Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 10598 |
| ensemblid | ENSG00000100591.8 |
| hgncid | 1189 |
| symbol | AHSA1 |
| name | activator of HSP90 ATPase activity 1 |
| refseq_nuc | NM_012111.3 |
| refseq_prot | NP_036243.1 |
| ensembl_nuc | ENST00000216479.8 |
| ensembl_prot | ENSP00000216479.3 |
| mane_status | MANE Select |
| chr | chr14 |
| start | 77458093 |
| end | 77469472 |
| strand | + |
| ver | v1.2 |
| region | chr14:77458093-77469472 |
| region5000 | chr14:77453093-77474472 |
| regionname0 | AHSA1_chr14_77458093_77469472 |
| regionname5000 | AHSA1_chr14_77453093_77474472 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1014 | 131 | 8 | 26 | 78 | 3 | 15 | AHSA1_chr14_77453093_77474472 | AHSA1 | ATGGC others(1009): Show |
chr14 | 77453093 | 77474472 | ||
| a0001c0002 | 1/0 | 1014 | 130 | 58 | 28 | 14 | 8 | 21 | AHSA1_chr14_77453093_77474472 | AHSA1 | ATGGC others(1009): Show |
chr14 | 77453093 | 77474472 | ||
| a0001c0003 | 0/0 | 1014 | 30 | 15 | 8 | 0 | 3 | 4 | AHSA1_chr14_77453093_77474472 | AHSA1 | ATGGC others(1009): Show |
chr14 | 77453093 | 77474472 | ||
| a0001c0004 | 0/0 | 1014 | 10 | 9 | 1 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | ATGGC others(1009): Show |
chr14 | 77453093 | 77474472 | ||
| a0001c0005 | 0/0 | 1014 | 2 | 2 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | ATGGC others(1009): Show |
chr14 | 77453093 | 77474472 | ||
| a0001c0006 | 0/0 | 1014 | 2 | 0 | 2 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | ATGGC others(1009): Show |
chr14 | 77453093 | 77474472 | ||
| a0001c0007 | 0/0 | 1014 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | ATGGC others(1009): Show |
chr14 | 77453093 | 77474472 | ||
| a0001c0008 | 0/0 | 1014 | 1 | 0 | 1 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | ATGGC others(1009): Show |
chr14 | 77453093 | 77474472 | ||
| a0001c0009 | 0/0 | 1014 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | ATGGC others(1009): Show |
chr14 | 77453093 | 77474472 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 1337 | 129 | 8 | 26 | 77 | 3 | 14 | AHSA1_chr14_77453093_77474472 | AHSA1 | AGTAG others(1332): Show |
chr14 | 77453093 | 77474472 |
| a0001c0001t0004 | 0/0 | 1337 | 1 | 0 | 0 | 0 | 0 | 1 | AHSA1_chr14_77453093_77474472 | AHSA1 | AGTAG others(1332): Show |
chr14 | 77453093 | 77474472 |
| a0001c0001t0005 | 0/0 | 1337 | 1 | 0 | 0 | 1 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | AGTAG others(1332): Show |
chr14 | 77453093 | 77474472 |
| a0001c0002t0001 | 1/0 | 1337 | 98 | 49 | 22 | 8 | 6 | 12 | AHSA1_chr14_77453093_77474472 | AHSA1 | AGTAG others(1332): Show |
chr14 | 77453093 | 77474472 |
| a0001c0002t0002 | 0/0 | 1337 | 32 | 9 | 6 | 6 | 2 | 9 | AHSA1_chr14_77453093_77474472 | AHSA1 | AGTAG others(1332): Show |
chr14 | 77453093 | 77474472 |
| a0001c0003t0001 | 0/0 | 1337 | 20 | 11 | 4 | 0 | 2 | 3 | AHSA1_chr14_77453093_77474472 | AHSA1 | AGTAG others(1332): Show |
chr14 | 77453093 | 77474472 |
| a0001c0003t0003 | 0/0 | 1337 | 10 | 4 | 4 | 0 | 1 | 1 | AHSA1_chr14_77453093_77474472 | AHSA1 | AGTAG others(1332): Show |
chr14 | 77453093 | 77474472 |
| a0001c0004t0001 | 0/0 | 1337 | 10 | 9 | 1 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | AGTAG others(1332): Show |
chr14 | 77453093 | 77474472 |
| a0001c0005t0001 | 0/0 | 1337 | 2 | 2 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | AGTAG others(1332): Show |
chr14 | 77453093 | 77474472 |
| a0001c0006t0001 | 0/0 | 1337 | 2 | 0 | 2 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | AGTAG others(1332): Show |
chr14 | 77453093 | 77474472 |
| a0001c0007t0001 | 0/0 | 1337 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | AGTAG others(1332): Show |
chr14 | 77453093 | 77474472 |
| a0001c0008t0001 | 0/0 | 1337 | 1 | 0 | 1 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | AGTAG others(1332): Show |
chr14 | 77453093 | 77474472 |
| a0001c0009t0001 | 0/0 | 1337 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | AGTAG others(1332): Show |
chr14 | 77453093 | 77474472 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 59 | 3 | 16 | 28 | 3 | 9 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0001t0001g0004 | 0/0 | 10 | 0 | 0 | 10 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0001t0001g0005 | 0/0 | 8 | 1 | 1 | 6 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0001t0001g0008 | 0/0 | 6 | 0 | 1 | 4 | 0 | 1 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0001t0001g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0001t0001g0024 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0001t0001g0050 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0001t0004g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0001t0005g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0002t0001g0002 | 0/0 | 19 | 4 | 8 | 0 | 0 | 7 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0002t0001g0003 | 1/0 | 14 | 13 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0002t0001g0009 | 0/0 | 6 | 1 | 3 | 0 | 0 | 2 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0002t0001g0013 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0002t0001g0016 | 0/0 | 3 | 0 | 0 | 0 | 3 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0002t0001g0017 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0002t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0002t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0002t0001g0022 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0002t0001g0025 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0002t0001g0026 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0002t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0002t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0002t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0002t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0002t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0002t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0002t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0002t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0002t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0002t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0002t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0002t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0002t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0002t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0002t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0002t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0002t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0002t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0002t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0002t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0002t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0002t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0002t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0002t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0002t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0002t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0002t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0002t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0002t0002g0012 | 0/0 | 4 | 1 | 0 | 1 | 0 | 2 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0002t0002g0018 | 0/0 | 3 | 1 | 1 | 1 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0002t0002g0028 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0002t0002g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0002t0002g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0002t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0002t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0002t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0002t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0002t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0002t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0002t0002g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0002t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0002t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0002t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0002t0002g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0002t0002g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0002t0002g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0002t0002g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0002t0002g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0002t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0003t0001g0007 | 0/0 | 6 | 0 | 3 | 0 | 1 | 2 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0003t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0003t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0003t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0003t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0003t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0003t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0003t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0003t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0003t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0003t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0003t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0003t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0003t0003g0006 | 0/0 | 7 | 4 | 2 | 0 | 1 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0003t0003g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0003t0003g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0003t0003g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0004t0001g0010 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0004t0001g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0004t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0004t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0005t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0005t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0006t0001g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0007t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0008t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| a0001c0009t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0003 | t0001 | g0007 | EUR | GBR | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG00099 | hp2 | a0001 | c0002 | t0001 | g0034 | EUR | GBR | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG00323 | hp1 | a0001 | c0003 | t0001 | g0043 | EUR | FIN | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | CHS | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | CHS | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG00639 | hp2 | a0001 | c0002 | t0001 | g0086 | AMR | PUR | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG00642 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG00642 | hp2 | a0001 | c0003 | t0003 | g0006 | AMR | PUR | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | CHS | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG00733 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG00735 | hp2 | a0001 | c0003 | t0003 | g0006 | AMR | PUR | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG00741 | hp1 | a0001 | c0002 | t0001 | g0013 | AMR | PUR | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG01069 | hp1 | a0001 | c0003 | t0001 | g0007 | AMR | PUR | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG01069 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG01070 | hp1 | a0001 | c0003 | t0001 | g0045 | AMR | PUR | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | PUR | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG01071 | hp2 | a0001 | c0003 | t0001 | g0007 | AMR | PUR | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG01081 | hp1 | a0001 | c0002 | t0002 | g0028 | AMR | PUR | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG01099 | hp2 | a0001 | c0002 | t0002 | g0107 | AMR | PUR | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG01106 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG01109 | hp1 | a0001 | c0002 | t0001 | g0022 | AMR | PUR | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG01109 | hp2 | a0001 | c0003 | t0003 | g0120 | AMR | PUR | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG01168 | hp2 | a0001 | c0002 | t0002 | g0018 | AMR | PUR | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG01169 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG01175 | hp2 | a0001 | c0002 | t0002 | g0136 | AMR | PUR | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG01243 | hp1 | a0001 | c0004 | t0001 | g0140 | AMR | PUR | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG01243 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG01255 | hp2 | a0001 | c0002 | t0001 | g0009 | AMR | CLM | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG01256 | hp2 | a0001 | c0006 | t0001 | g0023 | AMR | CLM | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG01257 | hp1 | a0001 | c0002 | t0001 | g0017 | AMR | CLM | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG01257 | hp2 | a0001 | c0002 | t0001 | g0139 | AMR | CLM | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG01258 | hp1 | a0001 | c0002 | t0001 | g0017 | AMR | CLM | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG01258 | hp2 | a0001 | c0006 | t0001 | g0023 | AMR | CLM | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG01261 | hp1 | a0001 | c0002 | t0001 | g0017 | AMR | CLM | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG01261 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | CLM | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG01358 | hp1 | a0001 | c0003 | t0001 | g0007 | AMR | CLM | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG01358 | hp2 | a0001 | c0002 | t0002 | g0099 | AMR | CLM | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG01515 | hp1 | a0001 | c0002 | t0001 | g0016 | EUR | IBS | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG01515 | hp2 | a0001 | c0002 | t0002 | g0108 | EUR | IBS | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG01516 | hp1 | a0001 | c0002 | t0001 | g0025 | EUR | IBS | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG01516 | hp2 | a0001 | c0002 | t0001 | g0016 | EUR | IBS | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG01517 | hp1 | a0001 | c0002 | t0001 | g0016 | EUR | IBS | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG01517 | hp2 | a0001 | c0002 | t0002 | g0105 | EUR | IBS | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG01884 | hp1 | a0001 | c0002 | t0001 | g0002 | AFR | ACB | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG01884 | hp2 | a0001 | c0003 | t0001 | g0031 | AFR | ACB | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG01891 | hp1 | a0001 | c0003 | t0001 | g0124 | AFR | ACB | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG01891 | hp2 | a0001 | c0002 | t0001 | g0003 | AFR | ACB | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG01934 | hp2 | a0001 | c0008 | t0001 | g0088 | AMR | PEL | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG01975 | hp2 | a0001 | c0002 | t0002 | g0101 | AMR | PEL | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0013 | AMR | PEL | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG01993 | hp1 | a0001 | c0002 | t0001 | g0009 | AMR | PEL | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | PEL | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG02055 | hp1 | a0001 | c0002 | t0001 | g0026 | AFR | ACB | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | ACB | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG02071 | hp1 | a0001 | c0002 | t0001 | g0089 | EAS | KHV | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG02074 | hp2 | a0001 | c0002 | t0002 | g0018 | EAS | KHV | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | KHV | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | KHV | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG02145 | hp1 | a0001 | c0003 | t0001 | g0121 | AFR | ACB | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG02145 | hp2 | a0001 | c0002 | t0001 | g0085 | AFR | ACB | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG02148 | hp1 | a0001 | c0002 | t0001 | g0135 | AMR | PEL | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG02148 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG02155 | hp2 | a0001 | c0002 | t0002 | g0012 | EAS | CDX | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | CDX | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | CDX | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG02257 | hp1 | a0001 | c0002 | t0001 | g0003 | AFR | ACB | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG02258 | hp1 | a0001 | c0002 | t0001 | g0097 | AFR | ACB | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG02258 | hp2 | a0001 | c0002 | t0001 | g0003 | AFR | ACB | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG02273 | hp1 | a0001 | c0002 | t0001 | g0009 | AMR | PEL | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG02280 | hp1 | a0001 | c0002 | t0001 | g0002 | AFR | ACB | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG02280 | hp2 | a0001 | c0004 | t0001 | g0141 | AFR | ACB | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG02293 | hp1 | a0001 | c0003 | t0003 | g0119 | AMR | PEL | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG02451 | hp1 | a0001 | c0002 | t0001 | g0025 | AFR | ACB | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG02451 | hp2 | a0001 | c0002 | t0001 | g0035 | AFR | ACB | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | KHV | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG02572 | hp1 | a0001 | c0002 | t0001 | g0021 | AFR | GWD | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG02572 | hp2 | a0001 | c0003 | t0001 | g0128 | AFR | GWD | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG02615 | hp1 | a0001 | c0002 | t0001 | g0003 | AFR | GWD | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG02615 | hp2 | a0001 | c0003 | t0001 | g0129 | AFR | GWD | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG02630 | hp1 | a0001 | c0002 | t0001 | g0091 | AFR | GWD | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG02630 | hp2 | a0001 | c0002 | t0001 | g0020 | AFR | GWD | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG02647 | hp1 | a0001 | c0002 | t0002 | g0028 | AFR | GWD | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG02647 | hp2 | a0001 | c0002 | t0001 | g0003 | AFR | GWD | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0049 | SAS | PJL | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG02698 | hp1 | a0001 | c0002 | t0001 | g0009 | SAS | PJL | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG02698 | hp2 | a0001 | c0003 | t0003 | g0122 | SAS | PJL | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG02717 | hp1 | a0001 | c0002 | t0001 | g0094 | AFR | GWD | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG02717 | hp2 | a0001 | c0003 | t0003 | g0006 | AFR | GWD | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG02723 | hp1 | a0001 | c0002 | t0002 | g0018 | AFR | GWD | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG02723 | hp2 | a0001 | c0002 | t0001 | g0003 | AFR | GWD | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG02735 | hp1 | a0001 | c0002 | t0001 | g0009 | SAS | PJL | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG02735 | hp2 | a0001 | c0002 | t0001 | g0002 | SAS | PJL | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG02738 | hp1 | a0001 | c0002 | t0002 | g0113 | SAS | PJL | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG02809 | hp1 | a0001 | c0002 | t0001 | g0125 | AFR | GWD | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG02809 | hp2 | a0001 | c0002 | t0001 | g0040 | AFR | GWD | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG02818 | hp1 | a0001 | c0003 | t0001 | g0118 | AFR | GWD | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG02818 | hp2 | a0001 | c0004 | t0001 | g0019 | AFR | GWD | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG02886 | hp1 | a0001 | c0003 | t0001 | g0031 | AFR | GWD | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG02886 | hp2 | a0001 | c0005 | t0001 | g0092 | AFR | GWD | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG02895 | hp1 | a0001 | c0004 | t0001 | g0010 | AFR | GWD | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG02897 | hp2 | a0001 | c0002 | t0001 | g0021 | AFR | GWD | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG02922 | hp1 | a0001 | c0004 | t0001 | g0019 | AFR | ESN | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG02922 | hp2 | a0001 | c0002 | t0001 | g0083 | AFR | ESN | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG02965 | hp1 | a0001 | c0002 | t0001 | g0082 | AFR | ESN | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG02965 | hp2 | a0001 | c0007 | t0001 | g0104 | AFR | ESN | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG02970 | hp1 | a0001 | c0004 | t0001 | g0019 | AFR | ESN | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG02970 | hp2 | a0001 | c0002 | t0002 | g0029 | AFR | ESN | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG02976 | hp1 | a0001 | c0002 | t0001 | g0126 | AFR | ESN | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG02976 | hp2 | a0001 | c0002 | t0002 | g0012 | AFR | ESN | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG03017 | hp1 | a0001 | c0002 | t0001 | g0002 | SAS | PJL | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG03017 | hp2 | a0001 | c0002 | t0002 | g0012 | SAS | PJL | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG03041 | hp1 | a0001 | c0002 | t0002 | g0100 | AFR | GWD | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG03041 | hp2 | a0001 | c0002 | t0001 | g0142 | AFR | GWD | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG03098 | hp1 | a0001 | c0002 | t0001 | g0080 | AFR | MSL | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG03098 | hp2 | a0001 | c0002 | t0001 | g0037 | AFR | MSL | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG03130 | hp1 | a0001 | c0004 | t0001 | g0010 | AFR | ESN | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG03130 | hp2 | a0001 | c0002 | t0001 | g0003 | AFR | ESN | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG03139 | hp1 | a0001 | c0005 | t0001 | g0084 | AFR | ESN | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG03139 | hp2 | a0001 | c0002 | t0001 | g0003 | AFR | ESN | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG03195 | hp1 | a0001 | c0002 | t0001 | g0103 | AFR | ESN | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG03195 | hp2 | a0001 | c0002 | t0002 | g0102 | AFR | ESN | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG03209 | hp1 | a0001 | c0002 | t0001 | g0003 | AFR | MSL | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG03209 | hp2 | a0001 | c0002 | t0001 | g0036 | AFR | MSL | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG03225 | hp1 | a0001 | c0004 | t0001 | g0010 | AFR | MSL | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG03225 | hp2 | a0001 | c0002 | t0001 | g0042 | AFR | MSL | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG03486 | hp1 | a0001 | c0003 | t0001 | g0032 | AFR | MSL | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG03486 | hp2 | a0001 | c0002 | t0001 | g0003 | AFR | MSL | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG03491 | hp2 | a0001 | c0003 | t0001 | g0007 | SAS | PJL | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG03516 | hp1 | a0001 | c0002 | t0001 | g0039 | AFR | ESN | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG03516 | hp2 | a0001 | c0002 | t0002 | g0029 | AFR | ESN | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG03540 | hp1 | a0001 | c0002 | t0001 | g0027 | AFR | GWD | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG03540 | hp2 | a0001 | c0009 | t0001 | g0079 | AFR | GWD | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG03579 | hp1 | a0001 | c0004 | t0001 | g0010 | AFR | MSL | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG03579 | hp2 | a0001 | c0003 | t0003 | g0006 | AFR | MSL | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG03654 | hp1 | a0001 | c0002 | t0002 | g0012 | SAS | PJL | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG03669 | hp1 | a0001 | c0002 | t0001 | g0002 | SAS | PJL | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG03688 | hp1 | a0001 | c0002 | t0002 | g0112 | SAS | STU | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG03704 | hp1 | a0001 | c0003 | t0001 | g0044 | SAS | PJL | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG03704 | hp2 | a0001 | c0002 | t0001 | g0002 | SAS | PJL | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG03710 | hp1 | a0001 | c0002 | t0002 | g0116 | SAS | PJL | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG03710 | hp2 | a0001 | c0002 | t0001 | g0002 | SAS | PJL | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG03831 | hp1 | a0001 | c0002 | t0001 | g0026 | SAS | BEB | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG03834 | hp1 | a0001 | c0002 | t0002 | g0106 | SAS | BEB | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG03927 | hp1 | a0001 | c0002 | t0001 | g0002 | SAS | BEB | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG03927 | hp2 | a0001 | c0002 | t0001 | g0093 | SAS | BEB | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG03942 | hp1 | a0001 | c0003 | t0001 | g0007 | SAS | BEB | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG03942 | hp2 | a0001 | c0002 | t0002 | g0114 | SAS | BEB | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG04115 | hp1 | a0001 | c0002 | t0002 | g0117 | SAS | STU | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | STU | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG04199 | hp1 | a0001 | c0002 | t0001 | g0002 | SAS | STU | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG04199 | hp2 | a0001 | c0002 | t0002 | g0115 | SAS | STU | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG04204 | hp1 | a0001 | c0002 | t0001 | g0013 | SAS | STU | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | STU | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| NA18522 | hp1 | a0001 | c0002 | t0001 | g0020 | AFR | YRI | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| NA18522 | hp2 | a0001 | c0003 | t0003 | g0006 | AFR | YRI | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| NA18906 | hp2 | a0001 | c0003 | t0001 | g0123 | AFR | YRI | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| NA18944 | hp2 | a0001 | c0002 | t0002 | g0030 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| NA18945 | hp1 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| NA18946 | hp2 | a0001 | c0002 | t0001 | g0131 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| NA18953 | hp1 | a0001 | c0002 | t0001 | g0033 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| NA18967 | hp2 | a0001 | c0002 | t0001 | g0133 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| NA18969 | hp2 | a0001 | c0002 | t0001 | g0134 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| NA18975 | hp1 | a0001 | c0002 | t0002 | g0030 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| NA18986 | hp2 | a0001 | c0002 | t0002 | g0110 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| NA18990 | hp1 | a0001 | c0002 | t0001 | g0033 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| NA18991 | hp1 | a0001 | c0002 | t0002 | g0109 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| NA19030 | hp1 | a0001 | c0002 | t0001 | g0041 | AFR | LWK | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | LWK | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| NA19043 | hp1 | a0001 | c0002 | t0001 | g0081 | AFR | LWK | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| NA19043 | hp2 | a0001 | c0002 | t0001 | g0003 | AFR | LWK | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| NA19058 | hp2 | a0001 | c0002 | t0001 | g0087 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| NA19081 | hp2 | a0001 | c0002 | t0001 | g0132 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| NA19240 | hp1 | a0001 | c0002 | t0001 | g0002 | AFR | YRI | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| NA19240 | hp2 | a0001 | c0003 | t0003 | g0006 | AFR | YRI | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | ASW | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| NA20129 | hp2 | a0001 | c0002 | t0001 | g0003 | AFR | ASW | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| NA20752 | hp1 | a0001 | c0002 | t0001 | g0130 | EUR | TSI | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| NA20805 | hp1 | a0001 | c0003 | t0003 | g0006 | EUR | TSI | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| NA20905 | hp1 | a0001 | c0001 | t0004 | g0063 | SAS | GIH | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0024 | SAS | GIH | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG01123 | hp1 | a0001 | c0002 | t0001 | g0013 | AMR | CLM | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG01123 | hp2 | a0001 | c0002 | t0001 | g0095 | AMR | CLM | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG02109 | hp1 | a0001 | c0002 | t0001 | g0003 | AFR | ACB | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG02109 | hp2 | a0001 | c0004 | t0001 | g0010 | AFR | ACB | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG02486 | hp1 | a0001 | c0002 | t0002 | g0111 | AFR | ACB | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | ACB | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG02559 | hp1 | a0001 | c0003 | t0001 | g0127 | AFR | ACB | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG02559 | hp2 | a0001 | c0002 | t0001 | g0002 | AFR | ACB | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG03471 | hp1 | a0001 | c0002 | t0001 | g0027 | AFR | MSL | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG03471 | hp2 | a0001 | c0002 | t0001 | g0038 | AFR | MSL | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG06807 | hp1 | a0001 | c0002 | t0001 | g0090 | AFR | USA | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| HG06807 | hp2 | a0001 | c0002 | t0001 | g0022 | AFR | USA | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| NA20300 | hp1 | a0001 | c0002 | t0001 | g0096 | AFR | USA | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| NA20300 | hp2 | a0001 | c0002 | t0001 | g0009 | AFR | USA | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| NA21309 | hp1 | a0001 | c0003 | t0001 | g0032 | AFR | LWK | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| NA21309 | hp2 | a0001 | c0002 | t0002 | g0098 | AFR | LWK | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0050 | REF | REF | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0001 | g0003 | REF | REF | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
| 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 |
|---|
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:77459668 | C | T | 2 | a0001c0001 a0001c0006 |
132 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(129): Show |
synonymous_variant | LOW | c.133C>T | p.Leu45Leu | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/9 | 230/1337 | 133/1017 | 45/338 | chr14 | 77459668 | |||
| chr14:77459712 | G | A | 1 | a0001c0007 | 1 | HG02965.hp2 | synonymous_variant | LOW | c.177G>A | p.Thr59Thr | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/9 | 274/1337 | 177/1017 | 59/338 | chr14 | 77459712 | |||
| chr14:77462182 | A | G | 6 | a0001c0001 a0001c0003 a0001c0004 others(3): Show |
174 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(171): Show |
synonymous_variant | LOW | c.294A>G | p.Gln98Gln | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 3/9 | 391/1337 | 294/1017 | 98/338 | chr14 | 77462182 | |||
| chr14:77462203 | C | T | 2 | a0001c0004 a0001c0009 |
11 | HG01243.hp1 HG02109.hp2 HG02280.hp2 others(8): Show |
synonymous_variant | LOW | c.315C>T | p.Ile105Ile | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 3/9 | 412/1337 | 315/1017 | 105/338 | chr14 | 77462203 | |||
| chr14:77468088 | G | A | 3 | a0001c0004 a0001c0005 a0001c0007 |
13 | HG01243.hp1 HG02109.hp2 HG02280.hp2 others(10): Show |
synonymous_variant | LOW | c.696G>A | p.Val232Val | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 7/9 | 793/1337 | 696/1017 | 232/338 | chr14 | 77468088 | |||
| chr14:77469177 | G | A | 3 | a0001c0001 a0001c0008 a0001c0009 |
132 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(129): Show |
synonymous_variant | LOW | c.945G>A | p.Thr315Thr | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 9/9 | 1042/1337 | 945/1017 | 315/338 | chr14 | 77469177 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:77458146 | G | T | 1 | a0001c0001t0005 | 1 | NA18945.hp1 | 5_prime_UTR_variant | MODIFIER | c.-44G>T | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 1/9 | 44 | chr14 | 77458146 | ||||||
