Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 2178 |
| ensemblid | ENSG00000112039.6 |
| hgncid | 3586 |
| symbol | FANCE |
| name | FA complementation group E |
| refseq_nuc | NM_021922.3 |
| refseq_prot | NP_068741.1 |
| ensembl_nuc | ENST00000229769.3 |
| ensembl_prot | ENSP00000229769.2 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 35452338 |
| end | 35467102 |
| strand | + |
| ver | v1.2 |
| region | chr6:35452338-35467102 |
| region5000 | chr6:35447338-35472102 |
| regionname0 | FANCE_chr6_35452338_35467102 |
| regionname5000 | FANCE_chr6_35447338_35472102 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 536 | 315 | 52 | 61 | 158 | 10 | 34 | 126 | FANCE_chr6_35447338_35472102 | FANCE | MATPD others(531): Show |
chr6 | 35447338 | 35472102 |
| a0002 | 0/0 | 536 | 54 | 22 | 5 | 18 | 2 | 7 | 8 | FANCE_chr6_35447338_35472102 | FANCE | MATPD others(531): Show |
chr6 | 35447338 | 35472102 |
| a0003 | 0/0 | 536 | 13 | 12 | 1 | 0 | 0 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | MATPD others(531): Show |
chr6 | 35447338 | 35472102 |
| a0004 | 0/0 | 536 | 5 | 0 | 0 | 5 | 0 | 0 | 5 | FANCE_chr6_35447338_35472102 | FANCE | MATPD others(531): Show |
chr6 | 35447338 | 35472102 |
| a0005 | 0/0 | 536 | 4 | 0 | 0 | 4 | 0 | 0 | 3 | FANCE_chr6_35447338_35472102 | FANCE | MATPD others(531): Show |
chr6 | 35447338 | 35472102 |
| a0006 | 0/0 | 536 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | MATPD others(531): Show |
chr6 | 35447338 | 35472102 |
| a0007 | 0/0 | 84 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | MATPD others(79): Show |
chr6 | 35447338 | 35472102 |
| a0008 | 0/0 | 536 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FANCE_chr6_35447338_35472102 | FANCE | MATPD others(531): Show |
chr6 | 35447338 | 35472102 |
| a0009 | 0/0 | 536 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FANCE_chr6_35447338_35472102 | FANCE | MATPD others(531): Show |
chr6 | 35447338 | 35472102 |
| a0010 | 0/0 | 536 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FANCE_chr6_35447338_35472102 | FANCE | MATPD others(531): Show |
chr6 | 35447338 | 35472102 |
| a0011 | 0/0 | 536 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FANCE_chr6_35447338_35472102 | FANCE | MATPD others(531): Show |
chr6 | 35447338 | 35472102 |
| a0012 | 0/0 | 11 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FANCE_chr6_35447338_35472102 | FANCE | MATPD others(6): Show |
chr6 | 35447338 | 35472102 |
| a0013 | 0/0 | 37 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FANCE_chr6_35447338_35472102 | FANCE | MATPD others(32): Show |
chr6 | 35447338 | 35472102 |
| a0014 | 0/0 | 37 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FANCE_chr6_35447338_35472102 | FANCE | MATPD others(32): Show |
chr6 | 35447338 | 35472102 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1608 | 184 | 45 | 40 | 74 | 7 | 18 | FANCE_chr6_35447338_35472102 | FANCE | ATGGC others(1603): Show |
chr6 | 35447338 | 35472102 | ||
| a0001c0002 | 0/0 | 1608 | 88 | 7 | 19 | 47 | 2 | 13 | FANCE_chr6_35447338_35472102 | FANCE | ATGGC others(1603): Show |
chr6 | 35447338 | 35472102 | ||
| a0001c0004 | 0/0 | 1608 | 37 | 0 | 1 | 32 | 1 | 3 | FANCE_chr6_35447338_35472102 | FANCE | ATGGC others(1603): Show |
chr6 | 35447338 | 35472102 | ||
| a0001c0006 | 0/0 | 1608 | 5 | 0 | 0 | 5 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | ATGGC others(1603): Show |
chr6 | 35447338 | 35472102 | ||
| a0001c0009 | 0/0 | 1608 | 1 | 0 | 1 | 0 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | ATGGC others(1603): Show |
chr6 | 35447338 | 35472102 | ||
| a0002c0003 | 0/0 | 1608 | 54 | 22 | 5 | 18 | 2 | 7 | FANCE_chr6_35447338_35472102 | FANCE | ATGGC others(1603): Show |
chr6 | 35447338 | 35472102 | ||
| a0003c0005 | 0/0 | 1608 | 13 | 12 | 1 | 0 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | ATGGC others(1603): Show |
chr6 | 35447338 | 35472102 | ||
| a0004c0007 | 0/0 | 1608 | 5 | 0 | 0 | 5 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | ATGGC others(1603): Show |
chr6 | 35447338 | 35472102 | ||
| a0005c0008 | 0/0 | 1608 | 4 | 0 | 0 | 4 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | ATGGC others(1603): Show |
chr6 | 35447338 | 35472102 | ||
| a0006c0012 | 0/0 | 1608 | 1 | 0 | 1 | 0 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | ATGGC others(1603): Show |
chr6 | 35447338 | 35472102 | ||
| a0007c0010 | 0/0 | 1613 | 1 | 0 | 0 | 1 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | ATGGC others(1608): Show |
chr6 | 35447338 | 35472102 | ||
| a0008c0011 | 0/0 | 1608 | 1 | 0 | 0 | 0 | 0 | 1 | FANCE_chr6_35447338_35472102 | FANCE | ATGGC others(1603): Show |
chr6 | 35447338 | 35472102 | ||
| a0009c0016 | 0/0 | 1608 | 1 | 0 | 0 | 0 | 0 | 1 | FANCE_chr6_35447338_35472102 | FANCE | ATGGC others(1603): Show |
chr6 | 35447338 | 35472102 | ||
| a0010c0014 | 0/0 | 1608 | 1 | 0 | 0 | 0 | 0 | 1 | FANCE_chr6_35447338_35472102 | FANCE | ATGGC others(1603): Show |
chr6 | 35447338 | 35472102 | ||
| a0011c0013 | 0/0 | 1608 | 1 | 0 | 0 | 1 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | ATGGC others(1603): Show |
chr6 | 35447338 | 35472102 | ||
| a0012c0018 | 0/0 | 1608 | 1 | 0 | 0 | 1 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | ATGGC others(1603): Show |
chr6 | 35447338 | 35472102 | ||
| a0013c0015 | 0/0 | 1610 | 1 | 0 | 0 | 1 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | ATGGC others(1605): Show |
chr6 | 35447338 | 35472102 | ||
| a0014c0017 | 0/0 | 1609 | 1 | 0 | 0 | 1 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | ATGGC others(1604): Show |
chr6 | 35447338 | 35472102 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2576 | 161 | 43 | 35 | 58 | 7 | 18 | FANCE_chr6_35447338_35472102 | FANCE | CCTTC others(2571): Show |
chr6 | 35447338 | 35472102 |
| a0001c0001t0003 | 0/0 | 2576 | 23 | 2 | 5 | 16 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | CCTTC others(2571): Show |
chr6 | 35447338 | 35472102 |
| a0001c0002t0001 | 0/0 | 2576 | 87 | 7 | 19 | 46 | 2 | 13 | FANCE_chr6_35447338_35472102 | FANCE | CCTTC others(2571): Show |
chr6 | 35447338 | 35472102 |
| a0001c0002t0007 | 0/0 | 2576 | 1 | 0 | 0 | 1 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | CCTTC others(2571): Show |
chr6 | 35447338 | 35472102 |
| a0001c0004t0001 | 0/0 | 2576 | 37 | 0 | 1 | 32 | 1 | 3 | FANCE_chr6_35447338_35472102 | FANCE | CCTTC others(2571): Show |
chr6 | 35447338 | 35472102 |
| a0001c0006t0001 | 0/0 | 2576 | 5 | 0 | 0 | 5 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | CCTTC others(2571): Show |
chr6 | 35447338 | 35472102 |
| a0001c0009t0001 | 0/0 | 2576 | 1 | 0 | 1 | 0 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | CCTTC others(2571): Show |
chr6 | 35447338 | 35472102 |
| a0002c0003t0001 | 0/0 | 2576 | 2 | 0 | 2 | 0 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | CCTTC others(2571): Show |
chr6 | 35447338 | 35472102 |
| a0002c0003t0002 | 0/0 | 2575 | 51 | 21 | 3 | 18 | 2 | 7 | FANCE_chr6_35447338_35472102 | FANCE | CCTTC others(2570): Show |
chr6 | 35447338 | 35472102 |
| a0002c0003t0004 | 0/0 | 2576 | 1 | 1 | 0 | 0 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | CCTTC others(2571): Show |
chr6 | 35447338 | 35472102 |
| a0003c0005t0004 | 0/0 | 2576 | 10 | 9 | 1 | 0 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | CCTTC others(2571): Show |
chr6 | 35447338 | 35472102 |
| a0003c0005t0005 | 0/0 | 2576 | 3 | 3 | 0 | 0 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | CCTTC others(2571): Show |
chr6 | 35447338 | 35472102 |
| a0004c0007t0001 | 0/0 | 2576 | 5 | 0 | 0 | 5 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | CCTTC others(2571): Show |
chr6 | 35447338 | 35472102 |
| a0005c0008t0001 | 0/0 | 2576 | 4 | 0 | 0 | 4 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | CCTTC others(2571): Show |
chr6 | 35447338 | 35472102 |
| a0006c0012t0001 | 0/0 | 2576 | 1 | 0 | 1 | 0 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | CCTTC others(2571): Show |
chr6 | 35447338 | 35472102 |
| a0007c0010t0001 | 0/0 | 2581 | 1 | 0 | 0 | 1 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | CCTTC others(2576): Show |
chr6 | 35447338 | 35472102 |
| a0008c0011t0002 | 0/0 | 2575 | 1 | 0 | 0 | 0 | 0 | 1 | FANCE_chr6_35447338_35472102 | FANCE | CCTTC others(2570): Show |
chr6 | 35447338 | 35472102 |
| a0009c0016t0001 | 0/0 | 2576 | 1 | 0 | 0 | 0 | 0 | 1 | FANCE_chr6_35447338_35472102 | FANCE | CCTTC others(2571): Show |
chr6 | 35447338 | 35472102 |
| a0010c0014t0002 | 0/0 | 2575 | 1 | 0 | 0 | 0 | 0 | 1 | FANCE_chr6_35447338_35472102 | FANCE | CCTTC others(2570): Show |
chr6 | 35447338 | 35472102 |
| a0011c0013t0001 | 0/0 | 2576 | 1 | 0 | 0 | 1 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | CCTTC others(2571): Show |
chr6 | 35447338 | 35472102 |
| a0012c0018t0001 | 0/0 | 2576 | 1 | 0 | 0 | 1 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | CCTTC others(2571): Show |
chr6 | 35447338 | 35472102 |
| a0013c0015t0001 | 0/0 | 2578 | 1 | 0 | 0 | 1 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | CCTTC others(2573): Show |
chr6 | 35447338 | 35472102 |
| a0014c0017t0006 | 0/0 | 2577 | 1 | 0 | 0 | 1 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | CCTTC others(2572): Show |
chr6 | 35447338 | 35472102 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 61 | 1 | 16 | 30 | 3 | 11 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0001c0001t0001g0005 | 0/0 | 18 | 1 | 11 | 6 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0001c0001t0001g0006 | 0/0 | 12 | 8 | 3 | 0 | 0 | 1 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0001c0001t0001g0011 | 0/0 | 8 | 1 | 1 | 6 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0001c0001t0001g0013 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0001c0001t0001g0017 | 0/0 | 4 | 0 | 0 | 2 | 1 | 1 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0001c0001t0001g0018 | 0/0 | 4 | 0 | 0 | 1 | 2 | 1 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0001c0001t0001g0020 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0001c0001t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0001c0001t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0001c0001t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0001c0001t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0001c0001t0003g0008 | 0/0 | 10 | 1 | 2 | 7 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0001c0001t0003g0012 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0001c0001t0003g0044 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0001c0001t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0001c0001t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0001c0001t0003g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0001c0001t0003g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0001c0001t0003g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0001c0002t0001g0002 | 0/0 | 40 | 1 | 7 | 24 | 1 | 7 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0001c0002t0001g0009 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0001c0002t0001g0010 | 0/0 | 7 | 2 | 4 | 1 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0001c0002t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0001c0002t0001g0022 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0001c0002t0001g0024 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0001c0002t0001g0028 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0001c0002t0001g0029 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0001c0002t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0001c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0001c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0001c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0001c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0001c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0001c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0001c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0001c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0001c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0001c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0001c0002t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0001c0002t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0001c0002t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0001c0002t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0001c0002t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0001c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0001c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0001c0002t0007g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0001c0004t0001g0004 | 0/0 | 21 | 0 | 0 | 19 | 1 | 1 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0001c0004t0001g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0001c0004t0001g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0001c0004t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0001c0004t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0001c0004t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0001c0004t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0001c0004t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0001c0004t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0001c0004t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0001c0004t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0001c0004t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0001c0006t0001g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0001c0006t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0001c0009t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0002c0003t0001g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0002c0003t0002g0003 | 0/0 | 25 | 13 | 2 | 7 | 1 | 2 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0002c0003t0002g0019 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0002c0003t0002g0025 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0002c0003t0002g0026 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0002c0003t0002g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0002c0003t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0002c0003t0002g0042 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0002c0003t0002g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0002c0003t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0002c0003t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0002c0003t0002g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0002c0003t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0002c0003t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0002c0003t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0002c0003t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0002c0003t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0002c0003t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0002c0003t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0002c0003t0004g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0003c0005t0004g0007 | 0/0 | 10 | 9 | 1 | 0 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0003c0005t0005g0027 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0004c0007t0001g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0004c0007t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0005c0008t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0005c0008t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0006c0012t0001g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0007c0010t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0008c0011t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0009c0016t0001g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0010c0014t0002g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0011c0013t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0012c0018t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0013c0015t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| a0014c0017t0006g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG00140 | hp2 | a0001 | c0002 | t0001 | g0002 | EUR | GBR | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG00323 | hp1 | a0001 | c0002 | t0001 | g0022 | EUR | FIN | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG00408 | hp2 | a0002 | c0003 | t0002 | g0003 | EAS | CHS | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG00423 | hp2 | a0002 | c0003 | t0002 | g0043 | EAS | CHS | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG00438 | hp1 | a0002 | c0003 | t0002 | g0019 | EAS | CHS | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG00438 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | CHS | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG00597 | hp1 | a0002 | c0003 | t0002 | g0003 | EAS | CHS | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG00609 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | CHS | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG00621 | hp1 | a0001 | c0002 | t0001 | g0052 | EAS | CHS | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | CHS | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG00639 | hp2 | a0001 | c0002 | t0001 | g0010 | AMR | PUR | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG00642 | hp1 | a0006 | c0012 | t0001 | g0006 | AMR | PUR | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG00673 | hp2 | a0002 | c0003 | t0002 | g0003 | EAS | CHS | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG00735 | hp1 | a0001 | c0002 | t0001 | g0024 | AMR | PUR | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG00738 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG00738 | hp2 | a0003 | c0005 | t0004 | g0007 | AMR | PUR | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG01069 | hp1 | a0001 | c0004 | t0001 | g0064 | AMR | PUR | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG01071 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG01081 | hp2 | a0001 | c0009 | t0001 | g0061 | AMR | PUR | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG01106 | hp1 | a0001 | c0002 | t0001 | g0010 | AMR | PUR | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG01106 | hp2 | a0001 | c0002 | t0001 | g0029 | AMR | PUR | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG01109 | hp2 | a0002 | c0003 | t0002 | g0042 | AMR | PUR | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG01167 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG01168 | hp1 | a0001 | c0002 | t0001 | g0059 | AMR | PUR | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG01169 | hp1 | a0001 | c0002 | t0001 | g0010 | AMR | PUR | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG01169 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG01175 | hp2 | a0002 | c0003 | t0001 | g0036 | AMR | PUR | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG01243 | hp1 | a0002 | c0003 | t0002 | g0003 | AMR | PUR | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG01243 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG01255 | hp1 | a0002 | c0003 | t0001 | g0036 | AMR | CLM | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG01256 | hp1 | a0001 | c0002 | t0001 | g0058 | AMR | CLM | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG01256 | hp2 | a0001 | c0002 | t0001 | g0022 | AMR | CLM | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG01258 | hp2 | a0001 | c0002 | t0001 | g0022 | AMR | CLM | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG01261 | hp1 | a0001 | c0002 | t0001 | g0073 | AMR | CLM | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | CLM | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG01433 | hp1 | a0001 | c0001 | t0003 | g0115 | AMR | CLM | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG01496 | hp1 | a0001 | c0002 | t0001 | g0010 | AMR | CLM | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0018 | EUR | IBS | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0017 | EUR | IBS | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG01516 | hp1 | a0002 | c0003 | t0002 | g0101 | EUR | IBS | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | ACB | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG01891 | hp2 | a0003 | c0005 | t0004 | g0007 | AFR | ACB | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG01934 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG01975 | hp1 | a0001 | c0001 | t0003 | g0116 | AMR | PEL | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG01975 | hp2 | a0001 | c0001 | t0003 | g0044 | AMR | PEL | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG01978 | hp1 | a0001 | c0001 | t0003 | g0008 | AMR | PEL | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PEL | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG02004 | hp2 | a0001 | c0001 | t0003 | g0008 | AMR | PEL | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | KHV | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG02027 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | KHV | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG02040 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | KHV | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | ACB | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG02055 | hp2 | a0002 | c0003 | t0002 | g0041 | AFR | ACB | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG02056 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | KHV | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG02071 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | KHV | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG02074 | hp1 | a0002 | c0003 | t0002 | g0003 | EAS | KHV | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG02074 | hp2 | a0001 | c0002 | t0007 | g0009 | EAS | KHV | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG02080 | hp1 | a0001 | c0001 | t0003 | g0113 | EAS | KHV | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG02080 | hp2 | a0002 | c0003 | t0002 | g0003 | EAS | KHV | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG02083 | hp1 | a0001 | c0004 | t0001 | g0014 | EAS | KHV | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG02129 | hp1 | a0002 | c0003 | t0002 | g0003 | EAS | KHV | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG02129 | hp2 | a0001 | c0002 | t0001 | g0050 | EAS | KHV | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG02132 | hp1 | a0001 | c0002 | t0001 | g0046 | EAS | KHV | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | KHV | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG02135 | hp2 | a0002 | c0003 | t0002 | g0026 | EAS | KHV | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | ACB | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG02148 | hp1 | a0001 | c0002 | t0001 | g0024 | AMR | PEL | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG02155 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | CDX | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG02155 | hp2 | a0001 | c0004 | t0001 | g0004 | EAS | CDX | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG02165 | hp1 | a0001 | c0002 | t0001 | g0010 | EAS | CDX | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG02165 | hp2 | a0005 | c0008 | t0001 | g0089 | EAS | CDX | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | ACB | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG02257 | hp2 | a0003 | c0005 | t0004 | g0007 | AFR | ACB | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG02273 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | ACB | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG02280 | hp2 | a0003 | c0005 | t0004 | g0007 | AFR | ACB | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG02451 | hp1 | a0001 | c0002 | t0001 | g0010 | AFR | ACB | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | ACB | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG02523 | hp1 | a0002 | c0003 | t0002 | g0003 | EAS | KHV | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG02523 | hp2 | a0007 | c0010 | t0001 | g0001 | EAS | KHV | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG02572 | hp1 | a0003 | c0005 | t0004 | g0007 | AFR | GWD | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG02602 | hp2 | a0001 | c0002 | t0001 | g0117 | SAS | PJL | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG02615 | hp2 | a0003 | c0005 | t0004 | g0007 | AFR | GWD | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG02622 | hp1 | a0002 | c0003 | t0002 | g0107 | AFR | GWD | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG02622 | hp2 | a0002 | c0003 | t0002 | g0108 | AFR | GWD | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG02630 | hp1 | a0002 | c0003 | t0002 | g0042 | AFR | GWD | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG02647 | hp1 | a0002 | c0003 | t0002 | g0003 | AFR | GWD | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG02647 | hp2 | a0002 | c0003 | t0002 | g0003 | AFR | GWD | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG02698 | hp2 | a0001 | c0002 | t0001 | g0002 | SAS | PJL | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG02717 | hp2 | a0002 | c0003 | t0002 | g0025 | AFR | GWD | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG02723 | hp2 | a0002 | c0003 | t0004 | g0007 | AFR | GWD | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG02735 | hp2 | a0002 | c0003 | t0002 | g0099 | SAS | PJL | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG02738 | hp1 | a0008 | c0011 | t0002 | g0041 | SAS | PJL | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG02738 | hp2 | a0001 | c0002 | t0001 | g0051 | SAS | PJL | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG02818 | hp1 | a0001 | c0002 | t0001 | g0057 | AFR | GWD | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG02895 | hp1 | a0002 | c0003 | t0002 | g0003 | AFR | GWD | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | GWD | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | GWD | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG02922 | hp1 | a0002 | c0003 | t0002 | g0003 | AFR | ESN | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG02922 | hp2 | a0002 | c0003 | t0002 | g0003 | AFR | ESN | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | ESN | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | ESN | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG02976 | hp1 | a0003 | c0005 | t0004 | g0007 | AFR | ESN | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | ESN | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG03017 | hp1 | a0009 | c0016 | t0001 | g0004 | SAS | PJL | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG03041 | hp1 | a0002 | c0003 | t0002 | g0003 | AFR | GWD | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | GWD | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG03098 | hp1 | a0003 | c0005 | t0005 | g0027 | AFR | MSL | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG03139 | hp1 | a0002 | c0003 | t0002 | g0003 | AFR | ESN | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ESN | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG03195 | hp2 | a0001 | c0002 | t0001 | g0060 | AFR | ESN | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG03209 | hp1 | a0002 | c0003 | t0002 | g0025 | AFR | MSL | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG03209 | hp2 | a0003 | c0005 | t0005 | g0027 | AFR | MSL | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG03225 | hp1 | a0003 | c0005 | t0004 | g0007 | AFR | MSL | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | MSL | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG03239 | hp2 | a0001 | c0002 | t0001 | g0002 | SAS | PJL | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG03453 | hp1 | a0002 | c0003 | t0002 | g0003 | AFR | MSL | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | MSL | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG03490 | hp2 | a0002 | c0003 | t0002 | g0003 | SAS | PJL | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG03491 | hp1 | a0001 | c0002 | t0001 | g0002 | SAS | PJL | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG03492 | hp1 | a0002 | c0003 | t0002 | g0003 | SAS | PJL | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG03492 | hp2 | a0001 | c0002 | t0001 | g0002 | SAS | PJL | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ESN | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG03516 | hp2 | a0003 | c0005 | t0004 | g0007 | AFR | ESN | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG03579 | hp1 | a0001 | c0002 | t0001 | g0030 | AFR | MSL | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG03579 | hp2 | a0002 | c0003 | t0002 | g0003 | AFR | MSL | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG03654 | hp1 | a0010 | c0014 | t0002 | g0040 | SAS | PJL | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0094 | SAS | PJL | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG03704 | hp1 | a0001 | c0002 | t0001 | g0028 | SAS | PJL | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG03710 | hp1 | a0001 | c0002 | t0001 | g0024 | SAS | PJL | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG03710 | hp2 | a0001 | c0004 | t0001 | g0004 | SAS | PJL | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG03831 | hp1 | a0001 | c0004 | t0001 | g0083 | SAS | BEB | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG03831 | hp2 | a0002 | c0003 | t0002 | g0105 | SAS | BEB | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG03927 | hp1 | a0001 | c0002 | t0001 | g0118 | SAS | BEB | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG03927 | hp2 | a0002 | c0003 | t0002 | g0026 | SAS | BEB | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG03942 | hp1 | a0001 | c0002 | t0001 | g0002 | SAS | BEB | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0075 | SAS | BEB | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG04184 | hp2 | a0001 | c0004 | t0001 | g0065 | SAS | BEB | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG04199 | hp1 | a0001 | c0002 | t0001 | g0002 | SAS | STU | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG04204 | hp1 | a0002 | c0003 | t0002 | g0040 | SAS | STU | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG04204 | hp2 | a0002 | c0003 | t0002 | g0106 | SAS | STU | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | STU | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA18522 | hp1 | a0002 | c0003 | t0002 | g0003 | AFR | YRI | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA18522 | hp2 | a0002 | c0003 | t0002 | g0102 | AFR | YRI | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA18747 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | CHB | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA18747 | hp2 | a0001 | c0004 | t0001 | g0066 | EAS | CHB | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA18939 | hp1 | a0001 | c0004 | t0001 | g0004 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA18939 | hp2 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA18940 | hp1 | a0002 | c0003 | t0002 | g0043 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA18941 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA18942 | hp1 | a0002 | c0003 | t0002 | g0103 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA18942 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA18945 | hp1 | a0001 | c0001 | t0003 | g0112 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA18945 | hp2 | a0011 | c0013 | t0001 | g0001 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA18947 | hp2 | a0001 | c0002 | t0001 | g0021 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA18950 | hp1 | a0002 | c0003 | t0002 | g0019 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA18950 | hp2 | a0001 | c0004 | t0001 | g0062 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA18951 | hp1 | a0001 | c0006 | t0001 | g0015 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA18951 | hp2 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA18952 | hp1 | a0001 | c0004 | t0001 | g0014 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA18952 | hp2 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA18953 | hp2 | a0001 | c0002 | t0001 | g0056 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA18954 | hp1 | a0002 | c0003 | t0002 | g0026 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA18960 | hp1 | a0004 | c0007 | t0001 | g0016 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA18960 | hp2 | a0001 | c0002 | t0001 | g0028 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA18961 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA18962 | hp2 | a0002 | c0003 | t0002 | g0100 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA18964 | hp2 | a0001 | c0004 | t0001 | g0004 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA18965 | hp2 | a0004 | c0007 | t0001 | g0016 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA18966 | hp1 | a0001 | c0004 | t0001 | g0004 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA18967 | hp1 | a0001 | c0004 | t0001 | g0004 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA18967 | hp2 | a0004 | c0007 | t0001 | g0016 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA18968 | hp1 | a0012 | c0018 | t0001 | g0087 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA18968 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA18969 | hp2 | a0001 | c0004 | t0001 | g0068 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA18970 | hp2 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA18971 | hp1 | a0001 | c0006 | t0001 | g0015 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA18971 | hp2 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA18972 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA18973 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA18973 | hp2 | a0001 | c0004 | t0001 | g0004 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA18974 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA18974 | hp2 | a0001 | c0004 | t0001 | g0004 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA18975 | hp1 | a0013 | c0015 | t0001 | g0021 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA18975 | hp2 | a0005 | c0008 | t0001 | g0001 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA18977 | hp1 | a0001 | c0004 | t0001 | g0014 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA18977 | hp2 | a0004 | c0007 | t0001 | g0016 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA18978 | hp1 | a0014 | c0017 | t0006 | g0055 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA18978 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA18980 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA18981 | hp1 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA18981 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA18982 | hp1 | a0001 | c0001 | t0003 | g0044 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA18983 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA18984 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA18984 | hp2 | a0001 | c0006 | t0001 | g0015 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA18986 | hp1 | a0001 | c0004 | t0001 | g0004 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA18988 | hp2 | a0001 | c0004 | t0001 | g0004 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA18992 | hp1 | a0001 | c0004 | t0001 | g0004 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA18992 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA18994 | hp2 | a0001 | c0002 | t0001 | g0029 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA18995 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA18999 | hp2 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA19000 | hp2 | a0002 | c0003 | t0002 | g0019 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA19002 | hp1 | a0001 | c0004 | t0001 | g0023 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA19003 | hp2 | a0005 | c0008 | t0001 | g0001 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA19005 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA19005 | hp2 | a0001 | c0004 | t0001 | g0004 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA19009 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA19010 | hp1 | a0001 | c0006 | t0001 | g0015 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA19010 | hp2 | a0001 | c0004 | t0001 | g0004 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA19011 | hp1 | a0002 | c0003 | t0002 | g0019 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | LWK | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA19030 | hp2 | a0003 | c0005 | t0005 | g0027 | AFR | LWK | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | LWK | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA19043 | hp2 | a0001 | c0001 | t0003 | g0114 | AFR | LWK | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA19054 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA19055 | hp2 | a0001 | c0004 | t0001 | g0067 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA19056 | hp1 | a0001 | c0004 | t0001 | g0004 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA19057 | hp1 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA19058 | hp1 | a0001 | c0004 | t0001 | g0004 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA19058 | hp2 | a0001 | c0004 | t0001 | g0072 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA19060 | hp2 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA19063 | hp1 | a0001 | c0002 | t0001 | g0045 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA19063 | hp2 | a0001 | c0004 | t0001 | g0014 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA19064 | hp1 | a0001 | c0004 | t0001 | g0004 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA19064 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA19065 | hp1 | a0001 | c0002 | t0001 | g0021 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA19065 | hp2 | a0005 | c0008 | t0001 | g0001 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA19067 | hp1 | a0001 | c0002 | t0001 | g0053 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA19067 | hp2 | a0001 | c0004 | t0001 | g0004 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA19068 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA19070 | hp2 | a0001 | c0004 | t0001 | g0004 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA19074 | hp2 | a0001 | c0004 | t0001 | g0023 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA19075 | hp1 | a0001 | c0002 | t0001 | g0048 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA19075 | hp2 | a0001 | c0006 | t0001 | g0069 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA19076 | hp1 | a0002 | c0003 | t0002 | g0104 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA19076 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA19077 | hp2 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA19080 | hp1 | a0001 | c0004 | t0001 | g0063 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA19080 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA19081 | hp2 | a0001 | c0004 | t0001 | g0023 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA19083 | hp1 | a0001 | c0004 | t0001 | g0004 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA19083 | hp2 | a0004 | c0007 | t0001 | g0074 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA19084 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA19084 | hp2 | a0001 | c0002 | t0001 | g0049 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA19086 | hp2 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA19088 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA19088 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA19090 | hp1 | a0001 | c0002 | t0001 | g0047 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA19090 | hp2 | a0001 | c0004 | t0001 | g0004 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA19091 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA19091 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA19240 | hp1 | a0002 | c0003 | t0002 | g0025 | AFR | YRI | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | YRI | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | ASW | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ASW | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0018 | EUR | TSI | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA20752 | hp2 | a0002 | c0003 | t0002 | g0003 | EUR | TSI | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA20805 | hp1 | a0001 | c0004 | t0001 | g0004 | EUR | TSI | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0034 | EUR | TSI | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA20905 | hp1 | a0001 | c0002 | t0001 | g0054 | SAS | GIH | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA20905 | hp2 | a0001 | c0002 | t0001 | g0002 | SAS | GIH | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG01123 | hp2 | a0002 | c0003 | t0002 | g0003 | AMR | CLM | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | ACB | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG02109 | hp2 | a0003 | c0005 | t0004 | g0007 | AFR | ACB | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG02486 | hp1 | a0002 | c0003 | t0002 | g0003 | AFR | ACB | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | ACB | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG02559 | hp1 | a0002 | c0003 | t0002 | g0003 | AFR | ACB | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | MSL | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG03471 | hp2 | a0002 | c0003 | t0002 | g0003 | AFR | MSL | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | USA | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0008 | AFR | USA | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | USA | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA20300 | hp2 | a0001 | c0002 | t0001 | g0030 | AFR | USA | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA21309 | hp1 | a0001 | c0002 | t0001 | g0002 | AFR | LWK | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| NA21309 | hp2 | a0001 | c0002 | t0001 | g0010 | AFR | LWK | FANCE_chr6_35447338_35472102 | FANCE | chr6 | 35447338 | 35472102 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:35452577 | C | CT | 1 | a0012 | 1 | NA18968.hp1 | frameshift_variant&stop_gained | HIGH | c.33dupT | p.Glu12fs | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 1/10 | 242/2576 | 34/1611 | 12/536 | INFO_REALIGN_3_PRIME | chr6 | 35452577 | ||
| chr6:35452615 | G | GC | 1 | a0007 | 1 | HG02523.hp2 | frameshift_variant | HIGH | c.75dupC | p.Ala26fs | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 1/10 | 284/2576 | 76/1611 | 26/536 | INFO_REALIGN_3_PRIME | chr6 | 35452615 | ||
| chr6:35452620 | C | CG | 1 | a0014 | 1 | NA18978.hp1 | frameshift_variant | HIGH | c.76dupG | p.Ala26fs | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 1/10 | 285/2576 | 77/1611 | 26/536 | INFO_REALIGN_3_PRIME | chr6 | 35452620 | ||
| chr6:35452641 | G | GC | 1 | a0007 | 1 | HG02523.hp2 | frameshift_variant | HIGH | c.97dupC | p.Leu33fs | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 1/10 | 306/2576 | 98/1611 | 33/536 | INFO_REALIGN_3_PRIME | chr6 | 35452641 | ||
| chr6:35452649 | C | CG | 1 | a0013 | 1 | NA18975.hp1 | frameshift_variant | HIGH | c.108dupG | p.Pro37fs | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 1/10 | 317/2576 | 109/1611 | 37/536 | INFO_REALIGN_3_PRIME | chr6 | 35452649 | ||
| chr6:35452649 | C | T | 1 | a0009 | 1 | HG03017.hp1 | missense_variant | MODERATE | c.104C>T | p.Ala35Val | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 1/10 | 312/2576 | 104/1611 | 35/536 | chr6 | 35452649 | |||
| chr6:35452658 | A | AG | 2 | a0007 a0013 |
2 | HG02523.hp2 NA18975.hp1 |
frameshift_variant | HIGH | c.118dupG | p.Ala40fs | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 1/10 | 327/2576 | 119/1611 | 40/536 | INFO_REALIGN_3_PRIME | chr6 | 35452658 | ||
| chr6:35452676 | T | TG | 1 | a0007 | 1 | HG02523.hp2 | frameshift_variant | HIGH | c.136dupG | p.Val46fs | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 1/10 | 345/2576 | 137/1611 | 46/536 | INFO_REALIGN_3_PRIME | chr6 | 35452676 | ||
