Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 4689 |
| ensemblid | ENSG00000100365.16 |
| hgncid | 7662 |
| symbol | NCF4 |
| name | neutrophil cytosolic factor 4 |
| refseq_nuc | NM_000631.5 |
| refseq_prot | NP_000622.2 |
| ensembl_nuc | ENST00000248899.11 |
| ensembl_prot | ENSP00000248899.6 |
| mane_status | MANE Select |
| chr | chr22 |
| start | 36861006 |
| end | 36878015 |
| strand | + |
| ver | v1.2 |
| region | chr22:36861006-36878015 |
| region5000 | chr22:36856006-36883015 |
| regionname0 | NCF4_chr22_36861006_36878015 |
| regionname5000 | NCF4_chr22_36856006_36883015 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 339 | 429 | 91 | 81 | 188 | 18 | 49 | 144 | NCF4_chr22_36856006_36883015 | NCF4 | MAVAQ others(334): Show |
chr22 | 36856006 | 36883015 |
| a0002 | 0/0 | 339 | 2 | 0 | 1 | 1 | 0 | 0 | 1 | NCF4_chr22_36856006_36883015 | NCF4 | MAVAQ others(334): Show |
chr22 | 36856006 | 36883015 |
| a0003 | 0/0 | 339 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | MAVAQ others(334): Show |
chr22 | 36856006 | 36883015 |
| a0004 | 0/0 | 339 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | MAVAQ others(334): Show |
chr22 | 36856006 | 36883015 |
| a0005 | 0/0 | 339 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NCF4_chr22_36856006_36883015 | NCF4 | MAVAQ others(334): Show |
chr22 | 36856006 | 36883015 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1017 | 333 | 33 | 67 | 171 | 16 | 44 | NCF4_chr22_36856006_36883015 | NCF4 | ATGGC others(1012): Show |
chr22 | 36856006 | 36883015 | ||
| a0001c0002 | 0/0 | 1017 | 36 | 21 | 9 | 6 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | ATGGC others(1012): Show |
chr22 | 36856006 | 36883015 | ||
| a0001c0003 | 0/0 | 1017 | 13 | 10 | 1 | 0 | 1 | 1 | NCF4_chr22_36856006_36883015 | NCF4 | ATGGC others(1012): Show |
chr22 | 36856006 | 36883015 | ||
| a0001c0004 | 0/0 | 1017 | 12 | 2 | 0 | 10 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | ATGGC others(1012): Show |
chr22 | 36856006 | 36883015 | ||
| a0001c0005 | 0/0 | 1017 | 12 | 3 | 3 | 1 | 1 | 4 | NCF4_chr22_36856006_36883015 | NCF4 | ATGGC others(1012): Show |
chr22 | 36856006 | 36883015 | ||
| a0001c0006 | 0/0 | 1017 | 10 | 10 | 0 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | ATGGC others(1012): Show |
chr22 | 36856006 | 36883015 | ||
| a0001c0007 | 0/0 | 1017 | 8 | 8 | 0 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | ATGGC others(1012): Show |
chr22 | 36856006 | 36883015 | ||
| a0001c0008 | 0/0 | 1017 | 3 | 3 | 0 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | ATGGC others(1012): Show |
chr22 | 36856006 | 36883015 | ||
| a0001c0012 | 0/0 | 1017 | 1 | 0 | 1 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | ATGGC others(1012): Show |
chr22 | 36856006 | 36883015 | ||
| a0001c0014 | 0/0 | 1017 | 1 | 1 | 0 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | ATGGC others(1012): Show |
chr22 | 36856006 | 36883015 | ||
| a0002c0009 | 0/0 | 1017 | 2 | 0 | 1 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | ATGGC others(1012): Show |
chr22 | 36856006 | 36883015 | ||
| a0003c0010 | 0/0 | 1017 | 1 | 1 | 0 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | ATGGC others(1012): Show |
chr22 | 36856006 | 36883015 | ||
| a0004c0013 | 0/0 | 1017 | 1 | 0 | 0 | 0 | 0 | 1 | NCF4_chr22_36856006_36883015 | NCF4 | ATGGC others(1012): Show |
chr22 | 36856006 | 36883015 | ||
| a0005c0011 | 0/0 | 1017 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | ATGGC others(1012): Show |
chr22 | 36856006 | 36883015 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1378 | 312 | 29 | 66 | 159 | 16 | 40 | NCF4_chr22_36856006_36883015 | NCF4 | AGACT others(1373): Show |
chr22 | 36856006 | 36883015 |
| a0001c0001t0002 | 0/0 | 1378 | 16 | 0 | 1 | 11 | 0 | 4 | NCF4_chr22_36856006_36883015 | NCF4 | AGACT others(1373): Show |
chr22 | 36856006 | 36883015 |
| a0001c0001t0003 | 0/0 | 1378 | 4 | 4 | 0 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | AGACT others(1373): Show |
chr22 | 36856006 | 36883015 |
| a0001c0001t0005 | 0/0 | 1378 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | AGGCT others(1373): Show |
chr22 | 36856006 | 36883015 |
| a0001c0002t0001 | 0/0 | 1378 | 32 | 19 | 9 | 4 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | AGACT others(1373): Show |
chr22 | 36856006 | 36883015 |
| a0001c0002t0002 | 0/0 | 1378 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | AGACT others(1373): Show |
chr22 | 36856006 | 36883015 |
| a0001c0002t0003 | 0/0 | 1378 | 2 | 2 | 0 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | AGACT others(1373): Show |
chr22 | 36856006 | 36883015 |
| a0001c0002t0004 | 0/0 | 1378 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | AGACT others(1373): Show |
chr22 | 36856006 | 36883015 |
| a0001c0003t0001 | 0/0 | 1378 | 13 | 10 | 1 | 0 | 1 | 1 | NCF4_chr22_36856006_36883015 | NCF4 | AGACT others(1373): Show |
chr22 | 36856006 | 36883015 |
| a0001c0004t0001 | 0/0 | 1378 | 12 | 2 | 0 | 10 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | AGACT others(1373): Show |
chr22 | 36856006 | 36883015 |
| a0001c0005t0001 | 0/0 | 1378 | 11 | 3 | 3 | 1 | 0 | 4 | NCF4_chr22_36856006_36883015 | NCF4 | AGACT others(1373): Show |
chr22 | 36856006 | 36883015 |
| a0001c0005t0002 | 0/0 | 1378 | 1 | 0 | 0 | 0 | 1 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | AGACT others(1373): Show |
chr22 | 36856006 | 36883015 |
| a0001c0006t0001 | 0/0 | 1378 | 9 | 9 | 0 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | AGACT others(1373): Show |
chr22 | 36856006 | 36883015 |
| a0001c0006t0003 | 0/0 | 1378 | 1 | 1 | 0 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | AGACT others(1373): Show |
chr22 | 36856006 | 36883015 |
| a0001c0007t0001 | 0/0 | 1378 | 7 | 7 | 0 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | AGACT others(1373): Show |
chr22 | 36856006 | 36883015 |
| a0001c0007t0003 | 0/0 | 1378 | 1 | 1 | 0 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | AGACT others(1373): Show |
chr22 | 36856006 | 36883015 |
| a0001c0008t0001 | 0/0 | 1378 | 3 | 3 | 0 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | AGACT others(1373): Show |
chr22 | 36856006 | 36883015 |
| a0001c0012t0001 | 0/0 | 1378 | 1 | 0 | 1 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | AGACT others(1373): Show |
chr22 | 36856006 | 36883015 |
| a0001c0014t0001 | 0/0 | 1378 | 1 | 1 | 0 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | AGACT others(1373): Show |
chr22 | 36856006 | 36883015 |
| a0002c0009t0001 | 0/0 | 1378 | 2 | 0 | 1 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | AGACT others(1373): Show |
chr22 | 36856006 | 36883015 |
| a0003c0010t0001 | 0/0 | 1378 | 1 | 1 | 0 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | AGACT others(1373): Show |
chr22 | 36856006 | 36883015 |
| a0004c0013t0001 | 0/0 | 1378 | 1 | 0 | 0 | 0 | 0 | 1 | NCF4_chr22_36856006_36883015 | NCF4 | AGACT others(1373): Show |
chr22 | 36856006 | 36883015 |
| a0005c0011t0001 | 0/0 | 1378 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | AGACT others(1373): Show |
chr22 | 36856006 | 36883015 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 1/0 | 20 | 0 | 3 | 12 | 1 | 3 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0002 | 0/0 | 18 | 0 | 0 | 17 | 0 | 1 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0003 | 0/0 | 13 | 0 | 6 | 6 | 0 | 1 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0004 | 0/0 | 9 | 0 | 3 | 5 | 0 | 1 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0006 | 0/0 | 7 | 0 | 1 | 5 | 0 | 1 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0007 | 0/0 | 7 | 0 | 3 | 3 | 1 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0008 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0009 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0019 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0021 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0047 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0049 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0105 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0002g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0002g0023 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0003g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0003g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0003g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0001t0005g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0002t0001g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0002t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0002t0001g0028 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0002t0001g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0002t0001g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0002t0001g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0002t0001g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0002t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0002t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0002t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0002t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0002t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0002t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0002t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0002t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0002t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0002t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0002t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0002t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0002t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0002t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0002t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0002t0003g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0002t0003g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0002t0004g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0003t0001g0011 | 0/0 | 3 | 2 | 0 | 0 | 1 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0003t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0003t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0003t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0003t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0003t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0003t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0003t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0003t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0003t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0003t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0004t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0004t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0004t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0004t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0004t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0004t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0004t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0004t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0004t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0004t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0004t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0004t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0005t0001g0027 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0005t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0005t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0005t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0005t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0005t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0005t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0005t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0005t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0005t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0005t0002g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0006t0001g0005 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0006t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0006t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0006t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0006t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0006t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0006t0003g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0007t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0007t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0007t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0007t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0007t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0007t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0007t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0007t0003g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0008t0001g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0012t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0001c0014t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0002c0009t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0002c0009t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0003c0010t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0004c0013t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| a0005c0011t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0005 | t0002 | g0050 | EUR | GBR | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0292 | EUR | GBR | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0103 | EUR | GBR | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0017 | EUR | GBR | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0033 | EUR | FIN | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0021 | EUR | FIN | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0088 | EUR | FIN | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | CHS | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | CHS | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | CHS | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | CHS | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | CHS | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | CHS | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | CHS | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | CHS | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG00639 | hp2 | a0001 | c0003 | t0001 | g0096 | AMR | PUR | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0293 | AMR | PUR | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG00673 | hp1 | a0001 | c0004 | t0001 | g0144 | EAS | CHS | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | CHS | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0259 | AMR | PUR | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0284 | AMR | PUR | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG01106 | hp2 | a0001 | c0005 | t0001 | g0176 | AMR | PUR | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0287 | AMR | PUR | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG01243 | hp1 | a0001 | c0012 | t0001 | g0040 | AMR | PUR | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0261 | AMR | PUR | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG01255 | hp1 | a0001 | c0002 | t0001 | g0126 | AMR | CLM | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | CLM | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG01261 | hp1 | a0001 | c0005 | t0001 | g0043 | AMR | CLM | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG01261 | hp2 | a0001 | c0002 | t0001 | g0029 | AMR | CLM | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | CLM | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | CLM | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG01358 | hp1 | a0001 | c0002 | t0001 | g0034 | AMR | CLM | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG01361 | hp2 | a0001 | c0002 | t0001 | g0029 | AMR | CLM | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0263 | AMR | CLM | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0249 | AMR | CLM | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0188 | EUR | IBS | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0015 | EUR | IBS | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0047 | EUR | IBS | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG01516 | hp2 | a0001 | c0003 | t0001 | g0011 | EUR | IBS | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0007 | EUR | IBS | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0047 | EUR | IBS | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | ACB | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | ACB | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG01891 | hp1 | a0001 | c0002 | t0001 | g0010 | AFR | ACB | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG01891 | hp2 | a0001 | c0005 | t0001 | g0083 | AFR | ACB | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0248 | AMR | PEL | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PEL | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG01943 | hp1 | a0001 | c0005 | t0001 | g0273 | AMR | PEL | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0245 | AMR | PEL | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG01952 | hp2 | a0001 | c0002 | t0001 | g0272 | AMR | PEL | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG01975 | hp1 | a0001 | c0002 | t0001 | g0136 | AMR | PEL | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG01975 | hp2 | a0002 | c0009 | t0001 | g0241 | AMR | PEL | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG01981 | hp2 | a0001 | c0002 | t0001 | g0110 | AMR | PEL | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PEL | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0059 | EAS | KHV | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | KHV | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG02055 | hp1 | a0001 | c0008 | t0001 | g0005 | AFR | ACB | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG02055 | hp2 | a0001 | c0006 | t0001 | g0005 | AFR | ACB | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | KHV | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | KHV | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | KHV | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | KHV | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | KHV | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | KHV | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | KHV | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | KHV | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | KHV | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0057 | EAS | KHV | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | ACB | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG02145 | hp2 | a0001 | c0003 | t0001 | g0077 | AFR | ACB | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0060 | AMR | PEL | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | CDX | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG02257 | hp1 | a0001 | c0002 | t0001 | g0072 | AFR | ACB | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | ACB | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG02258 | hp1 | a0001 | c0005 | t0001 | g0269 | AFR | ACB | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | ACB | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG02280 | hp1 | a0001 | c0002 | t0001 | g0046 | AFR | ACB | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG02280 | hp2 | a0001 | c0003 | t0001 | g0258 | AFR | ACB | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG02293 | hp2 | a0001 | c0002 | t0001 | g0028 | AMR | PEL | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG02451 | hp1 | a0001 | c0006 | t0001 | g0266 | AFR | ACB | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG02451 | hp2 | a0001 | c0006 | t0001 | g0081 | AFR | ACB | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | KHV | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0264 | AFR | GWD | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG02572 | hp2 | a0001 | c0002 | t0001 | g0045 | AFR | GWD | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0056 | SAS | PJL | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0237 | SAS | PJL | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | GWD | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG02615 | hp2 | a0001 | c0002 | t0001 | g0196 | AFR | GWD | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG02622 | hp1 | a0001 | c0003 | t0001 | g0208 | AFR | GWD | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0244 | AFR | GWD | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | GWD | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG02647 | hp1 | a0001 | c0006 | t0001 | g0005 | AFR | GWD | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG02647 | hp2 | a0001 | c0002 | t0003 | g0067 | AFR | GWD | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0089 | SAS | PJL | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0236 | SAS | PJL | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0063 | SAS | PJL | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG02723 | hp1 | a0001 | c0006 | t0001 | g0005 | AFR | GWD | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG02723 | hp2 | a0001 | c0002 | t0001 | g0200 | AFR | GWD | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0106 | SAS | PJL | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0211 | SAS | PJL | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG02738 | hp2 | a0001 | c0005 | t0001 | g0179 | SAS | PJL | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG02809 | hp1 | a0001 | c0004 | t0001 | g0076 | AFR | GWD | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG02809 | hp2 | a0001 | c0007 | t0001 | g0223 | AFR | GWD | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG02818 | hp1 | a0001 | c0002 | t0001 | g0045 | AFR | GWD | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | GWD | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG02886 | hp1 | a0001 | c0014 | t0001 | g0064 | AFR | GWD | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | GWD | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG02895 | hp1 | a0003 | c0010 | t0001 | g0074 | AFR | GWD | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG02895 | hp2 | a0001 | c0007 | t0001 | g0275 | AFR | GWD | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG02896 | hp1 | a0001 | c0003 | t0001 | g0182 | AFR | GWD | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0267 | AFR | GWD | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG02922 | hp1 | a0001 | c0007 | t0001 | g0040 | AFR | ESN | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | ESN | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG02965 | hp1 | a0001 | c0002 | t0003 | g0068 | AFR | ESN | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG02965 | hp2 | a0001 | c0006 | t0001 | g0278 | AFR | ESN | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0243 | AFR | ESN | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG02970 | hp2 | a0001 | c0002 | t0001 | g0084 | AFR | ESN | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG02976 | hp1 | a0001 | c0005 | t0001 | g0085 | AFR | ESN | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0024 | AFR | ESN | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0298 | SAS | PJL | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0285 | AFR | GWD | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG03041 | hp2 | a0001 | c0002 | t0001 | g0010 | AFR | GWD | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG03098 | hp1 | a0001 | c0008 | t0001 | g0005 | AFR | MSL | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | MSL | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG03130 | hp1 | a0001 | c0004 | t0001 | g0222 | AFR | ESN | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG03130 | hp2 | a0001 | c0003 | t0001 | g0204 | AFR | ESN | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0024 | AFR | ESN | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0276 | AFR | ESN | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG03195 | hp1 | a0001 | c0003 | t0001 | g0011 | AFR | ESN | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | ESN | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG03209 | hp1 | a0001 | c0002 | t0001 | g0070 | AFR | MSL | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG03209 | hp2 | a0001 | c0002 | t0001 | g0274 | AFR | MSL | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG03225 | hp1 | a0001 | c0002 | t0001 | g0010 | AFR | MSL | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG03225 | hp2 | a0001 | c0007 | t0001 | g0140 | AFR | MSL | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0181 | SAS | PJL | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | MSL | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG03486 | hp2 | a0001 | c0002 | t0001 | g0221 | AFR | MSL | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG03491 | hp1 | a0001 | c0003 | t0001 | g0242 | SAS | PJL | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG03516 | hp1 | a0001 | c0002 | t0001 | g0025 | AFR | ESN | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG03516 | hp2 | a0001 | c0002 | t0001 | g0071 | AFR | ESN | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | GWD | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG03540 | hp2 | a0001 | c0007 | t0003 | g0069 | AFR | GWD | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG03579 | hp1 | a0001 | c0006 | t0003 | g0065 | AFR | MSL | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG03579 | hp2 | a0001 | c0006 | t0001 | g0073 | AFR | MSL | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG03654 | hp2 | a0001 | c0005 | t0001 | g0277 | SAS | PJL | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0296 | SAS | PJL | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG03688 | hp1 | a0001 | c0005 | t0001 | g0027 | SAS | STU | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0108 | SAS | STU | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0239 | SAS | PJL | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0202 | SAS | PJL | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0256 | SAS | PJL | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0297 | SAS | PJL | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0207 | SAS | BEB | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0062 | SAS | BEB | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0299 | SAS | BEB | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0279 | SAS | BEB | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0049 | SAS | BEB | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0240 | SAS | BEB | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0148 | SAS | BEB | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0201 | SAS | BEB | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG04115 | hp1 | a0004 | c0013 | t0001 | g0171 | SAS | STU | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0210 | SAS | STU | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0023 | SAS | STU | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | STU | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0286 | SAS | STU | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | STU | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG04228 | hp1 | a0001 | c0005 | t0001 | g0027 | SAS | STU | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | STU | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | YRI | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0066 | AFR | YRI | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | CHB | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | CHB | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHB | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | CHB | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA18906 | hp1 | a0001 | c0006 | t0001 | g0005 | AFR | YRI | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA18906 | hp2 | a0001 | c0002 | t0001 | g0268 | AFR | YRI | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA18944 | hp1 | a0001 | c0004 | t0001 | g0251 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA18960 | hp1 | a0001 | c0002 | t0002 | g0054 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA18961 | hp2 | a0005 | c0011 | t0001 | g0043 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA18966 | hp1 | a0001 | c0002 | t0001 | g0158 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA18972 | hp1 | a0001 | c0004 | t0001 | g0143 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA18975 | hp2 | a0001 | c0004 | t0001 | g0295 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA18977 | hp1 | a0001 | c0004 | t0001 | g0225 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA18978 | hp1 | a0001 | c0004 | t0001 | g0260 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA18986 | hp1 | a0001 | c0005 | t0001 | g0288 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA18990 | hp1 | a0001 | c0004 | t0001 | g0280 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA18995 | hp1 | a0001 | c0002 | t0004 | g0214 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA18999 | hp1 | a0001 | c0004 | t0001 | g0125 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA19011 | hp2 | a0002 | c0009 | t0001 | g0001 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA19012 | hp2 | a0001 | c0002 | t0001 | g0166 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA19030 | hp1 | a0001 | c0002 | t0001 | g0046 | AFR | LWK | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | LWK | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA19056 | hp1 | a0001 | c0002 | t0001 | g0253 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA19068 | hp1 | a0001 | c0004 | t0001 | g0159 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA19070 | hp2 | a0001 | c0002 | t0001 | g0028 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA19080 | hp1 | a0001 | c0004 | t0001 | g0167 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA19081 | hp2 | a0001 | c0001 | t0005 | g0147 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA19240 | hp1 | a0001 | c0007 | t0001 | g0230 | AFR | YRI | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | YRI | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA20129 | hp1 | a0001 | c0006 | t0001 | g0198 | AFR | ASW | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA20129 | hp2 | a0001 | c0002 | t0001 | g0025 | AFR | ASW | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0174 | EUR | TSI | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0012 | EUR | TSI | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0218 | EUR | TSI | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0254 | EUR | TSI | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0163 | SAS | GIH | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0184 | SAS | GIH | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG01123 | hp2 | a0001 | c0002 | t0001 | g0034 | AMR | CLM | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG02109 | hp1 | a0001 | c0003 | t0001 | g0234 | AFR | ACB | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | ACB | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | ACB | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0265 | AFR | ACB | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG02559 | hp1 | a0001 | c0003 | t0001 | g0011 | AFR | ACB | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | ACB | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG03471 | hp1 | a0001 | c0008 | t0001 | g0005 | AFR | MSL | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG03471 | hp2 | a0001 | c0007 | t0001 | g0283 | AFR | MSL | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG06807 | hp1 | a0001 | c0007 | t0001 | g0232 | AFR | USA | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| HG06807 | hp2 | a0001 | c0002 | t0001 | g0104 | AFR | USA | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA20300 | hp1 | a0001 | c0003 | t0001 | g0078 | AFR | USA | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | USA | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0262 | AFR | LWK | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| NA21309 | hp2 | a0001 | c0003 | t0001 | g0291 | AFR | LWK | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0105 | REF | REF | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0001 | REF | REF | NCF4_chr22_36856006_36883015 | NCF4 | chr22 | 36856006 | 36883015 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:36864973 | C | T | 1 | a0002 | 2 | HG01975.hp2 NA19011.hp2 |
