Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 4802 |
| ensemblid | ENSG00000066136.21 |
| hgncid | 7806 |
| symbol | NFYC |
| name | nuclear transcription factor Y subunit gamma |
| refseq_nuc | NM_014223.5 |
| refseq_prot | NP_055038.2 |
| ensembl_nuc | ENST00000447388.8 |
| ensembl_prot | ENSP00000404427.3 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 40691704 |
| end | 40771603 |
| strand | + |
| ver | v1.2 |
| region | chr1:40691704-40771603 |
| region5000 | chr1:40686704-40776603 |
| regionname0 | NFYC_chr1_40691704_40771603 |
| regionname5000 | NFYC_chr1_40686704_40776603 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1005 | 174 | 49 | 34 | 63 | 5 | 21 | NFYC_chr1_40686704_40776603 | NFYC | ATGTC others(1000): Show |
chr1 | 40686704 | 40776603 | ||
| a0001c0002 | 0/0 | 1005 | 153 | 35 | 27 | 67 | 9 | 15 | NFYC_chr1_40686704_40776603 | NFYC | ATGTC others(1000): Show |
chr1 | 40686704 | 40776603 | ||
| a0001c0003 | 0/0 | 1005 | 3 | 3 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | ATGTC others(1000): Show |
chr1 | 40686704 | 40776603 | ||
| a0001c0004 | 0/0 | 1005 | 2 | 1 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | ATGTC others(1000): Show |
chr1 | 40686704 | 40776603 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1955 | 69 | 34 | 15 | 10 | 2 | 6 | NFYC_chr1_40686704_40776603 | NFYC | GCAAA others(1950): Show |
chr1 | 40686704 | 40776603 |
| a0001c0001t0002 | 0/0 | 1954 | 94 | 7 | 18 | 52 | 2 | 15 | NFYC_chr1_40686704_40776603 | NFYC | GCAAA others(1949): Show |
chr1 | 40686704 | 40776603 |
| a0001c0001t0003 | 0/0 | 1955 | 4 | 3 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | GCAAA others(1950): Show |
chr1 | 40686704 | 40776603 |
| a0001c0001t0004 | 0/0 | 1955 | 2 | 2 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | GCAAA others(1950): Show |
chr1 | 40686704 | 40776603 |
| a0001c0001t0005 | 0/0 | 1955 | 2 | 2 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | GCAAA others(1950): Show |
chr1 | 40686704 | 40776603 |
| a0001c0001t0006 | 0/0 | 1954 | 1 | 0 | 0 | 0 | 1 | 0 | NFYC_chr1_40686704_40776603 | NFYC | GCAAA others(1949): Show |
chr1 | 40686704 | 40776603 |
| a0001c0001t0007 | 0/0 | 1955 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | GCAAA others(1950): Show |
chr1 | 40686704 | 40776603 |
| a0001c0001t0010 | 0/0 | 1955 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | GCAAA others(1950): Show |
chr1 | 40686704 | 40776603 |
| a0001c0002t0001 | 0/0 | 1955 | 148 | 35 | 27 | 64 | 8 | 14 | NFYC_chr1_40686704_40776603 | NFYC | GCAAA others(1950): Show |
chr1 | 40686704 | 40776603 |
| a0001c0002t0002 | 0/0 | 1954 | 2 | 0 | 0 | 1 | 1 | 0 | NFYC_chr1_40686704_40776603 | NFYC | GCAAA others(1949): Show |
chr1 | 40686704 | 40776603 |
| a0001c0002t0008 | 0/0 | 1955 | 1 | 0 | 0 | 0 | 0 | 1 | NFYC_chr1_40686704_40776603 | NFYC | GCAAA others(1950): Show |
chr1 | 40686704 | 40776603 |
| a0001c0002t0009 | 0/0 | 1955 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | GCAAA others(1950): Show |
chr1 | 40686704 | 40776603 |
| a0001c0002t0011 | 0/0 | 1955 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | GCAAA others(1950): Show |
chr1 | 40686704 | 40776603 |
| a0001c0003t0001 | 0/0 | 1955 | 3 | 3 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | GCAAA others(1950): Show |
chr1 | 40686704 | 40776603 |
| a0001c0004t0001 | 0/0 | 1955 | 2 | 1 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | GCAAA others(1950): Show |
chr1 | 40686704 | 40776603 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0001g0077 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0001g0110 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0002g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0002g0002 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0002g0003 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0002g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0002g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0002g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0002g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0003g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0003g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0003g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0003g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0004g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0004g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0005g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0005g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0006g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0007g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0001t0010g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0002g0310 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0008g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0009g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0002t0011g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0003t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0003t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0003t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| a0001c0004t0001g0014 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0277 | EUR | GBR | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0034 | EUR | GBR | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG00140 | hp1 | a0001 | c0002 | t0001 | g0132 | EUR | GBR | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0062 | EUR | GBR | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG00280 | hp1 | a0001 | c0002 | t0001 | g0133 | EUR | FIN | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG00280 | hp2 | a0001 | c0001 | t0006 | g0050 | EUR | FIN | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | CHS | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG00423 | hp2 | a0001 | c0002 | t0001 | g0264 | EAS | CHS | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG00558 | hp1 | a0001 | c0002 | t0001 | g0238 | EAS | CHS | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | CHS | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG00597 | hp1 | a0001 | c0002 | t0001 | g0214 | EAS | CHS | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0082 | EAS | CHS | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0036 | AMR | PUR | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG00639 | hp2 | a0001 | c0001 | t0003 | g0280 | AMR | PUR | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG00642 | hp1 | a0001 | c0002 | t0001 | g0163 | AMR | PUR | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0275 | AMR | PUR | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0053 | AMR | PUR | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG00741 | hp2 | a0001 | c0002 | t0001 | g0241 | AMR | PUR | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG01069 | hp2 | a0001 | c0002 | t0001 | g0201 | AMR | PUR | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0064 | AMR | PUR | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG01074 | hp2 | a0001 | c0002 | t0001 | g0312 | AMR | PUR | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG01081 | hp1 | a0001 | c0002 | t0001 | g0168 | AMR | PUR | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0135 | AMR | PUR | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0070 | AMR | PUR | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG01099 | hp2 | a0001 | c0002 | t0001 | g0239 | AMR | PUR | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0270 | AMR | PUR | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG01106 | hp2 | a0001 | c0002 | t0001 | g0209 | AMR | PUR | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG01109 | hp1 | a0001 | c0002 | t0001 | g0234 | AMR | PUR | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0085 | AMR | PUR | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0094 | AMR | PUR | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG01167 | hp2 | a0001 | c0002 | t0001 | g0230 | AMR | PUR | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG01168 | hp1 | a0001 | c0002 | t0001 | g0252 | AMR | PUR | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0097 | AMR | PUR | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG01175 | hp2 | a0001 | c0002 | t0001 | g0305 | AMR | PUR | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG01192 | hp1 | a0001 | c0002 | t0001 | g0291 | AMR | PUR | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0035 | AMR | PUR | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG01243 | hp1 | a0001 | c0002 | t0001 | g0296 | AMR | PUR | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0086 | AMR | PUR | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | CLM | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG01256 | hp2 | a0001 | c0002 | t0001 | g0258 | AMR | CLM | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | CLM | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG01258 | hp2 | a0001 | c0002 | t0001 | g0012 | AMR | CLM | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG01261 | hp1 | a0001 | c0002 | t0001 | g0180 | AMR | CLM | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0276 | AMR | CLM | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG01346 | hp1 | a0001 | c0002 | t0001 | g0136 | AMR | CLM | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0066 | AMR | CLM | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG01358 | hp1 | a0001 | c0002 | t0001 | g0210 | AMR | CLM | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0060 | AMR | CLM | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG01515 | hp1 | a0001 | c0002 | t0001 | g0185 | EUR | IBS | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG01515 | hp2 | a0001 | c0002 | t0001 | g0248 | EUR | IBS | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG01516 | hp1 | a0001 | c0002 | t0002 | g0310 | EUR | IBS | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG01516 | hp2 | a0001 | c0002 | t0001 | g0257 | EUR | IBS | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | ACB | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG01884 | hp2 | a0001 | c0001 | t0005 | g0317 | AFR | ACB | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | ACB | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG01891 | hp2 | a0001 | c0002 | t0001 | g0183 | AFR | ACB | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG01934 | hp1 | a0001 | c0002 | t0001 | g0226 | AMR | PEL | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0032 | AMR | PEL | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PEL | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG01943 | hp2 | a0001 | c0004 | t0001 | g0014 | AMR | PEL | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG01952 | hp1 | a0001 | c0002 | t0001 | g0157 | AMR | PEL | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0073 | AMR | PEL | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0061 | AMR | PEL | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG01978 | hp2 | a0001 | c0002 | t0001 | g0178 | AMR | PEL | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0076 | AMR | PEL | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG01981 | hp2 | a0001 | c0002 | t0001 | g0186 | AMR | PEL | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0045 | AMR | PEL | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG01993 | hp2 | a0001 | c0002 | t0001 | g0221 | AMR | PEL | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG02004 | hp1 | a0001 | c0002 | t0001 | g0160 | AMR | PEL | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0063 | AMR | PEL | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | KHV | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG02015 | hp2 | a0001 | c0002 | t0001 | g0159 | EAS | KHV | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG02027 | hp1 | a0001 | c0002 | t0001 | g0262 | EAS | KHV | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0018 | EAS | KHV | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG02040 | hp1 | a0001 | c0002 | t0001 | g0217 | EAS | KHV | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG02040 | hp2 | a0001 | c0002 | t0001 | g0218 | EAS | KHV | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | ACB | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG02055 | hp2 | a0001 | c0002 | t0001 | g0176 | AFR | ACB | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG02056 | hp1 | a0001 | c0002 | t0001 | g0208 | EAS | KHV | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0056 | EAS | KHV | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG02083 | hp1 | a0001 | c0002 | t0001 | g0205 | EAS | KHV | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | KHV | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | KHV | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | KHV | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG02132 | hp1 | a0001 | c0002 | t0001 | g0253 | EAS | KHV | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | KHV | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG02135 | hp1 | a0001 | c0002 | t0009 | g0284 | EAS | KHV | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | KHV | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0303 | AFR | ACB | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG02145 | hp2 | a0001 | c0002 | t0001 | g0295 | AFR | ACB | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0067 | EAS | CDX | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG02155 | hp2 | a0001 | c0002 | t0001 | g0261 | EAS | CDX | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG02257 | hp1 | a0001 | c0002 | t0001 | g0267 | AFR | ACB | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | ACB | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0033 | AFR | ACB | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | ACB | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PEL | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG02273 | hp2 | a0001 | c0002 | t0001 | g0184 | AMR | PEL | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | ACB | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG02451 | hp2 | a0001 | c0002 | t0001 | g0151 | AFR | ACB | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG02602 | hp1 | a0001 | c0002 | t0001 | g0314 | SAS | PJL | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG02602 | hp2 | a0001 | c0002 | t0001 | g0223 | SAS | PJL | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG02615 | hp1 | a0001 | c0002 | t0001 | g0172 | AFR | GWD | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0078 | AFR | GWD | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0271 | AFR | GWD | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG02622 | hp2 | a0001 | c0002 | t0001 | g0179 | AFR | GWD | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0292 | AFR | GWD | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0282 | AFR | GWD | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0279 | AFR | GWD | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | GWD | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG02683 | hp1 | a0001 | c0002 | t0001 | g0236 | SAS | PJL | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0096 | SAS | PJL | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG02723 | hp1 | a0001 | c0002 | t0001 | g0174 | AFR | GWD | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0309 | AFR | GWD | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG02809 | hp1 | a0001 | c0002 | t0001 | g0161 | AFR | GWD | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0285 | AFR | GWD | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG02818 | hp1 | a0001 | c0002 | t0001 | g0195 | AFR | GWD | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG02818 | hp2 | a0001 | c0001 | t0007 | g0293 | AFR | GWD | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG02886 | hp1 | a0001 | c0002 | t0001 | g0203 | AFR | GWD | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0294 | AFR | GWD | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG02895 | hp1 | a0001 | c0002 | t0001 | g0194 | AFR | GWD | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0307 | AFR | GWD | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG02896 | hp1 | a0001 | c0002 | t0001 | g0177 | AFR | GWD | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0308 | AFR | GWD | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG02922 | hp1 | a0001 | c0002 | t0001 | g0202 | AFR | ESN | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG02922 | hp2 | a0001 | c0002 | t0001 | g0155 | AFR | ESN | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | ESN | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG02970 | hp2 | a0001 | c0002 | t0001 | g0149 | AFR | ESN | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG02976 | hp1 | a0001 | c0002 | t0001 | g0268 | AFR | ESN | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | ESN | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG03017 | hp1 | a0001 | c0002 | t0001 | g0231 | SAS | PJL | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG03017 | hp2 | a0001 | c0002 | t0001 | g0188 | SAS | PJL | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0281 | AFR | GWD | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0084 | AFR | GWD | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG03098 | hp1 | a0001 | c0002 | t0001 | g0181 | AFR | MSL | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0083 | AFR | MSL | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG03130 | hp1 | a0001 | c0002 | t0001 | g0152 | AFR | ESN | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG03130 | hp2 | a0001 | c0002 | t0001 | g0306 | AFR | ESN | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG03139 | hp1 | a0001 | c0002 | t0001 | g0156 | AFR | ESN | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG03139 | hp2 | a0001 | c0001 | t0005 | g0318 | AFR | ESN | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0040 | AFR | ESN | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | ESN | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | MSL | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | MSL | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0273 | AFR | MSL | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG03225 | hp2 | a0001 | c0002 | t0001 | g0164 | AFR | MSL | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0059 | SAS | PJL | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0269 | AFR | MSL | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0087 | AFR | MSL | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG03486 | hp1 | a0001 | c0002 | t0001 | g0204 | AFR | MSL | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG03486 | hp2 | a0001 | c0001 | t0004 | g0105 | AFR | MSL | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | PJL | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0080 | SAS | PJL | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG03516 | hp1 | a0001 | c0002 | t0001 | g0199 | AFR | ESN | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG03516 | hp2 | a0001 | c0002 | t0001 | g0266 | AFR | ESN | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG03540 | hp1 | a0001 | c0003 | t0001 | g0100 | AFR | GWD | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | GWD | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG03579 | hp1 | a0001 | c0002 | t0001 | g0200 | AFR | MSL | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG03579 | hp2 | a0001 | c0003 | t0001 | g0101 | AFR | MSL | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG03669 | hp1 | a0001 | c0002 | t0001 | g0182 | SAS | PJL | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG03669 | hp2 | a0001 | c0002 | t0001 | g0286 | SAS | PJL | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0027 | SAS | PJL | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG03710 | hp2 | a0001 | c0002 | t0001 | g0173 | SAS | PJL | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0090 | SAS | BEB | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG03831 | hp2 | a0001 | c0002 | t0001 | g0255 | SAS | BEB | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG03834 | hp1 | a0001 | c0002 | t0001 | g0144 | SAS | BEB | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG03834 | hp2 | a0001 | c0002 | t0001 | g0162 | SAS | BEB | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG03927 | hp1 | a0001 | c0002 | t0008 | g0298 | SAS | BEB | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0089 | SAS | BEB | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | BEB | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0046 | SAS | BEB | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0088 | SAS | STU | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0057 | SAS | STU | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG04184 | hp1 | a0001 | c0002 | t0001 | g0093 | SAS | BEB | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0316 | SAS | BEB | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0048 | SAS | STU | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG04199 | hp2 | a0001 | c0002 | t0001 | g0297 | SAS | STU | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | STU | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0095 | SAS | STU | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0047 | SAS | STU | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG04228 | hp2 | a0001 | c0002 | t0001 | g0283 | SAS | STU | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA18522 | hp1 | a0001 | c0003 | t0001 | g0102 | AFR | YRI | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA18522 | hp2 | a0001 | c0002 | t0001 | g0196 | AFR | YRI | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0278 | AFR | YRI | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA18906 | hp2 | a0001 | c0002 | t0001 | g0171 | AFR | YRI | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA18939 | hp1 | a0001 | c0002 | t0001 | g0250 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA18939 | hp2 | a0001 | c0002 | t0001 | g0187 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA18943 | hp1 | a0001 | c0002 | t0001 | g0211 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA18943 | hp2 | a0001 | c0002 | t0011 | g0150 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA18945 | hp2 | a0001 | c0002 | t0001 | g0237 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA18947 | hp1 | a0001 | c0002 | t0001 | g0170 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA18948 | hp2 | a0001 | c0002 | t0001 | g0219 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA18949 | hp1 | a0001 | c0002 | t0001 | g0244 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA18949 | hp2 | a0001 | c0002 | t0001 | g0158 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA18954 | hp1 | a0001 | c0002 | t0001 | g0166 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA18956 | hp1 | a0001 | c0002 | t0001 | g0311 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA18956 | hp2 | a0001 | c0002 | t0001 | g0206 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA18957 | hp2 | a0001 | c0002 | t0001 | g0137 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA18962 | hp1 | a0001 | c0002 | t0001 | g0099 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA18964 | hp1 | a0001 | c0002 | t0001 | g0254 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA18965 | hp1 | a0001 | c0002 | t0001 | g0299 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA18966 | hp1 | a0001 | c0002 | t0001 | g0216 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA18967 | hp2 | a0001 | c0002 | t0001 | g0215 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA18968 | hp2 | a0001 | c0002 | t0001 | g0247 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA18972 | hp1 | a0001 | c0002 | t0001 | g0213 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA18973 | hp1 | a0001 | c0002 | t0001 | g0207 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA18977 | hp2 | a0001 | c0002 | t0001 | g0235 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA18979 | hp1 | a0001 | c0002 | t0001 | g0167 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA18979 | hp2 | a0001 | c0002 | t0001 | g0192 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA18980 | hp1 | a0001 | c0002 | t0001 | g0153 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA18989 | hp1 | a0001 | c0002 | t0001 | g0212 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA18989 | hp2 | a0001 | c0002 | t0001 | g0175 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA18991 | hp2 | a0001 | c0002 | t0001 | g0313 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA18992 | hp1 | a0001 | c0002 | t0001 | g0227 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA18993 | hp2 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA18994 | hp1 | a0001 | c0001 | t0010 | g0107 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA18994 | hp2 | a0001 | c0002 | t0001 | g0165 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA18997 | hp1 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA18997 | hp2 | a0001 | c0002 | t0001 | g0302 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA18999 | hp2 | a0001 | c0002 | t0001 | g0191 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA19001 | hp2 | a0001 | c0002 | t0002 | g0249 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA19005 | hp1 | a0001 | c0002 | t0001 | g0225 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA19007 | hp1 | a0001 | c0002 | t0001 | g0222 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA19009 | hp2 | a0001 | c0002 | t0001 | g0224 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA19012 | hp1 | a0001 | c0002 | t0001 | g0190 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | LWK | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA19043 | hp2 | a0001 | c0004 | t0001 | g0014 | AFR | LWK | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA19054 | hp1 | a0001 | c0002 | t0001 | g0260 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA19060 | hp2 | a0001 | c0002 | t0001 | g0245 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA19062 | hp1 | a0001 | c0002 | t0001 | g0242 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA19065 | hp2 | a0001 | c0002 | t0001 | g0228 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA19070 | hp1 | a0001 | c0002 | t0001 | g0131 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA19075 | hp1 | a0001 | c0002 | t0001 | g0220 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA19079 | hp1 | a0001 | c0002 | t0001 | g0106 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA19082 | hp1 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA19084 | hp1 | a0001 | c0002 | t0001 | g0259 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA19085 | hp2 | a0001 | c0002 | t0001 | g0300 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA19086 | hp1 | a0001 | c0002 | t0001 | g0154 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA19086 | hp2 | a0001 | c0002 | t0001 | g0256 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA19088 | hp2 | a0001 | c0002 | t0001 | g0301 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA19089 | hp1 | a0001 | c0002 | t0001 | g0263 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA19089 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA19090 | hp1 | a0001 | c0002 | t0001 | g0315 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA19090 | hp2 | a0001 | c0002 | t0001 | g0233 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA19240 | hp1 | a0001 | c0002 | t0001 | g0189 | AFR | YRI | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | YRI | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA20752 | hp1 | a0001 | c0002 | t0001 | g0240 | EUR | TSI | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0118 | EUR | TSI | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA20805 | hp1 | a0001 | c0002 | t0001 | g0134 | EUR | TSI | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA20805 | hp2 | a0001 | c0002 | t0001 | g0169 | EUR | TSI | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | GIH | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0103 | SAS | GIH | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG01123 | hp1 | a0001 | c0002 | t0001 | g0012 | AMR | CLM | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG02109 | hp1 | a0001 | c0002 | t0001 | g0193 | AFR | ACB | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0272 | AFR | ACB | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG02486 | hp1 | a0001 | c0002 | t0001 | g0304 | AFR | ACB | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | ACB | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG02559 | hp1 | a0001 | c0002 | t0001 | g0265 | AFR | ACB | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0274 | AFR | ACB | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | MSL | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG03471 | hp2 | a0001 | c0002 | t0001 | g0198 | AFR | MSL | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG06807 | hp1 | a0001 | c0001 | t0004 | g0104 | AFR | USA | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0138 | AFR | USA | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA18955 | hp2 | a0001 | c0002 | t0001 | g0229 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA20300 | hp1 | a0001 | c0002 | t0001 | g0197 | AFR | USA | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | USA | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | LWK | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| NA21309 | hp2 | a0001 | c0002 | t0001 | g0243 | AFR | LWK | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0110 | REF | REF | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0077 | REF | REF | NFYC_chr1_40686704_40776603 | NFYC | chr1 | 40686704 | 40776603 |