| chr6:35452687 | C | CG | 1 | a0007 | 1 | HG02523.hp2 | frameshift_variant | HIGH | c.145dupG | p.Ala49fs | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 1/10 | 354/2576 | 146/1611 | 49/536 | INFO_REALIGN_3_PRIME | chr6 | 35452687 | ||
| chr6:35455764 | G | T | 1 | a0004 | 5 | NA18960.hp1 NA18965.hp2 NA18967.hp2 others(2): Show |
missense_variant | MODERATE | c.266G>T | p.Arg89Leu | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 2/10 | 474/2576 | 266/1611 | 89/536 | chr6 | 35455764 | |||
| chr6:35455856 | A | G | 1 | a0010 | 1 | HG03654.hp1 | missense_variant | MODERATE | c.358A>G | p.Ile120Val | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 2/10 | 566/2576 | 358/1611 | 120/536 | chr6 | 35455856 | |||
| chr6:35455881 | A | AC | 1 | a0012 | 1 | NA18968.hp1 | frameshift_variant | HIGH | c.386dupC | p.Asp130fs | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 2/10 | 595/2576 | 387/1611 | 129/536 | INFO_REALIGN_3_PRIME | chr6 | 35455881 | ||
| chr6:35455905 | TG | T | 1 | a0012 | 1 | NA18968.hp1 | frameshift_variant | HIGH | c.412delG | p.Glu138fs | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 2/10 | 620/2576 | 412/1611 | 138/536 | INFO_REALIGN_3_PRIME | chr6 | 35455905 | ||
| chr6:35456078 | TC | T | 1 | a0012 | 1 | NA18968.hp1 | frameshift_variant | HIGH | c.583delC | p.Gln195fs | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 2/10 | 791/2576 | 583/1611 | 195/536 | INFO_REALIGN_3_PRIME | chr6 | 35456078 | ||
| chr6:35456109 | C | T | 1 | a0003 | 13 | HG00738.hp2 HG01891.hp2 HG02109.hp2 others(10): Show |
missense_variant | MODERATE | c.611C>T | p.Ser204Leu | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 2/10 | 819/2576 | 611/1611 | 204/536 | chr6 | 35456109 | |||
| chr6:35458318 | C | G | 1 | a0011 | 1 | NA18945.hp2 | missense_variant | MODERATE | c.991C>G | p.Leu331Val | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 5/10 | 1199/2576 | 991/1611 | 331/536 | chr6 | 35458318 | |||
| chr6:35458355 | G | A | 1 | a0005 | 4 | HG02165.hp2 NA18975.hp2 NA19003.hp2 others(1): Show |
missense_variant | MODERATE | c.1028G>A | p.Arg343Gln | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 5/10 | 1236/2576 | 1028/1611 | 343/536 | chr6 | 35458355 | |||
| chr6:35458396 | C | T | 1 | a0006 | 1 | HG00642.hp1 | missense_variant | MODERATE | c.1069C>T | p.Leu357Phe | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 5/10 | 1277/2576 | 1069/1611 | 357/536 | chr6 | 35458396 | |||
| chr6:35460568 | C | T | 1 | a0008 | 1 | HG02738.hp1 | missense_variant | MODERATE | c.1333C>T | p.Pro445Ser | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 8/10 | 1541/2576 | 1333/1611 | 445/536 | chr6 | 35460568 | |||
| chr6:35462909 | G | A | 4 | a0002 a0003 a0008 others(1): Show |
69 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(66): Show |
missense_variant | MODERATE | c.1504G>A | p.Ala502Thr | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 9/10 | 1712/2576 | 1504/1611 | 502/536 | chr6 | 35462909 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:35455885 | A | C | 14 | a0001c0001 a0001c0004 a0001c0006 others(11): Show |
309 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(306): Show |
synonymous_variant | LOW | c.387A>C | p.Pro129Pro | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 2/10 | 595/2576 | 387/1611 | 129/536 | chr6 | 35455885 | |||
| chr6:35458398 | C | T | 3 | a0001c0004 a0001c0006 a0009c0016 |
43 | HG01069.hp1 HG02083.hp1 HG02155.hp2 others(40): Show |
synonymous_variant | LOW | c.1071C>T | p.Leu357Leu | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 5/10 | 1279/2576 | 1071/1611 | 357/536 | chr6 | 35458398 | |||
| chr6:35462914 | C | T | 1 | a0001c0006 | 5 | NA18951.hp1 NA18971.hp1 NA18984.hp2 others(2): Show |
splice_region_variant&synonymous_variant | LOW | c.1509C>T | p.Asn503Asn | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 9/10 | 1717/2576 | 1509/1611 | 503/536 | chr6 | 35462914 | |||
| chr6:35466306 | G | A | 1 | a0001c0009 | 2 | HG01081.hp2 homoSapiens_chm13v2.hp1 |
synonymous_variant | LOW | c.1572G>A | p.Arg524Arg | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 10/10 | 1780/2576 | 1572/1611 | 524/536 | chr6 | 35466306 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:35452490 | C | T | 1 | a0001c0001t0003 | 23 | HG01433.hp1 HG01975.hp1 HG01975.hp2 others(20): Show |
5_prime_UTR_variant | MODIFIER | c.-56C>T | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 1/10 | 56 | chr6 | 35452490 | ||||||
| chr6:35452507 | A | G | 1 | a0003c0005t0005 | 3 | HG03098.hp1 HG03209.hp2 NA19030.hp2 |
5_prime_UTR_variant | MODIFIER | c.-39A>G | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 1/10 | 39 | chr6 | 35452507 | ||||||
| chr6:35452513 | G | A | 1 | a0014c0017t0006 | 1 | NA18978.hp1 | 5_prime_UTR_variant | MODIFIER | c.-33G>A | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 1/10 | 33 | chr6 | 35452513 | ||||||
| chr6:35466496 | A | G | 3 | a0002c0003t0004 a0003c0005t0004 a0003c0005t0005 |
14 | HG00738.hp2 HG01891.hp2 HG02109.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*151A>G | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 10/10 | 151 | chr6 | 35466496 | ||||||
| chr6:35466560 | TC | T | 3 | a0002c0003t0002 a0008c0011t0002 a0010c0014t0002 |
53 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*216delC | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 10/10 | 216 | chr6 | 35466560 | ||||||
| chr6:35466956 | C | T | 1 | a0001c0002t0007 | 1 | HG02074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*611C>T | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 10/10 | 611 | chr6 | 35466956 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:35452851 | A | C | 67 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(64): Show |
225 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(222): Show |
intron_variant | MODIFIER | c.248+58A>C | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 1/9 | chr6 | 35452851 | |||||||
| chr6:35452902 | C | T | 1 | a0001c0004t0001g0083 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.248+109C>T | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 1/9 | chr6 | 35452902 | |||||||
| chr6:35452942 | T | A | 1 | a0002c0003t0002g0025 | 3 | HG02717.hp2 HG03209.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.248+149T>A | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 1/9 | chr6 | 35452942 | |||||||
| chr6:35453128 | A | G | 1 | a0001c0001t0001g0082 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.248+335A>G | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 1/9 | chr6 | 35453128 | |||||||
| chr6:35453146 | C | T | 83 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(80): Show |
263 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(260): Show |
intron_variant | MODIFIER | c.248+353C>T | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 1/9 | chr6 | 35453146 | |||||||
| chr6:35453190 | G | A | 53 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(50): Show |
193 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(190): Show |
intron_variant | MODIFIER | c.248+397G>A | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 1/9 | chr6 | 35453190 | |||||||
| chr6:35453283 | A | T | 3 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0121 |
3 | HG02698.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.248+490A>T | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 1/9 | chr6 | 35453283 | |||||||
| chr6:35453309 | G | T | 4 | a0001c0001t0001g0005 a0001c0001t0001g0109 a0001c0001t0001g0110 others(1): Show |
21 | HG00735.hp2 HG01109.hp1 HG01167.hp1 others(18): Show |
intron_variant | MODIFIER | c.248+516G>T | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 1/9 | chr6 | 35453309 | |||||||
| chr6:35453400 | TTATTGA | T | 7 | a0001c0002t0001g0009 a0001c0002t0001g0045 a0001c0002t0001g0046 others(4): Show |
14 | HG02074.hp2 HG02132.hp1 NA18939.hp2 others(11): Show |
intron_variant | MODIFIER | c.248+612_248+617del others(6): Show |
FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr6 | 35453400 | ||||||
| chr6:35453475 | T | TA | 9 | a0001c0001t0001g0084 a0001c0001t0003g0008 a0001c0001t0003g0012 others(6): Show |
24 | HG01361.hp1 HG01433.hp1 HG01975.hp1 others(21): Show |
intron_variant | MODIFIER | c.248+692dupA | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr6 | 35453475 | ||||||
| chr6:35453924 | C | T | 1 | a0002c0003t0002g0043 | 2 | HG00423.hp2 NA18940.hp1 |
intron_variant | MODIFIER | c.248+1131C>T | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 1/9 | chr6 | 35453924 | |||||||
| chr6:35454072 | G | GT | 25 | a0001c0002t0001g0024 a0001c0002t0001g0073 a0002c0003t0002g0003 others(22): Show |
71 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.248+1290dupT | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr6 | 35454072 | ||||||
| chr6:35454077 | T | G | 1 | a0001c0002t0001g0050 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.248+1284T>G | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 1/9 | chr6 | 35454077 | |||||||
| chr6:35454268 | G | T | 1 | a0001c0001t0001g0098 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.248+1475G>T | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 1/9 | chr6 | 35454268 | |||||||
| chr6:35454497 | A | G | 1 | a0001c0004t0001g0072 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.249-1250A>G | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 1/9 | chr6 | 35454497 | |||||||
| chr6:35454499 | G | A | 24 | a0001c0002t0001g0002 a0001c0002t0001g0009 a0001c0002t0001g0021 others(21): Show |
77 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.249-1248G>A | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 1/9 | chr6 | 35454499 | |||||||
| chr6:35454518 | C | T | 1 | a0001c0002t0001g0049 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.249-1229C>T | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 1/9 | chr6 | 35454518 | |||||||
| chr6:35454519 | G | A | 1 | a0002c0003t0002g0025 | 3 | HG02717.hp2 HG03209.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.249-1228G>A | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 1/9 | chr6 | 35454519 | |||||||
| chr6:35454523 | G | C | 1 | a0001c0001t0003g0112 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.249-1224G>C | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 1/9 | chr6 | 35454523 | |||||||
| chr6:35454577 | A | G | 1 | a0001c0006t0001g0015 | 4 | NA18951.hp1 NA18971.hp1 NA18984.hp2 others(1): Show |
intron_variant | MODIFIER | c.249-1170A>G | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 1/9 | chr6 | 35454577 | |||||||
| chr6:35454765 | C | T | 3 | a0002c0003t0004g0007 a0003c0005t0004g0007 a0003c0005t0005g0027 |
14 | HG00738.hp2 HG01891.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.249-982C>T | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 1/9 | chr6 | 35454765 | |||||||
| chr6:35454897 | C | T | 20 | a0002c0003t0002g0003 a0002c0003t0002g0019 a0002c0003t0002g0025 others(17): Show |
53 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.249-850C>T | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 1/9 | chr6 | 35454897 | |||||||