| chr14:77458150 | C | A | 1 | a0001c0001t0004 | 1 | NA20905.hp1 | 5_prime_UTR_variant | MODIFIER | c.-40C>A | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 1/9 | 40 | chr14 | 77458150 | ||||||
| chr14:77469316 | G | A | 1 | a0001c0002t0002 | 32 | HG01081.hp1 HG01099.hp2 HG01168.hp2 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*67G>A | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 9/9 | 67 | chr14 | 77469316 | ||||||
| chr14:77469334 | G | A | 1 | a0001c0003t0003 | 10 | HG00642.hp2 HG00735.hp2 HG01109.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*85G>A | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 9/9 | 85 | chr14 | 77469334 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:77458390 | T | G | 1 | a0001c0002t0001g0034 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.80+121T>G | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 1/8 | chr14 | 77458390 | |||||||
| chr14:77458567 | T | C | 10 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0022 others(7): Show |
13 | HG01109.hp1 HG02451.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.80+298T>C | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 1/8 | chr14 | 77458567 | |||||||
| chr14:77458663 | A | G | 1 | a0001c0002t0001g0142 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.80+394A>G | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 1/8 | chr14 | 77458663 | |||||||
| chr14:77458811 | T | C | 1 | a0001c0002t0001g0020 | 2 | HG02630.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.80+542T>C | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 1/8 | chr14 | 77458811 | |||||||
| chr14:77458854 | T | TA | 6 | a0001c0002t0001g0021 a0001c0002t0001g0035 a0001c0002t0001g0036 others(3): Show |
7 | HG02451.hp2 HG02572.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.80+589dupA | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr14 | 77458854 | ||||||
| chr14:77459140 | C | G | 4 | a0001c0004t0001g0010 a0001c0004t0001g0019 a0001c0004t0001g0140 others(1): Show |
10 | HG01243.hp1 HG02109.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.81-476C>G | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 1/8 | chr14 | 77459140 | |||||||
| chr14:77459181 | A | G | 6 | a0001c0002t0001g0021 a0001c0002t0001g0035 a0001c0002t0001g0036 others(3): Show |
7 | HG02451.hp2 HG02572.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.81-435A>G | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 1/8 | chr14 | 77459181 | |||||||
| chr14:77459337 | G | A | 1 | a0001c0002t0001g0042 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.81-279G>A | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 1/8 | chr14 | 77459337 | |||||||
| chr14:77459342 | A | G | 10 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0022 others(7): Show |
13 | HG01109.hp1 HG02451.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.81-274A>G | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 1/8 | chr14 | 77459342 | |||||||
| chr14:77459353 | C | T | 1 | a0001c0002t0001g0139 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.81-263C>T | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 1/8 | chr14 | 77459353 | |||||||
| chr14:77459401 | A | G | 6 | a0001c0002t0001g0021 a0001c0002t0001g0035 a0001c0002t0001g0036 others(3): Show |
7 | HG02451.hp2 HG02572.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.81-215A>G | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 1/8 | chr14 | 77459401 | |||||||
| chr14:77459442 | C | T | 1 | a0001c0001t0001g0138 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.81-174C>T | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 1/8 | chr14 | 77459442 | |||||||
| chr14:77459462 | A | C | 1 | a0001c0001t0001g0137 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.81-154A>C | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 1/8 | chr14 | 77459462 | |||||||
| chr14:77459540 | A | T | 1 | a0001c0002t0002g0136 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.81-76A>T | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 1/8 | chr14 | 77459540 | |||||||
| chr14:77460055 | C | T | 11 | a0001c0002t0001g0009 a0001c0002t0001g0013 a0001c0002t0001g0033 others(8): Show |
20 | HG00099.hp2 HG00741.hp1 HG01123.hp1 others(17): Show |
intron_variant | MODIFIER | c.271+249C>T | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | chr14 | 77460055 | |||||||
| chr14:77460219 | G | C | 4 | a0001c0003t0001g0007 a0001c0003t0001g0043 a0001c0003t0001g0044 others(1): Show |
9 | HG00099.hp1 HG00323.hp1 HG01069.hp1 others(6): Show |
intron_variant | MODIFIER | c.271+413G>C | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | chr14 | 77460219 | |||||||
| chr14:77460306 | G | A | 44 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(41): Show |
132 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(129): Show |
intron_variant | MODIFIER | c.271+500G>A | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | chr14 | 77460306 | |||||||
| chr14:77460390 | T | C | 1 | a0001c0001t0001g0014 | 3 | HG00597.hp2 HG01981.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.271+584T>C | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | chr14 | 77460390 | |||||||
| chr14:77460457 | T | TAAAGAAG others(316): Show |
1 | a0001c0002t0001g0103 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.271+664_271+665ins others(323): Show |
AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 77460457 | ||||||
| chr14:77460457 | T | TAAAGAAG others(317): Show |
4 | a0001c0002t0002g0029 a0001c0002t0002g0100 a0001c0002t0002g0101 others(1): Show |
5 | HG01975.hp2 HG02970.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.271+664_271+665ins others(324): Show |
AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 77460457 | ||||||
| chr14:77460457 | T | TAAAGAAG others(318): Show |
3 | a0001c0002t0002g0028 a0001c0002t0002g0098 a0001c0002t0002g0099 |
4 | HG01081.hp1 HG01358.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.271+664_271+665ins others(325): Show |
AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 77460457 | ||||||
| chr14:77460457 | T | TAAAGAAG others(303): Show |
1 | a0001c0007t0001g0104 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.271+663_271+664ins others(310): Show |
AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 77460457 | ||||||
| chr14:77460457 | T | TAAAGAAG others(302): Show |
3 | a0001c0003t0001g0045 a0001c0003t0001g0128 a0001c0003t0001g0129 |
3 | HG01070.hp1 HG02572.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.271+663_271+664ins others(309): Show |
AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 77460457 | ||||||
| chr14:77460457 | T | TAAAGAAG others(303): Show |
15 | a0001c0002t0001g0125 a0001c0002t0001g0126 a0001c0003t0001g0007 others(12): Show |
28 | HG00099.hp1 HG00323.hp1 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.271+663_271+664ins others(310): Show |
AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 77460457 | ||||||
| chr14:77460457 | T | TAAAGAAG others(304): Show |
1 | a0001c0003t0001g0118 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.271+663_271+664ins others(311): Show |
AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 77460457 | ||||||
| chr14:77460457 | T | TAAAGAAG others(307): Show |
1 | a0001c0002t0002g0117 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.271+663_271+664ins others(314): Show |
AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 77460457 | ||||||
| chr14:77460457 | T | TAAAGAAG others(316): Show |
4 | a0001c0002t0002g0012 a0001c0002t0002g0030 a0001c0002t0002g0115 others(1): Show |
8 | HG02155.hp2 HG02976.hp2 HG03017.hp2 others(5): Show |
intron_variant | MODIFIER | c.271+663_271+664ins others(323): Show |
AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 77460457 | ||||||
| chr14:77460457 | T | TAAAGAAG others(317): Show |
6 | a0001c0002t0002g0110 a0001c0002t0002g0111 a0001c0002t0002g0112 others(3): Show |
6 | HG01175.hp2 HG02486.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.271+663_271+664ins others(324): Show |
AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 77460457 | ||||||
| chr14:77460457 | T | TAAAGAAG others(318): Show |
2 | a0001c0002t0002g0018 a0001c0002t0002g0109 |
4 | HG01168.hp2 HG02074.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.271+663_271+664ins others(325): Show |
AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 77460457 | ||||||
| chr14:77460457 | T | TAAAGAAG others(319): Show |
3 | a0001c0002t0002g0106 a0001c0002t0002g0107 a0001c0002t0002g0108 |
3 | HG01099.hp2 HG01515.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.271+663_271+664ins others(326): Show |
AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 77460457 | ||||||
| chr14:77460457 | T | TAAAGAAG others(320): Show |
1 | a0001c0002t0002g0105 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.271+663_271+664ins others(327): Show |
AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 77460457 | ||||||
| chr14:77460572 | CT | C | 136 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(133): Show |
287 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(284): Show |
intron_variant | MODIFIER | c.271+779delT | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 77460572 | ||||||
| chr14:77460675 | C | A | 1 | a0001c0009t0001g0079 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.271+869C>A | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | chr14 | 77460675 | |||||||
| chr14:77460710 | C | A | 2 | a0001c0002t0001g0080 a0001c0002t0002g0098 |
2 | HG03098.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.271+904C>A | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | chr14 | 77460710 | |||||||
| chr14:77460718 | C | T | 1 | a0001c0002t0001g0093 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.271+912C>T | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | chr14 | 77460718 | |||||||
| chr14:77460798 | G | A | 1 | a0001c0002t0001g0142 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.271+992G>A | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | chr14 | 77460798 | |||||||
| chr14:77460829 | T | C | 1 | a0001c0002t0001g0142 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.271+1023T>C | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | chr14 | 77460829 | |||||||
| chr14:77460887 | T | C | 1 | a0001c0007t0001g0104 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.271+1081T>C | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | chr14 | 77460887 | |||||||
| chr14:77460895 | A | C | 26 | a0001c0001t0001g0015 a0001c0001t0001g0078 a0001c0002t0001g0125 others(23): Show |
41 | HG00099.hp1 HG00323.hp1 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.271+1089A>C | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | chr14 | 77460895 | |||||||