| 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 |
|---|
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:40738897 | C | T | 2 | a0001c0002 a0001c0004 |
155 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(152): Show |
synonymous_variant | LOW | c.54C>T | p.Ser18Ser | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 2/10 | 226/1955 | 54/1008 | 18/335 | chr1 | 40738897 | |||
| chr1:40738906 | G | A | 1 | a0001c0004 | 2 | HG01943.hp2 NA19043.hp2 |
synonymous_variant | LOW | c.63G>A | p.Ser21Ser | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 2/10 | 235/1955 | 63/1008 | 21/335 | chr1 | 40738906 | |||
| chr1:40758204 | C | T | 1 | a0001c0003 | 3 | HG03540.hp1 HG03579.hp2 NA18522.hp1 |
synonymous_variant | LOW | c.471C>T | p.Val157Val | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 6/10 | 643/1955 | 471/1008 | 157/335 | chr1 | 40758204 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:40691738 | C | G | 1 | a0001c0001t0005 | 2 | HG01884.hp2 HG03139.hp2 |
5_prime_UTR_variant | MODIFIER | c.-138C>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/10 | 47106 | chr1 | 40691738 | ||||||
| chr1:40691744 | G | T | 1 | a0001c0001t0004 | 2 | HG03486.hp2 HG06807.hp1 |
5_prime_UTR_variant | MODIFIER | c.-132G>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/10 | 47100 | chr1 | 40691744 | ||||||
| chr1:40691827 | C | T | 1 | a0001c0002t0011 | 1 | NA18943.hp2 | 5_prime_UTR_variant | MODIFIER | c.-49C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/10 | 47017 | chr1 | 40691827 | ||||||
| chr1:40770909 | C | A | 1 | a0001c0001t0006 | 1 | HG00280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*81C>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 10/10 | 81 | chr1 | 40770909 | ||||||
| chr1:40771017 | T | C | 1 | a0001c0001t0003 | 4 | HG00639.hp2 HG02622.hp1 HG02647.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*189T>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 10/10 | 189 | chr1 | 40771017 | ||||||
| chr1:40771039 | T | A | 1 | a0001c0001t0007 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*211T>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 10/10 | 211 | chr1 | 40771039 | ||||||
| chr1:40771067 | A | C | 1 | a0001c0001t0010 | 1 | NA18994.hp1 | 3_prime_UTR_variant | MODIFIER | c.*239A>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 10/10 | 239 | chr1 | 40771067 | ||||||
| chr1:40771165 | CT | C | 3 | a0001c0001t0002 a0001c0001t0006 a0001c0002t0002 |
97 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(94): Show |
3_prime_UTR_variant | MODIFIER | c.*347delT | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 10/10 | 347 | INFO_REALIGN_3_PRIME | chr1 | 40771165 | |||||
| chr1:40771243 | G | A | 1 | a0001c0002t0008 | 1 | HG03927.hp1 | 3_prime_UTR_variant | MODIFIER | c.*415G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 10/10 | 415 | chr1 | 40771243 | ||||||
| chr1:40771272 | G | A | 1 | a0001c0002t0009 | 1 | HG02135.hp1 | 3_prime_UTR_variant | MODIFIER | c.*444G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 10/10 | 444 | chr1 | 40771272 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:40691920 | G | T | 2 | a0001c0001t0005g0317 a0001c0001t0005g0318 |
2 | HG01884.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-9+53G>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40691920 | |||||||
| chr1:40691991 | C | G | 1 | a0001c0001t0002g0316 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-9+124C>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40691991 | |||||||
| chr1:40692185 | A | G | 5 | a0001c0002t0001g0311 a0001c0002t0001g0312 a0001c0002t0001g0313 others(2): Show |
5 | HG01074.hp2 HG02602.hp1 NA18956.hp1 others(2): Show |
intron_variant | MODIFIER | c.-9+318A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40692185 | |||||||
| chr1:40692486 | A | C | 226 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(223): Show |
234 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.-9+619A>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40692486 | |||||||
| chr1:40692701 | A | G | 226 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(223): Show |
234 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.-9+834A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40692701 | |||||||
| chr1:40692737 | G | A | 1 | a0001c0001t0002g0015 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-9+870G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40692737 | |||||||
| chr1:40692998 | G | A | 1 | a0001c0002t0001g0099 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.-9+1131G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40692998 | |||||||
| chr1:40693007 | T | C | 3 | a0001c0003t0001g0100 a0001c0003t0001g0101 a0001c0003t0001g0102 |
3 | HG03540.hp1 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-9+1140T>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40693007 | |||||||
| chr1:40693041 | C | T | 1 | a0001c0001t0002g0098 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.-9+1174C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40693041 | |||||||
| chr1:40693042 | T | C | 1 | a0001c0001t0002g0098 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.-9+1175T>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40693042 | |||||||
| chr1:40693394 | T | G | 1 | a0001c0001t0002g0103 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-9+1527T>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40693394 | |||||||
| chr1:40693469 | C | T | 1 | a0001c0002t0002g0310 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-9+1602C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40693469 | |||||||
| chr1:40693510 | T | C | 2 | a0001c0001t0004g0104 a0001c0001t0004g0105 |
2 | HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-9+1643T>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40693510 | |||||||
| chr1:40693557 | A | G | 226 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(223): Show |
234 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.-9+1690A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40693557 | |||||||
| chr1:40693559 | G | A | 1 | a0001c0002t0001g0106 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.-9+1692G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40693559 | |||||||
| chr1:40693591 | C | T | 1 | a0001c0001t0001g0309 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-9+1724C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40693591 | |||||||
| chr1:40693794 | A | G | 1 | a0001c0001t0001g0309 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-9+1927A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40693794 | |||||||
| chr1:40693875 | G | T | 2 | a0001c0001t0001g0307 a0001c0001t0001g0308 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-9+2008G>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40693875 | |||||||
| chr1:40694050 | T | TG | 222 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(219): Show |
230 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.-9+2184dupG | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40694050 | ||||||
| chr1:40694105 | G | A | 226 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(223): Show |
234 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.-9+2238G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40694105 | |||||||
| chr1:40694194 | G | C | 1 | a0001c0001t0010g0107 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-9+2327G>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40694194 | |||||||
| chr1:40694288 | A | G | 1 | a0001c0001t0010g0107 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-9+2421A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40694288 | |||||||
| chr1:40694352 | C | T | 4 | a0001c0001t0002g0094 a0001c0001t0002g0095 a0001c0001t0002g0096 others(1): Show |
4 | HG01167.hp1 HG01169.hp1 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.-9+2485C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40694352 | |||||||
| chr1:40694451 | A | G | 1 | a0001c0002t0001g0306 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-9+2584A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40694451 | |||||||
| chr1:40694459 | TCACTGTG others(11): Show |
T | 1 | a0001c0001t0002g0098 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.-9+2595_-9+2612del others(18): Show |
NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40694459 | ||||||
| chr1:40694532 | A | G | 196 | a0001c0001t0001g0013 a0001c0001t0001g0139 a0001c0001t0001g0140 others(193): Show |
200 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.-9+2665A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40694532 | |||||||
| chr1:40694609 | A | G | 26 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(23): Show |
30 | HG01069.hp1 HG01071.hp1 HG01168.hp2 others(27): Show |
intron_variant | MODIFIER | c.-9+2742A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40694609 | |||||||
| chr1:40694655 | T | G | 1 | a0001c0001t0010g0107 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-9+2788T>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40694655 | |||||||
| chr1:40694815 | T | C | 1 | a0001c0002t0001g0131 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.-9+2948T>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40694815 | |||||||
| chr1:40694887 | T | C | 235 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(232): Show |
243 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.-9+3020T>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40694887 | |||||||
| chr1:40694990 | C | T | 1 | a0001c0002t0001g0305 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-9+3123C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40694990 | |||||||
| chr1:40695482 | G | A | 1 | a0001c0002t0001g0132 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-9+3615G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40695482 | |||||||
| chr1:40695545 | C | T | 1 | a0001c0002t0001g0304 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-9+3678C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40695545 | |||||||
| chr1:40695579 | C | T | 26 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(23): Show |
30 | HG01069.hp1 HG01071.hp1 HG01168.hp2 others(27): Show |
intron_variant | MODIFIER | c.-9+3712C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40695579 | |||||||
| chr1:40696024 | G | GT | 6 | a0001c0001t0002g0021 a0001c0001t0002g0022 a0001c0001t0002g0090 others(3): Show |
6 | HG03831.hp1 HG06807.hp2 NA18957.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9+4173dupT | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40696024 | ||||||
| chr1:40696024 | G | GTT | 173 | a0001c0001t0001g0013 a0001c0001t0001g0139 a0001c0001t0001g0140 others(170): Show |
176 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(173): Show |
intron_variant | MODIFIER | c.-9+4172_-9+4173dup others(2): Show |
NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40696024 | ||||||
| chr1:40696024 | G | GTTT | 19 | a0001c0001t0001g0292 a0001c0001t0001g0294 a0001c0001t0001g0303 others(16): Show |
20 | HG01074.hp2 HG01192.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.-9+4171_-9+4173dup others(3): Show |
NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40696024 | ||||||
| chr1:40696126 | C | G | 5 | a0001c0001t0001g0013 a0001c0001t0001g0287 a0001c0001t0001g0288 others(2): Show |
6 | HG02129.hp1 NA18952.hp2 NA18967.hp1 others(3): Show |
intron_variant | MODIFIER | c.-9+4259C>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40696126 | |||||||
| chr1:40696271 | CT | C | 5 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 others(2): Show |
5 | HG02258.hp2 HG02976.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.-9+4406delT | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40696271 | ||||||
| chr1:40696275 | G | A | 2 | a0001c0001t0004g0104 a0001c0001t0004g0105 |
2 | HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-9+4408G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40696275 | |||||||
| chr1:40696302 | T | A | 1 | a0001c0002t0001g0144 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-9+4435T>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40696302 | |||||||
| chr1:40696360 | C | G | 1 | a0001c0001t0010g0107 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-9+4493C>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40696360 | |||||||
| chr1:40696620 | G | A | 1 | a0001c0002t0001g0291 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-9+4753G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40696620 | |||||||
| chr1:40697039 | C | T | 2 | a0001c0002t0001g0093 a0001c0002t0001g0286 |
2 | HG03669.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.-9+5172C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40697039 | |||||||
| chr1:40697113 | T | C | 1 | a0001c0001t0001g0145 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.-9+5246T>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40697113 | |||||||
| chr1:40697250 | G | A | 3 | a0001c0001t0002g0023 a0001c0001t0002g0024 a0001c0001t0002g0025 |
3 | HG00423.hp1 HG02135.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.-9+5383G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40697250 | |||||||
| chr1:40697490 | A | C | 1 | a0001c0001t0010g0107 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-9+5623A>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40697490 | |||||||
| chr1:40697560 | C | T | 1 | a0001c0001t0001g0285 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-9+5693C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40697560 | |||||||
| chr1:40698078 | T | A | 1 | a0001c0001t0002g0026 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-9+6211T>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40698078 | |||||||
| chr1:40698327 | A | C | 227 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(224): Show |
235 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.-9+6460A>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40698327 | |||||||
| chr1:40698460 | T | G | 2 | a0001c0001t0002g0027 a0001c0001t0002g0090 |
2 | HG03710.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.-9+6593T>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40698460 | |||||||
| chr1:40698465 | C | T | 1 | a0001c0001t0002g0089 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-9+6598C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40698465 | |||||||
| chr1:40698466 | G | A | 4 | a0001c0001t0002g0028 a0001c0001t0002g0029 a0001c0001t0002g0030 others(1): Show |
4 | NA18980.hp2 NA18993.hp1 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9+6599G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40698466 | |||||||
| chr1:40698557 | G | T | 1 | a0001c0002t0009g0284 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-9+6690G>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40698557 | |||||||
| chr1:40698574 | C | T | 3 | a0001c0003t0001g0100 a0001c0003t0001g0101 a0001c0003t0001g0102 |
3 | HG03540.hp1 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-9+6707C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40698574 | |||||||
| chr1:40698647 | C | G | 1 | a0001c0002t0001g0283 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-9+6780C>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40698647 | |||||||
| chr1:40698741 | C | T | 1 | a0001c0001t0001g0290 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-9+6874C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40698741 | |||||||
| chr1:40698743 | C | T | 2 | a0001c0001t0004g0104 a0001c0001t0004g0105 |
2 | HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-9+6876C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40698743 | |||||||
| chr1:40699056 | C | T | 1 | a0001c0002t0001g0306 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-9+7189C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40699056 | |||||||
| chr1:40699145 | C | T | 1 | a0001c0001t0002g0088 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-9+7278C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40699145 | |||||||
| chr1:40699160 | G | A | 12 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0108 others(9): Show |
14 | HG01168.hp2 HG01169.hp2 HG01175.hp1 others(11): Show |
intron_variant | MODIFIER | c.-9+7293G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40699160 | |||||||
| chr1:40699170 | AAAAAC | A | 24 | a0001c0001t0001g0013 a0001c0001t0001g0269 a0001c0001t0001g0270 others(21): Show |
25 | HG00099.hp1 HG00639.hp2 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.-9+7314_-9+7318del others(5): Show |
NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40699170 | ||||||
| chr1:40699282 | A | G | 1 | a0001c0001t0010g0107 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-9+7415A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40699282 | |||||||
| chr1:40699407 | C | A | 226 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(223): Show |
234 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.-9+7540C>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40699407 | |||||||
| chr1:40699426 | A | G | 3 | a0001c0002t0001g0265 a0001c0002t0001g0266 a0001c0002t0001g0267 |
3 | HG02257.hp1 HG02559.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-9+7559A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40699426 | |||||||
| chr1:40699498 | A | G | 1 | a0001c0001t0002g0316 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-9+7631A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40699498 | |||||||
| chr1:40699552 | T | G | 1 | a0001c0001t0001g0119 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-9+7685T>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40699552 | |||||||
| chr1:40699561 | T | G | 3 | a0001c0001t0001g0292 a0001c0001t0001g0294 a0001c0001t0007g0293 |
3 | HG02630.hp1 HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.-9+7694T>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40699561 | |||||||
| chr1:40699704 | G | T | 1 | a0001c0001t0010g0107 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-9+7837G>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40699704 | |||||||
| chr1:40699832 | A | T | 1 | a0001c0002t0001g0264 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-9+7965A>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40699832 | |||||||
| chr1:40699871 | A | G | 12 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0108 others(9): Show |
14 | HG01168.hp2 HG01169.hp2 HG01175.hp1 others(11): Show |
intron_variant | MODIFIER | c.-9+8004A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40699871 | |||||||
| chr1:40700043 | C | A | 1 | a0001c0001t0010g0107 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-9+8176C>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40700043 | |||||||
| chr1:40700088 | A | G | 12 | a0001c0002t0001g0265 a0001c0002t0001g0266 a0001c0002t0001g0267 others(9): Show |
12 | HG01074.hp2 HG02257.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.-9+8221A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40700088 | |||||||
| chr1:40700189 | A | C | 195 | a0001c0001t0001g0013 a0001c0001t0001g0139 a0001c0001t0001g0140 others(192): Show |
199 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.-9+8322A>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40700189 | |||||||
| chr1:40700204 | A | G | 94 | a0001c0001t0001g0232 a0001c0001t0001g0246 a0001c0001t0001g0251 others(91): Show |
96 | HG00280.hp1 HG00423.hp2 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.-9+8337A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40700204 | |||||||
| chr1:40700417 | A | G | 1 | a0001c0001t0002g0025 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-9+8550A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40700417 | |||||||
| chr1:40700811 | T | C | 26 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(23): Show |
30 | HG01069.hp1 HG01071.hp1 HG01168.hp2 others(27): Show |
intron_variant | MODIFIER | c.-9+8944T>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40700811 | |||||||
| chr1:40700949 | A | G | 1 | a0001c0001t0001g0130 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-9+9082A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40700949 | |||||||
| chr1:40700977 | A | G | 1 | a0001c0001t0002g0103 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-9+9110A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40700977 | |||||||
| chr1:40701081 | G | C | 1 | a0001c0001t0001g0007 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.-9+9214G>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40701081 | |||||||
| chr1:40701312 | A | G | 1 | a0001c0001t0002g0087 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-9+9445A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40701312 | |||||||
| chr1:40701317 | G | A | 4 | a0001c0001t0001g0285 a0001c0001t0001g0292 a0001c0001t0001g0294 others(1): Show |
4 | HG02630.hp1 HG02809.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.-9+9450G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40701317 | |||||||
| chr1:40701337 | A | G | 1 | a0001c0001t0002g0087 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-9+9470A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40701337 | |||||||
| chr1:40701349 | A | C | 59 | a0001c0002t0001g0132 a0001c0002t0001g0149 a0001c0002t0001g0151 others(56): Show |
59 | HG00140.hp1 HG00642.hp1 HG01074.hp2 others(56): Show |
intron_variant | MODIFIER | c.-9+9482A>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40701349 | |||||||
| chr1:40701446 | T | C | 1 | a0001c0002t0001g0192 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-9+9579T>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40701446 | |||||||
| chr1:40701456 | A | G | 1 | a0001c0001t0001g0309 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-9+9589A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40701456 | |||||||
| chr1:40701525 | A | G | 1 | a0001c0002t0001g0106 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.-9+9658A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40701525 | |||||||
| chr1:40701862 | A | G | 226 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(223): Show |
234 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.-9+9995A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40701862 | |||||||
| chr1:40701981 | C | G | 1 | a0001c0001t0010g0107 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-9+10114C>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40701981 | |||||||
| chr1:40701997 | T | G | 94 | a0001c0001t0001g0232 a0001c0001t0001g0246 a0001c0001t0001g0251 others(91): Show |
96 | HG00280.hp1 HG00423.hp2 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.-9+10130T>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40701997 | |||||||
| chr1:40702023 | C | T | 4 | a0001c0001t0001g0285 a0001c0001t0001g0292 a0001c0001t0001g0294 others(1): Show |
4 | HG02630.hp1 HG02809.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.-9+10156C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40702023 | |||||||
| chr1:40702198 | C | T | 10 | a0001c0001t0001g0020 a0001c0001t0002g0016 a0001c0001t0002g0017 others(7): Show |
10 | HG00423.hp1 HG02027.hp2 HG02135.hp2 others(7): Show |
intron_variant | MODIFIER | c.-9+10331C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40702198 | |||||||
| chr1:40702209 | A | G | 81 | a0001c0001t0001g0232 a0001c0001t0001g0246 a0001c0001t0001g0251 others(78): Show |
83 | HG00280.hp1 HG00423.hp2 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.-9+10342A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40702209 | |||||||
| chr1:40702341 | CT | C | 164 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 others(161): Show |
167 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(164): Show |
