Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 4800 |
| ensemblid | ENSG00000001167.15 |
| hgncid | 7804 |
| symbol | NFYA |
| name | nuclear transcription factor Y subunit alpha |
| refseq_nuc | NM_002505.5 |
| refseq_prot | NP_002496.1 |
| ensembl_nuc | ENST00000341376.11 |
| ensembl_prot | ENSP00000345702.6 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 41072974 |
| end | 41102403 |
| strand | + |
| ver | v1.2 |
| region | chr6:41072974-41102403 |
| region5000 | chr6:41067974-41107403 |
| regionname0 | NFYA_chr6_41072974_41102403 |
| regionname5000 | NFYA_chr6_41067974_41107403 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 347 | 319 | 90 | 52 | 125 | 12 | 40 | 105 | NFYA_chr6_41067974_41107403 | NFYA | MEQYT others(342): Show |
chr6 | 41067974 | 41107403 |
| a0002 | 0/0 | 347 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | MEQYT others(342): Show |
chr6 | 41067974 | 41107403 |
| a0003 | 0/0 | 347 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NFYA_chr6_41067974_41107403 | NFYA | MEQYT others(342): Show |
chr6 | 41067974 | 41107403 |
| a0004 | 0/0 | 347 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | MEQYT others(342): Show |
chr6 | 41067974 | 41107403 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1041 | 310 | 87 | 52 | 120 | 12 | 39 | NFYA_chr6_41067974_41107403 | NFYA | ATGGA others(1036): Show |
chr6 | 41067974 | 41107403 | ||
| a0001c0002 | 0/0 | 1041 | 5 | 0 | 0 | 5 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | ATGGA others(1036): Show |
chr6 | 41067974 | 41107403 | ||
| a0001c0003 | 0/0 | 1041 | 2 | 2 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | ATGGA others(1036): Show |
chr6 | 41067974 | 41107403 | ||
| a0001c0005 | 0/0 | 1041 | 1 | 0 | 0 | 0 | 0 | 1 | NFYA_chr6_41067974_41107403 | NFYA | ATGGA others(1036): Show |
chr6 | 41067974 | 41107403 | ||
| a0001c0008 | 0/0 | 1041 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | ATGGA others(1036): Show |
chr6 | 41067974 | 41107403 | ||
| a0002c0007 | 0/0 | 1041 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | ATGGA others(1036): Show |
chr6 | 41067974 | 41107403 | ||
| a0003c0004 | 0/0 | 1041 | 1 | 0 | 0 | 1 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | ATGGA others(1036): Show |
chr6 | 41067974 | 41107403 | ||
| a0004c0006 | 0/0 | 1041 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | ATGGA others(1036): Show |
chr6 | 41067974 | 41107403 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 6209 | 194 | 29 | 44 | 80 | 10 | 31 | NFYA_chr6_41067974_41107403 | NFYA | GCTAG others(6204): Show |
chr6 | 41067974 | 41107403 |
| a0001c0001t0002 | 0/0 | 6209 | 25 | 0 | 0 | 25 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | GCTAG others(6204): Show |
chr6 | 41067974 | 41107403 |
| a0001c0001t0003 | 0/0 | 6209 | 18 | 14 | 2 | 0 | 0 | 2 | NFYA_chr6_41067974_41107403 | NFYA | GCTAG others(6204): Show |
chr6 | 41067974 | 41107403 |
| a0001c0001t0004 | 0/0 | 6209 | 16 | 16 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | GCTAG others(6204): Show |
chr6 | 41067974 | 41107403 |
| a0001c0001t0005 | 0/0 | 6208 | 6 | 0 | 0 | 6 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | GCTAG others(6203): Show |
chr6 | 41067974 | 41107403 |
| a0001c0001t0006 | 0/0 | 6209 | 5 | 5 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | GCTAG others(6204): Show |
chr6 | 41067974 | 41107403 |
| a0001c0001t0007 | 0/0 | 6208 | 4 | 4 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | GCTAG others(6203): Show |
chr6 | 41067974 | 41107403 |
| a0001c0001t0008 | 0/0 | 6207 | 5 | 0 | 5 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | GCTAG others(6202): Show |
chr6 | 41067974 | 41107403 |
| a0001c0001t0009 | 0/0 | 6209 | 3 | 3 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | GCTAG others(6204): Show |
chr6 | 41067974 | 41107403 |
| a0001c0001t0010 | 0/0 | 6209 | 2 | 2 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | GCTAG others(6204): Show |
chr6 | 41067974 | 41107403 |
| a0001c0001t0011 | 0/0 | 6209 | 2 | 2 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | GCTAG others(6204): Show |
chr6 | 41067974 | 41107403 |
| a0001c0001t0012 | 0/0 | 6209 | 2 | 0 | 0 | 2 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | GCTAG others(6204): Show |
chr6 | 41067974 | 41107403 |
| a0001c0001t0013 | 0/0 | 6209 | 2 | 2 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | GCTAG others(6204): Show |
chr6 | 41067974 | 41107403 |
| a0001c0001t0014 | 0/0 | 6209 | 2 | 0 | 0 | 2 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | GCTAG others(6204): Show |
chr6 | 41067974 | 41107403 |
| a0001c0001t0015 | 0/0 | 6192 | 2 | 0 | 0 | 1 | 0 | 1 | NFYA_chr6_41067974_41107403 | NFYA | GCTAG others(6187): Show |
chr6 | 41067974 | 41107403 |
| a0001c0001t0016 | 0/0 | 6209 | 1 | 0 | 0 | 1 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | GCTAG others(6204): Show |
chr6 | 41067974 | 41107403 |
| a0001c0001t0017 | 0/0 | 6209 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | GCTAG others(6204): Show |
chr6 | 41067974 | 41107403 |
| a0001c0001t0019 | 0/0 | 6209 | 1 | 0 | 0 | 0 | 0 | 1 | NFYA_chr6_41067974_41107403 | NFYA | GCTAG others(6204): Show |
chr6 | 41067974 | 41107403 |
| a0001c0001t0020 | 0/0 | 6208 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | GCTAG others(6203): Show |
chr6 | 41067974 | 41107403 |
| a0001c0001t0021 | 0/0 | 6209 | 1 | 0 | 0 | 0 | 0 | 1 | NFYA_chr6_41067974_41107403 | NFYA | GCTAG others(6204): Show |
chr6 | 41067974 | 41107403 |
| a0001c0001t0022 | 0/0 | 6209 | 1 | 0 | 0 | 1 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | GCTAG others(6204): Show |
chr6 | 41067974 | 41107403 |
| a0001c0001t0023 | 0/0 | 6209 | 1 | 0 | 0 | 0 | 0 | 1 | NFYA_chr6_41067974_41107403 | NFYA | GCTAG others(6204): Show |
chr6 | 41067974 | 41107403 |
| a0001c0001t0024 | 0/0 | 6209 | 1 | 0 | 0 | 1 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | GCTAG others(6204): Show |
chr6 | 41067974 | 41107403 |
| a0001c0001t0025 | 0/0 | 6209 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | GCTAG others(6204): Show |
chr6 | 41067974 | 41107403 |
| a0001c0001t0026 | 0/0 | 6209 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | GCTAG others(6204): Show |
chr6 | 41067974 | 41107403 |
| a0001c0001t0027 | 0/0 | 6208 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | GCTAG others(6203): Show |
chr6 | 41067974 | 41107403 |
| a0001c0001t0028 | 0/0 | 6209 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | GCTAG others(6204): Show |
chr6 | 41067974 | 41107403 |
| a0001c0001t0029 | 0/0 | 6208 | 1 | 0 | 1 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | GCTAG others(6203): Show |
chr6 | 41067974 | 41107403 |
| a0001c0001t0030 | 0/0 | 6209 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | GCTAG others(6204): Show |
chr6 | 41067974 | 41107403 |
| a0001c0001t0031 | 0/0 | 6209 | 1 | 0 | 0 | 0 | 1 | 0 | NFYA_chr6_41067974_41107403 | NFYA | GCTAG others(6204): Show |
chr6 | 41067974 | 41107403 |
| a0001c0001t0032 | 0/0 | 6207 | 1 | 0 | 0 | 0 | 1 | 0 | NFYA_chr6_41067974_41107403 | NFYA | GCTAG others(6202): Show |
chr6 | 41067974 | 41107403 |
| a0001c0001t0033 | 0/0 | 6209 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | GCTAG others(6204): Show |
chr6 | 41067974 | 41107403 |
| a0001c0001t0034 | 0/0 | 6209 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | GCTAG others(6204): Show |
chr6 | 41067974 | 41107403 |
| a0001c0001t0035 | 0/0 | 6209 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | GCTAG others(6204): Show |
chr6 | 41067974 | 41107403 |
| a0001c0001t0036 | 0/0 | 6209 | 1 | 0 | 0 | 0 | 0 | 1 | NFYA_chr6_41067974_41107403 | NFYA | GCTAG others(6204): Show |
chr6 | 41067974 | 41107403 |
| a0001c0001t0037 | 0/0 | 6192 | 1 | 0 | 0 | 0 | 0 | 1 | NFYA_chr6_41067974_41107403 | NFYA | GCTAG others(6187): Show |
chr6 | 41067974 | 41107403 |
| a0001c0001t0038 | 0/0 | 6209 | 1 | 0 | 0 | 1 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | GCTAG others(6204): Show |
chr6 | 41067974 | 41107403 |
| a0001c0002t0001 | 0/0 | 6209 | 5 | 0 | 0 | 5 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | GCTAG others(6204): Show |
chr6 | 41067974 | 41107403 |
| a0001c0003t0001 | 0/0 | 6209 | 2 | 2 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | GCTAG others(6204): Show |
chr6 | 41067974 | 41107403 |
| a0001c0005t0001 | 0/0 | 6209 | 1 | 0 | 0 | 0 | 0 | 1 | NFYA_chr6_41067974_41107403 | NFYA | GCTAG others(6204): Show |
chr6 | 41067974 | 41107403 |
| a0001c0008t0018 | 0/0 | 6208 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | GCTAG others(6203): Show |
chr6 | 41067974 | 41107403 |
| a0002c0007t0007 | 0/0 | 6208 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | GCTAG others(6203): Show |
chr6 | 41067974 | 41107403 |
| a0003c0004t0001 | 0/0 | 6209 | 1 | 0 | 0 | 1 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | GCTAG others(6204): Show |
chr6 | 41067974 | 41107403 |
| a0004c0006t0006 | 0/0 | 6209 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | GCTAG others(6204): Show |
chr6 | 41067974 | 41107403 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 33 | 3 | 12 | 7 | 5 | 6 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0001g0002 | 0/0 | 28 | 1 | 9 | 9 | 3 | 6 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0001g0003 | 0/0 | 8 | 0 | 2 | 2 | 0 | 4 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0001g0004 | 0/0 | 24 | 0 | 0 | 24 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0001g0006 | 0/0 | 8 | 1 | 1 | 6 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0001g0007 | 0/0 | 7 | 6 | 1 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0001g0008 | 0/0 | 5 | 1 | 1 | 2 | 0 | 1 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0001g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0001g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0001g0027 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0002g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0002g0003 | 0/0 | 18 | 0 | 0 | 18 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0003g0010 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0003g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0003g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0003g0036 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0003g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0003g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0003g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0003g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0003g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0003g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0004g0005 | 0/0 | 10 | 10 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0004g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0004g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0004g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0004g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0005g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0005g0003 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0006g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0006g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0007g0015 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0008g0009 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0009g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0010g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0011g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0011g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0012g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0013g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0013g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0014g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0014g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0015g0021 