missense_variant | MODERATE | c.172C>T | p.Arg58Cys | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 3/10 | 338/1378 | 172/1020 | 58/339 | chr22 | 36864973 | |||
| chr22:36865055 | C | A | 1 | a0003 | 1 | HG02895.hp1 | missense_variant | MODERATE | c.254C>A | p.Thr85Asn | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 3/10 | 420/1378 | 254/1020 | 85/339 | chr22 | 36865055 | |||
| chr22:36870523 | C | T | 1 | a0004 | 1 | HG04115.hp1 | missense_variant | MODERATE | c.451C>T | p.Arg151Cys | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 5/10 | 617/1378 | 451/1020 | 151/339 | chr22 | 36870523 | |||
| chr22:36877737 | G | T | 1 | a0005 | 1 | NA18961.hp2 | missense_variant | MODERATE | c.934G>T | p.Gly312Cys | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 10/10 | 1100/1378 | 934/1020 | 312/339 | chr22 | 36877737 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:36864075 | C | T | 3 | a0001c0006 a0001c0008 a0001c0014 |
14 | HG02055.hp1 HG02055.hp2 HG02451.hp1 others(11): Show |
synonymous_variant | LOW | c.63C>T | p.Ala21Ala | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 2/10 | 229/1378 | 63/1020 | 21/339 | chr22 | 36864075 | |||
| chr22:36864081 | G | A | 2 | a0001c0002 a0001c0004 |
48 | HG00673.hp1 HG01123.hp2 HG01255.hp1 others(45): Show |
synonymous_variant | LOW | c.69G>A | p.Ser23Ser | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 2/10 | 235/1378 | 69/1020 | 23/339 | chr22 | 36864081 | |||
| chr22:36865041 | T | C | 1 | a0001c0008 | 3 | HG02055.hp1 HG03098.hp1 HG03471.hp1 |
synonymous_variant | LOW | c.240T>C | p.Ser80Ser | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 3/10 | 406/1378 | 240/1020 | 80/339 | chr22 | 36865041 | |||
| chr22:36875730 | C | T | 1 | a0001c0012 | 1 | HG01243.hp1 | synonymous_variant | LOW | c.705C>T | p.Asp235Asp | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 8/10 | 871/1378 | 705/1020 | 235/339 | chr22 | 36875730 | |||
| chr22:36875760 | C | T | 3 | a0001c0002 a0001c0005 a0005c0011 |
49 | HG00099.hp1 HG01106.hp2 HG01123.hp2 others(46): Show |
synonymous_variant | LOW | c.735C>T | p.Tyr245Tyr | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 8/10 | 901/1378 | 735/1020 | 245/339 | chr22 | 36875760 | |||
| chr22:36877700 | G | A | 5 | a0001c0002 a0001c0005 a0001c0014 others(2): Show |
51 | HG00099.hp1 HG01106.hp2 HG01123.hp2 others(48): Show |
synonymous_variant | LOW | c.897G>A | p.Ser299Ser | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 10/10 | 1063/1378 | 897/1020 | 299/339 | chr22 | 36877700 | |||
| chr22:36877763 | C | T | 1 | a0001c0003 | 13 | HG00639.hp2 HG01516.hp2 HG02109.hp1 others(10): Show |
synonymous_variant | LOW | c.960C>T | p.Phe320Phe | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 10/10 | 1126/1378 | 960/1020 | 320/339 | chr22 | 36877763 | |||
| chr22:36877814 | G | A | 2 | a0001c0007 a0001c0012 |
9 | HG01243.hp1 HG02809.hp2 HG02895.hp2 others(6): Show |
synonymous_variant | LOW | c.1011G>A | p.Thr337Thr | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 10/10 | 1177/1378 | 1011/1020 | 337/339 | chr22 | 36877814 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:36861008 | A | G | 1 | a0001c0001t0005 | 1 | NA19081.hp2 | 5_prime_UTR_variant | MODIFIER | c.-164A>G | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/10 | 164 | chr22 | 36861008 | ||||||
| chr22:36861077 | C | T | 4 | a0001c0001t0003 a0001c0002t0003 a0001c0006t0003 others(1): Show |
8 | HG02647.hp2 HG02965.hp1 HG02976.hp2 others(5): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-95C>T | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/10 | chr22 | 36861077 | |||||||
| chr22:36861135 | G | A | 3 | a0001c0001t0002 a0001c0002t0002 a0001c0005t0002 |
18 | HG00099.hp1 HG02015.hp1 HG02135.hp1 others(15): Show |
5_prime_UTR_variant | MODIFIER | c.-37G>A | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/10 | 37 | chr22 | 36861135 | ||||||
| chr22:36877919 | C | G | 1 | a0001c0002t0004 | 1 | NA18995.hp1 | 3_prime_UTR_variant | MODIFIER | c.*96C>G | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 10/10 | 96 | chr22 | 36877919 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:36861286 | C | T | 4 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0001t0001g0298 others(1): Show |
4 | HG03017.hp1 HG03669.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.32+83C>T | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | chr22 | 36861286 | |||||||
| chr22:36861670 | C | A | 26 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0051 others(23): Show |
36 | HG00099.hp1 HG01891.hp1 HG02015.hp1 others(33): Show |
intron_variant | MODIFIER | c.32+467C>A | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | chr22 | 36861670 | |||||||
| chr22:36861779 | G | T | 2 | a0001c0001t0001g0298 a0001c0001t0001g0299 |
2 | HG03017.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.32+576G>T | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | chr22 | 36861779 | |||||||
| chr22:36861780 | C | T | 65 | a0001c0001t0001g0044 a0001c0001t0001g0047 a0001c0001t0001g0048 others(62): Show |
81 | HG00099.hp2 HG00621.hp2 HG00642.hp1 others(78): Show |
intron_variant | MODIFIER | c.32+577C>T | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | chr22 | 36861780 | |||||||
| chr22:36861813 | G | A | 227 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(224): Show |
322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.32+610G>A | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | chr22 | 36861813 | |||||||
| chr22:36861865 | T | C | 3 | a0001c0001t0001g0201 a0001c0001t0001g0298 a0001c0001t0001g0299 |
3 | HG03017.hp1 HG03834.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.32+662T>C | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | chr22 | 36861865 | |||||||
| chr22:36861891 | A | C | 2 | a0001c0001t0001g0199 a0001c0002t0001g0200 |
2 | HG02723.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.32+688A>C | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | chr22 | 36861891 | |||||||
| chr22:36862134 | C | T | 1 | a0001c0006t0001g0198 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.32+931C>T | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | chr22 | 36862134 | |||||||
| chr22:36862192 | C | T | 1 | a0001c0001t0001g0021 | 3 | HG00280.hp2 HG01081.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.32+989C>T | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | chr22 | 36862192 | |||||||
| chr22:36862210 | G | T | 1 | a0001c0001t0001g0261 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.32+1007G>T | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | chr22 | 36862210 | |||||||
| chr22:36862217 | A | G | 1 | a0001c0001t0001g0197 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.32+1014A>G | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | chr22 | 36862217 | |||||||
| chr22:36862225 | G | A | 8 | a0001c0001t0001g0044 a0001c0001t0001g0262 a0001c0001t0001g0263 others(5): Show |
9 | HG01496.hp1 HG01884.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.32+1022G>A | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | chr22 | 36862225 | |||||||
| chr22:36862246 | G | A | 1 | a0001c0001t0001g0202 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.32+1043G>A | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | chr22 | 36862246 | |||||||
| chr22:36862250 | G | C | 1 | a0001c0001t0001g0202 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.32+1047G>C | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | chr22 | 36862250 | |||||||
| chr22:36862267 | T | C | 3 | a0001c0002t0001g0070 a0001c0002t0001g0071 a0001c0002t0001g0072 |
3 | HG02257.hp1 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.32+1064T>C | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | chr22 | 36862267 | |||||||
| chr22:36862333 | C | T | 8 | a0001c0001t0001g0044 a0001c0001t0001g0262 a0001c0001t0001g0263 others(5): Show |
9 | HG01496.hp1 HG01884.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.32+1130C>T | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | chr22 | 36862333 | |||||||
| chr22:36862461 | T | C | 107 | a0001c0001t0001g0012 a0001c0001t0001g0026 a0001c0001t0001g0044 others(104): Show |
130 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.32+1258T>C | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | chr22 | 36862461 | |||||||
| chr22:36862464 | T | C | 1 | a0001c0006t0001g0073 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.32+1261T>C | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | chr22 | 36862464 | |||||||
| chr22:36862609 | G | C | 40 | a0001c0001t0001g0012 a0001c0001t0001g0026 a0001c0001t0001g0075 others(37): Show |
47 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(44): Show |
intron_variant | MODIFIER | c.32+1406G>C | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | chr22 | 36862609 | |||||||
| chr22:36862655 | A | G | 1 | a0001c0006t0001g0198 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.33-1390A>G | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | chr22 | 36862655 | |||||||
| chr22:36862659 | G | A | 1 | a0001c0001t0001g0101 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.33-1386G>A | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | chr22 | 36862659 | |||||||
| chr22:36862768 | T | C | 1 | a0001c0003t0001g0204 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.33-1277T>C | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | chr22 | 36862768 | |||||||
| chr22:36862771 | A | G | 39 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(36): Show |
45 | HG00099.hp2 HG00621.hp2 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.33-1274A>G | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | chr22 | 36862771 | |||||||
| chr22:36862802 | G | A | 45 | a0001c0001t0001g0075 a0001c0001t0001g0079 a0001c0001t0001g0080 others(42): Show |
57 | HG00099.hp1 HG00140.hp1 HG01516.hp2 others(54): Show |
intron_variant | MODIFIER | c.33-1243G>A | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | chr22 | 36862802 | |||||||
| chr22:36862906 | C | T | 1 | a0001c0002t0001g0196 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.33-1139C>T | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | chr22 | 36862906 | |||||||
| chr22:36862944 | C | T | 102 | a0001c0001t0001g0012 a0001c0001t0001g0026 a0001c0001t0001g0044 others(99): Show |
124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.33-1101C>T | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | chr22 | 36862944 | |||||||
| chr22:36862947 | C | A | 2 | a0001c0001t0001g0107 a0001c0001t0001g0108 |
2 | HG03669.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.33-1098C>A | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | chr22 | 36862947 | |||||||
| chr22:36862996 | C | G | 1 | a0001c0001t0001g0087 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.33-1049C>G | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | chr22 | 36862996 | |||||||
| chr22:36863042 | C | T | 1 | a0001c0001t0001g0259 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.33-1003C>T | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | chr22 | 36863042 | |||||||
| chr22:36863063 | G | T | 1 | a0001c0001t0001g0195 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.33-982G>T | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | chr22 | 36863063 | |||||||
| chr22:36863189 | T | C | 1 | a0001c0001t0001g0201 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.33-856T>C | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | chr22 | 36863189 | |||||||
| chr22:36863231 | C | T | 114 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(111): Show |
180 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.33-814C>T | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | chr22 | 36863231 | |||||||
| chr22:36863266 | G | A | 1 | a0001c0001t0001g0087 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.33-779G>A | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | chr22 | 36863266 | |||||||
| chr22:36863297 | G | A | 8 | a0001c0001t0001g0019 a0001c0001t0001g0205 a0001c0001t0001g0206 others(5): Show |
11 | HG01109.hp2 HG01243.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.33-748G>A | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | chr22 | 36863297 | |||||||
| chr22:36863317 | T | C | 121 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0014 others(118): Show |
140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.33-728T>C | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | chr22 | 36863317 | |||||||
| chr22:36863478 | C | T | 1 | a0001c0001t0001g0250 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.33-567C>T | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | chr22 | 36863478 | |||||||
| chr22:36863492 | G | A | 2 | a0001c0001t0001g0210 a0001c0001t0001g0211 |
2 | HG02735.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.33-553G>A | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | chr22 | 36863492 | |||||||
| chr22:36863563 | T | C | 257 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(254): Show |
337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
intron_variant | MODIFIER | c.33-482T>C | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | chr22 | 36863563 | |||||||
| chr22:36863613 | A | AGCTGTGG others(3138): Show |
1 | a0001c0014t0001g0064 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.33-429_33-428insGT others(3143): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr22 | 36863613 | ||||||
| chr22:36863613 | A | AGCTGTGG others(3138): Show |
2 | a0001c0006t0001g0005 a0001c0008t0001g0005 |
7 | HG02055.hp1 HG02055.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.33-429_33-428insGT others(3143): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr22 | 36863613 | ||||||
| chr22:36863613 | A | AGCTGTGG others(3138): Show |
1 | a0001c0001t0001g0080 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.33-429_33-428insGT others(3143): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr22 | 36863613 | ||||||
| chr22:36863613 | A | AGCTGTGG others(3138): Show |
3 | a0001c0001t0001g0109 a0001c0001t0001g0122 a0001c0001t0002g0053 |
3 | NA19060.hp1 NA19082.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.33-429_33-428insGT others(3143): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr22 | 36863613 | ||||||
| chr22:36863613 | A | AGCTGTGG others(3138): Show |
2 | a0001c0001t0001g0123 a0001c0001t0001g0212 |
2 | NA18747.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.33-429_33-428insGT others(3143): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr22 | 36863613 | ||||||
| chr22:36863613 | A | AGCTGTGG others(3137): Show |
1 | a0001c0001t0001g0124 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.33-429_33-428insGT others(3142): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr22 | 36863613 | ||||||
| chr22:36863613 | A | AGCTGTGG others(3138): Show |
1 | a0001c0001t0001g0213 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.33-429_33-428insGT others(3143): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr22 | 36863613 | ||||||
| chr22:36863613 | A | AGCTGTGG others(3138): Show |
1 | a0001c0006t0001g0081 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.33-429_33-428insGT others(3143): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr22 | 36863613 | ||||||
| chr22:36863613 | A | AGCTGTGG others(3138): Show |
1 | a0001c0006t0003g0065 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.33-429_33-428insGT others(3143): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr22 | 36863613 | ||||||
| chr22:36863613 | A | AGCTGTGG others(3139): Show |
1 | a0001c0001t0001g0287 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.33-429_33-428insGT others(3144): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr22 | 36863613 | ||||||
| chr22:36863613 | A | AGCTGTGG others(3138): Show |
1 | a0001c0001t0001g0279 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.33-429_33-428insGT others(3143): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr22 | 36863613 | ||||||
| chr22:36863613 | A | AGCTGTGG others(3138): Show |
4 | a0001c0001t0001g0030 a0001c0001t0001g0127 a0001c0001t0001g0168 others(1): Show |
5 | NA18973.hp1 NA18977.hp2 NA19003.hp2 others(2): Show |