intron_variant | MODIFIER | c.-9+10492delT | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40702341 | ||||||
| chr1:40702341 | CTT | C | 30 | a0001c0001t0001g0013 a0001c0001t0001g0269 a0001c0001t0001g0270 others(27): Show |
31 | HG00099.hp1 HG00639.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.-9+10491_-9+10492d others(4): Show |
NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40702341 | ||||||
| chr1:40702483 | C | T | 1 | a0001c0001t0001g0148 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-9+10616C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40702483 | |||||||
| chr1:40702488 | G | GT | 4 | a0001c0002t0001g0259 a0001c0002t0001g0260 a0001c0002t0001g0261 others(1): Show |
4 | HG02027.hp1 HG02155.hp2 NA19054.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9+10622dupT | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40702488 | ||||||
| chr1:40702889 | T | C | 1 | a0001c0001t0001g0309 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-9+11022T>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40702889 | |||||||
| chr1:40702909 | C | G | 1 | a0001c0001t0010g0107 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-9+11042C>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40702909 | |||||||
| chr1:40703159 | G | T | 1 | a0001c0001t0001g0118 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-9+11292G>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40703159 | |||||||
| chr1:40703245 | C | T | 227 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(224): Show |
235 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.-9+11378C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40703245 | |||||||
| chr1:40703323 | C | G | 1 | a0001c0002t0001g0189 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-9+11456C>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40703323 | |||||||
| chr1:40703326 | C | CA | 26 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(23): Show |
30 | HG01069.hp1 HG01071.hp1 HG01168.hp2 others(27): Show |
intron_variant | MODIFIER | c.-9+11468dupA | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40703326 | ||||||
| chr1:40703335 | A | T | 1 | a0001c0001t0010g0107 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-9+11468A>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40703335 | |||||||
| chr1:40703336 | T | A | 59 | a0001c0002t0001g0132 a0001c0002t0001g0149 a0001c0002t0001g0151 others(56): Show |
59 | HG00140.hp1 HG00642.hp1 HG01074.hp2 others(56): Show |
intron_variant | MODIFIER | c.-9+11469T>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40703336 | |||||||
| chr1:40703448 | T | C | 223 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(220): Show |
230 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.-9+11581T>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40703448 | |||||||
| chr1:40703455 | G | A | 1 | a0001c0002t0001g0205 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-9+11588G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40703455 | |||||||
| chr1:40703480 | T | TAAAAAAA others(4): Show |
25 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(22): Show |
29 | HG01069.hp1 HG01071.hp1 HG01168.hp2 others(26): Show |
intron_variant | MODIFIER | c.-9+11617_-9+11627d others(13): Show |
NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40703480 | ||||||
| chr1:40703480 | T | TAAAAAAA others(5): Show |
8 | a0001c0001t0001g0120 a0001c0001t0001g0281 a0001c0001t0001g0309 others(5): Show |
8 | HG02486.hp2 HG02723.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.-9+11616_-9+11627d others(14): Show |
NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40703480 | ||||||
| chr1:40703480 | T | TAAAAAAA others(6): Show |
89 | a0001c0001t0001g0013 a0001c0001t0001g0140 a0001c0001t0001g0141 others(86): Show |
91 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(88): Show |
intron_variant | MODIFIER | c.-9+11615_-9+11627d others(15): Show |
NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40703480 | ||||||
| chr1:40703480 | T | TAAAAAAA others(7): Show |
85 | a0001c0001t0001g0139 a0001c0001t0001g0145 a0001c0001t0001g0146 others(82): Show |
87 | HG00280.hp1 HG00423.hp2 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.-9+11614_-9+11627d others(16): Show |
NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40703480 | ||||||
| chr1:40703480 | T | TAAAAAAA others(8): Show |
14 | a0001c0002t0001g0093 a0001c0002t0001g0192 a0001c0002t0001g0193 others(11): Show |
14 | HG00597.hp1 HG01106.hp2 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.-9+11627_-9+11628i others(17): Show |
NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40703480 | ||||||
| chr1:40703480 | T | TAAAAAAA others(9): Show |
2 | a0001c0002t0001g0206 a0001c0002t0001g0207 |
2 | NA18956.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.-9+11627_-9+11628i others(18): Show |
NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40703480 | ||||||
| chr1:40703897 | C | T | 3 | a0001c0001t0001g0292 a0001c0001t0001g0294 a0001c0001t0007g0293 |
3 | HG02630.hp1 HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.-9+12030C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40703897 | |||||||
| chr1:40704039 | G | A | 226 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(223): Show |
234 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.-9+12172G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40704039 | |||||||
| chr1:40704081 | GT | G | 197 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(194): Show |
205 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.-9+12228delT | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40704081 | ||||||
| chr1:40704081 | GTT | G | 20 | a0001c0002t0001g0099 a0001c0002t0001g0106 a0001c0002t0001g0192 others(17): Show |
20 | HG01934.hp1 HG01993.hp2 HG02027.hp1 others(17): Show |
intron_variant | MODIFIER | c.-9+12227_-9+12228d others(4): Show |
NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40704081 | ||||||
| chr1:40704228 | C | T | 26 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(23): Show |
30 | HG01069.hp1 HG01071.hp1 HG01168.hp2 others(27): Show |
intron_variant | MODIFIER | c.-9+12361C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40704228 | |||||||
| chr1:40704272 | C | T | 155 | a0001c0001t0001g0148 a0001c0001t0001g0232 a0001c0001t0001g0246 others(152): Show |
158 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(155): Show |
intron_variant | MODIFIER | c.-9+12405C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40704272 | |||||||
| chr1:40704290 | C | T | 2 | a0001c0002t0001g0185 a0001c0002t0001g0186 |
2 | HG01515.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.-9+12423C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40704290 | |||||||
| chr1:40704319 | C | G | 195 | a0001c0001t0001g0013 a0001c0001t0001g0139 a0001c0001t0001g0140 others(192): Show |
199 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.-9+12452C>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40704319 | |||||||
| chr1:40704684 | T | C | 26 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(23): Show |
30 | HG01069.hp1 HG01071.hp1 HG01168.hp2 others(27): Show |
intron_variant | MODIFIER | c.-9+12817T>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40704684 | |||||||
| chr1:40704756 | A | G | 1 | a0001c0002t0001g0144 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-9+12889A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40704756 | |||||||
| chr1:40704877 | C | A | 1 | a0001c0002t0001g0200 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-9+13010C>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40704877 | |||||||
| chr1:40704879 | G | GGCTAAGG others(14): Show |
1 | a0001c0002t0001g0200 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-9+13012_-9+13013i others(23): Show |
NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40704879 | |||||||
| chr1:40704880 | C | A | 1 | a0001c0002t0001g0200 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-9+13013C>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40704880 | |||||||
| chr1:40704996 | A | T | 1 | a0001c0002t0001g0184 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.-9+13129A>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40704996 | |||||||
| chr1:40704998 | T | C | 24 | a0001c0001t0001g0013 a0001c0001t0001g0269 a0001c0001t0001g0270 others(21): Show |
25 | HG00099.hp1 HG00639.hp2 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.-9+13131T>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40704998 | |||||||
| chr1:40705210 | C | G | 1 | a0001c0001t0002g0085 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-9+13343C>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40705210 | |||||||
| chr1:40705236 | G | C | 5 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 others(2): Show |
5 | HG02258.hp2 HG02976.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.-9+13369G>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40705236 | |||||||
| chr1:40705386 | T | A | 1 | a0001c0001t0001g0303 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-9+13519T>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40705386 | |||||||
| chr1:40705401 | T | G | 1 | a0001c0001t0002g0032 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-9+13534T>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40705401 | |||||||
| chr1:40706064 | A | G | 4 | a0001c0001t0003g0138 a0001c0001t0003g0271 a0001c0001t0003g0279 others(1): Show |
4 | HG00639.hp2 HG02622.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9+14197A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40706064 | |||||||
| chr1:40706176 | C | T | 226 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(223): Show |
234 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.-9+14309C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40706176 | |||||||
| chr1:40706177 | G | A | 1 | a0001c0001t0002g0033 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-9+14310G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40706177 | |||||||
| chr1:40706410 | G | A | 1 | a0001c0002t0001g0297 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-9+14543G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40706410 | |||||||
| chr1:40706441 | A | G | 1 | a0001c0002t0001g0253 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-9+14574A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40706441 | |||||||
| chr1:40706640 | A | G | 2 | a0001c0001t0001g0117 a0001c0001t0001g0118 |
2 | HG01258.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.-9+14773A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40706640 | |||||||
| chr1:40706776 | T | G | 2 | a0001c0002t0001g0227 a0001c0002t0001g0228 |
2 | NA18992.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.-9+14909T>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40706776 | |||||||
| chr1:40706838 | T | C | 3 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0001t0002g0035 |
3 | HG00099.hp2 HG01192.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.-9+14971T>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40706838 | |||||||
| chr1:40706867 | T | C | 59 | a0001c0002t0001g0132 a0001c0002t0001g0149 a0001c0002t0001g0151 others(56): Show |
59 | HG00140.hp1 HG00642.hp1 HG01074.hp2 others(56): Show |
intron_variant | MODIFIER | c.-9+15000T>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40706867 | |||||||
| chr1:40707029 | A | G | 226 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(223): Show |
234 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.-9+15162A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40707029 | |||||||
| chr1:40707062 | C | T | 154 | a0001c0001t0001g0232 a0001c0001t0001g0246 a0001c0001t0001g0251 others(151): Show |
157 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(154): Show |
intron_variant | MODIFIER | c.-9+15195C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40707062 | |||||||
| chr1:40707186 | A | T | 2 | a0001c0002t0001g0136 a0001c0002t0001g0188 |
2 | HG01346.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.-9+15319A>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40707186 | |||||||
| chr1:40707202 | A | G | 3 | a0001c0003t0001g0100 a0001c0003t0001g0101 a0001c0003t0001g0102 |
3 | HG03540.hp1 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-9+15335A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40707202 | |||||||
| chr1:40707260 | G | A | 3 | a0001c0001t0001g0292 a0001c0001t0001g0294 a0001c0001t0007g0293 |
3 | HG02630.hp1 HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.-9+15393G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40707260 | |||||||
| chr1:40707341 | A | G | 2 | a0001c0001t0002g0083 a0001c0001t0002g0084 |
2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-9+15474A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40707341 | |||||||
| chr1:40707376 | C | A | 26 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(23): Show |
30 | HG01069.hp1 HG01071.hp1 HG01168.hp2 others(27): Show |
intron_variant | MODIFIER | c.-9+15509C>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40707376 | |||||||
| chr1:40707493 | AAG | A | 152 | a0001c0001t0001g0232 a0001c0001t0001g0246 a0001c0001t0001g0251 others(149): Show |
155 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(152): Show |
intron_variant | MODIFIER | c.-9+15640_-9+15641d others(4): Show |
NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40707493 | ||||||
| chr1:40707493 | AAGAG | A | 26 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(23): Show |
30 | HG01069.hp1 HG01071.hp1 HG01168.hp2 others(27): Show |
intron_variant | MODIFIER | c.-9+15638_-9+15641d others(6): Show |
NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40707493 | ||||||
| chr1:40707539 | C | T | 26 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(23): Show |
30 | HG01069.hp1 HG01071.hp1 HG01168.hp2 others(27): Show |
intron_variant | MODIFIER | c.-9+15672C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40707539 | |||||||
| chr1:40707594 | A | G | 1 | a0001c0001t0002g0082 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-9+15727A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40707594 | |||||||
| chr1:40707620 | A | G | 27 | a0001c0001t0001g0013 a0001c0001t0001g0148 a0001c0001t0001g0269 others(24): Show |
28 | HG00099.hp1 HG00639.hp2 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.-9+15753A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40707620 | |||||||
| chr1:40707664 | A | G | 5 | a0001c0002t0001g0200 a0001c0002t0001g0201 a0001c0002t0001g0202 others(2): Show |
5 | HG01069.hp2 HG02886.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.-9+15797A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40707664 | |||||||
| chr1:40707771 | G | A | 1 | a0001c0002t0001g0268 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-9+15904G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40707771 | |||||||
| chr1:40707826 | G | A | 1 | a0001c0002t0001g0315 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.-9+15959G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40707826 | |||||||
| chr1:40707841 | C | T | 1 | a0001c0001t0002g0081 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-9+15974C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40707841 | |||||||
| chr1:40707849 | C | CA | 12 | a0001c0001t0001g0115 a0001c0001t0002g0001 a0001c0001t0002g0036 others(9): Show |
13 | HG00639.hp1 HG01106.hp2 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.-9+15999dupA | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40707849 | ||||||
| chr1:40707849 | C | CAA | 24 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(21): Show |
28 | HG01069.hp1 HG01071.hp1 HG01168.hp2 others(25): Show |
intron_variant | MODIFIER | c.-9+15998_-9+15999d others(4): Show |
NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40707849 | ||||||
| chr1:40707849 | CA | C | 8 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(5): Show |
8 | HG00738.hp1 HG01071.hp2 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.-9+15999delA | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40707849 | ||||||
| chr1:40708302 | A | G | 1 | a0001c0001t0002g0078 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-9+16435A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40708302 | |||||||
| chr1:40708327 | C | T | 226 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(223): Show |
234 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.-9+16460C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40708327 | |||||||
| chr1:40708475 | T | A | 1 | a0001c0001t0002g0026 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-9+16608T>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40708475 | |||||||
| chr1:40708508 | C | G | 196 | a0001c0001t0001g0013 a0001c0001t0001g0139 a0001c0001t0001g0140 others(193): Show |
200 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.-9+16641C>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40708508 | |||||||
| chr1:40708509 | C | T | 5 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 others(2): Show |
5 | HG02258.hp2 HG02976.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.-9+16642C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40708509 | |||||||
| chr1:40708959 | T | A | 5 | a0001c0002t0001g0200 a0001c0002t0001g0201 a0001c0002t0001g0202 others(2): Show |
5 | HG01069.hp2 HG02886.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.-9+17092T>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40708959 | |||||||
| chr1:40709097 | A | G | 1 | a0001c0004t0001g0014 | 2 | HG01943.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-9+17230A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40709097 | |||||||
| chr1:40709327 | G | A | 1 | a0001c0002t0001g0151 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-9+17460G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40709327 | |||||||
| chr1:40709460 | C | T | 1 | a0001c0002t0002g0249 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.-9+17593C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40709460 | |||||||
| chr1:40709507 | C | T | 4 | a0001c0001t0002g0028 a0001c0001t0002g0029 a0001c0001t0002g0030 others(1): Show |
4 | NA18980.hp2 NA18993.hp1 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9+17640C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40709507 | |||||||
| chr1:40709574 | G | T | 1 | a0001c0002t0001g0210 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-9+17707G>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40709574 | |||||||
| chr1:40709991 | T | C | 1 | a0001c0001t0001g0282 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-9+18124T>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40709991 | |||||||
| chr1:40710331 | C | T | 226 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(223): Show |
234 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.-9+18464C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40710331 | |||||||
| chr1:40710637 | A | G | 26 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(23): Show |
30 | HG01069.hp1 HG01071.hp1 HG01168.hp2 others(27): Show |
intron_variant | MODIFIER | c.-9+18770A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40710637 | |||||||
| chr1:40710704 | T | G | 1 | a0001c0001t0010g0107 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-9+18837T>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40710704 | |||||||
| chr1:40710794 | G | A | 26 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(23): Show |
30 | HG01069.hp1 HG01071.hp1 HG01168.hp2 others(27): Show |
intron_variant | MODIFIER | c.-9+18927G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40710794 | |||||||
| chr1:40710826 | C | T | 2 | a0001c0001t0004g0104 a0001c0001t0004g0105 |
2 | HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-9+18959C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40710826 | |||||||
| chr1:40711082 | T | C | 1 | a0001c0002t0001g0229 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-9+19215T>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40711082 | |||||||
| chr1:40711135 | T | C | 4 | a0001c0001t0003g0138 a0001c0001t0003g0271 a0001c0001t0003g0279 others(1): Show |
4 | HG00639.hp2 HG02622.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9+19268T>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40711135 | |||||||
| chr1:40711155 | A | G | 1 | a0001c0001t0002g0088 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-9+19288A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40711155 | |||||||
| chr1:40711174 | G | A | 1 | a0001c0001t0001g0121 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-9+19307G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40711174 | |||||||
| chr1:40711529 | G | C | 1 | a0001c0001t0001g0108 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.-9+19662G>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40711529 | |||||||
| chr1:40711613 | G | A | 1 | a0001c0004t0001g0014 | 2 | HG01943.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-9+19746G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40711613 | |||||||
| chr1:40711627 | C | T | 1 | a0001c0002t0001g0296 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-9+19760C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40711627 | |||||||
| chr1:40712013 | G | A | 2 | a0001c0001t0001g0122 a0001c0001t0001g0130 |
2 | HG01884.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.-9+20146G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40712013 | |||||||
| chr1:40712189 | A | C | 1 | a0001c0001t0001g0289 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-9+20322A>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40712189 | |||||||
| chr1:40712211 | A | G | 5 | a0001c0001t0001g0270 a0001c0001t0001g0275 a0001c0001t0001g0276 others(2): Show |
5 | HG00099.hp1 HG00738.hp2 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.-9+20344A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40712211 | |||||||
| chr1:40712271 | T | C | 227 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(224): Show |
235 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.-9+20404T>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40712271 | |||||||
| chr1:40712296 | A | G | 1 | a0001c0002t0001g0248 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-9+20429A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40712296 | |||||||
| chr1:40712556 | AT | A | 227 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(224): Show |
235 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.-9+20700delT | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40712556 | ||||||
| chr1:40712634 | G | A | 1 | a0001c0001t0010g0107 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-9+20767G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40712634 | |||||||
| chr1:40712658 | C | CT | 128 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0143 others(125): Show |
130 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.-9+20815dupT | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40712658 | ||||||
| chr1:40712658 | C | CTT | 40 | a0001c0001t0001g0246 a0001c0001t0005g0318 a0001c0001t0010g0107 others(37): Show |
41 | HG00597.hp1 HG01192.hp1 HG01261.hp1 others(38): Show |
intron_variant | MODIFIER | c.-9+20814_-9+20815d others(4): Show |
NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40712658 | ||||||
| chr1:40712658 | CT | C | 83 | a0001c0001t0001g0146 a0001c0001t0001g0270 a0001c0001t0001g0275 others(80): Show |
88 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(85): Show |
intron_variant | MODIFIER | c.-9+20815delT | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40712658 | ||||||
| chr1:40712746 | A | T | 1 | a0001c0001t0001g0285 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-9+20879A>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40712746 | |||||||
| chr1:40712851 | T | A | 74 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 others(71): Show |
74 | HG00140.hp1 HG00642.hp1 HG00738.hp1 others(71): Show |
intron_variant | MODIFIER | c.-9+20984T>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40712851 | |||||||
| chr1:40712876 | T | C | 1 | a0001c0001t0002g0041 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.-9+21009T>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40712876 | |||||||
| chr1:40713183 | A | G | 26 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(23): Show |
30 | HG01069.hp1 HG01071.hp1 HG01168.hp2 others(27): Show |
intron_variant | MODIFIER | c.-9+21316A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40713183 | |||||||
| chr1:40713244 | A | G | 1 | a0001c0001t0002g0040 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-9+21377A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40713244 | |||||||
| chr1:40713297 | T | C | 1 | a0001c0001t0002g0042 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-9+21430T>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40713297 | |||||||
| chr1:40713626 | A | T | 3 | a0001c0003t0001g0100 a0001c0003t0001g0101 a0001c0003t0001g0102 |
3 | HG03540.hp1 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-9+21759A>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40713626 | |||||||
| chr1:40713843 | T | C | 1 | a0001c0001t0001g0292 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-9+21976T>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40713843 | |||||||
| chr1:40713863 | A | G | 1 | a0001c0002t0001g0243 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-9+21996A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40713863 | |||||||
| chr1:40713915 | G | T | 59 | a0001c0002t0001g0132 a0001c0002t0001g0149 a0001c0002t0001g0151 others(56): Show |
59 | HG00140.hp1 HG00642.hp1 HG01074.hp2 others(56): Show |
intron_variant | MODIFIER | c.-9+22048G>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40713915 | |||||||
| chr1:40714065 | T | A | 1 | a0001c0001t0010g0107 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-9+22198T>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40714065 | |||||||
| chr1:40714093 | C | T | 2 | a0001c0001t0004g0104 a0001c0001t0004g0105 |
2 | HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-9+22226C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40714093 | |||||||
| chr1:40714221 | A | G | 26 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(23): Show |
30 | HG01069.hp1 HG01071.hp1 HG01168.hp2 others(27): Show |
intron_variant | MODIFIER | c.-9+22354A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40714221 | |||||||
| chr1:40714623 | C | T | 1 | a0001c0001t0002g0069 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.-9+22756C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40714623 | |||||||
