Search by Gene
| 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 |
Multiple Alignments (by translate haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
Multiple Alignments (by aa haplotype frequency)
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aa |
|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 335 | 332 | 88 | 62 | 130 | 14 | 36 | NFYC_chr1_40686704_40776603 | NFYC | copy fasta |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq |
|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1008 | 174 | 49 | 34 | 63 | 5 | 21 | NFYC_chr1_40686704_40776603 | NFYC | copy fasta |
| c0002 | 0/0 | 1008 | 153 | 35 | 27 | 67 | 9 | 15 | NFYC_chr1_40686704_40776603 | NFYC | copy fasta |
| c0003 | 0/0 | 1008 | 3 | 3 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | copy fasta |
| c0004 | 0/0 | 1008 | 2 | 1 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | copy fasta |
| thapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq |
|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 948 | 222 | 73 | 43 | 74 | 10 | 20 | NFYC_chr1_40686704_40776603 | NFYC | copy fasta |
| t0002 | 0/0 | 947 | 96 | 7 | 18 | 53 | 3 | 15 | NFYC_chr1_40686704_40776603 | NFYC | copy fasta |
| t0003 | 0/0 | 948 | 4 | 3 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | copy fasta |
| t0004 | 0/0 | 948 | 2 | 2 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | copy fasta |
| t0005 | 0/0 | 948 | 2 | 2 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | copy fasta |
| t0006 | 0/0 | 947 | 1 | 0 | 0 | 0 | 1 | 0 | NFYC_chr1_40686704_40776603 | NFYC | copy fasta |
| t0007 | 0/0 | 948 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | copy fasta |
| t0008 | 0/0 | 948 | 1 | 0 | 0 | 0 | 0 | 1 | NFYC_chr1_40686704_40776603 | NFYC | copy fasta |
| t0009 | 0/0 | 948 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | copy fasta |
| t0010 | 0/0 | 948 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | copy fasta |
| t0011 | 0/0 | 948 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | copy fasta |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename |
|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0002 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0003 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | NFYC_chr1_40686704_40776603 | NFYC |
| g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0008 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NFYC_chr1_40686704_40776603 | NFYC |
| g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0014 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYC_chr1_40686704_40776603 | NFYC |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYC_chr1_40686704_40776603 | NFYC |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYC_chr1_40686704_40776603 | NFYC |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYC_chr1_40686704_40776603 | NFYC |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYC_chr1_40686704_40776603 | NFYC |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYC_chr1_40686704_40776603 | NFYC |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0077 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYC_chr1_40686704_40776603 | NFYC |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYC_chr1_40686704_40776603 | NFYC |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYC_chr1_40686704_40776603 | NFYC |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYC_chr1_40686704_40776603 | NFYC |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYC_chr1_40686704_40776603 | NFYC |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYC_chr1_40686704_40776603 | NFYC |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYC_chr1_40686704_40776603 | NFYC |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYC_chr1_40686704_40776603 | NFYC |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYC_chr1_40686704_40776603 | NFYC |
| g0110 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYC_chr1_40686704_40776603 | NFYC |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYC_chr1_40686704_40776603 | NFYC |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYC_chr1_40686704_40776603 | NFYC |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYC_chr1_40686704_40776603 | NFYC |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYC_chr1_40686704_40776603 | NFYC |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYC_chr1_40686704_40776603 | NFYC |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYC_chr1_40686704_40776603 | NFYC |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYC_chr1_40686704_40776603 | NFYC |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYC_chr1_40686704_40776603 | NFYC |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYC_chr1_40686704_40776603 | NFYC |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYC_chr1_40686704_40776603 | NFYC |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYC_chr1_40686704_40776603 | NFYC |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYC_chr1_40686704_40776603 | NFYC |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0277 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYC_chr1_40686704_40776603 | NFYC |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYC_chr1_40686704_40776603 | NFYC |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYC_chr1_40686704_40776603 | NFYC |
| g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYC_chr1_40686704_40776603 | NFYC |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0310 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYC_chr1_40686704_40776603 | NFYC |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYC_chr1_40686704_40776603 | NFYC |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| achapid | ahapid | chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2 |
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | acseq |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | a0001 | c0001 | 1/1 | 174 | 49 | 34 | 63 | 5 | 21 | NFYC_chr1_40686704_40776603 | NFYC | copy fasta |
| a0001c0002 | a0001 | c0002 | 0/0 | 153 | 35 | 27 | 67 | 9 | 15 | NFYC_chr1_40686704_40776603 | NFYC | copy fasta |
| a0001c0003 | a0001 | c0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | copy fasta |
| a0001c0004 | a0001 | c0004 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | copy fasta |
| acthapid | ahapid | chapid | thapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2 |
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | actseq |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | a0001 | c0001 | t0001 | 1/1 | 69 | 34 | 15 | 10 | 2 | 6 | NFYC_chr1_40686704_40776603 | NFYC | copy fasta |
| a0001c0001t0002 | a0001 | c0001 | t0002 | 0/0 | 94 | 7 | 18 | 52 | 2 | 15 | NFYC_chr1_40686704_40776603 | NFYC | copy fasta |
| a0001c0001t0003 | a0001 | c0001 | t0003 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | copy fasta |
| a0001c0001t0004 | a0001 | c0001 | t0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | copy fasta |
| a0001c0001t0005 | a0001 | c0001 | t0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | copy fasta |
| a0001c0001t0006 | a0001 | c0001 | t0006 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFYC_chr1_40686704_40776603 | NFYC | copy fasta |
| a0001c0001t0007 | a0001 | c0001 | t0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | copy fasta |
| a0001c0001t0010 | a0001 | c0001 | t0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | copy fasta |
| a0001c0002t0001 | a0001 | c0002 | t0001 | 0/0 | 148 | 35 | 27 | 64 | 8 | 14 | NFYC_chr1_40686704_40776603 | NFYC | copy fasta |
| a0001c0002t0002 | a0001 | c0002 | t0002 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | NFYC_chr1_40686704_40776603 | NFYC | copy fasta |
| a0001c0002t0008 | a0001 | c0002 | t0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYC_chr1_40686704_40776603 | NFYC | copy fasta |
| a0001c0002t0009 | a0001 | c0002 | t0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | copy fasta |
| a0001c0002t0011 | a0001 | c0002 | t0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | copy fasta |
| a0001c0003t0001 | a0001 | c0003 | t0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | copy fasta |
| a0001c0004t0001 | a0001 | c0004 | t0001 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC | copy fasta |
| actghapid | ahapid | chapid | thapid | ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2 |
total | AFR | AMR | EAS | EUR | SAS | regionname | genename |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0007 | a0001 | c0001 | t0001 | g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0001g0008 | a0001 | c0001 | t0001 | g0008 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0001g0009 | a0001 | c0001 | t0001 | g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0001g0010 | a0001 | c0001 | t0001 | g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0001g0013 | a0001 | c0001 | t0001 | g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0001g0020 | a0001 | c0001 | t0001 | g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0001g0077 | a0001 | c0001 | t0001 | g0077 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0001g0108 | a0001 | c0001 | t0001 | g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0001g0109 | a0001 | c0001 | t0001 | g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0001g0110 | a0001 | c0001 | t0001 | g0110 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0001g0111 | a0001 | c0001 | t0001 | g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0001g0112 | a0001 | c0001 | t0001 | g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0001g0113 | a0001 | c0001 | t0001 | g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0001g0114 | a0001 | c0001 | t0001 | g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0001g0115 | a0001 | c0001 | t0001 | g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0001g0116 | a0001 | c0001 | t0001 | g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0001g0117 | a0001 | c0001 | t0001 | g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0001g0118 | a0001 | c0001 | t0001 | g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0001g0119 | a0001 | c0001 | t0001 | g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0001g0120 | a0001 | c0001 | t0001 | g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0001g0121 | a0001 | c0001 | t0001 | g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0001g0122 | a0001 | c0001 | t0001 | g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0001g0123 | a0001 | c0001 | t0001 | g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0001g0124 | a0001 | c0001 | t0001 | g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0001g0125 | a0001 | c0001 | t0001 | g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0001g0126 | a0001 | c0001 | t0001 | g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0001g0127 | a0001 | c0001 | t0001 | g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0001g0128 | a0001 | c0001 | t0001 | g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0001g0129 | a0001 | c0001 | t0001 | g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0001g0130 | a0001 | c0001 | t0001 | g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0001g0139 | a0001 | c0001 | t0001 | g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0001g0140 | a0001 | c0001 | t0001 | g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0001g0141 | a0001 | c0001 | t0001 | g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0001g0142 | a0001 | c0001 | t0001 | g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0001g0143 | a0001 | c0001 | t0001 | g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0001g0145 | a0001 | c0001 | t0001 | g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0001g0146 | a0001 | c0001 | t0001 | g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0001g0147 | a0001 | c0001 | t0001 | g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0001g0148 | a0001 | c0001 | t0001 | g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0001g0232 | a0001 | c0001 | t0001 | g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0001g0246 | a0001 | c0001 | t0001 | g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0001g0251 | a0001 | c0001 | t0001 | g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0001g0269 | a0001 | c0001 | t0001 | g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0001g0270 | a0001 | c0001 | t0001 | g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0001g0272 | a0001 | c0001 | t0001 | g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0001g0273 | a0001 | c0001 | t0001 | g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0001g0274 | a0001 | c0001 | t0001 | g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0001g0275 | a0001 | c0001 | t0001 | g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0001g0276 | a0001 | c0001 | t0001 | g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0001g0277 | a0001 | c0001 | t0001 | g0277 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0001g0278 | a0001 | c0001 | t0001 | g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0001g0281 | a0001 | c0001 | t0001 | g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0001g0282 | a0001 | c0001 | t0001 | g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0001g0285 | a0001 | c0001 | t0001 | g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0001g0287 | a0001 | c0001 | t0001 | g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0001g0288 | a0001 | c0001 | t0001 | g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0001g0289 | a0001 | c0001 | t0001 | g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0001g0290 | a0001 | c0001 | t0001 | g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0001g0292 | a0001 | c0001 | t0001 | g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0001g0294 | a0001 | c0001 | t0001 | g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0001g0303 | a0001 | c0001 | t0001 | g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0001g0307 | a0001 | c0001 | t0001 | g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0001g0308 | a0001 | c0001 | t0001 | g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0001g0309 | a0001 | c0001 | t0001 | g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0002g0001 | a0001 | c0001 | t0002 | g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0002g0002 | a0001 | c0001 | t0002 | g0002 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0002g0003 | a0001 | c0001 | t0002 | g0003 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0002g0004 | a0001 | c0001 | t0002 | g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0002g0005 | a0001 | c0001 | t0002 | g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0002g0006 | a0001 | c0001 | t0002 | g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0002g0015 | a0001 | c0001 | t0002 | g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0002g0016 | a0001 | c0001 | t0002 | g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0002g0017 | a0001 | c0001 | t0002 | g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0002g0018 | a0001 | c0001 | t0002 | g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0002g0019 | a0001 | c0001 | t0002 | g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0002g0021 | a0001 | c0001 | t0002 | g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0002g0022 | a0001 | c0001 | t0002 | g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0002g0023 | a0001 | c0001 | t0002 | g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0002g0024 | a0001 | c0001 | t0002 | g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0002g0025 | a0001 | c0001 | t0002 | g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0002g0026 | a0001 | c0001 | t0002 | g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0002g0027 | a0001 | c0001 | t0002 | g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0002g0028 | a0001 | c0001 | t0002 | g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0002g0029 | a0001 | c0001 | t0002 | g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0002g0030 | a0001 | c0001 | t0002 | g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0002g0031 | a0001 | c0001 | t0002 | g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0002g0032 | a0001 | c0001 | t0002 | g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0002g0033 | a0001 | c0001 | t0002 | g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0002g0034 | a0001 | c0001 | t0002 | g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0002g0035 | a0001 | c0001 | t0002 | g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0002g0036 | a0001 | c0001 | t0002 | g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0002g0037 | a0001 | c0001 | t0002 | g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0002g0038 | a0001 | c0001 | t0002 | g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0002g0039 | a0001 | c0001 | t0002 | g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0002g0040 | a0001 | c0001 | t0002 | g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0002g0041 | a0001 | c0001 | t0002 | g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0002g0042 | a0001 | c0001 | t0002 | g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0002g0043 | a0001 | c0001 | t0002 | g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0002g0044 | a0001 | c0001 | t0002 | g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0002g0045 | a0001 | c0001 | t0002 | g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0002g0046 | a0001 | c0001 | t0002 | g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0002g0047 | a0001 | c0001 | t0002 | g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0002g0048 | a0001 | c0001 | t0002 | g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0002g0049 | a0001 | c0001 | t0002 | g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0002g0051 | a0001 | c0001 | t0002 | g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0002g0052 | a0001 | c0001 | t0002 | g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0002g0053 | a0001 | c0001 | t0002 | g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0002g0054 | a0001 | c0001 | t0002 | g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0002g0055 | a0001 | c0001 | t0002 | g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0002g0056 | a0001 | c0001 | t0002 | g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0002g0057 | a0001 | c0001 | t0002 | g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0002g0058 | a0001 | c0001 | t0002 | g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0002g0059 | a0001 | c0001 | t0002 | g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0002g0060 | a0001 | c0001 | t0002 | g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0002g0061 | a0001 | c0001 | t0002 | g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0002g0062 | a0001 | c0001 | t0002 | g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0002g0063 | a0001 | c0001 | t0002 | g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0002g0064 | a0001 | c0001 | t0002 | g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0002g0065 | a0001 | c0001 | t0002 | g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0002g0066 | a0001 | c0001 | t0002 | g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0002g0067 | a0001 | c0001 | t0002 | g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0002g0068 | a0001 | c0001 | t0002 | g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0002g0069 | a0001 | c0001 | t0002 | g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0002g0070 | a0001 | c0001 | t0002 | g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0002g0071 | a0001 | c0001 | t0002 | g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0002g0072 | a0001 | c0001 | t0002 | g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0002g0073 | a0001 | c0001 | t0002 | g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0002g0074 | a0001 | c0001 | t0002 | g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0002g0075 | a0001 | c0001 | t0002 | g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0002g0076 | a0001 | c0001 | t0002 | g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0002g0078 | a0001 | c0001 | t0002 | g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0002g0079 | a0001 | c0001 | t0002 | g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0002g0080 | a0001 | c0001 | t0002 | g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0002g0081 | a0001 | c0001 | t0002 | g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0002g0082 | a0001 | c0001 | t0002 | g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0002g0083 | a0001 | c0001 | t0002 | g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0002g0084 | a0001 | c0001 | t0002 | g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0002g0085 | a0001 | c0001 | t0002 | g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0002g0086 | a0001 | c0001 | t0002 | g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0002g0087 | a0001 | c0001 | t0002 | g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0002g0088 | a0001 | c0001 | t0002 | g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0002g0089 | a0001 | c0001 | t0002 | g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0002g0090 | a0001 | c0001 | t0002 | g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0002g0091 | a0001 | c0001 | t0002 | g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0002g0092 | a0001 | c0001 | t0002 | g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0002g0094 | a0001 | c0001 | t0002 | g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0002g0095 | a0001 | c0001 | t0002 | g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0002g0096 | a0001 | c0001 | t0002 | g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0002g0097 | a0001 | c0001 | t0002 | g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0002g0098 | a0001 | c0001 | t0002 | g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0002g0103 | a0001 | c0001 | t0002 | g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0002g0316 | a0001 | c0001 | t0002 | g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0003g0138 | a0001 | c0001 | t0003 | g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0003g0271 | a0001 | c0001 | t0003 | g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0003g0279 | a0001 | c0001 | t0003 | g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0003g0280 | a0001 | c0001 | t0003 | g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0004g0104 | a0001 | c0001 | t0004 | g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0004g0105 | a0001 | c0001 | t0004 | g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0005g0317 | a0001 | c0001 | t0005 | g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0005g0318 | a0001 | c0001 | t0005 | g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0006g0050 | a0001 | c0001 | t0006 | g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0007g0293 | a0001 | c0001 | t0007 | g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0001t0010g0107 | a0001 | c0001 | t0010 | g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0011 | a0001 | c0002 | t0001 | g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0012 | a0001 | c0002 | t0001 | g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0093 | a0001 | c0002 | t0001 | g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0099 | a0001 | c0002 | t0001 | g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0106 | a0001 | c0002 | t0001 | g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0131 | a0001 | c0002 | t0001 | g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0132 | a0001 | c0002 | t0001 | g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0133 | a0001 | c0002 | t0001 | g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0134 | a0001 | c0002 | t0001 | g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0135 | a0001 | c0002 | t0001 | g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0136 | a0001 | c0002 | t0001 | g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0137 | a0001 | c0002 | t0001 | g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0144 | a0001 | c0002 | t0001 | g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0149 | a0001 | c0002 | t0001 | g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0151 | a0001 | c0002 | t0001 | g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0152 | a0001 | c0002 | t0001 | g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0153 | a0001 | c0002 | t0001 | g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0154 | a0001 | c0002 | t0001 | g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0155 | a0001 | c0002 | t0001 | g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0156 | a0001 | c0002 | t0001 | g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0157 | a0001 | c0002 | t0001 | g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0158 | a0001 | c0002 | t0001 | g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0159 | a0001 | c0002 | t0001 | g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0160 | a0001 | c0002 | t0001 | g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0161 | a0001 | c0002 | t0001 | g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0162 | a0001 | c0002 | t0001 | g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0163 | a0001 | c0002 | t0001 | g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0164 | a0001 | c0002 | t0001 | g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0165 | a0001 | c0002 | t0001 | g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0166 | a0001 | c0002 | t0001 | g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0167 | a0001 | c0002 | t0001 | g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0168 | a0001 | c0002 | t0001 | g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0169 | a0001 | c0002 | t0001 | g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0170 | a0001 | c0002 | t0001 | g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0171 | a0001 | c0002 | t0001 | g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0172 | a0001 | c0002 | t0001 | g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0173 | a0001 | c0002 | t0001 | g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0174 | a0001 | c0002 | t0001 | g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0175 | a0001 | c0002 | t0001 | g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0176 | a0001 | c0002 | t0001 | g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0177 | a0001 | c0002 | t0001 | g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0178 | a0001 | c0002 | t0001 | g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0179 | a0001 | c0002 | t0001 | g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0180 | a0001 | c0002 | t0001 | g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0181 | a0001 | c0002 | t0001 | g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0182 | a0001 | c0002 | t0001 | g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0183 | a0001 | c0002 | t0001 | g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0184 | a0001 | c0002 | t0001 | g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0185 | a0001 | c0002 | t0001 | g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0186 | a0001 | c0002 | t0001 | g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0187 | a0001 | c0002 | t0001 | g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0188 | a0001 | c0002 | t0001 | g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0189 | a0001 | c0002 | t0001 | g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0190 | a0001 | c0002 | t0001 | g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0191 | a0001 | c0002 | t0001 | g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0192 | a0001 | c0002 | t0001 | g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0193 | a0001 | c0002 | t0001 | g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0194 | a0001 | c0002 | t0001 | g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0195 | a0001 | c0002 | t0001 | g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0196 | a0001 | c0002 | t0001 | g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0197 | a0001 | c0002 | t0001 | g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0198 | a0001 | c0002 | t0001 | g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0199 | a0001 | c0002 | t0001 | g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0200 | a0001 | c0002 | t0001 | g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0201 | a0001 | c0002 | t0001 | g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0202 | a0001 | c0002 | t0001 | g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0203 | a0001 | c0002 | t0001 | g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0204 | a0001 | c0002 | t0001 | g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0205 | a0001 | c0002 | t0001 | g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0206 | a0001 | c0002 | t0001 | g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0207 | a0001 | c0002 | t0001 | g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0208 | a0001 | c0002 | t0001 | g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0209 | a0001 | c0002 | t0001 | g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0210 | a0001 | c0002 | t0001 | g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0211 | a0001 | c0002 | t0001 | g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0212 | a0001 | c0002 | t0001 | g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0213 | a0001 | c0002 | t0001 | g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0214 | a0001 | c0002 | t0001 | g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0215 | a0001 | c0002 | t0001 | g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0216 | a0001 | c0002 | t0001 | g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0217 | a0001 | c0002 | t0001 | g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0218 | a0001 | c0002 | t0001 | g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0219 | a0001 | c0002 | t0001 | g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0220 | a0001 | c0002 | t0001 | g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0221 | a0001 | c0002 | t0001 | g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0222 | a0001 | c0002 | t0001 | g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0223 | a0001 | c0002 | t0001 | g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0224 | a0001 | c0002 | t0001 | g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0225 | a0001 | c0002 | t0001 | g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0226 | a0001 | c0002 | t0001 | g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0227 | a0001 | c0002 | t0001 | g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0228 | a0001 | c0002 | t0001 | g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0229 | a0001 | c0002 | t0001 | g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0230 | a0001 | c0002 | t0001 | g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0231 | a0001 | c0002 | t0001 | g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0233 | a0001 | c0002 | t0001 | g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0234 | a0001 | c0002 | t0001 | g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0235 | a0001 | c0002 | t0001 | g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0236 | a0001 | c0002 | t0001 | g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0237 | a0001 | c0002 | t0001 | g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0238 | a0001 | c0002 | t0001 | g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0239 | a0001 | c0002 | t0001 | g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0240 | a0001 | c0002 | t0001 | g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0241 | a0001 | c0002 | t0001 | g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0242 | a0001 | c0002 | t0001 | g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0243 | a0001 | c0002 | t0001 | g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0244 | a0001 | c0002 | t0001 | g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0245 | a0001 | c0002 | t0001 | g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0247 | a0001 | c0002 | t0001 | g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0248 | a0001 | c0002 | t0001 | g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0250 | a0001 | c0002 | t0001 | g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0252 | a0001 | c0002 | t0001 | g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0253 | a0001 | c0002 | t0001 | g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0254 | a0001 | c0002 | t0001 | g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0255 | a0001 | c0002 | t0001 | g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0256 | a0001 | c0002 | t0001 | g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0257 | a0001 | c0002 | t0001 | g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0258 | a0001 | c0002 | t0001 | g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0259 | a0001 | c0002 | t0001 | g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0260 | a0001 | c0002 | t0001 | g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0261 | a0001 | c0002 | t0001 | g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0262 | a0001 | c0002 | t0001 | g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0263 | a0001 | c0002 | t0001 | g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0264 | a0001 | c0002 | t0001 | g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0265 | a0001 | c0002 | t0001 | g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0266 | a0001 | c0002 | t0001 | g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0267 | a0001 | c0002 | t0001 | g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0268 | a0001 | c0002 | t0001 | g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0283 | a0001 | c0002 | t0001 | g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0286 | a0001 | c0002 | t0001 | g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0291 | a0001 | c0002 | t0001 | g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0295 | a0001 | c0002 | t0001 | g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0296 | a0001 | c0002 | t0001 | g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0297 | a0001 | c0002 | t0001 | g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0299 | a0001 | c0002 | t0001 | g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0300 | a0001 | c0002 | t0001 | g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0301 | a0001 | c0002 | t0001 | g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0302 | a0001 | c0002 | t0001 | g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0304 | a0001 | c0002 | t0001 | g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0305 | a0001 | c0002 | t0001 | g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0306 | a0001 | c0002 | t0001 | g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0311 | a0001 | c0002 | t0001 | g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0312 | a0001 | c0002 | t0001 | g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0313 | a0001 | c0002 | t0001 | g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0314 | a0001 | c0002 | t0001 | g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0001g0315 | a0001 | c0002 | t0001 | g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0002g0249 | a0001 | c0002 | t0002 | g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0002g0310 | a0001 | c0002 | t0002 | g0310 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0008g0298 | a0001 | c0002 | t0008 | g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0009g0284 | a0001 | c0002 | t0009 | g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0002t0011g0150 | a0001 | c0002 | t0011 | g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0003t0001g0100 | a0001 | c0003 | t0001 | g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0003t0001g0101 | a0001 | c0003 | t0001 | g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0003t0001g0102 | a0001 | c0003 | t0001 | g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| a0001c0004t0001g0014 | a0001 | c0004 | t0001 | g0014 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NFYC_chr1_40686704_40776603 | NFYC |
| sampleid | haplotypeid | ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename |
|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0277 | EUR | GBR | NFYC_chr1_40686704_40776603 | NFYC |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0034 | EUR | GBR | NFYC_chr1_40686704_40776603 | NFYC |
| HG00140 | hp1 | a0001 | c0002 | t0001 | g0132 | EUR | GBR | NFYC_chr1_40686704_40776603 | NFYC |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0062 | EUR | GBR | NFYC_chr1_40686704_40776603 | NFYC |
| HG00280 | hp1 | a0001 | c0002 | t0001 | g0133 | EUR | FIN | NFYC_chr1_40686704_40776603 | NFYC |
| HG00280 | hp2 | a0001 | c0001 | t0006 | g0050 | EUR | FIN | NFYC_chr1_40686704_40776603 | NFYC |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | CHS | NFYC_chr1_40686704_40776603 | NFYC |
| HG00423 | hp2 | a0001 | c0002 | t0001 | g0264 | EAS | CHS | NFYC_chr1_40686704_40776603 | NFYC |
| HG00558 | hp1 | a0001 | c0002 | t0001 | g0238 | EAS | CHS | NFYC_chr1_40686704_40776603 | NFYC |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | CHS | NFYC_chr1_40686704_40776603 | NFYC |
| HG00597 | hp1 | a0001 | c0002 | t0001 | g0214 | EAS | CHS | NFYC_chr1_40686704_40776603 | NFYC |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0082 | EAS | CHS | NFYC_chr1_40686704_40776603 | NFYC |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0036 | AMR | PUR | NFYC_chr1_40686704_40776603 | NFYC |
| HG00639 | hp2 | a0001 | c0001 | t0003 | g0280 | AMR | PUR | NFYC_chr1_40686704_40776603 | NFYC |
| HG00642 | hp1 | a0001 | c0002 | t0001 | g0163 | AMR | PUR | NFYC_chr1_40686704_40776603 | NFYC |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | NFYC_chr1_40686704_40776603 | NFYC |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | NFYC_chr1_40686704_40776603 | NFYC |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0275 | AMR | PUR | NFYC_chr1_40686704_40776603 | NFYC |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0053 | AMR | PUR | NFYC_chr1_40686704_40776603 | NFYC |
| HG00741 | hp2 | a0001 | c0002 | t0001 | g0241 | AMR | PUR | NFYC_chr1_40686704_40776603 | NFYC |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | NFYC_chr1_40686704_40776603 | NFYC |
