Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 653361 |
| ensemblid | ENSG00000158517.16 |
| hgncid | 7660 |
| symbol | NCF1 |
| name | neutrophil cytosolic factor 1 |
| refseq_nuc | NM_000265.7 |
| refseq_prot | NP_000256.4 |
| ensembl_nuc | ENST00000289473.11 |
| ensembl_prot | ENSP00000289473.4 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 74774011 |
| end | 74789315 |
| strand | + |
| ver | v1.2 |
| region | chr7:74774011-74789315 |
| region5000 | chr7:74769011-74794315 |
| regionname0 | NCF1_chr7_74774011_74789315 |
| regionname5000 | NCF1_chr7_74769011_74794315 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 390 | 203 | 45 | 39 | 79 | 10 | 28 | 52 | NCF1_chr7_74769011_74794315 | NCF1 | MGDTF others(385): Show |
chr7 | 74769011 | 74794315 |
| a0002 | 0/0 | 390 | 65 | 29 | 17 | 16 | 0 | 3 | 12 | NCF1_chr7_74769011_74794315 | NCF1 | MGDTF others(385): Show |
chr7 | 74769011 | 74794315 |
| a0003 | 0/0 | 390 | 32 | 1 | 0 | 28 | 2 | 1 | 24 | NCF1_chr7_74769011_74794315 | NCF1 | MGDTF others(385): Show |
chr7 | 74769011 | 74794315 |
| a0004 | 0/0 | 390 | 13 | 3 | 3 | 7 | 0 | 0 | 7 | NCF1_chr7_74769011_74794315 | NCF1 | MGDTF others(385): Show |
chr7 | 74769011 | 74794315 |
| a0005 | 0/0 | 390 | 3 | 0 | 0 | 3 | 0 | 0 | 2 | NCF1_chr7_74769011_74794315 | NCF1 | MGDTF others(385): Show |
chr7 | 74769011 | 74794315 |
| a0006 | 0/0 | 390 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | MGDTF others(385): Show |
chr7 | 74769011 | 74794315 |
| a0007 | 0/0 | 390 | 3 | 0 | 0 | 3 | 0 | 0 | 2 | NCF1_chr7_74769011_74794315 | NCF1 | MGDTF others(385): Show |
chr7 | 74769011 | 74794315 |
| a0008 | 0/0 | 390 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | MGDTF others(385): Show |
chr7 | 74769011 | 74794315 |
| a0009 | 0/0 | 390 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | MGDTF others(385): Show |
chr7 | 74769011 | 74794315 |
| a0010 | 0/0 | 390 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | MGDTF others(385): Show |
chr7 | 74769011 | 74794315 |
| a0011 | 0/0 | 390 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | MGDTF others(385): Show |
chr7 | 74769011 | 74794315 |
| a0012 | 0/0 | 390 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NCF1_chr7_74769011_74794315 | NCF1 | MGDTF others(385): Show |
chr7 | 74769011 | 74794315 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1170 | 158 | 27 | 31 | 64 | 7 | 27 | NCF1_chr7_74769011_74794315 | NCF1 | ATGGG others(1165): Show |
chr7 | 74769011 | 74794315 | ||
| a0001c0003 | 0/0 | 1170 | 40 | 17 | 7 | 12 | 3 | 1 | NCF1_chr7_74769011_74794315 | NCF1 | ATGGG others(1165): Show |
chr7 | 74769011 | 74794315 | ||
| a0001c0013 | 0/0 | 1170 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | ATGGG others(1165): Show |
chr7 | 74769011 | 74794315 | ||
| a0001c0014 | 0/0 | 1170 | 1 | 0 | 1 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | ATGGG others(1165): Show |
chr7 | 74769011 | 74794315 | ||
| a0001c0015 | 0/0 | 1170 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | ATGGG others(1165): Show |
chr7 | 74769011 | 74794315 | ||
| a0001c0016 | 0/0 | 1170 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | ATGGG others(1165): Show |
chr7 | 74769011 | 74794315 | ||
| a0001c0017 | 0/0 | 1170 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | ATGGG others(1165): Show |
chr7 | 74769011 | 74794315 | ||
| a0002c0002 | 0/0 | 1170 | 44 | 12 | 14 | 16 | 0 | 2 | NCF1_chr7_74769011_74794315 | NCF1 | ATGGG others(1165): Show |
chr7 | 74769011 | 74794315 | ||
| a0002c0005 | 0/0 | 1170 | 21 | 17 | 3 | 0 | 0 | 1 | NCF1_chr7_74769011_74794315 | NCF1 | ATGGG others(1165): Show |
chr7 | 74769011 | 74794315 | ||
| a0003c0004 | 0/0 | 1170 | 32 | 1 | 0 | 28 | 2 | 1 | NCF1_chr7_74769011_74794315 | NCF1 | ATGGG others(1165): Show |
chr7 | 74769011 | 74794315 | ||
| a0004c0006 | 0/0 | 1170 | 12 | 3 | 2 | 7 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | ATGGG others(1165): Show |
chr7 | 74769011 | 74794315 | ||
| a0004c0012 | 0/0 | 1170 | 1 | 0 | 1 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | ATGGG others(1165): Show |
chr7 | 74769011 | 74794315 | ||
| a0005c0007 | 0/0 | 1170 | 3 | 0 | 0 | 3 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | ATGGG others(1165): Show |
chr7 | 74769011 | 74794315 | ||
| a0006c0010 | 0/0 | 1170 | 2 | 2 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | ATGGG others(1165): Show |
chr7 | 74769011 | 74794315 | ||
| a0006c0019 | 0/0 | 1170 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | ATGGG others(1165): Show |
chr7 | 74769011 | 74794315 | ||
| a0007c0008 | 0/0 | 1170 | 3 | 0 | 0 | 3 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | ATGGG others(1165): Show |
chr7 | 74769011 | 74794315 | ||
| a0008c0009 | 0/0 | 1170 | 3 | 3 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | ATGGG others(1165): Show |
chr7 | 74769011 | 74794315 | ||
| a0009c0021 | 0/0 | 1170 | 1 | 0 | 1 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | ATGGG others(1165): Show |
chr7 | 74769011 | 74794315 | ||
| a0009c0022 | 0/0 | 1170 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | ATGGG others(1165): Show |
chr7 | 74769011 | 74794315 | ||
| a0010c0011 | 0/0 | 1170 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | ATGGG others(1165): Show |
chr7 | 74769011 | 74794315 | ||
| a0011c0020 | 0/0 | 1170 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | ATGGG others(1165): Show |
chr7 | 74769011 | 74794315 | ||
| a0012c0018 | 0/0 | 1170 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | ATGGG others(1165): Show |
chr7 | 74769011 | 74794315 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 1349 | 136 | 24 | 22 | 63 | 6 | 21 | NCF1_chr7_74769011_74794315 | NCF1 | AGCAC others(1344): Show |
chr7 | 74769011 | 74794315 |
| a0001c0001t0002 | 1/1 | 1349 | 22 | 3 | 9 | 1 | 1 | 6 | NCF1_chr7_74769011_74794315 | NCF1 | AGCAC others(1344): Show |
chr7 | 74769011 | 74794315 |
| a0001c0003t0001 | 0/0 | 1349 | 40 | 17 | 7 | 12 | 3 | 1 | NCF1_chr7_74769011_74794315 | NCF1 | AGCAC others(1344): Show |
chr7 | 74769011 | 74794315 |
| a0001c0013t0001 | 0/0 | 1349 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | AGCAC others(1344): Show |
chr7 | 74769011 | 74794315 |
| a0001c0014t0001 | 0/0 | 1349 | 1 | 0 | 1 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | AGCAC others(1344): Show |
chr7 | 74769011 | 74794315 |
| a0001c0015t0001 | 0/0 | 1349 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | AGCAC others(1344): Show |
chr7 | 74769011 | 74794315 |
| a0001c0016t0001 | 0/0 | 1349 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | AGCAC others(1344): Show |
chr7 | 74769011 | 74794315 |
| a0001c0017t0001 | 0/0 | 1349 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | AGCAC others(1344): Show |
chr7 | 74769011 | 74794315 |
| a0002c0002t0001 | 0/0 | 1349 | 30 | 7 | 10 | 12 | 0 | 1 | NCF1_chr7_74769011_74794315 | NCF1 | AGCAC others(1344): Show |
chr7 | 74769011 | 74794315 |
| a0002c0002t0002 | 0/0 | 1349 | 14 | 5 | 4 | 4 | 0 | 1 | NCF1_chr7_74769011_74794315 | NCF1 | AGCAC others(1344): Show |
chr7 | 74769011 | 74794315 |
| a0002c0005t0001 | 0/0 | 1349 | 21 | 17 | 3 | 0 | 0 | 1 | NCF1_chr7_74769011_74794315 | NCF1 | AGCAC others(1344): Show |
chr7 | 74769011 | 74794315 |
| a0003c0004t0001 | 0/0 | 1349 | 32 | 1 | 0 | 28 | 2 | 1 | NCF1_chr7_74769011_74794315 | NCF1 | AGCAC others(1344): Show |
chr7 | 74769011 | 74794315 |
| a0004c0006t0001 | 0/0 | 1349 | 11 | 3 | 2 | 6 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | AGCAC others(1344): Show |
chr7 | 74769011 | 74794315 |
| a0004c0006t0002 | 0/0 | 1349 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | AGCAC others(1344): Show |
chr7 | 74769011 | 74794315 |
| a0004c0012t0001 | 0/0 | 1349 | 1 | 0 | 1 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | AGCAC others(1344): Show |
chr7 | 74769011 | 74794315 |
| a0005c0007t0001 | 0/0 | 1349 | 3 | 0 | 0 | 3 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | AGCAC others(1344): Show |
chr7 | 74769011 | 74794315 |
| a0006c0010t0001 | 0/0 | 1349 | 2 | 2 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | AGCAC others(1344): Show |
chr7 | 74769011 | 74794315 |
| a0006c0019t0001 | 0/0 | 1349 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | AGCAC others(1344): Show |
chr7 | 74769011 | 74794315 |
| a0007c0008t0001 | 0/0 | 1349 | 3 | 0 | 0 | 3 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | AGCAC others(1344): Show |
chr7 | 74769011 | 74794315 |
| a0008c0009t0001 | 0/0 | 1349 | 3 | 3 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | AGCAC others(1344): Show |
chr7 | 74769011 | 74794315 |
| a0009c0021t0001 | 0/0 | 1349 | 1 | 0 | 1 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | AGCAC others(1344): Show |
chr7 | 74769011 | 74794315 |
| a0009c0022t0001 | 0/0 | 1349 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | AGCAC others(1344): Show |
chr7 | 74769011 | 74794315 |
| a0010c0011t0001 | 0/0 | 1349 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | AGCAC others(1344): Show |
chr7 | 74769011 | 74794315 |
| a0011c0020t0001 | 0/0 | 1349 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | AGCAC others(1344): Show |
chr7 | 74769011 | 74794315 |
| a0012c0018t0001 | 0/0 | 1349 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | AGCAC others(1344): Show |