intron_variant | MODIFIER | c.33-429_33-428insGT others(3143): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr22 | 36863613 | ||||||
| chr22:36863613 | A | AGCTGTGG others(3137): Show |
3 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0169 |
3 | NA18959.hp2 NA19066.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.33-429_33-428insGT others(3142): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr22 | 36863613 | ||||||
| chr22:36863613 | A | AGCTGTGG others(3139): Show |
7 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0148 others(4): Show |
7 | HG03942.hp1 HG04115.hp1 NA18993.hp2 others(4): Show |
intron_variant | MODIFIER | c.33-429_33-428insGT others(3144): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr22 | 36863613 | ||||||
| chr22:36863613 | A | AGCTGTGG others(3138): Show |
1 | a0001c0001t0001g0149 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.33-429_33-428insGT others(3143): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr22 | 36863613 | ||||||
| chr22:36863613 | A | AGCTGTGG others(3138): Show |
64 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(61): Show |
94 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.33-429_33-428insGT others(3143): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr22 | 36863613 | ||||||
| chr22:36863613 | A | AGCTGTGG others(3138): Show |
1 | a0001c0001t0001g0220 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.33-429_33-428insGT others(3143): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr22 | 36863613 | ||||||
| chr22:36863613 | A | AGCTGTGG others(3137): Show |
2 | a0001c0001t0001g0094 a0001c0001t0001g0133 |
2 | HG01109.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.33-429_33-428insGT others(3142): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr22 | 36863613 | ||||||
| chr22:36863613 | A | AGCTGTGG others(3136): Show |
1 | a0001c0001t0001g0134 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.33-429_33-428insGT others(3141): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr22 | 36863613 | ||||||
| chr22:36863613 | A | AGCTGTGG others(3138): Show |
1 | a0001c0001t0002g0052 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.33-429_33-428insGT others(3143): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr22 | 36863613 | ||||||
| chr22:36863613 | A | AGCTGTGG others(3138): Show |
1 | a0001c0006t0001g0266 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.33-429_33-428insGT others(3143): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr22 | 36863613 | ||||||
| chr22:36863613 | A | AGCTGTGG others(3139): Show |
1 | a0001c0001t0001g0117 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.33-429_33-428insGT others(3144): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr22 | 36863613 | ||||||
| chr22:36863613 | A | AGCTGTGG others(3139): Show |
1 | a0001c0001t0001g0118 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.33-429_33-428insGT others(3144): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr22 | 36863613 | ||||||
| chr22:36863613 | A | AGCTGTGG others(3140): Show |
1 | a0001c0001t0001g0103 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.33-429_33-428insGT others(3145): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr22 | 36863613 | ||||||
| chr22:36863613 | A | AGCTGTGG others(3139): Show |
2 | a0001c0001t0001g0015 a0001c0001t0001g0108 |
4 | HG00738.hp2 HG01515.hp2 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-429_33-428insGT others(3144): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr22 | 36863613 | ||||||
| chr22:36863613 | A | AGCTGTGG others(3138): Show |
1 | a0001c0001t0001g0181 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.33-429_33-428insGT others(3143): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr22 | 36863613 | ||||||
| chr22:36863613 | A | AGCTGTGG others(3138): Show |
1 | a0001c0001t0001g0262 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.33-429_33-428insGT others(3143): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr22 | 36863613 | ||||||
| chr22:36863613 | A | AGCTGTGG others(3137): Show |
1 | a0001c0001t0001g0135 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.33-429_33-428insGT others(3142): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr22 | 36863613 | ||||||
| chr22:36863613 | A | AGCTGTGG others(3138): Show |
1 | a0001c0001t0002g0022 | 2 | NA18948.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.33-429_33-428insGT others(3143): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr22 | 36863613 | ||||||
| chr22:36863613 | A | AGCTGTGG others(3138): Show |
4 | a0001c0001t0001g0082 a0001c0001t0003g0066 a0001c0001t0003g0276 others(1): Show |
4 | HG01891.hp2 HG02818.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-429_33-428insGT others(3143): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr22 | 36863613 | ||||||
| chr22:36863613 | A | AGCTGTGG others(3138): Show |
1 | a0001c0001t0001g0100 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.33-429_33-428insGT others(3143): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr22 | 36863613 | ||||||
| chr22:36863613 | A | AGCTGTGG others(3139): Show |
1 | a0001c0001t0002g0062 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.33-429_33-428insGT others(3144): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr22 | 36863613 | ||||||
| chr22:36863613 | A | AGCTGTGG others(3138): Show |
1 | a0001c0003t0001g0291 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.33-429_33-428insGT others(3143): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr22 | 36863613 | ||||||
| chr22:36863613 | A | AGCTGTGG others(3138): Show |
2 | a0001c0006t0001g0073 a0001c0006t0001g0198 |
2 | HG03579.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.33-429_33-428insGT others(3143): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr22 | 36863613 | ||||||
| chr22:36863613 | A | AGCTGTGG others(3138): Show |
1 | a0001c0001t0001g0157 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.33-429_33-428insGT others(3143): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr22 | 36863613 | ||||||
| chr22:36863613 | A | AGCTGTGG others(3138): Show |
1 | a0001c0003t0001g0011 | 3 | HG01516.hp2 HG02559.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.33-429_33-428insGT others(3143): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr22 | 36863613 | ||||||
| chr22:36863613 | A | AGCTGTGG others(3137): Show |
1 | a0001c0003t0001g0182 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.33-429_33-428insGT others(3142): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr22 | 36863613 | ||||||
| chr22:36863613 | A | AGCTGTGG others(3138): Show |
2 | a0001c0001t0001g0263 a0001c0001t0001g0264 |
2 | HG01496.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.33-429_33-428insGT others(3143): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr22 | 36863613 | ||||||
| chr22:36863613 | A | AGCTGTGG others(3138): Show |
1 | a0001c0001t0001g0183 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.33-429_33-428insGT others(3143): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr22 | 36863613 | ||||||
| chr22:36863613 | A | AGCTGTGG others(3139): Show |
1 | a0001c0001t0001g0089 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.33-429_33-428insGT others(3144): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr22 | 36863613 | ||||||
| chr22:36863613 | A | AGCTGTGG others(3138): Show |
1 | a0001c0001t0001g0226 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.33-429_33-428insGT others(3143): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr22 | 36863613 | ||||||
| chr22:36863613 | A | AGCTGTGG others(3139): Show |
1 | a0001c0001t0001g0160 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.33-429_33-428insGT others(3144): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr22 | 36863613 | ||||||
| chr22:36863613 | A | AGCTGTGG others(3138): Show |
1 | a0001c0001t0001g0101 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.33-429_33-428insGT others(3143): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr22 | 36863613 | ||||||
| chr22:36863613 | A | AGCTGTGG others(3139): Show |
4 | a0001c0001t0001g0119 a0001c0001t0001g0137 a0001c0001t0001g0195 others(1): Show |
4 | HG02109.hp2 HG02257.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.33-429_33-428insGT others(3144): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr22 | 36863613 | ||||||
| chr22:36863613 | A | AGCTGTGG others(3137): Show |
1 | a0001c0001t0001g0297 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.33-429_33-428insGT others(3142): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr22 | 36863613 | ||||||
| chr22:36863613 | A | AGCTGTGG others(3138): Show |
43 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0012 others(40): Show |
72 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(69): Show |
intron_variant | MODIFIER | c.33-429_33-428insGT others(3143): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr22 | 36863613 | ||||||
| chr22:36863613 | A | AGCTGTGG others(3138): Show |
1 | a0001c0001t0001g0165 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.33-429_33-428insGT others(3143): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr22 | 36863613 | ||||||
| chr22:36863613 | A | AGCTGTGG others(3137): Show |
1 | a0001c0001t0001g0188 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.33-429_33-428insGT others(3142): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr22 | 36863613 | ||||||
| chr22:36863613 | A | AGCTGTGG others(3138): Show |
1 | a0001c0001t0001g0098 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.33-429_33-428insGT others(3143): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr22 | 36863613 | ||||||
| chr22:36863613 | A | AGCTGTGG others(3140): Show |
1 | a0001c0005t0001g0277 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.33-429_33-428insGT others(3145): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr22 | 36863613 | ||||||
| chr22:36863613 | A | AGCTGTGG others(3139): Show |
2 | a0001c0001t0001g0139 a0001c0001t0001g0256 |
2 | HG03710.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.33-429_33-428insGT others(3144): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr22 | 36863613 | ||||||
| chr22:36863613 | A | AGCTGTGG others(3139): Show |
1 | a0001c0001t0001g0037 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.33-429_33-428insGT others(3144): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr22 | 36863613 | ||||||
| chr22:36863613 | A | AGCTGTGG others(3138): Show |
2 | a0001c0001t0001g0233 a0001c0003t0001g0096 |
2 | HG00639.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.33-429_33-428insGT others(3143): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr22 | 36863613 | ||||||
| chr22:36863613 | A | AGCTGTGG others(3138): Show |
1 | a0001c0006t0001g0278 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.33-429_33-428insGT others(3143): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr22 | 36863613 | ||||||
| chr22:36863613 | A | AGCTGTGG others(3138): Show |
3 | a0001c0001t0001g0235 a0001c0001t0001g0265 a0001c0001t0001g0284 |
3 | HG01099.hp1 HG02486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.33-429_33-428insGT others(3143): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr22 | 36863613 | ||||||
| chr22:36863613 | A | AGCTGTGG others(3138): Show |
2 | a0001c0001t0001g0285 a0001c0001t0001g0293 |
2 | HG00642.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.33-429_33-428insGT others(3143): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr22 | 36863613 | ||||||
| chr22:36863613 | A | AGCTGTGG others(3138): Show |
1 | a0001c0001t0001g0254 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.33-429_33-428insGT others(3143): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr22 | 36863613 | ||||||
| chr22:36863613 | A | AGCTGTGG others(3138): Show |
1 | a0001c0001t0001g0286 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.33-429_33-428insGT others(3143): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr22 | 36863613 | ||||||
| chr22:36863616 | T | TGTGGCCT others(3137): Show |
1 | a0001c0002t0001g0010 | 3 | HG01891.hp1 HG03041.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.33-429_33-428insGT others(3142): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | chr22 | 36863616 | |||||||
| chr22:36863616 | T | TGTGGCCT others(3142): Show |
1 | a0003c0010t0001g0074 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.33-429_33-428insGT others(3147): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | chr22 | 36863616 | |||||||
| chr22:36863616 | T | TGTGGCCT others(3143): Show |
1 | a0001c0004t0001g0143 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.33-429_33-428insGT others(3148): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | chr22 | 36863616 | |||||||
| chr22:36863616 | T | TGTGGCCT others(3138): Show |
2 | a0001c0002t0001g0166 a0001c0004t0001g0125 |
2 | NA18999.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.33-429_33-428insGT others(3143): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | chr22 | 36863616 | |||||||
| chr22:36863616 | T | TGTGGCCT others(3137): Show |
12 | a0001c0002t0001g0028 a0001c0002t0001g0029 a0001c0002t0001g0034 others(9): Show |
15 | HG00673.hp1 HG01123.hp2 HG01255.hp1 others(12): Show |
intron_variant | MODIFIER | c.33-429_33-428insGT others(3142): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | chr22 | 36863616 | |||||||
| chr22:36863616 | T | TGTGGCCT others(3137): Show |
4 | a0001c0002t0001g0046 a0001c0002t0001g0070 a0001c0002t0001g0071 others(1): Show |
5 | HG02280.hp1 HG03209.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.33-429_33-428insGT others(3142): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | chr22 | 36863616 | |||||||
| chr22:36863616 | T | TGTGGCCT others(3140): Show |
1 | a0001c0001t0001g0075 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.33-429_33-428insGT others(3145): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | chr22 | 36863616 | |||||||
| chr22:36863616 | T | TGTGGCCT others(3142): Show |
1 | a0001c0007t0001g0275 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.33-429_33-428insGT others(3147): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | chr22 | 36863616 | |||||||
| chr22:36863616 | T | TGTGGCCT others(3137): Show |
1 | a0001c0002t0001g0196 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.33-429_33-428insGT others(3142): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | chr22 | 36863616 | |||||||
| chr22:36863616 | T | TGTGGCCT others(3137): Show |
2 | a0001c0002t0001g0072 a0001c0002t0001g0221 |
2 | HG02257.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.33-429_33-428insGT others(3142): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | chr22 | 36863616 | |||||||
| chr22:36863616 | T | TGTGGCCT others(3138): Show |
1 | a0001c0003t0001g0208 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.33-429_33-428insGT others(3143): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | chr22 | 36863616 | |||||||
| chr22:36863616 | T | TGTGGCCT others(3137): Show |
1 | a0001c0004t0001g0076 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.33-429_33-428insGT others(3142): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | chr22 | 36863616 | |||||||
| chr22:36863616 | T | TGTGGCCT others(3139): Show |
1 | a0001c0003t0001g0077 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.33-429_33-428insGT others(3144): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | chr22 | 36863616 | |||||||
| chr22:36863616 | T | TGTGGCCT others(3138): Show |
1 | a0001c0003t0001g0078 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.33-429_33-428insGT others(3143): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | chr22 | 36863616 | |||||||
| chr22:36863616 | T | TGTGGCCT others(3138): Show |
1 | a0001c0004t0001g0222 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.33-429_33-428insGT others(3143): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | chr22 | 36863616 | |||||||
| chr22:36863616 | T | TGTGGCCT others(3142): Show |
1 | a0001c0007t0001g0223 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.33-429_33-428insGT others(3147): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | chr22 | 36863616 | |||||||