| HG01069 | hp2 | a0001 | c0002 | t0001 | g0201 | AMR | PUR | NFYC_chr1_40686704_40776603 | NFYC |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | NFYC_chr1_40686704_40776603 | NFYC |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | NFYC_chr1_40686704_40776603 | NFYC |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0064 | AMR | PUR | NFYC_chr1_40686704_40776603 | NFYC |
| HG01074 | hp2 | a0001 | c0002 | t0001 | g0312 | AMR | PUR | NFYC_chr1_40686704_40776603 | NFYC |
| HG01081 | hp1 | a0001 | c0002 | t0001 | g0168 | AMR | PUR | NFYC_chr1_40686704_40776603 | NFYC |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0135 | AMR | PUR | NFYC_chr1_40686704_40776603 | NFYC |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0070 | AMR | PUR | NFYC_chr1_40686704_40776603 | NFYC |
| HG01099 | hp2 | a0001 | c0002 | t0001 | g0239 | AMR | PUR | NFYC_chr1_40686704_40776603 | NFYC |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0270 | AMR | PUR | NFYC_chr1_40686704_40776603 | NFYC |
| HG01106 | hp2 | a0001 | c0002 | t0001 | g0209 | AMR | PUR | NFYC_chr1_40686704_40776603 | NFYC |
| HG01109 | hp1 | a0001 | c0002 | t0001 | g0234 | AMR | PUR | NFYC_chr1_40686704_40776603 | NFYC |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0085 | AMR | PUR | NFYC_chr1_40686704_40776603 | NFYC |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0094 | AMR | PUR | NFYC_chr1_40686704_40776603 | NFYC |
| HG01167 | hp2 | a0001 | c0002 | t0001 | g0230 | AMR | PUR | NFYC_chr1_40686704_40776603 | NFYC |
| HG01168 | hp1 | a0001 | c0002 | t0001 | g0252 | AMR | PUR | NFYC_chr1_40686704_40776603 | NFYC |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | NFYC_chr1_40686704_40776603 | NFYC |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0097 | AMR | PUR | NFYC_chr1_40686704_40776603 | NFYC |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | NFYC_chr1_40686704_40776603 | NFYC |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | NFYC_chr1_40686704_40776603 | NFYC |
| HG01175 | hp2 | a0001 | c0002 | t0001 | g0305 | AMR | PUR | NFYC_chr1_40686704_40776603 | NFYC |
| HG01192 | hp1 | a0001 | c0002 | t0001 | g0291 | AMR | PUR | NFYC_chr1_40686704_40776603 | NFYC |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0035 | AMR | PUR | NFYC_chr1_40686704_40776603 | NFYC |
| HG01243 | hp1 | a0001 | c0002 | t0001 | g0296 | AMR | PUR | NFYC_chr1_40686704_40776603 | NFYC |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0086 | AMR | PUR | NFYC_chr1_40686704_40776603 | NFYC |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | CLM | NFYC_chr1_40686704_40776603 | NFYC |
| HG01256 | hp2 | a0001 | c0002 | t0001 | g0258 | AMR | CLM | NFYC_chr1_40686704_40776603 | NFYC |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | CLM | NFYC_chr1_40686704_40776603 | NFYC |
| HG01258 | hp2 | a0001 | c0002 | t0001 | g0012 | AMR | CLM | NFYC_chr1_40686704_40776603 | NFYC |
| HG01261 | hp1 | a0001 | c0002 | t0001 | g0180 | AMR | CLM | NFYC_chr1_40686704_40776603 | NFYC |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0276 | AMR | CLM | NFYC_chr1_40686704_40776603 | NFYC |
| HG01346 | hp1 | a0001 | c0002 | t0001 | g0136 | AMR | CLM | NFYC_chr1_40686704_40776603 | NFYC |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0066 | AMR | CLM | NFYC_chr1_40686704_40776603 | NFYC |
| HG01358 | hp1 | a0001 | c0002 | t0001 | g0210 | AMR | CLM | NFYC_chr1_40686704_40776603 | NFYC |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0060 | AMR | CLM | NFYC_chr1_40686704_40776603 | NFYC |
| HG01515 | hp1 | a0001 | c0002 | t0001 | g0185 | EUR | IBS | NFYC_chr1_40686704_40776603 | NFYC |
| HG01515 | hp2 | a0001 | c0002 | t0001 | g0248 | EUR | IBS | NFYC_chr1_40686704_40776603 | NFYC |
| HG01516 | hp1 | a0001 | c0002 | t0002 | g0310 | EUR | IBS | NFYC_chr1_40686704_40776603 | NFYC |
| HG01516 | hp2 | a0001 | c0002 | t0001 | g0257 | EUR | IBS | NFYC_chr1_40686704_40776603 | NFYC |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | ACB | NFYC_chr1_40686704_40776603 | NFYC |
| HG01884 | hp2 | a0001 | c0001 | t0005 | g0317 | AFR | ACB | NFYC_chr1_40686704_40776603 | NFYC |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | ACB | NFYC_chr1_40686704_40776603 | NFYC |
| HG01891 | hp2 | a0001 | c0002 | t0001 | g0183 | AFR | ACB | NFYC_chr1_40686704_40776603 | NFYC |
| HG01934 | hp1 | a0001 | c0002 | t0001 | g0226 | AMR | PEL | NFYC_chr1_40686704_40776603 | NFYC |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0032 | AMR | PEL | NFYC_chr1_40686704_40776603 | NFYC |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PEL | NFYC_chr1_40686704_40776603 | NFYC |
| HG01943 | hp2 | a0001 | c0004 | t0001 | g0014 | AMR | PEL | NFYC_chr1_40686704_40776603 | NFYC |
| HG01952 | hp1 | a0001 | c0002 | t0001 | g0157 | AMR | PEL | NFYC_chr1_40686704_40776603 | NFYC |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0073 | AMR | PEL | NFYC_chr1_40686704_40776603 | NFYC |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0061 | AMR | PEL | NFYC_chr1_40686704_40776603 | NFYC |
| HG01978 | hp2 | a0001 | c0002 | t0001 | g0178 | AMR | PEL | NFYC_chr1_40686704_40776603 | NFYC |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0076 | AMR | PEL | NFYC_chr1_40686704_40776603 | NFYC |
| HG01981 | hp2 | a0001 | c0002 | t0001 | g0186 | AMR | PEL | NFYC_chr1_40686704_40776603 | NFYC |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0045 | AMR | PEL | NFYC_chr1_40686704_40776603 | NFYC |
| HG01993 | hp2 | a0001 | c0002 | t0001 | g0221 | AMR | PEL | NFYC_chr1_40686704_40776603 | NFYC |
| HG02004 | hp1 | a0001 | c0002 | t0001 | g0160 | AMR | PEL | NFYC_chr1_40686704_40776603 | NFYC |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0063 | AMR | PEL | NFYC_chr1_40686704_40776603 | NFYC |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | KHV | NFYC_chr1_40686704_40776603 | NFYC |
| HG02015 | hp2 | a0001 | c0002 | t0001 | g0159 | EAS | KHV | NFYC_chr1_40686704_40776603 | NFYC |
| HG02027 | hp1 | a0001 | c0002 | t0001 | g0262 | EAS | KHV | NFYC_chr1_40686704_40776603 | NFYC |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0018 | EAS | KHV | NFYC_chr1_40686704_40776603 | NFYC |
| HG02040 | hp1 | a0001 | c0002 | t0001 | g0217 | EAS | KHV | NFYC_chr1_40686704_40776603 | NFYC |
| HG02040 | hp2 | a0001 | c0002 | t0001 | g0218 | EAS | KHV | NFYC_chr1_40686704_40776603 | NFYC |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | ACB | NFYC_chr1_40686704_40776603 | NFYC |
| HG02055 | hp2 | a0001 | c0002 | t0001 | g0176 | AFR | ACB | NFYC_chr1_40686704_40776603 | NFYC |
| HG02056 | hp1 | a0001 | c0002 | t0001 | g0208 | EAS | KHV | NFYC_chr1_40686704_40776603 | NFYC |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0056 | EAS | KHV | NFYC_chr1_40686704_40776603 | NFYC |
| HG02083 | hp1 | a0001 | c0002 | t0001 | g0205 | EAS | KHV | NFYC_chr1_40686704_40776603 | NFYC |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | KHV | NFYC_chr1_40686704_40776603 | NFYC |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | KHV | NFYC_chr1_40686704_40776603 | NFYC |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | KHV | NFYC_chr1_40686704_40776603 | NFYC |
| HG02132 | hp1 | a0001 | c0002 | t0001 | g0253 | EAS | KHV | NFYC_chr1_40686704_40776603 | NFYC |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | KHV | NFYC_chr1_40686704_40776603 | NFYC |
| HG02135 | hp1 | a0001 | c0002 | t0009 | g0284 | EAS | KHV | NFYC_chr1_40686704_40776603 | NFYC |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | KHV | NFYC_chr1_40686704_40776603 | NFYC |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0303 | AFR | ACB | NFYC_chr1_40686704_40776603 | NFYC |
| HG02145 | hp2 | a0001 | c0002 | t0001 | g0295 | AFR | ACB | NFYC_chr1_40686704_40776603 | NFYC |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0067 | EAS | CDX | NFYC_chr1_40686704_40776603 | NFYC |
| HG02155 | hp2 | a0001 | c0002 | t0001 | g0261 | EAS | CDX | NFYC_chr1_40686704_40776603 | NFYC |
| HG02257 | hp1 | a0001 | c0002 | t0001 | g0267 | AFR | ACB | NFYC_chr1_40686704_40776603 | NFYC |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | ACB | NFYC_chr1_40686704_40776603 | NFYC |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0033 | AFR | ACB | NFYC_chr1_40686704_40776603 | NFYC |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | ACB | NFYC_chr1_40686704_40776603 | NFYC |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PEL | NFYC_chr1_40686704_40776603 | NFYC |
| HG02273 | hp2 | a0001 | c0002 | t0001 | g0184 | AMR | PEL | NFYC_chr1_40686704_40776603 | NFYC |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | ACB | NFYC_chr1_40686704_40776603 | NFYC |
| HG02451 | hp2 | a0001 | c0002 | t0001 | g0151 | AFR | ACB | NFYC_chr1_40686704_40776603 | NFYC |
| HG02602 | hp1 | a0001 | c0002 | t0001 | g0314 | SAS | PJL | NFYC_chr1_40686704_40776603 | NFYC |
| HG02602 | hp2 | a0001 | c0002 | t0001 | g0223 | SAS | PJL | NFYC_chr1_40686704_40776603 | NFYC |
| HG02615 | hp1 | a0001 | c0002 | t0001 | g0172 | AFR | GWD | NFYC_chr1_40686704_40776603 | NFYC |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0078 | AFR | GWD | NFYC_chr1_40686704_40776603 | NFYC |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0271 | AFR | GWD | NFYC_chr1_40686704_40776603 | NFYC |
| HG02622 | hp2 | a0001 | c0002 | t0001 | g0179 | AFR | GWD | NFYC_chr1_40686704_40776603 | NFYC |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0292 | AFR | GWD | NFYC_chr1_40686704_40776603 | NFYC |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0282 | AFR | GWD | NFYC_chr1_40686704_40776603 | NFYC |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0279 | AFR | GWD | NFYC_chr1_40686704_40776603 | NFYC |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | GWD | NFYC_chr1_40686704_40776603 | NFYC |
| HG02683 | hp1 | a0001 | c0002 | t0001 | g0236 | SAS | PJL | NFYC_chr1_40686704_40776603 | NFYC |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | NFYC_chr1_40686704_40776603 | NFYC |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | NFYC_chr1_40686704_40776603 | NFYC |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0096 | SAS | PJL | NFYC_chr1_40686704_40776603 | NFYC |
| HG02723 | hp1 | a0001 | c0002 | t0001 | g0174 | AFR | GWD | NFYC_chr1_40686704_40776603 | NFYC |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0309 | AFR | GWD | NFYC_chr1_40686704_40776603 | NFYC |
| HG02809 | hp1 | a0001 | c0002 | t0001 | g0161 | AFR | GWD | NFYC_chr1_40686704_40776603 | NFYC |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0285 | AFR | GWD | NFYC_chr1_40686704_40776603 | NFYC |
| HG02818 | hp1 | a0001 | c0002 | t0001 | g0195 | AFR | GWD | NFYC_chr1_40686704_40776603 | NFYC |
| HG02818 | hp2 | a0001 | c0001 | t0007 | g0293 | AFR | GWD | NFYC_chr1_40686704_40776603 | NFYC |
| HG02886 | hp1 | a0001 | c0002 | t0001 | g0203 | AFR | GWD | NFYC_chr1_40686704_40776603 | NFYC |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0294 | AFR | GWD | NFYC_chr1_40686704_40776603 | NFYC |
| HG02895 | hp1 | a0001 | c0002 | t0001 | g0194 | AFR | GWD | NFYC_chr1_40686704_40776603 | NFYC |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0307 | AFR | GWD | NFYC_chr1_40686704_40776603 | NFYC |
| HG02896 | hp1 | a0001 | c0002 | t0001 | g0177 | AFR | GWD | NFYC_chr1_40686704_40776603 | NFYC |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | NFYC_chr1_40686704_40776603 | NFYC |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | NFYC_chr1_40686704_40776603 | NFYC |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0308 | AFR | GWD | NFYC_chr1_40686704_40776603 | NFYC |
| HG02922 | hp1 | a0001 | c0002 | t0001 | g0202 | AFR | ESN | NFYC_chr1_40686704_40776603 | NFYC |
| HG02922 | hp2 | a0001 | c0002 | t0001 | g0155 | AFR | ESN | NFYC_chr1_40686704_40776603 | NFYC |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | ESN | NFYC_chr1_40686704_40776603 | NFYC |
| HG02970 | hp2 | a0001 | c0002 | t0001 | g0149 | AFR | ESN | NFYC_chr1_40686704_40776603 | NFYC |
| HG02976 | hp1 | a0001 | c0002 | t0001 | g0268 | AFR | ESN | NFYC_chr1_40686704_40776603 | NFYC |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | ESN | NFYC_chr1_40686704_40776603 | NFYC |
| HG03017 | hp1 | a0001 | c0002 | t0001 | g0231 | SAS | PJL | NFYC_chr1_40686704_40776603 | NFYC |
| HG03017 | hp2 | a0001 | c0002 | t0001 | g0188 | SAS | PJL | NFYC_chr1_40686704_40776603 | NFYC |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0281 | AFR | GWD | NFYC_chr1_40686704_40776603 | NFYC |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0084 | AFR | GWD | NFYC_chr1_40686704_40776603 | NFYC |
| HG03098 | hp1 | a0001 | c0002 | t0001 | g0181 | AFR | MSL | NFYC_chr1_40686704_40776603 | NFYC |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0083 | AFR | MSL | NFYC_chr1_40686704_40776603 | NFYC |
| HG03130 | hp1 | a0001 | c0002 | t0001 | g0152 | AFR | ESN | NFYC_chr1_40686704_40776603 | NFYC |
| HG03130 | hp2 | a0001 | c0002 | t0001 | g0306 | AFR | ESN | NFYC_chr1_40686704_40776603 | NFYC |