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0016g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0017g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0019g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0020g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0021g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0022g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0023g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0024g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0025g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0026g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0027g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0028g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0029g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0030g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0031g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0032g0009 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0033g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0034g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0035g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0036g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0037g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0001t0038g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0002t0001g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0003t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0005t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0001c0008t0018g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0002c0007t0007g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0003c0004t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| a0004c0006t0006g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG00140 | hp1 | a0001 | c0001 | t0031 | g0088 | EUR | GBR | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0077 | EUR | FIN | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG00280 | hp2 | a0001 | c0001 | t0032 | g0009 | EUR | FIN | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | CHS | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG00597 | hp1 | a0001 | c0001 | t0014 | g0008 | EAS | CHS | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | CHS | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG00738 | hp1 | a0001 | c0001 | t0008 | g0009 | AMR | PUR | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG01069 | hp2 | a0001 | c0001 | t0008 | g0009 | AMR | PUR | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG01081 | hp1 | a0001 | c0001 | t0008 | g0009 | AMR | PUR | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG01175 | hp2 | a0001 | c0001 | t0003 | g0110 | AMR | PUR | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG01243 | hp1 | a0001 | c0001 | t0029 | g0090 | AMR | PUR | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG01255 | hp2 | a0001 | c0001 | t0003 | g0100 | AMR | CLM | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | CLM | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | CLM | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | CLM | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | CLM | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG01884 | hp1 | a0001 | c0001 | t0004 | g0005 | AFR | ACB | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | ACB | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG01891 | hp2 | a0001 | c0001 | t0004 | g0005 | AFR | ACB | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG01928 | hp2 | a0001 | c0001 | t0008 | g0009 | AMR | PEL | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PEL | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | PEL | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | PEL | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PEL | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PEL | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | PEL | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PEL | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG02027 | hp1 | a0001 | c0001 | t0024 | g0002 | EAS | KHV | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | KHV | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG02040 | hp1 | a0001 | c0001 | t0012 | g0002 | EAS | KHV | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | KHV | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0080 | EAS | KHV | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG02129 | hp1 | a0001 | c0001 | t0012 | g0002 | EAS | KHV | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG02145 | hp2 | a0001 | c0001 | t0004 | g0005 | AFR | ACB | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0010 | AFR | ACB | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG02258 | hp1 | a0001 | c0001 | t0004 | g0012 | AFR | ACB | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG02258 | hp2 | a0001 | c0001 | t0004 | g0106 | AFR | ACB | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | PEL | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG02273 | hp2 | a0001 | c0001 | t0008 | g0009 | AMR | PEL | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG02280 | hp2 | a0001 | c0001 | t0007 | g0015 | AFR | ACB | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG02451 | hp1 | a0001 | c0001 | t0004 | g0005 | AFR | ACB | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG02572 | hp1 | a0001 | c0001 | t0006 | g0105 | AFR | GWD | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG02572 | hp2 | a0001 | c0001 | t0013 | g0113 | AFR | GWD | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | GWD | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG02615 | hp2 | a0001 | c0001 | t0011 | g0091 | AFR | GWD | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0112 | AFR | GWD | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0020 | AFR | GWD | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0109 | AFR | GWD | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG02647 | hp2 | a0001 | c0001 | t0003 | g0020 | AFR | GWD | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG02683 | hp1 | a0001 | c0001 | t0003 | g0036 | SAS | PJL | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0059 | SAS | PJL | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG02717 | hp1 | a0001 | c0008 | t0018 | g0093 | AFR | GWD | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0102 | AFR | GWD | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG02738 | hp1 | a0001 | c0001 | t0003 | g0111 | SAS | PJL | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG02809 | hp1 | a0001 | c0001 | t0017 | g0099 | AFR | GWD | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0010 | AFR | GWD | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG02886 | hp1 | a0001 | c0001 | t0003 | g0010 | AFR | GWD | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG02886 | hp2 | a0001 | c0001 | t0004 | g0005 | AFR | GWD | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG02895 | hp1 | a0001 | c0003 | t0001 | g0030 | AFR | GWD | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG02895 | hp2 | a0001 | c0001 | t0027 | g0121 | AFR | GWD | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG02896 | hp1 | a0001 | c0001 | t0010 | g0034 | AFR | GWD | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG02896 | hp2 | a0001 | c0001 | t0009 | g0016 | AFR | GWD | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG02897 | hp1 | a0001 | c0001 | t0010 | g0034 | AFR | GWD | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG02897 | hp2 | a0001 | c0003 | t0001 | g0030 | AFR | GWD | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG02922 | hp1 | a0001 | c0001 | t0004 | g0012 | AFR | ESN | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG02922 | hp2 | a0001 | c0001 | t0004 | g0005 | AFR | ESN | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | ESN | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG02965 | hp2 | a0001 | c0001 | t0009 | g0016 | AFR | ESN | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG02970 | hp1 | a0001 | c0001 | t0020 | g0101 | AFR | ESN | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG02970 | hp2 | a0001 | c0001 | t0035 | g0094 | AFR | ESN | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | ESN | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG03017 | hp1 | a0001 | c0001 | t0036 | g0002 | SAS | PJL | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG03017 | hp2 | a0001 | c0005 | t0001 | g0084 | SAS | PJL | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0033 | AFR | GWD | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | MSL | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG03098 | hp2 | a0002 | c0007 | t0007 | g0108 | AFR | MSL | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG03130 | hp1 | a0001 | c0001 | t0034 | g0026 | AFR | ESN | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG03130 | hp2 | a0001 | c0001 | t0004 | g0107 | AFR | ESN | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG03139 | hp1 | a0001 | c0001 | t0011 | g0038 | AFR | ESN | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG03139 | hp2 | a0001 | c0001 | t0004 | g0005 | AFR | ESN | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG03195 | hp2 | a0001 | c0001 | t0007 | g0015 | AFR | ESN | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG03209 | hp2 | a0001 | c0001 | t0026 | g0104 | AFR | MSL | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | MSL | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG03225 | hp2 | a0001 | c0001 | t0004 | g0005 | AFR | MSL | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG03453 | hp1 | a0001 | c0001 | t0009 | g0016 | AFR | MSL | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG03453 | hp2 | a0001 | c0001 | t0006 | g0011 | AFR | MSL | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG03486 | hp1 | a0001 | c0001 | t0028 | g0012 | AFR | MSL | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG03486 | hp2 | a0001 | c0001 | t0025 | g0057 | AFR | MSL | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG03491 | hp2 | a0001 | c0001 | t0023 | g0002 | SAS | PJL | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | ESN | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG03516 | hp2 | a0001 | c0001 | t0004 | g0012 | AFR | ESN | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG03540 | hp1 | a0001 | c0001 | t0003 | g0010 | AFR | GWD | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0010 | AFR | MSL | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0069 | SAS | PJL | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG03669 | hp1 | a0001 | c0001 | t0037 | g0039 | SAS | PJL | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0089 | SAS | STU | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG03688 | hp2 | a0001 | c0001 | t0019 | g0006 | SAS | STU | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | BEB | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0081 | SAS | BEB | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0073 | SAS | BEB | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0075 | SAS | BEB | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | BEB | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0068 | SAS | BEB | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG03942 | hp2 | a0001 | c0001 | t0021 | g0001 | SAS | BEB | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | STU | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | STU | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | YRI | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA18522 | hp2 | a0001 | c0001 | t0006 | g0011 | AFR | YRI | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | CHB | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA18940 | hp1 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA18941 | hp1 | a0001 | c0002 | t0001 | g0078 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA18948 | hp1 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA18960 | hp1 | a0001 | c0001 | t0016 | g0096 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA18964 | hp2 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA18970 | hp1 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA18978 | hp1 | a0001 | c0001 | t0015 | g0021 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA18978 | hp2 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA18979 | hp1 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA18979 | hp2 | a0001 | c0001 | t0022 | g0002 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA18980 | hp1 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA19001 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA19004 | hp1 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | LWK | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA19030 | hp2 | a0001 | c0001 | t0003 | g0036 | AFR | LWK | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA19043 | hp1 | a0001 | c0001 | t0013 | g0114 | AFR | LWK | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA19043 | hp2 | a0001 | c0001 | t0007 | g0015 | AFR | LWK | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA19060 | hp1 | a0001 | c0001 | t0038 | g0053 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA19064 | hp2 | a0003 | c0004 | t0001 | g0079 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA19066 | hp2 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA19067 | hp1 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA19078 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA19240 | hp1 | a0001 | c0001 | t0006 | g0011 | AFR | YRI | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA19240 | hp2 | a0001 | c0001 | t0004 | g0040 | AFR | YRI | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ASW | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA20129 | hp2 | a0004 | c0006 | t0006 | g0011 | AFR | ASW | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0082 | EUR | TSI | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA20905 | hp2 | a0001 | c0001 | t0015 | g0021 | SAS | GIH | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG02109 | hp1 | a0001 | c0001 | t0004 | g0005 | AFR | ACB | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG02486 | hp1 | a0001 | c0001 | t0007 | g0015 | AFR | ACB | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | ACB | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG02559 | hp2 | a0001 | c0001 | t0003 | g0020 | AFR | ACB | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG03471 | hp1 | a0001 | c0001 | t0006 | g0011 | AFR | MSL | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0033 | AFR | MSL | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG06807 | hp1 | a0001 | c0001 | t0033 | g0103 | AFR | USA | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| HG06807 | hp2 | a0001 | c0001 | t0004 | g0005 | AFR | USA | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA18955 | hp2 | a0001 | c0001 | t0014 | g0003 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | USA | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| NA20300 | hp2 | a0001 | c0001 | t0030 | g0064 | AFR | USA | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:41084186 | G | T | 1 | a0002 | 1 | HG03098.hp2 | missense_variant | MODERATE | c.303G>T | p.Leu101Phe | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 4/10 | 475/6209 | 303/1044 | 101/347 | chr6 | 41084186 | |||
| chr6:41090211 | A | C | 1 | a0004 | 1 | NA20129.hp2 | missense_variant | MODERATE | c.449A>C | p.Gln150Pro | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 6/10 | 621/6209 | 449/1044 | 150/347 | chr6 | 41090211 | |||
| chr6:41094491 | T | G | 1 | a0003 | 1 | NA19064.hp2 | missense_variant | MODERATE | c.984T>G | p.His328Gln | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 9/10 | 1156/6209 | 984/1044 | 328/347 | chr6 | 41094491 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:41079131 | G | A | 1 | a0001c0003 | 2 | HG02895.hp1 HG02897.hp2 |
synonymous_variant | LOW | c.42G>A | p.Gln14Gln | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 2/10 | 214/6209 | 42/1044 | 14/347 | chr6 | 41079131 | |||
| chr6:41080864 | C | T | 1 | a0001c0008 | 1 | HG02717.hp1 | synonymous_variant | LOW | c.129C>T | p.Ser43Ser | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 3/10 | 301/6209 | 129/1044 | 43/347 | chr6 | 41080864 | |||
| chr6:41091619 | C | T | 1 | a0001c0005 | 1 | HG03017.hp2 | synonymous_variant | LOW | c.639C>T | p.Thr213Thr | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 7/10 | 811/6209 | 639/1044 | 213/347 | chr6 | 41091619 | |||
| chr6:41092965 | A | C | 1 | a0001c0002 | 5 | NA18941.hp1 NA18948.hp1 NA18978.hp2 others(2): Show |
synonymous_variant | LOW | c.768A>C | p.Gly256Gly | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 8/10 | 940/6209 | 768/1044 | 256/347 | chr6 | 41092965 | |||
| chr6:41094401 | C | T | 1 | a0001c0003 | 2 | HG02895.hp1 HG02897.hp2 |
synonymous_variant | LOW | c.894C>T | p.Tyr298Tyr | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 9/10 | 1066/6209 | 894/1044 | 298/347 | chr6 | 41094401 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:41097453 | C | T | 1 | a0001c0001t0038 | 1 | NA19060.hp1 | 3_prime_UTR_variant | MODIFIER | c.*43C>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 10/10 | 43 | chr6 | 41097453 | ||||||
| chr6:41097513 | A | T | 2 | a0001c0001t0015 a0001c0001t0037 |
3 | HG03669.hp1 NA18978.hp1 NA20905.hp2 |
3_prime_UTR_variant | MODIFIER | c.*103A>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 10/10 | 103 | chr6 | 41097513 | ||||||
| chr6:41097551 | T | C | 2 | a0001c0001t0007 a0002c0007t0007 |
5 | HG02280.hp2 HG02486.hp1 HG03098.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*141T>C | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 10/10 | 141 | chr6 | 41097551 | ||||||
| chr6:41097558 | T | C | 1 | a0001c0001t0016 | 1 | NA18960.hp1 | 3_prime_UTR_variant | MODIFIER | c.*148T>C | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 10/10 | 148 | chr6 | 41097558 | ||||||
| chr6:41097673 | A | G | 2 | a0001c0001t0015 a0001c0001t0037 |
3 | HG03669.hp1 NA18978.hp1 NA20905.hp2 |
3_prime_UTR_variant | MODIFIER | c.*263A>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 10/10 | 263 | chr6 | 41097673 | ||||||
| chr6:41097685 | C | A | 2 | a0001c0001t0015 a0001c0001t0037 |
3 | HG03669.hp1 NA18978.hp1 NA20905.hp2 |
3_prime_UTR_variant | MODIFIER | c.*275C>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 10/10 | 275 | chr6 | 41097685 | ||||||
| chr6:41097842 | A | C | 1 | a0001c0001t0036 | 1 | HG03017.hp1 | 3_prime_UTR_variant | MODIFIER | c.*432A>C | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 10/10 | 432 | chr6 | 41097842 | ||||||
| chr6:41097919 | C | T | 3 | a0001c0001t0014 a0001c0001t0015 a0001c0001t0037 |
5 | HG00597.hp1 HG03669.hp1 NA18955.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*509C>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 10/10 | 509 | chr6 | 41097919 | ||||||
| chr6:41098073 | A | G | 2 | a0001c0001t0013 a0001c0001t0035 |
3 | HG02572.hp2 HG02970.hp2 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*663A>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 10/10 | 663 | chr6 | 41098073 | ||||||
| chr6:41098479 | G | A | 1 | a0001c0001t0017 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1069G>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 10/10 | 1069 | chr6 | 41098479 | ||||||
| chr6:41098523 | A | G | 1 | a0001c0001t0034 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1113A>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 10/10 | 1113 | chr6 | 41098523 | ||||||
| chr6:41098559 | A | G | 3 | a0001c0001t0006 a0001c0001t0033 a0004c0006t0006 |
7 | HG02572.hp1 HG03453.hp2 HG03471.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1149A>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 10/10 | 1149 | chr6 | 41098559 | ||||||
| chr6:41098685 | G | A | 1 | a0001c0008t0018 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1275G>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 10/10 | 1275 | chr6 | 41098685 | ||||||
| chr6:41098871 | G | A | 2 | a0001c0001t0015 a0001c0001t0037 |
3 | HG03669.hp1 NA18978.hp1 NA20905.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1461G>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 10/10 | 1461 | chr6 | 41098871 | ||||||
| chr6:41098940 | A | G | 1 | a0001c0001t0032 | 1 | HG00280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1530A>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 10/10 | 1530 | chr6 | 41098940 | ||||||
| chr6:41099179 | G | A | 1 | a0001c0001t0019 | 1 | HG03688.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1769G>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 10/10 | 1769 | chr6 | 41099179 | ||||||
| chr6:41099583 | A | T | 1 | a0001c0008t0018 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2173A>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 10/10 | 2173 | chr6 | 41099583 | ||||||
| chr6:41099625 | A | T | 1 | a0001c0001t0031 | 1 | HG00140.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2215A>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 10/10 | 2215 | chr6 | 41099625 | ||||||
| chr6:41099716 | CT | C | 4 | a0001c0001t0005 a0001c0001t0008 a0001c0001t0020 others(1): Show |
13 | HG00280.hp2 HG00738.hp1 HG01069.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2320delT | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 10/10 | 2320 | INFO_REALIGN_3_PRIME | chr6 | 41099716 | |||||
| chr6:41099807 | C | G | 1 | a0001c0001t0030 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2397C>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 10/10 | 2397 | chr6 | 41099807 | ||||||
| chr6:41099943 | T | C | 2 | a0001c0001t0015 a0001c0001t0037 |
3 | HG03669.hp1 NA18978.hp1 NA20905.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2533T>C | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 10/10 | 2533 | chr6 | 41099943 | ||||||
| chr6:41100045 | T | A | 1 | a0001c0001t0021 | 1 | HG03942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2635T>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 10/10 | 2635 | chr6 | 41100045 | ||||||
| chr6:41100053 | G | A | 1 | a0001c0001t0022 | 1 | NA18979.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2643G>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 10/10 | 2643 | chr6 | 41100053 | ||||||
| chr6:41100270 | C | T | 1 | a0001c0001t0012 | 2 | HG02040.hp1 HG02129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2860C>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 10/10 | 2860 | chr6 | 41100270 | ||||||
| chr6:41100318 | G | T | 1 | a0001c0001t0029 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2908G>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 10/10 | 2908 | chr6 | 41100318 | ||||||
| chr6:41100402 | A | G | 2 | a0001c0001t0015 a0001c0001t0037 |
