T>C | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 11/11 | 1200 | chr18 | 24452047 | ||||||
| chr18:24452111 | G | C | 1 | a0001c0001t0020 | 1 | HG02040.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1264G>C | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 11/11 | 1264 | chr18 | 24452111 | ||||||
| chr18:24452161 | C | A | 1 | a0001c0001t0021 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1314C>A | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 11/11 | 1314 | chr18 | 24452161 | ||||||
| chr18:24452409 | A | G | 1 | a0001c0001t0023 | 1 | HG04204.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1562A>G | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 11/11 | 1562 | chr18 | 24452409 | ||||||
| chr18:24452482 | A | G | 1 | a0001c0001t0008 | 4 | NA18966.hp1 NA18975.hp1 NA18998.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1635A>G | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 11/11 | 1635 | chr18 | 24452482 | ||||||
| chr18:24452488 | G | A | 3 | a0001c0001t0004 a0001c0001t0009 a0001c0001t0013 |
18 | HG01109.hp1 HG01167.hp1 HG01169.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1641G>A | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 11/11 | 1641 | chr18 | 24452488 | ||||||
| chr18:24452622 | C | T | 1 | a0001c0001t0011 | 3 | HG00544.hp2 NA19056.hp2 NA19058.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1775C>T | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 11/11 | 1775 | chr18 | 24452622 | ||||||
| chr18:24452949 | G | T | 4 | a0001c0001t0005 a0001c0001t0007 a0001c0001t0016 others(1): Show |
17 | HG00735.hp1 HG01175.hp2 HG01891.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*2102G>T | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 11/11 | 2102 | chr18 | 24452949 | ||||||
| chr18:24453015 | G | A | 1 | a0001c0001t0022 | 1 | HG01496.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2168G>A | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 11/11 | 2168 | chr18 | 24453015 | ||||||
| chr18:24453297 | G | A | 16 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0015 others(13): Show |
229 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(226): Show |
3_prime_UTR_variant | MODIFIER | c.*2450G>A | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 11/11 | 2450 | chr18 | 24453297 | ||||||
| chr18:24453514 | ATTC | A | 3 | a0003c0003t0003 a0003c0003t0028 a0006c0005t0003 |
22 | HG00099.hp1 HG01106.hp1 HG01123.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*2672_*2674delTCT | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 11/11 | 2672 | INFO_REALIGN_3_PRIME | chr18 | 24453514 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:24426904 | G | C | 1 | a0002c0002t0002g0049 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.36+112G>C | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 1/10 | chr18 | 24426904 | |||||||
| chr18:24426925 | C | T | 5 | a0001c0001t0007g0048 a0001c0001t0007g0239 a0001c0001t0007g0240 others(2): Show |
5 | HG02559.hp2 HG02809.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.36+133C>T | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 1/10 | chr18 | 24426925 | |||||||
| chr18:24426997 | G | A | 1 | a0001c0001t0001g0050 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.36+205G>A | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 1/10 | chr18 | 24426997 | |||||||
| chr18:24426999 | T | G | 18 | a0001c0001t0002g0016 a0001c0001t0002g0057 a0001c0001t0004g0008 others(15): Show |
28 | HG01109.hp1 HG01167.hp1 HG01169.hp2 others(25): Show |
intron_variant | MODIFIER | c.36+207T>G | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 1/10 | chr18 | 24426999 | |||||||
| chr18:24427074 | C | T | 19 | a0001c0001t0002g0016 a0001c0001t0002g0057 a0001c0001t0004g0008 others(16): Show |
29 | HG01109.hp1 HG01167.hp1 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.36+282C>T | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 1/10 | chr18 | 24427074 | |||||||
| chr18:24427277 | C | T | 1 | a0001c0004t0019g0237 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.36+485C>T | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 1/10 | chr18 | 24427277 | |||||||
| chr18:24427352 | T | A | 2 | a0001c0001t0001g0017 a0001c0001t0001g0063 |
4 | NA18941.hp1 NA18948.hp1 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.36+560T>A | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 1/10 | chr18 | 24427352 | |||||||
| chr18:24427379 | A | G | 1 | a0001c0001t0001g0236 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.37-540A>G | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 1/10 | chr18 | 24427379 | |||||||
| chr18:24427442 | C | T | 1 | a0001c0001t0002g0235 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.37-477C>T | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 1/10 | chr18 | 24427442 | |||||||
| chr18:24427464 | C | G | 1 | a0003c0003t0003g0234 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.37-455C>G | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 1/10 | chr18 | 24427464 | |||||||
| chr18:24427663 | T | C | 2 | a0001c0001t0002g0033 a0001c0001t0002g0064 |
3 | HG02896.hp1 HG03195.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.37-256T>C | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 1/10 | chr18 | 24427663 | |||||||
| chr18:24427745 | C | A | 9 | a0001c0001t0004g0008 a0001c0001t0004g0015 a0001c0001t0004g0030 others(6): Show |
15 | HG01109.hp1 HG01167.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.37-174C>A | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 1/10 | chr18 | 24427745 | |||||||
| chr18:24427816 | G | T | 1 | a0001c0001t0001g0233 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.37-103G>T | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 1/10 | chr18 | 24427816 | |||||||
| chr18:24428185 | G | A | 1 | a0001c0001t0002g0065 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.165+138G>A | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 2/10 | chr18 | 24428185 | |||||||
| chr18:24428397 | C | T | 10 | a0003c0003t0003g0004 a0003c0003t0003g0029 a0003c0003t0003g0227 others(7): Show |
22 | HG00099.hp1 HG01106.hp1 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.165+350C>T | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 2/10 | chr18 | 24428397 | |||||||
| chr18:24428550 | A | C | 3 | a0001c0001t0004g0008 a0001c0001t0004g0030 a0001c0001t0004g0055 |
7 | HG01891.hp1 HG02451.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.166-319A>C | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 2/10 | chr18 | 24428550 | |||||||
| chr18:24428663 | G | A | 33 | a0001c0001t0001g0002 a0001c0001t0001g0034 a0001c0001t0001g0035 others(30): Show |
55 | HG00099.hp2 HG00544.hp1 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.166-206G>A | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 2/10 | chr18 | 24428663 | |||||||
| chr18:24428740 | T | C | 1 | a0001c0001t0006g0056 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.166-129T>C | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 2/10 | chr18 | 24428740 | |||||||
| chr18:24428949 | C | T | 212 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(209): Show |
330 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(327): Show |
intron_variant | MODIFIER | c.218+28C>T | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 3/10 | chr18 | 24428949 | |||||||
| chr18:24428994 | G | A | 5 | a0001c0001t0007g0048 a0001c0001t0007g0239 a0001c0001t0007g0240 others(2): Show |
5 | HG02559.hp2 HG02809.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.218+73G>A | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 3/10 | chr18 | 24428994 | |||||||
| chr18:24429211 | C | A | 212 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(209): Show |
330 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(327): Show |
intron_variant | MODIFIER | c.218+290C>A | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 3/10 | chr18 | 24429211 | |||||||
| chr18:24429310 | T | C | 2 | a0001c0001t0010g0037 a0001c0001t0010g0093 |
3 | HG02895.hp2 HG02897.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.218+389T>C | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 3/10 | chr18 | 24429310 | |||||||
| chr18:24429356 | C | T | 7 | a0002c0002t0002g0118 a0002c0002t0002g0119 a0002c0002t0002g0120 others(4): Show |
7 | HG00423.hp2 HG02015.hp2 NA18747.hp1 others(4): Show |
intron_variant | MODIFIER | c.218+435C>T | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 3/10 | chr18 | 24429356 | |||||||
| chr18:24429357 | G | A | 2 | a0001c0001t0010g0037 a0001c0001t0010g0093 |
3 | HG02895.hp2 HG02897.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.218+436G>A | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 3/10 | chr18 | 24429357 | |||||||
| chr18:24429502 | C | T | 1 | a0004c0008t0001g0092 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.218+581C>T | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 3/10 | chr18 | 24429502 | |||||||
| chr18:24429503 | C | T | 1 | a0001c0001t0001g0226 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.218+582C>T | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 3/10 | chr18 | 24429503 | |||||||
| chr18:24429595 | CTTAA | C | 65 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0012 others(62): Show |
109 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.218+678_218+681del others(4): Show |
IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr18 | 24429595 | ||||||
| chr18:24429614 | C | A | 204 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(201): Show |
311 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(308): Show |
intron_variant | MODIFIER | c.218+693C>A | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 3/10 | chr18 | 24429614 | |||||||
| chr18:24429657 | T | G | 8 | a0001c0001t0001g0024 a0001c0001t0008g0024 a0001c0001t0008g0180 others(5): Show |
9 | HG00544.hp2 NA18612.hp2 NA18966.hp1 others(6): Show |
intron_variant | MODIFIER | c.219-665T>G | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 3/10 | chr18 | 24429657 | |||||||
| chr18:24429695 | G | A | 213 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(210): Show |
331 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(328): Show |
intron_variant | MODIFIER | c.219-627G>A | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 3/10 | chr18 | 24429695 | |||||||