| chr1:40714723 | T | TC | 94 | a0001c0001t0001g0232 a0001c0001t0001g0246 a0001c0001t0001g0251 others(91): Show |
96 | HG00280.hp1 HG00423.hp2 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.-9+22859dupC | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40714723 | ||||||
| chr1:40714772 | C | T | 1 | a0001c0001t0002g0088 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-9+22905C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40714772 | |||||||
| chr1:40714863 | G | A | 1 | a0001c0001t0002g0070 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-9+22996G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40714863 | |||||||
| chr1:40714936 | C | T | 2 | a0001c0001t0010g0107 a0001c0002t0001g0174 |
2 | HG02723.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.-9+23069C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40714936 | |||||||
| chr1:40714937 | G | A | 3 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0130 |
3 | HG01884.hp1 HG02970.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-9+23070G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40714937 | |||||||
| chr1:40715011 | C | T | 6 | a0001c0002t0001g0099 a0001c0002t0001g0206 a0001c0002t0001g0221 others(3): Show |
6 | HG01934.hp1 HG01993.hp2 HG02602.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9+23144C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40715011 | |||||||
| chr1:40715086 | C | CAATA | 101 | a0001c0001t0001g0013 a0001c0001t0001g0020 a0001c0001t0001g0287 others(98): Show |
109 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.-9+23245_-9+23248d others(6): Show |
NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40715086 | ||||||
| chr1:40715086 | C | CAATAAAT others(1): Show |
50 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(47): Show |
54 | HG00140.hp1 HG00558.hp2 HG01069.hp1 others(51): Show |
intron_variant | MODIFIER | c.-9+23241_-9+23248d others(10): Show |
NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40715086 | ||||||
| chr1:40715086 | C | CAATAAAT others(5): Show |
23 | a0001c0001t0001g0121 a0001c0001t0001g0142 a0001c0001t0001g0147 others(20): Show |
23 | HG00738.hp1 HG01081.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.-9+23237_-9+23248d others(14): Show |
NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40715086 | ||||||
| chr1:40715086 | C | CAATAAAT others(9): Show |
36 | a0001c0001t0001g0108 a0001c0001t0001g0139 a0001c0001t0001g0140 others(33): Show |
36 | HG00642.hp1 HG01243.hp1 HG01261.hp1 others(33): Show |
intron_variant | MODIFIER | c.-9+23233_-9+23248d others(18): Show |
NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40715086 | ||||||
| chr1:40715086 | CAATA | C | 94 | a0001c0001t0001g0232 a0001c0001t0001g0246 a0001c0001t0001g0251 others(91): Show |
96 | HG00280.hp1 HG00423.hp2 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.-9+23245_-9+23248d others(6): Show |
NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40715086 | ||||||
| chr1:40715252 | C | T | 1 | a0001c0001t0002g0068 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-9+23385C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40715252 | |||||||
| chr1:40715378 | G | A | 1 | a0001c0001t0002g0002 | 2 | HG01123.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.-8-23458G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40715378 | |||||||
| chr1:40715504 | A | G | 1 | a0001c0001t0002g0086 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-8-23332A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40715504 | |||||||
| chr1:40715677 | TCAATAAT others(4): Show |
T | 5 | a0001c0002t0001g0151 a0001c0002t0001g0152 a0001c0002t0001g0181 others(2): Show |
5 | HG01891.hp2 HG02451.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.-8-23155_-8-23145d others(13): Show |
NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40715677 | ||||||
| chr1:40715879 | C | T | 1 | a0001c0001t0005g0317 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-8-22957C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40715879 | |||||||
| chr1:40715909 | A | G | 3 | a0001c0003t0001g0100 a0001c0003t0001g0101 a0001c0003t0001g0102 |
3 | HG03540.hp1 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-8-22927A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40715909 | |||||||
| chr1:40716381 | G | A | 4 | a0001c0001t0003g0138 a0001c0001t0003g0271 a0001c0001t0003g0279 others(1): Show |
4 | HG00639.hp2 HG02622.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-22455G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40716381 | |||||||
| chr1:40716386 | T | A | 1 | a0001c0004t0001g0014 | 2 | HG01943.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-8-22450T>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40716386 | |||||||
| chr1:40716498 | T | C | 6 | a0001c0002t0001g0193 a0001c0002t0001g0194 a0001c0002t0001g0195 others(3): Show |
6 | HG02109.hp1 HG02486.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.-8-22338T>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40716498 | |||||||
| chr1:40716738 | A | G | 94 | a0001c0001t0001g0232 a0001c0001t0001g0246 a0001c0001t0001g0251 others(91): Show |
96 | HG00280.hp1 HG00423.hp2 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.-8-22098A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40716738 | |||||||
| chr1:40716842 | A | G | 1 | a0001c0001t0002g0040 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-8-21994A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40716842 | |||||||
| chr1:40716940 | CAG | C | 59 | a0001c0002t0001g0132 a0001c0002t0001g0149 a0001c0002t0001g0151 others(56): Show |
59 | HG00140.hp1 HG00642.hp1 HG01074.hp2 others(56): Show |
intron_variant | MODIFIER | c.-8-21894_-8-21893d others(4): Show |
NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40716940 | ||||||
| chr1:40717162 | A | G | 1 | a0001c0002t0001g0172 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-8-21674A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40717162 | |||||||
| chr1:40717166 | AAG | A | 4 | a0001c0001t0003g0138 a0001c0001t0003g0271 a0001c0001t0003g0279 others(1): Show |
4 | HG00639.hp2 HG02622.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-21666_-8-21665d others(4): Show |
NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40717166 | ||||||
| chr1:40717433 | G | A | 26 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(23): Show |
30 | HG01069.hp1 HG01071.hp1 HG01168.hp2 others(27): Show |
intron_variant | MODIFIER | c.-8-21403G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40717433 | |||||||
| chr1:40717825 | T | C | 2 | a0001c0002t0001g0165 a0001c0002t0001g0175 |
2 | NA18989.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.-8-21011T>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40717825 | |||||||
| chr1:40717863 | G | A | 3 | a0001c0001t0002g0023 a0001c0001t0002g0024 a0001c0001t0002g0025 |
3 | HG00423.hp1 HG02135.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.-8-20973G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40717863 | |||||||
| chr1:40718272 | C | T | 3 | a0001c0003t0001g0100 a0001c0003t0001g0101 a0001c0003t0001g0102 |
3 | HG03540.hp1 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-8-20564C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40718272 | |||||||
| chr1:40718304 | A | G | 1 | a0001c0001t0010g0107 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-8-20532A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40718304 | |||||||
| chr1:40718317 | C | G | 1 | a0001c0001t0001g0117 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.-8-20519C>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40718317 | |||||||
| chr1:40718829 | A | T | 1 | a0001c0002t0002g0310 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-8-20007A>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40718829 | |||||||
| chr1:40718860 | T | G | 7 | a0001c0002t0001g0153 a0001c0002t0001g0154 a0001c0002t0001g0165 others(4): Show |
7 | NA18943.hp2 NA18954.hp1 NA18979.hp1 others(4): Show |
intron_variant | MODIFIER | c.-8-19976T>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40718860 | |||||||
| chr1:40718860 | TTTTTGTT others(3): Show |
T | 4 | a0001c0001t0001g0285 a0001c0001t0001g0292 a0001c0001t0001g0294 others(1): Show |
4 | HG02630.hp1 HG02809.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8-19956_-8-19947d others(12): Show |
NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40718860 | ||||||
| chr1:40718873 | T | C | 1 | a0001c0001t0002g0045 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-8-19963T>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40718873 | |||||||
| chr1:40719169 | C | T | 1 | a0001c0001t0010g0107 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-8-19667C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40719169 | |||||||
| chr1:40719204 | C | A | 1 | a0001c0002t0001g0188 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-8-19632C>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40719204 | |||||||
| chr1:40719371 | C | T | 1 | a0001c0001t0002g0080 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-8-19465C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40719371 | |||||||
| chr1:40719502 | A | G | 59 | a0001c0002t0001g0132 a0001c0002t0001g0149 a0001c0002t0001g0151 others(56): Show |
59 | HG00140.hp1 HG00642.hp1 HG01074.hp2 others(56): Show |
intron_variant | MODIFIER | c.-8-19334A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40719502 | |||||||
| chr1:40719523 | C | T | 2 | a0001c0002t0001g0151 a0001c0002t0001g0152 |
2 | HG02451.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-8-19313C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40719523 | |||||||
| chr1:40719647 | G | A | 1 | a0001c0002t0001g0210 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-8-19189G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40719647 | |||||||
| chr1:40719723 | G | A | 6 | a0001c0002t0001g0299 a0001c0002t0001g0300 a0001c0002t0001g0301 others(3): Show |
6 | NA18956.hp1 NA18965.hp1 NA18991.hp2 others(3): Show |
intron_variant | MODIFIER | c.-8-19113G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40719723 | |||||||
| chr1:40719850 | T | C | 1 | a0001c0001t0001g0109 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-8-18986T>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40719850 | |||||||
| chr1:40719853 | T | C | 1 | a0001c0001t0010g0107 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-8-18983T>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40719853 | |||||||
| chr1:40719862 | A | C | 227 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(224): Show |
235 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.-8-18974A>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40719862 | |||||||
| chr1:40719929 | T | C | 3 | a0001c0001t0001g0292 a0001c0001t0001g0294 a0001c0001t0007g0293 |
3 | HG02630.hp1 HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.-8-18907T>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40719929 | |||||||
| chr1:40720145 | T | C | 1 | a0001c0001t0010g0107 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-8-18691T>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40720145 | |||||||
| chr1:40720273 | T | G | 2 | a0001c0002t0001g0155 a0001c0002t0001g0176 |
2 | HG02055.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-8-18563T>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40720273 | |||||||
| chr1:40720288 | G | C | 1 | a0001c0001t0001g0142 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-8-18548G>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40720288 | |||||||
| chr1:40720291 | T | C | 1 | a0001c0001t0010g0107 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-8-18545T>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40720291 | |||||||
| chr1:40720377 | T | C | 1 | a0001c0001t0002g0033 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-8-18459T>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40720377 | |||||||
| chr1:40720517 | AT | A | 189 | a0001c0001t0001g0013 a0001c0001t0001g0139 a0001c0001t0001g0140 others(186): Show |
193 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.-8-18315delT | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40720517 | ||||||
| chr1:40720649 | T | C | 1 | a0001c0001t0001g0115 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-8-18187T>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40720649 | |||||||
| chr1:40720730 | T | C | 5 | a0001c0001t0002g0045 a0001c0001t0002g0094 a0001c0001t0002g0095 others(2): Show |
5 | HG01167.hp1 HG01169.hp1 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.-8-18106T>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40720730 | |||||||
| chr1:40720771 | G | A | 196 | a0001c0001t0001g0013 a0001c0001t0001g0139 a0001c0001t0001g0140 others(193): Show |
200 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.-8-18065G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40720771 | |||||||
| chr1:40720879 | T | A | 1 | a0001c0002t0001g0156 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-8-17957T>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40720879 | |||||||
| chr1:40721088 | T | C | 1 | a0001c0001t0010g0107 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-8-17748T>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40721088 | |||||||
| chr1:40721165 | A | C | 3 | a0001c0002t0001g0300 a0001c0002t0001g0301 a0001c0002t0001g0302 |
3 | NA18997.hp2 NA19085.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.-8-17671A>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40721165 | |||||||
| chr1:40721249 | T | C | 1 | a0001c0001t0002g0016 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.-8-17587T>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40721249 | |||||||
| chr1:40721393 | A | G | 1 | a0001c0001t0001g0148 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-8-17443A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40721393 | |||||||
| chr1:40721570 | G | GT | 96 | a0001c0001t0001g0232 a0001c0001t0001g0246 a0001c0001t0001g0251 others(93): Show |
98 | HG00280.hp1 HG00423.hp2 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.-8-17257dupT | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40721570 | ||||||
| chr1:40721570 | G | T | 1 | a0001c0001t0001g0120 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-8-17266G>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40721570 | |||||||
| chr1:40721656 | G | A | 1 | a0001c0001t0001g0309 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-8-17180G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40721656 | |||||||
| chr1:40721694 | G | A | 1 | a0001c0001t0010g0107 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-8-17142G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40721694 | |||||||
| chr1:40721816 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-8-17020G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40721816 | |||||||
| chr1:40721853 | G | A | 4 | a0001c0001t0001g0270 a0001c0001t0001g0275 a0001c0001t0001g0276 others(1): Show |
4 | HG00099.hp1 HG00738.hp2 HG01106.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-16983G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40721853 | |||||||
| chr1:40721898 | C | A | 1 | a0001c0001t0001g0309 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-8-16938C>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40721898 | |||||||
| chr1:40721899 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-8-16937G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40721899 | |||||||
| chr1:40721966 | G | C | 222 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(219): Show |
230 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.-8-16870G>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40721966 | |||||||
| chr1:40721967 | G | A | 1 | a0001c0002t0001g0182 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-8-16869G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40721967 | |||||||
| chr1:40721987 | G | A | 4 | a0001c0002t0001g0230 a0001c0002t0001g0231 a0001c0002t0001g0291 others(1): Show |
4 | HG01167.hp2 HG01192.hp1 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-16849G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40721987 | |||||||
| chr1:40721997 | T | C | 224 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(221): Show |
232 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.-8-16839T>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40721997 | |||||||
| chr1:40722022 | T | A | 3 | a0001c0003t0001g0100 a0001c0003t0001g0101 a0001c0003t0001g0102 |
3 | HG03540.hp1 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-8-16814T>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40722022 | |||||||
| chr1:40722063 | T | C | 1 | a0001c0002t0001g0299 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-8-16773T>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40722063 | |||||||
| chr1:40722127 | T | C | 226 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(223): Show |
234 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.-8-16709T>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40722127 | |||||||
| chr1:40722133 | T | A | 1 | a0001c0002t0001g0216 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-8-16703T>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40722133 | |||||||
| chr1:40722171 | A | C | 3 | a0001c0003t0001g0100 a0001c0003t0001g0101 a0001c0003t0001g0102 |
3 | HG03540.hp1 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-8-16665A>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40722171 | |||||||
| chr1:40722596 | A | G | 3 | a0001c0003t0001g0100 a0001c0003t0001g0101 a0001c0003t0001g0102 |
3 | HG03540.hp1 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-8-16240A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40722596 | |||||||
| chr1:40722675 | G | A | 290 | a0001c0001t0001g0013 a0001c0001t0001g0020 a0001c0001t0001g0139 others(287): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.-8-16161G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40722675 | |||||||
| chr1:40723017 | C | A | 4 | a0001c0001t0003g0138 a0001c0001t0003g0271 a0001c0001t0003g0279 others(1): Show |
4 | HG00639.hp2 HG02622.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-15819C>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40723017 | |||||||
| chr1:40723243 | A | G | 90 | a0001c0001t0001g0020 a0001c0001t0002g0001 a0001c0001t0002g0002 others(87): Show |
96 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.-8-15593A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40723243 | |||||||
| chr1:40723382 | A | G | 1 | a0001c0001t0001g0285 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-8-15454A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40723382 | |||||||
| chr1:40723672 | T | C | 1 | a0001c0001t0001g0020 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-8-15164T>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40723672 | |||||||
| chr1:40723734 | A | G | 1 | a0001c0001t0001g0127 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-8-15102A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40723734 | |||||||
| chr1:40723875 | C | T | 1 | a0001c0001t0002g0015 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-8-14961C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40723875 | |||||||
| chr1:40723913 | G | C | 1 | a0001c0001t0002g0015 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-8-14923G>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40723913 | |||||||
| chr1:40723957 | A | G | 290 | a0001c0001t0001g0013 a0001c0001t0001g0020 a0001c0001t0001g0139 others(287): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.-8-14879A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40723957 | |||||||
| chr1:40724123 | G | A | 313 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(310): Show |
327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.-8-14713G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40724123 | |||||||
| chr1:40724163 | A | G | 195 | a0001c0001t0001g0013 a0001c0001t0001g0139 a0001c0001t0001g0140 others(192): Show |
199 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.-8-14673A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40724163 | |||||||
| chr1:40724317 | G | A | 6 | a0001c0001t0002g0045 a0001c0001t0002g0046 a0001c0001t0002g0094 others(3): Show |
6 | HG01167.hp1 HG01169.hp1 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.-8-14519G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40724317 | |||||||
| chr1:40724451 | T | C | 1 | a0001c0001t0005g0318 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-8-14385T>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40724451 | |||||||
| chr1:40724682 | C | T | 90 | a0001c0001t0001g0020 a0001c0001t0002g0001 a0001c0001t0002g0002 others(87): Show |
96 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.-8-14154C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40724682 | |||||||
| chr1:40724789 | A | G | 1 | a0001c0004t0001g0014 | 2 | HG01943.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-8-14047A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40724789 | |||||||
| chr1:40724799 | AAAGT | A | 12 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0108 others(9): Show |
14 | HG01168.hp2 HG01169.hp2 HG01175.hp1 others(11): Show |
intron_variant | MODIFIER | c.-8-14035_-8-14032d others(6): Show |
NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40724799 | ||||||
| chr1:40725283 | G | A | 1 | a0001c0001t0002g0076 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-8-13553G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40725283 | |||||||
| chr1:40725528 | G | A | 90 | a0001c0001t0001g0020 a0001c0001t0002g0001 a0001c0001t0002g0002 others(87): Show |
96 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.-8-13308G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40725528 | |||||||
| chr1:40726107 | T | TTG | 175 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(172): Show |
181 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.-8-12711_-8-12710d others(4): Show |
NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40726107 | ||||||
| chr1:40726107 | T | TTGTG | 2 | a0001c0001t0002g0003 a0001c0001t0002g0048 |
3 | HG02683.hp2 HG03540.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.-8-12713_-8-12710d others(6): Show |
NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40726107 | ||||||
| chr1:40726126 | T | TGTG | 2 | a0001c0001t0002g0001 a0001c0001t0002g0038 |
3 | NA18947.hp2 NA18948.hp1 NA18997.hp1 |
intron_variant | MODIFIER | c.-8-12710_-8-12709i others(5): Show |
NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40726126 | |||||||
| chr1:40726127 | T | G | 103 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(100): Show |
105 | HG00280.hp1 HG00423.hp2 HG00558.hp1 others(102): Show |
intron_variant | MODIFIER | c.-8-12709T>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40726127 | |||||||
| chr1:40726129 | T | G | 94 | a0001c0001t0001g0232 a0001c0001t0001g0246 a0001c0001t0001g0251 others(91): Show |
96 | HG00280.hp1 HG00423.hp2 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.-8-12707T>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40726129 | |||||||
| chr1:40726153 | T | G | 1 | a0001c0001t0010g0107 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-8-12683T>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40726153 | |||||||
| chr1:40726221 | G | A | 1 | a0001c0001t0002g0076 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-8-12615G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40726221 | |||||||
| chr1:40726350 | T | C | 1 | a0001c0004t0001g0014 | 2 | HG01943.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-8-12486T>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40726350 | |||||||
| chr1:40726396 | G | A | 1 | a0001c0002t0001g0133 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-8-12440G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40726396 | |||||||
| chr1:40726397 | C | T | 3 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0115 |
3 | HG01256.hp1 HG01943.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.-8-12439C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40726397 | |||||||
| chr1:40726407 | C | T | 1 | a0001c0002t0001g0223 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-8-12429C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40726407 | |||||||
| chr1:40726431 | T | C | 5 | a0001c0001t0001g0269 a0001c0001t0001g0274 a0001c0001t0001g0281 others(2): Show |
5 | HG02559.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8-12405T>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40726431 | |||||||
| chr1:40726491 | C | A | 2 | a0001c0001t0004g0104 a0001c0001t0004g0105 |
2 | HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-8-12345C>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40726491 | |||||||
| chr1:40726520 | C | T | 1 | a0001c0001t0002g0087 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-8-12316C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40726520 | |||||||
| chr1:40726549 | A | G | 1 | a0001c0001t0001g0148 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-8-12287A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40726549 | |||||||
| chr1:40726561 | C | A | 3 | a0001c0003t0001g0100 a0001c0003t0001g0101 a0001c0003t0001g0102 |
3 | HG03540.hp1 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-8-12275C>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40726561 | |||||||
| chr1:40726573 | C | A | 1 | a0001c0002t0001g0177 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-8-12263C>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40726573 | |||||||
| chr1:40726825 | G | T | 90 | a0001c0001t0001g0020 a0001c0001t0002g0001 a0001c0001t0002g0002 others(87): Show |
96 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.-8-12011G>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40726825 | |||||||
| chr1:40727038 | C | T | 14 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 others(11): Show |
14 | HG00738.hp1 HG01071.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.-8-11798C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40727038 | |||||||
| chr1:40727171 | C | T | 4 | a0001c0001t0003g0138 a0001c0001t0003g0271 a0001c0001t0003g0279 others(1): Show |
4 | HG00639.hp2 HG02622.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-11665C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40727171 | |||||||
| chr1:40727208 | T | G | 1 | a0001c0002t0001g0313 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.-8-11628T>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40727208 | |||||||
| chr1:40727208 | T | TTTGG | 8 | a0001c0002t0001g0299 a0001c0002t0001g0300 a0001c0002t0001g0301 others(5): Show |