| chr14:77460941 | C | T | 1 | a0001c0003t0001g0032 | 2 | HG03486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.271+1135C>T | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | chr14 | 77460941 | |||||||
| chr14:77460942 | G | C | 1 | a0001c0002t0001g0094 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.271+1136G>C | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | chr14 | 77460942 | |||||||
| chr14:77460956 | A | G | 12 | a0001c0002t0001g0002 a0001c0002t0001g0016 a0001c0002t0001g0017 others(9): Show |
36 | HG00639.hp2 HG00642.hp1 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.271+1150A>G | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | chr14 | 77460956 | |||||||
| chr14:77460971 | G | A | 21 | a0001c0001t0001g0046 a0001c0002t0001g0002 a0001c0002t0001g0016 others(18): Show |
52 | HG00323.hp1 HG00621.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.271+1165G>A | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | chr14 | 77460971 | |||||||
| chr14:77460976 | A | G | 12 | a0001c0002t0001g0002 a0001c0002t0001g0016 a0001c0002t0001g0017 others(9): Show |
36 | HG00639.hp2 HG00642.hp1 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.271+1170A>G | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | chr14 | 77460976 | |||||||
| chr14:77460986 | C | T | 3 | a0001c0001t0001g0004 a0001c0001t0001g0076 a0001c0001t0001g0077 |
12 | HG02015.hp2 HG02523.hp2 NA18947.hp1 others(9): Show |
intron_variant | MODIFIER | c.272-1174C>T | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | chr14 | 77460986 | |||||||
| chr14:77460987 | G | A | 13 | a0001c0002t0001g0002 a0001c0002t0001g0016 a0001c0002t0001g0017 others(10): Show |
37 | HG00639.hp2 HG00642.hp1 HG00733.hp1 others(34): Show |
intron_variant | MODIFIER | c.272-1173G>A | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | chr14 | 77460987 | |||||||
| chr14:77460994 | C | CTTT | 13 | a0001c0002t0001g0002 a0001c0002t0001g0016 a0001c0002t0001g0017 others(10): Show |
37 | HG00639.hp2 HG00642.hp1 HG00733.hp1 others(34): Show |
intron_variant | MODIFIER | c.272-1165_272-1164i others(5): Show |
AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 77460994 | ||||||
| chr14:77461016 | C | G | 11 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0022 others(8): Show |
14 | HG01109.hp1 HG02145.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.272-1144C>G | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | chr14 | 77461016 | |||||||
| chr14:77461016 | C | T | 1 | a0001c0001t0001g0075 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.272-1144C>T | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | chr14 | 77461016 | |||||||
| chr14:77461017 | G | A | 1 | a0001c0002t0002g0098 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.272-1143G>A | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | chr14 | 77461017 | |||||||
| chr14:77461020 | G | A | 1 | a0001c0001t0001g0047 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.272-1140G>A | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | chr14 | 77461020 | |||||||
| chr14:77461028 | A | G | 1 | a0001c0001t0001g0074 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.272-1132A>G | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | chr14 | 77461028 | |||||||
| chr14:77461029 | T | G | 1 | a0001c0001t0001g0074 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.272-1131T>G | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | chr14 | 77461029 | |||||||
| chr14:77461031 | T | C | 1 | a0001c0001t0001g0074 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.272-1129T>C | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | chr14 | 77461031 | |||||||
| chr14:77461039 | G | A | 1 | a0001c0002t0001g0081 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.272-1121G>A | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | chr14 | 77461039 | |||||||
| chr14:77461042 | C | T | 2 | a0001c0005t0001g0084 a0001c0005t0001g0092 |
2 | HG02886.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.272-1118C>T | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | chr14 | 77461042 | |||||||
| chr14:77461052 | G | C | 45 | a0001c0002t0001g0086 a0001c0002t0001g0125 a0001c0002t0001g0126 others(42): Show |
67 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.272-1108G>C | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | chr14 | 77461052 | |||||||
| chr14:77461085 | G | T | 3 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 |
3 | HG01106.hp1 HG02055.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.272-1075G>T | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | chr14 | 77461085 | |||||||
| chr14:77461109 | G | T | 11 | a0001c0002t0001g0002 a0001c0002t0001g0016 a0001c0002t0001g0017 others(8): Show |
35 | HG00639.hp2 HG00642.hp1 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.272-1051G>T | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | chr14 | 77461109 | |||||||
| chr14:77461256 | C | T | 4 | a0001c0002t0001g0022 a0001c0002t0001g0040 a0001c0002t0001g0041 others(1): Show |
5 | HG01109.hp1 HG02145.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.272-904C>T | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | chr14 | 77461256 | |||||||
| chr14:77461268 | C | T | 1 | a0001c0003t0001g0127 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.272-892C>T | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | chr14 | 77461268 | |||||||
| chr14:77461400 | C | T | 29 | a0001c0002t0001g0009 a0001c0002t0001g0013 a0001c0002t0001g0017 others(26): Show |
46 | HG00099.hp2 HG00741.hp1 HG01081.hp1 others(43): Show |
intron_variant | MODIFIER | c.272-760C>T | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | chr14 | 77461400 | |||||||
| chr14:77461496 | A | C | 1 | a0001c0004t0001g0141 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.272-664A>C | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | chr14 | 77461496 | |||||||
| chr14:77461520 | ACT | A | 3 | a0001c0001t0001g0004 a0001c0001t0001g0070 a0001c0001t0001g0077 |
12 | HG02015.hp2 NA18947.hp1 NA18949.hp1 others(9): Show |
intron_variant | MODIFIER | c.272-637_272-636del others(2): Show |
AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 77461520 | ||||||
| chr14:77461531 | C | T | 1 | a0001c0002t0001g0103 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.272-629C>T | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | chr14 | 77461531 | |||||||
| chr14:77461549 | A | C | 1 | a0001c0001t0001g0069 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.272-611A>C | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | chr14 | 77461549 | |||||||
| chr14:77461627 | C | A | 7 | a0001c0002t0001g0033 a0001c0002t0001g0087 a0001c0002t0001g0094 others(4): Show |
10 | HG01081.hp1 HG02647.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.272-533C>A | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | chr14 | 77461627 | |||||||
| chr14:77461728 | G | A | 1 | a0001c0002t0001g0040 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.272-432G>A | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | chr14 | 77461728 | |||||||
| chr14:77461737 | C | T | 5 | a0001c0002t0001g0009 a0001c0002t0001g0013 a0001c0002t0001g0034 others(2): Show |
13 | HG00099.hp2 HG00741.hp1 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.272-423C>T | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | chr14 | 77461737 | |||||||
| chr14:77461940 | T | C | 107 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(104): Show |
249 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(246): Show |
intron_variant | MODIFIER | c.272-220T>C | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | chr14 | 77461940 | |||||||
| chr14:77461945 | T | C | 55 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(52): Show |
150 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(147): Show |
intron_variant | MODIFIER | c.272-215T>C | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | chr14 | 77461945 | |||||||
| chr14:77461973 | C | T | 12 | a0001c0003t0001g0007 a0001c0003t0001g0031 a0001c0003t0001g0043 others(9): Show |
25 | HG00099.hp1 HG00323.hp1 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.272-187C>T | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | chr14 | 77461973 | |||||||
| chr14:77462018 | C | T | 1 | a0001c0002t0001g0134 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.272-142C>T | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | chr14 | 77462018 | |||||||
| chr14:77462133 | C | T | 49 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(46): Show |
142 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(139): Show |
intron_variant | MODIFIER | c.272-27C>T | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | chr14 | 77462133 | |||||||
| chr14:77462254 | A | C | 1 | a0001c0002t0001g0016 | 3 | HG01515.hp1 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.354+12A>C | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 3/8 | chr14 | 77462254 | |||||||
| chr14:77462283 | T | G | 4 | a0001c0004t0001g0010 a0001c0004t0001g0019 a0001c0004t0001g0140 others(1): Show |
10 | HG01243.hp1 HG02109.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.354+41T>G | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 3/8 | chr14 | 77462283 | |||||||
| chr14:77462294 | G | C | 1 | a0001c0005t0001g0084 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.354+52G>C | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 3/8 | chr14 | 77462294 | |||||||
| chr14:77462392 | A | G | 45 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(42): Show |
132 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(129): Show |
intron_variant | MODIFIER | c.354+150A>G | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 3/8 | chr14 | 77462392 | |||||||
| chr14:77462524 | G | A | 5 | a0001c0001t0001g0048 a0001c0002t0001g0081 a0001c0002t0001g0082 others(2): Show |
5 | HG02083.hp2 HG02922.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.355-118G>A | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 3/8 | chr14 | 77462524 | |||||||
| chr14:77462560 | T | C | 1 | a0001c0002t0001g0089 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.355-82T>C | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 3/8 | chr14 | 77462560 | |||||||
| chr14:77462792 | A | G | 1 | a0001c0002t0001g0097 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.472+33A>G | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 4/8 | chr14 | 77462792 | |||||||
| chr14:77462826 | C | T | 2 | a0001c0001t0001g0067 a0001c0001t0001g0068 |
2 | NA18939.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.472+67C>T | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 4/8 | chr14 | 77462826 | |||||||
| chr14:77462985 | A | G | 92 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(89): Show |
220 | HG00099.hp2 HG00323.hp2 HG00544.hp1 others(217): Show |