| chr18:24429756 | TATAAAC | T | 1 | a0001c0001t0004g0015 | 3 | HG02109.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.219-560_219-555del others(6): Show |
IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr18 | 24429756 | ||||||
| chr18:24429782 | A | AT | 7 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0177 others(4): Show |
7 | HG01106.hp2 HG02145.hp2 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.219-525dupT | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr18 | 24429782 | ||||||
| chr18:24429782 | AT | A | 15 | a0001c0001t0001g0025 a0001c0001t0001g0066 a0001c0001t0001g0182 others(12): Show |
29 | HG00099.hp1 HG01106.hp1 HG01123.hp1 others(26): Show |
intron_variant | MODIFIER | c.219-525delT | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr18 | 24429782 | ||||||
| chr18:24429887 | C | T | 1 | a0001c0001t0009g0032 | 2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.219-435C>T | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 3/10 | chr18 | 24429887 | |||||||
| chr18:24429985 | G | A | 1 | a0001c0001t0001g0128 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.219-337G>A | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 3/10 | chr18 | 24429985 | |||||||
| chr18:24430018 | C | G | 1 | a0001c0004t0019g0237 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.219-304C>G | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 3/10 | chr18 | 24430018 | |||||||
| chr18:24430034 | C | T | 1 | a0001c0001t0002g0179 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.219-288C>T | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 3/10 | chr18 | 24430034 | |||||||
| chr18:24430057 | A | G | 1 | a0001c0001t0001g0089 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.219-265A>G | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 3/10 | chr18 | 24430057 | |||||||
| chr18:24430201 | A | G | 10 | a0003c0003t0003g0004 a0003c0003t0003g0029 a0003c0003t0003g0227 others(7): Show |
22 | HG00099.hp1 HG01106.hp1 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.219-121A>G | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 3/10 | chr18 | 24430201 | |||||||
| chr18:24430260 | T | A | 19 | a0001c0001t0002g0016 a0001c0001t0002g0057 a0001c0001t0004g0008 others(16): Show |
29 | HG01109.hp1 HG01167.hp1 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.219-62T>A | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 3/10 | chr18 | 24430260 | |||||||
| chr18:24430440 | T | C | 1 | a0003c0003t0003g0227 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.281+56T>C | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | chr18 | 24430440 | |||||||
| chr18:24430457 | C | T | 164 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(161): Show |
256 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(253): Show |
intron_variant | MODIFIER | c.281+73C>T | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | chr18 | 24430457 | |||||||
| chr18:24430535 | G | A | 1 | a0001c0001t0005g0129 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.281+151G>A | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | chr18 | 24430535 | |||||||
| chr18:24430536 | G | T | 1 | a0001c0001t0001g0176 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.281+152G>T | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | chr18 | 24430536 | |||||||
| chr18:24430771 | G | A | 1 | a0001c0001t0026g0130 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.281+387G>A | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | chr18 | 24430771 | |||||||
| chr18:24430843 | G | A | 1 | a0001c0001t0001g0184 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.281+459G>A | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | chr18 | 24430843 | |||||||
| chr18:24430862 | A | G | 1 | a0001c0001t0009g0032 | 2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.281+478A>G | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | chr18 | 24430862 | |||||||
| chr18:24430888 | A | C | 2 | a0001c0001t0001g0128 a0001c0001t0001g0175 |
2 | HG04115.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.281+504A>C | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | chr18 | 24430888 | |||||||
| chr18:24430970 | G | C | 5 | a0001c0001t0005g0010 a0001c0001t0005g0131 a0001c0001t0005g0132 others(2): Show |
8 | HG01891.hp2 HG02257.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.281+586G>C | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | chr18 | 24430970 | |||||||
| chr18:24431295 | G | A | 1 | a0001c0001t0002g0064 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.281+911G>A | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | chr18 | 24431295 | |||||||
| chr18:24431417 | A | G | 215 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(212): Show |
334 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(331): Show |
intron_variant | MODIFIER | c.281+1033A>G | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | chr18 | 24431417 | |||||||
| chr18:24431447 | G | A | 4 | a0001c0001t0011g0125 a0001c0001t0011g0126 a0001c0001t0011g0127 others(1): Show |
4 | HG00544.hp2 NA18991.hp2 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.281+1063G>A | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | chr18 | 24431447 | |||||||
| chr18:24431634 | T | C | 1 | a0002c0002t0002g0099 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.281+1250T>C | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | chr18 | 24431634 | |||||||
| chr18:24431659 | C | T | 2 | a0001c0001t0002g0173 a0001c0001t0002g0174 |
2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.281+1275C>T | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | chr18 | 24431659 | |||||||
| chr18:24431701 | T | A | 1 | a0001c0001t0001g0185 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.281+1317T>A | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | chr18 | 24431701 | |||||||
| chr18:24431708 | T | A | 5 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0188 others(2): Show |
6 | HG02896.hp1 HG03195.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.281+1324T>A | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | chr18 | 24431708 | |||||||
| chr18:24431818 | C | T | 146 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(143): Show |
229 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(226): Show |
intron_variant | MODIFIER | c.281+1434C>T | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | chr18 | 24431818 | |||||||
| chr18:24431957 | C | T | 1 | a0002c0002t0002g0117 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.281+1573C>T | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | chr18 | 24431957 | |||||||
| chr18:24431958 | T | C | 1 | a0002c0002t0002g0117 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.281+1574T>C | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | chr18 | 24431958 | |||||||
| chr18:24431959 | C | A | 1 | a0002c0002t0002g0117 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.281+1575C>A | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | chr18 | 24431959 | |||||||
| chr18:24432385 | G | A | 3 | a0001c0001t0013g0051 a0001c0001t0013g0052 a0001c0001t0013g0053 |
3 | HG01167.hp1 HG01169.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.281+2001G>A | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | chr18 | 24432385 | |||||||
| chr18:24432459 | A | G | 1 | a0002c0002t0002g0116 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.281+2075A>G | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | chr18 | 24432459 | |||||||
| chr18:24432504 | G | C | 3 | a0001c0001t0013g0051 a0001c0001t0013g0052 a0001c0001t0013g0053 |
3 | HG01167.hp1 HG01169.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.281+2120G>C | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | chr18 | 24432504 | |||||||
| chr18:24432752 | T | G | 164 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(161): Show |
256 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(253): Show |
intron_variant | MODIFIER | c.281+2368T>G | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | chr18 | 24432752 | |||||||
| chr18:24432753 | A | G | 3 | a0001c0001t0011g0125 a0001c0001t0011g0126 a0001c0001t0011g0127 |
3 | HG00544.hp2 NA19056.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.281+2369A>G | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | chr18 | 24432753 | |||||||
| chr18:24433039 | T | G | 1 | a0001c0001t0001g0143 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.281+2655T>G | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | chr18 | 24433039 | |||||||
| chr18:24433107 | C | T | 1 | a0001c0001t0002g0179 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.281+2723C>T | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | chr18 | 24433107 | |||||||
| chr18:24433184 | C | CT | 130 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(127): Show |
223 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.281+2826dupT | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr18 | 24433184 | ||||||
| chr18:24433184 | C | CTT | 35 | a0001c0001t0001g0014 a0001c0001t0001g0045 a0001c0001t0001g0085 others(32): Show |
38 | HG00438.hp1 HG00558.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.281+2825_281+2826d others(4): Show |
IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr18 | 24433184 | ||||||
| chr18:24433184 | CT | C | 12 | a0001c0001t0002g0033 a0001c0001t0002g0064 a0001c0001t0005g0129 others(9): Show |
15 | HG01169.hp2 HG02895.hp2 HG02896.hp1 others(12): Show |
intron_variant | MODIFIER | c.281+2826delT | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr18 | 24433184 | ||||||
| chr18:24433225 | C | T | 2 | a0001c0001t0002g0019 a0001c0001t0002g0041 |
5 | HG00733.hp1 HG01358.hp2 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.281+2841C>T | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | chr18 | 24433225 | |||||||
| chr18:24433256 | G | T | 10 | a0003c0003t0003g0004 a0003c0003t0003g0029 a0003c0003t0003g0227 others(7): Show |
22 | HG00099.hp1 HG01106.hp1 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.281+2872G>T | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | chr18 | 24433256 | |||||||
| chr18:24433261 | G | A | 4 | a0001c0001t0001g0020 a0001c0001t0001g0145 a0001c0001t0001g0146 others(1): Show |
6 | HG00735.hp2 HG00741.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.281+2877G>A | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | chr18 | 24433261 | |||||||