3 | HG03669.hp1 NA18978.hp1 NA20905.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2992A>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 10/10 | 2992 | chr6 | 41100402 | ||||||
| chr6:41100409 | C | T | 1 | a0001c0001t0028 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2999C>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 10/10 | 2999 | chr6 | 41100409 | ||||||
| chr6:41100435 | G | A | 1 | a0001c0001t0023 | 1 | HG03491.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3025G>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 10/10 | 3025 | chr6 | 41100435 | ||||||
| chr6:41100518 | CA | C | 9 | a0001c0001t0007 a0001c0001t0008 a0001c0001t0015 others(6): Show |
17 | HG00280.hp2 HG00738.hp1 HG01069.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*3110delA | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 10/10 | 3110 | INFO_REALIGN_3_PRIME | chr6 | 41100518 | |||||
| chr6:41100594 | G | A | 1 | a0001c0001t0037 | 1 | HG03669.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3184G>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 10/10 | 3184 | chr6 | 41100594 | ||||||
| chr6:41100684 | G | T | 12 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0006 others(9): Show |
49 | HG01175.hp2 HG01243.hp1 HG01255.hp2 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*3274G>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 10/10 | 3274 | chr6 | 41100684 | ||||||
| chr6:41100713 | C | T | 1 | a0001c0001t0030 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3303C>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 10/10 | 3303 | chr6 | 41100713 | ||||||
| chr6:41100761 | G | A | 8 | a0001c0001t0007 a0001c0001t0008 a0001c0001t0015 others(5): Show |
16 | HG00280.hp2 HG00738.hp1 HG01069.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*3351G>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 10/10 | 3351 | chr6 | 41100761 | ||||||
| chr6:41100768 | C | G | 2 | a0001c0001t0015 a0001c0001t0037 |
3 | HG03669.hp1 NA18978.hp1 NA20905.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3358C>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 10/10 | 3358 | chr6 | 41100768 | ||||||
| chr6:41100769 | C | G | 1 | a0001c0001t0025 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3359C>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 10/10 | 3359 | chr6 | 41100769 | ||||||
| chr6:41100802 | G | T | 2 | a0001c0001t0008 a0001c0001t0032 |
6 | HG00280.hp2 HG00738.hp1 HG01069.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3392G>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 10/10 | 3392 | chr6 | 41100802 | ||||||
| chr6:41100820 | A | T | 1 | a0001c0001t0035 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3410A>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 10/10 | 3410 | chr6 | 41100820 | ||||||
| chr6:41100841 | G | C | 8 | a0001c0001t0007 a0001c0001t0008 a0001c0001t0015 others(5): Show |
16 | HG00280.hp2 HG00738.hp1 HG01069.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*3431G>C | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 10/10 | 3431 | chr6 | 41100841 | ||||||
| chr6:41100861 | A | G | 9 | a0001c0001t0007 a0001c0001t0008 a0001c0001t0015 others(6): Show |
17 | HG00280.hp2 HG00738.hp1 HG01069.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*3451A>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 10/10 | 3451 | chr6 | 41100861 | ||||||
| chr6:41100862 | A | C | 9 | a0001c0001t0007 a0001c0001t0008 a0001c0001t0015 others(6): Show |
17 | HG00280.hp2 HG00738.hp1 HG01069.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*3452A>C | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 10/10 | 3452 | chr6 | 41100862 | ||||||
| chr6:41100960 | CCTGCTAG others(9): Show |
C | 2 | a0001c0001t0015 a0001c0001t0037 |
3 | HG03669.hp1 NA18978.hp1 NA20905.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3557_*3572delGGCG others(12): Show |
NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 10/10 | 3557 | INFO_REALIGN_3_PRIME | chr6 | 41100960 | |||||
| chr6:41100967 | G | T | 20 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0006 others(17): Show |
67 | HG00280.hp2 HG00738.hp1 HG01069.hp2 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*3557G>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 10/10 | 3557 | chr6 | 41100967 | ||||||
| chr6:41100972 | A | C | 1 | a0001c0001t0029 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3562A>C | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 10/10 | 3562 | chr6 | 41100972 | ||||||
| chr6:41100972 | A | G | 5 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0026 others(2): Show |
24 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*3562A>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 10/10 | 3562 | chr6 | 41100972 | ||||||
| chr6:41101050 | C | A | 7 | a0001c0001t0007 a0001c0001t0008 a0001c0001t0009 others(4): Show |
16 | HG00280.hp2 HG00738.hp1 HG01069.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*3640C>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 10/10 | 3640 | chr6 | 41101050 | ||||||
| chr6:41101256 | G | T | 2 | a0001c0001t0008 a0001c0001t0032 |
6 | HG00280.hp2 HG00738.hp1 HG01069.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3846G>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 10/10 | 3846 | chr6 | 41101256 | ||||||
| chr6:41101316 | C | T | 1 | a0001c0001t0027 | 1 | HG02895.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3906C>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 10/10 | 3906 | chr6 | 41101316 | ||||||
| chr6:41101381 | G | A | 3 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0038 |
32 | HG00609.hp1 HG02074.hp2 HG02129.hp2 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*3971G>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 10/10 | 3971 | chr6 | 41101381 | ||||||
| chr6:41101407 | G | T | 2 | a0001c0001t0015 a0001c0001t0037 |
3 | HG03669.hp1 NA18978.hp1 NA20905.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3997G>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 10/10 | 3997 | chr6 | 41101407 | ||||||
| chr6:41101454 | C | G | 9 | a0001c0001t0007 a0001c0001t0008 a0001c0001t0015 others(6): Show |
17 | HG00280.hp2 HG00738.hp1 HG01069.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*4044C>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 10/10 | 4044 | chr6 | 41101454 | ||||||
| chr6:41101455 | C | G | 9 | a0001c0001t0007 a0001c0001t0008 a0001c0001t0015 others(6): Show |
17 | HG00280.hp2 HG00738.hp1 HG01069.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*4045C>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 10/10 | 4045 | chr6 | 41101455 | ||||||
| chr6:41101551 | A | G | 1 | a0001c0001t0026 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4141A>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 10/10 | 4141 | chr6 | 41101551 | ||||||
| chr6:41101799 | G | C | 1 | a0001c0001t0029 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4389G>C | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 10/10 | 4389 | chr6 | 41101799 | ||||||
| chr6:41102060 | G | A | 1 | a0001c0001t0024 | 1 | HG02027.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4650G>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 10/10 | 4650 | chr6 | 41102060 | ||||||
| chr6:41102316 | T | G | 1 | a0001c0001t0010 | 2 | HG02896.hp1 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4906T>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 10/10 | 4906 | chr6 | 41102316 | ||||||
| chr6:41102369 | T | G | 1 | a0001c0001t0017 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4959T>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 10/10 | 4959 | chr6 | 41102369 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:41073222 | G | A | 1 | a0001c0001t0011g0038 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-62+138G>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 1/9 | chr6 | 41073222 | |||||||
| chr6:41073223 | C | G | 1 | a0001c0001t0011g0038 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-62+139C>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 1/9 | chr6 | 41073223 | |||||||
| chr6:41073239 | G | T | 1 | a0001c0001t0001g0122 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-62+155G>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 1/9 | chr6 | 41073239 | |||||||
| chr6:41073269 | G | A | 1 | a0001c0001t0009g0016 | 3 | HG02896.hp2 HG02965.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-62+185G>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 1/9 | chr6 | 41073269 | |||||||
| chr6:41073284 | G | C | 2 | a0001c0001t0015g0021 a0001c0001t0037g0039 |
3 | HG03669.hp1 NA18978.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.-62+200G>C | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 1/9 | chr6 | 41073284 | |||||||
| chr6:41073320 | G | C | 3 | a0001c0001t0004g0012 a0001c0001t0004g0040 a0001c0001t0028g0012 |
5 | HG02258.hp1 HG02922.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-62+236G>C | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 1/9 | chr6 | 41073320 | |||||||
| chr6:41073435 | A | G | 1 | a0001c0001t0027g0121 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-62+351A>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 1/9 | chr6 | 41073435 | |||||||
| chr6:41073491 | C | T | 1 | a0001c0001t0003g0020 | 3 | HG02559.hp2 HG02630.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-62+407C>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 1/9 | chr6 | 41073491 | |||||||
| chr6:41073622 | G | A | 11 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0017 others(8): Show |
23 | HG00558.hp2 HG01891.hp1 HG02074.hp1 others(20): Show |
intron_variant | MODIFIER | c.-62+538G>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 1/9 | chr6 | 41073622 | |||||||
| chr6:41073763 | C | T | 1 | a0001c0001t0001g0120 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.-62+679C>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 1/9 | chr6 | 41073763 | |||||||
| chr6:41073810 | C | T | 1 | a0001c0001t0027g0121 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-62+726C>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 1/9 | chr6 | 41073810 | |||||||
| chr6:41073924 | T | TCTCCGTT others(418): Show |
1 | a0001c0001t0001g0022 | 2 | HG02257.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.-62+852_-62+853ins others(425): Show |
NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr6 | 41073924 | ||||||
| chr6:41073939 | C | T | 1 | a0001c0001t0001g0047 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-62+855C>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 1/9 | chr6 | 41073939 | |||||||
| chr6:41074003 | C | T | 63 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0018 others(60): Show |
154 | HG00099.hp1 HG00280.hp2 HG00609.hp2 others(151): Show |
intron_variant | MODIFIER | c.-62+919C>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 1/9 | chr6 | 41074003 | |||||||
| chr6:41074013 | G | A | 63 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0018 others(60): Show |
154 | HG00099.hp1 HG00280.hp2 HG00609.hp2 others(151): Show |
intron_variant | MODIFIER | c.-62+929G>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 1/9 | chr6 | 41074013 | |||||||
| chr6:41074090 | A | G | 65 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0018 others(62): Show |
157 | HG00099.hp1 HG00280.hp2 HG00609.hp2 others(154): Show |
intron_variant | MODIFIER | c.-62+1006A>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 1/9 | chr6 | 41074090 | |||||||
| chr6:41074107 | G | T | 3 | a0001c0001t0001g0013 a0001c0001t0001g0046 a0001c0001t0001g0119 |