chr7 | 74769011 | 74794315 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 54 | 5 | 8 | 30 | 5 | 6 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0001c0001t0001g0003 | 0/0 | 8 | 0 | 6 | 2 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0001c0001t0001g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0001c0001t0001g0006 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0001c0001t0001g0010 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0001c0001t0001g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0001c0001t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0001c0001t0002g0014 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0001c0001t0002g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0001c0001t0002g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0001c0001t0002g0035 | 0/1 | 2 | 0 | 0 | 0 | 1 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0001c0001t0002g0036 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0001c0001t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0001c0001t0002g0136 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0001c0001t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0001c0003t0001g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0001c0003t0001g0002 | 0/0 | 6 | 5 | 1 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0001c0003t0001g0007 | 0/0 | 7 | 0 | 4 | 0 | 2 | 1 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0001c0003t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0001c0003t0001g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0001c0003t0001g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0001c0003t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0001c0003t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0001c0003t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0001c0003t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0001c0003t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0001c0003t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0001c0003t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0001c0003t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0001c0003t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0001c0003t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0001c0003t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0001c0003t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0001c0003t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0001c0003t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0001c0003t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0001c0003t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0001c0013t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0001c0014t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0001c0015t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0001c0016t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0001c0017t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0002c0002t0001g0001 | 0/0 | 10 | 1 | 5 | 3 | 0 | 1 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0002c0002t0001g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0002c0002t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0002c0002t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0002c0002t0001g0009 | 0/0 | 4 | 2 | 2 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0002c0002t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0002c0002t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0002c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0002c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0002c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0002c0002t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0002c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0002c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0002c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0002c0002t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0002c0002t0002g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0002c0002t0002g0019 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0002c0002t0002g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0002c0002t0002g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0002c0002t0002g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0002c0002t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0002c0002t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0002c0002t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0002c0002t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0002c0002t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0002c0002t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0002c0005t0001g0002 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0002c0005t0001g0008 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0002c0005t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0002c0005t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0002c0005t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0002c0005t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0002c0005t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0002c0005t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0002c0005t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0002c0005t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0002c0005t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0002c0005t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0002c0005t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0002c0005t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0003c0004t0001g0001 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0003c0004t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0003c0004t0001g0004 | 0/0 | 10 | 0 | 0 | 7 | 2 | 1 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0003c0004t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0003c0004t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0003c0004t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0003c0004t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0003c0004t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0003c0004t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0003c0004t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0003c0004t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0003c0004t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0003c0004t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0003c0004t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0004c0006t0001g0001 | 0/0 | 4 | 2 | 0 | 2 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0004c0006t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0004c0006t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0004c0006t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0004c0006t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0004c0006t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0004c0006t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0004c0006t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0004c0006t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0004c0012t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0005c0007t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0006c0010t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0006c0010t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0006c0019t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0007c0008t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0008c0009t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0008c0009t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0009c0021t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0009c0022t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0010c0011t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0011c0020t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| a0012c0018t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0003 | t0001 | g0007 | EUR | GBR | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG00280 | hp2 | a0003 | c0004 | t0001 | g0004 | EUR | FIN | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG00323 | hp2 | a0003 | c0004 | t0001 | g0004 | EUR | FIN | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG00408 | hp1 | a0003 | c0004 | t0001 | g0054 | EAS | CHS | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG00408 | hp2 | a0003 | c0004 | t0001 | g0004 | EAS | CHS | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG00423 | hp2 | a0003 | c0004 | t0001 | g0004 | EAS | CHS | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG00438 | hp2 | a0003 | c0004 | t0001 | g0023 | EAS | CHS | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG00544 | hp1 | a0001 | c0003 | t0001 | g0109 | EAS | CHS | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | CHS | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | CHS | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | CHS | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG00597 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | CHS | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | CHS | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG00639 | hp1 | a0001 | c0003 | t0001 | g0122 | AMR | PUR | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG00673 | hp1 | a0005 | c0007 | t0001 | g0012 | EAS | CHS | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG00673 | hp2 | a0001 | c0003 | t0001 | g0031 | EAS | CHS | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG00733 | hp2 | a0002 | c0005 | t0001 | g0022 | AMR | PUR | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG00735 | hp1 | a0001 | c0003 | t0001 | g0007 | AMR | PUR | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG01070 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG01070 | hp2 | a0002 | c0002 | t0002 | g0116 | AMR | PUR | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG01071 | hp2 | a0002 | c0002 | t0002 | g0032 | AMR | PUR | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG01074 | hp2 | a0002 | c0002 | t0001 | g0009 | AMR | PUR | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0141 | AMR | PUR | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG01109 | hp2 | a0001 | c0003 | t0001 | g0002 | AMR | PUR | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG01167 | hp1 | a0002 | c0002 | t0001 | g0078 | AMR | PUR | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG01167 | hp2 | a0001 | c0003 | t0001 | g0007 | AMR | PUR | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0036 | AMR | PUR | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG01169 | hp2 | a0001 | c0003 | t0001 | g0007 | AMR | PUR | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG01192 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG01192 | hp2 | a0009 | c0021 | t0001 | g0021 | AMR | PUR | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG01243 | hp1 | a0002 | c0005 | t0001 | g0002 | AMR | PUR | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG01243 | hp2 | a0002 | c0002 | t0001 | g0009 | AMR | PUR | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG01255 | hp1 | a0002 | c0002 | t0002 | g0032 | AMR | CLM | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | CLM | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0134 | AMR | CLM | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG01258 | hp1 | a0001 | c0003 | t0001 | g0029 | AMR | CLM | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0133 | AMR | CLM | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG01346 | hp1 | a0001 | c0014 | t0001 | g0001 | AMR | CLM | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0019 | AMR | CLM | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG01361 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | CLM | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG01433 | hp2 | a0002 | c0005 | t0001 | g0127 | AMR | CLM | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG01496 | hp2 | a0002 | c0002 | t0001 | g0003 | AMR | CLM | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0035 | EUR | IBS | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0085 | EUR | IBS | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG01884 | hp1 | a0001 | c0003 | t0001 | g0002 | AFR | ACB | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG01884 | hp2 | a0002 | c0005 | t0001 | g0097 | AFR | ACB | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG01891 | hp1 | a0006 | c0019 | t0001 | g0021 | AFR | ACB | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG01934 | hp1 | a0002 | c0002 | t0002 | g0019 | AMR | PEL | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG01934 | hp2 | a0002 | c0002 | t0001 | g0003 | AMR | PEL | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0147 | AMR | PEL | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG01978 | hp2 | a0001 | c0003 | t0001 | g0007 | AMR | PEL | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PEL | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0034 | AMR | PEL | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG02004 | hp1 | a0004 | c0006 | t0001 | g0062 | AMR | PEL | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG02004 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG02015 | hp1 | a0002 | c0002 | t0001 | g0056 | EAS | KHV | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG02055 | hp1 | a0002 | c0002 | t0001 | g0001 | AFR | ACB | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG02055 | hp2 | a0001 | c0003 | t0001 | g0033 | AFR | ACB | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | KHV | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG02056 | hp2 | a0001 | c0003 | t0001 | g0110 | EAS | KHV | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG02071 | hp1 | a0001 | c0013 | t0001 | g0073 | EAS | KHV | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG02071 | hp2 | a0002 | c0002 | t0002 | g0037 | EAS | KHV | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | KHV | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG02083 | hp1 | a0002 | c0002 | t0001 | g0071 | EAS | KHV | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | KHV | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG02132 | hp2 | a0007 | c0008 | t0001 | g0016 | EAS | KHV | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG02145 | hp1 | a0002 | c0002 | t0001 | g0042 | AFR | ACB | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG02145 | hp2 | a0002 | c0002 | t0001 | g0104 | AFR | ACB | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG02165 | hp1 | a0010 | c0011 | t0001 | g0012 | EAS | CDX | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG02257 | hp1 | a0002 | c0005 | t0001 | g0124 | AFR | ACB | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG02257 | hp2 | a0001 | c0003 | t0001 | g0098 | AFR | ACB | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG02258 | hp2 | a0002 | c0005 | t0001 | g0002 | AFR | ACB | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PEL | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG02280 | hp1 | a0002 | c0005 | t0001 | g0033 | AFR | ACB | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG02293 | hp1 | a0004 | c0006 | t0001 | g0081 | AMR | PEL | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG02293 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG02300 | hp2 | a0004 | c0012 | t0001 | g0049 | AMR | PEL | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG02451 | hp1 | a0001 | c0003 | t0001 | g0018 | AFR | ACB | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG02451 | hp2 | a0002 | c0005 | t0001 | g0011 | AFR | ACB | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG02572 | hp2 | a0011 | c0020 | t0001 | g0002 | AFR | GWD | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0139 | AFR | GWD | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG02615 | hp2 | a0002 | c0005 | t0001 | g0008 | AFR | GWD | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG02622 | hp1 | a0002 | c0005 | t0001 | g0008 | AFR | GWD | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG02622 | hp2 | a0008 | c0009 | t0001 | g0117 | AFR | GWD | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG02630 | hp1 | a0004 | c0006 | t0001 | g0001 | AFR | GWD | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG02630 | hp2 | a0001 | c0003 | t0001 | g0119 | AFR | GWD | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0055 | SAS | PJL | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG02698 | hp1 | a0002 | c0002 | t0002 | g0115 | SAS | PJL | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0080 | SAS | PJL | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0047 | SAS | PJL | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG02809 | hp1 | a0001 | c0003 | t0001 | g0018 | AFR | GWD | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG02818 | hp2 | a0006 | c0010 | t0001 | g0046 | AFR | GWD | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG02886 | hp1 | a0002 | c0005 | t0001 | g0008 | AFR | GWD | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | GWD | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG02895 | hp1 | a0008 | c0009 | t0001 | g0038 | AFR | GWD | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG02896 | hp2 | a0002 | c0002 | t0001 | g0009 | AFR | GWD | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG02897 | hp2 | a0008 | c0009 | t0001 | g0038 | AFR | GWD | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ESN | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG02922 | hp2 | a0003 | c0004 | t0001 | g0121 | AFR | ESN | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG02965 | hp1 | a0002 | c0002 | t0002 | g0130 | AFR | ESN | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | ESN | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG02970 | hp2 | a0001 | c0003 | t0001 | g0011 | AFR | ESN | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0135 | SAS | PJL | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG03041 | hp2 | a0002 | c0005 | t0001 | g0008 | AFR | GWD | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG03098 | hp1 | a0001 | c0017 | t0001 | g0002 | AFR | MSL | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG03130 | hp1 | a0002 | c0005 | t0001 | g0002 | AFR | ESN | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | ESN | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG03139 | hp1 | a0002 | c0002 | t0002 | g0129 | AFR | ESN | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG03139 | hp2 | a0001 | c0003 | t0001 | g0002 | AFR | ESN | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG03195 | hp1 | a0001 | c0003 | t0001 | g0011 | AFR | ESN | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG03195 | hp2 | a0002 | c0005 | t0001 | g0123 | AFR | ESN | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | MSL | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG03209 | hp2 | a0002 | c0005 | t0001 | g0008 | AFR | MSL | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG03225 | hp1 | a0002 | c0002 | t0001 | g0002 | AFR | MSL | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG03225 | hp2 | a0006 | c0010 | t0001 | g0090 | AFR | MSL | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG03453 | hp1 | a0001 | c0003 | t0001 | g0087 | AFR | MSL | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG03453 | hp2 | a0002 | c0005 | t0001 | g0125 | AFR | MSL | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG03486 | hp1 | a0001 | c0003 | t0001 | g0001 | AFR | MSL | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0146 | SAS | PJL | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0048 | SAS | PJL | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0064 | SAS | PJL | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG03540 | hp1 | a0002 | c0002 | t0001 | g0009 | AFR | GWD | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | GWD | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG03579 | hp1 | a0002 | c0005 | t0001 | g0126 | AFR | MSL | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG03579 | hp2 | a0001 | c0003 | t0001 | g0002 | AFR | MSL | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0066 | SAS | STU | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG03704 | hp1 | a0001 | c0003 | t0001 | g0007 | SAS | PJL | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG03704 | hp2 | a0003 | c0004 | t0001 | g0004 | SAS | PJL | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0014 | SAS | BEB | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0039 | SAS | BEB | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0145 | SAS | BEB | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | BEB | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0015 | SAS | STU | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG04115 | hp2 | a0002 | c0002 | t0001 | g0001 | SAS | STU | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | STU | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG04199 | hp2 | a0002 | c0005 | t0001 | g0075 | SAS | STU | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | STU | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0092 | SAS | STU | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0015 | SAS | STU | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0014 | SAS | STU | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA18522 | hp1 | a0002 | c0002 | t0001 | g0002 | AFR | YRI | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | YRI | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0137 | EAS | CHB | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA18939 | hp2 | a0002 | c0002 | t0002 | g0142 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA18944 | hp1 | a0003 | c0004 | t0001 | g0004 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA18945 | hp1 | a0003 | c0004 | t0001 | g0001 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA18948 | hp2 | a0002 | c0002 | t0001 | g0099 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA18949 | hp2 | a0004 | c0006 | t0002 | g0140 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA18959 | hp2 | a0004 | c0006 | t0001 | g0030 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA18960 | hp2 | a0012 | c0018 | t0001 | g0111 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA18962 | hp2 | a0002 | c0002 | t0001 | g0070 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA18964 | hp1 | a0001 | c0016 | t0001 | g0001 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA18966 | hp1 | a0003 | c0004 | t0001 | g0001 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA18966 | hp2 | a0003 | c0004 | t0001 | g0096 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA18968 | hp2 | a0004 | c0006 | t0001 | g0138 