8 | HG01074.hp2 HG02602.hp1 NA18956.hp1 others(5): Show |
intron_variant | MODIFIER | c.-8-11625_-8-11624i others(6): Show |
NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40727208 | ||||||
| chr1:40727212 | T | G | 14 | a0001c0002t0001g0265 a0001c0002t0001g0266 a0001c0002t0001g0267 others(11): Show |
14 | HG01074.hp2 HG02257.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.-8-11624T>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40727212 | |||||||
| chr1:40727216 | G | T | 94 | a0001c0001t0001g0020 a0001c0001t0002g0001 a0001c0001t0002g0002 others(91): Show |
100 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.-8-11620G>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40727216 | |||||||
| chr1:40727309 | G | C | 1 | a0001c0001t0002g0040 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-8-11527G>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40727309 | |||||||
| chr1:40727378 | C | CG | 156 | a0001c0001t0001g0148 a0001c0001t0001g0232 a0001c0001t0001g0246 others(153): Show |
159 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(156): Show |
intron_variant | MODIFIER | c.-8-11458_-8-11457i others(3): Show |
NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40727378 | |||||||
| chr1:40727382 | A | C | 290 | a0001c0001t0001g0013 a0001c0001t0001g0020 a0001c0001t0001g0139 others(287): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.-8-11454A>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40727382 | |||||||
| chr1:40727469 | C | T | 143 | a0001c0001t0001g0232 a0001c0001t0001g0246 a0001c0001t0001g0251 others(140): Show |
145 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.-8-11367C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40727469 | |||||||
| chr1:40727532 | C | CTTT | 82 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0003 others(79): Show |
87 | HG00099.hp2 HG00140.hp2 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.-8-11290_-8-11288d others(5): Show |
NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40727532 | ||||||
| chr1:40727549 | G | T | 1 | a0001c0001t0002g0067 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-8-11287G>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40727549 | |||||||
| chr1:40727587 | G | T | 1 | a0001c0001t0002g0076 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-8-11249G>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40727587 | |||||||
| chr1:40727875 | TAGA | T | 90 | a0001c0001t0001g0020 a0001c0001t0002g0001 a0001c0001t0002g0002 others(87): Show |
96 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.-8-10958_-8-10956d others(5): Show |
NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40727875 | ||||||
| chr1:40727955 | C | T | 90 | a0001c0001t0001g0020 a0001c0001t0002g0001 a0001c0001t0002g0002 others(87): Show |
96 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.-8-10881C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40727955 | |||||||
| chr1:40728134 | G | A | 4 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 others(1): Show |
4 | HG02258.hp2 HG02976.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-10702G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40728134 | |||||||
| chr1:40728194 | A | G | 2 | a0001c0001t0002g0044 a0001c0001t0002g0071 |
2 | HG00558.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.-8-10642A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40728194 | |||||||
| chr1:40728324 | C | T | 1 | a0001c0002t0001g0222 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-8-10512C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40728324 | |||||||
| chr1:40728412 | C | T | 1 | a0001c0001t0010g0107 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-8-10424C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40728412 | |||||||
| chr1:40728665 | T | G | 90 | a0001c0001t0001g0020 a0001c0001t0002g0001 a0001c0001t0002g0002 others(87): Show |
96 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.-8-10171T>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40728665 | |||||||
| chr1:40728745 | C | A | 1 | a0001c0001t0001g0303 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-8-10091C>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40728745 | |||||||
| chr1:40728852 | G | T | 1 | a0001c0002t0001g0198 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-8-9984G>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40728852 | |||||||
| chr1:40728881 | G | T | 1 | a0001c0002t0001g0198 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-8-9955G>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40728881 | |||||||
| chr1:40728961 | G | T | 81 | a0001c0001t0001g0232 a0001c0001t0001g0246 a0001c0001t0001g0251 others(78): Show |
83 | HG00280.hp1 HG00423.hp2 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.-8-9875G>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40728961 | |||||||
| chr1:40729042 | C | T | 1 | a0001c0002t0001g0203 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-8-9794C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40729042 | |||||||
| chr1:40729263 | A | G | 5 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 others(2): Show |
5 | HG02258.hp2 HG02976.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.-8-9573A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40729263 | |||||||
| chr1:40729300 | C | T | 11 | a0001c0002t0001g0193 a0001c0002t0001g0194 a0001c0002t0001g0195 others(8): Show |
11 | HG01069.hp2 HG02109.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.-8-9536C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40729300 | |||||||
| chr1:40729398 | A | G | 24 | a0001c0001t0001g0013 a0001c0001t0001g0269 a0001c0001t0001g0270 others(21): Show |
25 | HG00099.hp1 HG00639.hp2 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.-8-9438A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40729398 | |||||||
| chr1:40729463 | C | G | 1 | a0001c0001t0001g0116 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-8-9373C>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40729463 | |||||||
| chr1:40729551 | CT | C | 3 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 |
3 | HG00738.hp1 HG01071.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.-8-9284delT | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40729551 | |||||||
| chr1:40729634 | G | A | 1 | a0001c0002t0001g0182 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-8-9202G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40729634 | |||||||
| chr1:40729679 | C | T | 2 | a0001c0001t0002g0003 a0001c0001t0002g0048 |
3 | HG02683.hp2 HG03540.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.-8-9157C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40729679 | |||||||
| chr1:40729749 | G | T | 1 | a0001c0001t0001g0309 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-8-9087G>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40729749 | |||||||
| chr1:40729766 | C | A | 3 | a0001c0002t0001g0229 a0001c0002t0001g0250 a0001c0002t0002g0249 |
3 | NA18939.hp1 NA18955.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.-8-9070C>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40729766 | |||||||
| chr1:40730101 | C | A | 1 | a0001c0001t0002g0051 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.-8-8735C>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40730101 | |||||||
| chr1:40730146 | G | A | 1 | a0001c0001t0001g0121 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-8-8690G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40730146 | |||||||
| chr1:40730195 | C | CT | 21 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0109 others(18): Show |
24 | HG00642.hp1 HG01123.hp1 HG01168.hp2 others(21): Show |
intron_variant | MODIFIER | c.-8-8619dupT | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40730195 | ||||||
| chr1:40730195 | CT | C | 93 | a0001c0001t0001g0020 a0001c0001t0001g0120 a0001c0001t0001g0145 others(90): Show |
99 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.-8-8619delT | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40730195 | ||||||
| chr1:40730195 | CTT | C | 27 | a0001c0001t0001g0013 a0001c0001t0001g0269 a0001c0001t0001g0270 others(24): Show |
28 | HG00099.hp1 HG00558.hp2 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.-8-8620_-8-8619del others(2): Show |
NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40730195 | ||||||
| chr1:40730195 | CTTTTTTT | C | 11 | a0001c0002t0001g0157 a0001c0002t0001g0253 a0001c0002t0001g0299 others(8): Show |
11 | HG01074.hp2 HG01952.hp1 HG02132.hp1 others(8): Show |
intron_variant | MODIFIER | c.-8-8625_-8-8619del others(7): Show |
NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40730195 | ||||||
| chr1:40730195 | CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0001g0282 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-8-8629_-8-8619del others(11): Show |
NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40730195 | ||||||
| chr1:40730201 | T | C | 1 | a0001c0001t0002g0022 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-8-8635T>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40730201 | |||||||
| chr1:40730666 | A | G | 3 | a0001c0003t0001g0100 a0001c0003t0001g0101 a0001c0003t0001g0102 |
3 | HG03540.hp1 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-8-8170A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40730666 | |||||||
| chr1:40730684 | CA | C | 24 | a0001c0001t0001g0013 a0001c0001t0001g0269 a0001c0001t0001g0270 others(21): Show |
25 | HG00099.hp1 HG00639.hp2 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.-8-8147delA | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40730684 | ||||||
| chr1:40730754 | G | A | 2 | a0001c0001t0004g0104 a0001c0001t0004g0105 |
2 | HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-8-8082G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40730754 | |||||||
| chr1:40730779 | A | G | 2 | a0001c0001t0002g0004 a0001c0001t0002g0091 |
3 | NA18945.hp1 NA19068.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.-8-8057A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40730779 | |||||||
| chr1:40730974 | G | T | 4 | a0001c0002t0001g0230 a0001c0002t0001g0231 a0001c0002t0001g0291 others(1): Show |
4 | HG01167.hp2 HG01192.hp1 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-7862G>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40730974 | |||||||
| chr1:40731094 | C | T | 4 | a0001c0001t0001g0285 a0001c0001t0001g0292 a0001c0001t0001g0294 others(1): Show |
4 | HG02630.hp1 HG02809.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8-7742C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40731094 | |||||||
| chr1:40731194 | T | G | 1 | a0001c0001t0001g0285 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-8-7642T>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40731194 | |||||||
| chr1:40731300 | A | G | 290 | a0001c0001t0001g0013 a0001c0001t0001g0020 a0001c0001t0001g0139 others(287): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.-8-7536A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40731300 | |||||||
| chr1:40731439 | T | TGC | 290 | a0001c0001t0001g0013 a0001c0001t0001g0020 a0001c0001t0001g0139 others(287): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.-8-7397_-8-7396ins others(2): Show |
NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40731439 | |||||||
| chr1:40731450 | G | A | 3 | a0001c0003t0001g0100 a0001c0003t0001g0101 a0001c0003t0001g0102 |
3 | HG03540.hp1 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-8-7386G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40731450 | |||||||
| chr1:40731495 | C | T | 1 | a0001c0001t0002g0066 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-8-7341C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40731495 | |||||||
| chr1:40731530 | G | A | 1 | a0001c0001t0010g0107 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-8-7306G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40731530 | |||||||
| chr1:40731626 | A | G | 3 | a0001c0001t0001g0292 a0001c0001t0001g0294 a0001c0001t0007g0293 |
3 | HG02630.hp1 HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.-8-7210A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40731626 | |||||||
| chr1:40731634 | G | A | 90 | a0001c0001t0001g0020 a0001c0001t0002g0001 a0001c0001t0002g0002 others(87): Show |
96 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.-8-7202G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40731634 | |||||||
| chr1:40731719 | C | G | 195 | a0001c0001t0001g0013 a0001c0001t0001g0139 a0001c0001t0001g0140 others(192): Show |
199 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.-8-7117C>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40731719 | |||||||
| chr1:40731742 | T | C | 290 | a0001c0001t0001g0013 a0001c0001t0001g0020 a0001c0001t0001g0139 others(287): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.-8-7094T>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40731742 | |||||||
| chr1:40731776 | G | A | 1 | a0001c0002t0001g0254 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-8-7060G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40731776 | |||||||
| chr1:40731778 | C | T | 3 | a0001c0001t0001g0292 a0001c0001t0001g0294 a0001c0001t0007g0293 |
3 | HG02630.hp1 HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.-8-7058C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40731778 | |||||||
| chr1:40731821 | T | C | 2 | a0001c0001t0004g0104 a0001c0001t0004g0105 |
2 | HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-8-7015T>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40731821 | |||||||
| chr1:40731986 | G | A | 1 | a0001c0001t0002g0052 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.-8-6850G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40731986 | |||||||
| chr1:40732223 | G | A | 1 | a0001c0001t0002g0043 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-8-6613G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40732223 | |||||||
| chr1:40732627 | C | A | 5 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(2): Show |
5 | HG00738.hp1 HG01071.hp2 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8-6209C>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40732627 | |||||||
| chr1:40732736 | C | T | 2 | a0001c0002t0001g0213 a0001c0002t0001g0242 |
2 | NA18972.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.-8-6100C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40732736 | |||||||
| chr1:40732897 | C | T | 1 | a0001c0001t0001g0121 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-8-5939C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40732897 | |||||||
| chr1:40732988 | G | A | 24 | a0001c0001t0001g0013 a0001c0001t0001g0269 a0001c0001t0001g0270 others(21): Show |
25 | HG00099.hp1 HG00639.hp2 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.-8-5848G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40732988 | |||||||
| chr1:40733008 | G | GC | 13 | a0001c0001t0001g0007 a0001c0001t0001g0109 a0001c0001t0001g0116 others(10): Show |
15 | HG01168.hp2 HG01169.hp2 HG01943.hp2 others(12): Show |
intron_variant | MODIFIER | c.-8-5817dupC | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40733008 | ||||||
| chr1:40733019 | C | CCCT | 19 | a0001c0001t0001g0013 a0001c0001t0001g0269 a0001c0001t0001g0272 others(16): Show |
20 | HG00639.hp2 HG00738.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.-8-5817_-8-5816ins others(3): Show |
NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40733019 | |||||||
| chr1:40733019 | C | CCT | 78 | a0001c0001t0001g0232 a0001c0001t0001g0270 a0001c0001t0001g0277 others(75): Show |
78 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.-8-5817_-8-5816ins others(2): Show |
NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40733019 | |||||||
| chr1:40733019 | C | CT | 166 | a0001c0001t0001g0020 a0001c0001t0001g0246 a0001c0001t0001g0251 others(163): Show |
174 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.-8-5805dupT | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40733019 | ||||||
| chr1:40733019 | C | T | 7 | a0001c0002t0001g0213 a0001c0002t0001g0242 a0001c0002t0001g0261 others(4): Show |
7 | HG00423.hp2 HG02155.hp2 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.-8-5817C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40733019 | |||||||
| chr1:40733020 | T | C | 4 | a0001c0001t0001g0292 a0001c0001t0001g0294 a0001c0001t0001g0309 others(1): Show |
4 | HG02630.hp1 HG02723.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8-5816T>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40733020 | |||||||
| chr1:40733043 | A | T | 1 | a0001c0002t0001g0212 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-8-5793A>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40733043 | |||||||
| chr1:40733182 | G | A | 3 | a0001c0003t0001g0100 a0001c0003t0001g0101 a0001c0003t0001g0102 |
3 | HG03540.hp1 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-8-5654G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40733182 | |||||||
| chr1:40733272 | C | T | 1 | a0001c0001t0010g0107 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-8-5564C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40733272 | |||||||
| chr1:40733287 | C | T | 1 | a0001c0002t0001g0196 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-8-5549C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40733287 | |||||||
| chr1:40733299 | G | A | 90 | a0001c0001t0001g0020 a0001c0001t0002g0001 a0001c0001t0002g0002 others(87): Show |
96 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.-8-5537G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40733299 | |||||||
| chr1:40733451 | C | T | 6 | a0001c0002t0001g0193 a0001c0002t0001g0194 a0001c0002t0001g0195 others(3): Show |
6 | HG02109.hp1 HG02486.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.-8-5385C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40733451 | |||||||
| chr1:40733595 | G | T | 14 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 others(11): Show |
14 | HG00738.hp1 HG01071.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.-8-5241G>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40733595 | |||||||
| chr1:40733790 | C | T | 1 | a0001c0001t0010g0107 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-8-5046C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40733790 | |||||||
| chr1:40733829 | C | T | 1 | a0001c0001t0002g0088 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-8-5007C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40733829 | |||||||
| chr1:40733893 | G | A | 90 | a0001c0001t0001g0020 a0001c0001t0002g0001 a0001c0001t0002g0002 others(87): Show |
96 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.-8-4943G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40733893 | |||||||
| chr1:40733912 | G | T | 90 | a0001c0001t0001g0020 a0001c0001t0002g0001 a0001c0001t0002g0002 others(87): Show |
96 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.-8-4924G>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40733912 | |||||||
| chr1:40734340 | C | CTTTA | 61 | a0001c0001t0001g0009 a0001c0001t0001g0111 a0001c0001t0001g0124 others(58): Show |
62 | HG00639.hp2 HG00642.hp1 HG00738.hp2 others(59): Show |
intron_variant | MODIFIER | c.-8-4460_-8-4457dup others(4): Show |
NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40734340 | ||||||
| chr1:40734340 | C | CTTTATTT others(1): Show |
13 | a0001c0001t0001g0013 a0001c0001t0001g0139 a0001c0001t0001g0140 others(10): Show |
15 | HG00140.hp1 HG01943.hp2 HG01952.hp1 others(12): Show |
intron_variant | MODIFIER | c.-8-4464_-8-4457dup others(8): Show |
NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40734340 | ||||||
| chr1:40734340 | C | CTTTATTT others(9): Show |
1 | a0001c0003t0001g0101 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-8-4472_-8-4457dup others(16): Show |
NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40734340 | ||||||
| chr1:40734340 | CTTTA | C | 175 | a0001c0001t0001g0020 a0001c0001t0001g0116 a0001c0001t0001g0121 others(172): Show |
183 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.-8-4460_-8-4457del others(4): Show |
NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40734340 | ||||||
| chr1:40734340 | CTTTATTT others(1): Show |
C | 16 | a0001c0001t0001g0269 a0001c0001t0001g0274 a0001c0001t0001g0281 others(13): Show |
16 | HG01069.hp2 HG02559.hp2 HG02886.hp1 others(13): Show |
intron_variant | MODIFIER | c.-8-4464_-8-4457del others(8): Show |
NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40734340 | ||||||
| chr1:40734340 | CTTTATTT others(5): Show |
C | 1 | a0001c0001t0010g0107 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-8-4468_-8-4457del others(12): Show |
NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40734340 | ||||||
| chr1:40734508 | GTGCCACC others(16): Show |
G | 1 | a0001c0001t0001g0115 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-8-4324_-8-4302del others(23): Show |
NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40734508 | ||||||
| chr1:40734534 | C | T | 290 | a0001c0001t0001g0013 a0001c0001t0001g0020 a0001c0001t0001g0139 others(287): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.-8-4302C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40734534 | |||||||
| chr1:40734651 | G | A | 1 | a0001c0001t0002g0047 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-8-4185G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40734651 | |||||||
| chr1:40735089 | A | G | 90 | a0001c0001t0001g0020 a0001c0001t0002g0001 a0001c0001t0002g0002 others(87): Show |
96 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.-8-3747A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40735089 | |||||||
| chr1:40735109 | C | A | 1 | a0001c0001t0002g0030 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.-8-3727C>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40735109 | |||||||
| chr1:40735161 | GCCTGAGT others(4): Show |
G | 145 | a0001c0001t0001g0232 a0001c0001t0001g0246 a0001c0001t0001g0251 others(142): Show |
147 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(144): Show |
intron_variant | MODIFIER | c.-8-3671_-8-3661del others(11): Show |
NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40735161 | ||||||
| chr1:40735163 | CTGAGTGT others(5): Show |
C | 1 | a0001c0002t0001g0185 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-8-3671_-8-3660del others(12): Show |
NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40735163 | ||||||
| chr1:40735165 | G | T | 8 | a0001c0002t0001g0153 a0001c0002t0001g0193 a0001c0002t0001g0194 others(5): Show |
9 | HG01943.hp2 HG02109.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.-8-3671G>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40735165 | |||||||
| chr1:40735166 | AG | A | 8 | a0001c0002t0001g0153 a0001c0002t0001g0193 a0001c0002t0001g0194 others(5): Show |
9 | HG01943.hp2 HG02109.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.-8-3669delG | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40735166 | |||||||
| chr1:40735172 | TCCTTATG others(2): Show |
T | 8 | a0001c0002t0001g0153 a0001c0002t0001g0193 a0001c0002t0001g0194 others(5): Show |
9 | HG01943.hp2 HG02109.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.-8-3663_-8-3655del others(9): Show |
NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40735172 | |||||||
| chr1:40735181 | CT | C | 80 | a0001c0001t0001g0232 a0001c0001t0001g0246 a0001c0001t0001g0251 others(77): Show |
82 | HG00280.hp1 HG00423.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.-8-3640delT | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40735181 | ||||||
| chr1:40735183 | T | C | 5 | a0001c0001t0002g0045 a0001c0001t0002g0094 a0001c0001t0002g0095 others(2): Show |
5 | HG01167.hp1 HG01169.hp1 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.-8-3653T>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40735183 | |||||||
| chr1:40735457 | A | T | 1 | a0001c0001t0010g0107 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-8-3379A>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40735457 | |||||||
| chr1:40735463 | A | G | 4 | a0001c0001t0003g0138 a0001c0001t0003g0271 a0001c0001t0003g0279 others(1): Show |
4 | HG00639.hp2 HG02622.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-3373A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40735463 | |||||||
| chr1:40735585 | C | G | 90 | a0001c0001t0001g0020 a0001c0001t0002g0001 a0001c0001t0002g0002 others(87): Show |
96 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.-8-3251C>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40735585 | |||||||
| chr1:40735699 | C | T | 6 | a0001c0001t0002g0030 a0001c0001t0002g0058 a0001c0001t0002g0065 others(3): Show |
6 | NA18957.hp1 NA18966.hp2 NA18972.hp2 others(3): Show |
intron_variant | MODIFIER | c.-8-3137C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40735699 | |||||||
| chr1:40736067 | T | C | 90 | a0001c0001t0001g0020 a0001c0001t0002g0001 a0001c0001t0002g0002 others(87): Show |
96 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.-8-2769T>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40736067 | |||||||
| chr1:40736128 | T | C | 20 | a0001c0002t0001g0099 a0001c0002t0001g0106 a0001c0002t0001g0192 others(17): Show |
20 | HG01934.hp1 HG01993.hp2 HG02027.hp1 others(17): Show |
intron_variant | MODIFIER | c.-8-2708T>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40736128 | |||||||
| chr1:40736363 | A | G | 1 | a0001c0001t0002g0067 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-8-2473A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40736363 | |||||||
| chr1:40736630 | G | C | 2 | a0001c0002t0001g0152 a0001c0002t0001g0189 |
2 | HG03130.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-8-2206G>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40736630 | |||||||
| chr1:40736675 | A | G | 142 | a0001c0001t0001g0232 a0001c0001t0001g0246 a0001c0001t0001g0251 others(139): Show |
144 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.-8-2161A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40736675 | |||||||
| chr1:40736756 | C | T | 1 | a0001c0001t0002g0316 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-8-2080C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40736756 | |||||||
| chr1:40736817 | T | C | 5 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(2): Show |
5 | HG00738.hp1 HG01071.hp2 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8-2019T>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40736817 | |||||||
| chr1:40736820 | C | CA | 139 | a0001c0001t0001g0109 a0001c0001t0001g0111 a0001c0001t0001g0120 others(136): Show |
142 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.-8-1992dupA | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40736820 | ||||||
| chr1:40736820 | C | CAA | 42 | a0001c0001t0001g0010 a0001c0001t0005g0318 a0001c0002t0001g0106 others(39): Show |
