Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 57530 |
| ensemblid | ENSG00000143375.15 |
| hgncid | 17429 |
| symbol | CGN |
| name | cingulin |
| refseq_nuc | NM_020770.3 |
| refseq_prot | NP_065821.1 |
| ensembl_nuc | ENST00000271636.12 |
| ensembl_prot | ENSP00000271636.7 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 151511387 |
| end | 151538692 |
| strand | + |
| ver | v1.2 |
| region | chr1:151511387-151538692 |
| region5000 | chr1:151506387-151543692 |
| regionname0 | CGN_chr1_151511387_151538692 |
| regionname5000 | CGN_chr1_151506387_151543692 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1203 | 279 | 60 | 54 | 126 | 10 | 27 | 89 | CGN_chr1_151506387_151543692 | CGN | MEQAP others(1198): Show |
chr1 | 151506387 | 151543692 |
| a0002 | 0/0 | 1203 | 40 | 0 | 8 | 26 | 0 | 6 | 24 | CGN_chr1_151506387_151543692 | CGN | MEQAP others(1198): Show |
chr1 | 151506387 | 151543692 |
| a0003 | 0/0 | 1203 | 18 | 18 | 0 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | MEQAP others(1198): Show |
chr1 | 151506387 | 151543692 |
| a0004 | 0/0 | 1203 | 5 | 0 | 1 | 3 | 0 | 1 | 2 | CGN_chr1_151506387_151543692 | CGN | MEQAP others(1198): Show |
chr1 | 151506387 | 151543692 |
| a0005 | 0/0 | 1203 | 5 | 0 | 1 | 1 | 0 | 3 | 1 | CGN_chr1_151506387_151543692 | CGN | MEQAP others(1198): Show |
chr1 | 151506387 | 151543692 |
| a0006 | 0/0 | 1203 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | MEQAP others(1198): Show |
chr1 | 151506387 | 151543692 |
| a0007 | 0/0 | 1203 | 3 | 0 | 3 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | MEQAP others(1198): Show |
chr1 | 151506387 | 151543692 |
| a0008 | 0/0 | 1203 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | CGN_chr1_151506387_151543692 | CGN | MEQAP others(1198): Show |
chr1 | 151506387 | 151543692 |
| a0009 | 0/0 | 1203 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | MEQAP others(1198): Show |
chr1 | 151506387 | 151543692 |
| a0010 | 0/0 | 1203 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | CGN_chr1_151506387_151543692 | CGN | MEQAP others(1198): Show |
chr1 | 151506387 | 151543692 |
| a0011 | 0/0 | 1203 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | MEQAP others(1198): Show |
chr1 | 151506387 | 151543692 |
| a0012 | 0/0 | 1203 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | MEQAP others(1198): Show |
chr1 | 151506387 | 151543692 |
| a0013 | 0/0 | 1203 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | CGN_chr1_151506387_151543692 | CGN | MEQAP others(1198): Show |
chr1 | 151506387 | 151543692 |
| a0014 | 0/0 | 1203 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | MEQAP others(1198): Show |
chr1 | 151506387 | 151543692 |
| a0015 | 0/0 | 1203 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | MEQAP others(1198): Show |
chr1 | 151506387 | 151543692 |
| a0016 | 0/0 | 1203 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | MEQAP others(1198): Show |
chr1 | 151506387 | 151543692 |
| a0017 | 0/0 | 1203 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | MEQAP others(1198): Show |
chr1 | 151506387 | 151543692 |
| a0018 | 0/0 | 1203 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | MEQAP others(1198): Show |
chr1 | 151506387 | 151543692 |
| a0019 | 0/0 | 1203 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | MEQAP others(1198): Show |
chr1 | 151506387 | 151543692 |
| a0020 | 0/0 | 1203 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | MEQAP others(1198): Show |
chr1 | 151506387 | 151543692 |
| a0021 | 0/0 | 1203 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CGN_chr1_151506387_151543692 | CGN | MEQAP others(1198): Show |
chr1 | 151506387 | 151543692 |
| a0022 | 0/0 | 1203 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CGN_chr1_151506387_151543692 | CGN | MEQAP others(1198): Show |
chr1 | 151506387 | 151543692 |
| a0023 | 0/0 | 1203 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | MEQAP others(1198): Show |
chr1 | 151506387 | 151543692 |
| a0024 | 0/0 | 1203 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | MEQAP others(1198): Show |
chr1 | 151506387 | 151543692 |
| a0025 | 0/0 | 1203 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CGN_chr1_151506387_151543692 | CGN | MEQAP others(1198): Show |
chr1 | 151506387 | 151543692 |
| a0026 | 0/0 | 1203 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CGN_chr1_151506387_151543692 | CGN | MEQAP others(1198): Show |
chr1 | 151506387 | 151543692 |
| a0027 | 0/0 | 1203 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CGN_chr1_151506387_151543692 | CGN | MEQAP others(1198): Show |
chr1 | 151506387 | 151543692 |
| a0028 | 0/0 | 1203 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | MEQAP others(1198): Show |
chr1 | 151506387 | 151543692 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 3609 | 252 | 48 | 48 | 118 | 10 | 27 | CGN_chr1_151506387_151543692 | CGN | ATGGA others(3604): Show |
chr1 | 151506387 | 151543692 | ||
| a0001c0004 | 0/0 | 3609 | 13 | 1 | 5 | 7 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | ATGGA others(3604): Show |
chr1 | 151506387 | 151543692 | ||
| a0001c0007 | 0/0 | 3609 | 4 | 4 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | ATGGA others(3604): Show |
chr1 | 151506387 | 151543692 | ||
| a0001c0009 | 0/0 | 3609 | 4 | 4 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | ATGGA others(3604): Show |
chr1 | 151506387 | 151543692 | ||
| a0001c0023 | 0/0 | 3609 | 1 | 1 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | ATGGA others(3604): Show |
chr1 | 151506387 | 151543692 | ||
| a0001c0024 | 0/0 | 3609 | 1 | 0 | 0 | 1 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | ATGGA others(3604): Show |
chr1 | 151506387 | 151543692 | ||
| a0001c0025 | 0/1 | 3609 | 1 | 0 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | ATGGA others(3604): Show |
chr1 | 151506387 | 151543692 | ||
| a0001c0026 | 0/0 | 3609 | 1 | 1 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | ATGGA others(3604): Show |
chr1 | 151506387 | 151543692 | ||
| a0001c0034 | 0/0 | 3609 | 1 | 0 | 1 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | ATGGA others(3604): Show |
chr1 | 151506387 | 151543692 | ||
| a0001c0036 | 0/0 | 3609 | 1 | 1 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | ATGGA others(3604): Show |
chr1 | 151506387 | 151543692 | ||
| a0002c0002 | 0/0 | 3609 | 39 | 0 | 8 | 25 | 0 | 6 | CGN_chr1_151506387_151543692 | CGN | ATGGA others(3604): Show |
chr1 | 151506387 | 151543692 | ||
| a0002c0019 | 0/0 | 3609 | 1 | 0 | 0 | 1 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | ATGGA others(3604): Show |
chr1 | 151506387 | 151543692 | ||
| a0003c0003 | 0/0 | 3609 | 18 | 18 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | ATGGA others(3604): Show |
chr1 | 151506387 | 151543692 | ||
| a0004c0006 | 0/0 | 3609 | 5 | 0 | 1 | 3 | 0 | 1 | CGN_chr1_151506387_151543692 | CGN | ATGGA others(3604): Show |
chr1 | 151506387 | 151543692 | ||
| a0005c0005 | 0/0 | 3609 | 5 | 0 | 1 | 1 | 0 | 3 | CGN_chr1_151506387_151543692 | CGN | ATGGA others(3604): Show |
chr1 | 151506387 | 151543692 | ||
| a0006c0008 | 0/0 | 3609 | 4 | 4 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | ATGGA others(3604): Show |
chr1 | 151506387 | 151543692 | ||
| a0007c0011 | 0/0 | 3609 | 3 | 0 | 3 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | ATGGA others(3604): Show |
chr1 | 151506387 | 151543692 | ||
| a0008c0010 | 0/0 | 3609 | 3 | 0 | 0 | 3 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | ATGGA others(3604): Show |
chr1 | 151506387 | 151543692 | ||
| a0009c0016 | 0/0 | 3609 | 2 | 0 | 0 | 2 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | ATGGA others(3604): Show |
chr1 | 151506387 | 151543692 | ||
| a0010c0015 | 0/0 | 3609 | 2 | 0 | 1 | 0 | 0 | 1 | CGN_chr1_151506387_151543692 | CGN | ATGGA others(3604): Show |
chr1 | 151506387 | 151543692 | ||
| a0011c0012 | 0/0 | 3609 | 2 | 2 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | ATGGA others(3604): Show |
chr1 | 151506387 | 151543692 | ||
| a0012c0014 | 0/0 | 3609 | 2 | 2 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | ATGGA others(3604): Show |
chr1 | 151506387 | 151543692 | ||
| a0013c0013 | 0/0 | 3609 | 2 | 0 | 0 | 2 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | ATGGA others(3604): Show |
chr1 | 151506387 | 151543692 | ||
| a0014c0022 | 0/0 | 3609 | 1 | 0 | 1 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | ATGGA others(3604): Show |
chr1 | 151506387 | 151543692 | ||
| a0015c0029 | 0/0 | 3609 | 1 | 0 | 1 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | ATGGA others(3604): Show |
chr1 | 151506387 | 151543692 | ||
| a0016c0018 | 0/0 | 3609 | 1 | 0 | 0 | 1 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | ATGGA others(3604): Show |
chr1 | 151506387 | 151543692 | ||
| a0017c0030 | 0/0 | 3609 | 1 | 1 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | ATGGA others(3604): Show |
chr1 | 151506387 | 151543692 | ||
| a0018c0027 | 0/0 | 3609 | 1 | 0 | 0 | 1 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | ATGGA others(3604): Show |
chr1 | 151506387 | 151543692 | ||
| a0019c0033 | 0/0 | 3609 | 1 | 1 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | ATGGA others(3604): Show |
chr1 | 151506387 | 151543692 | ||
| a0020c0020 | 0/0 | 3609 | 1 | 1 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | ATGGA others(3604): Show |
chr1 | 151506387 | 151543692 | ||
| a0021c0017 | 0/0 | 3609 | 1 | 0 | 0 | 0 | 0 | 1 | CGN_chr1_151506387_151543692 | CGN | ATGGA others(3604): Show |
chr1 | 151506387 | 151543692 | ||
| a0022c0032 | 0/0 | 3609 | 1 | 0 | 0 | 0 | 0 | 1 | CGN_chr1_151506387_151543692 | CGN | ATGGA others(3604): Show |
chr1 | 151506387 | 151543692 | ||
| a0023c0021 | 0/0 | 3609 | 1 | 1 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | ATGGA others(3604): Show |
chr1 | 151506387 | 151543692 | ||
| a0024c0035 | 0/0 | 3609 | 1 | 1 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | ATGGA others(3604): Show |
chr1 | 151506387 | 151543692 | ||
| a0025c0028 | 0/0 | 3609 | 1 | 0 | 0 | 1 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | ATGGA others(3604): Show |
chr1 | 151506387 | 151543692 | ||
| a0026c0031 | 0/0 | 3609 | 1 | 0 | 0 | 1 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | ATGGA others(3604): Show |
chr1 | 151506387 | 151543692 | ||
| a0027c0037 | 0/0 | 3609 | 1 | 0 | 0 | 1 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | ATGGA others(3604): Show |
chr1 | 151506387 | 151543692 | ||
| a0028c0038 | 0/0 | 3609 | 1 | 1 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | ATGGA others(3604): Show |
chr1 | 151506387 | 151543692 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5108 | 149 | 14 | 28 | 82 | 6 | 19 | CGN_chr1_151506387_151543692 | CGN | AGGGA others(5103): Show |
chr1 | 151506387 | 151543692 |
| a0001c0001t0002 | 0/0 | 5107 | 5 | 5 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | AGGGA others(5102): Show |
chr1 | 151506387 | 151543692 |
| a0001c0001t0003 | 0/0 | 5108 | 36 | 0 | 10 | 22 | 2 | 2 | CGN_chr1_151506387_151543692 | CGN | AGGGA others(5103): Show |
chr1 | 151506387 | 151543692 |
| a0001c0001t0005 | 0/0 | 5114 | 4 | 1 | 1 | 1 | 1 | 0 | CGN_chr1_151506387_151543692 | CGN | AGGGA others(5109): Show |
chr1 | 151506387 | 151543692 |
| a0001c0001t0006 | 0/0 | 5103 | 8 | 8 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | AGGGA others(5098): Show |
chr1 | 151506387 | 151543692 |
| a0001c0001t0007 | 0/0 | 5107 | 4 | 1 | 0 | 3 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | AGGGA others(5102): Show |
chr1 | 151506387 | 151543692 |
| a0001c0001t0008 | 0/0 | 5102 | 5 | 4 | 1 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | AGGGA others(5097): Show |
chr1 | 151506387 | 151543692 |
| a0001c0001t0009 | 0/0 | 5096 | 2 | 1 | 0 | 1 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | AGGGA others(5091): Show |
chr1 | 151506387 | 151543692 |
| a0001c0001t0010 | 0/0 | 5101 | 6 | 1 | 0 | 0 | 0 | 5 | CGN_chr1_151506387_151543692 | CGN | AGGGA others(5096): Show |
chr1 | 151506387 | 151543692 |
| a0001c0001t0011 | 0/0 | 5114 | 6 | 0 | 4 | 1 | 0 | 1 | CGN_chr1_151506387_151543692 | CGN | AGGGA others(5109): Show |
chr1 | 151506387 | 151543692 |
| a0001c0001t0012 | 1/0 | 5101 | 5 | 4 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | AGGGA others(5096): Show |
chr1 | 151506387 | 151543692 |
| a0001c0001t0013 | 0/0 | 5108 | 3 | 0 | 2 | 0 | 1 | 0 | CGN_chr1_151506387_151543692 | CGN | AGGGA others(5103): Show |
chr1 | 151506387 | 151543692 |
| a0001c0001t0014 | 0/0 | 5113 | 1 | 1 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | AGGGA others(5108): Show |
chr1 | 151506387 | 151543692 |
| a0001c0001t0015 | 0/0 | 5113 | 3 | 1 | 0 | 2 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | AGGGA others(5108): Show |
chr1 | 151506387 | 151543692 |
| a0001c0001t0016 | 0/0 | 5109 | 2 | 0 | 1 | 1 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | AGGGA others(5104): Show |
chr1 | 151506387 | 151543692 |
| a0001c0001t0017 | 0/0 | 5108 | 1 | 0 | 0 | 1 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | AGGGA others(5103): Show |
chr1 | 151506387 | 151543692 |
| a0001c0001t0019 | 0/0 | 5126 | 2 | 0 | 0 | 2 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | AGGGA others(5121): Show |
chr1 | 151506387 | 151543692 |
| a0001c0001t0020 | 0/0 | 5102 | 2 | 2 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | AGGGA others(5097): Show |
chr1 | 151506387 | 151543692 |
| a0001c0001t0022 | 0/0 | 5084 | 1 | 1 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | AGGGA others(5079): Show |
chr1 | 151506387 | 151543692 |
| a0001c0001t0023 | 0/0 | 5096 | 1 | 0 | 1 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | AGGGA others(5091): Show |
chr1 | 151506387 | 151543692 |
| a0001c0001t0024 | 0/0 | 5101 | 1 | 1 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | AGGGA others(5096): Show |
chr1 | 151506387 | 151543692 |
| a0001c0001t0025 | 0/0 | 5108 | 1 | 0 | 0 | 1 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | AGGGA others(5103): Show |
chr1 | 151506387 | 151543692 |
| a0001c0001t0027 | 0/0 | 5108 | 1 | 0 | 0 | 1 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | AGGGA others(5103): Show |
chr1 | 151506387 | 151543692 |
| a0001c0001t0031 | 0/0 | 5115 | 1 | 1 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | AGGGA others(5110): Show |
chr1 | 151506387 | 151543692 |
| a0001c0001t0033 | 0/0 | 5113 | 1 | 1 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | AGGGA others(5108): Show |
chr1 | 151506387 | 151543692 |
| a0001c0001t0034 | 0/0 | 5101 | 1 | 1 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | AGGGA others(5096): Show |
chr1 | 151506387 | 151543692 |
| a0001c0004t0004 | 0/0 | 5114 | 12 | 1 | 5 | 6 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | AGGGA others(5109): Show |
chr1 | 151506387 | 151543692 |
| a0001c0004t0017 | 0/0 | 5108 | 1 | 0 | 0 | 1 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | AGGGA others(5103): Show |
chr1 | 151506387 | 151543692 |
| a0001c0007t0001 | 0/0 | 5108 | 3 | 3 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | AGGGA others(5103): Show |
chr1 | 151506387 | 151543692 |
| a0001c0007t0005 | 0/0 | 5114 | 1 | 1 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | AGGGA others(5109): Show |
chr1 | 151506387 | 151543692 |
| a0001c0009t0001 | 0/0 | 5108 | 2 | 2 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | AGGGA others(5103): Show |
chr1 | 151506387 | 151543692 |
| a0001c0009t0018 | 0/0 | 5107 | 2 | 2 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | AGGGA others(5102): Show |
chr1 | 151506387 | 151543692 |
| a0001c0023t0001 | 0/0 | 5108 | 1 | 1 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | AGGGA others(5103): Show |
chr1 | 151506387 | 151543692 |
| a0001c0024t0001 | 0/0 | 5108 | 1 | 0 | 0 | 1 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | AGGGA others(5103): Show |
chr1 | 151506387 | 151543692 |
| a0001c0025t0028 | 0/1 | 5108 | 1 | 0 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | AGGGA others(5103): Show |
chr1 | 151506387 | 151543692 |
| a0001c0026t0001 | 0/0 | 5108 | 1 | 1 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | AGGGA others(5103): Show |
chr1 | 151506387 | 151543692 |
| a0001c0034t0001 | 0/0 | 5108 | 1 | 0 | 1 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | AGGGA others(5103): Show |
chr1 | 151506387 | 151543692 |
| a0001c0036t0008 | 0/0 | 5102 | 1 | 1 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | AGGGA others(5097): Show |
chr1 | 151506387 | 151543692 |
| a0002c0002t0002 | 0/0 | 5107 | 36 | 0 | 8 | 22 | 0 | 6 | CGN_chr1_151506387_151543692 | CGN | AGGGA others(5102): Show |
chr1 | 151506387 | 151543692 |
| a0002c0002t0014 | 0/0 | 5113 | 1 | 0 | 0 | 1 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | AGGGA others(5108): Show |
chr1 | 151506387 | 151543692 |
| a0002c0002t0021 | 0/0 | 5107 | 2 | 0 | 0 | 2 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | AGGGA others(5102): Show |
chr1 | 151506387 | 151543692 |
| a0002c0019t0002 | 0/0 | 5107 | 1 | 0 | 0 | 1 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | AGGGA others(5102): Show |
chr1 | 151506387 | 151543692 |