| HG03139 | hp1 | a0001 | c0002 | t0001 | g0156 | AFR | ESN | NFYC_chr1_40686704_40776603 | NFYC |
| HG03139 | hp2 | a0001 | c0001 | t0005 | g0318 | AFR | ESN | NFYC_chr1_40686704_40776603 | NFYC |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0040 | AFR | ESN | NFYC_chr1_40686704_40776603 | NFYC |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | ESN | NFYC_chr1_40686704_40776603 | NFYC |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | MSL | NFYC_chr1_40686704_40776603 | NFYC |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | MSL | NFYC_chr1_40686704_40776603 | NFYC |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0273 | AFR | MSL | NFYC_chr1_40686704_40776603 | NFYC |
| HG03225 | hp2 | a0001 | c0002 | t0001 | g0164 | AFR | MSL | NFYC_chr1_40686704_40776603 | NFYC |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | NFYC_chr1_40686704_40776603 | NFYC |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0059 | SAS | PJL | NFYC_chr1_40686704_40776603 | NFYC |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0269 | AFR | MSL | NFYC_chr1_40686704_40776603 | NFYC |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0087 | AFR | MSL | NFYC_chr1_40686704_40776603 | NFYC |
| HG03486 | hp1 | a0001 | c0002 | t0001 | g0204 | AFR | MSL | NFYC_chr1_40686704_40776603 | NFYC |
| HG03486 | hp2 | a0001 | c0001 | t0004 | g0105 | AFR | MSL | NFYC_chr1_40686704_40776603 | NFYC |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | PJL | NFYC_chr1_40686704_40776603 | NFYC |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0080 | SAS | PJL | NFYC_chr1_40686704_40776603 | NFYC |
| HG03516 | hp1 | a0001 | c0002 | t0001 | g0199 | AFR | ESN | NFYC_chr1_40686704_40776603 | NFYC |
| HG03516 | hp2 | a0001 | c0002 | t0001 | g0266 | AFR | ESN | NFYC_chr1_40686704_40776603 | NFYC |
| HG03540 | hp1 | a0001 | c0003 | t0001 | g0100 | AFR | GWD | NFYC_chr1_40686704_40776603 | NFYC |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | GWD | NFYC_chr1_40686704_40776603 | NFYC |
| HG03579 | hp1 | a0001 | c0002 | t0001 | g0200 | AFR | MSL | NFYC_chr1_40686704_40776603 | NFYC |
| HG03579 | hp2 | a0001 | c0003 | t0001 | g0101 | AFR | MSL | NFYC_chr1_40686704_40776603 | NFYC |
| HG03669 | hp1 | a0001 | c0002 | t0001 | g0182 | SAS | PJL | NFYC_chr1_40686704_40776603 | NFYC |
| HG03669 | hp2 | a0001 | c0002 | t0001 | g0286 | SAS | PJL | NFYC_chr1_40686704_40776603 | NFYC |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0027 | SAS | PJL | NFYC_chr1_40686704_40776603 | NFYC |
| HG03710 | hp2 | a0001 | c0002 | t0001 | g0173 | SAS | PJL | NFYC_chr1_40686704_40776603 | NFYC |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0090 | SAS | BEB | NFYC_chr1_40686704_40776603 | NFYC |
| HG03831 | hp2 | a0001 | c0002 | t0001 | g0255 | SAS | BEB | NFYC_chr1_40686704_40776603 | NFYC |
| HG03834 | hp1 | a0001 | c0002 | t0001 | g0144 | SAS | BEB | NFYC_chr1_40686704_40776603 | NFYC |
| HG03834 | hp2 | a0001 | c0002 | t0001 | g0162 | SAS | BEB | NFYC_chr1_40686704_40776603 | NFYC |
| HG03927 | hp1 | a0001 | c0002 | t0008 | g0298 | SAS | BEB | NFYC_chr1_40686704_40776603 | NFYC |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0089 | SAS | BEB | NFYC_chr1_40686704_40776603 | NFYC |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | BEB | NFYC_chr1_40686704_40776603 | NFYC |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0046 | SAS | BEB | NFYC_chr1_40686704_40776603 | NFYC |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0088 | SAS | STU | NFYC_chr1_40686704_40776603 | NFYC |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0057 | SAS | STU | NFYC_chr1_40686704_40776603 | NFYC |
| HG04184 | hp1 | a0001 | c0002 | t0001 | g0093 | SAS | BEB | NFYC_chr1_40686704_40776603 | NFYC |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0316 | SAS | BEB | NFYC_chr1_40686704_40776603 | NFYC |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0048 | SAS | STU | NFYC_chr1_40686704_40776603 | NFYC |
| HG04199 | hp2 | a0001 | c0002 | t0001 | g0297 | SAS | STU | NFYC_chr1_40686704_40776603 | NFYC |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | STU | NFYC_chr1_40686704_40776603 | NFYC |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0095 | SAS | STU | NFYC_chr1_40686704_40776603 | NFYC |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0047 | SAS | STU | NFYC_chr1_40686704_40776603 | NFYC |
| HG04228 | hp2 | a0001 | c0002 | t0001 | g0283 | SAS | STU | NFYC_chr1_40686704_40776603 | NFYC |
| NA18522 | hp1 | a0001 | c0003 | t0001 | g0102 | AFR | YRI | NFYC_chr1_40686704_40776603 | NFYC |
| NA18522 | hp2 | a0001 | c0002 | t0001 | g0196 | AFR | YRI | NFYC_chr1_40686704_40776603 | NFYC |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0278 | AFR | YRI | NFYC_chr1_40686704_40776603 | NFYC |
| NA18906 | hp2 | a0001 | c0002 | t0001 | g0171 | AFR | YRI | NFYC_chr1_40686704_40776603 | NFYC |
| NA18939 | hp1 | a0001 | c0002 | t0001 | g0250 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC |
| NA18939 | hp2 | a0001 | c0002 | t0001 | g0187 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC |
| NA18943 | hp1 | a0001 | c0002 | t0001 | g0211 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC |
| NA18943 | hp2 | a0001 | c0002 | t0011 | g0150 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC |
| NA18945 | hp2 | a0001 | c0002 | t0001 | g0237 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC |
| NA18947 | hp1 | a0001 | c0002 | t0001 | g0170 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC |
| NA18948 | hp2 | a0001 | c0002 | t0001 | g0219 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC |
| NA18949 | hp1 | a0001 | c0002 | t0001 | g0244 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC |
| NA18949 | hp2 | a0001 | c0002 | t0001 | g0158 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC |
| NA18954 | hp1 | a0001 | c0002 | t0001 | g0166 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC |
| NA18956 | hp1 | a0001 | c0002 | t0001 | g0311 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC |
| NA18956 | hp2 | a0001 | c0002 | t0001 | g0206 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC |
| NA18957 | hp2 | a0001 | c0002 | t0001 | g0137 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC |
| NA18962 | hp1 | a0001 | c0002 | t0001 | g0099 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC |
| NA18964 | hp1 | a0001 | c0002 | t0001 | g0254 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC |
| NA18965 | hp1 | a0001 | c0002 | t0001 | g0299 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC |
| NA18966 | hp1 | a0001 | c0002 | t0001 | g0216 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC |
| NA18967 | hp2 | a0001 | c0002 | t0001 | g0215 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC |
| NA18968 | hp2 | a0001 | c0002 | t0001 | g0247 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC |
| NA18972 | hp1 | a0001 | c0002 | t0001 | g0213 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC |
| NA18973 | hp1 | a0001 | c0002 | t0001 | g0207 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC |
| NA18977 | hp2 | a0001 | c0002 | t0001 | g0235 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC |
| NA18979 | hp1 | a0001 | c0002 | t0001 | g0167 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC |
| NA18979 | hp2 | a0001 | c0002 | t0001 | g0192 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC |
| NA18980 | hp1 | a0001 | c0002 | t0001 | g0153 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC |
| NA18989 | hp1 | a0001 | c0002 | t0001 | g0212 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC |
| NA18989 | hp2 | a0001 | c0002 | t0001 | g0175 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC |
| NA18991 | hp2 | a0001 | c0002 | t0001 | g0313 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC |
| NA18992 | hp1 | a0001 | c0002 | t0001 | g0227 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC |
| NA18993 | hp2 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC |
| NA18994 | hp1 | a0001 | c0001 | t0010 | g0107 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC |
| NA18994 | hp2 | a0001 | c0002 | t0001 | g0165 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC |
| NA18997 | hp1 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC |
| NA18997 | hp2 | a0001 | c0002 | t0001 | g0302 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC |
| NA18999 | hp2 | a0001 | c0002 | t0001 | g0191 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC |
| NA19001 | hp2 | a0001 | c0002 | t0002 | g0249 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC |
| NA19005 | hp1 | a0001 | c0002 | t0001 | g0225 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC |
| NA19007 | hp1 | a0001 | c0002 | t0001 | g0222 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC |
| NA19009 | hp2 | a0001 | c0002 | t0001 | g0224 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC |
| NA19012 | hp1 | a0001 | c0002 | t0001 | g0190 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | LWK | NFYC_chr1_40686704_40776603 | NFYC |
| NA19043 | hp2 | a0001 | c0004 | t0001 | g0014 | AFR | LWK | NFYC_chr1_40686704_40776603 | NFYC |
| NA19054 | hp1 | a0001 | c0002 | t0001 | g0260 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC |
| NA19060 | hp2 | a0001 | c0002 | t0001 | g0245 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC |
| NA19062 | hp1 | a0001 | c0002 | t0001 | g0242 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC |
| NA19065 | hp2 | a0001 | c0002 | t0001 | g0228 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC |
| NA19070 | hp1 | a0001 | c0002 | t0001 | g0131 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC |
| NA19075 | hp1 | a0001 | c0002 | t0001 | g0220 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC |
| NA19079 | hp1 | a0001 | c0002 | t0001 | g0106 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC |
| NA19082 | hp1 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC |
| NA19084 | hp1 | a0001 | c0002 | t0001 | g0259 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC |
| NA19085 | hp2 | a0001 | c0002 | t0001 | g0300 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC |
| NA19086 | hp1 | a0001 | c0002 | t0001 | g0154 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC |
| NA19086 | hp2 | a0001 | c0002 | t0001 | g0256 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC |
| NA19088 | hp2 | a0001 | c0002 | t0001 | g0301 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC |
| NA19089 | hp1 | a0001 | c0002 | t0001 | g0263 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC |
| NA19089 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC |
| NA19090 | hp1 | a0001 | c0002 | t0001 | g0315 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC |
| NA19090 | hp2 | a0001 | c0002 | t0001 | g0233 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC |
| NA19240 | hp1 | a0001 | c0002 | t0001 | g0189 | AFR | YRI | NFYC_chr1_40686704_40776603 | NFYC |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | YRI | NFYC_chr1_40686704_40776603 | NFYC |
| NA20752 | hp1 | a0001 | c0002 | t0001 | g0240 | EUR | TSI | NFYC_chr1_40686704_40776603 | NFYC |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0118 | EUR | TSI | NFYC_chr1_40686704_40776603 | NFYC |
| NA20805 | hp1 | a0001 | c0002 | t0001 | g0134 | EUR | TSI | NFYC_chr1_40686704_40776603 | NFYC |
| NA20805 | hp2 | a0001 | c0002 | t0001 | g0169 | EUR | TSI | NFYC_chr1_40686704_40776603 | NFYC |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | GIH | NFYC_chr1_40686704_40776603 | NFYC |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0103 | SAS | GIH | NFYC_chr1_40686704_40776603 | NFYC |
| HG01123 | hp1 | a0001 | c0002 | t0001 | g0012 | AMR | CLM | NFYC_chr1_40686704_40776603 | NFYC |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | NFYC_chr1_40686704_40776603 | NFYC |
| HG02109 | hp1 | a0001 | c0002 | t0001 | g0193 | AFR | ACB | NFYC_chr1_40686704_40776603 | NFYC |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0272 | AFR | ACB | NFYC_chr1_40686704_40776603 | NFYC |
| HG02486 | hp1 | a0001 | c0002 | t0001 | g0304 | AFR | ACB | NFYC_chr1_40686704_40776603 | NFYC |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | ACB | NFYC_chr1_40686704_40776603 | NFYC |
| HG02559 | hp1 | a0001 | c0002 | t0001 | g0265 | AFR | ACB | NFYC_chr1_40686704_40776603 | NFYC |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0274 | AFR | ACB | NFYC_chr1_40686704_40776603 | NFYC |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | MSL | NFYC_chr1_40686704_40776603 | NFYC |
| HG03471 | hp2 | a0001 | c0002 | t0001 | g0198 | AFR | MSL | NFYC_chr1_40686704_40776603 | NFYC |
| HG06807 | hp1 | a0001 | c0001 | t0004 | g0104 | AFR | USA | NFYC_chr1_40686704_40776603 | NFYC |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0138 | AFR | USA | NFYC_chr1_40686704_40776603 | NFYC |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC |
| NA18955 | hp2 | a0001 | c0002 | t0001 | g0229 | EAS | JPT | NFYC_chr1_40686704_40776603 | NFYC |
| NA20300 | hp1 | a0001 | c0002 | t0001 | g0197 | AFR | USA | NFYC_chr1_40686704_40776603 | NFYC |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | USA | NFYC_chr1_40686704_40776603 | NFYC |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | LWK | NFYC_chr1_40686704_40776603 | NFYC |
| NA21309 | hp2 | a0001 | c0002 | t0001 | g0243 | AFR | LWK | NFYC_chr1_40686704_40776603 | NFYC |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0110 | REF | REF | NFYC_chr1_40686704_40776603 | NFYC |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0077 | REF | REF | NFYC_chr1_40686704_40776603 | NFYC |
| chr:pos | ref | alt | # # of ahapid:amio-acid(protein) level
|
ahapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|
| chr:pos | ref | alt | # # of chapid
|
chapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:40738897
|
C | T | 2 | a0001c0002a0001c0004 | 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 |
| 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_pos_length | cds_pos_length | 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 | a0001c0001t0002a0001c0001t0006a0001c0002t0002 | 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 |
| 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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:40691920
|
G | T | 2 | a0001c0001t0005g0317a0001c0001t0005g0318 | 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 | a0001c0002t0001g0311a0001c0002t0001g0312a0001c0002t0001g0313others(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 | 227 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(224): Show | 235 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.-9+619A>C | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40692486 | ||||||
| chr1:40692701
|
A | G | 227 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(224): Show | 235 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(232): 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 | a0001c0003t0001g0100a0001c0003t0001g0101a0001c0003t0001g0102 | 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 | a0001c0001t0004g0104a0001c0001t0004g0105 | 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 | 227 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(224): Show | 235 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(232): 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 | a0001c0001t0001g0307a0001c0001t0001g0308 | 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 | 223 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(220): Show | 231 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(228): 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 | 227 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(224): Show | 235 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(232): 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 | a0001c0001t0002g0094a0001c0001t0002g0095a0001c0001t0002g0096others(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 | a0001c0001t0001g0013a0001c0001t0001g0139a0001c0001t0001g0140others(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 | 27 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(24): Show | 31 | HG01069.hp1 HG01071.hp1 HG01168.hp2 others(28): 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 | 236 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(233): Show | 244 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(241): 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 | 27 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(24): Show | 31 | HG01069.hp1 HG01071.hp1 HG01168.hp2 others(28): 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 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0002g0090others(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 | a0001c0001t0001g0013a0001c0001t0001g0139a0001c0001t0001g0140others(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 | a0001c0001t0001g0292a0001c0001t0001g0294a0001c0001t0001g0303others(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 | a0001c0001t0001g0013a0001c0001t0001g0287a0001c0001t0001g0288others(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 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141others(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 | a0001c0001t0004g0104a0001c0001t0004g0105 | 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 | a0001c0002t0001g0093a0001c0002t0001g0286 | 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 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0025 | 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 | 228 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(225): Show | 236 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(233): 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 | a0001c0001t0002g0027a0001c0001t0002g0090 | 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 | a0001c0001t0002g0028a0001c0001t0002g0029a0001c0001t0002g0030others(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 | a0001c0003t0001g0100a0001c0003t0001g0101a0001c0003t0001g0102 | 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 | a0001c0001t0004g0104a0001c0001t0004g0105 | 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 | 13 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0108others(10): Show | 15 | HG01168.hp2 HG01169.hp2 HG01175.hp1 others(12): 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 | a0001c0001t0001g0013a0001c0001t0001g0269a0001c0001t0001g0270others(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 | 227 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(224): Show | 235 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(232): 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 | a0001c0002t0001g0265a0001c0002t0001g0266a0001c0002t0001g0267 | 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 | a0001c0001t0001g0292a0001c0001t0001g0294a0001c0001t0007g0293 | 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 | 13 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0108others(10): Show | 15 | HG01168.hp2 HG01169.hp2 HG01175.hp1 others(12): 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 | a0001c0002t0001g0265a0001c0002t0001g0266a0001c0002t0001g0267others(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 | a0001c0001t0001g0013a0001c0001t0001g0139a0001c0001t0001g0140others(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 | a0001c0001t0001g0232a0001c0001t0001g0246a0001c0001t0001g0251others(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 | 27 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(24): Show | 31 | HG01069.hp1 HG01071.hp1 HG01168.hp2 others(28): 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 | a0001c0001t0001g0285a0001c0001t0001g0292a0001c0001t0001g0294others(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 | a0001c0002t0001g0132a0001c0002t0001g0149a0001c0002t0001g0151others(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 | 227 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(224): Show | 235 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(232): 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 | a0001c0001t0001g0232a0001c0001t0001g0246a0001c0001t0001g0251others(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 | a0001c0001t0001g0285a0001c0001t0001g0292a0001c0001t0001g0294others(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 | a0001c0001t0001g0020a0001c0001t0002g0016a0001c0001t0002g0017others(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 | a0001c0001t0001g0232a0001c0001t0001g0246a0001c0001t0001g0251others(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 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141others(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 | a0001c0001t0001g0013a0001c0001t0001g0269a0001c0001t0001g0270others(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 | a0001c0002t0001g0259a0001c0002t0001g0260a0001c0002t0001g0261others(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 | 228 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(225): Show | 236 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(233): 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 | 27 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(24): Show | 31 | HG01069.hp1 HG01071.hp1 HG01168.hp2 others(28): 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 | a0001c0002t0001g0132a0001c0002t0001g0149a0001c0002t0001g0151others(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 | 224 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(221): Show | 231 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(228): 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 |
26 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(23): Show | 30 | HG01069.hp1 HG01071.hp1 HG01168.hp2 others(27): 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 | a0001c0001t0001g0120a0001c0001t0001g0281a0001c0001t0001g0309others(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 | a0001c0001t0001g0013a0001c0001t0001g0140a0001c0001t0001g0141others(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 | a0001c0001t0001g0139a0001c0001t0001g0145a0001c0001t0001g0146others(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 | a0001c0002t0001g0093a0001c0002t0001g0192a0001c0002t0001g0193others(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 | a0001c0002t0001g0206a0001c0002t0001g0207 | 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 | a0001c0001t0001g0292a0001c0001t0001g0294a0001c0001t0007g0293 | 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 | 227 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(224): Show | 235 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.-9+12172G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40704039 | ||||||
| chr1:40704081
|
GT | G | 198 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(195): Show | 206 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(203): 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 | a0001c0002t0001g0099a0001c0002t0001g0106a0001c0002t0001g0192others(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 | 27 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(24): Show | 31 | HG01069.hp1 HG01071.hp1 HG01168.hp2 others(28): 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 | a0001c0001t0001g0148a0001c0001t0001g0232a0001c0001t0001g0246others(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 | a0001c0002t0001g0185a0001c0002t0001g0186 | 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 | a0001c0001t0001g0013a0001c0001t0001g0139a0001c0001t0001g0140others(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 | 27 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(24): Show | 31 | HG01069.hp1 HG01071.hp1 HG01168.hp2 others(28): 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 | a0001c0001t0001g0013a0001c0001t0001g0269a0001c0001t0001g0270others(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 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141others(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 | a0001c0001t0003g0138a0001c0001t0003g0271a0001c0001t0003g0279others(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 | 227 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(224): Show | 235 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(232): 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 | a0001c0001t0001g0117a0001c0001t0001g0118 | 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 | a0001c0002t0001g0227a0001c0002t0001g0228 | 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 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0035 | 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 | a0001c0002t0001g0132a0001c0002t0001g0149a0001c0002t0001g0151others(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 | 227 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(224): Show | 235 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(232): 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 | a0001c0001t0001g0232a0001c0001t0001g0246a0001c0001t0001g0251others(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 | a0001c0002t0001g0136a0001c0002t0001g0188 | 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 | a0001c0003t0001g0100a0001c0003t0001g0101a0001c0003t0001g0102 | 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 | a0001c0001t0001g0292a0001c0001t0001g0294a0001c0001t0007g0293 | 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 | a0001c0001t0002g0083a0001c0001t0002g0084 | 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 | 27 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(24): Show | 31 | HG01069.hp1 HG01071.hp1 HG01168.hp2 others(28): 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 | a0001c0001t0001g0232a0001c0001t0001g0246a0001c0001t0001g0251others(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 | 27 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(24): Show | 31 | HG01069.hp1 HG01071.hp1 HG01168.hp2 others(28): 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 | 27 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(24): Show | 31 | HG01069.hp1 HG01071.hp1 HG01168.hp2 others(28): 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 | a0001c0001t0001g0013a0001c0001t0001g0148a0001c0001t0001g0269others(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 | a0001c0002t0001g0200a0001c0002t0001g0201a0001c0002t0001g0202others(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 | a0001c0001t0001g0115a0001c0001t0002g0001a0001c0001t0002g0036others(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 | 25 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(22): Show | 29 | HG01069.hp1 HG01071.hp1 HG01168.hp2 others(26): 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 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(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 | 227 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(224): Show | 235 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(232): 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 | a0001c0001t0001g0013a0001c0001t0001g0139a0001c0001t0001g0140others(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 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141others(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 | a0001c0002t0001g0200a0001c0002t0001g0201a0001c0002t0001g0202others(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 | a0001c0001t0002g0028a0001c0001t0002g0029a0001c0001t0002g0030others(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 | 227 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(224): Show | 235 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.-9+18464C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40710331 | ||||||