43 | HG00423.hp2 HG00597.hp1 HG01069.hp1 others(40): Show |
intron_variant | MODIFIER | c.-8-1993_-8-1992dup others(2): Show |
NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40736820 | ||||||
| chr1:40736820 | C | CAAA | 11 | a0001c0001t0001g0119 a0001c0001t0001g0125 a0001c0001t0001g0128 others(8): Show |
11 | HG01891.hp1 HG02055.hp1 HG02135.hp1 others(8): Show |
intron_variant | MODIFIER | c.-8-1994_-8-1992dup others(3): Show |
NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40736820 | ||||||
| chr1:40736820 | CA | C | 17 | a0001c0001t0001g0013 a0001c0001t0001g0020 a0001c0001t0001g0114 others(14): Show |
18 | HG01943.hp1 HG02129.hp1 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.-8-1992delA | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40736820 | ||||||
| chr1:40736954 | C | T | 1 | a0001c0001t0002g0088 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-8-1882C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40736954 | |||||||
| chr1:40737072 | A | C | 1 | a0001c0002t0001g0241 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-8-1764A>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40737072 | |||||||
| chr1:40737114 | C | T | 3 | a0001c0002t0001g0012 a0001c0002t0001g0258 a0001c0002t0002g0310 |
4 | HG01123.hp1 HG01256.hp2 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8-1722C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40737114 | |||||||
| chr1:40737127 | C | CA | 15 | a0001c0001t0001g0123 a0001c0001t0001g0130 a0001c0001t0001g0290 others(12): Show |
15 | HG00099.hp2 HG00280.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.-8-1687dupA | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40737127 | ||||||
| chr1:40737127 | CA | C | 36 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 others(33): Show |
36 | HG00738.hp1 HG01069.hp2 HG01071.hp2 others(33): Show |
intron_variant | MODIFIER | c.-8-1687delA | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40737127 | ||||||
| chr1:40737127 | CAA | C | 132 | a0001c0001t0001g0232 a0001c0001t0001g0246 a0001c0001t0001g0251 others(129): Show |
134 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.-8-1688_-8-1687del others(2): Show |
NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40737127 | ||||||
| chr1:40737180 | G | A | 1 | a0001c0002t0001g0295 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-8-1656G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40737180 | |||||||
| chr1:40737257 | C | T | 2 | a0001c0002t0001g0229 a0001c0002t0002g0249 |
2 | NA18955.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.-8-1579C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40737257 | |||||||
| chr1:40737313 | C | G | 3 | a0001c0003t0001g0100 a0001c0003t0001g0101 a0001c0003t0001g0102 |
3 | HG03540.hp1 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-8-1523C>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40737313 | |||||||
| chr1:40737333 | C | CT | 168 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0145 others(165): Show |
171 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(168): Show |
intron_variant | MODIFIER | c.-8-1490dupT | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40737333 | ||||||
| chr1:40737333 | C | CTT | 29 | a0001c0001t0001g0013 a0001c0001t0001g0139 a0001c0001t0001g0140 others(26): Show |
30 | HG00099.hp1 HG00639.hp2 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.-8-1491_-8-1490dup others(2): Show |
NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40737333 | ||||||
| chr1:40737351 | T | C | 24 | a0001c0001t0001g0013 a0001c0001t0001g0269 a0001c0001t0001g0270 others(21): Show |
25 | HG00099.hp1 HG00639.hp2 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.-8-1485T>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40737351 | |||||||
| chr1:40737473 | C | T | 5 | a0001c0001t0001g0269 a0001c0001t0001g0274 a0001c0001t0001g0281 others(2): Show |
5 | HG02559.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8-1363C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40737473 | |||||||
| chr1:40737581 | G | A | 1 | a0001c0004t0001g0014 | 2 | HG01943.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-8-1255G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40737581 | |||||||
| chr1:40737619 | G | A | 1 | a0001c0002t0001g0236 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-8-1217G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40737619 | |||||||
| chr1:40737761 | A | G | 2 | a0001c0001t0001g0122 a0001c0001t0001g0130 |
2 | HG01884.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.-8-1075A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40737761 | |||||||
| chr1:40737823 | A | C | 2 | a0001c0002t0001g0161 a0001c0002t0001g0179 |
2 | HG02622.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.-8-1013A>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40737823 | |||||||
| chr1:40737901 | C | CT | 8 | a0001c0001t0001g0020 a0001c0001t0001g0126 a0001c0001t0002g0015 others(5): Show |
8 | HG00423.hp1 HG03098.hp2 HG03209.hp2 others(5): Show |
intron_variant | MODIFIER | c.-8-916dupT | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40737901 | ||||||
| chr1:40737901 | C | T | 1 | a0001c0001t0010g0107 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-8-935C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40737901 | |||||||
| chr1:40737901 | CT | C | 13 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 others(10): Show |
13 | HG00738.hp1 HG01071.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.-8-916delT | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40737901 | ||||||
| chr1:40737901 | CTT | C | 178 | a0001c0001t0001g0013 a0001c0001t0001g0148 a0001c0001t0001g0232 others(175): Show |
181 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.-8-917_-8-916delTT | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40737901 | ||||||
| chr1:40737925 | C | T | 195 | a0001c0001t0001g0013 a0001c0001t0001g0139 a0001c0001t0001g0140 others(192): Show |
199 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.-8-911C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40737925 | |||||||
| chr1:40737972 | G | A | 1 | a0001c0001t0002g0051 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.-8-864G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40737972 | |||||||
| chr1:40738026 | C | G | 1 | a0001c0004t0001g0014 | 2 | HG01943.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-8-810C>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40738026 | |||||||
| chr1:40738034 | C | G | 1 | a0001c0001t0002g0064 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-8-802C>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40738034 | |||||||
| chr1:40738051 | C | G | 9 | a0001c0002t0001g0299 a0001c0002t0001g0300 a0001c0002t0001g0301 others(6): Show |
9 | HG01074.hp2 HG02602.hp1 NA18956.hp1 others(6): Show |
intron_variant | MODIFIER | c.-8-785C>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40738051 | |||||||
| chr1:40738123 | C | T | 14 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 others(11): Show |
14 | HG00738.hp1 HG01071.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.-8-713C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40738123 | |||||||
| chr1:40738196 | C | A | 1 | a0001c0002t0001g0191 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-8-640C>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40738196 | |||||||
| chr1:40738198 | G | A | 1 | a0001c0001t0001g0148 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-8-638G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40738198 | |||||||
| chr1:40738225 | A | G | 1 | a0001c0001t0002g0088 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-8-611A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40738225 | |||||||
| chr1:40738227 | G | A | 14 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 others(11): Show |
14 | HG00738.hp1 HG01071.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.-8-609G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40738227 | |||||||
| chr1:40738303 | A | G | 1 | a0001c0002t0008g0298 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-8-533A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40738303 | |||||||
| chr1:40738323 | G | A | 1 | a0001c0001t0001g0148 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-8-513G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40738323 | |||||||
| chr1:40738426 | G | A | 3 | a0001c0002t0001g0214 a0001c0002t0001g0253 a0001c0002t0001g0256 |
3 | HG00597.hp1 HG02132.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.-8-410G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40738426 | |||||||
| chr1:40738792 | A | G | 1 | a0001c0001t0001g0116 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-8-44A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40738792 | |||||||
| chr1:40739162 | C | T | 3 | a0001c0003t0001g0100 a0001c0003t0001g0101 a0001c0003t0001g0102 |
3 | HG03540.hp1 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.105+214C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 2/9 | chr1 | 40739162 | |||||||
| chr1:40739335 | A | G | 3 | a0001c0003t0001g0100 a0001c0003t0001g0101 a0001c0003t0001g0102 |
3 | HG03540.hp1 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.105+387A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 2/9 | chr1 | 40739335 | |||||||
| chr1:40739604 | T | C | 290 | a0001c0001t0001g0013 a0001c0001t0001g0020 a0001c0001t0001g0139 others(287): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.105+656T>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 2/9 | chr1 | 40739604 | |||||||
| chr1:40739619 | G | C | 4 | a0001c0002t0001g0137 a0001c0002t0001g0211 a0001c0002t0001g0237 others(1): Show |
4 | NA18943.hp1 NA18945.hp2 NA18957.hp2 others(1): Show |
intron_variant | MODIFIER | c.105+671G>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 2/9 | chr1 | 40739619 | |||||||
| chr1:40739780 | G | T | 90 | a0001c0001t0001g0020 a0001c0001t0002g0001 a0001c0001t0002g0002 others(87): Show |
96 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.105+832G>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 2/9 | chr1 | 40739780 | |||||||
| chr1:40740228 | A | G | 290 | a0001c0001t0001g0013 a0001c0001t0001g0020 a0001c0001t0001g0139 others(287): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.105+1280A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 2/9 | chr1 | 40740228 | |||||||
| chr1:40740252 | C | T | 14 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 others(11): Show |
14 | HG00738.hp1 HG01071.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.105+1304C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 2/9 | chr1 | 40740252 | |||||||
| chr1:40740260 | T | C | 3 | a0001c0001t0002g0023 a0001c0001t0002g0024 a0001c0001t0002g0025 |
3 | HG00423.hp1 HG02135.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.105+1312T>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 2/9 | chr1 | 40740260 | |||||||
| chr1:40740409 | TAATGA | T | 195 | a0001c0001t0001g0013 a0001c0001t0001g0139 a0001c0001t0001g0140 others(192): Show |
199 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.105+1470_105+1474d others(7): Show |
NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 40740409 | ||||||
| chr1:40740803 | A | G | 12 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0108 others(9): Show |
14 | HG01168.hp2 HG01169.hp2 HG01175.hp1 others(11): Show |
intron_variant | MODIFIER | c.105+1855A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 2/9 | chr1 | 40740803 | |||||||
| chr1:40740912 | G | C | 1 | a0001c0001t0001g0290 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.105+1964G>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 2/9 | chr1 | 40740912 | |||||||
| chr1:40740968 | G | A | 59 | a0001c0002t0001g0132 a0001c0002t0001g0149 a0001c0002t0001g0151 others(56): Show |
59 | HG00140.hp1 HG00642.hp1 HG01074.hp2 others(56): Show |
intron_variant | MODIFIER | c.105+2020G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 2/9 | chr1 | 40740968 | |||||||
| chr1:40741054 | T | G | 2 | a0001c0001t0001g0246 a0001c0001t0001g0251 |
2 | NA19056.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.105+2106T>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 2/9 | chr1 | 40741054 | |||||||
| chr1:40741149 | G | A | 4 | a0001c0002t0001g0222 a0001c0002t0001g0265 a0001c0002t0001g0266 others(1): Show |
4 | HG02257.hp1 HG02559.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.105+2201G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 2/9 | chr1 | 40741149 | |||||||
| chr1:40741176 | A | G | 3 | a0001c0003t0001g0100 a0001c0003t0001g0101 a0001c0003t0001g0102 |
3 | HG03540.hp1 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.105+2228A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 2/9 | chr1 | 40741176 | |||||||
| chr1:40741333 | G | C | 1 | a0001c0001t0002g0030 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.105+2385G>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 2/9 | chr1 | 40741333 | |||||||
| chr1:40741486 | G | C | 1 | a0001c0001t0001g0285 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.105+2538G>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 2/9 | chr1 | 40741486 | |||||||
| chr1:40741523 | C | T | 2 | a0001c0001t0006g0050 a0001c0002t0001g0154 |
2 | HG00280.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.105+2575C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 2/9 | chr1 | 40741523 | |||||||
| chr1:40741814 | G | A | 1 | a0001c0002t0001g0286 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.105+2866G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 2/9 | chr1 | 40741814 | |||||||
| chr1:40741930 | G | A | 5 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(2): Show |
5 | HG00738.hp1 HG01071.hp2 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.105+2982G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 2/9 | chr1 | 40741930 | |||||||
| chr1:40742237 | A | G | 1 | a0001c0001t0002g0070 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.105+3289A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 2/9 | chr1 | 40742237 | |||||||
| chr1:40742489 | T | C | 1 | a0001c0002t0001g0256 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.105+3541T>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 2/9 | chr1 | 40742489 | |||||||
| chr1:40742709 | A | G | 90 | a0001c0001t0001g0020 a0001c0001t0002g0001 a0001c0001t0002g0002 others(87): Show |
96 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.105+3761A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 2/9 | chr1 | 40742709 | |||||||
| chr1:40742713 | T | C | 1 | a0001c0002t0001g0169 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.105+3765T>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 2/9 | chr1 | 40742713 | |||||||
| chr1:40742756 | A | G | 290 | a0001c0001t0001g0013 a0001c0001t0001g0020 a0001c0001t0001g0139 others(287): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.105+3808A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 2/9 | chr1 | 40742756 | |||||||
| chr1:40742811 | C | T | 1 | a0001c0001t0001g0309 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.105+3863C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 2/9 | chr1 | 40742811 | |||||||
| chr1:40742827 | T | A | 1 | a0001c0001t0002g0015 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.105+3879T>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 2/9 | chr1 | 40742827 | |||||||
| chr1:40742888 | A | G | 1 | a0001c0001t0007g0293 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.105+3940A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 2/9 | chr1 | 40742888 | |||||||
| chr1:40742980 | T | A | 4 | a0001c0001t0002g0058 a0001c0001t0002g0065 a0001c0001t0002g0074 others(1): Show |
4 | NA18957.hp1 NA18966.hp2 NA18991.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+4032T>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 2/9 | chr1 | 40742980 | |||||||
| chr1:40743201 | A | G | 2 | a0001c0001t0004g0104 a0001c0001t0004g0105 |
2 | HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.105+4253A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 2/9 | chr1 | 40743201 | |||||||
| chr1:40743230 | G | A | 1 | a0001c0001t0002g0057 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.105+4282G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 2/9 | chr1 | 40743230 | |||||||
| chr1:40743467 | T | C | 3 | a0001c0002t0001g0265 a0001c0002t0001g0266 a0001c0002t0001g0267 |
3 | HG02257.hp1 HG02559.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.106-4067T>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 2/9 | chr1 | 40743467 | |||||||
| chr1:40743700 | G | A | 1 | a0001c0002t0001g0174 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.106-3834G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 2/9 | chr1 | 40743700 | |||||||
| chr1:40744116 | T | C | 290 | a0001c0001t0001g0013 a0001c0001t0001g0020 a0001c0001t0001g0139 others(287): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.106-3418T>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 2/9 | chr1 | 40744116 | |||||||
| chr1:40744361 | A | G | 5 | a0001c0001t0001g0270 a0001c0001t0001g0275 a0001c0001t0001g0276 others(2): Show |
5 | HG00099.hp1 HG00738.hp2 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.106-3173A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 2/9 | chr1 | 40744361 | |||||||
| chr1:40744379 | C | G | 1 | a0001c0001t0001g0294 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.106-3155C>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 2/9 | chr1 | 40744379 | |||||||
| chr1:40744673 | T | C | 1 | a0001c0001t0001g0309 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.106-2861T>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 2/9 | chr1 | 40744673 | |||||||
| chr1:40745399 | A | C | 1 | a0001c0002t0001g0261 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.106-2135A>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 2/9 | chr1 | 40745399 | |||||||
| chr1:40745445 | C | G | 1 | a0001c0001t0001g0010 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.106-2089C>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 2/9 | chr1 | 40745445 | |||||||
| chr1:40745716 | A | G | 1 | a0001c0002t0001g0171 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.106-1818A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 2/9 | chr1 | 40745716 | |||||||
| chr1:40746498 | T | G | 290 | a0001c0001t0001g0013 a0001c0001t0001g0020 a0001c0001t0001g0139 others(287): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.106-1036T>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 2/9 | chr1 | 40746498 | |||||||
| chr1:40746499 | A | C | 290 | a0001c0001t0001g0013 a0001c0001t0001g0020 a0001c0001t0001g0139 others(287): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.106-1035A>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 2/9 | chr1 | 40746499 | |||||||
| chr1:40746598 | T | G | 1 | a0001c0001t0001g0148 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.106-936T>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 2/9 | chr1 | 40746598 | |||||||
| chr1:40746935 | A | G | 2 | a0001c0001t0004g0104 a0001c0001t0004g0105 |
2 | HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.106-599A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 2/9 | chr1 | 40746935 | |||||||
| chr1:40747198 | GA | G | 284 | a0001c0001t0001g0013 a0001c0001t0001g0020 a0001c0001t0001g0139 others(281): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.106-327delA | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 40747198 | ||||||
| chr1:40747198 | GAA | G | 6 | a0001c0001t0001g0232 a0001c0002t0001g0234 a0001c0002t0001g0239 others(3): Show |
6 | HG00642.hp2 HG01099.hp2 HG01109.hp1 others(3): Show |
intron_variant | MODIFIER | c.106-328_106-327del others(2): Show |
NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 40747198 | ||||||
| chr1:40747218 | A | C | 1 | a0001c0001t0001g0148 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.106-316A>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 2/9 | chr1 | 40747218 | |||||||
| chr1:40747233 | G | A | 1 | a0001c0002t0001g0099 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.106-301G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 2/9 | chr1 | 40747233 | |||||||
| chr1:40747244 | G | GA | 281 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(278): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.106-275dupA | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 40747244 | ||||||
| chr1:40747244 | G | GAA | 8 | a0001c0001t0001g0290 a0001c0001t0002g0024 a0001c0001t0002g0086 others(5): Show |
8 | HG01243.hp2 HG02135.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.106-276_106-275dup others(2): Show |
NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 40747244 | ||||||
| chr1:40747278 | G | A | 290 | a0001c0001t0001g0013 a0001c0001t0001g0020 a0001c0001t0001g0139 others(287): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.106-256G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 2/9 | chr1 | 40747278 | |||||||
| chr1:40747290 | A | G | 90 | a0001c0001t0001g0020 a0001c0001t0002g0001 a0001c0001t0002g0002 others(87): Show |
96 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.106-244A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 2/9 | chr1 | 40747290 | |||||||
| chr1:40747292 | C | T | 1 | a0001c0004t0001g0014 | 2 | HG01943.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.106-242C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 2/9 | chr1 | 40747292 | |||||||
| chr1:40747296 | G | GT | 27 | a0001c0001t0001g0013 a0001c0001t0001g0148 a0001c0001t0001g0269 others(24): Show |
28 | HG00099.hp1 HG00639.hp2 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.106-236dupT | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 40747296 | ||||||
| chr1:40747370 | T | A | 4 | a0001c0001t0003g0138 a0001c0001t0003g0271 a0001c0001t0003g0279 others(1): Show |
4 | HG00639.hp2 HG02622.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.106-164T>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 2/9 | chr1 | 40747370 | |||||||
| chr1:40747488 | T | C | 4 | a0001c0001t0002g0043 a0001c0001t0002g0044 a0001c0001t0002g0071 others(1): Show |
4 | HG00558.hp2 HG00597.hp2 HG02083.hp2 others(1): Show |
intron_variant | MODIFIER | c.106-46T>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 2/9 | chr1 | 40747488 | |||||||
| chr1:40747774 | G | C | 11 | a0001c0002t0001g0193 a0001c0002t0001g0194 a0001c0002t0001g0195 others(8): Show |
11 | HG01069.hp2 HG02109.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.177+169G>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 3/9 | chr1 | 40747774 | |||||||
| chr1:40747802 | T | C | 4 | a0001c0002t0001g0213 a0001c0002t0001g0242 a0001c0002t0001g0244 others(1): Show |
4 | HG00423.hp2 NA18949.hp1 NA18972.hp1 others(1): Show |
intron_variant | MODIFIER | c.177+197T>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 3/9 | chr1 | 40747802 | |||||||
| chr1:40747818 | G | A | 2 | a0001c0002t0001g0134 a0001c0002t0001g0135 |
2 | HG01081.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.177+213G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 3/9 | chr1 | 40747818 | |||||||
| chr1:40747820 | T | G | 3 | a0001c0001t0001g0292 a0001c0001t0001g0294 a0001c0001t0007g0293 |
3 | HG02630.hp1 HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.177+215T>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 3/9 | chr1 | 40747820 | |||||||
| chr1:40747841 | G | GT | 12 | a0001c0001t0002g0016 a0001c0001t0002g0018 a0001c0001t0002g0019 others(9): Show |
12 | HG01346.hp1 HG02027.hp2 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.177+252dupT | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr1 | 40747841 | ||||||
| chr1:40747841 | GT | G | 13 | a0001c0001t0010g0107 a0001c0002t0001g0193 a0001c0002t0001g0194 others(10): Show |
13 | HG01069.hp2 HG01256.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.177+252delT | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr1 | 40747841 | ||||||
| chr1:40747876 | T | C | 90 | a0001c0001t0001g0020 a0001c0001t0002g0001 a0001c0001t0002g0002 others(87): Show |
96 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.177+271T>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 3/9 | chr1 | 40747876 | |||||||
| chr1:40747883 | C | T | 3 | a0001c0003t0001g0100 a0001c0003t0001g0101 a0001c0003t0001g0102 |
3 | HG03540.hp1 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.177+278C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 3/9 | chr1 | 40747883 | |||||||
| chr1:40747923 | C | T | 1 | a0001c0002t0001g0255 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.177+318C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 3/9 | chr1 | 40747923 | |||||||
| chr1:40747980 | C | T | 9 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 others(6): Show |
9 | HG02258.hp2 HG02630.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.177+375C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 3/9 | chr1 | 40747980 | |||||||
| chr1:40747994 | C | G | 11 | a0001c0002t0001g0193 a0001c0002t0001g0194 a0001c0002t0001g0195 others(8): Show |
11 | HG01069.hp2 HG02109.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.177+389C>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 3/9 | chr1 | 40747994 | |||||||
| chr1:40748122 | C | T | 1 | a0001c0001t0010g0107 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.177+517C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 3/9 | chr1 | 40748122 | |||||||
| chr1:40748125 | C | T | 2 | a0001c0002t0001g0185 a0001c0002t0001g0186 |
2 | HG01515.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.177+520C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 3/9 | chr1 | 40748125 | |||||||
| chr1:40748289 | G | A | 1 | a0001c0002t0001g0230 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.177+684G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 3/9 | chr1 | 40748289 | |||||||
| chr1:40748308 | G | GT | 7 | a0001c0001t0001g0111 a0001c0001t0001g0270 a0001c0001t0001g0272 others(4): Show |
7 | HG00099.hp1 HG00738.hp2 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.177+710dupT | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr1 | 40748308 | ||||||
| chr1:40748519 | C | T | 90 | a0001c0001t0001g0020 a0001c0001t0002g0001 a0001c0001t0002g0002 others(87): Show |
96 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.177+914C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 3/9 | chr1 | 40748519 | |||||||
| chr1:40748897 | G | A | 3 | a0001c0002t0001g0206 a0001c0002t0001g0221 a0001c0002t0001g0226 |
3 | HG01934.hp1 HG01993.hp2 NA18956.hp2 |
intron_variant | MODIFIER | c.178-676G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 3/9 | chr1 | 40748897 | |||||||