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA18970 | hp2 | a0003 | c0004 | t0001 | g0086 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA18971 | hp1 | a0003 | c0004 | t0001 | g0001 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA18973 | hp1 | a0002 | c0002 | t0001 | g0091 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA18973 | hp2 | a0001 | c0003 | t0001 | g0112 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA18974 | hp1 | a0003 | c0004 | t0001 | g0001 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA18974 | hp2 | a0003 | c0004 | t0001 | g0001 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA18979 | hp1 | a0002 | c0002 | t0002 | g0037 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA18981 | hp2 | a0003 | c0004 | t0001 | g0003 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA18983 | hp1 | a0004 | c0006 | t0001 | g0059 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA18984 | hp2 | a0003 | c0004 | t0001 | g0004 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA18989 | hp1 | a0002 | c0002 | t0001 | g0082 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA18993 | hp1 | a0003 | c0004 | t0001 | g0053 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA18993 | hp2 | a0004 | c0006 | t0001 | g0101 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA18995 | hp1 | a0002 | c0002 | t0002 | g0019 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA18995 | hp2 | a0001 | c0003 | t0001 | g0013 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA18998 | hp1 | a0007 | c0008 | t0001 | g0016 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA18998 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA19001 | hp1 | a0004 | c0006 | t0001 | g0001 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA19001 | hp2 | a0005 | c0007 | t0001 | g0012 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA19002 | hp1 | a0003 | c0004 | t0001 | g0004 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA19003 | hp1 | a0003 | c0004 | t0001 | g0005 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA19004 | hp1 | a0003 | c0004 | t0001 | g0079 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA19004 | hp2 | a0001 | c0003 | t0001 | g0108 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA19007 | hp2 | a0003 | c0004 | t0001 | g0004 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA19009 | hp1 | a0003 | c0004 | t0001 | g0050 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA19009 | hp2 | a0001 | c0015 | t0001 | g0005 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA19012 | hp2 | a0001 | c0003 | t0001 | g0031 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA19030 | hp1 | a0002 | c0005 | t0001 | g0040 | AFR | LWK | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA19030 | hp2 | a0002 | c0005 | t0001 | g0002 | AFR | LWK | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA19043 | hp1 | a0002 | c0002 | t0002 | g0118 | AFR | LWK | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA19043 | hp2 | a0002 | c0005 | t0001 | g0128 | AFR | LWK | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA19054 | hp1 | a0003 | c0004 | t0001 | g0001 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA19056 | hp1 | a0001 | c0003 | t0001 | g0013 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA19057 | hp1 | a0005 | c0007 | t0001 | g0012 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA19058 | hp1 | a0003 | c0004 | t0001 | g0001 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA19058 | hp2 | a0007 | c0008 | t0001 | g0016 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA19060 | hp1 | a0004 | c0006 | t0001 | g0001 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA19060 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA19062 | hp1 | a0003 | c0004 | t0001 | g0052 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA19064 | hp1 | a0003 | c0004 | t0001 | g0004 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA19065 | hp1 | a0001 | c0003 | t0001 | g0013 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA19065 | hp2 | a0003 | c0004 | t0001 | g0001 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA19066 | hp1 | a0001 | c0003 | t0001 | g0106 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA19082 | hp2 | a0001 | c0003 | t0001 | g0013 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA19085 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA19085 | hp2 | a0003 | c0004 | t0001 | g0023 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA19088 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA19088 | hp2 | a0003 | c0004 | t0001 | g0051 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA19090 | hp1 | a0002 | c0002 | t0001 | g0025 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA19090 | hp2 | a0001 | c0003 | t0001 | g0107 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA19240 | hp1 | a0001 | c0003 | t0001 | g0002 | AFR | YRI | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA19240 | hp2 | a0009 | c0022 | t0001 | g0008 | AFR | YRI | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA20129 | hp1 | a0001 | c0003 | t0001 | g0018 | AFR | ASW | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA20129 | hp2 | a0001 | c0003 | t0001 | g0105 | AFR | ASW | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA20752 | hp2 | a0001 | c0003 | t0001 | g0113 | EUR | TSI | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA20805 | hp2 | a0001 | c0003 | t0001 | g0007 | EUR | TSI | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0034 | AMR | CLM | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0014 | AMR | CLM | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG02486 | hp1 | a0001 | c0003 | t0001 | g0002 | AFR | ACB | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0036 | AFR | ACB | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0131 | AFR | ACB | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG03471 | hp1 | a0002 | c0002 | t0002 | g0014 | AFR | MSL | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG06807 | hp1 | a0004 | c0006 | t0001 | g0074 | AFR | USA | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | USA | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA18955 | hp1 | a0003 | c0004 | t0001 | g0001 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | USA | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA20300 | hp2 | a0004 | c0006 | t0001 | g0001 | AFR | USA | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA21309 | hp1 | a0001 | c0003 | t0001 | g0114 | AFR | LWK | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| NA21309 | hp2 | a0002 | c0002 | t0002 | g0132 | AFR | LWK | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0035 | REF | REF | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0136 | REF | REF | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:74779138 | G | C | 2 | a0005 a0010 |
4 | HG00673.hp1 HG02165.hp1 NA19001.hp2 others(1): Show |
missense_variant | MODERATE | c.210G>C | p.Arg70Ser | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 3/11 | 231/1349 | 210/1173 | 70/390 | chr7 | 74779138 | |||
| chr7:74779296 | G | A | 2 | a0003 a0004 |
45 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(42): Show |
missense_variant | MODERATE | c.269G>A | p.Arg90His | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 4/11 | 290/1349 | 269/1173 | 90/390 | chr7 | 74779296 | |||
| chr7:74779322 | A | G | 5 | a0002 a0003 a0008 others(2): Show |
103 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(100): Show |
missense_variant | MODERATE | c.295A>G | p.Ser99Gly | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 4/11 | 316/1349 | 295/1173 | 99/390 | chr7 | 74779322 | |||
| chr7:74779326 | C | T | 1 | a0011 | 1 | HG02572.hp2 | missense_variant | MODERATE | c.299C>T | p.Thr100Met | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 4/11 | 320/1349 | 299/1173 | 100/390 | chr7 | 74779326 | |||
| chr7:74782983 | A | G | 3 | a0006 a0008 a0009 |
8 | HG01192.hp2 HG01891.hp1 HG02622.hp2 others(5): Show |
missense_variant | MODERATE | c.496A>G | p.Asn166Asp | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 6/11 | 517/1349 | 496/1173 | 166/390 | chr7 | 74782983 | |||
| chr7:74788576 | C | T | 1 | a0007 | 3 | HG02132.hp2 NA18998.hp1 NA19058.hp2 |
missense_variant | MODERATE | c.923C>T | p.Ala308Val | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 10/11 | 944/1349 | 923/1173 | 308/390 | chr7 | 74788576 | |||
| chr7:74788604 | G | C | 1 | a0008 | 3 | HG02622.hp2 HG02895.hp1 HG02897.hp2 |
missense_variant | MODERATE | c.951G>C | p.Lys317Asn | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 10/11 | 972/1349 | 951/1173 | 317/390 | chr7 | 74788604 | |||
| chr7:74789048 | G | T | 1 | a0012 | 1 | NA18960.hp2 | missense_variant | MODERATE | c.1061G>T | p.Arg354Leu | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 11/11 | 1082/1349 | 1061/1173 | 354/390 | chr7 | 74789048 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:74779372 | C | T | 9 | a0001c0003 a0001c0016 a0001c0017 others(6): Show |
68 | HG00140.hp1 HG00544.hp1 HG00639.hp1 others(65): Show |
synonymous_variant | LOW | c.345C>T | p.Leu115Leu | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 4/11 | 366/1349 | 345/1173 | 115/390 | chr7 | 74779372 | |||
| chr7:74779414 | G | A | 2 | a0001c0013 a0001c0016 |
2 | HG02071.hp1 NA18964.hp1 |
synonymous_variant | LOW | c.387G>A | p.Thr129Thr | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 4/11 | 408/1349 | 387/1173 | 129/390 | chr7 | 74779414 | |||
| chr7:74783045 | A | G | 4 | a0001c0015 a0006c0010 a0006c0019 others(1): Show |
5 | HG01192.hp2 HG01891.hp1 HG02818.hp2 others(2): Show |
synonymous_variant | LOW | c.558A>G | p.Val186Val | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 6/11 | 579/1349 | 558/1173 | 186/390 | chr7 | 74783045 | |||
| chr7:74783571 | G | A | 1 | a0001c0017 | 1 | HG03098.hp1 | synonymous_variant | LOW | c.621G>A | p.Ala207Ala | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 7/11 | 642/1349 | 621/1173 | 207/390 | chr7 | 74783571 | |||
| chr7:74785285 | C | T | 1 | a0001c0014 | 1 | HG01346.hp1 | synonymous_variant | LOW | c.786C>T | p.Gly262Gly | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 8/11 | 807/1349 | 786/1173 | 262/390 | chr7 | 74785285 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:74789215 | T | C | 22 | a0001c0001t0001 a0001c0003t0001 a0001c0013t0001 others(19): Show |
293 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(290): Show |
3_prime_UTR_variant | MODIFIER | c.*55T>C | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 11/11 | 55 | chr7 | 74789215 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:74774463 | C | T | 1 | a0008c0009t0001g0038 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.72+360C>T | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 1/10 | chr7 | 74774463 | |||||||