| a0003c0003t0001 | 0/0 | 5108 | 11 | 11 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | AGGGA others(5103): Show |
chr1 | 151506387 | 151543692 |
| a0003c0003t0002 | 0/0 | 5107 | 1 | 1 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | AGGGA others(5102): Show |
chr1 | 151506387 | 151543692 |
| a0003c0003t0005 | 0/0 | 5114 | 2 | 2 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | AGGGA others(5109): Show |
chr1 | 151506387 | 151543692 |
| a0003c0003t0009 | 0/0 | 5096 | 4 | 4 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | AGGGA others(5091): Show |
chr1 | 151506387 | 151543692 |
| a0004c0006t0002 | 0/0 | 5107 | 3 | 0 | 1 | 2 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | AGGGA others(5102): Show |
chr1 | 151506387 | 151543692 |
| a0004c0006t0014 | 0/0 | 5113 | 1 | 0 | 0 | 1 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | AGGGA others(5108): Show |
chr1 | 151506387 | 151543692 |
| a0004c0006t0030 | 0/0 | 5107 | 1 | 0 | 0 | 0 | 0 | 1 | CGN_chr1_151506387_151543692 | CGN | AGGGA others(5102): Show |
chr1 | 151506387 | 151543692 |
| a0005c0005t0001 | 0/0 | 5108 | 3 | 0 | 1 | 1 | 0 | 1 | CGN_chr1_151506387_151543692 | CGN | AGGGA others(5103): Show |
chr1 | 151506387 | 151543692 |
| a0005c0005t0003 | 0/0 | 5108 | 2 | 0 | 0 | 0 | 0 | 2 | CGN_chr1_151506387_151543692 | CGN | AGGGA others(5103): Show |
chr1 | 151506387 | 151543692 |
| a0006c0008t0007 | 0/0 | 5107 | 4 | 4 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | AGGGA others(5102): Show |
chr1 | 151506387 | 151543692 |
| a0007c0011t0001 | 0/0 | 5108 | 3 | 0 | 3 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | AGGGA others(5103): Show |
chr1 | 151506387 | 151543692 |
| a0008c0010t0001 | 0/0 | 5108 | 3 | 0 | 0 | 3 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | AGGGA others(5103): Show |
chr1 | 151506387 | 151543692 |
| a0009c0016t0003 | 0/0 | 5108 | 2 | 0 | 0 | 2 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | AGGGA others(5103): Show |
chr1 | 151506387 | 151543692 |
| a0010c0015t0003 | 0/0 | 5108 | 2 | 0 | 1 | 0 | 0 | 1 | CGN_chr1_151506387_151543692 | CGN | AGGGA others(5103): Show |
chr1 | 151506387 | 151543692 |
| a0011c0012t0005 | 0/0 | 5114 | 2 | 2 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | AGGGA others(5109): Show |
chr1 | 151506387 | 151543692 |
| a0012c0014t0001 | 0/0 | 5108 | 2 | 2 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | AGGGA others(5103): Show |
chr1 | 151506387 | 151543692 |
| a0013c0013t0002 | 0/0 | 5107 | 2 | 0 | 0 | 2 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | AGGGA others(5102): Show |
chr1 | 151506387 | 151543692 |
| a0014c0022t0001 | 0/0 | 5108 | 1 | 0 | 1 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | AGGGA others(5103): Show |
chr1 | 151506387 | 151543692 |
| a0015c0029t0032 | 0/0 | 5120 | 1 | 0 | 1 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | AGGGA others(5115): Show |
chr1 | 151506387 | 151543692 |
| a0016c0018t0002 | 0/0 | 5107 | 1 | 0 | 0 | 1 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | AGGGA others(5102): Show |
chr1 | 151506387 | 151543692 |
| a0017c0030t0029 | 0/0 | 5107 | 1 | 1 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | AGGGA others(5102): Show |
chr1 | 151506387 | 151543692 |
| a0018c0027t0001 | 0/0 | 5108 | 1 | 0 | 0 | 1 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | AGGGA others(5103): Show |
chr1 | 151506387 | 151543692 |
| a0019c0033t0001 | 0/0 | 5108 | 1 | 1 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | AGGGA others(5103): Show |
chr1 | 151506387 | 151543692 |
| a0020c0020t0001 | 0/0 | 5108 | 1 | 1 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | AGGGA others(5103): Show |
chr1 | 151506387 | 151543692 |
| a0021c0017t0001 | 0/0 | 5108 | 1 | 0 | 0 | 0 | 0 | 1 | CGN_chr1_151506387_151543692 | CGN | AGGGA others(5103): Show |
chr1 | 151506387 | 151543692 |
| a0022c0032t0001 | 0/0 | 5108 | 1 | 0 | 0 | 0 | 0 | 1 | CGN_chr1_151506387_151543692 | CGN | AGGGA others(5103): Show |
chr1 | 151506387 | 151543692 |
| a0023c0021t0001 | 0/0 | 5108 | 1 | 1 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | AGGGA others(5103): Show |
chr1 | 151506387 | 151543692 |
| a0024c0035t0008 | 0/0 | 5102 | 1 | 1 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | AGGGA others(5097): Show |
chr1 | 151506387 | 151543692 |
| a0025c0028t0001 | 0/0 | 5108 | 1 | 0 | 0 | 1 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | AGGGA others(5103): Show |
chr1 | 151506387 | 151543692 |
| a0026c0031t0004 | 0/0 | 5114 | 1 | 0 | 0 | 1 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | AGGGA others(5109): Show |
chr1 | 151506387 | 151543692 |
| a0027c0037t0001 | 0/0 | 5108 | 1 | 0 | 0 | 1 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | AGGGA others(5103): Show |
chr1 | 151506387 | 151543692 |
| a0028c0038t0026 | 0/0 | 5108 | 1 | 1 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | AGGGA others(5103): Show |
chr1 | 151506387 | 151543692 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 12 | 0 | 0 | 11 | 0 | 1 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0001g0003 | 0/0 | 12 | 0 | 2 | 10 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0001g0004 | 0/0 | 9 | 2 | 4 | 1 | 0 | 2 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0001g0007 | 0/0 | 5 | 0 | 3 | 0 | 1 | 1 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0001g0008 | 0/0 | 5 | 0 | 1 | 0 | 1 | 3 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0001g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0001g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0001g0021 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0001g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0001g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0003g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0003g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0003g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0003g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0003g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0003g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0003g0049 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0003g0052 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0003g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0003g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0003g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0003g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0003g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0003g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0003g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0003g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0003g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0005g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0005g0007 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0005g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0005g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0006g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0006g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0006g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0006g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0007g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0007g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0007g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0007g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0008g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0008g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0008g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0009g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0009g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0010g0006 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0010g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0010g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0010g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0011g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0011g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0011g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0011g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0011g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0012g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0012g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0012g0099 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0013g0012 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0014g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0015g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0015g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0015g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0016g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0016g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0017g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0019g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0019g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0020g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0020g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0022g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0023g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0024g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0025g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0027g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0031g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0033g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0001t0034g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0004t0004g0005 | 0/0 | 9 | 1 | 3 | 5 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0004t0004g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0004t0004g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0004t0004g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0004t0017g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0007t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0007t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0007t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0007t0005g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0009t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0009t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0009t0018g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0023t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0024t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0025t0028g0179 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0026t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0034t0001g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0001c0036t0008g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0002c0002t0002g0001 | 0/0 | 18 | 0 | 6 | 9 | 0 | 3 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0002c0002t0002g0009 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0002c0002t0002g0034 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0002c0002t0002g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0002c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0002c0002t0002g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0002c0002t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0002c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0002c0002t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0002c0002t0002g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0002c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0002c0002t0002g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0002c0002t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0002c0002t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0002c0002t0014g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0002c0002t0021g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0002c0019t0002g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0003c0003t0001g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0003c0003t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0003c0003t0001g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0003c0003t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0003c0003t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0003c0003t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0003c0003t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0003c0003t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0003c0003t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0003c0003t0005g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0003c0003t0005g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0003c0003t0009g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0003c0003t0009g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0003c0003t0009g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0004c0006t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0004c0006t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0004c0006t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0004c0006t0014g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0004c0006t0030g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0005c0005t0001g0037 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0005c0005t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0005c0005t0003g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0005c0005t0003g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0006c0008t0007g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0006c0008t0007g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0006c0008t0007g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0007c0011t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0007c0011t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0008c0010t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0009c0016t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0009c0016t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0010c0015t0003g0022 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0011c0012t0005g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0012c0014t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0012c0014t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0013c0013t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0013c0013t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0014c0022t0001g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0015c0029t0032g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0016c0018t0002g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0017c0030t0029g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0018c0027t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0019c0033t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0020c0020t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0021c0017t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0022c0032t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0023c0021t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0024c0035t0008g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0025c0028t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0026c0031t0004g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0027c0037t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| a0028c0038t0026g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0007 | EUR | GBR | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG00099 | hp2 | a0001 | c0001 | t0003 | g0055 | EUR | GBR | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0008 | EUR | FIN | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0047 | EUR | FIN | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG00323 | hp1 | a0001 | c0001 | t0005 | g0007 | EUR | FIN | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0231 | EUR | FIN | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | CHS | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG00544 | hp2 | a0001 | c0001 | t0003 | g0223 | EAS | CHS | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG00558 | hp2 | a0002 | c0002 | t0002 | g0038 | EAS | CHS | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | CHS | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG00597 | hp2 | a0009 | c0016 | t0003 | g0114 | EAS | CHS | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG00609 | hp2 | a0001 | c0001 | t0003 | g0033 | EAS | CHS | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0048 | EAS | CHS | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG00673 | hp1 | a0001 | c0004 | t0004 | g0005 | EAS | CHS | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG00741 | hp2 | a0002 | c0002 | t0002 | g0001 | AMR | PUR | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG01070 | hp1 | a0002 | c0002 | t0002 | g0001 | AMR | PUR | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG01070 | hp2 | a0001 | c0001 | t0003 | g0107 | AMR | PUR | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG01071 | hp2 | a0002 | c0002 | t0002 | g0001 | AMR | PUR | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG01074 | hp2 | a0014 | c0022 | t0001 | g0004 | AMR | PUR | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG01081 | hp1 | a0007 | c0011 | t0001 | g0006 | AMR | PUR | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG01106 | hp1 | a0001 | c0001 | t0013 | g0012 | AMR | PUR | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG01109 | hp2 | a0001 | c0034 | t0001 | g0004 | AMR | PUR | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG01167 | hp2 | a0001 | c0004 | t0004 | g0090 | AMR | PUR | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG01168 | hp1 | a0001 | c0001 | t0011 | g0032 | AMR | PUR | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG01169 | hp1 | a0001 | c0004 | t0004 | g0086 | AMR | PUR | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG01169 | hp2 | a0001 | c0001 | t0011 | g0032 | AMR | PUR | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG01175 | hp1 | a0001 | c0001 | t0013 | g0012 | AMR | PUR | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG01175 | hp2 | a0001 | c0001 | t0003 | g0166 | AMR | PUR | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG01192 | hp1 | a0015 | c0029 | t0032 | g0208 | AMR | PUR | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG01192 | hp2 | a0007 | c0011 | t0001 | g0006 | AMR | PUR | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG01243 | hp1 | a0010 | c0015 | t0003 | g0022 | AMR | PUR | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG01255 | hp1 | a0002 | c0002 | t0002 | g0001 | AMR | CLM | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG01255 | hp2 | a0001 | c0001 | t0003 | g0052 | AMR | CLM | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG01256 | hp2 | a0002 | c0002 | t0002 | g0001 | AMR | CLM | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG01257 | hp2 | a0001 | c0001 | t0003 | g0052 | AMR | CLM | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | CLM | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG01261 | hp2 | a0001 | c0004 | t0004 | g0005 | AMR | CLM | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG01346 | hp2 | a0001 | c0004 | t0004 | g0005 | AMR | CLM | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | CLM | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG01361 | hp2 | a0001 | c0001 | t0005 | g0002 | AMR | CLM | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG01433 | hp1 | a0004 | c0006 | t0002 | g0077 | AMR | CLM | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | CLM | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG01496 | hp1 | a0001 | c0001 | t0023 | g0036 | AMR | CLM | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG01496 | hp2 | a0007 | c0011 | t0001 | g0233 | AMR | CLM | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG01517 | hp1 | a0001 | c0001 | t0013 | g0012 | EUR | IBS | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0187 | EUR | IBS | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG01884 | hp1 | a0001 | c0001 | t0008 | g0019 | AFR | ACB | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG01891 | hp1 | a0003 | c0003 | t0009 | g0044 | AFR | ACB | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG01891 | hp2 | a0001 | c0001 | t0012 | g0029 | AFR | ACB | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG01928 | hp2 | a0005 | c0005 | t0001 | g0037 | AMR | PEL | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG01943 | hp1 | a0001 | c0001 | t0003 | g0201 | AMR | PEL | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG01943 | hp2 | a0001 | c0001 | t0011 | g0087 | AMR | PEL | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG01952 | hp1 | a0001 | c0001 | t0003 | g0190 | AMR | PEL | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | PEL | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG01975 | hp1 | a0001 | c0001 | t0016 | g0022 | AMR | PEL | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG01975 | hp2 | a0001 | c0004 | t0004 | g0005 | AMR | PEL | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | PEL | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | PEL | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG01981 | hp2 | a0001 | c0001 | t0003 | g0204 | AMR | PEL | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG01993 | hp1 | a0001 | c0001 | t0011 | g0036 | AMR | PEL | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG01993 | hp2 | a0001 | c0001 | t0003 | g0049 | AMR | PEL | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG02015 | hp2 | a0001 | c0001 | t0011 | g0015 | EAS | KHV | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG02027 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | KHV | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG02027 | hp2 | a0001 | c0001 | t0007 | g0078 | EAS | KHV | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | KHV | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG02040 | hp2 | a0001 | c0001 | t0003 | g0171 | EAS | KHV | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG02055 | hp1 | a0001 | c0026 | t0001 | g0221 | AFR | ACB | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG02055 | hp2 | a0003 | c0003 | t0001 | g0134 | AFR | ACB | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG02071 | hp1 | a0016 | c0018 | t0002 | g0001 | EAS | KHV | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG02071 | hp2 | a0001 | c0001 | t0003 | g0031 | EAS | KHV | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | KHV | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG02074 | hp2 | a0001 | c0001 | t0007 | g0006 | EAS | KHV | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG02080 | hp1 | a0009 | c0016 | t0003 | g0113 | EAS | KHV | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG02080 | hp2 | a0001 | c0001 | t0015 | g0096 | EAS | KHV | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG02083 | hp1 | a0001 | c0001 | t0005 | g0213 | EAS | KHV | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG02083 | hp2 | a0001 | c0004 | t0004 | g0005 | EAS | KHV | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | KHV | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG02129 | hp2 | a0001 | c0001 | t0007 | g0215 | EAS | KHV | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | KHV | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | KHV | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG02135 | hp2 | a0001 | c0024 | t0001 | g0003 | EAS | KHV | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG02145 | hp1 | a0001 | c0007 | t0005 | g0056 | AFR | ACB | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG02145 | hp2 | a0001 | c0001 | t0014 | g0200 | AFR | ACB | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | PEL | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG02148 | hp2 | a0002 | c0002 | t0002 | g0065 | AMR | PEL | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | CDX | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG02155 | hp2 | a0018 | c0027 | t0001 | g0220 | EAS | CDX | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG02165 | hp1 | a0001 | c0001 | t0003 | g0033 | EAS | CDX | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | CDX | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG02258 | hp1 | a0001 | c0001 | t0006 | g0018 | AFR | ACB | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG02258 | hp2 | a0001 | c0001 | t0009 | g0199 | AFR | ACB | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG02273 | hp1 | a0002 | c0002 | t0002 | g0009 | AMR | PEL | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | PEL | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG02280 | hp1 | a0001 | c0001 | t0022 | g0211 | AFR | ACB | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG02280 | hp2 | a0001 | c0001 | t0006 | g0018 | AFR | ACB | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG02300 | hp1 | a0002 | c0002 | t0002 | g0001 | AMR | PEL | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG02300 | hp2 | a0001 | c0001 | t0008 | g0054 | AMR | PEL | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG02451 | hp1 | a0019 | c0033 | t0001 | g0098 | AFR | ACB | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG02451 | hp2 | a0001 | c0007 | t0001 | g0151 | AFR | ACB | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG02523 | hp1 | a0001 | c0001 | t0003 | g0195 | EAS | KHV | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | KHV | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG02572 | hp1 | a0003 | c0003 | t0002 | g0093 | AFR | GWD | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG02572 | hp2 | a0020 | c0020 | t0001 | g0035 | AFR | GWD | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG02602 | hp1 | a0021 | c0017 | t0001 | g0047 | SAS | PJL | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG02602 | hp2 | a0005 | c0005 | t0003 | g0105 | SAS | PJL | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG02615 | hp1 | a0001 | c0001 | t0010 | g0155 | AFR | GWD | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG02615 | hp2 | a0001 | c0001 | t0008 | g0019 | AFR | GWD | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG02647 | hp1 | a0001 | c0001 | t0020 | g0146 | AFR | GWD | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG02683 | hp1 | a0002 | c0002 | t0002 | g0001 | SAS | PJL | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG02683 | hp2 | a0010 | c0015 | t0003 | g0022 | SAS | PJL | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG02698 | hp1 | a0004 | c0006 | t0030 | g0198 | SAS | PJL | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG02698 | hp2 | a0022 | c0032 | t0001 | g0202 | SAS | PJL | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG02717 | hp1 | a0003 | c0003 | t0009 | g0161 | AFR | GWD | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0143 | AFR | GWD | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0210 | AFR | GWD | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG02723 | hp2 | a0003 | c0003 | t0001 | g0133 | AFR | GWD | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0197 | SAS | PJL | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG02809 | hp1 | a0001 | c0009 | t0001 | g0219 | AFR | GWD | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG02809 | hp2 | a0001 | c0001 | t0012 | g0030 | AFR | GWD | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG02818 | hp1 | a0001 | c0001 | t0008 | g0019 | AFR | GWD | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG02818 | hp2 | a0001 | c0001 | t0034 | g0100 | AFR | GWD | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG02886 | hp1 | a0003 | c0003 | t0005 | g0040 | AFR | GWD | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG02886 | hp2 | a0023 | c0021 | t0001 | g0216 | AFR | GWD | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | GWD | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG02895 | hp2 | a0001 | c0009 | t0018 | g0046 | AFR | GWD | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG02896 | hp1 | a0011 | c0012 | t0005 | g0028 | AFR | GWD | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG02896 | hp2 | a0001 | c0001 | t0031 | g0109 | AFR | GWD | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG02897 | hp1 | a0001 | c0009 | t0018 | g0046 | AFR | GWD | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG02897 | hp2 | a0011 | c0012 | t0005 | g0028 | AFR | GWD | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG02922 | hp1 | a0001 | c0001 | t0024 | g0011 | AFR | ESN | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | ESN | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG02965 | hp1 | a0003 | c0003 | t0001 | g0017 | AFR | ESN | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG02965 | hp2 | a0003 | c0003 | t0001 | g0132 | AFR | ESN | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG02970 | hp1 | a0001 | c0009 | t0001 | g0174 | AFR | ESN | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG02970 | hp2 | a0006 | c0008 | t0007 | g0157 | AFR | ESN | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | ESN | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG02976 | hp2 | a0001 | c0001 | t0006 | g0135 | AFR | ESN | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG03017 | hp1 | a0001 | c0001 | t0010 | g0175 | SAS | PJL | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0185 | SAS | PJL | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | GWD | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | GWD | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG03098 | hp1 | a0012 | c0014 | t0001 | g0035 | AFR | MSL | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG03098 | hp2 | a0003 | c0003 | t0001 | g0017 | AFR | MSL | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG03130 | hp1 | a0001 | c0001 | t0008 | g0083 | AFR | ESN | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG03130 | hp2 | a0001 | c0001 | t0033 | g0154 | AFR | ESN | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | ESN | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG03139 | hp2 | a0012 | c0014 | t0001 | g0015 | AFR | ESN | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG03195 | hp1 | a0001 | c0001 | t0015 | g0209 | AFR | ESN | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG03195 | hp2 | a0001 | c0001 | t0005 | g0180 | AFR | ESN | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG03209 | hp1 | a0001 | c0001 | t0012 | g0030 | AFR | MSL | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG03209 | hp2 | a0003 | c0003 | t0001 | g0041 | AFR | MSL | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG03225 | hp1 | a0001 | c0007 | t0001 | g0148 | AFR | MSL | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG03225 | hp2 | a0003 | c0003 | t0001 | g0017 | AFR | MSL | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0188 | SAS | PJL | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG03453 | hp1 | a0024 | c0035 | t0008 | g0232 | AFR | MSL | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG03453 | hp2 | a0006 | c0008 | t0007 | g0144 | AFR | MSL | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG03486 | hp1 | a0001 | c0036 | t0008 | g0158 | AFR | MSL | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | MSL | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG03490 | hp1 | a0001 | c0001 | t0010 | g0050 | SAS | PJL | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG03491 | hp1 | a0005 | c0005 | t0001 | g0121 | SAS | PJL | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG03492 | hp2 | a0001 | c0001 | t0010 | g0006 | SAS | PJL | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG03540 | hp1 | a0003 | c0003 | t0001 | g0137 | AFR | GWD | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG03540 | hp2 | a0006 | c0008 | t0007 | g0043 | AFR | GWD | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG03579 | hp1 | a0003 | c0003 | t0009 | g0044 | AFR | MSL | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG03579 | hp2 | a0001 | c0001 | t0006 | g0011 | AFR | MSL | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0225 | SAS | PJL | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG03654 | hp2 | a0001 | c0001 | t0010 | g0006 | SAS | PJL | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG03669 | hp2 | a0002 | c0002 | t0002 | g0001 | SAS | PJL | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG03688 | hp1 | a0002 | c0002 | t0002 | g0115 | SAS | STU | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG03688 | hp2 | a0001 | c0001 | t0003 | g0116 | SAS | STU | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0167 | SAS | PJL | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0129 | SAS | BEB | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG03834 | hp1 | a0001 | c0001 | t0010 | g0006 | SAS | BEB | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | BEB | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | BEB | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0072 | SAS | BEB | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | STU | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG04115 | hp2 | a0002 | c0002 | t0002 | g0001 | SAS | STU | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG04184 | hp1 | a0005 | c0005 | t0003 | g0145 | SAS | BEB | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0186 | SAS | BEB | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG04199 | hp1 | a0002 | c0002 | t0002 | g0120 | SAS | STU | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | STU | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG04228 | hp1 | a0002 | c0002 | t0002 | g0034 | SAS | STU | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG04228 | hp2 | a0001 | c0001 | t0011 | g0125 | SAS | STU | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0156 | AFR | YRI | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA18522 | hp2 | a0001 | c0001 | t0020 | g0101 | AFR | YRI | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | CHB | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | CHB | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | CHB | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA18747 | hp2 | a0004 | c0006 | t0014 | g0183 | EAS | CHB | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA18906 | hp1 | a0006 | c0008 | t0007 | g0043 | AFR | YRI | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA18906 | hp2 | a0001 | c0001 | t0012 | g0029 | AFR | YRI | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA18939 | hp2 | a0013 | c0013 | t0002 | g0147 