| chr22:36863616 | T | TGTGGCCT others(3137): Show |
4 | a0001c0002t0001g0025 a0001c0002t0001g0045 a0001c0002t0001g0104 others(1): Show |
6 | HG02572.hp2 HG02818.hp1 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.33-429_33-428insGT others(3142): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | chr22 | 36863616 | |||||||
| chr22:36863616 | T | TGTGGCCT others(3137): Show |
1 | a0001c0002t0001g0084 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.33-429_33-428insGT others(3142): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | chr22 | 36863616 | |||||||
| chr22:36863616 | T | TGTGGCCT others(3139): Show |
1 | a0001c0001t0001g0224 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.33-429_33-428insGT others(3144): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | chr22 | 36863616 | |||||||
| chr22:36863616 | T | TGTGGCCT others(3138): Show |
2 | a0001c0001t0001g0079 a0001c0001t0001g0199 |
2 | HG02922.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.33-429_33-428insGT others(3143): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | chr22 | 36863616 | |||||||
| chr22:36863616 | T | TGTGGCCT others(3137): Show |
7 | a0001c0002t0001g0136 a0001c0002t0001g0158 a0001c0002t0001g0253 others(4): Show |
7 | HG01975.hp1 NA18966.hp1 NA18975.hp2 others(4): Show |
intron_variant | MODIFIER | c.33-429_33-428insGT others(3142): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | chr22 | 36863616 | |||||||
| chr22:36863616 | T | TGTGGCCT others(3137): Show |
2 | a0001c0002t0003g0067 a0001c0002t0003g0068 |
2 | HG02647.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.33-429_33-428insGT others(3142): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | chr22 | 36863616 | |||||||
| chr22:36863616 | T | TGTGGCCT others(3140): Show |
2 | a0001c0001t0001g0203 a0001c0001t0001g0267 |
2 | HG02896.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.33-429_33-428insGT others(3145): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | chr22 | 36863616 | |||||||
| chr22:36863616 | T | TGTGGCCT others(3142): Show |
8 | a0001c0001t0001g0231 a0001c0007t0001g0040 a0001c0007t0001g0140 others(5): Show |
8 | HG01243.hp1 HG02922.hp1 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.33-429_33-428insGT others(3147): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | chr22 | 36863616 | |||||||
| chr22:36863616 | T | TGTGGCCT others(3140): Show |
2 | a0001c0003t0001g0204 a0001c0003t0001g0234 |
2 | HG02109.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.33-429_33-428insGT others(3145): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | chr22 | 36863616 | |||||||
| chr22:36863616 | T | TGTGGCCT others(3143): Show |
1 | a0001c0001t0001g0044 | 2 | HG01884.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.33-429_33-428insGT others(3148): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | chr22 | 36863616 | |||||||
| chr22:36863616 | T | TGTGGCCT others(3137): Show |
1 | a0001c0002t0001g0200 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.33-429_33-428insGT others(3142): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | chr22 | 36863616 | |||||||
| chr22:36863616 | T | TGTGGCCT others(3138): Show |
1 | a0001c0001t0001g0141 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.33-429_33-428insGT others(3143): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | chr22 | 36863616 | |||||||
| chr22:36863773 | C | CTTCCCAT others(9): Show |
1 | a0001c0001t0001g0194 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.33-271_33-256dupTT others(14): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr22 | 36863773 | ||||||
| chr22:36863879 | C | T | 2 | a0001c0001t0001g0009 a0001c0001t0001g0249 |
5 | HG00741.hp2 HG01070.hp2 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.33-166C>T | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | chr22 | 36863879 | |||||||
| chr22:36863965 | T | A | 1 | a0003c0010t0001g0074 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.33-80T>A | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | chr22 | 36863965 | |||||||
| chr22:36863972 | T | TAACCTCA others(26): Show |
1 | a0001c0004t0001g0143 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.33-72_33-71insACCT others(29): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr22 | 36863972 | ||||||
| chr22:36864175 | A | C | 1 | a0001c0001t0001g0248 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.117+46A>C | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 2/9 | chr22 | 36864175 | |||||||
| chr22:36864180 | GCTGACCT others(14): Show |
G | 49 | a0001c0001t0001g0044 a0001c0001t0001g0079 a0001c0001t0001g0141 others(46): Show |
58 | HG00673.hp1 HG01123.hp2 HG01255.hp1 others(55): Show |
intron_variant | MODIFIER | c.117+67_117+87delTG others(19): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr22 | 36864180 | ||||||
| chr22:36864213 | ACCTCCAA others(7): Show |
A | 1 | a0001c0007t0001g0283 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.117+85_117+98delCC others(12): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 2/9 | chr22 | 36864213 | |||||||
| chr22:36864230 | C | G | 1 | a0001c0007t0001g0283 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.117+101C>G | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 2/9 | chr22 | 36864230 | |||||||
| chr22:36864231 | T | C | 1 | a0001c0007t0001g0283 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.117+102T>C | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 2/9 | chr22 | 36864231 | |||||||
| chr22:36864242 | A | G | 1 | a0001c0007t0001g0283 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.117+113A>G | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 2/9 | chr22 | 36864242 | |||||||
| chr22:36864252 | T | C | 1 | a0001c0007t0001g0283 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.117+123T>C | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 2/9 | chr22 | 36864252 | |||||||
| chr22:36864254 | C | A | 1 | a0001c0007t0001g0283 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.117+125C>A | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 2/9 | chr22 | 36864254 | |||||||
| chr22:36864256 | C | A | 1 | a0001c0007t0001g0283 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.117+127C>A | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 2/9 | chr22 | 36864256 | |||||||
| chr22:36864257 | A | G | 1 | a0001c0007t0001g0283 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.117+128A>G | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 2/9 | chr22 | 36864257 | |||||||
| chr22:36864258 | A | C | 1 | a0001c0007t0001g0283 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.117+129A>C | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 2/9 | chr22 | 36864258 | |||||||
| chr22:36864262 | G | T | 1 | a0001c0001t0001g0086 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.117+133G>T | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 2/9 | chr22 | 36864262 | |||||||
| chr22:36864266 | G | C | 1 | a0001c0007t0001g0283 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.117+137G>C | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 2/9 | chr22 | 36864266 | |||||||
| chr22:36864268 | T | C | 1 | a0001c0007t0001g0283 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.117+139T>C | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 2/9 | chr22 | 36864268 | |||||||
| chr22:36864272 | G | A | 1 | a0001c0007t0001g0283 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.117+143G>A | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 2/9 | chr22 | 36864272 | |||||||
| chr22:36864277 | T | G | 1 | a0001c0007t0001g0283 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.117+148T>G | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 2/9 | chr22 | 36864277 | |||||||
| chr22:36864278 | T | C | 1 | a0001c0007t0001g0283 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.117+149T>C | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 2/9 | chr22 | 36864278 | |||||||
| chr22:36864279 | T | A | 1 | a0001c0007t0001g0283 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.117+150T>A | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 2/9 | chr22 | 36864279 | |||||||
| chr22:36864282 | C | G | 1 | a0001c0007t0001g0283 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.117+153C>G | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 2/9 | chr22 | 36864282 | |||||||
| chr22:36864283 | A | G | 1 | a0001c0007t0001g0283 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.117+154A>G | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 2/9 | chr22 | 36864283 | |||||||
| chr22:36864288 | C | A | 1 | a0001c0007t0001g0283 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.117+159C>A | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 2/9 | chr22 | 36864288 | |||||||
| chr22:36864289 | C | G | 1 | a0001c0007t0001g0283 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.117+160C>G | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 2/9 | chr22 | 36864289 | |||||||
| chr22:36864292 | G | A | 1 | a0001c0007t0001g0283 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.117+163G>A | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 2/9 | chr22 | 36864292 | |||||||
| chr22:36864303 | T | C | 1 | a0001c0007t0001g0283 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.117+174T>C | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 2/9 | chr22 | 36864303 | |||||||
| chr22:36864313 | T | G | 1 | a0001c0007t0001g0283 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.117+184T>G | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 2/9 | chr22 | 36864313 | |||||||
| chr22:36864314 | T | A | 1 | a0001c0007t0001g0283 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.117+185T>A | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 2/9 | chr22 | 36864314 | |||||||
| chr22:36864316 | G | T | 1 | a0001c0007t0001g0283 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.117+187G>T | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 2/9 | chr22 | 36864316 | |||||||
| chr22:36864318 | G | A | 1 | a0001c0007t0001g0283 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.117+189G>A | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 2/9 | chr22 | 36864318 | |||||||
| chr22:36864324 | C | A | 1 | a0001c0007t0001g0283 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.117+195C>A | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 2/9 | chr22 | 36864324 | |||||||
| chr22:36864325 | T | G | 1 | a0001c0007t0001g0283 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.117+196T>G | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 2/9 | chr22 | 36864325 | |||||||
| chr22:36864330 | C | T | 1 | a0001c0007t0001g0283 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.117+201C>T | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 2/9 | chr22 | 36864330 | |||||||
| chr22:36864331 | A | G | 1 | a0001c0007t0001g0283 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.117+202A>G | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 2/9 | chr22 | 36864331 | |||||||
| chr22:36864332 | C | T | 1 | a0001c0007t0001g0283 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.117+203C>T | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 2/9 | chr22 | 36864332 | |||||||
| chr22:36864336 | T | A | 1 | a0001c0007t0001g0283 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.117+207T>A | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 2/9 | chr22 | 36864336 | |||||||
| chr22:36864345 | G | A | 1 | a0001c0007t0001g0283 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.117+216G>A | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 2/9 | chr22 | 36864345 | |||||||
| chr22:36864348 | T | A | 1 | a0001c0007t0001g0283 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.117+219T>A | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 2/9 | chr22 | 36864348 | |||||||
| chr22:36864432 | A | G | 48 | a0001c0001t0001g0079 a0001c0001t0001g0141 a0001c0001t0001g0199 others(45): Show |
56 | HG00673.hp1 HG01123.hp2 HG01255.hp1 others(53): Show |
intron_variant | MODIFIER | c.117+303A>G | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 2/9 | chr22 | 36864432 | |||||||
| chr22:36864451 | G | A | 5 | a0001c0001t0001g0019 a0001c0001t0001g0087 a0001c0001t0001g0236 others(2): Show |
7 | HG01109.hp2 HG01243.hp2 HG02602.hp2 others(4): Show |
intron_variant | MODIFIER | c.117+322G>A | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 2/9 | chr22 | 36864451 | |||||||
| chr22:36864559 | A | G | 267 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(264): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.118-360A>G | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 2/9 | chr22 | 36864559 | |||||||
| chr22:36864635 | A | G | 48 | a0001c0001t0001g0079 a0001c0001t0001g0141 a0001c0001t0001g0199 others(45): Show |
56 | HG00673.hp1 HG01123.hp2 HG01255.hp1 others(53): Show |
intron_variant | MODIFIER | c.118-284A>G | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 2/9 | chr22 | 36864635 | |||||||
| chr22:36864667 | C | T | 1 | a0001c0001t0001g0211 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.118-252C>T | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 2/9 | chr22 | 36864667 | |||||||
| chr22:36864703 | G | GT | 41 | a0001c0002t0001g0010 a0001c0002t0001g0025 a0001c0002t0001g0028 others(38): Show |
49 | HG00673.hp1 HG01123.hp2 HG01255.hp1 others(46): Show |
intron_variant | MODIFIER | c.118-206dupT | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr22 | 36864703 | ||||||
| chr22:36864709 | T | C | 1 | a0001c0001t0001g0183 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.118-210T>C | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 2/9 | chr22 | 36864709 | |||||||
| chr22:36864744 | G | A | 1 | a0001c0001t0002g0056 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.118-175G>A | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 2/9 | chr22 | 36864744 | |||||||
| chr22:36864764 | C | A | 1 | a0001c0001t0001g0238 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.118-155C>A | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 2/9 | chr22 | 36864764 | |||||||
| chr22:36864771 | A | G | 48 | a0001c0001t0001g0079 a0001c0001t0001g0141 a0001c0001t0001g0199 others(45): Show |
56 | HG00673.hp1 HG01123.hp2 HG01255.hp1 others(53): Show |
intron_variant | MODIFIER | c.118-148A>G | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 2/9 | chr22 | 36864771 | |||||||
| chr22:36864847 | T | C | 1 | a0001c0001t0001g0044 | 2 | HG01884.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.118-72T>C | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 2/9 | chr22 | 36864847 | |||||||
| chr22:36864860 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.118-59C>T | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 2/9 | chr22 | 36864860 | |||||||
| chr22:36865292 | C | G | 1 | a0001c0001t0001g0044 | 2 | HG01884.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.271+220C>G | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 3/9 | chr22 | 36865292 | |||||||
| chr22:36865459 | C | T | 1 | a0001c0001t0001g0256 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.271+387C>T | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 3/9 | chr22 | 36865459 | |||||||
| chr22:36865498 | G | A | 1 | a0001c0005t0001g0288 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.271+426G>A | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 3/9 | chr22 | 36865498 | |||||||
| chr22:36865520 | T | C | 1 | a0003c0010t0001g0074 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.271+448T>C | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 3/9 | chr22 | 36865520 | |||||||
| chr22:36865528 | C | T | 5 | a0001c0006t0001g0081 a0001c0006t0001g0198 a0001c0006t0001g0266 others(2): Show |
5 | HG02451.hp1 HG02451.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.271+456C>T | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 3/9 | chr22 | 36865528 | |||||||
| chr22:36865529 | G | A | 2 | a0001c0001t0001g0228 a0001c0001t0001g0229 |
2 | NA18981.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.271+457G>A | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 3/9 | chr22 | 36865529 | |||||||