| chr7:74774752 | T | G | 111 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(108): Show |
238 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(235): Show |
intron_variant | MODIFIER | c.72+649T>G | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 1/10 | chr7 | 74774752 | |||||||
| chr7:74774819 | A | G | 2 | a0001c0001t0001g0103 a0002c0002t0001g0104 |
2 | HG02145.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.72+716A>G | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 1/10 | chr7 | 74774819 | |||||||
| chr7:74774884 | G | A | 1 | a0001c0001t0001g0039 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.72+781G>A | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 1/10 | chr7 | 74774884 | |||||||
| chr7:74774887 | C | T | 2 | a0005c0007t0001g0012 a0010c0011t0001g0012 |
4 | HG00673.hp1 HG02165.hp1 NA19001.hp2 others(1): Show |
intron_variant | MODIFIER | c.72+784C>T | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 1/10 | chr7 | 74774887 | |||||||
| chr7:74775097 | G | A | 1 | a0001c0001t0001g0039 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.72+994G>A | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 1/10 | chr7 | 74775097 | |||||||
| chr7:74775104 | C | A | 10 | a0001c0003t0001g0007 a0001c0003t0001g0013 a0001c0003t0001g0031 others(7): Show |
20 | HG00140.hp1 HG00544.hp1 HG00673.hp2 others(17): Show |
intron_variant | MODIFIER | c.72+1001C>A | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 1/10 | chr7 | 74775104 | |||||||
| chr7:74775131 | C | T | 3 | a0001c0001t0002g0145 a0001c0001t0002g0146 a0001c0001t0002g0147 |
3 | HG01975.hp1 HG03490.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.72+1028C>T | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 1/10 | chr7 | 74775131 | |||||||
| chr7:74775134 | C | G | 1 | a0001c0001t0001g0102 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.72+1031C>G | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 1/10 | chr7 | 74775134 | |||||||
| chr7:74775218 | T | C | 2 | a0002c0002t0001g0009 a0002c0005t0001g0040 |
5 | HG01074.hp2 HG01243.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.72+1115T>C | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 1/10 | chr7 | 74775218 | |||||||
| chr7:74775318 | C | A | 1 | a0001c0001t0001g0041 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.72+1215C>A | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 1/10 | chr7 | 74775318 | |||||||
| chr7:74775471 | T | C | 2 | a0001c0003t0001g0007 a0001c0003t0001g0105 |
8 | HG00140.hp1 HG00735.hp1 HG01167.hp2 others(5): Show |
intron_variant | MODIFIER | c.72+1368T>C | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 1/10 | chr7 | 74775471 | |||||||
| chr7:74775607 | C | T | 3 | a0001c0001t0001g0020 a0001c0001t0001g0143 a0001c0001t0001g0144 |
5 | HG01891.hp2 HG02280.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.72+1504C>T | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 1/10 | chr7 | 74775607 | |||||||
| chr7:74775881 | G | A | 3 | a0001c0003t0001g0112 a0001c0003t0001g0113 a0001c0003t0001g0114 |
3 | NA18973.hp2 NA20752.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.73-1386G>A | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 1/10 | chr7 | 74775881 | |||||||
| chr7:74775882 | C | T | 7 | a0001c0001t0001g0020 a0001c0001t0001g0143 a0001c0001t0001g0144 others(4): Show |
11 | HG01346.hp2 HG01891.hp2 HG01934.hp1 others(8): Show |
intron_variant | MODIFIER | c.73-1385C>T | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 1/10 | chr7 | 74775882 | |||||||
| chr7:74775890 | T | C | 5 | a0001c0001t0001g0039 a0002c0002t0002g0032 a0002c0002t0002g0115 others(2): Show |
7 | HG01070.hp2 HG01071.hp2 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.73-1377T>C | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 1/10 | chr7 | 74775890 | |||||||
| chr7:74775900 | GCAT | G | 5 | a0001c0001t0001g0039 a0002c0002t0002g0032 a0002c0002t0002g0115 others(2): Show |
7 | HG01070.hp2 HG01071.hp2 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.73-1366_73-1364del others(3): Show |
NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 1/10 | chr7 | 74775900 | |||||||
| chr7:74775948 | C | CT | 6 | a0001c0001t0002g0019 a0002c0002t0002g0019 a0002c0002t0002g0032 others(3): Show |
9 | HG01070.hp2 HG01071.hp2 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.73-1305dupT | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 74775948 | ||||||
| chr7:74775948 | C | CTT | 4 | a0001c0001t0001g0020 a0001c0001t0001g0143 a0001c0001t0001g0144 others(1): Show |
7 | HG01891.hp2 HG02280.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.73-1306_73-1305dup others(2): Show |
NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 74775948 | ||||||
| chr7:74775948 | C | T | 1 | a0001c0001t0001g0039 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.73-1319C>T | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 1/10 | chr7 | 74775948 | |||||||
| chr7:74775948 | CT | C | 137 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(134): Show |
282 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.73-1305delT | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 74775948 | ||||||
| chr7:74776003 | A | G | 1 | a0002c0002t0001g0099 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.73-1264A>G | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 1/10 | chr7 | 74776003 | |||||||
| chr7:74776011 | A | G | 1 | a0001c0001t0002g0141 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.73-1256A>G | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 1/10 | chr7 | 74776011 | |||||||
| chr7:74776039 | C | T | 28 | a0001c0001t0001g0120 a0001c0003t0001g0002 a0001c0003t0001g0007 others(25): Show |
52 | HG00140.hp1 HG00544.hp1 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.73-1228C>T | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 1/10 | chr7 | 74776039 | |||||||
| chr7:74776132 | A | T | 1 | a0001c0001t0001g0102 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.73-1135A>T | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 1/10 | chr7 | 74776132 | |||||||
| chr7:74776509 | A | C | 145 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(142): Show |
291 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.73-758A>C | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 1/10 | chr7 | 74776509 | |||||||
| chr7:74776619 | C | T | 1 | a0003c0004t0001g0096 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.73-648C>T | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 1/10 | chr7 | 74776619 | |||||||
| chr7:74776701 | C | T | 1 | a0001c0001t0001g0095 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.73-566C>T | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 1/10 | chr7 | 74776701 | |||||||
| chr7:74776707 | G | GCCCCTCC others(23): Show |
1 | a0002c0002t0001g0042 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.73-551_73-522dupGT others(28): Show |
NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 74776707 | ||||||
| chr7:74776711 | C | T | 2 | a0002c0002t0002g0032 a0002c0002t0002g0116 |
3 | HG01070.hp2 HG01071.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.73-556C>T | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 1/10 | chr7 | 74776711 | |||||||
| chr7:74776716 | G | GTCCCCTC others(23): Show |
89 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(86): Show |
206 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.73-538_73-509dupTC others(28): Show |
NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 74776716 | ||||||
| chr7:74776716 | G | GTCCCCTC others(53): Show |
1 | a0001c0001t0001g0094 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.73-509_73-508insTC others(58): Show |
NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 74776716 | ||||||
| chr7:74776716 | G | T | 7 | a0001c0001t0002g0019 a0002c0002t0002g0019 a0002c0002t0002g0032 others(4): Show |
10 | HG01070.hp2 HG01071.hp2 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.73-551G>T | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 1/10 | chr7 | 74776716 | |||||||
| chr7:74776717 | T | C | 7 | a0001c0001t0002g0019 a0002c0002t0002g0019 a0002c0002t0002g0032 others(4): Show |
10 | HG01070.hp2 HG01071.hp2 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.73-550T>C | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 1/10 | chr7 | 74776717 | |||||||
| chr7:74777114 | C | T | 1 | a0001c0001t0001g0093 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.73-153C>T | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 1/10 | chr7 | 74777114 | |||||||
| chr7:74777361 | T | C | 143 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(140): Show |
289 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.153+14T>C | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 2/10 | chr7 | 74777361 | |||||||
| chr7:74777502 | A | ACAGGGTC others(13): Show |
5 | a0001c0001t0002g0035 a0001c0001t0002g0036 a0002c0005t0001g0126 others(2): Show |
6 | HG01169.hp1 HG01433.hp2 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.153+156_153+175dup others(20): Show |
NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 74777502 | ||||||
| chr7:74777567 | C | T | 1 | a0002c0002t0001g0091 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.153+220C>T | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 2/10 | chr7 | 74777567 | |||||||
| chr7:74777569 | C | G | 1 | a0001c0001t0002g0036 | 2 | HG01169.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.153+222C>G | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 2/10 | chr7 | 74777569 | |||||||
| chr7:74777616 | G | A | 1 | a0001c0001t0002g0036 | 2 | HG01169.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.153+269G>A | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 2/10 | chr7 | 74777616 | |||||||
| chr7:74777927 | AAAAC | A | 2 | a0008c0009t0001g0038 a0008c0009t0001g0117 |
3 | HG02622.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.153+582_153+585del others(4): Show |
NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 74777927 | ||||||
| chr7:74778106 | G | A | 1 | a0002c0002t0002g0130 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.153+759G>A | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 2/10 | chr7 | 74778106 | |||||||
| chr7:74778319 | G | A | 3 | a0001c0001t0001g0020 a0001c0001t0001g0143 a0001c0001t0001g0144 |
5 | HG01891.hp2 HG02280.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.154-763G>A | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 2/10 | chr7 | 74778319 | |||||||