| chr18:24433290 | C | T | 1 | a0001c0001t0001g0191 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.281+2906C>T | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | chr18 | 24433290 | |||||||
| chr18:24433301 | G | A | 1 | a0001c0001t0029g0217 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.281+2917G>A | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | chr18 | 24433301 | |||||||
| chr18:24433324 | C | G | 1 | a0001c0001t0001g0172 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.281+2940C>G | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | chr18 | 24433324 | |||||||
| chr18:24433345 | G | A | 3 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0002g0142 |
3 | HG01070.hp1 HG01109.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.281+2961G>A | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | chr18 | 24433345 | |||||||
| chr18:24433356 | C | T | 19 | a0001c0001t0002g0016 a0001c0001t0002g0057 a0001c0001t0004g0008 others(16): Show |
29 | HG01109.hp1 HG01167.hp1 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.281+2972C>T | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | chr18 | 24433356 | |||||||
| chr18:24433360 | C | T | 1 | a0001c0001t0001g0147 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.281+2976C>T | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | chr18 | 24433360 | |||||||
| chr18:24433389 | C | T | 4 | a0001c0001t0010g0037 a0001c0001t0010g0093 a0002c0002t0014g0095 others(1): Show |
5 | HG02895.hp2 HG02897.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.281+3005C>T | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | chr18 | 24433389 | |||||||
| chr18:24433423 | T | C | 1 | a0001c0001t0009g0061 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.281+3039T>C | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | chr18 | 24433423 | |||||||
| chr18:24433488 | C | T | 3 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0188 |
3 | HG03471.hp1 HG03540.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.281+3104C>T | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | chr18 | 24433488 | |||||||
| chr18:24433494 | C | T | 2 | a0001c0001t0001g0216 a0001c0001t0001g0224 |
2 | HG01192.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.281+3110C>T | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | chr18 | 24433494 | |||||||
| chr18:24433495 | G | A | 1 | a0001c0001t0001g0186 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.281+3111G>A | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | chr18 | 24433495 | |||||||
| chr18:24433665 | A | AT | 23 | a0001c0001t0002g0016 a0001c0001t0002g0057 a0001c0001t0005g0129 others(20): Show |
38 | HG00099.hp1 HG01123.hp1 HG01168.hp2 others(35): Show |
intron_variant | MODIFIER | c.281+3302dupT | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr18 | 24433665 | ||||||
| chr18:24433665 | AT | A | 161 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(158): Show |
259 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(256): Show |
intron_variant | MODIFIER | c.281+3302delT | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr18 | 24433665 | ||||||
| chr18:24433665 | ATT | A | 7 | a0001c0001t0001g0070 a0001c0001t0001g0148 a0001c0001t0001g0149 others(4): Show |
7 | HG00323.hp2 HG01069.hp1 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.281+3301_281+3302d others(4): Show |
IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr18 | 24433665 | ||||||
| chr18:24433694 | C | T | 5 | a0001c0001t0002g0011 a0001c0001t0002g0065 a0001c0001t0002g0138 others(2): Show |
8 | HG01167.hp2 HG02647.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.281+3310C>T | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | chr18 | 24433694 | |||||||
| chr18:24433767 | T | C | 1 | a0001c0001t0002g0179 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.281+3383T>C | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | chr18 | 24433767 | |||||||
| chr18:24433794 | C | T | 1 | a0001c0001t0001g0047 | 2 | HG01261.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.281+3410C>T | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | chr18 | 24433794 | |||||||
| chr18:24434048 | A | G | 3 | a0001c0001t0011g0125 a0001c0001t0011g0126 a0001c0001t0011g0127 |
3 | HG00544.hp2 NA19056.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.281+3664A>G | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | chr18 | 24434048 | |||||||
| chr18:24434169 | C | T | 1 | a0001c0001t0009g0061 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.281+3785C>T | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | chr18 | 24434169 | |||||||
| chr18:24434188 | A | T | 1 | a0001c0001t0002g0235 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.282-3767A>T | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | chr18 | 24434188 | |||||||
| chr18:24434283 | G | A | 164 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(161): Show |
256 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(253): Show |
intron_variant | MODIFIER | c.282-3672G>A | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | chr18 | 24434283 | |||||||
| chr18:24434499 | G | A | 1 | a0001c0001t0002g0179 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.282-3456G>A | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | chr18 | 24434499 | |||||||
| chr18:24434599 | C | T | 1 | a0001c0001t0001g0146 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.282-3356C>T | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | chr18 | 24434599 | |||||||
| chr18:24434703 | C | T | 1 | a0001c0001t0009g0061 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.282-3252C>T | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | chr18 | 24434703 | |||||||
| chr18:24434763 | C | CA | 64 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0013 others(61): Show |
91 | HG00558.hp1 HG00639.hp1 HG00673.hp1 others(88): Show |
intron_variant | MODIFIER | c.282-3178dupA | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr18 | 24434763 | ||||||
| chr18:24434763 | C | CAA | 9 | a0001c0001t0001g0143 a0001c0001t0001g0216 a0001c0001t0004g0054 others(6): Show |
10 | HG01109.hp1 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.282-3179_282-3178d others(4): Show |
IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr18 | 24434763 | ||||||
| chr18:24434774 | A | T | 1 | a0001c0004t0019g0237 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.282-3181A>T | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | chr18 | 24434774 | |||||||
| chr18:24434776 | A | AAAATATA others(5): Show |
2 | a0001c0001t0011g0125 a0001c0001t0011g0126 |
2 | NA19056.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.282-3178_282-3177i others(14): Show |
IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr18 | 24434776 | ||||||
| chr18:24434776 | A | AAAT | 5 | a0001c0001t0001g0017 a0001c0001t0001g0183 a0001c0001t0001g0185 others(2): Show |
7 | HG00323.hp2 HG00597.hp1 HG02523.hp1 others(4): Show |
intron_variant | MODIFIER | c.282-3178_282-3177i others(5): Show |
IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr18 | 24434776 | ||||||
| chr18:24434776 | A | AAT | 3 | a0001c0001t0004g0008 a0001c0001t0004g0030 a0001c0001t0004g0238 |
6 | HG01891.hp1 HG02280.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.282-3160_282-3159d others(4): Show |
IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr18 | 24434776 | ||||||
| chr18:24434776 | A | AATATATA others(5): Show |
1 | a0001c0001t0011g0127 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.282-3170_282-3159d others(14): Show |
IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr18 | 24434776 | ||||||
| chr18:24434776 | A | AT | 9 | a0001c0001t0001g0161 a0001c0001t0002g0016 a0001c0001t0002g0057 others(6): Show |
12 | HG00741.hp2 HG02055.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.282-3179_282-3178i others(3): Show |
IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | chr18 | 24434776 | |||||||
| chr18:24434776 | A | T | 1 | a0001c0004t0019g0237 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.282-3179A>T | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | chr18 | 24434776 | |||||||
| chr18:24434776 | AAT | A | 11 | a0001c0001t0005g0010 a0001c0001t0005g0129 a0001c0001t0005g0131 others(8): Show |
14 | HG01891.hp2 HG02257.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.282-3160_282-3159d others(4): Show |
IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr18 | 24434776 | ||||||
| chr18:24434777 | AT | A | 40 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0149 others(37): Show |
64 | HG00323.hp1 HG00408.hp2 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.282-3177delT | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | chr18 | 24434777 | |||||||
| chr18:24434777 | ATAT | A | 2 | a0001c0001t0005g0039 a0001c0001t0005g0134 |
3 | HG00735.hp1 HG01175.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.282-3177_282-3175d others(5): Show |
IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | chr18 | 24434777 | |||||||
| chr18:24434778 | T | A | 136 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(133): Show |
211 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(208): Show |
intron_variant | MODIFIER | c.282-3177T>A | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | chr18 | 24434778 | |||||||
| chr18:24434780 | T | A | 65 | a0001c0001t0001g0002 a0001c0001t0001g0034 a0001c0001t0001g0066 others(62): Show |
97 | HG00423.hp1 HG00544.hp1 HG00642.hp1 others(94): Show |
intron_variant | MODIFIER | c.282-3175T>A | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | chr18 | 24434780 | |||||||
| chr18:24434782 | T | A | 5 | a0001c0001t0002g0011 a0001c0001t0002g0065 a0001c0001t0002g0138 others(2): Show |
8 | HG01167.hp2 HG02647.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.282-3173T>A | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | chr18 | 24434782 | |||||||
| chr18:24434784 | T | A | 4 | a0001c0001t0002g0011 a0001c0001t0002g0065 a0001c0001t0002g0138 others(1): Show |
7 | HG02647.hp2 HG02976.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.282-3171T>A | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | chr18 | 24434784 | |||||||
| chr18:24434793 | ATATG | A | 2 | a0001c0001t0001g0028 a0001c0001t0001g0191 |
4 | HG02809.hp1 HG02895.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.282-3160_282-3157d others(6): Show |
IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr18 | 24434793 | ||||||
| chr18:24434795 | A | ATATATAT others(3): Show |
2 | a0002c0002t0014g0095 a0002c0002t0014g0096 |
2 | HG03098.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.282-3159_282-3158i others(12): Show |
IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr18 | 24434795 | ||||||
| chr18:24434795 | A | G | 2 | a0001c0004t0019g0237 a0002c0002t0002g0007 |
2 | HG00438.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.282-3160A>G | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | chr18 | 24434795 | |||||||
| chr18:24434795 | ATG | A | 12 | a0001c0001t0001g0184 a0001c0001t0002g0140 a0003c0003t0003g0004 others(9): Show |
23 | HG00099.hp1 HG01106.hp1 HG01123.hp1 others(20): Show |
intron_variant | MODIFIER | c.282-3146_282-3145d others(4): Show |
IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr18 | 24434795 | ||||||
| chr18:24434797 | G | A | 158 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(155): Show |
247 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(244): Show |
intron_variant | MODIFIER | c.282-3158G>A | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | chr18 | 24434797 | |||||||
| chr18:24434831 | AGTGTATA others(31): Show |
A | 8 | a0001c0001t0002g0016 a0001c0001t0002g0057 a0001c0001t0006g0031 others(5): Show |
11 | HG02055.hp1 HG02145.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.282-3107_282-3070d others(40): Show |
IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr18 | 24434831 | ||||||
| chr18:24434844 | G | GTGTGTAT others(17): Show |
4 | a0002c0002t0002g0001 a0002c0002t0002g0103 a0002c0002t0002g0104 others(1): Show |
4 | NA18953.hp1 NA18956.hp1 NA19059.hp1 others(1): Show |
intron_variant | MODIFIER | c.282-3069_282-3046d others(26): Show |
IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr18 | 24434844 | ||||||
| chr18:24434844 | GTGTGTAT others(5): Show |
G | 4 | a0002c0002t0002g0001 a0002c0002t0002g0007 a0002c0002t0002g0097 others(1): Show |
6 | HG02683.hp2 NA18940.hp1 NA18942.hp2 others(3): Show |
intron_variant | MODIFIER | c.282-3057_282-3046d others(14): Show |
IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr18 | 24434844 | ||||||
| chr18:24434880 | ATGTGTAT others(19): Show |
A | 3 | a0001c0001t0011g0125 a0001c0001t0011g0126 a0001c0001t0011g0127 |
3 | HG00544.hp2 NA19056.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.282-3069_282-3044d others(28): Show |
IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr18 | 24434880 | ||||||
| chr18:24434892 | ATGTGTAT others(7): Show |
A | 34 | a0001c0001t0001g0028 a0001c0001t0001g0169 a0001c0001t0001g0194 others(31): Show |
49 | HG00733.hp1 HG01069.hp2 HG01071.hp2 others(46): Show |
intron_variant | MODIFIER | c.282-3057_282-3044d others(16): Show |
IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr18 | 24434892 | ||||||
| chr18:24434906 | G | GTGTATAT others(3): Show |
11 | a0003c0003t0003g0004 a0003c0003t0003g0029 a0003c0003t0003g0227 others(8): Show |
23 | HG00099.hp1 HG00642.hp2 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.282-3046_282-3045i others(12): Show |
IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr18 | 24434906 | ||||||
| chr18:24434912 | GTA | G | 166 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(163): Show |
258 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(255): Show |
intron_variant | MODIFIER | c.282-3030_282-3029d others(4): Show |
IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr18 | 24434912 | ||||||
| chr18:24434914 | A | G | 48 | a0001c0001t0001g0028 a0001c0001t0001g0169 a0001c0001t0001g0194 others(45): Show |
75 | HG00099.hp1 HG00544.hp2 HG00642.hp2 others(72): Show |
intron_variant | MODIFIER | c.282-3041A>G | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | chr18 | 24434914 | |||||||
| chr18:24434945 | T | C | 164 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(161): Show |
256 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(253): Show |
intron_variant | MODIFIER | c.282-3010T>C | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | chr18 | 24434945 | |||||||
| chr18:24434977 | C | CT | 19 | a0001c0001t0002g0016 a0001c0001t0002g0057 a0001c0001t0004g0008 others(16): Show |
29 | HG01109.hp1 HG01167.hp1 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.282-2966dupT | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr18 | 24434977 | ||||||
| chr18:24435117 | G | C | 10 | a0003c0003t0003g0004 a0003c0003t0003g0029 a0003c0003t0003g0227 others(7): Show |
22 | HG00099.hp1 HG01106.hp1 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.282-2838G>C | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | chr18 | 24435117 | |||||||
| chr18:24435219 | C | A | 1 | a0001c0001t0001g0202 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.282-2736C>A | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | chr18 | 24435219 | |||||||
| chr18:24435349 | C | T | 2 | a0002c0002t0002g0009 a0002c0002t0002g0108 |
5 | NA18947.hp2 NA18971.hp2 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.282-2606C>T | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | chr18 | 24435349 | |||||||
| chr18:24435439 | A | G | 5 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0090 others(2): Show |
8 | HG01123.hp2 HG01515.hp1 HG01517.hp2 others(5): Show |
intron_variant | MODIFIER | c.282-2516A>G | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | chr18 | 24435439 | |||||||
| chr18:24435526 | G | A | 214 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(211): Show |
333 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(330): Show |
intron_variant | MODIFIER | c.282-2429G>A | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | chr18 | 24435526 | |||||||
| chr18:24435744 | G | A | 2 | a0001c0001t0010g0037 a0001c0001t0010g0093 |
3 | HG02895.hp2 HG02897.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.282-2211G>A | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | chr18 | 24435744 | |||||||
| chr18:24435827 | C | T | 1 | a0001c0001t0009g0061 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.282-2128C>T | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | chr18 | 24435827 | |||||||
| chr18:24435871 | G | GGGCAGTG others(132): Show |
5 | a0001c0001t0001g0026 a0001c0001t0001g0189 a0001c0001t0001g0196 others(2): Show |
7 | HG00597.hp1 HG01074.hp1 HG02083.hp1 others(4): Show |
intron_variant | MODIFIER | c.282-2068_282-2067i others(141): Show |
IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr18 | 24435871 | ||||||
| chr18:24435871 | G | GGGCAGTG others(132): Show |
20 | a0001c0001t0001g0013 a0001c0001t0001g0017 a0001c0001t0001g0025 others(17): Show |
27 | HG00323.hp2 HG00558.hp1 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.282-2068_282-2067i others(141): Show |
IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr18 | 24435871 | ||||||
| chr18:24436095 | C | T | 2 | a0001c0001t0010g0037 a0001c0001t0010g0093 |
3 | HG02895.hp2 HG02897.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.282-1860C>T | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | chr18 | 24436095 | |||||||
| chr18:24436097 | A | G | 1 | a0001c0001t0001g0175 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.282-1858A>G | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | chr18 | 24436097 | |||||||
| chr18:24436311 | C | T | 1 | a0001c0001t0001g0012 | 4 | HG02055.hp2 HG03209.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.282-1644C>T | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | chr18 | 24436311 | |||||||
| chr18:24436338 | C | G | 1 | a0001c0001t0004g0238 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.282-1617C>G | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | chr18 | 24436338 | |||||||
| chr18:24436419 | T | A | 8 | a0001c0001t0002g0016 a0001c0001t0002g0057 a0001c0001t0006g0031 others(5): Show |
11 | HG02055.hp1 HG02145.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.282-1536T>A | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | chr18 | 24436419 | |||||||
| chr18:24436515 | TG | T | 13 | a0001c0001t0002g0179 a0001c0001t0002g0235 a0001c0004t0019g0237 others(10): Show |
25 | HG00099.hp1 HG01106.hp1 HG01123.hp1 others(22): Show |
intron_variant | MODIFIER | c.282-1439delG | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | chr18 | 24436515 | |||||||
| chr18:24436520 | T | C | 32 | a0001c0001t0002g0016 a0001c0001t0002g0057 a0001c0001t0002g0179 others(29): Show |
54 | HG00099.hp1 HG01106.hp1 HG01109.hp1 others(51): Show |
intron_variant | MODIFIER | c.282-1435T>C | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | chr18 | 24436520 | |||||||
| chr18:24436752 | A | T | 1 | a0001c0001t0002g0179 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.282-1203A>T | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | chr18 | 24436752 | |||||||
| chr18:24436756 | G | A | 1 | a0002c0002t0002g0119 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.282-1199G>A | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | chr18 | 24436756 | |||||||
| chr18:24436803 | G | A | 5 | a0001c0001t0004g0008 a0001c0001t0004g0015 a0001c0001t0004g0030 others(2): Show |
11 | HG01891.hp1 HG02109.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.282-1152G>A | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | chr18 | 24436803 | |||||||
| chr18:24436825 | A | G | 1 | a0002c0002t0002g0107 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.282-1130A>G | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | chr18 | 24436825 | |||||||
| chr18:24436885 | T | C | 35 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0017 others(32): Show |
49 | HG00323.hp2 HG00558.hp1 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.282-1070T>C | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | chr18 | 24436885 | |||||||
| chr18:24436891 | A | G | 1 | a0001c0001t0001g0201 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.282-1064A>G | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | chr18 | 24436891 | |||||||
| chr18:24437037 | G | T | 19 | a0001c0001t0002g0016 a0001c0001t0002g0057 a0001c0001t0004g0008 others(16): Show |
29 | HG01109.hp1 HG01167.hp1 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.282-918G>T | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | chr18 | 24437037 | |||||||