| chr22:36865529 | G | C | 1 | a0001c0004t0001g0143 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.271+457G>C | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 3/9 | chr22 | 36865529 | |||||||
| chr22:36865530 | C | G | 1 | a0001c0004t0001g0143 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.271+458C>G | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 3/9 | chr22 | 36865530 | |||||||
| chr22:36865658 | A | C | 10 | a0001c0001t0001g0231 a0001c0007t0001g0040 a0001c0007t0001g0140 others(7): Show |
10 | HG01243.hp1 HG02809.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.271+586A>C | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 3/9 | chr22 | 36865658 | |||||||
| chr22:36865666 | C | T | 10 | a0001c0001t0001g0231 a0001c0007t0001g0040 a0001c0007t0001g0140 others(7): Show |
10 | HG01243.hp1 HG02809.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.271+594C>T | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 3/9 | chr22 | 36865666 | |||||||
| chr22:36865686 | C | T | 2 | a0001c0001t0001g0044 a0001c0002t0001g0010 |
5 | HG01884.hp1 HG01891.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.271+614C>T | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 3/9 | chr22 | 36865686 | |||||||
| chr22:36865724 | C | T | 1 | a0001c0001t0001g0219 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.271+652C>T | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 3/9 | chr22 | 36865724 | |||||||
| chr22:36865944 | G | A | 1 | a0003c0010t0001g0074 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.271+872G>A | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 3/9 | chr22 | 36865944 | |||||||
| chr22:36866018 | A | G | 1 | a0003c0010t0001g0074 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.271+946A>G | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 3/9 | chr22 | 36866018 | |||||||
| chr22:36866189 | C | A | 1 | a0001c0004t0001g0143 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.271+1117C>A | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 3/9 | chr22 | 36866189 | |||||||
| chr22:36866189 | C | T | 1 | a0001c0001t0001g0036 | 2 | HG00642.hp2 HG00741.hp1 |
intron_variant | MODIFIER | c.271+1117C>T | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 3/9 | chr22 | 36866189 | |||||||
| chr22:36866251 | C | A | 1 | a0001c0001t0001g0189 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.272-1141C>A | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 3/9 | chr22 | 36866251 | |||||||
| chr22:36866284 | C | T | 2 | a0001c0001t0001g0132 a0001c0001t0001g0180 |
2 | HG00423.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.272-1108C>T | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 3/9 | chr22 | 36866284 | |||||||
| chr22:36866391 | C | G | 5 | a0001c0002t0001g0072 a0001c0002t0001g0221 a0001c0002t0001g0268 others(2): Show |
5 | HG02257.hp1 HG02647.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.272-1001C>G | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 3/9 | chr22 | 36866391 | |||||||
| chr22:36866602 | C | T | 1 | a0001c0001t0001g0141 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.272-790C>T | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 3/9 | chr22 | 36866602 | |||||||
| chr22:36866711 | G | T | 4 | a0001c0005t0001g0027 a0001c0005t0001g0043 a0001c0005t0001g0277 others(1): Show |
5 | HG01261.hp1 HG03654.hp2 HG03688.hp1 others(2): Show |
intron_variant | MODIFIER | c.272-681G>T | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 3/9 | chr22 | 36866711 | |||||||
| chr22:36866727 | C | T | 10 | a0001c0001t0001g0231 a0001c0007t0001g0040 a0001c0007t0001g0140 others(7): Show |
10 | HG01243.hp1 HG02809.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.272-665C>T | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 3/9 | chr22 | 36866727 | |||||||
| chr22:36866900 | C | T | 15 | a0001c0001t0001g0075 a0001c0001t0001g0203 a0001c0001t0001g0231 others(12): Show |
15 | HG01243.hp1 HG02109.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.272-492C>T | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 3/9 | chr22 | 36866900 | |||||||
| chr22:36866914 | T | C | 1 | a0001c0001t0001g0151 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.272-478T>C | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 3/9 | chr22 | 36866914 | |||||||
| chr22:36866924 | C | T | 1 | a0001c0001t0001g0009 | 4 | HG00741.hp2 HG01070.hp2 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.272-468C>T | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 3/9 | chr22 | 36866924 | |||||||
| chr22:36867110 | C | CGT | 27 | a0001c0001t0001g0020 a0001c0001t0001g0037 a0001c0001t0001g0044 others(24): Show |
31 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(28): Show |
intron_variant | MODIFIER | c.272-250_272-249dup others(2): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr22 | 36867110 | ||||||
| chr22:36867110 | C | CGTGT | 53 | a0001c0001t0001g0012 a0001c0001t0001g0015 a0001c0001t0001g0016 others(50): Show |
64 | HG00099.hp2 HG00597.hp1 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.272-252_272-249dup others(4): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr22 | 36867110 | ||||||
| chr22:36867110 | C | CGTGTGT | 84 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(81): Show |
131 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.272-254_272-249dup others(6): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr22 | 36867110 | ||||||
| chr22:36867110 | C | CGTGTGTG others(1): Show |
27 | a0001c0001t0001g0014 a0001c0001t0001g0017 a0001c0001t0001g0031 others(24): Show |
35 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(32): Show |
intron_variant | MODIFIER | c.272-256_272-249dup others(8): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr22 | 36867110 | ||||||
| chr22:36867110 | C | CGTGTGTG others(3): Show |
32 | a0001c0001t0001g0030 a0001c0001t0001g0101 a0001c0001t0001g0146 others(29): Show |
39 | HG01346.hp2 HG01891.hp1 HG01891.hp2 others(36): Show |
intron_variant | MODIFIER | c.272-258_272-249dup others(10): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr22 | 36867110 | ||||||
| chr22:36867110 | C | CGTGTGTG others(5): Show |
15 | a0001c0001t0001g0019 a0001c0001t0001g0049 a0001c0001t0001g0294 others(12): Show |
20 | HG01109.hp2 HG01123.hp2 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.272-260_272-249dup others(12): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr22 | 36867110 | ||||||
| chr22:36867110 | C | CGTGTGTG others(7): Show |
2 | a0001c0002t0001g0126 a0001c0002t0001g0166 |
2 | HG01255.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.272-262_272-249dup others(14): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr22 | 36867110 | ||||||
| chr22:36867110 | CGT | C | 6 | a0001c0001t0001g0041 a0001c0001t0001g0111 a0001c0001t0001g0113 others(3): Show |
12 | HG02055.hp1 HG02055.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.272-250_272-249del others(2): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr22 | 36867110 | ||||||
| chr22:36867142 | T | C | 1 | a0001c0003t0001g0258 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.272-250T>C | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 3/9 | chr22 | 36867142 | |||||||
| chr22:36867142 | T | TGTGTGTG others(3): Show |
10 | a0001c0001t0001g0231 a0001c0005t0001g0027 a0001c0005t0001g0043 others(7): Show |
11 | HG01243.hp1 HG01261.hp1 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.272-249_272-248ins others(10): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr22 | 36867142 | ||||||
| chr22:36867142 | T | TGTGTGTG others(5): Show |
3 | a0001c0004t0001g0144 a0001c0007t0001g0140 a0001c0007t0001g0232 |
3 | HG00673.hp1 HG03225.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.272-249_272-248ins others(12): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr22 | 36867142 | ||||||
| chr22:36867323 | T | C | 7 | a0001c0002t0001g0025 a0001c0002t0001g0045 a0001c0002t0001g0084 others(4): Show |
9 | HG01891.hp2 HG02258.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.272-69T>C | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 3/9 | chr22 | 36867323 | |||||||
| chr22:36867491 | G | A | 1 | a0001c0001t0001g0044 | 2 | HG01884.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.342+29G>A | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 4/9 | chr22 | 36867491 | |||||||
| chr22:36867576 | G | A | 9 | a0001c0001t0001g0015 a0001c0001t0001g0037 a0001c0001t0001g0089 others(6): Show |
12 | HG00140.hp1 HG00639.hp2 HG00738.hp2 others(9): Show |
intron_variant | MODIFIER | c.342+114G>A | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 4/9 | chr22 | 36867576 | |||||||
| chr22:36867595 | C | T | 1 | a0001c0006t0001g0081 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.342+133C>T | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 4/9 | chr22 | 36867595 | |||||||
| chr22:36867646 | A | G | 1 | a0003c0010t0001g0074 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.342+184A>G | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 4/9 | chr22 | 36867646 | |||||||
| chr22:36867664 | C | T | 249 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(246): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.342+202C>T | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 4/9 | chr22 | 36867664 | |||||||
| chr22:36867804 | T | C | 199 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(196): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.342+342T>C | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 4/9 | chr22 | 36867804 | |||||||
| chr22:36867885 | C | T | 2 | a0001c0001t0001g0243 a0001c0001t0001g0244 |
2 | HG02622.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.342+423C>T | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 4/9 | chr22 | 36867885 | |||||||
| chr22:36867955 | G | C | 1 | a0003c0010t0001g0074 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.342+493G>C | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 4/9 | chr22 | 36867955 | |||||||
| chr22:36868024 | G | A | 4 | a0001c0001t0001g0014 a0001c0001t0001g0017 a0001c0001t0001g0185 others(1): Show |
8 | HG00140.hp2 HG01069.hp2 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.342+562G>A | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 4/9 | chr22 | 36868024 | |||||||
| chr22:36868404 | G | A | 9 | a0001c0001t0001g0015 a0001c0001t0001g0037 a0001c0001t0001g0089 others(6): Show |
12 | HG00140.hp1 HG00639.hp2 HG00738.hp2 others(9): Show |
intron_variant | MODIFIER | c.342+942G>A | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 4/9 | chr22 | 36868404 | |||||||
| chr22:36868474 | G | A | 1 | a0001c0001t0001g0227 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.342+1012G>A | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 4/9 | chr22 | 36868474 | |||||||
| chr22:36868788 | A | G | 13 | a0001c0001t0001g0015 a0001c0001t0001g0037 a0001c0001t0001g0079 others(10): Show |
16 | HG00140.hp1 HG00639.hp2 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.342+1326A>G | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 4/9 | chr22 | 36868788 | |||||||
| chr22:36868874 | G | A | 1 | a0001c0001t0001g0271 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.342+1412G>A | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 4/9 | chr22 | 36868874 | |||||||
| chr22:36868979 | G | A | 1 | a0003c0010t0001g0074 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.343-1436G>A | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 4/9 | chr22 | 36868979 | |||||||
| chr22:36868986 | T | G | 2 | a0001c0004t0001g0222 a0001c0006t0001g0266 |
2 | HG02451.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.343-1429T>G | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 4/9 | chr22 | 36868986 | |||||||
| chr22:36869019 | C | G | 11 | a0001c0001t0001g0047 a0001c0001t0001g0090 a0001c0001t0001g0093 others(8): Show |
12 | HG00642.hp1 HG00733.hp1 HG00735.hp2 others(9): Show |
intron_variant | MODIFIER | c.343-1396C>G | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 4/9 | chr22 | 36869019 | |||||||
| chr22:36869037 | G | C | 182 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(179): Show |
248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.343-1378G>C | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 4/9 | chr22 | 36869037 | |||||||
| chr22:36869077 | T | G | 1 | a0003c0010t0001g0074 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.343-1338T>G | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 4/9 | chr22 | 36869077 | |||||||
| chr22:36869130 | A | C | 48 | a0001c0001t0001g0079 a0001c0001t0001g0141 a0001c0001t0001g0199 others(45): Show |
56 | HG00673.hp1 HG01123.hp2 HG01255.hp1 others(53): Show |
intron_variant | MODIFIER | c.343-1285A>C | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 4/9 | chr22 | 36869130 | |||||||
| chr22:36869243 | C | T | 1 | a0003c0010t0001g0074 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.343-1172C>T | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 4/9 | chr22 | 36869243 | |||||||
| chr22:36869272 | G | A | 4 | a0001c0005t0001g0027 a0001c0005t0001g0043 a0001c0005t0001g0277 others(1): Show |
5 | HG01261.hp1 HG03654.hp2 HG03688.hp1 others(2): Show |
intron_variant | MODIFIER | c.343-1143G>A | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 4/9 | chr22 | 36869272 | |||||||
| chr22:36869301 | T | C | 6 | a0001c0001t0001g0075 a0001c0001t0001g0087 a0001c0001t0001g0203 others(3): Show |
6 | HG02109.hp1 HG02486.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.343-1114T>C | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 4/9 | chr22 | 36869301 | |||||||
| chr22:36869333 | G | A | 1 | a0003c0010t0001g0074 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.343-1082G>A | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 4/9 | chr22 | 36869333 | |||||||
| chr22:36869344 | T | C | 48 | a0001c0001t0001g0079 a0001c0001t0001g0141 a0001c0001t0001g0199 others(45): Show |
56 | HG00673.hp1 HG01123.hp2 HG01255.hp1 others(53): Show |
intron_variant | MODIFIER | c.343-1071T>C | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 4/9 | chr22 | 36869344 | |||||||
| chr22:36869519 | A | C | 1 | a0001c0001t0001g0183 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.343-896A>C | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 4/9 | chr22 | 36869519 | |||||||
| chr22:36869525 | T | G | 1 | a0001c0004t0001g0225 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.343-890T>G | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 4/9 | chr22 | 36869525 | |||||||
| chr22:36869759 | G | A | 1 | a0001c0001t0001g0138 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.343-656G>A | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 4/9 | chr22 | 36869759 | |||||||
| chr22:36869894 | G | C | 1 | a0001c0001t0001g0019 | 3 | HG01109.hp2 HG02630.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.343-521G>C | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 4/9 | chr22 | 36869894 | |||||||
| chr22:36869981 | C | T | 3 | a0001c0001t0001g0088 a0001c0001t0001g0115 a0001c0001t0001g0195 |
3 | HG00323.hp1 HG01070.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.343-434C>T | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 4/9 | chr22 | 36869981 | |||||||
| chr22:36870053 | A | T | 1 | a0001c0001t0002g0058 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.343-362A>T | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 4/9 | chr22 | 36870053 | |||||||
| chr22:36870067 | A | T | 1 | a0001c0001t0001g0191 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.343-348A>T | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 4/9 | chr22 | 36870067 | |||||||
| chr22:36870076 | G | A | 21 | a0001c0001t0001g0079 a0001c0001t0001g0087 a0001c0001t0001g0231 others(18): Show |
26 | HG01243.hp1 HG02055.hp1 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.343-339G>A | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 4/9 | chr22 | 36870076 | |||||||
| chr22:36870078 | G | A | 10 | a0001c0001t0001g0231 a0001c0007t0001g0040 a0001c0007t0001g0140 others(7): Show |
10 | HG01243.hp1 HG02809.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.343-337G>A | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 4/9 | chr22 | 36870078 | |||||||