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA18942 | hp1 | a0002 | c0002 | t0002 | g0034 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA18942 | hp2 | a0001 | c0001 | t0019 | g0002 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA18944 | hp1 | a0001 | c0004 | t0004 | g0005 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA18944 | hp2 | a0013 | c0013 | t0002 | g0119 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA18945 | hp2 | a0002 | c0002 | t0021 | g0001 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA18947 | hp1 | a0008 | c0010 | t0001 | g0002 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA18947 | hp2 | a0001 | c0001 | t0017 | g0002 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA18948 | hp1 | a0002 | c0002 | t0002 | g0106 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA18951 | hp1 | a0025 | c0028 | t0001 | g0169 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA18952 | hp2 | a0002 | c0002 | t0002 | g0009 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA18954 | hp1 | a0005 | c0005 | t0001 | g0037 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA18954 | hp2 | a0001 | c0001 | t0003 | g0118 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA18957 | hp2 | a0002 | c0002 | t0002 | g0038 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA18960 | hp2 | a0001 | c0001 | t0019 | g0062 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA18963 | hp1 | a0004 | c0006 | t0002 | g0203 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA18965 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA18965 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA18967 | hp1 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA18967 | hp2 | a0001 | c0001 | t0009 | g0214 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA18968 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA18970 | hp1 | a0001 | c0001 | t0003 | g0102 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA18972 | hp1 | a0001 | c0001 | t0015 | g0097 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA18972 | hp2 | a0001 | c0001 | t0016 | g0226 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA18974 | hp2 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA18977 | hp2 | a0008 | c0010 | t0001 | g0002 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA18981 | hp1 | a0002 | c0002 | t0014 | g0039 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA18981 | hp2 | a0026 | c0031 | t0004 | g0130 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA18982 | hp2 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA18983 | hp2 | a0002 | c0002 | t0002 | g0042 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA18985 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA18986 | hp1 | a0001 | c0004 | t0004 | g0005 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA18986 | hp2 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA18987 | hp1 | a0002 | c0002 | t0002 | g0009 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA18991 | hp1 | a0008 | c0010 | t0001 | g0002 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA18991 | hp2 | a0002 | c0002 | t0002 | g0122 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA18998 | hp2 | a0004 | c0006 | t0002 | g0189 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA18999 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA19001 | hp1 | a0002 | c0002 | t0002 | g0131 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA19001 | hp2 | a0001 | c0004 | t0004 | g0005 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA19003 | hp2 | a0001 | c0001 | t0027 | g0058 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA19006 | hp1 | a0001 | c0001 | t0003 | g0049 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA19009 | hp2 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA19010 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA19010 | hp2 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA19012 | hp2 | a0001 | c0001 | t0003 | g0172 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | LWK | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA19030 | hp2 | a0003 | c0003 | t0001 | g0138 | AFR | LWK | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA19043 | hp1 | a0001 | c0001 | t0007 | g0165 | AFR | LWK | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA19043 | hp2 | a0001 | c0001 | t0006 | g0018 | AFR | LWK | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA19055 | hp2 | a0001 | c0001 | t0003 | g0031 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA19056 | hp2 | a0027 | c0037 | t0001 | g0003 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA19060 | hp2 | a0001 | c0001 | t0003 | g0123 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA19062 | hp1 | a0002 | c0002 | t0002 | g0110 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA19063 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA19063 | hp2 | a0001 | c0001 | t0025 | g0205 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA19066 | hp1 | a0001 | c0001 | t0003 | g0048 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA19067 | hp1 | a0002 | c0002 | t0021 | g0001 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA19068 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA19079 | hp2 | a0001 | c0001 | t0003 | g0207 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA19080 | hp1 | a0001 | c0004 | t0017 | g0005 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA19080 | hp2 | a0002 | c0002 | t0002 | g0039 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA19081 | hp1 | a0001 | c0001 | t0003 | g0112 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA19085 | hp2 | a0002 | c0002 | t0002 | g0042 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA19087 | hp1 | a0002 | c0019 | t0002 | g0009 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA19087 | hp2 | a0002 | c0002 | t0002 | g0117 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA19090 | hp2 | a0001 | c0004 | t0004 | g0089 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0153 | AFR | YRI | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA19240 | hp2 | a0003 | c0003 | t0005 | g0095 | AFR | YRI | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA20129 | hp1 | a0003 | c0003 | t0009 | g0159 | AFR | ASW | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | ASW | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0181 | EUR | TSI | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0164 | EUR | TSI | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG01123 | hp1 | a0001 | c0001 | t0003 | g0230 | AMR | CLM | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG01123 | hp2 | a0001 | c0001 | t0003 | g0015 | AMR | CLM | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG02109 | hp1 | a0017 | c0030 | t0029 | g0149 | AFR | ACB | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG02109 | hp2 | a0001 | c0001 | t0006 | g0011 | AFR | ACB | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0152 | AFR | ACB | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | ACB | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG02559 | hp1 | a0001 | c0007 | t0001 | g0150 | AFR | ACB | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | ACB | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG03471 | hp1 | a0003 | c0003 | t0001 | g0041 | AFR | MSL | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | MSL | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG06807 | hp1 | a0003 | c0003 | t0001 | g0040 | AFR | USA | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| HG06807 | hp2 | a0001 | c0023 | t0001 | g0108 | AFR | USA | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA20300 | hp1 | a0001 | c0004 | t0004 | g0005 | AFR | USA | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA20300 | hp2 | a0001 | c0001 | t0006 | g0011 | AFR | USA | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA21309 | hp1 | a0028 | c0038 | t0026 | g0160 | AFR | LWK | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| NA21309 | hp2 | a0001 | c0001 | t0006 | g0136 | AFR | LWK | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| homoSapiens | chm13v2 | a0001 | c0025 | t0028 | g0179 | REF | REF | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0012 | g0099 | REF | REF | CGN_chr1_151506387_151543692 | CGN | chr1 | 151506387 | 151543692 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:151518625 | C | T | 1 | a0027 | 1 | NA19056.hp2 | missense_variant | MODERATE | c.106C>T | p.Arg36Cys | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 2/21 | 249/5101 | 106/3612 | 36/1203 | chr1 | 151518625 | |||
| chr1:151518842 | T | G | 1 | a0011 | 2 | HG02896.hp1 HG02897.hp2 |
missense_variant | MODERATE | c.323T>G | p.Val108Gly | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 2/21 | 466/5101 | 323/3612 | 108/1203 | chr1 | 151518842 | |||
| chr1:151518935 | C | T | 1 | a0009 | 2 | HG00597.hp2 HG02080.hp1 |
missense_variant | MODERATE | c.416C>T | p.Ala139Val | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 2/21 | 559/5101 | 416/3612 | 139/1203 | chr1 | 151518935 | |||
| chr1:151519051 | G | C | 1 | a0021 | 1 | HG02602.hp1 | missense_variant | MODERATE | c.532G>C | p.Val178Leu | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 2/21 | 675/5101 | 532/3612 | 178/1203 | chr1 | 151519051 | |||
| chr1:151519312 | C | T | 1 | a0024 | 1 | HG03453.hp1 | missense_variant | MODERATE | c.793C>T | p.Arg265Cys | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 2/21 | 936/5101 | 793/3612 | 265/1203 | chr1 | 151519312 | |||
| chr1:151524242 | C | T | 3 | a0003 a0019 a0028 |
20 | HG01891.hp1 HG02055.hp2 HG02451.hp1 others(17): Show |
missense_variant | MODERATE | c.1285C>T | p.Arg429Cys | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 7/21 | 1428/5101 | 1285/3612 | 429/1203 | chr1 | 151524242 | |||
| chr1:151524726 | G | A | 4 | a0002 a0005 a0013 others(1): Show |
48 | HG00558.hp2 HG00741.hp2 HG01070.hp1 others(45): Show |
missense_variant | MODERATE | c.1454G>A | p.Arg485Gln | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 8/21 | 1597/5101 | 1454/3612 | 485/1203 | chr1 | 151524726 | |||
| chr1:151524803 | C | T | 1 | a0022 | 1 | HG02698.hp2 | missense_variant | MODERATE | c.1531C>T | p.Arg511Cys | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 8/21 | 1674/5101 | 1531/3612 | 511/1203 | chr1 | 151524803 | |||
| chr1:151526989 | G | A | 1 | a0008 | 3 | NA18947.hp1 NA18977.hp2 NA18991.hp1 |
missense_variant | MODERATE | c.1778G>A | p.Arg593Gln | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 10/21 | 1921/5101 | 1778/3612 | 593/1203 | chr1 | 151526989 | |||
| chr1:151527034 | A | G | 1 | a0028 | 1 | NA21309.hp1 | missense_variant | MODERATE | c.1823A>G | p.Glu608Gly | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 10/21 | 1966/5101 | 1823/3612 | 608/1203 | chr1 | 151527034 | |||
| chr1:151529365 | C | G | 5 | a0002 a0004 a0013 others(2): Show |
49 | HG00558.hp2 HG00741.hp2 HG01070.hp1 others(46): Show |
missense_variant | MODERATE | c.1912C>G | p.Gln638Glu | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 11/21 | 2055/5101 | 1912/3612 | 638/1203 | chr1 | 151529365 | |||
| chr1:151529420 | G | A | 1 | a0020 | 1 | HG02572.hp2 | missense_variant | MODERATE | c.1967G>A | p.Arg656Gln | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 11/21 | 2110/5101 | 1967/3612 | 656/1203 | chr1 | 151529420 | |||
| chr1:151529432 | G | A | 2 | a0012 a0020 |
3 | HG02572.hp2 HG03098.hp1 HG03139.hp2 |
missense_variant | MODERATE | c.1979G>A | p.Arg660Gln | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 11/21 | 2122/5101 | 1979/3612 | 660/1203 | chr1 | 151529432 | |||
| chr1:151529924 | G | A | 1 | a0013 | 2 | NA18939.hp2 NA18944.hp2 |
missense_variant | MODERATE | c.2122G>A | p.Glu708Lys | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 12/21 | 2265/5101 | 2122/3612 | 708/1203 | chr1 | 151529924 | |||
| chr1:151529951 | C | T | 1 | a0010 | 2 | HG01243.hp1 HG02683.hp2 |
missense_variant | MODERATE | c.2149C>T | p.Arg717Trp | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 12/21 | 2292/5101 | 2149/3612 | 717/1203 | chr1 | 151529951 | |||
| chr1:151529954 | C | T | 3 | a0011 a0019 a0024 |
4 | HG02451.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
missense_variant | MODERATE | c.2152C>T | p.Arg718Trp | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 12/21 | 2295/5101 | 2152/3612 | 718/1203 | chr1 | 151529954 | |||
| chr1:151530490 | C | G | 1 | a0015 | 1 | HG01192.hp1 | missense_variant&splice_region_variant | MODERATE | c.2315C>G | p.Ala772Gly | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 13/21 | 2458/5101 | 2315/3612 | 772/1203 | chr1 | 151530490 | |||
| chr1:151530502 | A | G | 1 | a0006 | 4 | HG02970.hp2 HG03453.hp2 HG03540.hp2 others(1): Show |
missense_variant | MODERATE | c.2327A>G | p.Gln776Arg | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 13/21 | 2470/5101 | 2327/3612 | 776/1203 | chr1 | 151530502 | |||
| chr1:151530562 | G | A | 1 | a0023 | 1 | HG02886.hp2 | missense_variant | MODERATE | c.2387G>A | p.Arg796Gln | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 13/21 | 2530/5101 | 2387/3612 | 796/1203 | chr1 | 151530562 | |||
| chr1:151530595 | G | A | 1 | a0014 | 1 | HG01074.hp2 | missense_variant | MODERATE | c.2420G>A | p.Arg807Gln | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 13/21 | 2563/5101 | 2420/3612 | 807/1203 | chr1 | 151530595 | |||
| chr1:151530607 | G | T | 1 | a0025 | 1 | NA18951.hp1 | missense_variant | MODERATE | c.2432G>T | p.Arg811Leu | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 13/21 | 2575/5101 | 2432/3612 | 811/1203 | chr1 | 151530607 | |||
| chr1:151530636 | C | T | 1 | a0018 | 1 | HG02155.hp2 | missense_variant | MODERATE | c.2461C>T | p.Arg821Trp | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 13/21 | 2604/5101 | 2461/3612 | 821/1203 | chr1 | 151530636 | |||
| chr1:151530663 | C | T | 1 | a0026 | 1 | NA18981.hp2 | missense_variant | MODERATE | c.2488C>T | p.Arg830Trp | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 13/21 | 2631/5101 | 2488/3612 | 830/1203 | chr1 | 151530663 | |||
| chr1:151532559 | G | A | 1 | a0006 | 4 | HG02970.hp2 HG03453.hp2 HG03540.hp2 others(1): Show |
missense_variant | MODERATE | c.2729G>A | p.Arg910Gln | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 14/21 | 2872/5101 | 2729/3612 | 910/1203 | chr1 | 151532559 | |||
| chr1:151534050 | G | A | 1 | a0007 | 3 | HG01081.hp1 HG01192.hp2 HG01496.hp2 |
missense_variant | MODERATE | c.2818G>A | p.Ala940Thr | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 15/21 | 2961/5101 | 2818/3612 | 940/1203 | chr1 | 151534050 | |||
| chr1:151535055 | G | A | 1 | a0017 | 1 | HG02109.hp1 | missense_variant | MODERATE | c.2918G>A | p.Arg973Gln | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 16/21 | 3061/5101 | 2918/3612 | 973/1203 | chr1 | 151535055 | |||
| chr1:151536791 | G | A | 1 | a0016 | 1 | HG02071.hp1 | missense_variant | MODERATE | c.3368G>A | p.Arg1123Gln | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 20/21 | 3511/5101 | 3368/3612 | 1123/1203 | chr1 | 151536791 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:151518558 | C | T | 1 | a0028c0038 | 1 | NA21309.hp1 | synonymous_variant | LOW | c.39C>T | p.Pro13Pro | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 2/21 | 182/5101 | 39/3612 | 13/1203 | chr1 | 151518558 | |||
| chr1:151518699 | C | T | 2 | a0001c0036 a0028c0038 |
2 | HG03486.hp1 NA21309.hp1 |
synonymous_variant | LOW | c.180C>T | p.Ile60Ile | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 2/21 | 323/5101 | 180/3612 | 60/1203 | chr1 | 151518699 | |||
| chr1:151520622 | C | T | 1 | a0001c0009 | 4 | HG02809.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
synonymous_variant | LOW | c.1071C>T | p.Ala357Ala | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 5/21 | 1214/5101 | 1071/3612 | 357/1203 | chr1 | 151520622 | |||
| chr1:151523508 | A | G | 1 | a0001c0034 | 1 | HG01109.hp2 | synonymous_variant | LOW | c.1215A>G | p.Arg405Arg | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 6/21 | 1358/5101 | 1215/3612 | 405/1203 | chr1 | 151523508 | |||
| chr1:151525662 | C | G | 2 | a0001c0004 a0026c0031 |
14 | HG00673.hp1 HG01167.hp2 HG01169.hp1 others(11): Show |
synonymous_variant | LOW | c.1635C>G | p.Ala545Ala | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 9/21 | 1778/5101 | 1635/3612 | 545/1203 | chr1 | 151525662 | |||
| chr1:151532434 | C | T | 1 | a0001c0026 | 1 | HG02055.hp1 | synonymous_variant | LOW | c.2604C>T | p.Ala868Ala | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 14/21 | 2747/5101 | 2604/3612 | 868/1203 | chr1 | 151532434 | |||
| chr1:151536312 | C | T | 2 | a0001c0024 a0002c0019 |
2 | HG02135.hp2 NA19087.hp1 |
synonymous_variant | LOW | c.3273C>T | p.Asp1091Asp | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 19/21 | 3416/5101 | 3273/3612 | 1091/1203 | chr1 | 151536312 | |||
| chr1:151536795 | G | A | 1 | a0001c0007 | 4 | HG02145.hp1 HG02451.hp2 HG02559.hp1 others(1): Show |
synonymous_variant | LOW | c.3372G>A | p.Leu1124Leu | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 20/21 | 3515/5101 | 3372/3612 | 1124/1203 | chr1 | 151536795 | |||