| chr18:24437059 | A | G | 76 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(73): Show |
115 | HG00099.hp2 HG00544.hp1 HG00639.hp1 others(112): Show |
intron_variant | MODIFIER | c.282-896A>G | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | chr18 | 24437059 | |||||||
| chr18:24437059 | ATGT | A | 8 | a0001c0001t0002g0016 a0001c0001t0002g0057 a0001c0001t0006g0031 others(5): Show |
11 | HG02055.hp1 HG02145.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.282-891_282-889del others(3): Show |
IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr18 | 24437059 | ||||||
| chr18:24437217 | T | C | 1 | a0003c0003t0003g0227 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.282-738T>C | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | chr18 | 24437217 | |||||||
| chr18:24437253 | G | A | 1 | a0001c0001t0001g0202 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.282-702G>A | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | chr18 | 24437253 | |||||||
| chr18:24437280 | A | G | 1 | a0001c0001t0001g0213 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.282-675A>G | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | chr18 | 24437280 | |||||||
| chr18:24437555 | A | G | 1 | a0001c0001t0001g0083 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.282-400A>G | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | chr18 | 24437555 | |||||||
| chr18:24437581 | C | G | 184 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(181): Show |
281 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(278): Show |
intron_variant | MODIFIER | c.282-374C>G | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | chr18 | 24437581 | |||||||
| chr18:24437598 | G | A | 203 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(200): Show |
310 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(307): Show |
intron_variant | MODIFIER | c.282-357G>A | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | chr18 | 24437598 | |||||||
| chr18:24437611 | G | A | 20 | a0001c0001t0002g0016 a0001c0001t0002g0057 a0001c0001t0002g0138 others(17): Show |
30 | HG01109.hp1 HG01167.hp1 HG01169.hp2 others(27): Show |
intron_variant | MODIFIER | c.282-344G>A | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | chr18 | 24437611 | |||||||
| chr18:24437772 | C | T | 41 | a0001c0001t0001g0005 a0001c0001t0001g0020 a0001c0001t0001g0021 others(38): Show |
58 | HG00639.hp1 HG00673.hp1 HG00735.hp2 others(55): Show |
intron_variant | MODIFIER | c.282-183C>T | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | chr18 | 24437772 | |||||||
| chr18:24437787 | A | G | 1 | a0001c0001t0006g0060 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.282-168A>G | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | chr18 | 24437787 | |||||||
| chr18:24437788 | C | A | 203 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(200): Show |
310 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(307): Show |
intron_variant | MODIFIER | c.282-167C>A | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | chr18 | 24437788 | |||||||
| chr18:24437836 | T | A | 10 | a0003c0003t0003g0004 a0003c0003t0003g0029 a0003c0003t0003g0227 others(7): Show |
22 | HG00099.hp1 HG01106.hp1 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.282-119T>A | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 4/10 | chr18 | 24437836 | |||||||
| chr18:24438165 | A | C | 213 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(210): Show |
332 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(329): Show |
intron_variant | MODIFIER | c.367+125A>C | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 5/10 | chr18 | 24438165 | |||||||
| chr18:24438273 | G | T | 215 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(212): Show |
334 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(331): Show |
intron_variant | MODIFIER | c.367+233G>T | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 5/10 | chr18 | 24438273 | |||||||
| chr18:24438352 | GT | G | 1 | a0001c0001t0001g0028 | 3 | HG02809.hp1 HG02895.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.367+316delT | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr18 | 24438352 | ||||||
| chr18:24438771 | A | G | 19 | a0001c0001t0002g0016 a0001c0001t0002g0057 a0001c0001t0004g0008 others(16): Show |
29 | HG01109.hp1 HG01167.hp1 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.367+731A>G | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 5/10 | chr18 | 24438771 | |||||||
| chr18:24438815 | G | A | 2 | a0001c0001t0001g0189 a0001c0001t0001g0196 |
2 | NA18954.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.367+775G>A | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 5/10 | chr18 | 24438815 | |||||||
| chr18:24438820 | T | C | 3 | a0001c0001t0011g0125 a0001c0001t0011g0126 a0001c0001t0011g0127 |
3 | HG00544.hp2 NA19056.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.367+780T>C | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 5/10 | chr18 | 24438820 | |||||||
| chr18:24438822 | T | C | 10 | a0003c0003t0003g0004 a0003c0003t0003g0029 a0003c0003t0003g0227 others(7): Show |
22 | HG00099.hp1 HG01106.hp1 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.367+782T>C | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 5/10 | chr18 | 24438822 | |||||||
| chr18:24438854 | T | A | 13 | a0001c0001t0002g0179 a0001c0001t0002g0235 a0001c0004t0019g0237 others(10): Show |
25 | HG00099.hp1 HG01106.hp1 HG01123.hp1 others(22): Show |
intron_variant | MODIFIER | c.367+814T>A | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 5/10 | chr18 | 24438854 | |||||||
| chr18:24438910 | GTA | G | 8 | a0001c0001t0002g0016 a0001c0001t0002g0057 a0001c0001t0006g0031 others(5): Show |
11 | HG02055.hp1 HG02145.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.367+872_367+873del others(2): Show |
IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr18 | 24438910 | ||||||
| chr18:24438914 | G | T | 8 | a0001c0001t0002g0016 a0001c0001t0002g0057 a0001c0001t0006g0031 others(5): Show |
11 | HG02055.hp1 HG02145.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.367+874G>T | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 5/10 | chr18 | 24438914 | |||||||
| chr18:24439010 | G | C | 1 | a0002c0002t0002g0116 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.367+970G>C | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 5/10 | chr18 | 24439010 | |||||||
| chr18:24439110 | C | T | 2 | a0001c0001t0010g0037 a0001c0001t0010g0093 |
3 | HG02895.hp2 HG02897.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.367+1070C>T | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 5/10 | chr18 | 24439110 | |||||||
| chr18:24439112 | A | G | 215 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(212): Show |
334 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(331): Show |
intron_variant | MODIFIER | c.367+1072A>G | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 5/10 | chr18 | 24439112 | |||||||
| chr18:24439238 | A | G | 2 | a0001c0001t0002g0136 a0001c0001t0002g0137 |
2 | HG01884.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.367+1198A>G | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 5/10 | chr18 | 24439238 | |||||||
| chr18:24439242 | G | A | 1 | a0001c0001t0001g0150 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.367+1202G>A | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 5/10 | chr18 | 24439242 | |||||||
| chr18:24439249 | G | A | 147 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(144): Show |
230 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(227): Show |
intron_variant | MODIFIER | c.367+1209G>A | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 5/10 | chr18 | 24439249 | |||||||
| chr18:24439362 | C | G | 1 | a0001c0001t0001g0233 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.368-1134C>G | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 5/10 | chr18 | 24439362 | |||||||
| chr18:24439374 | T | C | 4 | a0001c0001t0001g0021 a0001c0001t0001g0151 a0001c0001t0001g0164 others(1): Show |
6 | HG01255.hp2 HG01257.hp2 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.368-1122T>C | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 5/10 | chr18 | 24439374 | |||||||
| chr18:24439408 | C | T | 1 | a0001c0001t0002g0135 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.368-1088C>T | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 5/10 | chr18 | 24439408 | |||||||
| chr18:24439409 | G | A | 13 | a0001c0001t0002g0179 a0001c0001t0002g0235 a0001c0004t0019g0237 others(10): Show |
25 | HG00099.hp1 HG01106.hp1 HG01123.hp1 others(22): Show |
intron_variant | MODIFIER | c.368-1087G>A | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 5/10 | chr18 | 24439409 | |||||||
| chr18:24439465 | G | A | 1 | a0001c0001t0001g0233 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.368-1031G>A | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 5/10 | chr18 | 24439465 | |||||||
| chr18:24439509 | T | C | 1 | a0001c0001t0002g0235 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.368-987T>C | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 5/10 | chr18 | 24439509 | |||||||
| chr18:24439553 | C | T | 1 | a0002c0002t0002g0112 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.368-943C>T | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 5/10 | chr18 | 24439553 | |||||||
| chr18:24439556 | GA | G | 2 | a0001c0001t0002g0016 a0001c0001t0002g0057 |
4 | HG03139.hp2 HG06807.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.368-938delA | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr18 | 24439556 | ||||||
| chr18:24439561 | C | T | 3 | a0001c0001t0011g0125 a0001c0001t0011g0126 a0001c0001t0011g0127 |
3 | HG00544.hp2 NA19056.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.368-935C>T | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 5/10 | chr18 | 24439561 | |||||||
| chr18:24439588 | G | T | 13 | a0001c0001t0005g0010 a0001c0001t0005g0039 a0001c0001t0005g0129 others(10): Show |
17 | HG00735.hp1 HG01175.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.368-908G>T | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 5/10 | chr18 | 24439588 | |||||||
| chr18:24439592 | G | A | 1 | a0003c0003t0003g0229 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.368-904G>A | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 5/10 | chr18 | 24439592 | |||||||