| chr1:40710637
|
A | G | 27 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(24): Show | 31 | HG01069.hp1 HG01071.hp1 HG01168.hp2 others(28): 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 | 27 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(24): Show | 31 | HG01069.hp1 HG01071.hp1 HG01168.hp2 others(28): 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 | a0001c0001t0004g0104a0001c0001t0004g0105 | 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 | a0001c0001t0003g0138a0001c0001t0003g0271a0001c0001t0003g0279others(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 | a0001c0001t0001g0122a0001c0001t0001g0130 | 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 | a0001c0001t0001g0270a0001c0001t0001g0275a0001c0001t0001g0276others(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 | 228 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(225): Show | 236 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(233): 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 | 228 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(225): Show | 236 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(233): 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 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0143others(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 | a0001c0001t0001g0246a0001c0001t0005g0318a0001c0001t0010g0107others(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 | a0001c0001t0001g0146a0001c0001t0001g0270a0001c0001t0001g0275others(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 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141others(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 | 27 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(24): Show | 31 | HG01069.hp1 HG01071.hp1 HG01168.hp2 others(28): 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 | a0001c0003t0001g0100a0001c0003t0001g0101a0001c0003t0001g0102 | 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 | a0001c0002t0001g0132a0001c0002t0001g0149a0001c0002t0001g0151others(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 | a0001c0001t0004g0104a0001c0001t0004g0105 | 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 | 27 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(24): Show | 31 | HG01069.hp1 HG01071.hp1 HG01168.hp2 others(28): 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 | a0001c0001t0001g0232a0001c0001t0001g0246a0001c0001t0001g0251others(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 | a0001c0001t0010g0107a0001c0002t0001g0174 | 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 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0130 | 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 | a0001c0002t0001g0099a0001c0002t0001g0206a0001c0002t0001g0221others(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 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0287others(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 |
51 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(48): Show | 55 | HG00140.hp1 HG00558.hp2 HG01069.hp1 others(52): 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 | a0001c0001t0001g0121a0001c0001t0001g0142a0001c0001t0001g0147others(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 | a0001c0001t0001g0108a0001c0001t0001g0139a0001c0001t0001g0140others(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 | a0001c0001t0001g0232a0001c0001t0001g0246a0001c0001t0001g0251others(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 | a0001c0002t0001g0151a0001c0002t0001g0152a0001c0002t0001g0181others(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 | a0001c0003t0001g0100a0001c0003t0001g0101a0001c0003t0001g0102 | 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 | a0001c0001t0003g0138a0001c0001t0003g0271a0001c0001t0003g0279others(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 | a0001c0002t0001g0193a0001c0002t0001g0194a0001c0002t0001g0195others(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 | a0001c0001t0001g0232a0001c0001t0001g0246a0001c0001t0001g0251others(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 | a0001c0002t0001g0132a0001c0002t0001g0149a0001c0002t0001g0151others(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 | a0001c0001t0003g0138a0001c0001t0003g0271a0001c0001t0003g0279others(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 | 27 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(24): Show | 31 | HG01069.hp1 HG01071.hp1 HG01168.hp2 others(28): 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 | a0001c0002t0001g0165a0001c0002t0001g0175 | 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 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0025 | 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 | a0001c0003t0001g0100a0001c0003t0001g0101a0001c0003t0001g0102 | 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 | a0001c0002t0001g0153a0001c0002t0001g0154a0001c0002t0001g0165others(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 | a0001c0001t0001g0285a0001c0001t0001g0292a0001c0001t0001g0294others(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 | a0001c0002t0001g0132a0001c0002t0001g0149a0001c0002t0001g0151others(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 | a0001c0002t0001g0151a0001c0002t0001g0152 | 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 | a0001c0002t0001g0299a0001c0002t0001g0300a0001c0002t0001g0301others(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 | 228 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(225): Show | 236 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(233): 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 | a0001c0001t0001g0292a0001c0001t0001g0294a0001c0001t0007g0293 | 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 | a0001c0002t0001g0155a0001c0002t0001g0176 | 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 | a0001c0001t0001g0013a0001c0001t0001g0139a0001c0001t0001g0140others(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 | a0001c0001t0002g0045a0001c0001t0002g0094a0001c0001t0002g0095others(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 | a0001c0001t0001g0013a0001c0001t0001g0139a0001c0001t0001g0140others(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 | a0001c0002t0001g0300a0001c0002t0001g0301a0001c0002t0001g0302 | 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 | ||||||
| chr1:40721234
|
G | A | 1 | a0001c0001t0001g0110 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-8-17602G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 1/9 | chr1 | 40721234 | ||||||
| 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 | a0001c0001t0001g0232a0001c0001t0001g0246a0001c0001t0001g0251others(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 | a0001c0001t0001g0270a0001c0001t0001g0275a0001c0001t0001g0276others(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 | 223 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(220): Show | 231 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(228): 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 | a0001c0002t0001g0230a0001c0002t0001g0231a0001c0002t0001g0291others(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 | 225 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(222): Show | 233 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(230): 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 | a0001c0003t0001g0100a0001c0003t0001g0101a0001c0003t0001g0102 | 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 | 227 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(224): Show | 235 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(232): 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 | a0001c0003t0001g0100a0001c0003t0001g0101a0001c0003t0001g0102 | 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 | a0001c0003t0001g0100a0001c0003t0001g0101a0001c0003t0001g0102 | 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 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0139others(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 | a0001c0001t0003g0138a0001c0001t0003g0271a0001c0001t0003g0279others(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 | a0001c0001t0001g0020a0001c0001t0002g0001a0001c0001t0002g0002others(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 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0139others(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 | 314 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(311): Show | 328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): 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 | a0001c0001t0001g0013a0001c0001t0001g0139a0001c0001t0001g0140others(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 | a0001c0001t0002g0045a0001c0001t0002g0046a0001c0001t0002g0094others(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 | a0001c0001t0001g0020a0001c0001t0002g0001a0001c0001t0002g0002others(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 | 13 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0108others(10): Show | 15 | HG01168.hp2 HG01169.hp2 HG01175.hp1 others(12): 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 | a0001c0001t0001g0020a0001c0001t0002g0001a0001c0001t0002g0002others(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 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(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 | a0001c0001t0002g0003a0001c0001t0002g0048 | 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 | a0001c0001t0002g0001a0001c0001t0002g0038 | 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 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(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 | a0001c0001t0001g0232a0001c0001t0001g0246a0001c0001t0001g0251others(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 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115 | 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 | a0001c0001t0001g0269a0001c0001t0001g0274a0001c0001t0001g0281others(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 | a0001c0001t0004g0104a0001c0001t0004g0105 | 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 | a0001c0003t0001g0100a0001c0003t0001g0101a0001c0003t0001g0102 | 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 | a0001c0001t0001g0020a0001c0001t0002g0001a0001c0001t0002g0002others(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 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141others(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 | a0001c0001t0003g0138a0001c0001t0003g0271a0001c0001t0003g0279others(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 | a0001c0002t0001g0299a0001c0002t0001g0300a0001c0002t0001g0301others(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 | a0001c0002t0001g0265a0001c0002t0001g0266a0001c0002t0001g0267others(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 | a0001c0001t0001g0020a0001c0001t0002g0001a0001c0001t0002g0002others(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 | a0001c0001t0001g0148a0001c0001t0001g0232a0001c0001t0001g0246others(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 