| chr1:151536798 | C | T | 1 | a0001c0023 | 1 | HG06807.hp2 | synonymous_variant | LOW | c.3375C>T | p.Asp1125Asp | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 20/21 | 3518/5101 | 3375/3612 | 1125/1203 | chr1 | 151536798 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:151511402 | C | T | 1 | a0002c0002t0021 | 2 | NA18945.hp2 NA19067.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-128C>T | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 1/21 | chr1 | 151511402 | |||||||
| chr1:151511416 | G | A | 70 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(67): Show |
373 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(370): Show |
5_prime_UTR_variant | MODIFIER | c.-114G>A | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 1/21 | 7104 | chr1 | 151511416 | ||||||
| chr1:151511435 | T | TGCCCGA | 45 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(42): Show |
304 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(301): Show |
5_prime_UTR_variant | MODIFIER | c.-52_-47dupGCCCGA | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 1/21 | 7036 | INFO_REALIGN_3_PRIME | chr1 | 151511435 | |||||
| chr1:151511435 | T | TGCCCGAG others(5): Show |
12 | a0001c0001t0005 a0001c0001t0011 a0001c0001t0014 others(9): Show |
35 | HG00323.hp1 HG00673.hp1 HG01167.hp2 others(32): Show |
5_prime_UTR_variant | MODIFIER | c.-58_-47dupGCCCGAGC others(4): Show |
CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 1/21 | 7036 | INFO_REALIGN_3_PRIME | chr1 | 151511435 | |||||
| chr1:151511435 | T | TGCCCGAG others(11): Show |
1 | a0015c0029t0032 | 1 | HG01192.hp1 | 5_prime_UTR_variant | MODIFIER | c.-64_-47dupGCCCGAGC others(10): Show |
CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 1/21 | 7036 | INFO_REALIGN_3_PRIME | chr1 | 151511435 | |||||
| chr1:151511435 | T | TGCCCGAG others(17): Show |
1 | a0001c0001t0019 | 2 | NA18942.hp2 NA18960.hp2 |
5_prime_UTR_variant | MODIFIER | c.-70_-47dupGCCCGAGC others(16): Show |
CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 1/21 | 7036 | INFO_REALIGN_3_PRIME | chr1 | 151511435 | |||||
| chr1:151511435 | TGCCCGA | T | 3 | a0001c0001t0009 a0001c0001t0023 a0003c0003t0009 |
7 | HG01496.hp1 HG01891.hp1 HG02258.hp2 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-52_-47delGCCCGA | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 1/21 | 7037 | INFO_REALIGN_3_PRIME | chr1 | 151511435 | |||||
| chr1:151511435 | TGCCCGAG others(11): Show |
T | 1 | a0001c0001t0022 | 1 | HG02280.hp1 | 5_prime_UTR_variant | MODIFIER | c.-64_-47delGCCCGAGC others(10): Show |
CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 1/21 | 7037 | INFO_REALIGN_3_PRIME | chr1 | 151511435 | |||||
| chr1:151511463 | C | CGAGCCCG others(5): Show |
1 | a0001c0001t0033 | 1 | HG03130.hp2 | 5_prime_UTR_variant | MODIFIER | c.-56_-55insTGAGCCCG others(4): Show |
CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 1/21 | 7045 | INFO_REALIGN_3_PRIME | chr1 | 151511463 | |||||
| chr1:151511501 | C | T | 2 | a0001c0001t0013 a0004c0006t0030 |
4 | HG01106.hp1 HG01175.hp1 HG01517.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-29C>T | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 1/21 | 7019 | chr1 | 151511501 | ||||||
| chr1:151537490 | T | TA | 48 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(45): Show |
287 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(284): Show |
3_prime_UTR_variant | MODIFIER | c.*156dupA | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 21/21 | 157 | INFO_REALIGN_3_PRIME | chr1 | 151537490 | |||||
| chr1:151537490 | T | TAA | 3 | a0001c0001t0006 a0001c0001t0016 a0001c0001t0031 |
11 | HG01975.hp1 HG02109.hp2 HG02258.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*155_*156dupAA | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 21/21 | 157 | INFO_REALIGN_3_PRIME | chr1 | 151537490 | |||||
| chr1:151537550 | A | G | 51 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(48): Show |
292 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(289): Show |
3_prime_UTR_variant | MODIFIER | c.*204A>G | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 21/21 | 204 | chr1 | 151537550 | ||||||
| chr1:151537551 | T | G | 1 | a0001c0001t0025 | 1 | NA19063.hp2 | 3_prime_UTR_variant | MODIFIER | c.*205T>G | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 21/21 | 205 | chr1 | 151537551 | ||||||
| chr1:151537853 | C | T | 2 | a0001c0001t0034 a0001c0009t0018 |
3 | HG02818.hp2 HG02895.hp2 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*507C>T | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 21/21 | 507 | chr1 | 151537853 | ||||||
| chr1:151537938 | T | C | 1 | a0028c0038t0026 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*592T>C | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 21/21 | 592 | chr1 | 151537938 | ||||||
| chr1:151537962 | A | G | 1 | a0017c0030t0029 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*616A>G | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 21/21 | 616 | chr1 | 151537962 | ||||||
| chr1:151538341 | A | G | 1 | a0017c0030t0029 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*995A>G | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 21/21 | 995 | chr1 | 151538341 | ||||||
| chr1:151538345 | G | C | 4 | a0001c0001t0017 a0001c0004t0004 a0001c0004t0017 others(1): Show |
15 | HG00673.hp1 HG01167.hp2 HG01169.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*999G>C | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 21/21 | 999 | chr1 | 151538345 | ||||||
| chr1:151538349 | C | T | 6 | a0001c0001t0003 a0001c0001t0011 a0001c0001t0023 others(3): Show |
49 | HG00099.hp2 HG00323.hp2 HG00544.hp2 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*1003C>T | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 21/21 | 1003 | chr1 | 151538349 | ||||||
| chr1:151538582 | G | A | 1 | a0001c0001t0027 | 1 | NA19003.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1236G>A | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 21/21 | 1236 | chr1 | 151538582 | ||||||
| chr1:151538633 | T | C | 14 | a0001c0001t0002 a0001c0001t0010 a0001c0001t0014 others(11): Show |
62 | HG00558.hp2 HG00741.hp2 HG01070.hp1 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*1287T>C | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 21/21 | 1287 | chr1 | 151538633 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:151511535 | G | A | 1 | a0001c0001t0001g0053 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.-15+20G>A | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 1/20 | chr1 | 151511535 | |||||||
| chr1:151511672 | T | A | 1 | a0001c0001t0008g0054 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-15+157T>A | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 1/20 | chr1 | 151511672 | |||||||
| chr1:151511743 | A | C | 106 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(103): Show |
147 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.-15+228A>C | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 1/20 | chr1 | 151511743 | |||||||
| chr1:151511803 | G | A | 1 | a0001c0001t0003g0055 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-15+288G>A | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 1/20 | chr1 | 151511803 | |||||||
| chr1:151511821 | G | A | 1 | a0001c0001t0001g0024 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-15+306G>A | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 1/20 | chr1 | 151511821 | |||||||
| chr1:151511845 | C | A | 1 | a0001c0007t0005g0056 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-15+330C>A | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 1/20 | chr1 | 151511845 | |||||||
| chr1:151511923 | C | G | 1 | a0006c0008t0007g0157 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-15+408C>G | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 1/20 | chr1 | 151511923 | |||||||
| chr1:151511940 | C | T | 1 | a0006c0008t0007g0157 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-15+425C>T | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 1/20 | chr1 | 151511940 | |||||||
| chr1:151512017 | G | C | 1 | a0001c0007t0005g0056 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-15+502G>C | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 1/20 | chr1 | 151512017 | |||||||
| chr1:151512189 | T | TGA | 53 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0024 others(50): Show |
91 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.-15+688_-15+689dup others(2): Show |
CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 151512189 | ||||||
| chr1:151512239 | G | A | 1 | a0001c0001t0001g0057 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-15+724G>A | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 1/20 | chr1 | 151512239 | |||||||
| chr1:151512252 | C | T | 2 | a0001c0001t0001g0027 a0001c0001t0001g0092 |
3 | HG02135.hp1 NA18968.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.-15+737C>T | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 1/20 | chr1 | 151512252 | |||||||
| chr1:151512395 | A | G | 5 | a0001c0001t0002g0152 a0001c0001t0002g0153 a0001c0001t0002g0156 others(2): Show |
5 | HG02486.hp1 HG02615.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-15+880A>G | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 1/20 | chr1 | 151512395 | |||||||
| chr1:151512442 | C | T | 1 | a0007c0011t0001g0233 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-15+927C>T | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 1/20 | chr1 | 151512442 | |||||||
| chr1:151512639 | G | GAACTAGA others(21): Show |
1 | a0001c0001t0008g0054 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-15+1125_-15+1152d others(30): Show |
CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 151512639 | ||||||
| chr1:151512831 | G | A | 5 | a0001c0036t0008g0158 a0003c0003t0009g0044 a0003c0003t0009g0159 others(2): Show |
6 | HG01891.hp1 HG02717.hp1 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.-15+1316G>A | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 1/20 | chr1 | 151512831 | |||||||
| chr1:151512916 | G | A | 1 | a0003c0003t0002g0093 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-15+1401G>A | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 1/20 | chr1 | 151512916 | |||||||
| chr1:151513311 | T | C | 1 | a0001c0001t0027g0058 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-15+1796T>C | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 1/20 | chr1 | 151513311 | |||||||
| chr1:151513419 | G | A | 5 | a0001c0001t0002g0152 a0001c0001t0002g0153 a0001c0001t0002g0156 others(2): Show |
5 | HG02486.hp1 HG02615.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-15+1904G>A | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 1/20 | chr1 | 151513419 | |||||||
| chr1:151513540 | A | T | 4 | a0001c0007t0001g0148 a0001c0007t0001g0150 a0001c0007t0001g0151 others(1): Show |
4 | HG02109.hp1 HG02451.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.-15+2025A>T | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 1/20 | chr1 | 151513540 | |||||||
| chr1:151513550 | T | A | 97 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(94): Show |
137 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.-15+2035T>A | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 1/20 | chr1 | 151513550 | |||||||
| chr1:151513564 | A | G | 1 | a0013c0013t0002g0147 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-15+2049A>G | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 1/20 | chr1 | 151513564 | |||||||
| chr1:151513844 | G | C | 1 | a0003c0003t0005g0095 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-15+2329G>C | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 1/20 | chr1 | 151513844 | |||||||
| chr1:151513999 | C | G | 1 | a0001c0001t0020g0146 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-15+2484C>G | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 1/20 | chr1 | 151513999 | |||||||
| chr1:151513999 | C | T | 1 | a0003c0003t0009g0161 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-15+2484C>T | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 1/20 | chr1 | 151513999 | |||||||
| chr1:151514084 | C | T | 1 | a0024c0035t0008g0232 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-15+2569C>T | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 1/20 | chr1 | 151514084 | |||||||
| chr1:151514221 | TG | T | 97 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(94): Show |
137 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.-15+2711delG | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 151514221 | ||||||
| chr1:151514353 | T | G | 2 | a0001c0001t0015g0096 a0001c0001t0015g0097 |
2 | HG02080.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.-15+2838T>G | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 1/20 | chr1 | 151514353 | |||||||
| chr1:151514622 | C | T | 1 | a0005c0005t0003g0145 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-15+3107C>T | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 1/20 | chr1 | 151514622 | |||||||
| chr1:151514650 | A | T | 1 | a0006c0008t0007g0157 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-15+3135A>T | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 1/20 | chr1 | 151514650 | |||||||
| chr1:151514855 | A | C | 4 | a0001c0007t0001g0148 a0001c0007t0001g0150 a0001c0007t0001g0151 others(1): Show |
4 | HG02109.hp1 HG02451.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.-15+3340A>C | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 1/20 | chr1 | 151514855 | |||||||
| chr1:151515016 | C | CT | 12 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(9): Show |
13 | HG00735.hp1 HG02109.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.-14-3475dupT | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 151515016 | ||||||
| chr1:151515120 | G | A | 1 | a0011c0012t0005g0028 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-14-3386G>A | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 1/20 | chr1 | 151515120 | |||||||
| chr1:151515148 | G | A | 1 | a0011c0012t0005g0028 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-14-3358G>A | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 1/20 | chr1 | 151515148 | |||||||
| chr1:151515159 | C | T | 2 | a0001c0001t0003g0230 a0001c0001t0003g0231 |
2 | HG00323.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.-14-3347C>T | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 1/20 | chr1 | 151515159 | |||||||
| chr1:151515190 | G | T | 1 | a0002c0002t0002g0042 | 2 | NA18983.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.-14-3316G>T | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 1/20 | chr1 | 151515190 | |||||||
| chr1:151515300 | G | A | 5 | a0001c0001t0002g0152 a0001c0001t0002g0153 a0001c0001t0002g0156 others(2): Show |
5 | HG02486.hp1 HG02615.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-14-3206G>A | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 1/20 | chr1 | 151515300 | |||||||
| chr1:151515510 | A | G | 2 | a0001c0001t0001g0091 a0028c0038t0026g0160 |
2 | HG02148.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-14-2996A>G | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 1/20 | chr1 | 151515510 | |||||||
| chr1:151515547 | C | T | 98 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(95): Show |
138 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.-14-2959C>T | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 1/20 | chr1 | 151515547 | |||||||
| chr1:151515604 | G | A | 4 | a0001c0001t0001g0020 a0001c0001t0001g0162 a0001c0001t0001g0163 others(1): Show |
6 | HG01074.hp1 HG01167.hp1 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.-14-2902G>A | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 1/20 | chr1 | 151515604 | |||||||
| chr1:151515631 | A | C | 1 | a0007c0011t0001g0233 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-14-2875A>C | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 1/20 | chr1 | 151515631 | |||||||
| chr1:151515677 | A | G | 248 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(245): Show |
367 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(364): Show |
intron_variant | MODIFIER | c.-14-2829A>G | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 1/20 | chr1 | 151515677 | |||||||
| chr1:151515685 | G | C | 98 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(95): Show |
138 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.-14-2821G>C | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 1/20 | chr1 | 151515685 | |||||||
| chr1:151515941 | T | G | 1 | a0001c0001t0007g0165 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-14-2565T>G | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 1/20 | chr1 | 151515941 | |||||||
| chr1:151516128 | C | A | 1 | a0024c0035t0008g0232 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-14-2378C>A | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 1/20 | chr1 | 151516128 | |||||||
| chr1:151516293 | G | A | 1 | a0001c0001t0003g0166 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-14-2213G>A | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 1/20 | chr1 | 151516293 | |||||||
| chr1:151516306 | T | G | 115 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0016 others(112): Show |