| chr18:24439593 | C | T | 1 | a0001c0001t0021g0082 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.368-903C>T | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 5/10 | chr18 | 24439593 | |||||||
| chr18:24439615 | C | T | 7 | a0001c0001t0006g0031 a0001c0001t0006g0056 a0001c0001t0006g0058 others(4): Show |
8 | HG02055.hp1 HG02145.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.368-881C>T | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 5/10 | chr18 | 24439615 | |||||||
| chr18:24439623 | C | T | 3 | a0001c0001t0002g0019 a0001c0001t0002g0041 a0002c0002t0002g0123 |
6 | HG00733.hp1 HG01358.hp2 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.368-873C>T | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 5/10 | chr18 | 24439623 | |||||||
| chr18:24439636 | C | CA | 15 | a0001c0001t0001g0159 a0001c0001t0001g0197 a0001c0001t0001g0198 others(12): Show |
19 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(16): Show |
intron_variant | MODIFIER | c.368-837dupA | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr18 | 24439636 | ||||||
| chr18:24439636 | CA | C | 118 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(115): Show |
186 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(183): Show |
intron_variant | MODIFIER | c.368-837delA | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr18 | 24439636 | ||||||
| chr18:24439636 | CAA | C | 14 | a0001c0001t0002g0019 a0001c0001t0002g0033 a0001c0001t0002g0040 others(11): Show |
20 | HG00733.hp1 HG01069.hp2 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.368-838_368-837del others(2): Show |
IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr18 | 24439636 | ||||||
| chr18:24439743 | C | T | 1 | a0001c0001t0002g0235 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.368-753C>T | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 5/10 | chr18 | 24439743 | |||||||
| chr18:24439776 | C | T | 12 | a0001c0001t0002g0019 a0001c0001t0002g0033 a0001c0001t0002g0040 others(9): Show |
18 | HG00733.hp1 HG01069.hp2 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.368-720C>T | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 5/10 | chr18 | 24439776 | |||||||
| chr18:24439782 | A | T | 147 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(144): Show |
230 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(227): Show |
intron_variant | MODIFIER | c.368-714A>T | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 5/10 | chr18 | 24439782 | |||||||
| chr18:24439832 | A | G | 3 | a0001c0001t0013g0051 a0001c0001t0013g0052 a0001c0001t0013g0053 |
3 | HG01167.hp1 HG01169.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.368-664A>G | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 5/10 | chr18 | 24439832 | |||||||
| chr18:24440078 | T | C | 1 | a0001c0001t0004g0054 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.368-418T>C | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 5/10 | chr18 | 24440078 | |||||||
| chr18:24440142 | GACTC | G | 35 | a0001c0001t0001g0002 a0001c0001t0001g0034 a0001c0001t0001g0035 others(32): Show |
57 | HG00099.hp2 HG00544.hp1 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.368-352_368-349del others(4): Show |
IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr18 | 24440142 | ||||||
| chr18:24440149 | G | A | 35 | a0001c0001t0001g0002 a0001c0001t0001g0034 a0001c0001t0001g0035 others(32): Show |
57 | HG00099.hp2 HG00544.hp1 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.368-347G>A | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 5/10 | chr18 | 24440149 | |||||||
| chr18:24440150 | T | A | 5 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0161 others(2): Show |
5 | HG00741.hp2 HG01358.hp1 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.368-346T>A | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 5/10 | chr18 | 24440150 | |||||||
| chr18:24440154 | TTATTTCA others(14): Show |
T | 35 | a0001c0001t0001g0002 a0001c0001t0001g0034 a0001c0001t0001g0035 others(32): Show |
57 | HG00099.hp2 HG00544.hp1 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.368-341_368-321del others(21): Show |
IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 5/10 | chr18 | 24440154 | |||||||
| chr18:24440158 | T | A | 1 | a0001c0001t0001g0210 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.368-338T>A | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 5/10 | chr18 | 24440158 | |||||||
| chr18:24440175 | A | T | 1 | a0001c0001t0001g0210 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.368-321A>T | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 5/10 | chr18 | 24440175 | |||||||
| chr18:24440395 | G | A | 19 | a0001c0001t0002g0016 a0001c0001t0002g0057 a0001c0001t0004g0008 others(16): Show |
29 | HG01109.hp1 HG01167.hp1 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.368-101G>A | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 5/10 | chr18 | 24440395 | |||||||
| chr18:24440657 | G | T | 5 | a0001c0001t0007g0048 a0001c0001t0007g0239 a0001c0001t0007g0240 others(2): Show |
5 | HG02559.hp2 HG02809.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.490+39G>T | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 6/10 | chr18 | 24440657 | |||||||
| chr18:24441052 | G | A | 13 | a0001c0001t0002g0179 a0001c0001t0002g0235 a0001c0004t0019g0237 others(10): Show |
25 | HG00099.hp1 HG01106.hp1 HG01123.hp1 others(22): Show |
intron_variant | MODIFIER | c.490+434G>A | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 6/10 | chr18 | 24441052 | |||||||
| chr18:24441053 | G | T | 213 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(210): Show |
331 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(328): Show |
intron_variant | MODIFIER | c.490+435G>T | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 6/10 | chr18 | 24441053 | |||||||
| chr18:24441076 | C | T | 12 | a0001c0001t0001g0080 a0001c0001t0001g0088 a0003c0003t0003g0004 others(9): Show |
24 | HG00099.hp1 HG01106.hp1 HG01123.hp1 others(21): Show |
intron_variant | MODIFIER | c.490+458C>T | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 6/10 | chr18 | 24441076 | |||||||
| chr18:24441127 | A | G | 5 | a0001c0001t0007g0048 a0001c0001t0007g0239 a0001c0001t0007g0240 others(2): Show |
5 | HG02559.hp2 HG02809.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.490+509A>G | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 6/10 | chr18 | 24441127 | |||||||
| chr18:24441138 | C | T | 1 | a0001c0001t0004g0015 | 3 | HG02109.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.490+520C>T | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 6/10 | chr18 | 24441138 | |||||||
| chr18:24441209 | T | G | 1 | a0001c0001t0002g0235 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.490+591T>G | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 6/10 | chr18 | 24441209 | |||||||
| chr18:24441234 | G | T | 2 | a0001c0001t0001g0066 a0001c0001t0001g0079 |
2 | NA18941.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.490+616G>T | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 6/10 | chr18 | 24441234 | |||||||
| chr18:24441270 | A | G | 19 | a0001c0001t0002g0016 a0001c0001t0002g0057 a0001c0001t0004g0008 others(16): Show |
29 | HG01109.hp1 HG01167.hp1 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.490+652A>G | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 6/10 | chr18 | 24441270 | |||||||
| chr18:24441323 | T | G | 217 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(214): Show |
336 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(333): Show |
intron_variant | MODIFIER | c.490+705T>G | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 6/10 | chr18 | 24441323 | |||||||
| chr18:24441390 | G | A | 12 | a0001c0001t0002g0019 a0001c0001t0002g0033 a0001c0001t0002g0040 others(9): Show |
18 | HG00733.hp1 HG01069.hp2 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.490+772G>A | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 6/10 | chr18 | 24441390 | |||||||
| chr18:24441413 | A | G | 3 | a0001c0001t0001g0044 a0001c0001t0001g0167 a0001c0001t0001g0226 |
4 | HG01074.hp2 HG02735.hp2 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.490+795A>G | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 6/10 | chr18 | 24441413 | |||||||
| chr18:24441433 | C | T | 1 | a0001c0001t0001g0158 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.490+815C>T | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 6/10 | chr18 | 24441433 | |||||||
| chr18:24441461 | C | T | 2 | a0001c0001t0001g0171 a0001c0001t0001g0177 |
2 | NA18985.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.490+843C>T | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 6/10 | chr18 | 24441461 | |||||||
| chr18:24441473 | C | T | 1 | a0001c0001t0001g0233 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.490+855C>T | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 6/10 | chr18 | 24441473 | |||||||
| chr18:24441607 | C | T | 3 | a0001c0001t0001g0027 a0001c0001t0001g0221 a0001c0001t0001g0236 |
5 | NA18939.hp2 NA19055.hp2 NA19056.hp1 others(2): Show |
intron_variant | MODIFIER | c.490+989C>T | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 6/10 | chr18 | 24441607 | |||||||
| chr18:24441661 | G | T | 2 | a0001c0001t0002g0138 a0001c0001t0002g0139 |
2 | HG02647.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.490+1043G>T | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 6/10 | chr18 | 24441661 | |||||||
| chr18:24441822 | A | G | 6 | a0001c0001t0004g0008 a0001c0001t0004g0015 a0001c0001t0004g0030 others(3): Show |
12 | HG01109.hp1 HG01891.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.490+1204A>G | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 6/10 | chr18 | 24441822 | |||||||
| chr18:24441975 | T | A | 1 | a0002c0002t0002g0108 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.491-1074T>A | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 6/10 | chr18 | 24441975 | |||||||
| chr18:24441990 | C | G | 5 | a0001c0001t0007g0048 a0001c0001t0007g0239 a0001c0001t0007g0240 others(2): Show |
5 | HG02559.hp2 HG02809.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.491-1059C>G | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 6/10 | chr18 | 24441990 | |||||||
| chr18:24442104 | C | G | 1 | a0001c0001t0002g0179 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.491-945C>G | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 6/10 | chr18 | 24442104 | |||||||