intron_variant | MODIFIER | c.472+226A>G | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 4/8 | chr14 | 77462985 | |||||||
| chr14:77463008 | G | A | 1 | a0001c0002t0001g0022 | 2 | HG01109.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.472+249G>A | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 4/8 | chr14 | 77463008 | |||||||
| chr14:77463109 | G | T | 45 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(42): Show |
132 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(129): Show |
intron_variant | MODIFIER | c.472+350G>T | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 4/8 | chr14 | 77463109 | |||||||
| chr14:77463323 | TCA | T | 4 | a0001c0002t0001g0022 a0001c0002t0001g0040 a0001c0002t0001g0041 others(1): Show |
5 | HG01109.hp1 HG02145.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.472+568_472+569del others(2): Show |
AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr14 | 77463323 | ||||||
| chr14:77463327 | A | G | 45 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(42): Show |
132 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(129): Show |
intron_variant | MODIFIER | c.472+568A>G | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 4/8 | chr14 | 77463327 | |||||||
| chr14:77463345 | T | C | 1 | a0001c0001t0001g0049 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.472+586T>C | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 4/8 | chr14 | 77463345 | |||||||
| chr14:77463386 | C | T | 1 | a0001c0003t0003g0120 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.472+627C>T | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 4/8 | chr14 | 77463386 | |||||||
| chr14:77463540 | C | T | 1 | a0001c0001t0001g0066 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.472+781C>T | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 4/8 | chr14 | 77463540 | |||||||
| chr14:77463585 | C | CA | 7 | a0001c0002t0001g0022 a0001c0002t0001g0037 a0001c0002t0001g0040 others(4): Show |
8 | HG01109.hp1 HG02145.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.472+840dupA | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr14 | 77463585 | ||||||
| chr14:77463585 | C | CAA | 16 | a0001c0002t0001g0002 a0001c0002t0001g0016 a0001c0002t0001g0017 others(13): Show |
46 | HG00639.hp2 HG00642.hp1 HG00733.hp1 others(43): Show |
intron_variant | MODIFIER | c.472+839_472+840dup others(2): Show |
AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr14 | 77463585 | ||||||
| chr14:77463585 | CA | C | 11 | a0001c0002t0001g0009 a0001c0002t0001g0013 a0001c0002t0001g0033 others(8): Show |
20 | HG00099.hp2 HG00741.hp1 HG01123.hp1 others(17): Show |
intron_variant | MODIFIER | c.472+840delA | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr14 | 77463585 | ||||||
| chr14:77463595 | AAAAAC | A | 44 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(41): Show |
127 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.472+841_472+845del others(5): Show |
AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr14 | 77463595 | ||||||
| chr14:77463600 | C | A | 12 | a0001c0002t0001g0021 a0001c0002t0001g0022 a0001c0002t0001g0035 others(9): Show |
16 | HG01081.hp1 HG01109.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.472+841C>A | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 4/8 | chr14 | 77463600 | |||||||
| chr14:77463648 | C | T | 5 | a0001c0004t0001g0010 a0001c0004t0001g0019 a0001c0004t0001g0140 others(2): Show |
11 | HG01243.hp1 HG02109.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.472+889C>T | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 4/8 | chr14 | 77463648 | |||||||
| chr14:77463708 | T | C | 1 | a0001c0002t0001g0085 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.473-890T>C | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 4/8 | chr14 | 77463708 | |||||||
| chr14:77463803 | G | A | 2 | a0001c0002t0002g0099 a0001c0002t0002g0101 |
2 | HG01358.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.473-795G>A | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 4/8 | chr14 | 77463803 | |||||||
| chr14:77463845 | G | C | 45 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(42): Show |
132 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(129): Show |
intron_variant | MODIFIER | c.473-753G>C | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 4/8 | chr14 | 77463845 | |||||||
| chr14:77463950 | C | T | 45 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(42): Show |
132 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(129): Show |
intron_variant | MODIFIER | c.473-648C>T | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 4/8 | chr14 | 77463950 | |||||||
| chr14:77463969 | T | G | 11 | a0001c0002t0001g0009 a0001c0002t0001g0013 a0001c0002t0001g0033 others(8): Show |
20 | HG00099.hp2 HG00741.hp1 HG01123.hp1 others(17): Show |
intron_variant | MODIFIER | c.473-629T>G | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 4/8 | chr14 | 77463969 | |||||||
| chr14:77464012 | T | A | 1 | a0001c0001t0001g0051 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.473-586T>A | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 4/8 | chr14 | 77464012 | |||||||
| chr14:77464064 | G | A | 45 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(42): Show |
132 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(129): Show |
intron_variant | MODIFIER | c.473-534G>A | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 4/8 | chr14 | 77464064 | |||||||
| chr14:77464188 | C | G | 11 | a0001c0002t0001g0022 a0001c0002t0001g0040 a0001c0002t0001g0041 others(8): Show |
18 | HG01109.hp1 HG01243.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.473-410C>G | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 4/8 | chr14 | 77464188 | |||||||
| chr14:77464222 | C | T | 11 | a0001c0002t0001g0002 a0001c0002t0001g0016 a0001c0002t0001g0017 others(8): Show |
35 | HG00639.hp2 HG00642.hp1 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.473-376C>T | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 4/8 | chr14 | 77464222 | |||||||
| chr14:77464249 | C | T | 56 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(53): Show |
167 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(164): Show |
intron_variant | MODIFIER | c.473-349C>T | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 4/8 | chr14 | 77464249 | |||||||
| chr14:77464334 | G | T | 1 | a0001c0001t0001g0065 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.473-264G>T | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 4/8 | chr14 | 77464334 | |||||||
| chr14:77464369 | A | G | 45 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(42): Show |
132 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(129): Show |
intron_variant | MODIFIER | c.473-229A>G | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 4/8 | chr14 | 77464369 | |||||||
| chr14:77464381 | A | T | 4 | a0001c0004t0001g0010 a0001c0004t0001g0019 a0001c0004t0001g0140 others(1): Show |
10 | HG01243.hp1 HG02109.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.473-217A>T | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 4/8 | chr14 | 77464381 | |||||||
| chr14:77464409 | G | A | 91 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(88): Show |
219 | HG00099.hp2 HG00323.hp2 HG00544.hp1 others(216): Show |
intron_variant | MODIFIER | c.473-189G>A | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 4/8 | chr14 | 77464409 | |||||||
| chr14:77464512 | A | T | 11 | a0001c0002t0001g0002 a0001c0002t0001g0016 a0001c0002t0001g0017 others(8): Show |
35 | HG00639.hp2 HG00642.hp1 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.473-86A>T | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 4/8 | chr14 | 77464512 | |||||||
| chr14:77464518 | G | C | 1 | a0001c0009t0001g0079 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.473-80G>C | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 4/8 | chr14 | 77464518 | |||||||
| chr14:77464535 | A | G | 15 | a0001c0002t0001g0009 a0001c0002t0001g0013 a0001c0002t0001g0033 others(12): Show |
24 | HG00099.hp2 HG00741.hp1 HG01123.hp1 others(21): Show |
intron_variant | MODIFIER | c.473-63A>G | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 4/8 | chr14 | 77464535 | |||||||
| chr14:77464545 | A | G | 3 | a0001c0001t0001g0046 a0001c0001t0001g0064 a0001c0001t0001g0070 |
3 | HG00621.hp1 HG02135.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.473-53A>G | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 4/8 | chr14 | 77464545 | |||||||
| chr14:77464549 | C | A | 7 | a0001c0002t0001g0021 a0001c0002t0001g0035 a0001c0002t0001g0036 others(4): Show |
8 | HG02451.hp2 HG02572.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.473-49C>A | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 4/8 | chr14 | 77464549 | |||||||
| chr14:77464722 | A | G | 1 | a0001c0001t0004g0063 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.561+36A>G | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 5/8 | chr14 | 77464722 | |||||||
| chr14:77464739 | G | A | 2 | a0001c0002t0001g0125 a0001c0002t0001g0126 |
2 | HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.561+53G>A | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 5/8 | chr14 | 77464739 | |||||||
| chr14:77464880 | C | T | 24 | a0001c0002t0002g0012 a0001c0002t0002g0018 a0001c0002t0002g0028 others(21): Show |
32 | HG01081.hp1 HG01099.hp2 HG01168.hp2 others(29): Show |
intron_variant | MODIFIER | c.561+194C>T | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 5/8 | chr14 | 77464880 | |||||||
| chr14:77464888 | T | C | 45 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(42): Show |
132 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(129): Show |
intron_variant | MODIFIER | c.561+202T>C | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 5/8 | chr14 | 77464888 | |||||||
| chr14:77464910 | A | T | 6 | a0001c0002t0001g0022 a0001c0002t0001g0040 a0001c0002t0001g0041 others(3): Show |
7 | HG01109.hp1 HG02145.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.561+224A>T | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 5/8 | chr14 | 77464910 | |||||||
| chr14:77464949 | A | AG | 45 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(42): Show |
132 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(129): Show |
intron_variant | MODIFIER | c.561+264dupG | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr14 | 77464949 | ||||||
| chr14:77465057 | G | A | 1 | a0001c0009t0001g0079 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.561+371G>A | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 5/8 | chr14 | 77465057 | |||||||
| chr14:77465158 | G | T | 4 | a0001c0004t0001g0010 a0001c0004t0001g0019 a0001c0004t0001g0140 others(1): Show |
10 | HG01243.hp1 HG02109.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.562-381G>T | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 5/8 | chr14 | 77465158 | |||||||