| chr6:35454977 | G | T | 29 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(26): Show |
124 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.249-770G>T | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 1/9 | chr6 | 35454977 | |||||||
| chr6:35455063 | G | A | 1 | a0001c0001t0001g0032 | 2 | HG02809.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.249-684G>A | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 1/9 | chr6 | 35455063 | |||||||
| chr6:35455079 | A | G | 14 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0032 others(11): Show |
33 | HG00642.hp1 HG00741.hp1 HG01074.hp1 others(30): Show |
intron_variant | MODIFIER | c.249-668A>G | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 1/9 | chr6 | 35455079 | |||||||
| chr6:35455241 | A | T | 3 | a0001c0001t0001g0039 a0001c0001t0001g0096 a0001c0001t0001g0097 |
4 | HG02257.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.249-506A>T | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 1/9 | chr6 | 35455241 | |||||||
| chr6:35455319 | T | A | 12 | a0001c0001t0001g0020 a0001c0001t0001g0119 a0001c0001t0001g0120 others(9): Show |
30 | HG01433.hp1 HG01975.hp1 HG01975.hp2 others(27): Show |
intron_variant | MODIFIER | c.249-428T>A | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 1/9 | chr6 | 35455319 | |||||||
| chr6:35455639 | G | A | 8 | a0001c0001t0003g0008 a0001c0001t0003g0012 a0001c0001t0003g0044 others(5): Show |
23 | HG01433.hp1 HG01975.hp1 HG01975.hp2 others(20): Show |
intron_variant | MODIFIER | c.249-108G>A | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 1/9 | chr6 | 35455639 | |||||||
| chr6:35455640 | T | C | 1 | a0002c0003t0001g0036 | 2 | HG01175.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.249-107T>C | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 1/9 | chr6 | 35455640 | |||||||
| chr6:35455661 | C | T | 3 | a0001c0001t0001g0038 a0001c0001t0001g0095 a0001c0002t0001g0056 |
4 | HG00621.hp2 NA18940.hp2 NA18953.hp2 others(1): Show |
intron_variant | MODIFIER | c.249-86C>T | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 1/9 | chr6 | 35455661 | |||||||
| chr6:35455712 | A | G | 100 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(97): Show |
309 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(306): Show |
intron_variant | MODIFIER | c.249-35A>G | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 1/9 | chr6 | 35455712 | |||||||
| chr6:35455725 | T | G | 1 | a0001c0004t0001g0062 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.249-22T>G | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 1/9 | chr6 | 35455725 | |||||||
| chr6:35456411 | A | G | 85 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(82): Show |
266 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(263): Show |
intron_variant | MODIFIER | c.855+58A>G | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 2/9 | chr6 | 35456411 | |||||||
| chr6:35456427 | G | A | 2 | a0004c0007t0001g0016 a0004c0007t0001g0074 |
5 | NA18960.hp1 NA18965.hp2 NA18967.hp2 others(2): Show |
intron_variant | MODIFIER | c.855+74G>A | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 2/9 | chr6 | 35456427 | |||||||
| chr6:35456491 | A | G | 100 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(97): Show |
309 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(306): Show |
intron_variant | MODIFIER | c.855+138A>G | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 2/9 | chr6 | 35456491 | |||||||
| chr6:35456506 | C | T | 6 | a0001c0001t0003g0008 a0001c0001t0003g0012 a0001c0001t0003g0044 others(3): Show |
21 | HG01433.hp1 HG01975.hp1 HG01975.hp2 others(18): Show |
intron_variant | MODIFIER | c.855+153C>T | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 2/9 | chr6 | 35456506 | |||||||
| chr6:35456797 | G | A | 1 | a0001c0001t0001g0085 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.855+444G>A | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 2/9 | chr6 | 35456797 | |||||||
| chr6:35457048 | A | G | 1 | a0001c0009t0001g0061 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.856-508A>G | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 2/9 | chr6 | 35457048 | |||||||
| chr6:35457116 | A | G | 1 | a0001c0001t0001g0094 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.856-440A>G | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 2/9 | chr6 | 35457116 | |||||||
| chr6:35457126 | C | CT | 5 | a0001c0001t0001g0032 a0001c0001t0001g0035 a0001c0001t0001g0079 others(2): Show |
7 | HG02809.hp2 HG02896.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.856-419dupT | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr6 | 35457126 | ||||||
| chr6:35457191 | A | G | 1 | a0001c0002t0001g0060 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.856-365A>G | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 2/9 | chr6 | 35457191 | |||||||
| chr6:35457430 | T | C | 2 | a0001c0001t0001g0119 a0001c0001t0001g0120 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.856-126T>C | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 2/9 | chr6 | 35457430 | |||||||
| chr6:35457486 | G | A | 24 | a0002c0003t0001g0036 a0002c0003t0002g0003 a0002c0003t0002g0019 others(21): Show |
69 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.856-70G>A | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 2/9 | chr6 | 35457486 | |||||||
| chr6:35457639 | A | G | 27 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(24): Show |
121 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.900+39A>G | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 3/9 | chr6 | 35457639 | |||||||
| chr6:35457710 | G | A | 1 | a0001c0004t0001g0063 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.900+110G>A | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 3/9 | chr6 | 35457710 | |||||||
| chr6:35458213 | T | C | 19 | a0002c0003t0002g0003 a0002c0003t0002g0019 a0002c0003t0002g0026 others(16): Show |
50 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.970-84T>C | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 4/9 | chr6 | 35458213 | |||||||
| chr6:35458264 | G | A | 1 | a0001c0001t0001g0033 | 2 | HG02109.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.970-33G>A | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 4/9 | chr6 | 35458264 | |||||||
| chr6:35458281 | C | T | 2 | a0001c0006t0001g0015 a0001c0006t0001g0069 |
5 | NA18951.hp1 NA18971.hp1 NA18984.hp2 others(2): Show |
intron_variant | MODIFIER | c.970-16C>T | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 4/9 | chr6 | 35458281 | |||||||
| chr6:35458470 | C | T | 2 | a0004c0007t0001g0016 a0004c0007t0001g0074 |
5 | NA18960.hp1 NA18965.hp2 NA18967.hp2 others(2): Show |
intron_variant | MODIFIER | c.1113+30C>T | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 5/9 | chr6 | 35458470 | |||||||
| chr6:35458603 | A | G | 8 | a0001c0001t0003g0008 a0001c0001t0003g0012 a0001c0001t0003g0044 others(5): Show |
23 | HG01433.hp1 HG01975.hp1 HG01975.hp2 others(20): Show |
intron_variant | MODIFIER | c.1113+163A>G | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 5/9 | chr6 | 35458603 | |||||||
| chr6:35458639 | C | CT | 17 | a0001c0001t0001g0095 a0001c0002t0001g0048 a0002c0003t0002g0003 others(14): Show |
48 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(45): Show |
intron_variant | MODIFIER | c.1113+215dupT | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr6 | 35458639 | ||||||
| chr6:35458655 | TGAGA | T | 1 | a0001c0001t0001g0020 | 4 | HG02809.hp1 HG03195.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1113+221_1113+224d others(6): Show |
FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr6 | 35458655 | ||||||
| chr6:35458675 | T | C | 1 | a0002c0003t0002g0100 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1113+235T>C | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 5/9 | chr6 | 35458675 | |||||||
| chr6:35458876 | G | T | 2 | a0004c0007t0001g0016 a0004c0007t0001g0074 |
5 | NA18960.hp1 NA18965.hp2 NA18967.hp2 others(2): Show |
intron_variant | MODIFIER | c.1113+436G>T | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 5/9 | chr6 | 35458876 | |||||||
| chr6:35459014 | C | T | 3 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0121 |
3 | HG02698.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1114-317C>T | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 5/9 | chr6 | 35459014 | |||||||
| chr6:35459213 | A | C | 1 | a0001c0001t0001g0078 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1114-118A>C | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 5/9 | chr6 | 35459213 | |||||||
| chr6:35459616 | C | T | 1 | a0001c0002t0001g0022 | 3 | HG00323.hp1 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1238-66C>T | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 6/9 | chr6 | 35459616 | |||||||
| chr6:35459647 | C | A | 2 | a0004c0007t0001g0016 a0004c0007t0001g0074 |
5 | NA18960.hp1 NA18965.hp2 NA18967.hp2 others(2): Show |
intron_variant | MODIFIER | c.1238-35C>A | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 6/9 | chr6 | 35459647 | |||||||
| chr6:35459779 | G | A | 24 | a0002c0003t0001g0036 a0002c0003t0002g0003 a0002c0003t0002g0019 others(21): Show |
69 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.1316+19G>A | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 7/9 | chr6 | 35459779 | |||||||
| chr6:35459809 | G | A | 1 | a0001c0001t0001g0075 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1316+49G>A | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 7/9 | chr6 | 35459809 | |||||||
| chr6:35459981 | C | T | 8 | a0001c0001t0003g0008 a0001c0001t0003g0012 a0001c0001t0003g0044 others(5): Show |
23 | HG01433.hp1 HG01975.hp1 HG01975.hp2 others(20): Show |
intron_variant | MODIFIER | c.1316+221C>T | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 7/9 | chr6 | 35459981 | |||||||
| chr6:35460055 | C | T | 1 | a0002c0003t0002g0025 | 3 | HG02717.hp2 HG03209.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1316+295C>T | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 7/9 | chr6 | 35460055 | |||||||
| chr6:35460104 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1316+344C>T | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 7/9 | chr6 | 35460104 | |||||||
| chr6:35460123 | G | A | 1 | a0002c0003t0002g0101 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1316+363G>A | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 7/9 | chr6 | 35460123 | |||||||
| chr6:35460139 | G | A | 1 | a0002c0003t0002g0025 | 3 | HG02717.hp2 HG03209.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1316+379G>A | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 7/9 | chr6 | 35460139 | |||||||
| chr6:35460232 | C | T | 1 | a0001c0001t0001g0018 | 4 | HG01515.hp1 HG02135.hp1 HG04228.hp2 others(1): Show |
intron_variant | MODIFIER | c.1317-320C>T | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 7/9 | chr6 | 35460232 | |||||||