182 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(179): Show |
intron_variant | MODIFIER | c.-14-2200T>G | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 1/20 | chr1 | 151516306 | |||||||
| chr1:151516542 | CT | C | 231 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(228): Show |
341 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(338): Show |
intron_variant | MODIFIER | c.-14-1947delT | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 151516542 | ||||||
| chr1:151516552 | T | C | 2 | a0001c0001t0003g0031 a0001c0001t0003g0102 |
3 | HG02071.hp2 NA18970.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.-14-1954T>C | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 1/20 | chr1 | 151516552 | |||||||
| chr1:151516646 | G | A | 4 | a0001c0001t0002g0143 a0006c0008t0007g0043 a0006c0008t0007g0144 others(1): Show |
5 | HG02717.hp2 HG02970.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.-14-1860G>A | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 1/20 | chr1 | 151516646 | |||||||
| chr1:151516842 | G | A | 2 | a0001c0001t0001g0103 a0001c0001t0001g0104 |
2 | HG02486.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-14-1664G>A | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 1/20 | chr1 | 151516842 | |||||||
| chr1:151516881 | C | T | 1 | a0001c0001t0001g0225 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-14-1625C>T | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 1/20 | chr1 | 151516881 | |||||||
| chr1:151517051 | G | A | 3 | a0001c0001t0001g0059 a0001c0001t0001g0167 a0001c0001t0001g0168 |
3 | HG01261.hp1 HG03710.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.-14-1455G>A | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 1/20 | chr1 | 151517051 | |||||||
| chr1:151517187 | A | G | 1 | a0001c0001t0001g0057 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-14-1319A>G | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 1/20 | chr1 | 151517187 | |||||||
| chr1:151517442 | G | A | 1 | a0001c0001t0001g0060 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-14-1064G>A | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 1/20 | chr1 | 151517442 | |||||||
| chr1:151517508 | G | GT | 12 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0104 others(9): Show |
13 | HG00544.hp2 HG00558.hp2 HG01261.hp1 others(10): Show |
intron_variant | MODIFIER | c.-14-980dupT | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 151517508 | ||||||
| chr1:151517508 | GT | G | 14 | a0003c0003t0001g0017 a0003c0003t0001g0040 a0003c0003t0001g0041 others(11): Show |
18 | HG01891.hp1 HG02055.hp2 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.-14-980delT | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 151517508 | ||||||
| chr1:151517579 | C | T | 1 | a0001c0001t0001g0222 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-14-927C>T | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 1/20 | chr1 | 151517579 | |||||||
| chr1:151517659 | C | T | 1 | a0001c0026t0001g0221 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-14-847C>T | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 1/20 | chr1 | 151517659 | |||||||
| chr1:151517704 | G | T | 2 | a0001c0001t0001g0103 a0001c0001t0001g0104 |
2 | HG02486.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-14-802G>T | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 1/20 | chr1 | 151517704 | |||||||
| chr1:151517752 | T | C | 2 | a0005c0005t0003g0105 a0005c0005t0003g0145 |
2 | HG02602.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.-14-754T>C | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 1/20 | chr1 | 151517752 | |||||||
| chr1:151517853 | C | CT | 38 | a0001c0001t0001g0063 a0001c0001t0001g0227 a0001c0001t0002g0143 others(35): Show |
44 | HG01169.hp1 HG01891.hp1 HG02055.hp2 others(41): Show |
intron_variant | MODIFIER | c.-14-638dupT | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 151517853 | ||||||
| chr1:151517853 | C | CTT | 109 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0016 others(106): Show |
177 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(174): Show |
intron_variant | MODIFIER | c.-14-639_-14-638dup others(2): Show |
CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 151517853 | ||||||
| chr1:151517983 | A | G | 5 | a0001c0001t0002g0152 a0001c0001t0002g0153 a0001c0001t0002g0156 others(2): Show |
5 | HG02486.hp1 HG02615.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-14-523A>G | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 1/20 | chr1 | 151517983 | |||||||
| chr1:151518151 | A | G | 1 | a0011c0012t0005g0028 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-14-355A>G | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 1/20 | chr1 | 151518151 | |||||||
| chr1:151518254 | G | A | 1 | a0001c0001t0001g0064 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-14-252G>A | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 1/20 | chr1 | 151518254 | |||||||
| chr1:151519405 | C | A | 1 | a0001c0001t0034g0100 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.873+13C>A | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 2/20 | chr1 | 151519405 | |||||||
| chr1:151519674 | C | A | 15 | a0003c0003t0001g0017 a0003c0003t0001g0040 a0003c0003t0001g0041 others(12): Show |
19 | HG01891.hp1 HG02055.hp2 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.873+282C>A | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 2/20 | chr1 | 151519674 | |||||||
| chr1:151519745 | G | A | 1 | a0001c0001t0003g0107 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.873+353G>A | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 2/20 | chr1 | 151519745 | |||||||
| chr1:151519992 | C | T | 2 | a0001c0001t0003g0031 a0001c0001t0003g0102 |
3 | HG02071.hp2 NA18970.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.874-174C>T | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 2/20 | chr1 | 151519992 | |||||||
| chr1:151520138 | T | C | 17 | a0002c0002t0002g0065 a0003c0003t0001g0017 a0003c0003t0001g0040 others(14): Show |
21 | HG01891.hp1 HG02055.hp2 HG02148.hp2 others(18): Show |
intron_variant | MODIFIER | c.874-28T>C | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 2/20 | chr1 | 151520138 | |||||||
| chr1:151520145 | C | T | 1 | a0001c0001t0008g0083 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.874-21C>T | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 2/20 | chr1 | 151520145 | |||||||
| chr1:151520514 | G | A | 1 | a0024c0035t0008g0232 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1044+31G>A | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 4/20 | chr1 | 151520514 | |||||||
| chr1:151520549 | A | C | 2 | a0001c0001t0015g0096 a0001c0001t0015g0097 |
2 | HG02080.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.1045-47A>C | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 4/20 | chr1 | 151520549 | |||||||
| chr1:151520932 | C | T | 2 | a0003c0003t0005g0095 a0019c0033t0001g0098 |
2 | HG02451.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1140+241C>T | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 5/20 | chr1 | 151520932 | |||||||
| chr1:151520992 | T | A | 1 | a0028c0038t0026g0160 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1140+301T>A | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 5/20 | chr1 | 151520992 | |||||||
| chr1:151520995 | AT | A | 5 | a0001c0001t0002g0143 a0002c0002t0002g0131 a0006c0008t0007g0043 others(2): Show |
6 | HG02717.hp2 HG02970.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.1140+313delT | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr1 | 151520995 | ||||||
| chr1:151521099 | T | G | 1 | a0001c0001t0001g0025 | 2 | NA19005.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.1140+408T>G | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 5/20 | chr1 | 151521099 | |||||||
| chr1:151521122 | A | G | 2 | a0001c0007t0001g0151 a0001c0007t0005g0056 |
2 | HG02145.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1140+431A>G | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 5/20 | chr1 | 151521122 | |||||||
| chr1:151521160 | AAGTAAAT others(10): Show |
A | 1 | a0001c0001t0003g0052 | 2 | HG01255.hp2 HG01257.hp2 |
intron_variant | MODIFIER | c.1140+475_1140+491d others(19): Show |
CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr1 | 151521160 | ||||||
| chr1:151521173 | A | G | 1 | a0001c0001t0001g0003 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1140+482A>G | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 5/20 | chr1 | 151521173 | |||||||
| chr1:151521338 | C | T | 95 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(92): Show |
135 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.1140+647C>T | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 5/20 | chr1 | 151521338 | |||||||
| chr1:151521570 | C | A | 16 | a0003c0003t0001g0017 a0003c0003t0001g0040 a0003c0003t0001g0041 others(13): Show |
20 | HG01891.hp1 HG02055.hp2 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.1140+879C>A | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 5/20 | chr1 | 151521570 | |||||||
| chr1:151521570 | C | T | 2 | a0001c0001t0001g0023 a0018c0027t0001g0220 |
4 | HG00438.hp1 HG02155.hp2 NA18985.hp2 others(1): Show |
intron_variant | MODIFIER | c.1140+879C>T | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 5/20 | chr1 | 151521570 | |||||||
| chr1:151521693 | C | T | 2 | a0001c0004t0004g0086 a0001c0004t0004g0090 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1140+1002C>T | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 5/20 | chr1 | 151521693 | |||||||
| chr1:151521724 | G | A | 3 | a0001c0001t0001g0021 a0001c0001t0001g0045 a0025c0028t0001g0169 |
6 | HG03927.hp1 NA18939.hp1 NA18948.hp2 others(3): Show |
intron_variant | MODIFIER | c.1140+1033G>A | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 5/20 | chr1 | 151521724 | |||||||
| chr1:151521838 | C | CA | 4 | a0001c0001t0002g0143 a0006c0008t0007g0043 a0006c0008t0007g0144 others(1): Show |
5 | HG02717.hp2 HG02970.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1140+1156dupA | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr1 | 151521838 | ||||||
| chr1:151521888 | T | C | 1 | a0001c0036t0008g0158 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1140+1197T>C | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 5/20 | chr1 | 151521888 | |||||||
| chr1:151522016 | G | A | 95 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(92): Show |
135 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.1140+1325G>A | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 5/20 | chr1 | 151522016 | |||||||
| chr1:151522107 | G | A | 7 | a0001c0001t0006g0011 a0001c0001t0006g0018 a0001c0001t0006g0135 others(4): Show |
14 | HG01884.hp1 HG02109.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.1141-1327G>A | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 5/20 | chr1 | 151522107 | |||||||
| chr1:151522147 | G | A | 1 | a0006c0008t0007g0157 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1141-1287G>A | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 5/20 | chr1 | 151522147 | |||||||
| chr1:151522244 | T | C | 1 | a0001c0001t0003g0172 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1141-1190T>C | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 5/20 | chr1 | 151522244 | |||||||
| chr1:151522441 | A | G | 12 | a0003c0003t0001g0017 a0003c0003t0001g0040 a0003c0003t0001g0041 others(9): Show |
15 | HG02055.hp2 HG02451.hp1 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.1141-993A>G | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 5/20 | chr1 | 151522441 | |||||||
| chr1:151522566 | C | G | 15 | a0003c0003t0001g0017 a0003c0003t0001g0040 a0003c0003t0001g0041 others(12): Show |
19 | HG01891.hp1 HG02055.hp2 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.1141-868C>G | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 5/20 | chr1 | 151522566 | |||||||
| chr1:151522583 | G | A | 1 | a0001c0001t0001g0170 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1141-851G>A | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 5/20 | chr1 | 151522583 | |||||||
| chr1:151522639 | AC | A | 28 | a0001c0001t0002g0143 a0001c0001t0015g0096 a0001c0001t0015g0097 others(25): Show |
33 | HG01891.hp1 HG02055.hp2 HG02080.hp2 others(30): Show |
intron_variant | MODIFIER | c.1141-794delC | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 5/20 | chr1 | 151522639 | |||||||
| chr1:151522640 | C | A | 116 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0016 others(113): Show |
183 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(180): Show |
intron_variant | MODIFIER | c.1141-794C>A | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 5/20 | chr1 | 151522640 | |||||||
| chr1:151522640 | CA | C | 7 | a0001c0001t0006g0011 a0001c0001t0006g0018 a0001c0001t0006g0135 others(4): Show |
14 | HG01884.hp1 HG02109.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.1141-786delA | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr1 | 151522640 | ||||||
| chr1:151522642 | A | C | 2 | a0001c0001t0003g0129 a0001c0001t0011g0125 |
2 | HG03831.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1141-792A>C | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 5/20 | chr1 | 151522642 | |||||||
| chr1:151522854 | C | T | 52 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0024 others(49): Show |
88 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.1141-580C>T | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 5/20 | chr1 | 151522854 | |||||||
| chr1:151522855 | G | A | 4 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0173 others(1): Show |
4 | HG02486.hp2 HG02976.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1141-579G>A | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 5/20 | chr1 | 151522855 | |||||||
| chr1:151522927 | GA | G | 25 | a0001c0001t0015g0096 a0001c0001t0015g0097 a0001c0007t0001g0148 others(22): Show |
29 | HG01891.hp1 HG02055.hp2 HG02080.hp2 others(26): Show |
intron_variant | MODIFIER | c.1141-495delA | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr1 | 151522927 | ||||||
| chr1:151522927 | GAA | G | 129 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0016 others(126): Show |
204 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(201): Show |
intron_variant | MODIFIER | c.1141-496_1141-495d others(4): Show |
CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr1 | 151522927 | ||||||
| chr1:151523074 | G | A | 1 | a0001c0001t0001g0140 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1141-360G>A | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 5/20 | chr1 | 151523074 | |||||||
| chr1:151523142 | C | T | 2 | a0001c0001t0001g0026 a0001c0001t0001g0063 |
3 | NA18960.hp1 NA19057.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.1141-292C>T | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 5/20 | chr1 | 151523142 | |||||||
| chr1:151523320 | T | C | 154 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0016 others(151): Show |
233 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(230): Show |
intron_variant | MODIFIER | c.1141-114T>C | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 5/20 | chr1 | 151523320 | |||||||
| chr1:151523368 | T | C | 2 | a0001c0001t0015g0096 a0001c0001t0015g0097 |
2 | HG02080.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.1141-66T>C | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 5/20 | chr1 | 151523368 | |||||||
| chr1:151523949 | C | T | 1 | a0001c0009t0001g0219 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1269-277C>T | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 6/20 | chr1 | 151523949 | |||||||
| chr1:151523952 | T | C | 7 | a0001c0001t0006g0011 a0001c0001t0006g0018 a0001c0001t0006g0135 others(4): Show |
14 | HG01884.hp1 HG02109.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.1269-274T>C | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 6/20 | chr1 | 151523952 | |||||||
| chr1:151524081 | C | T | 1 | a0028c0038t0026g0160 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1269-145C>T | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 6/20 | chr1 | 151524081 | |||||||
| chr1:151524410 | T | C | 1 | a0001c0001t0020g0101 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1401+52T>C | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 7/20 | chr1 | 151524410 | |||||||
| chr1:151524580 | G | C | 1 | a0011c0012t0005g0028 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1402-94G>C | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 7/20 | chr1 | 151524580 | |||||||
| chr1:151524664 | T | C | 154 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0016 others(151): Show |
233 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(230): Show |
intron_variant | MODIFIER | c.1402-10T>C | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 7/20 | chr1 | 151524664 | |||||||
| chr1:151524900 | G | A | 118 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0016 others(115): Show |
185 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(182): Show |
intron_variant | MODIFIER | c.1614+14G>A | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 8/20 | chr1 | 151524900 | |||||||