| chr7:74778377 | C | T | 8 | a0001c0001t0001g0022 a0001c0001t0001g0047 a0001c0001t0001g0048 others(5): Show |
9 | HG00733.hp2 HG01169.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.154-705C>T | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 2/10 | chr7 | 74778377 | |||||||
| chr7:74778595 | G | A | 5 | a0001c0001t0001g0120 a0001c0001t0002g0036 a0001c0003t0001g0119 others(2): Show |
6 | HG01169.hp1 HG02486.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.154-487G>A | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 2/10 | chr7 | 74778595 | |||||||
| chr7:74778644 | C | T | 10 | a0001c0001t0001g0022 a0001c0001t0001g0047 a0001c0001t0001g0048 others(7): Show |
11 | HG00733.hp2 HG01169.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.154-438C>T | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 2/10 | chr7 | 74778644 | |||||||
| chr7:74778736 | A | G | 145 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(142): Show |
292 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.154-346A>G | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 2/10 | chr7 | 74778736 | |||||||
| chr7:74778776 | G | A | 10 | a0001c0001t0001g0022 a0001c0001t0001g0047 a0001c0001t0001g0048 others(7): Show |
11 | HG00733.hp2 HG01169.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.154-306G>A | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 2/10 | chr7 | 74778776 | |||||||
| chr7:74779020 | C | A | 37 | a0001c0003t0001g0002 a0001c0003t0001g0007 a0001c0003t0001g0013 others(34): Show |
66 | HG00140.hp1 HG00544.hp1 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.154-62C>A | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 2/10 | chr7 | 74779020 | |||||||
| chr7:74779221 | C | A | 2 | a0003c0004t0001g0121 a0004c0012t0001g0049 |
2 | HG02300.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.230-36C>A | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 3/10 | chr7 | 74779221 | |||||||
| chr7:74779228 | G | A | 2 | a0001c0001t0001g0020 a0001c0001t0001g0143 |
4 | HG01891.hp2 HG02280.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.230-29G>A | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 3/10 | chr7 | 74779228 | |||||||
| chr7:74779594 | C | T | 2 | a0001c0001t0001g0047 a0001c0001t0001g0048 |
2 | HG02738.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.395+172C>T | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 4/10 | chr7 | 74779594 | |||||||
| chr7:74779691 | C | T | 2 | a0001c0001t0002g0137 a0002c0005t0001g0125 |
2 | HG03453.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.395+269C>T | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 4/10 | chr7 | 74779691 | |||||||
| chr7:74779878 | C | G | 1 | a0006c0010t0001g0090 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.395+456C>G | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 4/10 | chr7 | 74779878 | |||||||
| chr7:74779935 | C | T | 2 | a0001c0001t0001g0088 a0001c0001t0001g0089 |
2 | HG02965.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.395+513C>T | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 4/10 | chr7 | 74779935 | |||||||
| chr7:74780048 | C | T | 17 | a0001c0001t0001g0011 a0001c0001t0001g0022 a0001c0001t0001g0047 others(14): Show |
21 | HG00733.hp2 HG01074.hp2 HG01192.hp2 others(18): Show |
intron_variant | MODIFIER | c.395+626C>T | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 4/10 | chr7 | 74780048 | |||||||
| chr7:74780073 | G | C | 5 | a0003c0004t0001g0004 a0003c0004t0001g0050 a0003c0004t0001g0051 others(2): Show |
14 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(11): Show |
intron_variant | MODIFIER | c.395+651G>C | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 4/10 | chr7 | 74780073 | |||||||
| chr7:74780103 | G | A | 5 | a0001c0001t0001g0022 a0001c0001t0001g0047 a0001c0001t0001g0048 others(2): Show |
5 | HG00733.hp2 HG02735.hp1 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.396-677G>A | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 4/10 | chr7 | 74780103 | |||||||
| chr7:74780132 | C | T | 5 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0002g0036 others(2): Show |
6 | HG01169.hp1 HG01975.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.396-648C>T | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 4/10 | chr7 | 74780132 | |||||||
| chr7:74780137 | C | T | 4 | a0001c0001t0001g0029 a0001c0001t0001g0085 a0001c0001t0001g0102 others(1): Show |
4 | HG00642.hp2 HG00735.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.396-643C>T | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 4/10 | chr7 | 74780137 | |||||||
| chr7:74780198 | G | C | 172 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(169): Show |
326 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.396-582G>C | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 4/10 | chr7 | 74780198 | |||||||
| chr7:74780234 | G | A | 4 | a0001c0001t0001g0010 a0001c0001t0001g0043 a0001c0001t0001g0044 others(1): Show |
7 | HG02559.hp2 HG02809.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.396-546G>A | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 4/10 | chr7 | 74780234 | |||||||
| chr7:74780384 | G | C | 2 | a0008c0009t0001g0038 a0008c0009t0001g0117 |
3 | HG02622.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.396-396G>C | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 4/10 | chr7 | 74780384 | |||||||
| chr7:74780405 | G | C | 2 | a0002c0002t0001g0009 a0002c0005t0001g0040 |
5 | HG01074.hp2 HG01243.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.396-375G>C | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 4/10 | chr7 | 74780405 | |||||||
| chr7:74780556 | G | T | 1 | a0001c0001t0001g0084 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.396-224G>T | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 4/10 | chr7 | 74780556 | |||||||
| chr7:74780639 | C | G | 3 | a0001c0001t0001g0011 a0001c0003t0001g0011 a0002c0005t0001g0011 |
4 | HG02451.hp2 HG02970.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.396-141C>G | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 4/10 | chr7 | 74780639 | |||||||
| chr7:74780859 | C | CG | 30 | a0001c0001t0001g0017 a0001c0001t0001g0083 a0001c0001t0001g0095 others(27): Show |
57 | HG00140.hp1 HG00544.hp2 HG00673.hp2 others(54): Show |
intron_variant | MODIFIER | c.451+32dupG | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr7 | 74780859 | ||||||
| chr7:74780989 | G | A | 1 | a0004c0006t0001g0081 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.451+154G>A | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 5/10 | chr7 | 74780989 | |||||||
| chr7:74781244 | CA | C | 131 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(128): Show |
265 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.451+430delA | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr7 | 74781244 | ||||||
| chr7:74781244 | CAA | C | 13 | a0001c0001t0001g0006 a0001c0001t0001g0028 a0001c0001t0001g0044 others(10): Show |
20 | HG00558.hp2 HG01167.hp1 HG01515.hp2 others(17): Show |
intron_variant | MODIFIER | c.451+429_451+430del others(2): Show |
NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr7 | 74781244 | ||||||
| chr7:74781342 | A | T | 1 | a0001c0001t0001g0080 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.451+507A>T | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 5/10 | chr7 | 74781342 | |||||||
| chr7:74781375 | G | A | 1 | a0004c0006t0001g0081 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.451+540G>A | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 5/10 | chr7 | 74781375 | |||||||
| chr7:74781407 | T | C | 143 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(140): Show |
289 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.451+572T>C | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 5/10 | chr7 | 74781407 | |||||||
| chr7:74781422 | C | T | 1 | a0002c0005t0001g0128 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.451+587C>T | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 5/10 | chr7 | 74781422 | |||||||
| chr7:74781492 | C | T | 110 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(107): Show |
230 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.451+657C>T | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 5/10 | chr7 | 74781492 | |||||||
| chr7:74781555 | C | T | 2 | a0001c0001t0001g0020 a0001c0001t0001g0144 |
4 | HG01891.hp2 HG02280.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.451+720C>T | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 5/10 | chr7 | 74781555 | |||||||
| chr7:74781580 | T | C | 2 | a0008c0009t0001g0038 a0008c0009t0001g0117 |
3 | HG02622.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.451+745T>C | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 5/10 | chr7 | 74781580 | |||||||
| chr7:74781617 | C | T | 1 | a0002c0005t0001g0040 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.451+782C>T | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 5/10 | chr7 | 74781617 | |||||||
| chr7:74781642 | C | T | 1 | a0001c0003t0001g0114 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.451+807C>T | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 5/10 | chr7 | 74781642 | |||||||
| chr7:74781743 | A | G | 136 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(133): Show |
275 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.451+908A>G | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 5/10 | chr7 | 74781743 | |||||||
| chr7:74781745 | CT | C | 26 | a0001c0001t0001g0120 a0001c0003t0001g0002 a0001c0003t0001g0007 others(23): Show |
45 | HG00140.hp1 HG00544.hp1 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.451+911delT | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 5/10 | chr7 | 74781745 | |||||||
| chr7:74781755 | G | A | 102 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(99): Show |
219 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.451+920G>A | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 5/10 | chr7 | 74781755 | |||||||
| chr7:74781786 | G | C | 11 | a0001c0001t0001g0022 a0001c0001t0001g0047 a0001c0001t0001g0048 others(8): Show |
14 | HG00733.hp2 HG01074.hp2 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.451+951G>C | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 5/10 | chr7 | 74781786 | |||||||
| chr7:74781840 | C | A | 8 | a0003c0004t0001g0004 a0003c0004t0001g0023 a0003c0004t0001g0050 others(5): Show |
18 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(15): Show |
intron_variant | MODIFIER | c.451+1005C>A | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 5/10 | chr7 | 74781840 | |||||||
| chr7:74781899 | T | C | 153 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(150): Show |