6 | HG00558.hp2 NA18970.hp2 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.-62+1023G>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 1/9 | chr6 | 41074107 | |||||||
| chr6:41074108 | T | G | 1 | a0001c0001t0001g0018 | 3 | HG03927.hp2 HG04199.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.-62+1024T>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 1/9 | chr6 | 41074108 | |||||||
| chr6:41074208 | T | A | 2 | a0001c0001t0008g0009 a0001c0001t0032g0009 |
6 | HG00280.hp2 HG00738.hp1 HG01069.hp2 others(3): Show |
intron_variant | MODIFIER | c.-62+1124T>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 1/9 | chr6 | 41074208 | |||||||
| chr6:41074491 | A | T | 1 | a0001c0001t0009g0016 | 3 | HG02896.hp2 HG02965.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-62+1407A>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 1/9 | chr6 | 41074491 | |||||||
| chr6:41074652 | T | A | 2 | a0001c0001t0015g0021 a0001c0001t0037g0039 |
3 | HG03669.hp1 NA18978.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.-62+1568T>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 1/9 | chr6 | 41074652 | |||||||
| chr6:41074773 | T | G | 1 | a0001c0001t0001g0048 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-62+1689T>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 1/9 | chr6 | 41074773 | |||||||
| chr6:41074811 | A | T | 1 | a0001c0001t0031g0088 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-62+1727A>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 1/9 | chr6 | 41074811 | |||||||
| chr6:41074851 | T | G | 63 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0018 others(60): Show |
154 | HG00099.hp1 HG00280.hp2 HG00609.hp2 others(151): Show |
intron_variant | MODIFIER | c.-62+1767T>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 1/9 | chr6 | 41074851 | |||||||
| chr6:41075254 | G | A | 65 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0018 others(62): Show |
157 | HG00099.hp1 HG00280.hp2 HG00609.hp2 others(154): Show |
intron_variant | MODIFIER | c.-62+2170G>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 1/9 | chr6 | 41075254 | |||||||
| chr6:41075261 | A | G | 1 | a0001c0001t0001g0118 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-62+2177A>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 1/9 | chr6 | 41075261 | |||||||
| chr6:41075301 | T | C | 2 | a0001c0001t0015g0021 a0001c0001t0037g0039 |
3 | HG03669.hp1 NA18978.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.-62+2217T>C | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 1/9 | chr6 | 41075301 | |||||||
| chr6:41075409 | T | A | 1 | a0001c0001t0001g0023 | 2 | HG01496.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-62+2325T>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 1/9 | chr6 | 41075409 | |||||||
| chr6:41075464 | T | C | 1 | a0001c0001t0001g0031 | 2 | HG00639.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.-62+2380T>C | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 1/9 | chr6 | 41075464 | |||||||
| chr6:41075475 | A | G | 7 | a0001c0001t0001g0004 a0001c0001t0001g0019 a0001c0001t0001g0037 others(4): Show |
33 | HG02523.hp1 NA18747.hp1 NA18948.hp2 others(30): Show |
intron_variant | MODIFIER | c.-62+2391A>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 1/9 | chr6 | 41075475 | |||||||
| chr6:41075510 | C | A | 1 | a0001c0001t0001g0024 | 2 | NA18960.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.-62+2426C>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 1/9 | chr6 | 41075510 | |||||||
| chr6:41075595 | G | C | 1 | a0001c0001t0001g0089 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-62+2511G>C | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 1/9 | chr6 | 41075595 | |||||||
| chr6:41075726 | G | A | 63 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0018 others(60): Show |
154 | HG00099.hp1 HG00280.hp2 HG00609.hp2 others(151): Show |
intron_variant | MODIFIER | c.-62+2642G>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 1/9 | chr6 | 41075726 | |||||||
| chr6:41075733 | C | CT | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(135): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.-62+2660dupT | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr6 | 41075733 | ||||||
| chr6:41075805 | T | G | 1 | a0001c0001t0029g0090 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-62+2721T>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 1/9 | chr6 | 41075805 | |||||||
| chr6:41075837 | G | C | 2 | a0001c0001t0015g0021 a0001c0001t0037g0039 |
3 | HG03669.hp1 NA18978.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.-62+2753G>C | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 1/9 | chr6 | 41075837 | |||||||
| chr6:41075929 | T | A | 2 | a0001c0001t0015g0021 a0001c0001t0037g0039 |
3 | HG03669.hp1 NA18978.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.-62+2845T>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 1/9 | chr6 | 41075929 | |||||||
| chr6:41076037 | C | T | 1 | a0001c0001t0001g0087 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-62+2953C>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 1/9 | chr6 | 41076037 | |||||||
| chr6:41076155 | C | A | 2 | a0001c0001t0015g0021 a0001c0001t0037g0039 |
3 | HG03669.hp1 NA18978.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.-61-2874C>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 1/9 | chr6 | 41076155 | |||||||
| chr6:41076244 | A | G | 1 | a0001c0001t0001g0086 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-61-2785A>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 1/9 | chr6 | 41076244 | |||||||
| chr6:41076332 | A | G | 2 | a0001c0001t0013g0113 a0001c0001t0013g0114 |
2 | HG02572.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-61-2697A>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 1/9 | chr6 | 41076332 | |||||||
| chr6:41076445 | C | A | 1 | a0001c0001t0001g0050 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-61-2584C>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 1/9 | chr6 | 41076445 | |||||||
| chr6:41076841 | T | C | 1 | a0001c0001t0002g0051 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-61-2188T>C | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 1/9 | chr6 | 41076841 | |||||||
| chr6:41077218 | A | T | 63 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0018 others(60): Show |
154 | HG00099.hp1 HG00280.hp2 HG00609.hp2 others(151): Show |
intron_variant | MODIFIER | c.-61-1811A>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 1/9 | chr6 | 41077218 | |||||||
| chr6:41077236 | G | A | 1 | a0001c0001t0029g0090 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-61-1793G>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 1/9 | chr6 | 41077236 | |||||||
| chr6:41077247 | A | T | 65 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0018 others(62): Show |
157 | HG00099.hp1 HG00280.hp2 HG00609.hp2 others(154): Show |
intron_variant | MODIFIER | c.-61-1782A>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 1/9 | chr6 | 41077247 | |||||||
| chr6:41077531 | T | C | 63 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0018 others(60): Show |
154 | HG00099.hp1 HG00280.hp2 HG00609.hp2 others(151): Show |
intron_variant | MODIFIER | c.-61-1498T>C | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 1/9 | chr6 | 41077531 | |||||||
| chr6:41077540 | ATGTAT | A | 54 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0018 others(51): Show |
139 | HG00099.hp1 HG00609.hp2 HG00639.hp2 others(136): Show |
intron_variant | MODIFIER | c.-61-1485_-61-1481d others(7): Show |
NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr6 | 41077540 | ||||||
| chr6:41077827 | C | G | 4 | a0001c0001t0003g0020 a0001c0001t0003g0036 a0001c0001t0003g0111 others(1): Show |
7 | HG02559.hp2 HG02622.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.-61-1202C>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 1/9 | chr6 | 41077827 | |||||||
| chr6:41078438 | G | A | 63 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0018 others(60): Show |
154 | HG00099.hp1 HG00280.hp2 HG00609.hp2 others(151): Show |
intron_variant | MODIFIER | c.-61-591G>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 1/9 | chr6 | 41078438 | |||||||
| chr6:41078480 | CTT | C | 55 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0018 others(52): Show |
140 | HG00099.hp1 HG00609.hp2 HG00639.hp2 others(137): Show |
intron_variant | MODIFIER | c.-61-548_-61-547del others(2): Show |
NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 1/9 | chr6 | 41078480 | |||||||
| chr6:41078666 | A | C | 2 | a0001c0001t0015g0021 a0001c0001t0037g0039 |
3 | HG03669.hp1 NA18978.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.-61-363A>C | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 1/9 | chr6 | 41078666 | |||||||
| chr6:41078910 | C | T | 1 | a0001c0001t0003g0110 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-61-119C>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 1/9 | chr6 | 41078910 | |||||||
| chr6:41079283 | G | A | 4 | a0001c0001t0008g0009 a0001c0001t0011g0038 a0001c0001t0011g0091 others(1): Show |
8 | HG00280.hp2 HG00738.hp1 HG01069.hp2 others(5): Show |
intron_variant | MODIFIER | c.75+119G>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 2/9 | chr6 | 41079283 | |||||||
| chr6:41079588 | C | T | 1 | a0001c0001t0001g0035 | 2 | HG01943.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.75+424C>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 2/9 | chr6 | 41079588 | |||||||
| chr6:41079639 | T | C | 3 | a0001c0001t0013g0113 a0001c0001t0013g0114 a0001c0001t0035g0094 |
3 | HG02572.hp2 HG02970.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.75+475T>C | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 2/9 | chr6 | 41079639 | |||||||
| chr6:41079800 | A | G | 1 | a0001c0001t0001g0085 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.75+636A>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 2/9 | chr6 | 41079800 | |||||||
| chr6:41080053 | G | C | 1 | a0001c0001t0003g0110 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.76-758G>C | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 2/9 | chr6 | 41080053 | |||||||
| chr6:41080326 | G | A | 1 | a0001c0001t0009g0016 | 3 | HG02896.hp2 HG02965.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.76-485G>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 2/9 | chr6 | 41080326 | |||||||
| chr6:41080386 | C | T | 2 | a0001c0001t0015g0021 a0001c0001t0037g0039 |
3 | HG03669.hp1 NA18978.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.76-425C>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 2/9 | chr6 | 41080386 | |||||||
| chr6:41080505 | C | T | 2 | a0001c0001t0015g0021 a0001c0001t0037g0039 |
3 | HG03669.hp1 NA18978.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.76-306C>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 2/9 | chr6 | 41080505 | |||||||
| chr6:41080718 | C | T | 2 | a0001c0001t0013g0113 a0001c0001t0013g0114 |
2 | HG02572.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.76-93C>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 2/9 | chr6 | 41080718 | |||||||
| chr6:41081125 | T | G | 1 | a0001c0001t0001g0041 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.162+228T>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 3/9 | chr6 | 41081125 | |||||||
| chr6:41081155 | A | G | 1 | a0001c0005t0001g0084 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.162+258A>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 3/9 | chr6 | 41081155 | |||||||
| chr6:41081218 | G | A | 30 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0018 others(27): Show |