| chr6:35460396 | G | A | 1 | a0001c0002t0001g0057 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1317-156G>A | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 7/9 | chr6 | 35460396 | |||||||
| chr6:35460504 | G | T | 1 | a0001c0002t0001g0057 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1317-48G>T | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 7/9 | chr6 | 35460504 | |||||||
| chr6:35460541 | C | T | 2 | a0001c0004t0001g0023 a0001c0004t0001g0068 |
4 | NA18969.hp2 NA19002.hp1 NA19074.hp2 others(1): Show |
intron_variant | MODIFIER | c.1317-11C>T | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 7/9 | chr6 | 35460541 | |||||||
| chr6:35460834 | C | G | 1 | a0001c0001t0001g0121 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1383+216C>G | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 8/9 | chr6 | 35460834 | |||||||
| chr6:35460837 | G | T | 1 | a0001c0002t0001g0056 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1383+219G>T | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 8/9 | chr6 | 35460837 | |||||||
| chr6:35460850 | G | C | 24 | a0002c0003t0001g0036 a0002c0003t0002g0003 a0002c0003t0002g0019 others(21): Show |
69 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.1383+232G>C | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 8/9 | chr6 | 35460850 | |||||||
| chr6:35460909 | C | G | 1 | a0001c0002t0001g0054 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1383+291C>G | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 8/9 | chr6 | 35460909 | |||||||
| chr6:35460922 | AT | A | 39 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0031 others(36): Show |
91 | HG00642.hp1 HG00741.hp1 HG01069.hp1 others(88): Show |
intron_variant | MODIFIER | c.1383+319delT | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr6 | 35460922 | ||||||
| chr6:35460966 | C | T | 2 | a0004c0007t0001g0016 a0004c0007t0001g0074 |
5 | NA18960.hp1 NA18965.hp2 NA18967.hp2 others(2): Show |
intron_variant | MODIFIER | c.1383+348C>T | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 8/9 | chr6 | 35460966 | |||||||
| chr6:35461005 | G | A | 26 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(23): Show |
120 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.1383+387G>A | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 8/9 | chr6 | 35461005 | |||||||
| chr6:35461063 | C | T | 1 | a0001c0001t0001g0093 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1383+445C>T | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 8/9 | chr6 | 35461063 | |||||||
| chr6:35461115 | G | A | 1 | a0002c0003t0002g0102 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1383+497G>A | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 8/9 | chr6 | 35461115 | |||||||
| chr6:35461123 | C | T | 24 | a0002c0003t0001g0036 a0002c0003t0002g0003 a0002c0003t0002g0019 others(21): Show |
69 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.1383+505C>T | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 8/9 | chr6 | 35461123 | |||||||
| chr6:35461176 | G | A | 1 | a0001c0001t0001g0097 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1383+558G>A | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 8/9 | chr6 | 35461176 | |||||||
| chr6:35461180 | G | A | 1 | a0001c0004t0001g0014 | 4 | HG02083.hp1 NA18952.hp1 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.1383+562G>A | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 8/9 | chr6 | 35461180 | |||||||
| chr6:35461378 | A | C | 1 | a0001c0001t0001g0097 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1383+760A>C | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 8/9 | chr6 | 35461378 | |||||||
| chr6:35461448 | G | A | 24 | a0002c0003t0001g0036 a0002c0003t0002g0003 a0002c0003t0002g0019 others(21): Show |
69 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.1383+830G>A | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 8/9 | chr6 | 35461448 | |||||||
| chr6:35461607 | A | G | 2 | a0004c0007t0001g0016 a0004c0007t0001g0074 |
5 | NA18960.hp1 NA18965.hp2 NA18967.hp2 others(2): Show |
intron_variant | MODIFIER | c.1383+989A>G | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 8/9 | chr6 | 35461607 | |||||||
| chr6:35461650 | C | CT | 37 | a0001c0001t0001g0031 a0001c0001t0001g0039 a0001c0001t0001g0070 others(34): Show |
85 | HG01175.hp1 HG01433.hp1 HG01975.hp1 others(82): Show |
intron_variant | MODIFIER | c.1383+1047dupT | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr6 | 35461650 | ||||||
| chr6:35461795 | C | G | 2 | a0001c0001t0001g0033 a0001c0001t0001g0077 |
3 | HG02109.hp1 HG02145.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1384-994C>G | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 8/9 | chr6 | 35461795 | |||||||
| chr6:35461797 | A | G | 2 | a0001c0001t0001g0033 a0001c0001t0001g0077 |
3 | HG02109.hp1 HG02145.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1384-992A>G | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 8/9 | chr6 | 35461797 | |||||||
| chr6:35461870 | A | G | 1 | a0001c0001t0001g0091 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1384-919A>G | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 8/9 | chr6 | 35461870 | |||||||
| chr6:35461927 | G | A | 24 | a0002c0003t0001g0036 a0002c0003t0002g0003 a0002c0003t0002g0019 others(21): Show |
69 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.1384-862G>A | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 8/9 | chr6 | 35461927 | |||||||
| chr6:35461996 | A | G | 22 | a0001c0001t0001g0031 a0001c0001t0001g0039 a0001c0001t0001g0070 others(19): Show |
52 | HG01069.hp1 HG02055.hp1 HG02083.hp1 others(49): Show |
intron_variant | MODIFIER | c.1384-793A>G | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 8/9 | chr6 | 35461996 | |||||||
| chr6:35462097 | A | AAATAAT | 5 | a0002c0003t0001g0036 a0002c0003t0002g0019 a0002c0003t0002g0100 others(2): Show |
12 | HG00438.hp1 HG01175.hp2 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.1384-682_1384-677d others(8): Show |
FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr6 | 35462097 | ||||||
| chr6:35462110 | A | AATAATT | 32 | a0001c0001t0001g0020 a0001c0001t0001g0119 a0001c0001t0001g0120 others(29): Show |
89 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.1384-677_1384-676i others(8): Show |
FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr6 | 35462110 | ||||||
| chr6:35462110 | A | AATTATT | 22 | a0001c0001t0001g0031 a0001c0001t0001g0039 a0001c0001t0001g0070 others(19): Show |
52 | HG01069.hp1 HG02055.hp1 HG02083.hp1 others(49): Show |
intron_variant | MODIFIER | c.1384-675_1384-670d others(8): Show |
FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr6 | 35462110 | ||||||
| chr6:35462110 | A | T | 1 | a0001c0002t0001g0053 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1384-679A>T | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 8/9 | chr6 | 35462110 | |||||||
| chr6:35462113 | T | A | 8 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0033 others(5): Show |
25 | HG00642.hp1 HG00741.hp1 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.1384-676T>A | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 8/9 | chr6 | 35462113 | |||||||
| chr6:35462117 | A | ATTAT | 14 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0032 others(11): Show |
33 | HG00642.hp1 HG00741.hp1 HG01074.hp1 others(30): Show |
intron_variant | MODIFIER | c.1384-670_1384-669i others(6): Show |
FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr6 | 35462117 | ||||||
| chr6:35462117 | A | T | 23 | a0002c0003t0001g0036 a0002c0003t0002g0003 a0002c0003t0002g0019 others(20): Show |
66 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.1384-672A>T | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 8/9 | chr6 | 35462117 | |||||||
| chr6:35462297 | G | A | 24 | a0002c0003t0001g0036 a0002c0003t0002g0003 a0002c0003t0002g0019 others(21): Show |
69 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.1384-492G>A | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 8/9 | chr6 | 35462297 | |||||||
| chr6:35462353 | C | T | 2 | a0001c0001t0001g0033 a0001c0001t0001g0077 |
3 | HG02109.hp1 HG02145.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1384-436C>T | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 8/9 | chr6 | 35462353 | |||||||
| chr6:35462381 | A | G | 1 | a0001c0001t0001g0077 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1384-408A>G | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 8/9 | chr6 | 35462381 | |||||||
| chr6:35462388 | T | C | 1 | a0001c0004t0001g0063 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1384-401T>C | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 8/9 | chr6 | 35462388 | |||||||
| chr6:35462723 | A | C | 2 | a0004c0007t0001g0016 a0004c0007t0001g0074 |
5 | NA18960.hp1 NA18965.hp2 NA18967.hp2 others(2): Show |
intron_variant | MODIFIER | c.1384-66A>C | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 8/9 | chr6 | 35462723 | |||||||
| chr6:35462922 | T | C | 1 | a0001c0001t0003g0113 | 1 | HG02080.hp1 | splice_region_variant&intron_variant | LOW | c.1509+8T>C | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 9/9 | chr6 | 35462922 | |||||||
| chr6:35463144 | C | G | 8 | a0001c0001t0003g0008 a0001c0001t0003g0012 a0001c0001t0003g0044 others(5): Show |
23 | HG01433.hp1 HG01975.hp1 HG01975.hp2 others(20): Show |
intron_variant | MODIFIER | c.1509+230C>G | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 9/9 | chr6 | 35463144 | |||||||
| chr6:35463325 | A | T | 2 | a0001c0002t0001g0021 a0013c0015t0001g0021 |
3 | NA18947.hp2 NA18975.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.1509+411A>T | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 9/9 | chr6 | 35463325 | |||||||
| chr6:35463412 | C | A | 1 | a0001c0001t0001g0076 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1509+498C>A | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 9/9 | chr6 | 35463412 | |||||||
| chr6:35463433 | G | C | 3 | a0001c0001t0003g0012 a0001c0001t0003g0044 a0001c0001t0003g0115 |
9 | HG01433.hp1 HG01975.hp2 NA18968.hp2 others(6): Show |
intron_variant | MODIFIER | c.1509+519G>C | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 9/9 | chr6 | 35463433 | |||||||
| chr6:35463524 | A | C | 1 | a0002c0003t0002g0106 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1509+610A>C | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 9/9 | chr6 | 35463524 | |||||||
| chr6:35463584 | G | A | 1 | a0001c0001t0001g0109 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1509+670G>A | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 9/9 | chr6 | 35463584 | |||||||
| chr6:35463612 | G | A | 25 | a0001c0001t0001g0086 a0002c0003t0001g0036 a0002c0003t0002g0003 others(22): Show |
70 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.1509+698G>A | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 9/9 | chr6 | 35463612 | |||||||
| chr6:35463625 | G | A | 1 | a0001c0001t0001g0070 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1509+711G>A | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 9/9 | chr6 | 35463625 | |||||||