304 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(301): Show |
intron_variant | MODIFIER | c.452-1040T>C | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 5/10 | chr7 | 74781899 | |||||||
| chr7:74781928 | G | C | 1 | a0002c0002t0001g0082 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.452-1011G>C | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 5/10 | chr7 | 74781928 | |||||||
| chr7:74782011 | G | A | 2 | a0001c0001t0001g0088 a0001c0001t0001g0089 |
2 | HG02965.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.452-928G>A | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 5/10 | chr7 | 74782011 | |||||||
| chr7:74782019 | T | C | 143 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(140): Show |
289 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.452-920T>C | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 5/10 | chr7 | 74782019 | |||||||
| chr7:74782181 | G | A | 1 | a0001c0001t0001g0055 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.452-758G>A | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 5/10 | chr7 | 74782181 | |||||||
| chr7:74782209 | C | T | 1 | a0002c0005t0001g0075 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.452-730C>T | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 5/10 | chr7 | 74782209 | |||||||
| chr7:74782432 | CAA | C | 138 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(135): Show |
282 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.452-490_452-489del others(2): Show |
NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr7 | 74782432 | ||||||
| chr7:74782482 | A | G | 150 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(147): Show |
300 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.452-457A>G | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 5/10 | chr7 | 74782482 | |||||||
| chr7:74782501 | T | C | 1 | a0001c0003t0001g0114 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.452-438T>C | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 5/10 | chr7 | 74782501 | |||||||
| chr7:74782613 | A | G | 2 | a0008c0009t0001g0038 a0008c0009t0001g0117 |
3 | HG02622.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.452-326A>G | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 5/10 | chr7 | 74782613 | |||||||
| chr7:74782668 | C | T | 2 | a0008c0009t0001g0038 a0008c0009t0001g0117 |
3 | HG02622.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.452-271C>T | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 5/10 | chr7 | 74782668 | |||||||
| chr7:74782846 | C | A | 1 | a0008c0009t0001g0038 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.452-93C>A | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 5/10 | chr7 | 74782846 | |||||||
| chr7:74783128 | G | A | 1 | a0002c0005t0001g0040 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.574+67G>A | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 6/10 | chr7 | 74783128 | |||||||
| chr7:74783215 | G | C | 4 | a0001c0001t0001g0010 a0001c0001t0001g0043 a0001c0001t0001g0044 others(1): Show |
7 | HG02559.hp2 HG02809.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.574+154G>C | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 6/10 | chr7 | 74783215 | |||||||
| chr7:74783255 | A | T | 31 | a0001c0001t0001g0120 a0001c0003t0001g0002 a0001c0003t0001g0007 others(28): Show |
56 | HG00140.hp1 HG00544.hp1 HG00639.hp1 others(53): Show |
intron_variant | MODIFIER | c.574+194A>T | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 6/10 | chr7 | 74783255 | |||||||
| chr7:74783387 | A | G | 31 | a0001c0001t0001g0120 a0001c0003t0001g0002 a0001c0003t0001g0007 others(28): Show |
56 | HG00140.hp1 HG00544.hp1 HG00639.hp1 others(53): Show |
intron_variant | MODIFIER | c.575-138A>G | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 6/10 | chr7 | 74783387 | |||||||
| chr7:74783439 | G | C | 5 | a0001c0001t0001g0022 a0001c0001t0001g0047 a0001c0001t0001g0048 others(2): Show |
5 | HG00733.hp2 HG02735.hp1 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.575-86G>C | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 6/10 | chr7 | 74783439 | |||||||
| chr7:74783476 | G | A | 1 | a0002c0002t0001g0009 | 4 | HG01074.hp2 HG01243.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.575-49G>A | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 6/10 | chr7 | 74783476 | |||||||
| chr7:74783481 | G | A | 1 | a0002c0005t0001g0128 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.575-44G>A | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 6/10 | chr7 | 74783481 | |||||||
| chr7:74783649 | G | A | 3 | a0001c0001t0001g0020 a0001c0001t0001g0143 a0001c0001t0001g0144 |
5 | HG01891.hp2 HG02280.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.682+17G>A | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 7/10 | chr7 | 74783649 | |||||||
| chr7:74784054 | T | A | 1 | a0002c0002t0001g0056 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.682+422T>A | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 7/10 | chr7 | 74784054 | |||||||
| chr7:74784109 | C | T | 143 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(140): Show |
289 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.682+477C>T | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 7/10 | chr7 | 74784109 | |||||||
| chr7:74784210 | T | C | 1 | a0001c0001t0001g0057 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.682+578T>C | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 7/10 | chr7 | 74784210 | |||||||
| chr7:74784315 | T | C | 172 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(169): Show |
327 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.682+683T>C | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 7/10 | chr7 | 74784315 | |||||||
| chr7:74784418 | C | CTTG | 162 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(159): Show |
312 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.683-762_683-761ins others(3): Show |
NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr7 | 74784418 | ||||||
| chr7:74784418 | C | CTTGT | 8 | a0001c0001t0001g0083 a0001c0003t0001g0098 a0001c0013t0001g0073 others(5): Show |
13 | HG02056.hp1 HG02071.hp1 HG02071.hp2 others(10): Show |
intron_variant | MODIFIER | c.683-762_683-761ins others(4): Show |
NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr7 | 74784418 | ||||||
| chr7:74784553 | A | G | 170 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(167): Show |
324 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(321): Show |
intron_variant | MODIFIER | c.683-629A>G | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 7/10 | chr7 | 74784553 | |||||||
| chr7:74784667 | C | G | 170 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(167): Show |
324 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(321): Show |
intron_variant | MODIFIER | c.683-515C>G | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 7/10 | chr7 | 74784667 | |||||||
| chr7:74784709 | T | C | 170 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(167): Show |
324 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(321): Show |
intron_variant | MODIFIER | c.683-473T>C | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 7/10 | chr7 | 74784709 | |||||||
| chr7:74784815 | C | G | 170 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(167): Show |
324 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(321): Show |
intron_variant | MODIFIER | c.683-367C>G | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 7/10 | chr7 | 74784815 | |||||||
| chr7:74784878 | G | A | 29 | a0001c0001t0002g0014 a0001c0001t0002g0019 a0001c0001t0002g0034 others(26): Show |
37 | HG01070.hp2 HG01071.hp2 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.683-304G>A | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 7/10 | chr7 | 74784878 | |||||||
| chr7:74784945 | A | G | 1 | a0001c0001t0001g0120 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.683-237A>G | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 7/10 | chr7 | 74784945 | |||||||
| chr7:74784972 | C | T | 5 | a0001c0001t0001g0027 a0001c0001t0001g0072 a0001c0001t0001g0088 others(2): Show |
6 | HG02886.hp2 HG02895.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.683-210C>T | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 7/10 | chr7 | 74784972 | |||||||
| chr7:74785049 | G | C | 8 | a0001c0001t0001g0006 a0001c0001t0001g0028 a0001c0001t0001g0058 others(5): Show |
15 | HG00558.hp2 HG02135.hp2 NA18944.hp2 others(12): Show |
intron_variant | MODIFIER | c.683-133G>C | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 7/10 | chr7 | 74785049 | |||||||
| chr7:74785092 | C | G | 30 | a0001c0001t0001g0120 a0001c0003t0001g0002 a0001c0003t0001g0007 others(27): Show |
55 | HG00140.hp1 HG00544.hp1 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.683-90C>G | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 7/10 | chr7 | 74785092 | |||||||
| chr7:74785099 | G | A | 2 | a0008c0009t0001g0038 a0008c0009t0001g0117 |
3 | HG02622.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.683-83G>A | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 7/10 | chr7 | 74785099 | |||||||
| chr7:74785106 | G | A | 1 | a0001c0001t0002g0092 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.683-76G>A | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 7/10 | chr7 | 74785106 | |||||||
| chr7:74785126 | C | T | 1 | a0008c0009t0001g0117 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.683-56C>T | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 7/10 | chr7 | 74785126 | |||||||
| chr7:74785354 | C | T | 3 | a0001c0003t0001g0018 a0001c0003t0001g0098 a0002c0005t0001g0097 |
5 | HG01884.hp2 HG02257.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.800+55C>T | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 8/10 | chr7 | 74785354 | |||||||
| chr7:74785449 | A | G | 3 | a0001c0001t0001g0011 a0001c0003t0001g0011 a0002c0005t0001g0011 |
4 | HG02451.hp2 HG02970.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.800+150A>G | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 8/10 | chr7 | 74785449 | |||||||
| chr7:74785602 | G | A | 1 | a0004c0006t0001g0059 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.800+303G>A | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 8/10 | chr7 | 74785602 | |||||||
| chr7:74785617 | T | C | 3 | a0001c0001t0001g0011 a0001c0003t0001g0011 a0002c0005t0001g0011 |
4 | HG02451.hp2 HG02970.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.800+318T>C | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 8/10 | chr7 | 74785617 | |||||||
| chr7:74785652 | A | G | 3 | a0001c0001t0001g0011 a0001c0003t0001g0011 a0002c0005t0001g0011 |