| chr18:24442136 | G | A | 1 | a0001c0001t0009g0032 | 2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.491-913G>A | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 6/10 | chr18 | 24442136 | |||||||
| chr18:24442150 | C | CT | 43 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0024 others(40): Show |
72 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.491-879dupT | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr18 | 24442150 | ||||||
| chr18:24442150 | C | CTT | 6 | a0001c0001t0001g0074 a0001c0001t0001g0208 a0001c0001t0001g0209 others(3): Show |
7 | HG03225.hp2 HG03453.hp2 HG03579.hp2 others(4): Show |
intron_variant | MODIFIER | c.491-880_491-879dup others(2): Show |
IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr18 | 24442150 | ||||||
| chr18:24442150 | CT | C | 21 | a0001c0001t0001g0068 a0001c0001t0001g0151 a0001c0001t0002g0016 others(18): Show |
28 | HG00735.hp1 HG01070.hp1 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.491-879delT | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr18 | 24442150 | ||||||
| chr18:24442231 | G | A | 2 | a0002c0002t0014g0095 a0002c0002t0014g0096 |
2 | HG03098.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.491-818G>A | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 6/10 | chr18 | 24442231 | |||||||
| chr18:24442346 | G | T | 1 | a0001c0001t0001g0216 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.491-703G>T | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 6/10 | chr18 | 24442346 | |||||||
| chr18:24442398 | C | T | 1 | a0001c0001t0002g0041 | 2 | HG00733.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.491-651C>T | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 6/10 | chr18 | 24442398 | |||||||
| chr18:24442497 | T | C | 2 | a0002c0002t0014g0095 a0002c0002t0014g0096 |
2 | HG03098.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.491-552T>C | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 6/10 | chr18 | 24442497 | |||||||
| chr18:24442620 | A | G | 7 | a0001c0001t0005g0010 a0001c0001t0005g0039 a0001c0001t0005g0129 others(4): Show |
11 | HG00735.hp1 HG01175.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.491-429A>G | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 6/10 | chr18 | 24442620 | |||||||
| chr18:24442710 | T | C | 251 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(248): Show |
398 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(395): Show |
intron_variant | MODIFIER | c.491-339T>C | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 6/10 | chr18 | 24442710 | |||||||
| chr18:24442739 | G | C | 1 | a0002c0002t0002g0097 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.491-310G>C | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 6/10 | chr18 | 24442739 | |||||||
| chr18:24442744 | T | C | 164 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(161): Show |
256 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(253): Show |
intron_variant | MODIFIER | c.491-305T>C | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 6/10 | chr18 | 24442744 | |||||||
| chr18:24442745 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.491-304G>A | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 6/10 | chr18 | 24442745 | |||||||
| chr18:24442768 | C | G | 1 | a0004c0008t0001g0092 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.491-281C>G | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 6/10 | chr18 | 24442768 | |||||||
| chr18:24442980 | C | T | 5 | a0001c0001t0002g0011 a0001c0001t0002g0065 a0001c0001t0002g0138 others(2): Show |
8 | HG01167.hp2 HG02647.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.491-69C>T | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 6/10 | chr18 | 24442980 | |||||||
| chr18:24443405 | A | G | 1 | a0001c0001t0011g0126 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.594+253A>G | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 7/10 | chr18 | 24443405 | |||||||
| chr18:24443452 | C | T | 7 | a0001c0001t0005g0010 a0001c0001t0005g0039 a0001c0001t0005g0129 others(4): Show |
11 | HG00735.hp1 HG01175.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.594+300C>T | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 7/10 | chr18 | 24443452 | |||||||
| chr18:24443457 | A | G | 3 | a0001c0001t0001g0148 a0001c0001t0001g0155 a0001c0001t0001g0166 |
3 | NA18948.hp2 NA18974.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.594+305A>G | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 7/10 | chr18 | 24443457 | |||||||
| chr18:24443570 | A | G | 1 | a0001c0001t0009g0032 | 2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.594+418A>G | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 7/10 | chr18 | 24443570 | |||||||
| chr18:24443700 | C | A | 1 | a0001c0001t0026g0130 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.594+548C>A | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 7/10 | chr18 | 24443700 | |||||||
| chr18:24443779 | G | A | 1 | a0001c0001t0001g0035 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.594+627G>A | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 7/10 | chr18 | 24443779 | |||||||
| chr18:24443803 | G | A | 19 | a0001c0001t0002g0016 a0001c0001t0002g0057 a0001c0001t0004g0008 others(16): Show |
29 | HG01109.hp1 HG01167.hp1 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.594+651G>A | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 7/10 | chr18 | 24443803 | |||||||
| chr18:24443863 | T | C | 1 | a0001c0001t0006g0059 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.594+711T>C | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 7/10 | chr18 | 24443863 | |||||||
| chr18:24443904 | T | C | 1 | a0001c0001t0001g0075 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.594+752T>C | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 7/10 | chr18 | 24443904 | |||||||
| chr18:24444024 | A | G | 3 | a0001c0001t0013g0051 a0001c0001t0013g0052 a0001c0001t0013g0053 |
3 | HG01167.hp1 HG01169.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.594+872A>G | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 7/10 | chr18 | 24444024 | |||||||
| chr18:24444241 | T | G | 36 | a0001c0001t0001g0005 a0001c0001t0001g0020 a0001c0001t0001g0021 others(33): Show |
50 | HG00673.hp1 HG00735.hp2 HG00738.hp1 others(47): Show |
intron_variant | MODIFIER | c.594+1089T>G | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 7/10 | chr18 | 24444241 | |||||||
| chr18:24444354 | A | G | 10 | a0003c0003t0003g0004 a0003c0003t0003g0029 a0003c0003t0003g0227 others(7): Show |
22 | HG00099.hp1 HG01106.hp1 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.595-1039A>G | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 7/10 | chr18 | 24444354 | |||||||
| chr18:24444596 | C | T | 1 | a0001c0001t0001g0212 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.595-797C>T | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 7/10 | chr18 | 24444596 | |||||||
| chr18:24444765 | T | C | 7 | a0002c0002t0002g0118 a0002c0002t0002g0119 a0002c0002t0002g0120 others(4): Show |
7 | HG00423.hp2 HG02015.hp2 NA18747.hp1 others(4): Show |
intron_variant | MODIFIER | c.595-628T>C | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 7/10 | chr18 | 24444765 | |||||||
| chr18:24444801 | A | C | 165 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(162): Show |
257 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(254): Show |
intron_variant | MODIFIER | c.595-592A>C | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 7/10 | chr18 | 24444801 | |||||||
| chr18:24444826 | T | C | 2 | a0001c0001t0010g0037 a0001c0001t0010g0093 |
3 | HG02895.hp2 HG02897.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.595-567T>C | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 7/10 | chr18 | 24444826 | |||||||
| chr18:24445030 | G | C | 1 | a0001c0001t0001g0153 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.595-363G>C | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 7/10 | chr18 | 24445030 | |||||||
| chr18:24445172 | A | T | 1 | a0001c0001t0023g0200 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.595-221A>T | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 7/10 | chr18 | 24445172 | |||||||
| chr18:24445226 | C | T | 1 | a0001c0001t0001g0216 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.595-167C>T | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 7/10 | chr18 | 24445226 | |||||||
| chr18:24445493 | T | C | 8 | a0001c0001t0002g0016 a0001c0001t0002g0057 a0001c0001t0006g0031 others(5): Show |
11 | HG02055.hp1 HG02145.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.668+27T>C | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 8/10 | chr18 | 24445493 | |||||||
| chr18:24445568 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.668+102G>A | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 8/10 | chr18 | 24445568 | |||||||
| chr18:24445586 | G | A | 1 | a0001c0001t0001g0012 | 4 | HG02055.hp2 HG03209.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.668+120G>A | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 8/10 | chr18 | 24445586 | |||||||
| chr18:24445836 | C | G | 10 | a0003c0003t0003g0004 a0003c0003t0003g0029 a0003c0003t0003g0227 others(7): Show |
22 | HG00099.hp1 HG01106.hp1 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.668+370C>G | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 8/10 | chr18 | 24445836 | |||||||
| chr18:24445983 | A | C | 19 | a0001c0001t0002g0016 a0001c0001t0002g0057 a0001c0001t0004g0008 others(16): Show |
29 | HG01109.hp1 HG01167.hp1 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.668+517A>C | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 8/10 | chr18 | 24445983 | |||||||
| chr18:24446021 | A | G | 147 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(144): Show |
230 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(227): Show |
intron_variant | MODIFIER | c.668+555A>G | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 8/10 | chr18 | 24446021 | |||||||
| chr18:24446027 | T | C | 2 | a0001c0001t0010g0037 a0001c0001t0010g0093 |
3 | HG02895.hp2 HG02897.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.668+561T>C | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 8/10 | chr18 | 24446027 | |||||||
| chr18:24446107 | A | G | 1 | a0002c0002t0002g0105 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.668+641A>G | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 8/10 | chr18 | 24446107 | |||||||