89 | HG00099.hp1 HG00609.hp2 HG00639.hp2 others(86): Show |
intron_variant | MODIFIER | c.162+321G>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 3/9 | chr6 | 41081218 | |||||||
| chr6:41081264 | C | T | 1 | a0001c0001t0003g0109 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.162+367C>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 3/9 | chr6 | 41081264 | |||||||
| chr6:41081406 | C | T | 2 | a0001c0001t0015g0021 a0001c0001t0037g0039 |
3 | HG03669.hp1 NA18978.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.162+509C>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 3/9 | chr6 | 41081406 | |||||||
| chr6:41081415 | A | G | 2 | a0001c0001t0011g0038 a0001c0001t0011g0091 |
2 | HG02615.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.162+518A>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 3/9 | chr6 | 41081415 | |||||||
| chr6:41081418 | A | G | 2 | a0001c0001t0015g0021 a0001c0001t0037g0039 |
3 | HG03669.hp1 NA18978.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.162+521A>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 3/9 | chr6 | 41081418 | |||||||
| chr6:41081429 | G | T | 1 | a0001c0001t0009g0016 | 3 | HG02896.hp2 HG02965.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.162+532G>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 3/9 | chr6 | 41081429 | |||||||
| chr6:41081447 | G | A | 1 | a0001c0001t0038g0053 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.162+550G>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 3/9 | chr6 | 41081447 | |||||||
| chr6:41081501 | A | C | 1 | a0001c0001t0010g0034 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.162+604A>C | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 3/9 | chr6 | 41081501 | |||||||
| chr6:41081571 | C | T | 7 | a0001c0001t0008g0009 a0001c0001t0011g0038 a0001c0001t0011g0091 others(4): Show |
12 | HG00280.hp2 HG00738.hp1 HG01069.hp2 others(9): Show |
intron_variant | MODIFIER | c.162+674C>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 3/9 | chr6 | 41081571 | |||||||
| chr6:41081700 | ATCTTGTT others(4): Show |
A | 2 | a0001c0001t0001g0092 a0001c0008t0018g0093 |
2 | HG02717.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.162+813_162+823del others(11): Show |
NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 41081700 | ||||||
| chr6:41081769 | T | C | 26 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0018 others(23): Show |
85 | HG00099.hp1 HG00609.hp2 HG00639.hp2 others(82): Show |
intron_variant | MODIFIER | c.162+872T>C | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 3/9 | chr6 | 41081769 | |||||||
| chr6:41081903 | G | GGCTAA | 2 | a0001c0001t0015g0021 a0001c0001t0037g0039 |
3 | HG03669.hp1 NA18978.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.162+1008_162+1012d others(7): Show |
NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 41081903 | ||||||
| chr6:41081952 | C | T | 2 | a0001c0001t0015g0021 a0001c0001t0037g0039 |
3 | HG03669.hp1 NA18978.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.162+1055C>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 3/9 | chr6 | 41081952 | |||||||
| chr6:41081961 | C | G | 2 | a0001c0001t0015g0021 a0001c0001t0037g0039 |
3 | HG03669.hp1 NA18978.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.162+1064C>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 3/9 | chr6 | 41081961 | |||||||
| chr6:41082148 | A | G | 2 | a0001c0001t0011g0091 a0001c0008t0018g0093 |
2 | HG02615.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.162+1251A>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 3/9 | chr6 | 41082148 | |||||||
| chr6:41082156 | T | C | 52 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(49): Show |
137 | HG00099.hp1 HG00609.hp2 HG00639.hp2 others(134): Show |
intron_variant | MODIFIER | c.162+1259T>C | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 3/9 | chr6 | 41082156 | |||||||
| chr6:41082202 | A | G | 1 | a0001c0001t0001g0083 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.162+1305A>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 3/9 | chr6 | 41082202 | |||||||
| chr6:41082300 | T | C | 1 | a0001c0001t0025g0057 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.162+1403T>C | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 3/9 | chr6 | 41082300 | |||||||
| chr6:41082541 | A | G | 1 | a0001c0001t0001g0082 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.163-1505A>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 3/9 | chr6 | 41082541 | |||||||
| chr6:41082760 | T | C | 1 | a0001c0001t0003g0111 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.163-1286T>C | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 3/9 | chr6 | 41082760 | |||||||
| chr6:41082982 | C | T | 5 | a0001c0001t0001g0013 a0001c0001t0001g0046 a0001c0001t0009g0016 others(2): Show |
11 | HG00558.hp2 HG02896.hp2 HG02965.hp2 others(8): Show |
intron_variant | MODIFIER | c.163-1064C>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 3/9 | chr6 | 41082982 | |||||||
| chr6:41083132 | A | G | 1 | a0001c0001t0001g0081 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.163-914A>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 3/9 | chr6 | 41083132 | |||||||
| chr6:41083348 | A | G | 1 | a0001c0001t0002g0080 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.163-698A>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 3/9 | chr6 | 41083348 | |||||||
| chr6:41083362 | A | G | 1 | a0001c0001t0003g0033 | 2 | HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.163-684A>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 3/9 | chr6 | 41083362 | |||||||
| chr6:41083381 | G | A | 1 | a0001c0001t0029g0090 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.163-665G>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 3/9 | chr6 | 41083381 | |||||||
| chr6:41083483 | G | GTA | 15 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0017 others(12): Show |
28 | HG00558.hp2 HG01891.hp1 HG02074.hp1 others(25): Show |
intron_variant | MODIFIER | c.163-560_163-559dup others(2): Show |
NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 41083483 | ||||||
| chr6:41083687 | C | A | 1 | a0001c0001t0027g0121 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.163-359C>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 3/9 | chr6 | 41083687 | |||||||
| chr6:41083813 | A | G | 1 | a0001c0008t0018g0093 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.163-233A>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 3/9 | chr6 | 41083813 | |||||||
| chr6:41084001 | T | C | 1 | a0001c0001t0001g0058 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.163-45T>C | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 3/9 | chr6 | 41084001 | |||||||
| chr6:41084263 | A | G | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(135): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.309+71A>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 4/9 | chr6 | 41084263 | |||||||
| chr6:41084341 | A | G | 1 | a0001c0001t0001g0077 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.309+149A>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 4/9 | chr6 | 41084341 | |||||||
| chr6:41084375 | A | C | 1 | a0001c0001t0001g0029 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.309+183A>C | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 4/9 | chr6 | 41084375 | |||||||
| chr6:41084458 | A | G | 2 | a0001c0001t0015g0021 a0001c0001t0037g0039 |
3 | HG03669.hp1 NA18978.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.309+266A>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 4/9 | chr6 | 41084458 | |||||||
| chr6:41084485 | G | A | 3 | a0001c0001t0015g0021 a0001c0001t0029g0090 a0001c0001t0037g0039 |
4 | HG01243.hp1 HG03669.hp1 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.309+293G>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 4/9 | chr6 | 41084485 | |||||||
| chr6:41084804 | A | C | 1 | a0001c0001t0003g0112 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.309+612A>C | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 4/9 | chr6 | 41084804 | |||||||
| chr6:41084822 | C | G | 2 | a0001c0001t0004g0005 a0001c0001t0004g0107 |
11 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.309+630C>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 4/9 | chr6 | 41084822 | |||||||
| chr6:41084989 | T | C | 1 | a0001c0001t0001g0059 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.309+797T>C | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 4/9 | chr6 | 41084989 | |||||||
| chr6:41085130 | A | G | 2 | a0001c0001t0015g0021 a0001c0001t0037g0039 |
3 | HG03669.hp1 NA18978.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.309+938A>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 4/9 | chr6 | 41085130 | |||||||
| chr6:41085135 | A | C | 39 | a0001c0001t0003g0010 a0001c0001t0003g0020 a0001c0001t0003g0033 others(36): Show |
72 | HG00280.hp2 HG00738.hp1 HG01069.hp2 others(69): Show |
intron_variant | MODIFIER | c.309+943A>C | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 4/9 | chr6 | 41085135 | |||||||
| chr6:41085476 | C | G | 1 | a0001c0001t0029g0090 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.309+1284C>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 4/9 | chr6 | 41085476 | |||||||
| chr6:41085682 | G | A | 1 | a0001c0001t0003g0033 | 2 | HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.309+1490G>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 4/9 | chr6 | 41085682 | |||||||
| chr6:41085752 | AT | A | 38 | a0001c0001t0003g0010 a0001c0001t0003g0020 a0001c0001t0003g0033 others(35): Show |
73 | HG00280.hp2 HG00738.hp1 HG01069.hp2 others(70): Show |
intron_variant | MODIFIER | c.309+1572delT | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 41085752 | ||||||
| chr6:41085784 | G | A | 11 | a0001c0001t0003g0010 a0001c0001t0003g0020 a0001c0001t0003g0033 others(8): Show |
20 | HG01175.hp2 HG02257.hp2 HG02559.hp2 others(17): Show |
intron_variant | MODIFIER | c.309+1592G>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 4/9 | chr6 | 41085784 | |||||||
| chr6:41085829 | G | C | 1 | a0001c0001t0027g0121 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.309+1637G>C | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 4/9 | chr6 | 41085829 | |||||||
| chr6:41086206 | CA | C | 39 | a0001c0001t0003g0010 a0001c0001t0003g0020 a0001c0001t0003g0033 others(36): Show |
72 | HG00280.hp2 HG00738.hp1 HG01069.hp2 others(69): Show |
intron_variant | MODIFIER | c.309+2016delA | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 41086206 | ||||||
| chr6:41086522 | G | GT | 18 | a0001c0001t0001g0003 a0001c0001t0001g0056 a0001c0001t0001g0058 others(15): Show |
46 | HG00280.hp1 HG00597.hp2 HG00609.hp1 others(43): Show |
intron_variant | MODIFIER | c.309+2338dupT | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 41086522 | ||||||
| chr6:41086549 | C | T | 1 | a0001c0001t0001g0082 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.309+2357C>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 4/9 | chr6 | 41086549 | |||||||
| chr6:41086671 | A | G | 2 | a0001c0001t0015g0021 a0001c0001t0037g0039 |
3 | HG03669.hp1 NA18978.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.309+2479A>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 4/9 | chr6 | 41086671 | |||||||
| chr6:41086734 | A | G | 1 | a0001c0001t0003g0109 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.309+2542A>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 4/9 | chr6 | 41086734 | |||||||