| chr14:77465262 | G | C | 20 | a0001c0002t0001g0125 a0001c0002t0001g0126 a0001c0003t0001g0007 others(17): Show |
34 | HG00099.hp1 HG00323.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.562-277G>C | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 5/8 | chr14 | 77465262 | |||||||
| chr14:77465320 | T | G | 2 | a0001c0002t0001g0094 a0001c0002t0001g0103 |
2 | HG02717.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.562-219T>G | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 5/8 | chr14 | 77465320 | |||||||
| chr14:77465408 | A | C | 1 | a0001c0001t0001g0047 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.562-131A>C | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 5/8 | chr14 | 77465408 | |||||||
| chr14:77465482 | G | A | 2 | a0001c0002t0001g0038 a0001c0002t0001g0039 |
2 | HG03471.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.562-57G>A | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 5/8 | chr14 | 77465482 | |||||||
| chr14:77465674 | A | C | 45 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(42): Show |
132 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(129): Show |
splice_region_variant&intron_variant | LOW | c.690+7A>C | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 6/8 | chr14 | 77465674 | |||||||
| chr14:77465734 | A | G | 4 | a0001c0002t0001g0022 a0001c0002t0001g0040 a0001c0002t0001g0041 others(1): Show |
5 | HG01109.hp1 HG02145.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.690+67A>G | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 6/8 | chr14 | 77465734 | |||||||
| chr14:77465768 | A | G | 48 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(45): Show |
135 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(132): Show |
intron_variant | MODIFIER | c.690+101A>G | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 6/8 | chr14 | 77465768 | |||||||
| chr14:77465827 | C | CT | 8 | a0001c0002t0002g0114 a0001c0002t0002g0116 a0001c0003t0003g0122 others(5): Show |
14 | HG01243.hp1 HG02109.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.690+173dupT | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr14 | 77465827 | ||||||
| chr14:77465853 | C | T | 3 | a0001c0002t0001g0081 a0001c0002t0001g0082 a0001c0002t0001g0083 |
3 | HG02922.hp2 HG02965.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.690+186C>T | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 6/8 | chr14 | 77465853 | |||||||
| chr14:77465947 | G | A | 1 | a0001c0002t0001g0090 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.690+280G>A | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 6/8 | chr14 | 77465947 | |||||||
| chr14:77466137 | A | G | 3 | a0001c0002t0001g0020 a0001c0002t0001g0080 a0001c0002t0001g0097 |
4 | HG02258.hp1 HG02630.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.690+470A>G | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 6/8 | chr14 | 77466137 | |||||||
| chr14:77466266 | G | A | 1 | a0001c0002t0002g0029 | 2 | HG02970.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.690+599G>A | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 6/8 | chr14 | 77466266 | |||||||
| chr14:77466276 | C | T | 91 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(88): Show |
219 | HG00099.hp2 HG00323.hp2 HG00544.hp1 others(216): Show |
intron_variant | MODIFIER | c.690+609C>T | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 6/8 | chr14 | 77466276 | |||||||
| chr14:77466438 | C | T | 11 | a0001c0002t0001g0009 a0001c0002t0001g0013 a0001c0002t0001g0033 others(8): Show |
20 | HG00099.hp2 HG00741.hp1 HG01123.hp1 others(17): Show |
intron_variant | MODIFIER | c.690+771C>T | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 6/8 | chr14 | 77466438 | |||||||
| chr14:77466439 | G | A | 3 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0138 |
3 | HG01070.hp2 HG01071.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.690+772G>A | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 6/8 | chr14 | 77466439 | |||||||
| chr14:77466480 | T | C | 91 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(88): Show |
219 | HG00099.hp2 HG00323.hp2 HG00544.hp1 others(216): Show |
intron_variant | MODIFIER | c.690+813T>C | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 6/8 | chr14 | 77466480 | |||||||
| chr14:77466623 | G | A | 1 | a0001c0002t0001g0089 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.690+956G>A | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 6/8 | chr14 | 77466623 | |||||||
| chr14:77466624 | A | T | 11 | a0001c0002t0001g0009 a0001c0002t0001g0013 a0001c0002t0001g0033 others(8): Show |
20 | HG00099.hp2 HG00741.hp1 HG01123.hp1 others(17): Show |
intron_variant | MODIFIER | c.690+957A>T | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 6/8 | chr14 | 77466624 | |||||||
| chr14:77466798 | G | A | 11 | a0001c0002t0001g0009 a0001c0002t0001g0013 a0001c0002t0001g0033 others(8): Show |
20 | HG00099.hp2 HG00741.hp1 HG01123.hp1 others(17): Show |
intron_variant | MODIFIER | c.690+1131G>A | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 6/8 | chr14 | 77466798 | |||||||
| chr14:77466819 | G | A | 11 | a0001c0002t0001g0009 a0001c0002t0001g0013 a0001c0002t0001g0033 others(8): Show |
20 | HG00099.hp2 HG00741.hp1 HG01123.hp1 others(17): Show |
intron_variant | MODIFIER | c.690+1152G>A | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 6/8 | chr14 | 77466819 | |||||||
| chr14:77466959 | G | A | 5 | a0001c0004t0001g0010 a0001c0004t0001g0019 a0001c0004t0001g0140 others(2): Show |
11 | HG01243.hp1 HG02109.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.691-1124G>A | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 6/8 | chr14 | 77466959 | |||||||
| chr14:77467108 | T | C | 24 | a0001c0002t0002g0012 a0001c0002t0002g0018 a0001c0002t0002g0028 others(21): Show |
32 | HG01081.hp1 HG01099.hp2 HG01168.hp2 others(29): Show |
intron_variant | MODIFIER | c.691-975T>C | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 6/8 | chr14 | 77467108 | |||||||
| chr14:77467146 | C | T | 7 | a0001c0002t0001g0125 a0001c0002t0001g0126 a0001c0003t0001g0032 others(4): Show |
8 | HG02559.hp1 HG02572.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.691-937C>T | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 6/8 | chr14 | 77467146 | |||||||
| chr14:77467163 | C | A | 1 | a0001c0002t0001g0125 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.691-920C>A | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 6/8 | chr14 | 77467163 | |||||||
| chr14:77467265 | G | A | 1 | a0001c0003t0003g0119 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.691-818G>A | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 6/8 | chr14 | 77467265 | |||||||
| chr14:77467271 | C | T | 1 | a0001c0001t0001g0062 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.691-812C>T | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 6/8 | chr14 | 77467271 | |||||||
| chr14:77467376 | G | A | 1 | a0001c0002t0002g0102 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.691-707G>A | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 6/8 | chr14 | 77467376 | |||||||
| chr14:77467457 | G | T | 1 | a0001c0002t0002g0115 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.691-626G>T | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 6/8 | chr14 | 77467457 | |||||||
| chr14:77467552 | G | C | 45 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(42): Show |
132 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(129): Show |
intron_variant | MODIFIER | c.691-531G>C | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 6/8 | chr14 | 77467552 | |||||||
| chr14:77467567 | G | T | 1 | a0001c0001t0001g0061 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.691-516G>T | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 6/8 | chr14 | 77467567 | |||||||
| chr14:77467627 | G | A | 1 | a0001c0001t0001g0054 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.691-456G>A | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 6/8 | chr14 | 77467627 | |||||||
| chr14:77467643 | G | A | 45 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(42): Show |
132 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(129): Show |
intron_variant | MODIFIER | c.691-440G>A | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 6/8 | chr14 | 77467643 | |||||||
| chr14:77467650 | C | T | 7 | a0001c0002t0001g0021 a0001c0002t0001g0035 a0001c0002t0001g0036 others(4): Show |
8 | HG02451.hp2 HG02572.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.691-433C>T | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 6/8 | chr14 | 77467650 | |||||||
| chr14:77467689 | G | A | 11 | a0001c0002t0001g0009 a0001c0002t0001g0013 a0001c0002t0001g0033 others(8): Show |
20 | HG00099.hp2 HG00741.hp1 HG01123.hp1 others(17): Show |
intron_variant | MODIFIER | c.691-394G>A | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 6/8 | chr14 | 77467689 | |||||||
| chr14:77467700 | T | A | 10 | a0001c0002t0001g0021 a0001c0002t0001g0035 a0001c0002t0001g0036 others(7): Show |
11 | HG02451.hp2 HG02572.hp1 HG02897.hp2 others(8): Show |
intron_variant | MODIFIER | c.691-383T>A | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 6/8 | chr14 | 77467700 | |||||||
| chr14:77467703 | A | AT | 10 | a0001c0002t0001g0021 a0001c0002t0001g0035 a0001c0002t0001g0036 others(7): Show |
11 | HG02451.hp2 HG02572.hp1 HG02897.hp2 others(8): Show |
intron_variant | MODIFIER | c.691-380_691-379ins others(1): Show |
AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 6/8 | chr14 | 77467703 | |||||||
| chr14:77467703 | AAAAAT | A | 44 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(41): Show |
131 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.691-365_691-361del others(5): Show |
AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr14 | 77467703 | ||||||
| chr14:77467816 | A | T | 1 | a0001c0003t0001g0129 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.691-267A>T | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 6/8 | chr14 | 77467816 | |||||||
| chr14:77467938 | G | A | 1 | a0001c0001t0001g0051 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.691-145G>A | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 6/8 | chr14 | 77467938 | |||||||
| chr14:77467950 | A | G | 4 | a0001c0002t0001g0081 a0001c0002t0001g0082 a0001c0002t0001g0083 others(1): Show |
4 | HG02922.hp2 HG02965.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.691-133A>G | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 6/8 | chr14 | 77467950 | |||||||
| chr14:77468049 | C | CT | 9 | a0001c0001t0001g0005 a0001c0001t0001g0058 a0001c0001t0001g0059 others(6): Show |
16 | HG00621.hp2 HG00673.hp1 HG00673.hp2 others(13): Show |
intron_variant | MODIFIER | c.691-33dupT | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr14 | 77468049 | ||||||
| chr14:77468050 | TC | T | 3 | a0001c0001t0001g0053 a0001c0001t0001g0060 a0001c0009t0001g0079 |