| chr1:40749060 | T | C | 1 | a0001c0001t0002g0063 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.178-513T>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 3/9 | chr1 | 40749060 | |||||||
| chr1:40749115 | A | G | 1 | a0001c0001t0005g0318 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.178-458A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 3/9 | chr1 | 40749115 | |||||||
| chr1:40749403 | T | A | 83 | a0001c0001t0001g0232 a0001c0001t0001g0246 a0001c0001t0001g0251 others(80): Show |
85 | HG00280.hp1 HG00423.hp2 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.178-170T>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 3/9 | chr1 | 40749403 | |||||||
| chr1:40749493 | A | G | 3 | a0001c0003t0001g0100 a0001c0003t0001g0101 a0001c0003t0001g0102 |
3 | HG03540.hp1 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.178-80A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 3/9 | chr1 | 40749493 | |||||||
| chr1:40749761 | GAAAGATT others(16): Show |
G | 3 | a0001c0001t0001g0272 a0001c0001t0005g0318 a0001c0001t0010g0107 |
3 | HG02109.hp2 HG03139.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.291+119_291+141del others(23): Show |
NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr1 | 40749761 | ||||||
| chr1:40749840 | T | G | 1 | a0001c0002t0001g0315 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.291+154T>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 4/9 | chr1 | 40749840 | |||||||
| chr1:40749844 | G | C | 1 | a0001c0001t0001g0309 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.291+158G>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 4/9 | chr1 | 40749844 | |||||||
| chr1:40749900 | G | A | 1 | a0001c0001t0002g0076 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.291+214G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 4/9 | chr1 | 40749900 | |||||||
| chr1:40750031 | C | T | 94 | a0001c0001t0001g0232 a0001c0001t0001g0246 a0001c0001t0001g0251 others(91): Show |
96 | HG00280.hp1 HG00423.hp2 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.291+345C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 4/9 | chr1 | 40750031 | |||||||
| chr1:40750036 | T | A | 291 | a0001c0001t0001g0013 a0001c0001t0001g0020 a0001c0001t0001g0121 others(288): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.291+350T>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 4/9 | chr1 | 40750036 | |||||||
| chr1:40750183 | G | A | 2 | a0001c0001t0002g0004 a0001c0001t0002g0091 |
3 | NA18945.hp1 NA19068.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.291+497G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 4/9 | chr1 | 40750183 | |||||||
| chr1:40750353 | T | A | 1 | a0001c0002t0001g0238 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.291+667T>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 4/9 | chr1 | 40750353 | |||||||
| chr1:40750430 | C | G | 2 | a0001c0002t0001g0181 a0001c0002t0001g0183 |
2 | HG01891.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.291+744C>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 4/9 | chr1 | 40750430 | |||||||
| chr1:40750482 | A | G | 14 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 others(11): Show |
14 | HG00738.hp1 HG01071.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.291+796A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 4/9 | chr1 | 40750482 | |||||||
| chr1:40750587 | TAAAGCAA others(2): Show |
T | 90 | a0001c0001t0001g0020 a0001c0001t0002g0001 a0001c0001t0002g0002 others(87): Show |
96 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.291+913_291+921del others(9): Show |
NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr1 | 40750587 | ||||||
| chr1:40750685 | G | A | 1 | a0001c0002t0001g0187 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.291+999G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 4/9 | chr1 | 40750685 | |||||||
| chr1:40750761 | A | G | 1 | a0001c0002t0001g0191 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.291+1075A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 4/9 | chr1 | 40750761 | |||||||
| chr1:40750887 | G | A | 1 | a0001c0004t0001g0014 | 2 | HG01943.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.291+1201G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 4/9 | chr1 | 40750887 | |||||||
| chr1:40750908 | T | G | 81 | a0001c0001t0001g0232 a0001c0001t0001g0246 a0001c0001t0001g0251 others(78): Show |
83 | HG00280.hp1 HG00423.hp2 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.291+1222T>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 4/9 | chr1 | 40750908 | |||||||
| chr1:40751277 | AAATT | A | 3 | a0001c0002t0001g0093 a0001c0002t0001g0255 a0001c0002t0001g0286 |
3 | HG03669.hp2 HG03831.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.291+1593_291+1596d others(6): Show |
NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr1 | 40751277 | ||||||
| chr1:40751331 | A | G | 1 | a0001c0001t0002g0316 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.291+1645A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 4/9 | chr1 | 40751331 | |||||||
| chr1:40751372 | T | A | 1 | a0001c0001t0001g0309 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.291+1686T>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 4/9 | chr1 | 40751372 | |||||||
| chr1:40751428 | T | C | 90 | a0001c0001t0001g0020 a0001c0001t0002g0001 a0001c0001t0002g0002 others(87): Show |
96 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.292-1723T>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 4/9 | chr1 | 40751428 | |||||||
| chr1:40751495 | T | A | 2 | a0001c0001t0004g0104 a0001c0001t0004g0105 |
2 | HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.292-1656T>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 4/9 | chr1 | 40751495 | |||||||
| chr1:40751718 | A | G | 90 | a0001c0001t0001g0020 a0001c0001t0002g0001 a0001c0001t0002g0002 others(87): Show |
96 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.292-1433A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 4/9 | chr1 | 40751718 | |||||||
| chr1:40751749 | A | T | 3 | a0001c0003t0001g0100 a0001c0003t0001g0101 a0001c0003t0001g0102 |
3 | HG03540.hp1 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.292-1402A>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 4/9 | chr1 | 40751749 | |||||||
| chr1:40751813 | A | T | 90 | a0001c0001t0001g0020 a0001c0001t0002g0001 a0001c0001t0002g0002 others(87): Show |
96 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.292-1338A>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 4/9 | chr1 | 40751813 | |||||||
| chr1:40751902 | T | C | 1 | a0001c0001t0001g0120 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.292-1249T>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 4/9 | chr1 | 40751902 | |||||||
| chr1:40752035 | C | T | 3 | a0001c0003t0001g0100 a0001c0003t0001g0101 a0001c0003t0001g0102 |
3 | HG03540.hp1 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.292-1116C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 4/9 | chr1 | 40752035 | |||||||
| chr1:40752054 | G | T | 1 | a0001c0001t0001g0309 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.292-1097G>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 4/9 | chr1 | 40752054 | |||||||
| chr1:40752221 | C | G | 1 | a0001c0002t0001g0169 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.292-930C>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 4/9 | chr1 | 40752221 | |||||||
| chr1:40752377 | A | G | 1 | a0001c0002t0001g0216 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.292-774A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 4/9 | chr1 | 40752377 | |||||||
| chr1:40752539 | C | G | 1 | a0001c0001t0001g0148 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.292-612C>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 4/9 | chr1 | 40752539 | |||||||
| chr1:40752782 | G | A | 83 | a0001c0001t0001g0232 a0001c0001t0001g0246 a0001c0001t0001g0251 others(80): Show |
85 | HG00280.hp1 HG00423.hp2 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.292-369G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 4/9 | chr1 | 40752782 | |||||||
| chr1:40752907 | T | C | 5 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(2): Show |
5 | HG00738.hp1 HG01071.hp2 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.292-244T>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 4/9 | chr1 | 40752907 | |||||||
| chr1:40752925 | A | G | 1 | a0001c0001t0001g0113 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.292-226A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 4/9 | chr1 | 40752925 | |||||||
| chr1:40753032 | A | G | 1 | a0001c0002t0001g0245 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.292-119A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 4/9 | chr1 | 40753032 | |||||||
| chr1:40753040 | G | T | 1 | a0001c0002t0001g0311 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.292-111G>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 4/9 | chr1 | 40753040 | |||||||
| chr1:40753116 | A | G | 3 | a0001c0003t0001g0100 a0001c0003t0001g0101 a0001c0003t0001g0102 |
3 | HG03540.hp1 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.292-35A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 4/9 | chr1 | 40753116 | |||||||
| chr1:40753252 | C | T | 1 | a0001c0002t0001g0179 | 1 | HG02622.hp2 | splice_region_variant&intron_variant | LOW | c.387+6C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 5/9 | chr1 | 40753252 | |||||||
| chr1:40753287 | C | T | 5 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 others(2): Show |
5 | HG02258.hp2 HG02976.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.387+41C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 5/9 | chr1 | 40753287 | |||||||
| chr1:40753301 | G | T | 3 | a0001c0001t0002g0023 a0001c0001t0002g0024 a0001c0001t0002g0025 |
3 | HG00423.hp1 HG02135.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.387+55G>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 5/9 | chr1 | 40753301 | |||||||
| chr1:40753389 | C | A | 1 | a0001c0002t0001g0217 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.387+143C>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 5/9 | chr1 | 40753389 | |||||||
| chr1:40753411 | T | G | 5 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 others(2): Show |
5 | HG02258.hp2 HG02976.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.387+165T>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 5/9 | chr1 | 40753411 | |||||||
| chr1:40753511 | G | A | 10 | a0001c0001t0002g0032 a0001c0001t0002g0036 a0001c0001t0002g0053 others(7): Show |
10 | HG00639.hp1 HG00741.hp1 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.387+265G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 5/9 | chr1 | 40753511 | |||||||
| chr1:40753535 | C | T | 1 | a0001c0001t0010g0107 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.387+289C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 5/9 | chr1 | 40753535 | |||||||
| chr1:40753612 | C | T | 1 | a0001c0001t0004g0105 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.387+366C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 5/9 | chr1 | 40753612 | |||||||
| chr1:40753617 | G | C | 5 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 others(2): Show |
5 | HG02258.hp2 HG02976.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.387+371G>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 5/9 | chr1 | 40753617 | |||||||
| chr1:40753888 | C | T | 1 | a0001c0002t0001g0268 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.387+642C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 5/9 | chr1 | 40753888 | |||||||
| chr1:40753930 | C | T | 1 | a0001c0001t0001g0309 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.387+684C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 5/9 | chr1 | 40753930 | |||||||
| chr1:40754022 | A | G | 4 | a0001c0002t0001g0213 a0001c0002t0001g0242 a0001c0002t0001g0244 others(1): Show |
4 | HG00423.hp2 NA18949.hp1 NA18972.hp1 others(1): Show |
intron_variant | MODIFIER | c.387+776A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 5/9 | chr1 | 40754022 | |||||||
| chr1:40754047 | G | A | 5 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 others(2): Show |
5 | HG02258.hp2 HG02976.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.387+801G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 5/9 | chr1 | 40754047 | |||||||
| chr1:40754405 | C | T | 1 | a0001c0001t0010g0107 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.387+1159C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 5/9 | chr1 | 40754405 | |||||||
| chr1:40754504 | C | G | 2 | a0001c0001t0002g0061 a0001c0001t0002g0085 |
2 | HG01109.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.387+1258C>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 5/9 | chr1 | 40754504 | |||||||
| chr1:40754564 | C | T | 4 | a0001c0001t0002g0028 a0001c0001t0002g0029 a0001c0001t0002g0031 others(1): Show |
4 | NA18980.hp2 NA18993.hp1 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.387+1318C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 5/9 | chr1 | 40754564 | |||||||
| chr1:40754724 | G | A | 290 | a0001c0001t0001g0013 a0001c0001t0001g0020 a0001c0001t0001g0139 others(287): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.387+1478G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 5/9 | chr1 | 40754724 | |||||||
| chr1:40754729 | C | T | 16 | a0001c0001t0002g0030 a0001c0001t0002g0032 a0001c0001t0002g0036 others(13): Show |
16 | HG00639.hp1 HG00741.hp1 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.387+1483C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 5/9 | chr1 | 40754729 | |||||||
| chr1:40754765 | C | T | 1 | a0001c0001t0002g0059 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.387+1519C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 5/9 | chr1 | 40754765 | |||||||
| chr1:40754801 | G | C | 1 | a0001c0002t0001g0235 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.387+1555G>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 5/9 | chr1 | 40754801 | |||||||
| chr1:40754810 | G | A | 2 | a0001c0002t0001g0197 a0001c0002t0001g0198 |
2 | HG03471.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.387+1564G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 5/9 | chr1 | 40754810 | |||||||
| chr1:40754820 | A | T | 3 | a0001c0003t0001g0100 a0001c0003t0001g0101 a0001c0003t0001g0102 |
3 | HG03540.hp1 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.387+1574A>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 5/9 | chr1 | 40754820 | |||||||
| chr1:40754821 | CAG | C | 3 | a0001c0003t0001g0100 a0001c0003t0001g0101 a0001c0003t0001g0102 |
3 | HG03540.hp1 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.387+1576_387+1577d others(4): Show |
NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 5/9 | chr1 | 40754821 | |||||||
| chr1:40754825 | T | A | 3 | a0001c0003t0001g0100 a0001c0003t0001g0101 a0001c0003t0001g0102 |
3 | HG03540.hp1 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.387+1579T>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 5/9 | chr1 | 40754825 | |||||||
| chr1:40754826 | C | T | 3 | a0001c0003t0001g0100 a0001c0003t0001g0101 a0001c0003t0001g0102 |
3 | HG03540.hp1 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.387+1580C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 5/9 | chr1 | 40754826 | |||||||
| chr1:40754833 | C | T | 1 | a0001c0001t0010g0107 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.387+1587C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 5/9 | chr1 | 40754833 | |||||||
| chr1:40754858 | A | G | 1 | a0001c0001t0002g0062 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.387+1612A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 5/9 | chr1 | 40754858 | |||||||
| chr1:40754937 | G | T | 1 | a0001c0002t0001g0315 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.387+1691G>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 5/9 | chr1 | 40754937 | |||||||
| chr1:40755043 | G | A | 1 | a0001c0001t0002g0088 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.387+1797G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 5/9 | chr1 | 40755043 | |||||||
| chr1:40755064 | T | C | 90 | a0001c0001t0001g0020 a0001c0001t0002g0001 a0001c0001t0002g0002 others(87): Show |
96 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.387+1818T>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 5/9 | chr1 | 40755064 | |||||||
| chr1:40755099 | C | T | 90 | a0001c0001t0001g0020 a0001c0001t0002g0001 a0001c0001t0002g0002 others(87): Show |
96 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.387+1853C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 5/9 | chr1 | 40755099 | |||||||
| chr1:40755116 | C | G | 1 | a0001c0001t0002g0096 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.387+1870C>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 5/9 | chr1 | 40755116 | |||||||
| chr1:40755347 | A | G | 1 | a0001c0001t0002g0018 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.387+2101A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 5/9 | chr1 | 40755347 | |||||||
| chr1:40755352 | A | G | 5 | a0001c0001t0001g0269 a0001c0001t0001g0274 a0001c0001t0001g0281 others(2): Show |
5 | HG02559.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.387+2106A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 5/9 | chr1 | 40755352 | |||||||
| chr1:40755624 | G | A | 290 | a0001c0001t0001g0013 a0001c0001t0001g0020 a0001c0001t0001g0139 others(287): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.387+2378G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 5/9 | chr1 | 40755624 | |||||||
| chr1:40756164 | A | G | 3 | a0001c0003t0001g0100 a0001c0003t0001g0101 a0001c0003t0001g0102 |
3 | HG03540.hp1 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.388-1957A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 5/9 | chr1 | 40756164 | |||||||
| chr1:40756191 | C | T | 3 | a0001c0003t0001g0100 a0001c0003t0001g0101 a0001c0003t0001g0102 |
3 | HG03540.hp1 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.388-1930C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 5/9 | chr1 | 40756191 | |||||||
| chr1:40756227 | T | C | 290 | a0001c0001t0001g0013 a0001c0001t0001g0020 a0001c0001t0001g0139 others(287): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.388-1894T>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 5/9 | chr1 | 40756227 | |||||||
| chr1:40756258 | G | A | 1 | a0001c0001t0002g0316 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.388-1863G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 5/9 | chr1 | 40756258 | |||||||
| chr1:40756543 | C | T | 3 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0001t0002g0035 |
3 | HG00099.hp2 HG01192.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.388-1578C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 5/9 | chr1 | 40756543 | |||||||
| chr1:40756641 | G | C | 1 | a0001c0001t0001g0309 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.388-1480G>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 5/9 | chr1 | 40756641 | |||||||
| chr1:40756826 | C | T | 1 | a0001c0001t0002g0006 | 2 | NA18954.hp2 NA18965.hp2 |
intron_variant | MODIFIER | c.388-1295C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 5/9 | chr1 | 40756826 | |||||||
| chr1:40756857 | A | G | 1 | a0001c0001t0001g0309 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.388-1264A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 5/9 | chr1 | 40756857 | |||||||
| chr1:40756910 | C | T | 1 | a0001c0002t0001g0162 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.388-1211C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 5/9 | chr1 | 40756910 | |||||||
| chr1:40757086 | C | T | 1 | a0001c0002t0001g0155 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.388-1035C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 5/9 | chr1 | 40757086 | |||||||
| chr1:40757153 | A | G | 1 | a0001c0001t0010g0107 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.388-968A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 5/9 | chr1 | 40757153 | |||||||
| chr1:40757217 | C | T | 26 | a0001c0001t0001g0013 a0001c0001t0001g0269 a0001c0001t0001g0270 others(23): Show |
27 | HG00099.hp1 HG00639.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.388-904C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 5/9 | chr1 | 40757217 | |||||||
| chr1:40757413 | C | T | 1 | a0001c0004t0001g0014 | 2 | HG01943.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.388-708C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 5/9 | chr1 | 40757413 | |||||||
| chr1:40757488 | C | T | 5 | a0001c0002t0001g0207 a0001c0002t0001g0215 a0001c0002t0001g0233 others(2): Show |
5 | NA18967.hp2 NA18968.hp2 NA18973.hp1 others(2): Show |
intron_variant | MODIFIER | c.388-633C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 5/9 | chr1 | 40757488 | |||||||
| chr1:40757636 | G | T | 3 | a0001c0003t0001g0100 a0001c0003t0001g0101 a0001c0003t0001g0102 |
3 | HG03540.hp1 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.388-485G>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 5/9 | chr1 | 40757636 | |||||||
| chr1:40757742 | G | A | 142 | a0001c0001t0001g0232 a0001c0001t0001g0246 a0001c0001t0001g0251 others(139): Show |
144 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.388-379G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 5/9 | chr1 | 40757742 | |||||||
| chr1:40757784 | C | T | 5 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(2): Show |
5 | HG00738.hp1 HG01071.hp2 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.388-337C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 5/9 | chr1 | 40757784 | |||||||
| chr1:40757840 | G | A | 1 | a0001c0001t0001g0129 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.388-281G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 5/9 | chr1 | 40757840 | |||||||
| chr1:40757871 | G | A | 1 | a0001c0002t0001g0314 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.388-250G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 5/9 | chr1 | 40757871 | |||||||
| chr1:40758336 | C | T | 90 | a0001c0001t0001g0020 a0001c0001t0002g0001 a0001c0001t0002g0002 others(87): Show |
96 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.561+42C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 6/9 | chr1 | 40758336 | |||||||
| chr1:40758566 | A | G | 2 | a0001c0001t0010g0107 a0001c0002t0001g0240 |
2 | NA18994.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.561+272A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 6/9 | chr1 | 40758566 | |||||||
| chr1:40758899 | T | C | 1 | a0001c0001t0001g0309 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.561+605T>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 6/9 | chr1 | 40758899 | |||||||
| chr1:40758950 | T | G | 1 | a0001c0001t0001g0309 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.561+656T>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 6/9 | chr1 | 40758950 | |||||||
| chr1:40759233 | T | TA | 171 | a0001c0001t0001g0020 a0001c0001t0001g0232 a0001c0001t0001g0246 others(168): Show |
179 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.561+955dupA | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr1 | 40759233 | ||||||
| chr1:40759234 | A | T | 1 | a0001c0002t0001g0173 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.561+940A>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 6/9 | chr1 | 40759234 | |||||||
| chr1:40759251 | G | T | 142 | a0001c0001t0001g0232 a0001c0001t0001g0246 a0001c0001t0001g0251 others(139): Show |
144 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.561+957G>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 6/9 | chr1 | 40759251 | |||||||
| chr1:40759362 | T | C | 94 | a0001c0001t0001g0020 a0001c0001t0002g0001 a0001c0001t0002g0002 others(91): Show |
100 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.561+1068T>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 6/9 | chr1 | 40759362 | |||||||
| chr1:40759421 | A | G | 1 | a0001c0004t0001g0014 | 2 | HG01943.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.561+1127A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 6/9 | chr1 | 40759421 | |||||||
| chr1:40759512 | G | A | 3 | a0001c0003t0001g0100 a0001c0003t0001g0101 a0001c0003t0001g0102 |
3 | HG03540.hp1 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.561+1218G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 6/9 | chr1 | 40759512 | |||||||
| chr1:40759548 | A | G | 1 | a0001c0001t0001g0281 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.561+1254A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 6/9 | chr1 | 40759548 | |||||||
| chr1:40759559 | A | ATG | 186 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 others(183): Show |
189 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.561+1281_561+1282d others(4): Show |
NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr1 | 40759559 | ||||||
| chr1:40759559 | A | ATGTG | 95 | a0001c0001t0001g0020 a0001c0001t0002g0001 a0001c0001t0002g0002 others(92): Show |
101 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.561+1279_561+1282d others(6): Show |
NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr1 | 40759559 | ||||||
| chr1:40759567 | GTGTGTGT others(3): Show |
G | 4 | a0001c0001t0001g0013 a0001c0001t0001g0287 a0001c0001t0001g0288 others(1): Show |
5 | NA18952.hp2 NA18967.hp1 NA18995.hp2 others(2): Show |
intron_variant | MODIFIER | c.561+1283_561+1292d others(12): Show |
NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr1 | 40759567 | ||||||
| chr1:40759682 | A | C | 115 | a0001c0001t0001g0020 a0001c0001t0001g0246 a0001c0001t0001g0251 others(112): Show |
122 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.561+1388A>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 6/9 | chr1 | 40759682 | |||||||
| chr1:40759780 | G | A | 1 | a0001c0001t0001g0010 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.561+1486G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 6/9 | chr1 | 40759780 | |||||||
| chr1:40759848 | C | T | 30 | a0001c0001t0001g0013 a0001c0001t0001g0269 a0001c0001t0001g0270 others(27): Show |
32 | HG00099.hp1 HG00639.hp2 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.561+1554C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 6/9 | chr1 | 40759848 | |||||||
| chr1:40760187 | C | T | 1 | a0001c0001t0010g0107 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.561+1893C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 6/9 | chr1 | 40760187 | |||||||
| chr1:40760225 | G | A | 1 | a0001c0001t0001g0281 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.561+1931G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 6/9 | chr1 | 40760225 | |||||||