| chr6:35463663 | C | CTTT | 21 | a0002c0003t0002g0003 a0002c0003t0002g0019 a0002c0003t0002g0025 others(18): Show |
64 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.1509+763_1509+765d others(5): Show |
FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr6 | 35463663 | ||||||
| chr6:35463725 | G | A | 1 | a0012c0018t0001g0087 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1509+811G>A | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 9/9 | chr6 | 35463725 | |||||||
| chr6:35463854 | C | T | 2 | a0004c0007t0001g0016 a0004c0007t0001g0074 |
5 | NA18960.hp1 NA18965.hp2 NA18967.hp2 others(2): Show |
intron_variant | MODIFIER | c.1509+940C>T | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 9/9 | chr6 | 35463854 | |||||||
| chr6:35463934 | G | A | 24 | a0002c0003t0001g0036 a0002c0003t0002g0003 a0002c0003t0002g0019 others(21): Show |
69 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.1509+1020G>A | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 9/9 | chr6 | 35463934 | |||||||
| chr6:35464036 | C | T | 1 | a0001c0001t0001g0111 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1509+1122C>T | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 9/9 | chr6 | 35464036 | |||||||
| chr6:35464062 | G | A | 24 | a0002c0003t0001g0036 a0002c0003t0002g0003 a0002c0003t0002g0019 others(21): Show |
69 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.1509+1148G>A | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 9/9 | chr6 | 35464062 | |||||||
| chr6:35464116 | G | T | 14 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0032 others(11): Show |
33 | HG00642.hp1 HG00741.hp1 HG01074.hp1 others(30): Show |
intron_variant | MODIFIER | c.1509+1202G>T | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 9/9 | chr6 | 35464116 | |||||||
| chr6:35464155 | T | A | 24 | a0002c0003t0001g0036 a0002c0003t0002g0003 a0002c0003t0002g0019 others(21): Show |
69 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.1509+1241T>A | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 9/9 | chr6 | 35464155 | |||||||
| chr6:35464234 | CT | C | 67 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(64): Show |
245 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(242): Show |
intron_variant | MODIFIER | c.1509+1342delT | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr6 | 35464234 | ||||||
| chr6:35464234 | CTT | C | 20 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0020 others(17): Show |
43 | HG00642.hp1 HG00741.hp1 HG01074.hp1 others(40): Show |
intron_variant | MODIFIER | c.1509+1341_1509+134 others(6): Show |
FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr6 | 35464234 | ||||||
| chr6:35464234 | CTTTT | C | 22 | a0002c0003t0001g0036 a0002c0003t0002g0003 a0002c0003t0002g0019 others(19): Show |
65 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.1509+1339_1509+134 others(8): Show |
FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr6 | 35464234 | ||||||
| chr6:35464261 | C | T | 19 | a0002c0003t0002g0003 a0002c0003t0002g0019 a0002c0003t0002g0026 others(16): Show |
50 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.1509+1347C>T | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 9/9 | chr6 | 35464261 | |||||||
| chr6:35464299 | C | T | 1 | a0001c0001t0001g0080 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1509+1385C>T | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 9/9 | chr6 | 35464299 | |||||||
| chr6:35464306 | C | T | 1 | a0001c0001t0001g0078 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1509+1392C>T | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 9/9 | chr6 | 35464306 | |||||||
| chr6:35464394 | T | C | 75 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0020 others(72): Show |
190 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(187): Show |
intron_variant | MODIFIER | c.1509+1480T>C | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 9/9 | chr6 | 35464394 | |||||||
| chr6:35464527 | G | A | 24 | a0002c0003t0001g0036 a0002c0003t0002g0003 a0002c0003t0002g0019 others(21): Show |
69 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.1509+1613G>A | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 9/9 | chr6 | 35464527 | |||||||
| chr6:35464533 | G | A | 24 | a0002c0003t0001g0036 a0002c0003t0002g0003 a0002c0003t0002g0019 others(21): Show |
69 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.1509+1619G>A | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 9/9 | chr6 | 35464533 | |||||||
| chr6:35464672 | C | G | 1 | a0001c0001t0001g0090 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1510-1572C>G | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 9/9 | chr6 | 35464672 | |||||||
| chr6:35464724 | T | C | 1 | a0001c0001t0003g0115 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1510-1520T>C | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 9/9 | chr6 | 35464724 | |||||||
| chr6:35464725 | ATTCTT | A | 6 | a0001c0001t0003g0008 a0001c0001t0003g0012 a0001c0001t0003g0112 others(3): Show |
20 | HG01433.hp1 HG01978.hp1 HG02004.hp2 others(17): Show |
intron_variant | MODIFIER | c.1510-1516_1510-151 others(9): Show |
FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr6 | 35464725 | ||||||
| chr6:35464728 | C | CT | 12 | a0001c0001t0001g0011 a0001c0001t0001g0092 a0001c0001t0001g0110 others(9): Show |
19 | HG00558.hp2 HG00621.hp1 HG00673.hp1 others(16): Show |
intron_variant | MODIFIER | c.1510-1494dupT | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr6 | 35464728 | ||||||
| chr6:35464728 | CT | C | 23 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0017 others(20): Show |
46 | HG00642.hp1 HG00741.hp1 HG01074.hp1 others(43): Show |
intron_variant | MODIFIER | c.1510-1494delT | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr6 | 35464728 | ||||||
| chr6:35464728 | CTT | C | 5 | a0001c0001t0001g0020 a0001c0001t0001g0071 a0001c0004t0001g0064 others(2): Show |
11 | HG01069.hp1 HG02055.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.1510-1495_1510-149 others(6): Show |
FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr6 | 35464728 | ||||||
| chr6:35464728 | CTTT | C | 17 | a0001c0001t0001g0031 a0001c0001t0001g0039 a0001c0001t0001g0070 others(14): Show |
44 | HG02083.hp1 HG02155.hp2 HG02257.hp1 others(41): Show |
intron_variant | MODIFIER | c.1510-1496_1510-149 others(7): Show |
FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr6 | 35464728 | ||||||
| chr6:35464772 | G | A | 22 | a0001c0001t0001g0031 a0001c0001t0001g0039 a0001c0001t0001g0070 others(19): Show |
52 | HG01069.hp1 HG02055.hp1 HG02083.hp1 others(49): Show |
intron_variant | MODIFIER | c.1510-1472G>A | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 9/9 | chr6 | 35464772 | |||||||
| chr6:35464877 | C | T | 14 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0032 others(11): Show |
33 | HG00642.hp1 HG00741.hp1 HG01074.hp1 others(30): Show |
intron_variant | MODIFIER | c.1510-1367C>T | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 9/9 | chr6 | 35464877 | |||||||
| chr6:35464908 | G | T | 1 | a0001c0002t0001g0073 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1510-1336G>T | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 9/9 | chr6 | 35464908 | |||||||
| chr6:35464941 | A | G | 24 | a0002c0003t0001g0036 a0002c0003t0002g0003 a0002c0003t0002g0019 others(21): Show |
69 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.1510-1303A>G | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 9/9 | chr6 | 35464941 | |||||||
| chr6:35464980 | C | G | 8 | a0001c0001t0003g0008 a0001c0001t0003g0012 a0001c0001t0003g0044 others(5): Show |
23 | HG01433.hp1 HG01975.hp1 HG01975.hp2 others(20): Show |
intron_variant | MODIFIER | c.1510-1264C>G | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 9/9 | chr6 | 35464980 | |||||||
| chr6:35465025 | C | T | 1 | a0001c0002t0001g0051 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1510-1219C>T | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 9/9 | chr6 | 35465025 | |||||||
| chr6:35465165 | A | ATATG | 3 | a0001c0001t0001g0039 a0002c0003t0002g0103 a0002c0003t0002g0104 |
4 | HG02895.hp2 HG02897.hp2 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.1510-1061_1510-105 others(8): Show |
FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr6 | 35465165 | ||||||
| chr6:35465185 | G | T | 1 | a0001c0006t0001g0069 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.1510-1059G>T | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 9/9 | chr6 | 35465185 | |||||||
| chr6:35465186 | T | G | 1 | a0001c0006t0001g0069 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.1510-1058T>G | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 9/9 | chr6 | 35465186 | |||||||
| chr6:35465194 | GAC | G | 1 | a0003c0005t0005g0027 | 3 | HG03098.hp1 HG03209.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1510-1048_1510-104 others(6): Show |
FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr6 | 35465194 | ||||||
| chr6:35465237 | G | A | 3 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0121 |
3 | HG02698.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1510-1007G>A | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 9/9 | chr6 | 35465237 | |||||||
| chr6:35465309 | G | T | 14 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0032 others(11): Show |
33 | HG00642.hp1 HG00741.hp1 HG01074.hp1 others(30): Show |
intron_variant | MODIFIER | c.1510-935G>T | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 9/9 | chr6 | 35465309 | |||||||
| chr6:35465330 | C | T | 1 | a0001c0001t0001g0013 | 5 | HG02145.hp1 HG02717.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1510-914C>T | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 9/9 | chr6 | 35465330 | |||||||
| chr6:35465331 | G | A | 50 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0020 others(47): Show |
120 | HG00642.hp1 HG00741.hp1 HG01069.hp1 others(117): Show |
intron_variant | MODIFIER | c.1510-913G>A | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 9/9 | chr6 | 35465331 | |||||||
| chr6:35465348 | A | G | 1 | a0001c0001t0001g0090 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1510-896A>G | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 9/9 | chr6 | 35465348 | |||||||
| chr6:35465447 | G | T | 24 | a0002c0003t0001g0036 a0002c0003t0002g0003 a0002c0003t0002g0019 others(21): Show |
69 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.1510-797G>T | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 9/9 | chr6 | 35465447 | |||||||
| chr6:35465661 | G | A | 1 | a0001c0001t0001g0034 | 2 | HG02735.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1510-583G>A | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 9/9 | chr6 | 35465661 | |||||||
| chr6:35465908 | A | G | 19 | a0001c0001t0001g0031 a0001c0001t0001g0070 a0001c0001t0001g0071 others(16): Show |
48 | HG01069.hp1 HG02055.hp1 HG02083.hp1 others(45): Show |
intron_variant | MODIFIER | c.1510-336A>G | FANCE | ENSG00000112039.6 | transcript | ENST00000229769.3 | protein_coding | 9/9 | chr6 | 35465908 |