| chr22:36870187 | C | T | 1 | a0001c0001t0001g0184 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.343-228C>T | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 4/9 | chr22 | 36870187 | |||||||
| chr22:36870192 | G | A | 1 | a0001c0001t0001g0267 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.343-223G>A | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 4/9 | chr22 | 36870192 | |||||||
| chr22:36870280 | A | G | 201 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(198): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.343-135A>G | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 4/9 | chr22 | 36870280 | |||||||
| chr22:36870336 | C | T | 1 | a0001c0001t0001g0298 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.343-79C>T | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 4/9 | chr22 | 36870336 | |||||||
| chr22:36870342 | C | T | 10 | a0001c0001t0001g0231 a0001c0007t0001g0040 a0001c0007t0001g0140 others(7): Show |
10 | HG01243.hp1 HG02809.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.343-73C>T | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 4/9 | chr22 | 36870342 | |||||||
| chr22:36870562 | G | C | 13 | a0001c0001t0001g0087 a0001c0001t0001g0231 a0001c0003t0001g0204 others(10): Show |
13 | HG01243.hp1 HG02109.hp1 HG02809.hp2 others(10): Show |
intron_variant | MODIFIER | c.470+20G>C | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 5/9 | chr22 | 36870562 | |||||||
| chr22:36870731 | C | T | 1 | a0001c0001t0001g0261 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.470+189C>T | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 5/9 | chr22 | 36870731 | |||||||
| chr22:36870839 | G | A | 13 | a0001c0001t0001g0079 a0001c0001t0001g0205 a0001c0001t0001g0206 others(10): Show |
18 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.470+297G>A | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 5/9 | chr22 | 36870839 | |||||||
| chr22:36870846 | T | C | 4 | a0001c0002t0001g0046 a0001c0002t0001g0070 a0001c0002t0001g0071 others(1): Show |
5 | HG02280.hp1 HG03209.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.470+304T>C | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 5/9 | chr22 | 36870846 | |||||||
| chr22:36870851 | G | A | 1 | a0001c0001t0001g0215 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.470+309G>A | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 5/9 | chr22 | 36870851 | |||||||
| chr22:36870936 | C | T | 3 | a0001c0001t0001g0131 a0001c0003t0001g0204 a0001c0003t0001g0234 |
3 | HG02109.hp1 HG03130.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.470+394C>T | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 5/9 | chr22 | 36870936 | |||||||
| chr22:36870937 | A | G | 203 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(200): Show |
270 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.470+395A>G | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 5/9 | chr22 | 36870937 | |||||||
| chr22:36871120 | C | A | 8 | a0001c0001t0001g0015 a0001c0001t0001g0037 a0001c0001t0001g0089 others(5): Show |
11 | HG00140.hp1 HG00738.hp2 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.471-532C>A | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 5/9 | chr22 | 36871120 | |||||||
| chr22:36871200 | G | A | 2 | a0001c0003t0001g0204 a0001c0003t0001g0234 |
2 | HG02109.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.471-452G>A | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 5/9 | chr22 | 36871200 | |||||||
| chr22:36871209 | G | C | 3 | a0001c0006t0001g0198 a0001c0006t0001g0278 a0001c0006t0003g0065 |
3 | HG02965.hp2 HG03579.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.471-443G>C | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 5/9 | chr22 | 36871209 | |||||||
| chr22:36871265 | C | T | 1 | a0001c0001t0001g0244 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.471-387C>T | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 5/9 | chr22 | 36871265 | |||||||
| chr22:36871320 | T | G | 1 | a0001c0001t0001g0120 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.471-332T>G | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 5/9 | chr22 | 36871320 | |||||||
| chr22:36871385 | C | T | 10 | a0001c0001t0001g0231 a0001c0007t0001g0040 a0001c0007t0001g0140 others(7): Show |
10 | HG01243.hp1 HG02809.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.471-267C>T | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 5/9 | chr22 | 36871385 | |||||||
| chr22:36871411 | C | A | 1 | a0001c0001t0001g0086 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.471-241C>A | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 5/9 | chr22 | 36871411 | |||||||
| chr22:36871516 | A | T | 2 | a0001c0001t0001g0154 a0001c0001t0001g0297 |
2 | HG02132.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.471-136A>T | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 5/9 | chr22 | 36871516 | |||||||
| chr22:36871520 | C | T | 1 | a0002c0009t0001g0241 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.471-132C>T | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 5/9 | chr22 | 36871520 | |||||||
| chr22:36871725 | A | G | 200 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(197): Show |
265 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.528+16A>G | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 6/9 | chr22 | 36871725 | |||||||
| chr22:36871726 | C | A | 10 | a0001c0001t0001g0079 a0001c0004t0001g0222 a0001c0006t0001g0005 others(7): Show |
15 | HG02055.hp1 HG02055.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.528+17C>A | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 6/9 | chr22 | 36871726 | |||||||
| chr22:36871727 | G | C | 18 | a0001c0002t0001g0010 a0001c0002t0001g0025 a0001c0002t0001g0045 others(15): Show |
23 | HG01891.hp1 HG01891.hp2 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.528+18G>C | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 6/9 | chr22 | 36871727 | |||||||
| chr22:36871785 | C | T | 1 | a0001c0002t0001g0272 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.528+76C>T | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 6/9 | chr22 | 36871785 | |||||||
| chr22:36871865 | C | T | 1 | a0001c0001t0002g0053 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.528+156C>T | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 6/9 | chr22 | 36871865 | |||||||
| chr22:36871881 | G | A | 23 | a0001c0001t0001g0177 a0001c0002t0001g0010 a0001c0002t0001g0025 others(20): Show |
30 | HG01516.hp2 HG01891.hp1 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.528+172G>A | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 6/9 | chr22 | 36871881 | |||||||
| chr22:36871901 | C | A | 222 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(219): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.528+192C>A | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 6/9 | chr22 | 36871901 | |||||||
| chr22:36871912 | C | G | 1 | a0001c0001t0001g0199 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.528+203C>G | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 6/9 | chr22 | 36871912 | |||||||
| chr22:36871917 | G | A | 10 | a0001c0001t0001g0231 a0001c0007t0001g0040 a0001c0007t0001g0140 others(7): Show |
10 | HG01243.hp1 HG02809.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.528+208G>A | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 6/9 | chr22 | 36871917 | |||||||
| chr22:36872037 | A | G | 200 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(197): Show |
265 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.529-290A>G | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 6/9 | chr22 | 36872037 | |||||||
| chr22:36872087 | C | A | 1 | a0001c0001t0001g0240 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.529-240C>A | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 6/9 | chr22 | 36872087 | |||||||
| chr22:36872215 | C | T | 177 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(174): Show |
238 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.529-112C>T | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 6/9 | chr22 | 36872215 | |||||||
| chr22:36872273 | T | C | 2 | a0001c0002t0001g0010 a0001c0005t0001g0085 |
4 | HG01891.hp1 HG02976.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.529-54T>C | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 6/9 | chr22 | 36872273 | |||||||
| chr22:36872459 | A | G | 200 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(197): Show |
265 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.627+34A>G | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 7/9 | chr22 | 36872459 | |||||||
| chr22:36872513 | A | G | 253 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(250): Show |
336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.627+88A>G | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 7/9 | chr22 | 36872513 | |||||||
| chr22:36872609 | G | A | 2 | a0001c0003t0001g0011 a0001c0003t0001g0182 |
4 | HG01516.hp2 HG02559.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.627+184G>A | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 7/9 | chr22 | 36872609 | |||||||
| chr22:36872623 | TTGGAGGT others(41): Show |
T | 173 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(170): Show |
234 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.627+209_627+256del others(48): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr22 | 36872623 | ||||||
| chr22:36872634 | G | A | 4 | a0001c0001t0001g0116 a0001c0001t0001g0130 a0001c0001t0001g0131 others(1): Show |
4 | NA18957.hp2 NA18983.hp2 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.627+209G>A | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 7/9 | chr22 | 36872634 | |||||||
| chr22:36872635 | G | T | 4 | a0001c0001t0001g0116 a0001c0001t0001g0130 a0001c0001t0001g0131 others(1): Show |
4 | NA18957.hp2 NA18983.hp2 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.627+210G>T | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 7/9 | chr22 | 36872635 | |||||||
| chr22:36872646 | A | G | 4 | a0001c0001t0001g0116 a0001c0001t0001g0130 a0001c0001t0001g0131 others(1): Show |
4 | NA18957.hp2 NA18983.hp2 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.627+221A>G | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 7/9 | chr22 | 36872646 | |||||||
| chr22:36872647 | G | T | 4 | a0001c0001t0001g0116 a0001c0001t0001g0130 a0001c0001t0001g0131 others(1): Show |
4 | NA18957.hp2 NA18983.hp2 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.627+222G>T | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 7/9 | chr22 | 36872647 | |||||||
| chr22:36872653 | A | G | 4 | a0001c0001t0001g0116 a0001c0001t0001g0130 a0001c0001t0001g0131 others(1): Show |
4 | NA18957.hp2 NA18983.hp2 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.627+228A>G | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 7/9 | chr22 | 36872653 | |||||||
| chr22:36872671 | ATGGAGGT others(17): Show |
A | 3 | a0001c0001t0001g0141 a0001c0001t0001g0224 a0001c0003t0001g0208 |
3 | HG01884.hp2 HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.627+266_627+289del others(24): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr22 | 36872671 | ||||||
| chr22:36872691 | A | AAGGTTGG others(17): Show |
4 | a0001c0005t0001g0027 a0001c0005t0001g0043 a0001c0005t0001g0277 others(1): Show |
5 | HG01261.hp1 HG03654.hp2 HG03688.hp1 others(2): Show |
intron_variant | MODIFIER | c.627+288_627+311dup others(24): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr22 | 36872691 | ||||||
| chr22:36872807 | G | A | 11 | a0001c0001t0001g0102 a0001c0001t0001g0141 a0001c0001t0001g0216 others(8): Show |
11 | HG00639.hp2 HG01884.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.627+382G>A | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 7/9 | chr22 | 36872807 | |||||||
| chr22:36872826 | G | A | 196 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(193): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(258): Show |
intron_variant | MODIFIER | c.627+401G>A | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 7/9 | chr22 | 36872826 | |||||||
| chr22:36872829 | T | C | 5 | a0001c0001t0001g0048 a0001c0001t0001g0162 a0001c0001t0001g0194 others(2): Show |
6 | HG00597.hp1 NA18946.hp2 NA18947.hp2 others(3): Show |
intron_variant | MODIFIER | c.627+404T>C | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 7/9 | chr22 | 36872829 | |||||||
| chr22:36872830 | G | A | 1 | a0001c0001t0001g0142 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.627+405G>A | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 7/9 | chr22 | 36872830 | |||||||
| chr22:36872830 | G | T | 1 | a0001c0001t0001g0194 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.627+405G>T | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 7/9 | chr22 | 36872830 | |||||||
| chr22:36872835 | T | G | 1 | a0001c0001t0001g0194 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.627+410T>G | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 7/9 | chr22 | 36872835 | |||||||
| chr22:36872836 | A | G | 1 | a0001c0001t0001g0194 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.627+411A>G | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 7/9 | chr22 | 36872836 | |||||||
| chr22:36872855 | G | T | 1 | a0001c0001t0001g0194 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.627+430G>T | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 7/9 | chr22 | 36872855 | |||||||
| chr22:36872856 | G | A | 249 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(246): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.627+431G>A | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 7/9 | chr22 | 36872856 | |||||||
| chr22:36872892 | A | C | 1 | a0001c0001t0001g0194 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.627+467A>C | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 7/9 | chr22 | 36872892 | |||||||
| chr22:36872900 | T | G | 1 | a0001c0001t0001g0194 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.627+475T>G | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 7/9 | chr22 | 36872900 | |||||||
| chr22:36872902 | G | A | 1 | a0001c0001t0001g0194 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.627+477G>A | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 7/9 | chr22 | 36872902 | |||||||
| chr22:36872919 | T | C | 4 | a0001c0001t0001g0079 a0001c0006t0001g0005 a0001c0006t0001g0073 others(1): Show |
9 | HG02055.hp1 HG02055.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.627+494T>C | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 7/9 | chr22 | 36872919 | |||||||
| chr22:36872927 | G | A | 1 | a0001c0001t0001g0194 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.627+502G>A | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 7/9 | chr22 | 36872927 | |||||||
| chr22:36872936 | ATGGAGGT others(5): Show |
A | 22 | a0001c0002t0001g0010 a0001c0002t0001g0025 a0001c0002t0001g0045 others(19): Show |
29 | HG01516.hp2 HG01891.hp1 HG01891.hp2 others(26): Show |
intron_variant | MODIFIER | c.627+534_627+545del others(12): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr22 | 36872936 | ||||||
| chr22:36872944 | G | A | 196 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(193): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(258): Show |
intron_variant | MODIFIER | c.627+519G>A | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 7/9 | chr22 | 36872944 | |||||||
| chr22:36872957 | A | C | 1 | a0001c0001t0001g0194 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.627+532A>C | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 7/9 | chr22 | 36872957 | |||||||
| chr22:36873020 | C | A | 17 | a0001c0001t0001g0015 a0001c0001t0001g0037 a0001c0001t0001g0089 others(14): Show |
20 | HG00140.hp1 HG00639.hp2 HG00738.hp2 others(17): Show |
intron_variant | MODIFIER | c.627+595C>A | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 7/9 | chr22 | 36873020 | |||||||
| chr22:36873030 | G | C | 1 | a0001c0001t0001g0185 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.627+605G>C | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 7/9 | chr22 | 36873030 | |||||||
| chr22:36873031 | A | ATTGGAGG others(29): Show |
1 | a0001c0001t0002g0056 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.627+639_627+674dup others(36): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr22 | 36873031 | ||||||