3 | HG01070.hp2 HG03540.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.691-32delC | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 6/8 | chr14 | 77468050 | |||||||
| chr14:77468051 | C | CT | 41 | a0001c0002t0001g0020 a0001c0002t0001g0022 a0001c0002t0001g0026 others(38): Show |
61 | HG00099.hp1 HG00323.hp1 HG00642.hp2 others(58): Show |
splice_region_variant&intron_variant | LOW | c.691-9dupT | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr14 | 77468051 | ||||||
| chr14:77468051 | C | CTT | 8 | a0001c0002t0002g0029 a0001c0002t0002g0107 a0001c0002t0002g0113 others(5): Show |
8 | HG01099.hp2 HG01109.hp2 HG01891.hp1 others(5): Show |
splice_region_variant&intron_variant | LOW | c.691-10_691-9dupTT | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr14 | 77468051 | ||||||
| chr14:77468051 | C | T | 42 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(39): Show |
129 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(126): Show |
intron_variant | MODIFIER | c.691-32C>T | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 6/8 | chr14 | 77468051 | |||||||
| chr14:77468051 | CT | C | 11 | a0001c0002t0001g0002 a0001c0002t0001g0017 a0001c0002t0001g0021 others(8): Show |
14 | HG01169.hp2 HG01257.hp2 HG01261.hp1 others(11): Show |
intron_variant | MODIFIER | c.691-9delT | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr14 | 77468051 | ||||||
| chr14:77468051 | CTTTTTTT others(4): Show |
C | 1 | a0001c0002t0001g0095 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.691-19_691-9delTTT others(8): Show |
AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr14 | 77468051 | ||||||
| chr14:77468074 | T | C | 1 | a0001c0002t0001g0095 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.691-9T>C | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 6/8 | chr14 | 77468074 | |||||||
| chr14:77468244 | T | C | 11 | a0001c0002t0001g0002 a0001c0002t0001g0016 a0001c0002t0001g0017 others(8): Show |
35 | HG00639.hp2 HG00642.hp1 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.792+60T>C | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 7/8 | chr14 | 77468244 | |||||||
| chr14:77468258 | CTA | C | 11 | a0001c0002t0001g0009 a0001c0002t0001g0013 a0001c0002t0001g0033 others(8): Show |
20 | HG00099.hp2 HG00741.hp1 HG01123.hp1 others(17): Show |
intron_variant | MODIFIER | c.792+77_792+78delTA | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr14 | 77468258 | ||||||
| chr14:77468374 | G | A | 4 | a0001c0004t0001g0010 a0001c0004t0001g0019 a0001c0004t0001g0140 others(1): Show |
10 | HG01243.hp1 HG02109.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.793-83G>A | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 7/8 | chr14 | 77468374 | |||||||
| chr14:77468415 | A | G | 45 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(42): Show |
132 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(129): Show |
intron_variant | MODIFIER | c.793-42A>G | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 7/8 | chr14 | 77468415 | |||||||
| chr14:77468562 | A | AT | 66 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(63): Show |
157 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(154): Show |
intron_variant | MODIFIER | c.844+73dupT | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr14 | 77468562 | ||||||
| chr14:77468562 | A | ATT | 5 | a0001c0001t0001g0011 a0001c0001t0001g0057 a0001c0001t0001g0059 others(2): Show |
8 | HG01175.hp2 HG02080.hp1 HG02080.hp2 others(5): Show |
intron_variant | MODIFIER | c.844+72_844+73dupTT | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr14 | 77468562 | ||||||
| chr14:77468562 | AT | A | 14 | a0001c0002t0001g0021 a0001c0002t0001g0025 a0001c0002t0001g0035 others(11): Show |
17 | HG01516.hp1 HG02148.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.844+73delT | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr14 | 77468562 | ||||||
| chr14:77468629 | C | T | 4 | a0001c0004t0001g0010 a0001c0004t0001g0019 a0001c0004t0001g0140 others(1): Show |
10 | HG01243.hp1 HG02109.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.844+121C>T | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 8/8 | chr14 | 77468629 | |||||||
| chr14:77468685 | C | T | 2 | a0001c0005t0001g0084 a0001c0005t0001g0092 |
2 | HG02886.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.844+177C>T | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 8/8 | chr14 | 77468685 | |||||||
| chr14:77468721 | C | CT | 6 | a0001c0002t0001g0096 a0001c0002t0002g0105 a0001c0002t0002g0107 others(3): Show |
6 | HG01099.hp2 HG01517.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.844+237dupT | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr14 | 77468721 | ||||||
| chr14:77468721 | C | CTTTT | 10 | a0001c0002t0001g0002 a0001c0002t0001g0016 a0001c0002t0001g0017 others(7): Show |
33 | HG00639.hp2 HG00642.hp1 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.844+234_844+237dup others(4): Show |
AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr14 | 77468721 | ||||||
| chr14:77468721 | C | CTTTTTTT | 8 | a0001c0002t0001g0022 a0001c0002t0001g0040 a0001c0002t0001g0042 others(5): Show |
9 | HG01109.hp1 HG02280.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.844+231_844+237dup others(7): Show |
AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr14 | 77468721 | ||||||
| chr14:77468721 | C | CTTTTTTT others(1): Show |
10 | a0001c0002t0001g0009 a0001c0002t0001g0033 a0001c0002t0001g0034 others(7): Show |
20 | HG00099.hp2 HG01255.hp2 HG01257.hp2 others(17): Show |
intron_variant | MODIFIER | c.844+230_844+237dup others(8): Show |
AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr14 | 77468721 | ||||||
| chr14:77468721 | C | CTTTTTTT others(2): Show |
4 | a0001c0002t0001g0013 a0001c0002t0001g0134 a0001c0004t0001g0019 others(1): Show |
9 | HG00741.hp1 HG01123.hp1 HG01981.hp1 others(6): Show |
intron_variant | MODIFIER | c.844+229_844+237dup others(9): Show |
AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr14 | 77468721 | ||||||
| chr14:77468721 | C | CTTTTTTT others(3): Show |
2 | a0001c0002t0001g0133 a0001c0004t0001g0140 |
2 | HG01243.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.844+228_844+237dup others(10): Show |
AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr14 | 77468721 | ||||||
| chr14:77468721 | C | CTTTTTTT others(7): Show |
1 | a0001c0002t0001g0082 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.844+224_844+237dup others(14): Show |
AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr14 | 77468721 | ||||||
| chr14:77468721 | C | CTTTTTTT others(8): Show |
1 | a0001c0002t0001g0083 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.844+223_844+237dup others(15): Show |
AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr14 | 77468721 | ||||||
| chr14:77468721 | C | CTTTTTTT others(9): Show |
1 | a0001c0002t0001g0081 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.844+222_844+237dup others(16): Show |
AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr14 | 77468721 | ||||||
| chr14:77468721 | C | CTTTTTTT others(15): Show |
1 | a0001c0005t0001g0084 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.844+216_844+237dup others(22): Show |
AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr14 | 77468721 | ||||||
| chr14:77468721 | C | CTTTTTTT others(16): Show |
1 | a0001c0005t0001g0092 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.844+215_844+237dup others(23): Show |
AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr14 | 77468721 | ||||||
| chr14:77468721 | CT | C | 18 | a0001c0001t0001g0056 a0001c0002t0001g0125 a0001c0002t0001g0126 others(15): Show |
32 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(29): Show |
intron_variant | MODIFIER | c.844+237delT | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr14 | 77468721 | ||||||
| chr14:77468721 | CTT | C | 8 | a0001c0001t0001g0008 a0001c0001t0001g0057 a0001c0001t0001g0072 others(5): Show |
13 | HG00323.hp1 HG00639.hp1 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.844+236_844+237del others(2): Show |
AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr14 | 77468721 | ||||||
| chr14:77468721 | CTTT | C | 34 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(31): Show |
116 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(113): Show |
intron_variant | MODIFIER | c.844+235_844+237del others(3): Show |
AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr14 | 77468721 | ||||||
| chr14:77468721 | CTTTT | C | 8 | a0001c0001t0001g0053 a0001c0001t0001g0055 a0001c0002t0001g0021 others(5): Show |
9 | HG01070.hp2 HG02451.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.844+234_844+237del others(4): Show |
AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr14 | 77468721 | ||||||
| chr14:77468743 | T | A | 1 | a0001c0001t0001g0068 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.844+235T>A | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 8/8 | chr14 | 77468743 | |||||||
| chr14:77468744 | T | C | 1 | a0001c0001t0001g0068 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.844+236T>C | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 8/8 | chr14 | 77468744 | |||||||
| chr14:77468745 | T | A | 3 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 |
3 | HG01106.hp1 HG02055.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.844+237T>A | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 8/8 | chr14 | 77468745 | |||||||
| chr14:77468754 | A | T | 45 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(42): Show |
132 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(129): Show |
intron_variant | MODIFIER | c.844+246A>T | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 8/8 | chr14 | 77468754 | |||||||
| chr14:77468755 | C | T | 45 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(42): Show |
132 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(129): Show |
intron_variant | MODIFIER | c.844+247C>T | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 8/8 | chr14 | 77468755 | |||||||
| chr14:77468802 | G | A | 44 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(41): Show |
131 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.845-275G>A | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 8/8 | chr14 | 77468802 | |||||||
| chr14:77468893 | A | G | 5 | a0001c0004t0001g0010 a0001c0004t0001g0019 a0001c0004t0001g0140 others(2): Show |
11 | HG01243.hp1 HG02109.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.845-184A>G | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 8/8 | chr14 | 77468893 | |||||||
| chr14:77468896 | T | TG | 45 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(42): Show |
132 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(129): Show |
intron_variant | MODIFIER | c.845-179dupG | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr14 | 77468896 |