| chr1:151524901 | C | T | 15 | a0003c0003t0001g0017 a0003c0003t0001g0040 a0003c0003t0001g0041 others(12): Show |
19 | HG01891.hp1 HG02055.hp2 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.1614+15C>T | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 8/20 | chr1 | 151524901 | |||||||
| chr1:151525008 | G | A | 4 | a0001c0001t0002g0143 a0006c0008t0007g0043 a0006c0008t0007g0144 others(1): Show |
5 | HG02717.hp2 HG02970.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1614+122G>A | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 8/20 | chr1 | 151525008 | |||||||
| chr1:151525275 | T | C | 1 | a0001c0007t0001g0148 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1615-367T>C | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 8/20 | chr1 | 151525275 | |||||||
| chr1:151525314 | G | A | 2 | a0001c0001t0015g0096 a0001c0001t0015g0097 |
2 | HG02080.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.1615-328G>A | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 8/20 | chr1 | 151525314 | |||||||
| chr1:151525341 | G | T | 7 | a0001c0001t0006g0011 a0001c0001t0006g0018 a0001c0001t0006g0135 others(4): Show |
14 | HG01884.hp1 HG02109.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.1615-301G>T | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 8/20 | chr1 | 151525341 | |||||||
| chr1:151525370 | C | G | 254 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(251): Show |
373 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(370): Show |
intron_variant | MODIFIER | c.1615-272C>G | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 8/20 | chr1 | 151525370 | |||||||
| chr1:151525443 | C | A | 3 | a0001c0009t0001g0174 a0001c0009t0001g0219 a0001c0009t0018g0046 |
4 | HG02809.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1615-199C>A | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 8/20 | chr1 | 151525443 | |||||||
| chr1:151525520 | CAG | C | 4 | a0001c0001t0002g0143 a0006c0008t0007g0043 a0006c0008t0007g0144 others(1): Show |
5 | HG02717.hp2 HG02970.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1615-121_1615-120d others(4): Show |
CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 8/20 | chr1 | 151525520 | |||||||
| chr1:151525590 | A | G | 2 | a0001c0001t0015g0096 a0001c0001t0015g0097 |
2 | HG02080.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.1615-52A>G | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 8/20 | chr1 | 151525590 | |||||||
| chr1:151525903 | G | A | 1 | a0001c0001t0010g0175 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1763+113G>A | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 9/20 | chr1 | 151525903 | |||||||
| chr1:151525916 | A | G | 1 | a0001c0001t0001g0045 | 2 | NA18948.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.1763+126A>G | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 9/20 | chr1 | 151525916 | |||||||
| chr1:151526093 | G | A | 3 | a0001c0001t0001g0025 a0001c0001t0001g0067 a0001c0001t0001g0088 |
4 | NA18952.hp1 NA18974.hp1 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.1763+303G>A | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 9/20 | chr1 | 151526093 | |||||||
| chr1:151526148 | G | A | 155 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0016 others(152): Show |
234 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(231): Show |
intron_variant | MODIFIER | c.1763+358G>A | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 9/20 | chr1 | 151526148 | |||||||
| chr1:151526181 | CT | C | 98 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(95): Show |
138 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.1763+406delT | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chr1 | 151526181 | ||||||
| chr1:151526181 | CTT | C | 150 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0016 others(147): Show |
228 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(225): Show |
intron_variant | MODIFIER | c.1763+405_1763+406d others(4): Show |
CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chr1 | 151526181 | ||||||
| chr1:151526181 | CTTT | C | 5 | a0001c0001t0031g0109 a0002c0002t0002g0110 a0003c0003t0009g0044 others(2): Show |
6 | HG01891.hp1 HG02717.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1763+404_1763+406d others(5): Show |
CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chr1 | 151526181 | ||||||
| chr1:151526408 | T | G | 1 | a0001c0001t0001g0068 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1764-567T>G | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 9/20 | chr1 | 151526408 | |||||||
| chr1:151526663 | G | A | 1 | a0001c0001t0002g0152 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1764-312G>A | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 9/20 | chr1 | 151526663 | |||||||
| chr1:151526777 | T | C | 2 | a0001c0001t0015g0096 a0001c0001t0015g0097 |
2 | HG02080.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.1764-198T>C | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 9/20 | chr1 | 151526777 | |||||||
| chr1:151527159 | C | T | 100 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(97): Show |
140 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.1896+52C>T | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 10/20 | chr1 | 151527159 | |||||||
| chr1:151527255 | G | A | 156 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0016 others(153): Show |
235 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(232): Show |
intron_variant | MODIFIER | c.1896+148G>A | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 10/20 | chr1 | 151527255 | |||||||
| chr1:151527317 | C | G | 2 | a0001c0001t0001g0139 a0001c0001t0001g0217 |
2 | NA18970.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.1896+210C>G | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 10/20 | chr1 | 151527317 | |||||||
| chr1:151527348 | C | T | 1 | a0023c0021t0001g0216 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1896+241C>T | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 10/20 | chr1 | 151527348 | |||||||
| chr1:151527607 | C | A | 246 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(243): Show |
365 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(362): Show |
intron_variant | MODIFIER | c.1896+500C>A | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 10/20 | chr1 | 151527607 | |||||||
| chr1:151527750 | C | T | 1 | a0024c0035t0008g0232 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1896+643C>T | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 10/20 | chr1 | 151527750 | |||||||
| chr1:151527808 | T | TAC | 92 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0024 others(89): Show |
160 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(157): Show |
intron_variant | MODIFIER | c.1896+730_1896+731d others(4): Show |
CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 151527808 | ||||||
| chr1:151527808 | T | TACAC | 112 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(109): Show |
144 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.1896+728_1896+731d others(6): Show |
CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 151527808 | ||||||
| chr1:151527808 | T | TACACAC | 28 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0023 others(25): Show |
41 | HG00280.hp1 HG00438.hp1 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.1896+726_1896+731d others(8): Show |
CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 151527808 | ||||||
| chr1:151527808 | T | TACACACA others(1): Show |
2 | a0001c0001t0006g0018 a0001c0001t0011g0032 |
5 | HG01168.hp1 HG01169.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.1896+724_1896+731d others(10): Show |
CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 151527808 | ||||||
| chr1:151527808 | TACAC | T | 7 | a0001c0001t0001g0128 a0001c0001t0001g0164 a0001c0007t0001g0148 others(4): Show |
7 | HG02109.hp1 HG02145.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1896+728_1896+731d others(6): Show |
CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 151527808 | ||||||
| chr1:151527839 | G | C | 1 | a0002c0002t0002g0110 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1896+732G>C | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 10/20 | chr1 | 151527839 | |||||||
| chr1:151527840 | A | G | 1 | a0002c0002t0002g0110 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1896+733A>G | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 10/20 | chr1 | 151527840 | |||||||
| chr1:151527879 | C | T | 9 | a0001c0001t0001g0128 a0001c0001t0008g0019 a0001c0007t0001g0148 others(6): Show |
12 | HG01884.hp1 HG02109.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.1896+772C>T | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 10/20 | chr1 | 151527879 | |||||||
| chr1:151527924 | C | T | 2 | a0002c0002t0002g0120 a0005c0005t0001g0121 |
2 | HG03491.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1896+817C>T | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 10/20 | chr1 | 151527924 | |||||||
| chr1:151527948 | A | AT | 10 | a0001c0001t0001g0126 a0001c0001t0003g0112 a0001c0001t0003g0118 others(7): Show |
11 | HG01123.hp1 HG02155.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1896+842dupT | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 151527948 | ||||||
| chr1:151527948 | A | ATT | 28 | a0001c0001t0001g0016 a0001c0001t0001g0103 a0001c0001t0001g0104 others(25): Show |
36 | HG00099.hp2 HG00323.hp2 HG00544.hp2 others(33): Show |
intron_variant | MODIFIER | c.1896+842_1896+843i others(4): Show |
CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 151527948 | ||||||
| chr1:151527948 | A | T | 1 | a0001c0001t0003g0116 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1896+841A>T | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 10/20 | chr1 | 151527948 | |||||||
| chr1:151527950 | A | AT | 10 | a0001c0001t0001g0004 a0001c0001t0002g0143 a0001c0001t0002g0152 others(7): Show |
10 | HG01258.hp1 HG02080.hp2 HG02129.hp2 others(7): Show |
intron_variant | MODIFIER | c.1896+866dupT | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 151527950 | ||||||
| chr1:151527950 | A | ATATATAT others(6): Show |
2 | a0001c0001t0001g0003 a0001c0001t0001g0073 |
2 | HG00438.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.1896+844_1896+845i others(15): Show |
CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 151527950 | ||||||
| chr1:151527950 | A | ATATATAT others(2): Show |
5 | a0001c0001t0001g0003 a0002c0002t0002g0001 a0002c0002t0002g0065 others(2): Show |
10 | HG00558.hp1 HG01071.hp2 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.1896+844_1896+845i others(11): Show |
CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 151527950 | ||||||
| chr1:151527950 | A | ATATATAT others(3): Show |
1 | a0001c0001t0001g0082 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1896+844_1896+845i others(12): Show |
CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 151527950 | ||||||
| chr1:151527950 | A | ATATATAT others(4): Show |
2 | a0001c0001t0001g0026 a0001c0001t0001g0063 |
2 | NA18960.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.1896+844_1896+845i others(13): Show |
CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 151527950 | ||||||
| chr1:151527950 | A | ATATATAT others(5): Show |
1 | a0001c0001t0001g0026 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1896+844_1896+845i others(14): Show |
CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 151527950 | ||||||
| chr1:151527950 | A | ATATATTT others(1): Show |
12 | a0001c0001t0001g0003 a0001c0001t0001g0068 a0001c0001t0001g0071 others(9): Show |
13 | HG00558.hp2 HG01167.hp2 HG02273.hp2 others(10): Show |
intron_variant | MODIFIER | c.1896+844_1896+845i others(10): Show |
CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 151527950 | ||||||
| chr1:151527950 | A | ATATATTT others(2): Show |
46 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0025 others(43): Show |
74 | HG00544.hp1 HG00673.hp1 HG01169.hp1 others(71): Show |
intron_variant | MODIFIER | c.1896+844_1896+845i others(11): Show |
CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 151527950 | ||||||
| chr1:151527950 | A | ATATATTT others(3): Show |
12 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0027 others(9): Show |
18 | HG00597.hp1 HG00609.hp1 HG00621.hp2 others(15): Show |
intron_variant | MODIFIER | c.1896+844_1896+845i others(12): Show |
CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 151527950 | ||||||
| chr1:151527950 | A | ATATATTT others(4): Show |
2 | a0001c0001t0001g0003 a0001c0001t0001g0085 |
2 | NA18992.hp2 NA18997.hp1 |
intron_variant | MODIFIER | c.1896+844_1896+845i others(13): Show |
CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 151527950 | ||||||
| chr1:151527950 | A | ATATTTTT others(2): Show |
4 | a0001c0001t0001g0003 a0002c0002t0002g0001 a0002c0002t0002g0009 others(1): Show |
7 | HG00741.hp2 HG01256.hp2 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.1896+844_1896+845i others(11): Show |
CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 151527950 | ||||||
| chr1:151527950 | A | ATATTTTT others(3): Show |
1 | a0001c0009t0001g0174 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1896+844_1896+845i others(12): Show |
CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 151527950 | ||||||
| chr1:151527950 | A | T | 43 | a0001c0001t0001g0016 a0001c0001t0001g0021 a0001c0001t0001g0103 others(40): Show |
53 | HG00099.hp2 HG00323.hp2 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.1896+843A>T | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 10/20 | chr1 | 151527950 | |||||||
| chr1:151527950 | AT | A | 23 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(20): Show |
25 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(22): Show |
intron_variant | MODIFIER | c.1896+866delT | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 151527950 | ||||||
| chr1:151527951 | T | TA | 14 | a0001c0001t0001g0186 a0001c0001t0001g0191 a0001c0001t0001g0192 others(11): Show |
21 | HG01106.hp2 HG01884.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.1896+844_1896+845i others(3): Show |
CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 10/20 | chr1 | 151527951 | |||||||
| chr1:151527951 | T | TATATA | 2 | a0003c0003t0009g0044 a0003c0003t0009g0161 |
3 | HG01891.hp1 HG02717.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1896+844_1896+845i others(7): Show |
CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 10/20 | chr1 | 151527951 | |||||||
| chr1:151527952 | T | A | 22 | a0001c0001t0001g0020 a0001c0001t0001g0128 a0001c0001t0001g0162 others(19): Show |
28 | HG01074.hp1 HG01167.hp1 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.1896+845T>A | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 10/20 | chr1 | 151527952 | |||||||
| chr1:151527953 | T | A | 15 | a0001c0001t0001g0186 a0001c0001t0001g0193 a0001c0001t0001g0225 others(12): Show |
23 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.1896+846T>A | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 10/20 | chr1 | 151527953 | |||||||
| chr1:151527954 | T | A | 2 | a0001c0001t0001g0162 a0003c0003t0009g0159 |
2 | HG01074.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1896+847T>A | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 10/20 | chr1 | 151527954 | |||||||
| chr1:151527955 | T | A | 4 | a0001c0001t0008g0019 a0003c0003t0009g0044 a0003c0003t0009g0161 others(1): Show |
8 | HG01884.hp1 HG01891.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.1896+848T>A | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 10/20 | chr1 | 151527955 | |||||||
| chr1:151527956 | T | A | 1 | a0003c0003t0009g0159 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1896+849T>A | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 10/20 | chr1 | 151527956 | |||||||
| chr1:151527957 | T | A | 6 | a0001c0001t0001g0061 a0001c0001t0001g0081 a0001c0001t0001g0091 others(3): Show |
9 | HG01884.hp1 HG01891.hp1 HG01952.hp2 others(6): Show |
intron_variant | MODIFIER | c.1896+850T>A | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 10/20 | chr1 | 151527957 | |||||||
| chr1:151527958 | T | A | 1 | a0003c0003t0009g0159 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1896+851T>A | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 10/20 | chr1 | 151527958 | |||||||
| chr1:151527959 | T | A | 3 | a0001c0001t0001g0061 a0001c0001t0001g0081 a0001c0001t0001g0091 |
3 | HG01952.hp2 HG01978.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.1896+852T>A | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 10/20 | chr1 | 151527959 | |||||||
| chr1:151527978 | C | T | 248 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(245): Show |
366 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(363): Show |
intron_variant | MODIFIER | c.1896+871C>T | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 10/20 | chr1 | 151527978 | |||||||
| chr1:151528162 | TGTTTCAC others(11): Show |
T | 1 | a0001c0001t0001g0218 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1896+1067_1896+108 others(22): Show |
CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 151528162 | ||||||
| chr1:151528218 | A | AC | 3 | a0001c0001t0001g0194 a0001c0001t0003g0172 a0001c0001t0003g0195 |