4 | HG02451.hp2 HG02970.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.800+353A>G | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 8/10 | chr7 | 74785652 | |||||||
| chr7:74785664 | T | C | 3 | a0001c0001t0001g0011 a0001c0003t0001g0011 a0002c0005t0001g0011 |
4 | HG02451.hp2 HG02970.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.800+365T>C | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 8/10 | chr7 | 74785664 | |||||||
| chr7:74785708 | C | A | 1 | a0001c0001t0001g0060 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.800+409C>A | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 8/10 | chr7 | 74785708 | |||||||
| chr7:74785746 | G | T | 1 | a0002c0002t0001g0071 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.800+447G>T | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 8/10 | chr7 | 74785746 | |||||||
| chr7:74785883 | CA | C | 25 | a0001c0001t0001g0003 a0001c0001t0001g0028 a0001c0001t0001g0047 others(22): Show |
38 | HG00639.hp1 HG01070.hp2 HG01071.hp2 others(35): Show |
intron_variant | MODIFIER | c.800+605delA | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr7 | 74785883 | ||||||
| chr7:74785883 | CAA | C | 121 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(118): Show |
259 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.800+604_800+605del others(2): Show |
NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr7 | 74785883 | ||||||
| chr7:74785883 | CAAA | C | 7 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0077 others(4): Show |
7 | HG02083.hp2 HG02965.hp2 NA18960.hp1 others(4): Show |
intron_variant | MODIFIER | c.800+603_800+605del others(3): Show |
NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr7 | 74785883 | ||||||
| chr7:74785914 | C | A | 1 | a0006c0010t0001g0046 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.800+615C>A | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 8/10 | chr7 | 74785914 | |||||||
| chr7:74786081 | A | T | 1 | a0001c0001t0001g0063 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.800+782A>T | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 8/10 | chr7 | 74786081 | |||||||
| chr7:74786173 | T | A | 144 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(141): Show |
291 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.800+874T>A | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 8/10 | chr7 | 74786173 | |||||||
| chr7:74786191 | C | T | 1 | a0003c0004t0001g0054 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.800+892C>T | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 8/10 | chr7 | 74786191 | |||||||
| chr7:74786227 | C | G | 1 | a0002c0002t0001g0070 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.800+928C>G | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 8/10 | chr7 | 74786227 | |||||||
| chr7:74786234 | C | CA | 9 | a0001c0001t0001g0064 a0001c0001t0002g0131 a0001c0001t0002g0141 others(6): Show |
13 | HG01074.hp2 HG01109.hp1 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.800+956dupA | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr7 | 74786234 | ||||||
| chr7:74786234 | CA | C | 88 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(85): Show |
192 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.800+956delA | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr7 | 74786234 | ||||||
| chr7:74786234 | CAA | C | 5 | a0001c0001t0001g0027 a0001c0001t0001g0067 a0001c0001t0001g0076 others(2): Show |
6 | HG00558.hp2 HG01993.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.800+955_800+956del others(2): Show |
NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr7 | 74786234 | ||||||
| chr7:74786349 | G | A | 1 | a0002c0002t0001g0104 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.800+1050G>A | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 8/10 | chr7 | 74786349 | |||||||
| chr7:74786576 | G | A | 1 | a0002c0002t0002g0132 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.800+1277G>A | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 8/10 | chr7 | 74786576 | |||||||
| chr7:74786809 | T | A | 2 | a0001c0001t0002g0133 a0001c0001t0002g0134 |
2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.801-1175T>A | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 8/10 | chr7 | 74786809 | |||||||
| chr7:74786994 | T | G | 31 | a0001c0001t0001g0120 a0001c0003t0001g0002 a0001c0003t0001g0007 others(28): Show |
56 | HG00140.hp1 HG00544.hp1 HG00639.hp1 others(53): Show |
intron_variant | MODIFIER | c.801-990T>G | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 8/10 | chr7 | 74786994 | |||||||
| chr7:74787035 | G | GA | 12 | a0001c0001t0002g0139 a0001c0003t0001g0007 a0001c0003t0001g0013 others(9): Show |
22 | HG00140.hp1 HG00544.hp1 HG00673.hp2 others(19): Show |
intron_variant | MODIFIER | c.801-935dupA | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr7 | 74787035 | ||||||
| chr7:74787035 | G | GAA | 7 | a0001c0001t0002g0019 a0002c0002t0002g0019 a0002c0002t0002g0032 others(4): Show |
10 | HG01070.hp2 HG01071.hp2 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.801-936_801-935dup others(2): Show |
NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr7 | 74787035 | ||||||
| chr7:74787135 | C | A | 2 | a0008c0009t0001g0038 a0008c0009t0001g0117 |
3 | HG02622.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.801-849C>A | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 8/10 | chr7 | 74787135 | |||||||
| chr7:74787238 | G | A | 1 | a0001c0001t0001g0041 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.801-746G>A | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 8/10 | chr7 | 74787238 | |||||||
| chr7:74787254 | C | T | 144 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(141): Show |
291 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.801-730C>T | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 8/10 | chr7 | 74787254 | |||||||
| chr7:74787400 | A | G | 1 | a0004c0006t0001g0062 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.801-584A>G | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 8/10 | chr7 | 74787400 | |||||||
| chr7:74787450 | C | T | 1 | a0001c0001t0001g0061 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.801-534C>T | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 8/10 | chr7 | 74787450 | |||||||
| chr7:74787698 | G | A | 1 | a0008c0009t0001g0117 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.801-286G>A | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 8/10 | chr7 | 74787698 | |||||||
| chr7:74787871 | T | A | 1 | a0001c0001t0001g0057 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.801-113T>A | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 8/10 | chr7 | 74787871 | |||||||
| chr7:74787889 | G | C | 1 | a0001c0003t0001g0114 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.801-95G>C | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 8/10 | chr7 | 74787889 | |||||||
| chr7:74788133 | C | T | 1 | a0008c0009t0001g0038 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.905+45C>T | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 9/10 | chr7 | 74788133 | |||||||
| chr7:74788173 | G | A | 31 | a0001c0001t0001g0120 a0001c0003t0001g0002 a0001c0003t0001g0007 others(28): Show |
56 | HG00140.hp1 HG00544.hp1 HG00639.hp1 others(53): Show |
intron_variant | MODIFIER | c.905+85G>A | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 9/10 | chr7 | 74788173 | |||||||
| chr7:74788213 | C | T | 1 | a0003c0004t0001g0051 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.905+125C>T | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 9/10 | chr7 | 74788213 | |||||||
| chr7:74788262 | G | C | 1 | a0002c0002t0002g0129 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.905+174G>C | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 9/10 | chr7 | 74788262 | |||||||
| chr7:74788320 | G | C | 146 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(143): Show |
294 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(291): Show |
intron_variant | MODIFIER | c.905+232G>C | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 9/10 | chr7 | 74788320 | |||||||
| chr7:74788340 | C | T | 1 | a0001c0001t0001g0026 | 2 | HG03017.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.906-219C>T | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 9/10 | chr7 | 74788340 | |||||||
| chr7:74788363 | G | A | 4 | a0001c0001t0001g0027 a0001c0001t0001g0072 a0001c0001t0001g0088 others(1): Show |
5 | HG02895.hp2 HG02922.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.906-196G>A | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 9/10 | chr7 | 74788363 | |||||||
| chr7:74788441 | T | C | 1 | a0001c0001t0001g0065 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.906-118T>C | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 9/10 | chr7 | 74788441 | |||||||
| chr7:74788740 | C | G | 134 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(131): Show |
277 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.1051+36C>G | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 10/10 | chr7 | 74788740 | |||||||
| chr7:74788744 | A | G | 10 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0047 others(7): Show |
14 | HG00733.hp2 HG01891.hp2 HG02132.hp2 others(11): Show |
intron_variant | MODIFIER | c.1051+40A>G | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 10/10 | chr7 | 74788744 | |||||||
| chr7:74788777 | T | C | 1 | a0002c0002t0002g0118 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1051+73T>C | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 10/10 | chr7 | 74788777 | |||||||
| chr7:74788845 | T | G | 2 | a0002c0002t0002g0118 a0002c0005t0001g0126 |
2 | HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1051+141T>G | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 10/10 | chr7 | 74788845 | |||||||
| chr7:74788952 | C | A | 144 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(141): Show |
292 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.1052-87C>A | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 10/10 | chr7 | 74788952 | |||||||
| chr7:74788979 | T | TGTGGGCG others(6): Show |
4 | a0001c0001t0001g0025 a0002c0002t0001g0025 a0002c0002t0001g0091 others(1): Show |
4 | NA18948.hp1 NA18948.hp2 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.1052-56_1052-44dup others(13): Show |
NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 74788979 | ||||||
| chr7:74788996 | T | G | 144 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(141): Show |
292 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.1052-43T>G | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 10/10 | chr7 | 74788996 |