| chr6:41086740 | T | A | 1 | a0001c0001t0003g0109 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.309+2548T>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 4/9 | chr6 | 41086740 | |||||||
| chr6:41087172 | A | G | 1 | a0001c0001t0001g0028 | 2 | HG02630.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.310-2407A>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 4/9 | chr6 | 41087172 | |||||||
| chr6:41087252 | G | C | 2 | a0001c0001t0011g0038 a0001c0001t0011g0091 |
2 | HG02615.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.310-2327G>C | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 4/9 | chr6 | 41087252 | |||||||
| chr6:41087465 | A | T | 2 | a0001c0001t0013g0113 a0001c0001t0013g0114 |
2 | HG02572.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.310-2114A>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 4/9 | chr6 | 41087465 | |||||||
| chr6:41087475 | A | G | 1 | a0001c0001t0001g0027 | 2 | HG01081.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.310-2104A>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 4/9 | chr6 | 41087475 | |||||||
| chr6:41087555 | A | G | 2 | a0001c0001t0015g0021 a0001c0001t0037g0039 |
3 | HG03669.hp1 NA18978.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.310-2024A>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 4/9 | chr6 | 41087555 | |||||||
| chr6:41087716 | T | TA | 2 | a0001c0001t0008g0009 a0001c0001t0032g0009 |
6 | HG00280.hp2 HG00738.hp1 HG01069.hp2 others(3): Show |
intron_variant | MODIFIER | c.310-1853dupA | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 41087716 | ||||||
| chr6:41087733 | A | G | 1 | a0001c0001t0027g0121 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.310-1846A>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 4/9 | chr6 | 41087733 | |||||||
| chr6:41087880 | A | C | 1 | a0001c0001t0001g0071 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.310-1699A>C | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 4/9 | chr6 | 41087880 | |||||||
| chr6:41087889 | G | T | 2 | a0001c0001t0008g0009 a0001c0001t0032g0009 |
6 | HG00280.hp2 HG00738.hp1 HG01069.hp2 others(3): Show |
intron_variant | MODIFIER | c.310-1690G>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 4/9 | chr6 | 41087889 | |||||||
| chr6:41088142 | G | A | 27 | a0001c0001t0003g0010 a0001c0001t0003g0020 a0001c0001t0003g0033 others(24): Show |
50 | HG01175.hp2 HG01255.hp2 HG01884.hp1 others(47): Show |
intron_variant | MODIFIER | c.310-1437G>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 4/9 | chr6 | 41088142 | |||||||
| chr6:41088183 | C | T | 1 | a0001c0001t0001g0087 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.310-1396C>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 4/9 | chr6 | 41088183 | |||||||
| chr6:41088189 | C | T | 1 | a0001c0001t0001g0070 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.310-1390C>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 4/9 | chr6 | 41088189 | |||||||
| chr6:41088217 | G | A | 1 | a0001c0003t0001g0030 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.310-1362G>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 4/9 | chr6 | 41088217 | |||||||
| chr6:41088423 | C | CA | 13 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0001g0031 others(10): Show |
20 | HG00597.hp1 HG00639.hp2 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.310-1134dupA | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 41088423 | ||||||
| chr6:41088423 | C | CAA | 9 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0115 others(6): Show |
11 | HG01175.hp1 HG01243.hp1 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.310-1135_310-1134d others(4): Show |
NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 41088423 | ||||||
| chr6:41088423 | C | CAAA | 17 | a0001c0001t0003g0010 a0001c0001t0003g0033 a0001c0001t0003g0102 others(14): Show |
37 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(34): Show |
intron_variant | MODIFIER | c.310-1136_310-1134d others(5): Show |
NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 41088423 | ||||||
| chr6:41088423 | C | CAAAA | 10 | a0001c0001t0003g0020 a0001c0001t0003g0036 a0001c0001t0003g0111 others(7): Show |
20 | HG00280.hp2 HG00738.hp1 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.310-1137_310-1134d others(6): Show |
NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 41088423 | ||||||
| chr6:41088423 | CA | C | 7 | a0001c0001t0001g0023 a0001c0001t0001g0026 a0001c0001t0001g0070 others(4): Show |
8 | HG00558.hp1 HG01261.hp2 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.310-1134delA | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 41088423 | ||||||
| chr6:41088446 | T | A | 1 | a0001c0001t0001g0116 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.310-1133T>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 4/9 | chr6 | 41088446 | |||||||
| chr6:41088504 | A | G | 2 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
2 | HG03654.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.310-1075A>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 4/9 | chr6 | 41088504 | |||||||
| chr6:41088610 | T | C | 2 | a0001c0001t0015g0021 a0001c0001t0037g0039 |
3 | HG03669.hp1 NA18978.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.310-969T>C | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 4/9 | chr6 | 41088610 | |||||||
| chr6:41088766 | A | C | 13 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0017 others(10): Show |
25 | HG00558.hp2 HG02074.hp1 HG02132.hp2 others(22): Show |
intron_variant | MODIFIER | c.310-813A>C | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 4/9 | chr6 | 41088766 | |||||||
| chr6:41088953 | A | G | 2 | a0001c0001t0007g0015 a0002c0007t0007g0108 |
5 | HG02280.hp2 HG02486.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.310-626A>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 4/9 | chr6 | 41088953 | |||||||
| chr6:41088988 | A | G | 1 | a0001c0001t0037g0039 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.310-591A>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 4/9 | chr6 | 41088988 | |||||||
| chr6:41089047 | G | A | 2 | a0001c0001t0015g0021 a0001c0001t0037g0039 |
3 | HG03669.hp1 NA18978.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.310-532G>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 4/9 | chr6 | 41089047 | |||||||
| chr6:41089377 | T | C | 1 | a0001c0001t0001g0037 | 2 | NA18956.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.310-202T>C | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 4/9 | chr6 | 41089377 | |||||||
| chr6:41089398 | C | T | 1 | a0001c0001t0001g0082 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.310-181C>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 4/9 | chr6 | 41089398 | |||||||
| chr6:41089555 | C | G | 2 | a0001c0001t0015g0021 a0001c0001t0037g0039 |
3 | HG03669.hp1 NA18978.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.310-24C>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 4/9 | chr6 | 41089555 | |||||||
| chr6:41089809 | G | A | 1 | a0001c0001t0001g0073 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.441+99G>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 5/9 | chr6 | 41089809 | |||||||
| chr6:41089886 | G | A | 1 | a0001c0001t0003g0102 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.441+176G>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 5/9 | chr6 | 41089886 | |||||||
| chr6:41090066 | C | T | 2 | a0001c0001t0007g0015 a0002c0007t0007g0108 |
5 | HG02280.hp2 HG02486.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.442-138C>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 5/9 | chr6 | 41090066 | |||||||
| chr6:41090578 | A | T | 39 | a0001c0001t0003g0010 a0001c0001t0003g0020 a0001c0001t0003g0033 others(36): Show |
72 | HG00280.hp2 HG00738.hp1 HG01069.hp2 others(69): Show |
intron_variant | MODIFIER | c.547+269A>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 6/9 | chr6 | 41090578 | |||||||
| chr6:41090598 | G | A | 2 | a0001c0001t0015g0021 a0001c0001t0037g0039 |
3 | HG03669.hp1 NA18978.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.547+289G>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 6/9 | chr6 | 41090598 | |||||||
| chr6:41090688 | G | T | 1 | a0001c0001t0004g0106 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.547+379G>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 6/9 | chr6 | 41090688 | |||||||
| chr6:41090691 | T | A | 1 | a0001c0001t0001g0060 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.547+382T>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 6/9 | chr6 | 41090691 | |||||||
| chr6:41090692 | A | C | 1 | a0001c0001t0001g0060 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.547+383A>C | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 6/9 | chr6 | 41090692 | |||||||
| chr6:41090751 | A | G | 39 | a0001c0001t0003g0010 a0001c0001t0003g0020 a0001c0001t0003g0033 others(36): Show |
72 | HG00280.hp2 HG00738.hp1 HG01069.hp2 others(69): Show |
intron_variant | MODIFIER | c.547+442A>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 6/9 | chr6 | 41090751 | |||||||
| chr6:41090850 | A | G | 1 | a0001c0001t0026g0104 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.547+541A>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 6/9 | chr6 | 41090850 | |||||||
| chr6:41091045 | C | G | 1 | a0001c0008t0018g0093 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.548-483C>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 6/9 | chr6 | 41091045 | |||||||
| chr6:41091076 | A | G | 1 | a0001c0001t0017g0099 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.548-452A>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 6/9 | chr6 | 41091076 | |||||||
| chr6:41091174 | A | T | 37 | a0001c0001t0003g0010 a0001c0001t0003g0020 a0001c0001t0003g0033 others(34): Show |
69 | HG00280.hp2 HG00738.hp1 HG01069.hp2 others(66): Show |
intron_variant | MODIFIER | c.548-354A>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 6/9 | chr6 | 41091174 | |||||||
| chr6:41091229 | G | A | 39 | a0001c0001t0003g0010 a0001c0001t0003g0020 a0001c0001t0003g0033 others(36): Show |
72 | HG00280.hp2 HG00738.hp1 HG01069.hp2 others(69): Show |
intron_variant | MODIFIER | c.548-299G>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 6/9 | chr6 | 41091229 | |||||||
| chr6:41091287 | G | C | 1 | a0001c0008t0018g0093 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.548-241G>C | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 6/9 | chr6 | 41091287 | |||||||
| chr6:41091430 | G | A | 39 | a0001c0001t0003g0010 a0001c0001t0003g0020 a0001c0001t0003g0033 others(36): Show |
72 | HG00280.hp2 HG00738.hp1 HG01069.hp2 others(69): Show |
intron_variant | MODIFIER | c.548-98G>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 6/9 | chr6 | 41091430 | |||||||
| chr6:41091719 | T | G | 37 | a0001c0001t0003g0010 a0001c0001t0003g0020 a0001c0001t0003g0033 others(34): Show |
69 | HG00280.hp2 HG00738.hp1 HG01069.hp2 others(66): Show |
intron_variant | MODIFIER | c.714+25T>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 7/9 | chr6 | 41091719 | |||||||
| chr6:41091752 | T | C | 1 | a0001c0001t0009g0016 | 3 | HG02896.hp2 HG02965.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.714+58T>C | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 7/9 | chr6 | 41091752 | |||||||
| chr6:41091791 | G | A | 1 | a0001c0001t0001g0085 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.714+97G>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 7/9 | chr6 | 41091791 | |||||||