| chr1:40760294 | C | T | 1 | a0001c0001t0002g0040 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.561+2000C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 6/9 | chr1 | 40760294 | |||||||
| chr1:40760295 | G | A | 1 | a0001c0004t0001g0014 | 2 | HG01943.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.561+2001G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 6/9 | chr1 | 40760295 | |||||||
| chr1:40760479 | G | A | 165 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 others(162): Show |
168 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(165): Show |
intron_variant | MODIFIER | c.561+2185G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 6/9 | chr1 | 40760479 | |||||||
| chr1:40760487 | G | A | 1 | a0001c0001t0001g0287 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.561+2193G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 6/9 | chr1 | 40760487 | |||||||
| chr1:40760496 | G | A | 1 | a0001c0001t0007g0293 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.561+2202G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 6/9 | chr1 | 40760496 | |||||||
| chr1:40760538 | G | A | 1 | a0001c0004t0001g0014 | 2 | HG01943.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.561+2244G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 6/9 | chr1 | 40760538 | |||||||
| chr1:40760587 | C | T | 1 | a0001c0002t0001g0195 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.561+2293C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 6/9 | chr1 | 40760587 | |||||||
| chr1:40760611 | C | T | 1 | a0001c0001t0006g0050 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.562-2277C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 6/9 | chr1 | 40760611 | |||||||
| chr1:40760717 | C | CA | 29 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0119 others(26): Show |
31 | HG00099.hp1 HG00639.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.562-2158dupA | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr1 | 40760717 | ||||||
| chr1:40760719 | A | G | 4 | a0001c0001t0002g0043 a0001c0001t0002g0044 a0001c0001t0002g0071 others(1): Show |
4 | HG00558.hp2 HG00597.hp2 HG02083.hp2 others(1): Show |
intron_variant | MODIFIER | c.562-2169A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 6/9 | chr1 | 40760719 | |||||||
| chr1:40760781 | A | G | 8 | a0001c0001t0001g0270 a0001c0001t0001g0272 a0001c0001t0001g0273 others(5): Show |
8 | HG00099.hp1 HG00738.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.562-2107A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 6/9 | chr1 | 40760781 | |||||||
| chr1:40760842 | G | C | 1 | a0001c0001t0001g0285 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.562-2046G>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 6/9 | chr1 | 40760842 | |||||||
| chr1:40760930 | G | A | 58 | a0001c0002t0001g0132 a0001c0002t0001g0149 a0001c0002t0001g0151 others(55): Show |
58 | HG00140.hp1 HG00642.hp1 HG01074.hp2 others(55): Show |
intron_variant | MODIFIER | c.562-1958G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 6/9 | chr1 | 40760930 | |||||||
| chr1:40761238 | C | T | 1 | a0001c0002t0001g0312 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.562-1650C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 6/9 | chr1 | 40761238 | |||||||
| chr1:40761655 | G | T | 90 | a0001c0001t0001g0020 a0001c0001t0002g0001 a0001c0001t0002g0002 others(87): Show |
96 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.562-1233G>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 6/9 | chr1 | 40761655 | |||||||
| chr1:40761750 | G | A | 1 | a0001c0002t0001g0171 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.562-1138G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 6/9 | chr1 | 40761750 | |||||||
| chr1:40762050 | G | A | 5 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(2): Show |
5 | HG00738.hp1 HG01071.hp2 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.562-838G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 6/9 | chr1 | 40762050 | |||||||
| chr1:40762548 | G | A | 1 | a0001c0001t0001g0127 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.562-340G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 6/9 | chr1 | 40762548 | |||||||
| chr1:40762571 | C | T | 3 | a0001c0003t0001g0100 a0001c0003t0001g0101 a0001c0003t0001g0102 |
3 | HG03540.hp1 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.562-317C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 6/9 | chr1 | 40762571 | |||||||
| chr1:40762727 | G | A | 3 | a0001c0003t0001g0100 a0001c0003t0001g0101 a0001c0003t0001g0102 |
3 | HG03540.hp1 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.562-161G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 6/9 | chr1 | 40762727 | |||||||
| chr1:40762744 | T | C | 2 | a0001c0001t0004g0104 a0001c0001t0004g0105 |
2 | HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.562-144T>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 6/9 | chr1 | 40762744 | |||||||
| chr1:40762771 | C | G | 290 | a0001c0001t0001g0013 a0001c0001t0001g0020 a0001c0001t0001g0139 others(287): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.562-117C>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 6/9 | chr1 | 40762771 | |||||||
| chr1:40762828 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.562-60G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 6/9 | chr1 | 40762828 | |||||||
| chr1:40762868 | C | G | 1 | a0001c0001t0001g0130 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.562-20C>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 6/9 | chr1 | 40762868 | |||||||
| chr1:40763101 | GATATATA others(57): Show |
G | 1 | a0001c0001t0001g0112 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.720+80_720+143delG others(63): Show |
NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr1 | 40763101 | ||||||
| chr1:40763152 | G | GTATATCT others(25): Show |
2 | a0001c0001t0002g0078 a0001c0001t0002g0087 |
2 | HG02615.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.720+144_720+175dup others(32): Show |
NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr1 | 40763152 | ||||||
| chr1:40763184 | A | G | 1 | a0001c0002t0001g0200 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.720+138A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 7/9 | chr1 | 40763184 | |||||||
| chr1:40763196 | C | CTA | 3 | a0001c0001t0001g0292 a0001c0001t0001g0294 a0001c0001t0007g0293 |
3 | HG02630.hp1 HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.720+159_720+160dup others(2): Show |
NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr1 | 40763196 | ||||||
| chr1:40763199 | T | G | 1 | a0001c0001t0010g0107 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.720+153T>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 7/9 | chr1 | 40763199 | |||||||
| chr1:40763226 | G | A | 290 | a0001c0001t0001g0013 a0001c0001t0001g0020 a0001c0001t0001g0139 others(287): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.720+180G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 7/9 | chr1 | 40763226 | |||||||
| chr1:40763256 | A | ATAGCTAT others(25): Show |
1 | a0001c0001t0001g0309 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.720+240_720+271dup others(32): Show |
NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr1 | 40763256 | ||||||
| chr1:40763288 | G | A | 94 | a0001c0001t0001g0020 a0001c0001t0002g0001 a0001c0001t0002g0002 others(91): Show |
100 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.720+242G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 7/9 | chr1 | 40763288 | |||||||
| chr1:40763307 | G | T | 2 | a0001c0001t0004g0104 a0001c0001t0004g0105 |
2 | HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.720+261G>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 7/9 | chr1 | 40763307 | |||||||
| chr1:40763317 | T | G | 2 | a0001c0001t0001g0282 a0001c0001t0010g0107 |
2 | HG02630.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.720+271T>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 7/9 | chr1 | 40763317 | |||||||
| chr1:40763450 | G | T | 90 | a0001c0001t0001g0020 a0001c0001t0002g0001 a0001c0001t0002g0002 others(87): Show |
96 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.720+404G>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 7/9 | chr1 | 40763450 | |||||||
| chr1:40763471 | C | T | 1 | a0001c0001t0001g0309 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.720+425C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 7/9 | chr1 | 40763471 | |||||||
| chr1:40763472 | G | T | 5 | a0001c0001t0001g0269 a0001c0001t0001g0274 a0001c0001t0001g0281 others(2): Show |
5 | HG02559.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.720+426G>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 7/9 | chr1 | 40763472 | |||||||
| chr1:40763508 | G | A | 290 | a0001c0001t0001g0013 a0001c0001t0001g0020 a0001c0001t0001g0139 others(287): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.720+462G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 7/9 | chr1 | 40763508 | |||||||
| chr1:40763594 | G | A | 1 | a0001c0001t0002g0023 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.720+548G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 7/9 | chr1 | 40763594 | |||||||
| chr1:40763710 | G | A | 1 | a0001c0001t0002g0067 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.720+664G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 7/9 | chr1 | 40763710 | |||||||
| chr1:40763760 | T | A | 1 | a0001c0001t0002g0041 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.720+714T>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 7/9 | chr1 | 40763760 | |||||||
| chr1:40763775 | A | G | 1 | a0001c0001t0001g0121 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.720+729A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 7/9 | chr1 | 40763775 | |||||||
| chr1:40763788 | G | A | 47 | a0001c0002t0001g0132 a0001c0002t0001g0149 a0001c0002t0001g0151 others(44): Show |
47 | HG00140.hp1 HG00642.hp1 HG01081.hp1 others(44): Show |
intron_variant | MODIFIER | c.720+742G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 7/9 | chr1 | 40763788 | |||||||
| chr1:40763797 | C | T | 2 | a0001c0002t0001g0161 a0001c0002t0001g0179 |
2 | HG02622.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.720+751C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 7/9 | chr1 | 40763797 | |||||||
| chr1:40763798 | G | A | 1 | a0001c0001t0002g0030 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.720+752G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 7/9 | chr1 | 40763798 | |||||||
| chr1:40763812 | C | G | 3 | a0001c0003t0001g0100 a0001c0003t0001g0101 a0001c0003t0001g0102 |
3 | HG03540.hp1 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.720+766C>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 7/9 | chr1 | 40763812 | |||||||
| chr1:40764115 | C | G | 19 | a0001c0001t0002g0001 a0001c0001t0002g0033 a0001c0001t0002g0034 others(16): Show |
20 | HG00099.hp2 HG00558.hp2 HG00597.hp2 others(17): Show |
intron_variant | MODIFIER | c.720+1069C>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 7/9 | chr1 | 40764115 | |||||||
| chr1:40764286 | C | T | 1 | a0001c0001t0010g0107 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.720+1240C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 7/9 | chr1 | 40764286 | |||||||
| chr1:40764406 | G | A | 2 | a0001c0001t0002g0080 a0001c0002t0001g0179 |
2 | HG02622.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.720+1360G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 7/9 | chr1 | 40764406 | |||||||
| chr1:40764542 | G | A | 91 | a0001c0001t0001g0020 a0001c0001t0002g0001 a0001c0001t0002g0002 others(88): Show |
97 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.720+1496G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 7/9 | chr1 | 40764542 | |||||||
| chr1:40764646 | C | T | 1 | a0001c0002t0001g0312 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.720+1600C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 7/9 | chr1 | 40764646 | |||||||
| chr1:40764673 | C | G | 1 | a0001c0001t0001g0020 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.720+1627C>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 7/9 | chr1 | 40764673 | |||||||
| chr1:40764678 | T | C | 91 | a0001c0001t0001g0020 a0001c0001t0002g0001 a0001c0001t0002g0002 others(88): Show |
97 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.720+1632T>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 7/9 | chr1 | 40764678 | |||||||
| chr1:40764813 | G | A | 1 | a0001c0001t0001g0275 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.720+1767G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 7/9 | chr1 | 40764813 | |||||||
| chr1:40764979 | G | A | 90 | a0001c0001t0001g0020 a0001c0001t0002g0001 a0001c0001t0002g0002 others(87): Show |
96 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.721-1617G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 7/9 | chr1 | 40764979 | |||||||
| chr1:40765078 | C | T | 1 | a0001c0001t0006g0050 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.721-1518C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 7/9 | chr1 | 40765078 | |||||||
| chr1:40765360 | G | A | 90 | a0001c0001t0001g0020 a0001c0001t0002g0001 a0001c0001t0002g0002 others(87): Show |
96 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.721-1236G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 7/9 | chr1 | 40765360 | |||||||
| chr1:40765376 | G | A | 1 | a0001c0002t0001g0296 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.721-1220G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 7/9 | chr1 | 40765376 | |||||||
| chr1:40765385 | C | T | 290 | a0001c0001t0001g0013 a0001c0001t0001g0020 a0001c0001t0001g0139 others(287): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.721-1211C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 7/9 | chr1 | 40765385 | |||||||
| chr1:40765618 | T | C | 1 | a0001c0002t0001g0259 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.721-978T>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 7/9 | chr1 | 40765618 | |||||||
| chr1:40765620 | T | A | 1 | a0001c0002t0001g0259 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.721-976T>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 7/9 | chr1 | 40765620 | |||||||
| chr1:40765621 | C | A | 1 | a0001c0002t0001g0259 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.721-975C>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 7/9 | chr1 | 40765621 | |||||||
| chr1:40765623 | G | A | 1 | a0001c0002t0001g0259 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.721-973G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 7/9 | chr1 | 40765623 | |||||||
| chr1:40765624 | G | A | 1 | a0001c0002t0001g0259 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.721-972G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 7/9 | chr1 | 40765624 | |||||||
| chr1:40765627 | C | T | 1 | a0001c0002t0001g0259 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.721-969C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 7/9 | chr1 | 40765627 | |||||||
| chr1:40765629 | C | A | 1 | a0001c0002t0001g0259 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.721-967C>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 7/9 | chr1 | 40765629 | |||||||
| chr1:40765630 | G | T | 1 | a0001c0002t0001g0259 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.721-966G>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 7/9 | chr1 | 40765630 | |||||||
| chr1:40765631 | C | G | 1 | a0001c0002t0001g0259 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.721-965C>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 7/9 | chr1 | 40765631 | |||||||
| chr1:40765634 | A | T | 1 | a0001c0002t0001g0259 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.721-962A>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 7/9 | chr1 | 40765634 | |||||||
| chr1:40765638 | A | T | 1 | a0001c0002t0001g0259 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.721-958A>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 7/9 | chr1 | 40765638 | |||||||
| chr1:40765639 | G | C | 1 | a0001c0002t0001g0259 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.721-957G>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 7/9 | chr1 | 40765639 | |||||||
| chr1:40765642 | C | T | 1 | a0001c0002t0001g0259 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.721-954C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 7/9 | chr1 | 40765642 | |||||||
| chr1:40765645 | G | A | 1 | a0001c0002t0001g0259 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.721-951G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 7/9 | chr1 | 40765645 | |||||||
| chr1:40765646 | T | TTAGGCTT others(5): Show |
1 | a0001c0002t0001g0259 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.721-950_721-949ins others(12): Show |
NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 7/9 | chr1 | 40765646 | |||||||
| chr1:40765651 | C | T | 1 | a0001c0002t0001g0259 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.721-945C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 7/9 | chr1 | 40765651 | |||||||
| chr1:40765655 | G | C | 1 | a0001c0002t0001g0259 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.721-941G>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 7/9 | chr1 | 40765655 | |||||||
| chr1:40765669 | T | A | 1 | a0001c0002t0001g0259 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.721-927T>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 7/9 | chr1 | 40765669 | |||||||
| chr1:40765674 | T | A | 1 | a0001c0002t0001g0259 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.721-922T>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 7/9 | chr1 | 40765674 | |||||||
| chr1:40765752 | T | C | 290 | a0001c0001t0001g0013 a0001c0001t0001g0020 a0001c0001t0001g0139 others(287): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.721-844T>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 7/9 | chr1 | 40765752 | |||||||
| chr1:40765872 | G | T | 4 | a0001c0002t0001g0200 a0001c0002t0001g0201 a0001c0002t0001g0203 others(1): Show |
4 | HG01069.hp2 HG02886.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.721-724G>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 7/9 | chr1 | 40765872 | |||||||
| chr1:40765996 | G | A | 1 | a0001c0001t0001g0129 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.721-600G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 7/9 | chr1 | 40765996 | |||||||
| chr1:40765998 | G | A | 1 | a0001c0002t0001g0248 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.721-598G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 7/9 | chr1 | 40765998 | |||||||
| chr1:40766044 | A | G | 2 | a0001c0001t0002g0003 a0001c0001t0002g0048 |
3 | HG02683.hp2 HG03540.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.721-552A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 7/9 | chr1 | 40766044 | |||||||
| chr1:40766048 | A | AC | 91 | a0001c0001t0001g0020 a0001c0001t0002g0001 a0001c0001t0002g0002 others(88): Show |
97 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.721-543dupC | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr1 | 40766048 | ||||||
| chr1:40766150 | C | T | 1 | a0001c0002t0001g0136 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.721-446C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 7/9 | chr1 | 40766150 | |||||||
| chr1:40766345 | A | G | 7 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0026 others(4): Show |
9 | HG01123.hp2 HG02015.hp1 HG02056.hp2 others(6): Show |
intron_variant | MODIFIER | c.721-251A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 7/9 | chr1 | 40766345 | |||||||
| chr1:40766522 | T | C | 91 | a0001c0001t0001g0020 a0001c0001t0002g0001 a0001c0001t0002g0002 others(88): Show |
97 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.721-74T>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 7/9 | chr1 | 40766522 | |||||||
| chr1:40766575 | T | C | 1 | a0001c0002t0001g0182 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.721-21T>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 7/9 | chr1 | 40766575 | |||||||
| chr1:40766723 | A | C | 1 | a0001c0001t0010g0107 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.828+20A>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 8/9 | chr1 | 40766723 | |||||||
| chr1:40767212 | T | C | 26 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(23): Show |
30 | HG01069.hp1 HG01071.hp1 HG01168.hp2 others(27): Show |
intron_variant | MODIFIER | c.828+509T>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 8/9 | chr1 | 40767212 | |||||||
| chr1:40767240 | T | C | 1 | a0001c0001t0002g0086 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.828+537T>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 8/9 | chr1 | 40767240 | |||||||
| chr1:40767323 | C | T | 1 | a0001c0001t0002g0046 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.828+620C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 8/9 | chr1 | 40767323 | |||||||
| chr1:40767359 | T | C | 94 | a0001c0001t0001g0020 a0001c0001t0002g0001 a0001c0001t0002g0002 others(91): Show |
100 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.828+656T>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 8/9 | chr1 | 40767359 | |||||||
| chr1:40767397 | G | C | 1 | a0001c0001t0001g0309 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.828+694G>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 8/9 | chr1 | 40767397 | |||||||
| chr1:40767398 | A | T | 1 | a0001c0001t0001g0309 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.828+695A>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 8/9 | chr1 | 40767398 | |||||||
| chr1:40767541 | G | T | 90 | a0001c0001t0001g0020 a0001c0001t0002g0001 a0001c0001t0002g0002 others(87): Show |
96 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.828+838G>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 8/9 | chr1 | 40767541 | |||||||
| chr1:40767542 | C | T | 26 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(23): Show |
30 | HG01069.hp1 HG01071.hp1 HG01168.hp2 others(27): Show |
intron_variant | MODIFIER | c.828+839C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 8/9 | chr1 | 40767542 | |||||||
| chr1:40767555 | G | A | 257 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(254): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.828+852G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 8/9 | chr1 | 40767555 | |||||||
| chr1:40767634 | C | T | 1 | a0001c0002t0001g0210 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.828+931C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 8/9 | chr1 | 40767634 | |||||||
| chr1:40767768 | C | T | 1 | a0001c0001t0001g0278 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.828+1065C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 8/9 | chr1 | 40767768 | |||||||
| chr1:40768273 | G | C | 1 | a0001c0001t0001g0272 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.829-1083G>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 8/9 | chr1 | 40768273 | |||||||
| chr1:40768464 | G | T | 90 | a0001c0001t0001g0020 a0001c0001t0002g0001 a0001c0001t0002g0002 others(87): Show |
96 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.829-892G>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 8/9 | chr1 | 40768464 | |||||||
| chr1:40768530 | G | T | 1 | a0001c0002t0001g0144 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.829-826G>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 8/9 | chr1 | 40768530 | |||||||
| chr1:40768606 | C | T | 3 | a0001c0002t0001g0234 a0001c0002t0001g0248 a0001c0002t0001g0305 |
3 | HG01109.hp1 HG01175.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.829-750C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 8/9 | chr1 | 40768606 | |||||||
| chr1:40768760 | C | G | 1 | a0001c0002t0001g0188 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.829-596C>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 8/9 | chr1 | 40768760 | |||||||
| chr1:40768792 | T | G | 24 | a0001c0001t0001g0013 a0001c0001t0001g0269 a0001c0001t0001g0270 others(21): Show |
25 | HG00099.hp1 HG00639.hp2 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.829-564T>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 8/9 | chr1 | 40768792 | |||||||
| chr1:40768849 | A | G | 257 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(254): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.829-507A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 8/9 | chr1 | 40768849 | |||||||
| chr1:40768857 | C | T | 4 | a0001c0001t0001g0010 a0001c0001t0001g0119 a0001c0001t0001g0125 others(1): Show |
5 | HG01069.hp1 HG01071.hp1 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.829-499C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 8/9 | chr1 | 40768857 | |||||||
| chr1:40769027 | A | G | 1 | a0001c0004t0001g0014 | 2 | HG01943.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.829-329A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 8/9 | chr1 | 40769027 | |||||||
| chr1:40769040 | T | G | 313 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(310): Show |
327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.829-316T>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 8/9 | chr1 | 40769040 | |||||||
| chr1:40769183 | A | G | 1 | a0001c0001t0002g0076 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.829-173A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 8/9 | chr1 | 40769183 | |||||||
| chr1:40769505 | G | C | 124 | a0001c0001t0001g0013 a0001c0001t0001g0139 a0001c0001t0001g0140 others(121): Show |
127 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.888+90G>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 9/9 | chr1 | 40769505 | |||||||
| chr1:40769692 | T | C | 1 | a0001c0001t0010g0107 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.888+277T>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 9/9 | chr1 | 40769692 | |||||||
| chr1:40769812 | C | T | 1 | a0001c0001t0010g0107 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.888+397C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 9/9 | chr1 | 40769812 | |||||||
| chr1:40769876 | C | T | 3 | a0001c0001t0002g0005 a0001c0001t0002g0026 a0001c0001t0002g0056 |
4 | HG02015.hp1 HG02056.hp2 HG02129.hp2 others(1): Show |
intron_variant | MODIFIER | c.888+461C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 9/9 | chr1 | 40769876 | |||||||
| chr1:40769891 | C | T | 1 | a0001c0001t0006g0050 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.888+476C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 9/9 | chr1 | 40769891 | |||||||
| chr1:40770274 | G | A | 97 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 others(94): Show |
99 | HG00280.hp1 HG00423.hp2 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.889-435G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 9/9 | chr1 | 40770274 |