| chr18:24446146 | G | T | 3 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0188 |
3 | HG03471.hp1 HG03540.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.668+680G>T | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 8/10 | chr18 | 24446146 | |||||||
| chr18:24446252 | G | A | 5 | a0001c0001t0007g0048 a0001c0001t0007g0239 a0001c0001t0007g0240 others(2): Show |
5 | HG02559.hp2 HG02809.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.668+786G>A | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 8/10 | chr18 | 24446252 | |||||||
| chr18:24446276 | G | T | 3 | a0001c0001t0011g0125 a0001c0001t0011g0126 a0001c0001t0011g0127 |
3 | HG00544.hp2 NA19056.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.668+810G>T | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 8/10 | chr18 | 24446276 | |||||||
| chr18:24446310 | C | T | 4 | a0001c0001t0010g0037 a0001c0001t0010g0093 a0002c0002t0014g0095 others(1): Show |
5 | HG02895.hp2 HG02897.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.668+844C>T | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 8/10 | chr18 | 24446310 | |||||||
| chr18:24446312 | A | C | 216 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(213): Show |
335 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(332): Show |
intron_variant | MODIFIER | c.668+846A>C | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 8/10 | chr18 | 24446312 | |||||||
| chr18:24446345 | G | T | 1 | a0001c0001t0001g0145 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.668+879G>T | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 8/10 | chr18 | 24446345 | |||||||
| chr18:24446559 | C | T | 216 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(213): Show |
335 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(332): Show |
intron_variant | MODIFIER | c.668+1093C>T | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 8/10 | chr18 | 24446559 | |||||||
| chr18:24446570 | T | G | 10 | a0003c0003t0003g0004 a0003c0003t0003g0029 a0003c0003t0003g0227 others(7): Show |
22 | HG00099.hp1 HG01106.hp1 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.668+1104T>G | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 8/10 | chr18 | 24446570 | |||||||
| chr18:24446807 | T | G | 5 | a0001c0001t0001g0034 a0001c0001t0001g0071 a0001c0001t0001g0072 others(2): Show |
6 | HG02735.hp1 HG04184.hp2 NA18952.hp1 others(3): Show |
intron_variant | MODIFIER | c.669-1286T>G | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 8/10 | chr18 | 24446807 | |||||||
| chr18:24446834 | C | T | 1 | a0001c0001t0001g0191 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.669-1259C>T | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 8/10 | chr18 | 24446834 | |||||||
| chr18:24446977 | A | G | 10 | a0003c0003t0003g0004 a0003c0003t0003g0029 a0003c0003t0003g0227 others(7): Show |
22 | HG00099.hp1 HG01106.hp1 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.669-1116A>G | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 8/10 | chr18 | 24446977 | |||||||
| chr18:24446993 | T | C | 2 | a0002c0002t0014g0095 a0002c0002t0014g0096 |
2 | HG03098.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.669-1100T>C | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 8/10 | chr18 | 24446993 | |||||||
| chr18:24447024 | C | T | 10 | a0003c0003t0003g0004 a0003c0003t0003g0029 a0003c0003t0003g0227 others(7): Show |
22 | HG00099.hp1 HG01106.hp1 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.669-1069C>T | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 8/10 | chr18 | 24447024 | |||||||
| chr18:24447055 | A | G | 1 | a0001c0001t0001g0199 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.669-1038A>G | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 8/10 | chr18 | 24447055 | |||||||
| chr18:24447180 | T | C | 19 | a0001c0001t0002g0016 a0001c0001t0002g0057 a0001c0001t0004g0008 others(16): Show |
29 | HG01109.hp1 HG01167.hp1 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.669-913T>C | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 8/10 | chr18 | 24447180 | |||||||
| chr18:24447259 | A | G | 1 | a0001c0001t0009g0032 | 2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.669-834A>G | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 8/10 | chr18 | 24447259 | |||||||
| chr18:24447353 | G | T | 3 | a0002c0002t0002g0103 a0002c0002t0002g0104 a0002c0002t0002g0117 |
3 | NA18953.hp1 NA19059.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.669-740G>T | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 8/10 | chr18 | 24447353 | |||||||
| chr18:24447478 | T | G | 1 | a0001c0001t0002g0136 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.669-615T>G | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 8/10 | chr18 | 24447478 | |||||||
| chr18:24447482 | T | C | 8 | a0001c0001t0002g0016 a0001c0001t0002g0057 a0001c0001t0006g0031 others(5): Show |
11 | HG02055.hp1 HG02145.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.669-611T>C | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 8/10 | chr18 | 24447482 | |||||||
| chr18:24447497 | C | T | 4 | a0001c0001t0010g0037 a0001c0001t0010g0093 a0002c0002t0014g0095 others(1): Show |
5 | HG02895.hp2 HG02897.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.669-596C>T | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 8/10 | chr18 | 24447497 | |||||||
| chr18:24447809 | A | C | 1 | a0001c0001t0011g0126 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.669-284A>C | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 8/10 | chr18 | 24447809 | |||||||
| chr18:24448206 | A | G | 1 | a0002c0002t0002g0111 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.759+23A>G | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 9/10 | chr18 | 24448206 | |||||||
| chr18:24448449 | G | A | 146 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(143): Show |
229 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(226): Show |
intron_variant | MODIFIER | c.759+266G>A | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 9/10 | chr18 | 24448449 | |||||||
| chr18:24448560 | G | A | 215 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(212): Show |
334 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(331): Show |
intron_variant | MODIFIER | c.759+377G>A | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 9/10 | chr18 | 24448560 | |||||||
| chr18:24448896 | A | G | 1 | a0001c0001t0001g0215 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.759+713A>G | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 9/10 | chr18 | 24448896 | |||||||
| chr18:24449158 | C | T | 1 | a0001c0001t0001g0211 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.760-661C>T | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 9/10 | chr18 | 24449158 | |||||||
| chr18:24449218 | C | T | 1 | a0001c0001t0001g0077 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.760-601C>T | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 9/10 | chr18 | 24449218 | |||||||
| chr18:24449400 | G | A | 1 | a0001c0001t0004g0054 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.760-419G>A | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 9/10 | chr18 | 24449400 | |||||||
| chr18:24449415 | G | A | 38 | a0001c0001t0001g0005 a0001c0001t0001g0020 a0001c0001t0001g0021 others(35): Show |
54 | HG00639.hp1 HG00673.hp1 HG00735.hp2 others(51): Show |
intron_variant | MODIFIER | c.760-404G>A | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 9/10 | chr18 | 24449415 | |||||||
| chr18:24449447 | G | GT | 5 | a0001c0001t0001g0154 a0001c0001t0001g0164 a0001c0001t0001g0209 others(2): Show |
5 | HG02293.hp1 NA18956.hp2 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.760-364dupT | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr18 | 24449447 | ||||||
| chr18:24449574 | C | G | 2 | a0001c0001t0001g0070 a0001c0001t0001g0086 |
2 | HG00642.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.760-245C>G | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 9/10 | chr18 | 24449574 | |||||||
| chr18:24449964 | C | G | 13 | a0001c0001t0005g0010 a0001c0001t0005g0039 a0001c0001t0005g0129 others(10): Show |
17 | HG00735.hp1 HG01175.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.894+11C>G | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 10/10 | chr18 | 24449964 | |||||||
| chr18:24450005 | A | AT | 2 | a0003c0003t0003g0029 a0003c0003t0003g0229 |
4 | HG00099.hp1 HG01975.hp1 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.894+58dupT | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr18 | 24450005 | ||||||
| chr18:24450042 | A | G | 1 | a0001c0001t0001g0076 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.894+89A>G | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 10/10 | chr18 | 24450042 | |||||||
| chr18:24450065 | C | T | 5 | a0001c0001t0007g0048 a0001c0001t0007g0239 a0001c0001t0007g0240 others(2): Show |
5 | HG02559.hp2 HG02809.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.894+112C>T | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 10/10 | chr18 | 24450065 | |||||||
| chr18:24450134 | G | A | 2 | a0001c0001t0002g0138 a0001c0001t0002g0139 |
2 | HG02647.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.894+181G>A | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 10/10 | chr18 | 24450134 | |||||||
| chr18:24450364 | C | T | 1 | a0001c0001t0005g0129 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.894+411C>T | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 10/10 | chr18 | 24450364 | |||||||
| chr18:24450379 | A | G | 1 | a0001c0004t0019g0237 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.895-400A>G | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 10/10 | chr18 | 24450379 | |||||||
| chr18:24450621 | A | G | 204 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(201): Show |
311 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(308): Show |
intron_variant | MODIFIER | c.895-158A>G | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 10/10 | chr18 | 24450621 | |||||||
| chr18:24450636 | C | T | 29 | a0001c0001t0001g0005 a0001c0001t0001g0020 a0001c0001t0001g0021 others(26): Show |
43 | HG00639.hp1 HG00673.hp1 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.895-143C>T | IMPACT | ENSG00000154059.11 | transcript | ENST00000284202.9 | protein_coding | 10/10 | chr18 | 24450636 |