| chr6:41091846 | C | G | 1 | a0001c0001t0001g0082 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.714+152C>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 7/9 | chr6 | 41091846 | |||||||
| chr6:41091871 | A | G | 24 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0018 others(21): Show |
83 | HG00099.hp1 HG00609.hp2 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.714+177A>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 7/9 | chr6 | 41091871 | |||||||
| chr6:41091900 | T | C | 1 | a0001c0001t0016g0096 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.714+206T>C | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 7/9 | chr6 | 41091900 | |||||||
| chr6:41091969 | C | T | 1 | a0001c0001t0001g0092 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.714+275C>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 7/9 | chr6 | 41091969 | |||||||
| chr6:41092134 | C | T | 39 | a0001c0001t0003g0010 a0001c0001t0003g0020 a0001c0001t0003g0033 others(36): Show |
72 | HG00280.hp2 HG00738.hp1 HG01069.hp2 others(69): Show |
intron_variant | MODIFIER | c.714+440C>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 7/9 | chr6 | 41092134 | |||||||
| chr6:41092184 | TAAGAATG others(6): Show |
T | 1 | a0001c0003t0001g0030 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.714+492_714+504del others(13): Show |
NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr6 | 41092184 | ||||||
| chr6:41092199 | G | T | 1 | a0001c0003t0001g0030 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.714+505G>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 7/9 | chr6 | 41092199 | |||||||
| chr6:41092200 | A | T | 1 | a0001c0003t0001g0030 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.714+506A>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 7/9 | chr6 | 41092200 | |||||||
| chr6:41092233 | G | A | 2 | a0001c0001t0015g0021 a0001c0001t0037g0039 |
3 | HG03669.hp1 NA18978.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.714+539G>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 7/9 | chr6 | 41092233 | |||||||
| chr6:41092277 | A | G | 1 | a0001c0001t0001g0067 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.714+583A>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 7/9 | chr6 | 41092277 | |||||||
| chr6:41092473 | C | G | 39 | a0001c0001t0003g0010 a0001c0001t0003g0020 a0001c0001t0003g0033 others(36): Show |
72 | HG00280.hp2 HG00738.hp1 HG01069.hp2 others(69): Show |
intron_variant | MODIFIER | c.715-439C>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 7/9 | chr6 | 41092473 | |||||||
| chr6:41092540 | T | C | 5 | a0001c0001t0003g0100 a0001c0001t0013g0113 a0001c0001t0013g0114 others(2): Show |
5 | HG01255.hp2 HG02572.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.715-372T>C | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 7/9 | chr6 | 41092540 | |||||||
| chr6:41092552 | T | C | 1 | a0001c0001t0027g0121 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.715-360T>C | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 7/9 | chr6 | 41092552 | |||||||
| chr6:41092776 | T | C | 1 | a0001c0001t0001g0062 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.715-136T>C | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 7/9 | chr6 | 41092776 | |||||||
| chr6:41093220 | G | A | 1 | a0001c0001t0001g0068 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.888+135G>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 8/9 | chr6 | 41093220 | |||||||
| chr6:41093362 | T | C | 2 | a0001c0001t0015g0021 a0001c0001t0037g0039 |
3 | HG03669.hp1 NA18978.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.888+277T>C | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 8/9 | chr6 | 41093362 | |||||||
| chr6:41093369 | G | A | 1 | a0001c0001t0001g0018 | 3 | HG03927.hp2 HG04199.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.888+284G>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 8/9 | chr6 | 41093369 | |||||||
| chr6:41093415 | A | G | 1 | a0001c0001t0029g0090 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.888+330A>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 8/9 | chr6 | 41093415 | |||||||
| chr6:41093457 | G | C | 1 | a0001c0001t0027g0121 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.888+372G>C | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 8/9 | chr6 | 41093457 | |||||||
| chr6:41093478 | T | A | 1 | a0001c0003t0001g0030 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.888+393T>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 8/9 | chr6 | 41093478 | |||||||
| chr6:41093564 | A | G | 1 | a0001c0001t0001g0059 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.888+479A>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 8/9 | chr6 | 41093564 | |||||||
| chr6:41093628 | G | A | 1 | a0001c0001t0011g0038 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.888+543G>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 8/9 | chr6 | 41093628 | |||||||
| chr6:41093690 | C | T | 1 | a0001c0001t0001g0066 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.888+605C>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 8/9 | chr6 | 41093690 | |||||||
| chr6:41093751 | G | A | 1 | a0001c0001t0016g0096 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.889-645G>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 8/9 | chr6 | 41093751 | |||||||
| chr6:41093766 | C | T | 1 | a0001c0001t0025g0057 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.889-630C>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 8/9 | chr6 | 41093766 | |||||||
| chr6:41093809 | G | A | 27 | a0001c0001t0003g0010 a0001c0001t0003g0020 a0001c0001t0003g0033 others(24): Show |
50 | HG01175.hp2 HG01255.hp2 HG01884.hp1 others(47): Show |
intron_variant | MODIFIER | c.889-587G>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 8/9 | chr6 | 41093809 | |||||||
| chr6:41093854 | T | C | 27 | a0001c0001t0003g0010 a0001c0001t0003g0020 a0001c0001t0003g0033 others(24): Show |
50 | HG01175.hp2 HG01255.hp2 HG01884.hp1 others(47): Show |
intron_variant | MODIFIER | c.889-542T>C | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 8/9 | chr6 | 41093854 | |||||||
| chr6:41094009 | T | C | 1 | a0001c0001t0029g0090 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.889-387T>C | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 8/9 | chr6 | 41094009 | |||||||
| chr6:41094090 | G | A | 1 | a0001c0001t0027g0121 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.889-306G>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 8/9 | chr6 | 41094090 | |||||||
| chr6:41094143 | G | GTC | 3 | a0001c0001t0004g0012 a0001c0001t0004g0040 a0001c0001t0028g0012 |
5 | HG02258.hp1 HG02922.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.889-252_889-251ins others(2): Show |
NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr6 | 41094143 | ||||||
| chr6:41094164 | T | A | 3 | a0001c0001t0011g0038 a0001c0001t0011g0091 a0001c0001t0013g0113 |
3 | HG02572.hp2 HG02615.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.889-232T>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 8/9 | chr6 | 41094164 | |||||||
| chr6:41094165 | A | T | 1 | a0001c0001t0001g0117 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.889-231A>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 8/9 | chr6 | 41094165 | |||||||
| chr6:41094266 | T | C | 1 | a0001c0001t0001g0074 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.889-130T>C | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 8/9 | chr6 | 41094266 | |||||||
| chr6:41094624 | A | G | 1 | a0001c0001t0029g0090 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.990+127A>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 9/9 | chr6 | 41094624 | |||||||
| chr6:41094950 | C | G | 26 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0018 others(23): Show |
86 | HG00099.hp1 HG00609.hp2 HG00639.hp2 others(83): Show |
intron_variant | MODIFIER | c.990+453C>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 9/9 | chr6 | 41094950 | |||||||
| chr6:41095326 | C | T | 39 | a0001c0001t0003g0010 a0001c0001t0003g0020 a0001c0001t0003g0033 others(36): Show |
72 | HG00280.hp2 HG00738.hp1 HG01069.hp2 others(69): Show |
intron_variant | MODIFIER | c.990+829C>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 9/9 | chr6 | 41095326 | |||||||
| chr6:41095392 | T | C | 1 | a0001c0001t0001g0063 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.990+895T>C | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 9/9 | chr6 | 41095392 | |||||||
| chr6:41095678 | G | A | 2 | a0001c0001t0015g0021 a0001c0001t0037g0039 |
3 | HG03669.hp1 NA18978.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.990+1181G>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 9/9 | chr6 | 41095678 | |||||||
| chr6:41095710 | C | T | 1 | a0001c0001t0001g0098 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.990+1213C>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 9/9 | chr6 | 41095710 | |||||||
| chr6:41095711 | G | A | 1 | a0001c0001t0001g0046 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.990+1214G>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 9/9 | chr6 | 41095711 | |||||||
| chr6:41095767 | A | G | 1 | a0001c0001t0001g0082 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.990+1270A>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 9/9 | chr6 | 41095767 | |||||||
| chr6:41096188 | T | A | 2 | a0001c0001t0011g0038 a0001c0001t0011g0091 |
2 | HG02615.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.991-1169T>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 9/9 | chr6 | 41096188 | |||||||
| chr6:41096244 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.991-1113C>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 9/9 | chr6 | 41096244 | |||||||
| chr6:41096281 | A | G | 2 | a0001c0001t0015g0021 a0001c0001t0037g0039 |
3 | HG03669.hp1 NA18978.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.991-1076A>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 9/9 | chr6 | 41096281 | |||||||
| chr6:41096741 | C | T | 2 | a0001c0001t0015g0021 a0001c0001t0037g0039 |
3 | HG03669.hp1 NA18978.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.991-616C>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 9/9 | chr6 | 41096741 | |||||||
| chr6:41096787 | A | T | 1 | a0001c0001t0001g0067 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.991-570A>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 9/9 | chr6 | 41096787 | |||||||
| chr6:41096907 | C | T | 3 | a0001c0001t0001g0056 a0001c0001t0001g0075 a0001c0001t0030g0064 |
3 | HG01981.hp2 HG03834.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.991-450C>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 9/9 | chr6 | 41096907 | |||||||
| chr6:41096954 | T | C | 1 | a0001c0001t0001g0025 | 2 | NA19063.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.991-403T>C | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 9/9 | chr6 | 41096954 | |||||||
| chr6:41097067 | G | A | 2 | a0001c0001t0001g0032 a0001c0001t0001g0089 |
3 | HG01099.hp1 HG02738.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.991-290G>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 9/9 | chr6 | 41097067 | |||||||
| chr6:41097114 | C | A | 2 | a0001c0001t0008g0009 a0001c0001t0032g0009 |
6 | HG00280.hp2 HG00738.hp1 HG01069.hp2 others(3): Show |
intron_variant | MODIFIER | c.991-243C>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 9/9 | chr6 | 41097114 | |||||||
| chr6:41097300 | A | G | 1 | a0001c0001t0001g0045 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.991-57A>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 9/9 | chr6 | 41097300 |