| chr22:36873032 | T | C | 1 | a0001c0001t0001g0267 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.627+607T>C | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 7/9 | chr22 | 36873032 | |||||||
| chr22:36873064 | A | G | 4 | a0001c0005t0001g0027 a0001c0005t0001g0043 a0001c0005t0001g0277 others(1): Show |
5 | HG01261.hp1 HG03654.hp2 HG03688.hp1 others(2): Show |
intron_variant | MODIFIER | c.627+639A>G | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 7/9 | chr22 | 36873064 | |||||||
| chr22:36873136 | A | G | 196 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(193): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(258): Show |
intron_variant | MODIFIER | c.627+711A>G | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 7/9 | chr22 | 36873136 | |||||||
| chr22:36873142 | A | G | 1 | a0001c0001t0002g0059 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.627+717A>G | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 7/9 | chr22 | 36873142 | |||||||
| chr22:36873218 | G | A | 1 | a0001c0001t0001g0210 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.627+793G>A | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 7/9 | chr22 | 36873218 | |||||||
| chr22:36873260 | G | C | 1 | a0001c0001t0001g0199 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.627+835G>C | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 7/9 | chr22 | 36873260 | |||||||
| chr22:36873274 | G | A | 2 | a0001c0014t0001g0064 a0003c0010t0001g0074 |
2 | HG02886.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.627+849G>A | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 7/9 | chr22 | 36873274 | |||||||
| chr22:36873292 | G | C | 4 | a0001c0005t0001g0027 a0001c0005t0001g0043 a0001c0005t0001g0277 others(1): Show |
5 | HG01261.hp1 HG03654.hp2 HG03688.hp1 others(2): Show |
intron_variant | MODIFIER | c.627+867G>C | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 7/9 | chr22 | 36873292 | |||||||
| chr22:36873426 | G | T | 2 | a0001c0003t0001g0077 a0001c0003t0001g0078 |
2 | HG02145.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.627+1001G>T | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 7/9 | chr22 | 36873426 | |||||||
| chr22:36873465 | T | C | 162 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(159): Show |
223 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.627+1040T>C | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 7/9 | chr22 | 36873465 | |||||||
| chr22:36873499 | GCTAT | G | 41 | a0001c0001t0001g0015 a0001c0001t0001g0019 a0001c0001t0001g0037 others(38): Show |
54 | HG00140.hp1 HG00639.hp2 HG00738.hp2 others(51): Show |
intron_variant | MODIFIER | c.627+1077_627+1080d others(6): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr22 | 36873499 | ||||||
| chr22:36873514 | C | T | 249 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(246): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.627+1089C>T | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 7/9 | chr22 | 36873514 | |||||||
| chr22:36873591 | A | T | 3 | a0001c0001t0001g0133 a0001c0001t0001g0156 a0001c0004t0001g0260 |
3 | NA18978.hp1 NA18984.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.627+1166A>T | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 7/9 | chr22 | 36873591 | |||||||
| chr22:36873593 | T | C | 1 | a0001c0001t0001g0212 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.627+1168T>C | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 7/9 | chr22 | 36873593 | |||||||
| chr22:36873716 | G | C | 22 | a0001c0002t0001g0028 a0001c0002t0001g0029 a0001c0002t0001g0034 others(19): Show |
26 | HG00099.hp1 HG01106.hp2 HG01123.hp2 others(23): Show |
intron_variant | MODIFIER | c.627+1291G>C | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 7/9 | chr22 | 36873716 | |||||||
| chr22:36873734 | T | G | 1 | a0001c0001t0001g0129 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.627+1309T>G | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 7/9 | chr22 | 36873734 | |||||||
| chr22:36873737 | G | T | 1 | a0001c0001t0001g0129 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.627+1312G>T | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 7/9 | chr22 | 36873737 | |||||||
| chr22:36873772 | C | G | 12 | a0001c0001t0001g0079 a0001c0001t0001g0205 a0001c0001t0001g0206 others(9): Show |
17 | HG02055.hp1 HG02055.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.627+1347C>G | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 7/9 | chr22 | 36873772 | |||||||
| chr22:36873799 | G | A | 1 | a0001c0001t0001g0298 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.627+1374G>A | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 7/9 | chr22 | 36873799 | |||||||
| chr22:36873811 | T | C | 1 | a0001c0001t0001g0244 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.627+1386T>C | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 7/9 | chr22 | 36873811 | |||||||
| chr22:36873862 | AAC | A | 207 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(204): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(274): Show |
intron_variant | MODIFIER | c.627+1438_627+1439d others(4): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 7/9 | chr22 | 36873862 | |||||||
| chr22:36873903 | A | G | 249 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(246): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.627+1478A>G | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 7/9 | chr22 | 36873903 | |||||||
| chr22:36874048 | G | A | 22 | a0001c0002t0001g0028 a0001c0002t0001g0029 a0001c0002t0001g0034 others(19): Show |
26 | HG00099.hp1 HG01106.hp2 HG01123.hp2 others(23): Show |
intron_variant | MODIFIER | c.628-1605G>A | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 7/9 | chr22 | 36874048 | |||||||
| chr22:36874083 | C | T | 206 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(203): Show |
276 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(273): Show |
intron_variant | MODIFIER | c.628-1570C>T | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 7/9 | chr22 | 36874083 | |||||||
| chr22:36874106 | G | A | 207 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(204): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(274): Show |
intron_variant | MODIFIER | c.628-1547G>A | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 7/9 | chr22 | 36874106 | |||||||
| chr22:36874143 | G | T | 4 | a0001c0002t0001g0046 a0001c0002t0001g0070 a0001c0002t0001g0071 others(1): Show |
5 | HG02280.hp1 HG03209.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.628-1510G>T | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 7/9 | chr22 | 36874143 | |||||||
| chr22:36874326 | T | C | 1 | a0001c0001t0001g0201 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.628-1327T>C | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 7/9 | chr22 | 36874326 | |||||||
| chr22:36874401 | G | T | 40 | a0001c0002t0001g0010 a0001c0002t0001g0025 a0001c0002t0001g0028 others(37): Show |
49 | HG00099.hp1 HG01106.hp2 HG01123.hp2 others(46): Show |
intron_variant | MODIFIER | c.628-1252G>T | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 7/9 | chr22 | 36874401 | |||||||
| chr22:36874411 | G | A | 2 | a0001c0001t0001g0141 a0001c0001t0001g0224 |
2 | HG01884.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.628-1242G>A | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 7/9 | chr22 | 36874411 | |||||||
| chr22:36874460 | A | G | 164 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(161): Show |
225 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.628-1193A>G | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 7/9 | chr22 | 36874460 | |||||||
| chr22:36874842 | G | T | 6 | a0001c0004t0001g0222 a0001c0006t0001g0081 a0001c0006t0001g0198 others(3): Show |
6 | HG02451.hp1 HG02451.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.628-811G>T | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 7/9 | chr22 | 36874842 | |||||||
| chr22:36874971 | G | C | 238 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(235): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(312): Show |
intron_variant | MODIFIER | c.628-682G>C | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 7/9 | chr22 | 36874971 | |||||||
| chr22:36875147 | C | T | 2 | a0001c0003t0001g0011 a0001c0003t0001g0182 |
4 | HG01516.hp2 HG02559.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.628-506C>T | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 7/9 | chr22 | 36875147 | |||||||
| chr22:36875265 | A | G | 173 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(170): Show |
234 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.628-388A>G | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 7/9 | chr22 | 36875265 | |||||||
| chr22:36875389 | C | A | 213 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(210): Show |
283 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(280): Show |
intron_variant | MODIFIER | c.628-264C>A | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 7/9 | chr22 | 36875389 | |||||||
| chr22:36875456 | A | G | 14 | a0001c0002t0001g0028 a0001c0002t0001g0029 a0001c0002t0001g0034 others(11): Show |
17 | HG01123.hp2 HG01255.hp1 HG01261.hp2 others(14): Show |
intron_variant | MODIFIER | c.628-197A>G | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 7/9 | chr22 | 36875456 | |||||||
| chr22:36875504 | G | A | 1 | a0001c0001t0001g0281 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.628-149G>A | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 7/9 | chr22 | 36875504 | |||||||
| chr22:36875630 | G | A | 4 | a0001c0001t0001g0124 a0001c0001t0001g0134 a0001c0001t0001g0186 others(1): Show |
4 | HG00558.hp2 HG02056.hp1 HG02083.hp2 others(1): Show |
intron_variant | MODIFIER | c.628-23G>A | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 7/9 | chr22 | 36875630 | |||||||
| chr22:36875639 | C | A | 2 | a0001c0001t0001g0249 a0001c0001t0001g0286 |
2 | HG01496.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.628-14C>A | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 7/9 | chr22 | 36875639 | |||||||
| chr22:36875822 | T | C | 1 | a0004c0013t0001g0171 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.758+39T>C | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 8/9 | chr22 | 36875822 | |||||||
| chr22:36875840 | T | C | 249 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(246): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.758+57T>C | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 8/9 | chr22 | 36875840 | |||||||
| chr22:36876099 | G | A | 2 | a0001c0014t0001g0064 a0003c0010t0001g0074 |
2 | HG02886.hp1 HG02895.hp1 |
splice_region_variant&intron_variant | LOW | c.824+5G>A | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 9/9 | chr22 | 36876099 | |||||||
| chr22:36876131 | T | G | 1 | a0001c0001t0001g0215 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.824+37T>G | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 9/9 | chr22 | 36876131 | |||||||
| chr22:36876144 | G | A | 9 | a0001c0007t0001g0040 a0001c0007t0001g0140 a0001c0007t0001g0223 others(6): Show |
9 | HG01243.hp1 HG02809.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.824+50G>A | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 9/9 | chr22 | 36876144 | |||||||
| chr22:36876166 | C | G | 1 | a0001c0001t0001g0175 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.824+72C>G | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 9/9 | chr22 | 36876166 | |||||||
| chr22:36876171 | A | G | 3 | a0001c0001t0001g0137 a0001c0001t0001g0139 a0001c0001t0001g0164 |
3 | NA18959.hp1 NA18967.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.824+77A>G | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 9/9 | chr22 | 36876171 | |||||||
| chr22:36876308 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.824+214C>T | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 9/9 | chr22 | 36876308 | |||||||
| chr22:36876330 | G | T | 2 | a0001c0001t0001g0019 a0001c0001t0001g0044 |
5 | HG01109.hp2 HG01884.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.824+236G>T | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 9/9 | chr22 | 36876330 | |||||||
| chr22:36876383 | A | G | 1 | a0001c0001t0002g0060 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.824+289A>G | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 9/9 | chr22 | 36876383 | |||||||
| chr22:36876408 | C | G | 2 | a0001c0014t0001g0064 a0003c0010t0001g0074 |
2 | HG02886.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.824+314C>G | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 9/9 | chr22 | 36876408 | |||||||
| chr22:36877002 | GTC | G | 9 | a0001c0001t0001g0141 a0001c0001t0001g0224 a0001c0003t0001g0077 others(6): Show |
9 | HG00639.hp2 HG01884.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.825-620_825-619del others(2): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 36877002 | ||||||
| chr22:36877023 | G | A | 6 | a0001c0004t0001g0222 a0001c0006t0001g0081 a0001c0006t0001g0198 others(3): Show |
6 | HG02451.hp1 HG02451.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.825-605G>A | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 9/9 | chr22 | 36877023 | |||||||
| chr22:36877028 | ACT | A | 51 | a0001c0002t0001g0010 a0001c0002t0001g0025 a0001c0002t0001g0028 others(48): Show |
60 | HG00099.hp1 HG01106.hp2 HG01123.hp2 others(57): Show |
intron_variant | MODIFIER | c.825-597_825-596del others(2): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 36877028 | ||||||
| chr22:36877031 | C | G | 51 | a0001c0002t0001g0010 a0001c0002t0001g0025 a0001c0002t0001g0028 others(48): Show |
60 | HG00099.hp1 HG01106.hp2 HG01123.hp2 others(57): Show |
intron_variant | MODIFIER | c.825-597C>G | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 9/9 | chr22 | 36877031 | |||||||
| chr22:36877032 | T | A | 51 | a0001c0002t0001g0010 a0001c0002t0001g0025 a0001c0002t0001g0028 others(48): Show |
60 | HG00099.hp1 HG01106.hp2 HG01123.hp2 others(57): Show |
intron_variant | MODIFIER | c.825-596T>A | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 9/9 | chr22 | 36877032 | |||||||
| chr22:36877070 | T | G | 12 | a0001c0001t0001g0079 a0001c0001t0001g0205 a0001c0001t0001g0206 others(9): Show |
17 | HG02055.hp1 HG02055.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.825-558T>G | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 9/9 | chr22 | 36877070 | |||||||
| chr22:36877138 | T | G | 51 | a0001c0002t0001g0010 a0001c0002t0001g0025 a0001c0002t0001g0028 others(48): Show |
60 | HG00099.hp1 HG01106.hp2 HG01123.hp2 others(57): Show |
intron_variant | MODIFIER | c.825-490T>G | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 9/9 | chr22 | 36877138 | |||||||
| chr22:36877143 | C | CT | 9 | a0001c0007t0001g0040 a0001c0007t0001g0140 a0001c0007t0001g0223 others(6): Show |
9 | HG01243.hp1 HG02809.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.825-474dupT | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 36877143 | ||||||
| chr22:36877163 | G | A | 2 | a0001c0003t0001g0011 a0001c0003t0001g0182 |
4 | HG01516.hp2 HG02559.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.825-465G>A | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 9/9 | chr22 | 36877163 | |||||||
| chr22:36877188 | G | A | 12 | a0001c0001t0001g0079 a0001c0001t0001g0205 a0001c0001t0001g0206 others(9): Show |
17 | HG02055.hp1 HG02055.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.825-440G>A | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 9/9 | chr22 | 36877188 | |||||||
| chr22:36877267 | G | A | 3 | a0001c0004t0001g0222 a0001c0006t0001g0081 a0001c0006t0001g0266 |
3 | HG02451.hp1 HG02451.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.825-361G>A | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 9/9 | chr22 | 36877267 | |||||||
| chr22:36877414 | A | G | 63 | a0001c0001t0001g0079 a0001c0001t0001g0205 a0001c0001t0001g0206 others(60): Show |
77 | HG00099.hp1 HG01106.hp2 HG01123.hp2 others(74): Show |
intron_variant | MODIFIER | c.825-214A>G | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 9/9 | chr22 | 36877414 | |||||||
| chr22:36877535 | C | T | 1 | a0001c0001t0002g0063 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.825-93C>T | NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 9/9 | chr22 | 36877535 |