3 | HG02523.hp1 NA18977.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.1896+1113dupC | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 151528218 | ||||||
| chr1:151528278 | C | T | 4 | a0002c0002t0002g0106 a0002c0002t0002g0117 a0009c0016t0003g0113 others(1): Show |
4 | HG00597.hp2 HG02080.hp1 NA18948.hp1 others(1): Show |
intron_variant | MODIFIER | c.1897-1072C>T | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 10/20 | chr1 | 151528278 | |||||||
| chr1:151528279 | A | G | 72 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0014 others(69): Show |
103 | HG00280.hp2 HG00544.hp1 HG00597.hp1 others(100): Show |
intron_variant | MODIFIER | c.1897-1071A>G | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 10/20 | chr1 | 151528279 | |||||||
| chr1:151528419 | GT | G | 217 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(214): Show |
328 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(325): Show |
intron_variant | MODIFIER | c.1897-921delT | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 151528419 | ||||||
| chr1:151528431 | T | C | 1 | a0002c0002t0002g0110 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1897-919T>C | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 10/20 | chr1 | 151528431 | |||||||
| chr1:151528543 | A | G | 11 | a0001c0001t0006g0011 a0001c0001t0006g0018 a0001c0001t0006g0135 others(8): Show |
18 | HG02055.hp2 HG02109.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.1897-807A>G | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 10/20 | chr1 | 151528543 | |||||||
| chr1:151528836 | A | G | 1 | a0004c0006t0014g0183 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1897-514A>G | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 10/20 | chr1 | 151528836 | |||||||
| chr1:151528904 | T | C | 1 | a0003c0003t0002g0093 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1897-446T>C | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 10/20 | chr1 | 151528904 | |||||||
| chr1:151528927 | T | G | 1 | a0001c0001t0011g0032 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1897-423T>G | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 10/20 | chr1 | 151528927 | |||||||
| chr1:151528961 | G | A | 16 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0021 others(13): Show |
29 | HG00280.hp1 HG00438.hp1 HG01081.hp2 others(26): Show |
intron_variant | MODIFIER | c.1897-389G>A | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 10/20 | chr1 | 151528961 | |||||||
| chr1:151529079 | GGCTATAA others(8): Show |
G | 1 | a0001c0001t0001g0076 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1897-266_1897-252d others(17): Show |
CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 151529079 | ||||||
| chr1:151529222 | A | G | 243 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(240): Show |
359 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(356): Show |
intron_variant | MODIFIER | c.1897-128A>G | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 10/20 | chr1 | 151529222 | |||||||
| chr1:151529249 | G | C | 1 | a0001c0001t0001g0073 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1897-101G>C | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 10/20 | chr1 | 151529249 | |||||||
| chr1:151529261 | T | C | 244 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(241): Show |
362 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(359): Show |
intron_variant | MODIFIER | c.1897-89T>C | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 10/20 | chr1 | 151529261 | |||||||
| chr1:151529314 | T | C | 1 | a0001c0001t0001g0194 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1897-36T>C | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 10/20 | chr1 | 151529314 | |||||||
| chr1:151529588 | G | A | 3 | a0006c0008t0007g0043 a0006c0008t0007g0144 a0006c0008t0007g0157 |
4 | HG02970.hp2 HG03453.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.2106+29G>A | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 11/20 | chr1 | 151529588 | |||||||
| chr1:151529589 | G | A | 1 | a0001c0001t0001g0187 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.2106+30G>A | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 11/20 | chr1 | 151529589 | |||||||
| chr1:151529604 | G | T | 1 | a0015c0029t0032g0208 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2106+45G>T | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 11/20 | chr1 | 151529604 | |||||||
| chr1:151530128 | G | A | 5 | a0001c0001t0003g0049 a0001c0001t0003g0166 a0001c0001t0003g0190 others(2): Show |
6 | HG01175.hp2 HG01943.hp1 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.2313+13G>A | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 12/20 | chr1 | 151530128 | |||||||
| chr1:151530445 | A | C | 1 | a0001c0001t0003g0204 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.2314-44A>C | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 12/20 | chr1 | 151530445 | |||||||
| chr1:151530754 | A | G | 1 | a0009c0016t0003g0114 | 1 | HG00597.hp2 | splice_region_variant&intron_variant | LOW | c.2571+8A>G | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 13/20 | chr1 | 151530754 | |||||||
| chr1:151530825 | G | GGGA | 6 | a0003c0003t0009g0044 a0003c0003t0009g0159 a0003c0003t0009g0161 others(3): Show |
8 | HG01891.hp1 HG02717.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.2571+81_2571+83dup others(3): Show |
CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr1 | 151530825 | ||||||
| chr1:151530869 | G | A | 27 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0047 others(24): Show |
38 | HG00280.hp2 HG00639.hp1 HG00673.hp2 others(35): Show |
intron_variant | MODIFIER | c.2571+123G>A | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 13/20 | chr1 | 151530869 | |||||||
| chr1:151531001 | C | G | 1 | a0001c0001t0001g0140 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2571+255C>G | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 13/20 | chr1 | 151531001 | |||||||
| chr1:151531124 | G | C | 30 | a0001c0001t0002g0156 a0001c0001t0002g0210 a0001c0001t0007g0165 others(27): Show |
53 | HG00558.hp2 HG00741.hp2 HG01070.hp1 others(50): Show |
intron_variant | MODIFIER | c.2571+378G>C | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 13/20 | chr1 | 151531124 | |||||||
| chr1:151531143 | G | GA | 9 | a0001c0001t0001g0066 a0001c0001t0003g0033 a0001c0001t0003g0107 others(6): Show |
10 | HG00597.hp2 HG00609.hp2 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.2571+410dupA | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr1 | 151531143 | ||||||
| chr1:151531422 | T | C | 1 | a0028c0038t0026g0160 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2571+676T>C | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 13/20 | chr1 | 151531422 | |||||||
| chr1:151531619 | C | T | 1 | a0001c0001t0001g0164 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2572-783C>T | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 13/20 | chr1 | 151531619 | |||||||
| chr1:151531808 | T | A | 3 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0023t0001g0108 |
3 | HG02486.hp2 HG02976.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2572-594T>A | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 13/20 | chr1 | 151531808 | |||||||
| chr1:151531808 | T | TTTATCAT others(22): Show |
4 | a0001c0001t0001g0013 a0001c0001t0001g0068 a0001c0001t0001g0224 others(1): Show |
7 | HG02922.hp2 NA18982.hp1 NA18994.hp2 others(4): Show |
intron_variant | MODIFIER | c.2572-507_2572-479d others(31): Show |
CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr1 | 151531808 | ||||||
| chr1:151531808 | TTTATCAT others(22): Show |
T | 5 | a0001c0001t0001g0182 a0001c0007t0001g0148 a0001c0007t0001g0150 others(2): Show |
5 | HG01978.hp1 HG02145.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.2572-507_2572-479d others(31): Show |
CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr1 | 151531808 | ||||||
| chr1:151532007 | G | A | 1 | a0003c0003t0005g0095 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2572-395G>A | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 13/20 | chr1 | 151532007 | |||||||
| chr1:151532213 | T | C | 13 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0021 others(10): Show |
25 | HG00280.hp1 HG00438.hp1 HG01081.hp2 others(22): Show |
intron_variant | MODIFIER | c.2572-189T>C | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 13/20 | chr1 | 151532213 | |||||||
| chr1:151532214 | G | A | 61 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0013 others(58): Show |
78 | HG00280.hp2 HG00639.hp1 HG00673.hp2 others(75): Show |
intron_variant | MODIFIER | c.2572-188G>A | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 13/20 | chr1 | 151532214 | |||||||
| chr1:151532302 | C | T | 118 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(115): Show |
175 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.2572-100C>T | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 13/20 | chr1 | 151532302 | |||||||
| chr1:151532326 | G | A | 1 | a0001c0001t0001g0196 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.2572-76G>A | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 13/20 | chr1 | 151532326 | |||||||
| chr1:151532395 | G | A | 1 | a0001c0001t0015g0209 | 1 | HG03195.hp1 | splice_region_variant&intron_variant | LOW | c.2572-7G>A | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 13/20 | chr1 | 151532395 | |||||||
| chr1:151532612 | C | CT | 27 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0021 others(24): Show |
39 | HG00280.hp1 HG00438.hp1 HG01081.hp2 others(36): Show |
intron_variant | MODIFIER | c.2742+61dupT | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr1 | 151532612 | ||||||
| chr1:151532612 | CT | C | 124 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(121): Show |
184 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.2742+61delT | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr1 | 151532612 | ||||||
| chr1:151532682 | C | T | 4 | a0001c0001t0006g0011 a0001c0001t0006g0018 a0001c0001t0006g0135 others(1): Show |
8 | HG02109.hp2 HG02258.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.2742+110C>T | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 14/20 | chr1 | 151532682 | |||||||
| chr1:151532919 | C | G | 1 | a0001c0001t0003g0207 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.2742+347C>G | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 14/20 | chr1 | 151532919 | |||||||
| chr1:151533006 | T | C | 2 | a0001c0001t0001g0074 a0001c0001t0001g0084 |
2 | NA18945.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.2742+434T>C | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 14/20 | chr1 | 151533006 | |||||||
| chr1:151533087 | A | G | 1 | a0017c0030t0029g0149 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2742+515A>G | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 14/20 | chr1 | 151533087 | |||||||
| chr1:151533119 | A | T | 1 | a0001c0001t0001g0212 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2742+547A>T | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 14/20 | chr1 | 151533119 | |||||||
| chr1:151533205 | C | T | 1 | a0001c0001t0001g0080 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.2742+633C>T | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 14/20 | chr1 | 151533205 | |||||||
| chr1:151533232 | C | T | 117 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(114): Show |
174 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.2742+660C>T | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 14/20 | chr1 | 151533232 | |||||||
| chr1:151533336 | C | T | 1 | a0001c0001t0001g0163 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2743-639C>T | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 14/20 | chr1 | 151533336 | |||||||
| chr1:151533588 | A | C | 4 | a0001c0001t0006g0011 a0001c0001t0006g0018 a0001c0001t0006g0135 others(1): Show |
8 | HG02109.hp2 HG02258.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.2743-387A>C | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 14/20 | chr1 | 151533588 | |||||||
| chr1:151533846 | A | G | 2 | a0001c0009t0001g0174 a0001c0009t0001g0219 |
2 | HG02809.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2743-129A>G | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 14/20 | chr1 | 151533846 | |||||||
| chr1:151534201 | C | T | 4 | a0001c0007t0001g0148 a0001c0007t0001g0150 a0001c0007t0001g0151 others(1): Show |
4 | HG02145.hp1 HG02451.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.2904+65C>T | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 15/20 | chr1 | 151534201 | |||||||
| chr1:151534405 | G | A | 1 | a0001c0001t0001g0064 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2904+269G>A | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 15/20 | chr1 | 151534405 | |||||||
| chr1:151534427 | A | G | 1 | a0003c0003t0001g0133 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2904+291A>G | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 15/20 | chr1 | 151534427 | |||||||
| chr1:151534448 | T | C | 2 | a0001c0001t0001g0071 a0001c0001t0001g0079 |
2 | NA19003.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.2904+312T>C | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 15/20 | chr1 | 151534448 | |||||||
| chr1:151534601 | G | T | 4 | a0003c0003t0009g0044 a0003c0003t0009g0159 a0003c0003t0009g0161 others(1): Show |
5 | HG01891.hp1 HG02109.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.2905-441G>T | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 15/20 | chr1 | 151534601 | |||||||
| chr1:151534686 | C | T | 1 | a0001c0001t0001g0206 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.2905-356C>T | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 15/20 | chr1 | 151534686 | |||||||
| chr1:151534762 | T | C | 1 | a0024c0035t0008g0232 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2905-280T>C | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 15/20 | chr1 | 151534762 | |||||||
| chr1:151534864 | C | A | 1 | a0022c0032t0001g0202 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2905-178C>A | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 15/20 | chr1 | 151534864 | |||||||
| chr1:151534889 | A | G | 1 | a0001c0001t0001g0066 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2905-153A>G | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 15/20 | chr1 | 151534889 | |||||||
| chr1:151535178 | C | T | 1 | a0002c0002t0002g0115 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2994+47C>T | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 16/20 | chr1 | 151535178 | |||||||
| chr1:151535243 | G | A | 1 | a0001c0001t0001g0197 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2994+112G>A | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 16/20 | chr1 | 151535243 | |||||||
| chr1:151535316 | A | G | 1 | a0002c0002t0002g0110 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.2994+185A>G | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 16/20 | chr1 | 151535316 | |||||||
| chr1:151535467 | T | G | 5 | a0001c0007t0001g0148 a0001c0007t0001g0150 a0001c0007t0001g0151 others(2): Show |
5 | HG02145.hp1 HG02451.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.2995-133T>G | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 16/20 | chr1 | 151535467 | |||||||
| chr1:151535585 | A | C | 60 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0013 others(57): Show |
77 | HG00280.hp2 HG00639.hp1 HG00673.hp2 others(74): Show |
intron_variant | MODIFIER | c.2995-15A>C | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 16/20 | chr1 | 151535585 | |||||||
| chr1:151536501 | G | T | 4 | a0001c0001t0007g0078 a0001c0001t0007g0215 a0001c0001t0015g0096 others(1): Show |
4 | HG02027.hp2 HG02080.hp2 HG02129.hp2 others(1): Show |
intron_variant | MODIFIER | c.3306+156G>T | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 19/20 | chr1 | 151536501 | |||||||
| chr1:151536634 | A | C | 3 | a0006c0008t0007g0043 a0006c0008t0007g0144 a0006c0008t0007g0157 |
4 | HG02970.hp2 HG03453.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.3307-96A>C | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 19/20 | chr1 | 151536634 | |||||||
| chr1:151537027 | ATATT | A | 5 | a0001c0036t0008g0158 a0003c0003t0001g0017 a0003c0003t0001g0041 others(2): Show |
8 | HG02055.hp2 HG02723.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.3470+143_3470+146d others(6): Show |
CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr1 | 151537027 | ||||||
| chr1:151537119 | A | T | 1 | a0001c0001t0025g0205 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.3471-86A>T | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 20/20 | chr1 | 151537119 | |||||||
| chr1:151537181 | C | T | 1 | a0017c0030t0029g0149 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3471-24C>T | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 20/20 | chr1 | 151537181 | |||||||
| chr1:151537183 | A | G | 3 | a0001c0036t0008g0158 a0003c0003t0001g0041 a0003c0003t0001g0133 |
4 | HG02723.hp2 HG03209.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.3471-22A>G | CGN | ENSG00000143375.15 | transcript | ENST00000271636.12 | protein_coding | 20/20 | chr1 | 151537183 |