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0139others(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 | a0001c0001t0001g0232a0001c0001t0001g0246a0001c0001t0001g0251others(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 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(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 | a0001c0001t0001g0020a0001c0001t0002g0001a0001c0001t0002g0002others(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 | a0001c0001t0001g0020a0001c0001t0002g0001a0001c0001t0002g0002others(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 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141others(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 | a0001c0001t0002g0044a0001c0001t0002g0071 | 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 | a0001c0001t0001g0020a0001c0001t0002g0001a0001c0001t0002g0002others(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 | a0001c0001t0001g0232a0001c0001t0001g0246a0001c0001t0001g0251others(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 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141others(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 | a0001c0002t0001g0193a0001c0002t0001g0194a0001c0002t0001g0195others(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 | a0001c0001t0001g0013a0001c0001t0001g0269a0001c0001t0001g0270others(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 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147 | 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 | a0001c0001t0002g0003a0001c0001t0002g0048 | 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 | a0001c0002t0001g0229a0001c0002t0001g0250a0001c0002t0002g0249 | 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 | 22 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0109others(19): Show | 25 | HG00642.hp1 HG01123.hp1 HG01168.hp2 others(22): 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 | a0001c0001t0001g0020a0001c0001t0001g0120a0001c0001t0001g0145others(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 | a0001c0001t0001g0013a0001c0001t0001g0269a0001c0001t0001g0270others(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 | a0001c0002t0001g0157a0001c0002t0001g0253a0001c0002t0001g0299others(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 | a0001c0003t0001g0100a0001c0003t0001g0101a0001c0003t0001g0102 | 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 | a0001c0001t0001g0013a0001c0001t0001g0269a0001c0001t0001g0270others(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 | a0001c0001t0004g0104a0001c0001t0004g0105 | 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 | a0001c0001t0002g0004a0001c0001t0002g0091 | 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 | a0001c0002t0001g0230a0001c0002t0001g0231a0001c0002t0001g0291others(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 | a0001c0001t0001g0285a0001c0001t0001g0292a0001c0001t0001g0294others(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 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0139others(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 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0139others(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 | a0001c0003t0001g0100a0001c0003t0001g0101a0001c0003t0001g0102 | 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 | a0001c0001t0001g0292a0001c0001t0001g0294a0001c0001t0007g0293 | 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 | a0001c0001t0001g0020a0001c0001t0002g0001a0001c0001t0002g0002others(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 | a0001c0001t0001g0013a0001c0001t0001g0139a0001c0001t0001g0140others(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 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0139others(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 | a0001c0001t0001g0292a0001c0001t0001g0294a0001c0001t0007g0293 | 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 | a0001c0001t0004g0104a0001c0001t0004g0105 | 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 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(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 | a0001c0002t0001g0213a0001c0002t0001g0242 | 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 | a0001c0001t0001g0013a0001c0001t0001g0269a0001c0001t0001g0270others(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 | a0001c0001t0001g0007a0001c0001t0001g0109a0001c0001t0001g0116others(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 | a0001c0001t0001g0013a0001c0001t0001g0269a0001c0001t0001g0272others(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 | a0001c0001t0001g0232a0001c0001t0001g0270a0001c0001t0001g0277others(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 | 167 | a0001c0001t0001g0020a0001c0001t0001g0110a0001c0001t0001g0246others(164): Show | 175 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(172): 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 | a0001c0002t0001g0213a0001c0002t0001g0242a0001c0002t0001g0261others(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 | a0001c0001t0001g0292a0001c0001t0001g0294a0001c0001t0001g0309others(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 | a0001c0003t0001g0100a0001c0003t0001g0101a0001c0003t0001g0102 | 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 | a0001c0001t0001g0020a0001c0001t0002g0001a0001c0001t0002g0002others(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 | a0001c0002t0001g0193a0001c0002t0001g0194a0001c0002t0001g0195others(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 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141others(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 | a0001c0001t0001g0020a0001c0001t0002g0001a0001c0001t0002g0002others(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 | a0001c0001t0001g0020a0001c0001t0002g0001a0001c0001t0002g0002others(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 | a0001c0001t0001g0009a0001c0001t0001g0111a0001c0001t0001g0124others(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 | a0001c0001t0001g0013a0001c0001t0001g0139a0001c0001t0001g0140others(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 | a0001c0001t0001g0020a0001c0001t0001g0116a0001c0001t0001g0121others(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 | a0001c0001t0001g0269a0001c0001t0001g0274a0001c0001t0001g0281others(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 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0139others(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 | a0001c0001t0001g0020a0001c0001t0002g0001a0001c0001t0002g0002others(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 | a0001c0001t0001g0232a0001c0001t0001g0246a0001c0001t0001g0251others(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 | a0001c0002t0001g0153a0001c0002t0001g0193a0001c0002t0001g0194others(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 | a0001c0002t0001g0153a0001c0002t0001g0193a0001c0002t0001g0194others(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 | a0001c0002t0001g0153a0001c0002t0001g0193a0001c0002t0001g0194others(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 | a0001c0001t0001g0232a0001c0001t0001g0246a0001c0001t0001g0251others(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 | a0001c0001t0002g0045a0001c0001t0002g0094a0001c0001t0002g0095others(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 | a0001c0001t0003g0138a0001c0001t0003g0271a0001c0001t0003g0279others(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 | a0001c0001t0001g0020a0001c0001t0002g0001a0001c0001t0002g0002others(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 | a0001c0001t0002g0030a0001c0001t0002g0058a0001c0001t0002g0065others(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 | a0001c0001t0001g0020a0001c0001t0002g0001a0001c0001t0002g0002others(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 | a0001c0002t0001g0099a0001c0002t0001g0106a0001c0002t0001g0192others(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 | a0001c0002t0001g0152a0001c0002t0001g0189 | 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 | a0001c0001t0001g0232a0001c0001t0001g0246a0001c0001t0001g0251others(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 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(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 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0120others(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 | a0001c0001t0001g0010a0001c0001t0005g0318a0001c0002t0001g0106others(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 | a0001c0001t0001g0119a0001c0001t0001g0125a0001c0001t0001g0128others(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 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0114others(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 | a0001c0002t0001g0012a0001c0002t0001g0258a0001c0002t0002g0310 | 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 | a0001c0001t0001g0123a0001c0001t0001g0130a0001c0001t0001g0290others(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 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141others(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 | a0001c0001t0001g0232a0001c0001t0001g0246a0001c0001t0001g0251others(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 | a0001c0002t0001g0229a0001c0002t0002g0249 | 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 | a0001c0003t0001g0100a0001c0003t0001g0101a0001c0003t0001g0102 | 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 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0145others(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 | a0001c0001t0001g0013a0001c0001t0001g0139a0001c0001t0001g0140others(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 | a0001c0001t0001g0013a0001c0001t0001g0269a0001c0001t0001g0270others(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 | a0001c0001t0001g0269a0001c0001t0001g0274a0001c0001t0001g0281others(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 | a0001c0001t0001g0122a0001c0001t0001g0130 | 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 | a0001c0002t0001g0161a0001c0002t0001g0179 | 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 | a0001c0001t0001g0020a0001c0001t0001g0126a0001c0001t0002g0015others(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 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141others(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 | a0001c0001t0001g0013a0001c0001t0001g0148a0001c0001t0001g0232others(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 | a0001c0001t0001g0013a0001c0001t0001g0139a0001c0001t0001g0140others(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 | a0001c0002t0001g0299a0001c0002t0001g0300a0001c0002t0001g0301others(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 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141others(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 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141others(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 | a0001c0002t0001g0214a0001c0002t0001g0253a0001c0002t0001g0256 | 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 | a0001c0003t0001g0100a0001c0003t0001g0101a0001c0003t0001g0102 | 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 | a0001c0003t0001g0100a0001c0003t0001g0101a0001c0003t0001g0102 | 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 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0139others(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 | a0001c0002t0001g0137a0001c0002t0001g0211a0001c0002t0001g0237others(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 | a0001c0001t0001g0020a0001c0001t0002g0001a0001c0001t0002g0002others(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 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0139others(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 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141others(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 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0025 | 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 | a0001c0001t0001g0013a0001c0001t0001g0139a0001c0001t0001g0140others(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 | 13 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0108others(10): Show | 15 | HG01168.hp2 HG01169.hp2 HG01175.hp1 others(12): 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 | a0001c0002t0001g0132a0001c0002t0001g0149a0001c0002t0001g0151others(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 | a0001c0001t0001g0246a0001c0001t0001g0251 | 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 | a0001c0002t0001g0222a0001c0002t0001g0265a0001c0002t0001g0266others(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 | a0001c0003t0001g0100a0001c0003t0001g0101a0001c0003t0001g0102 | 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 | a0001c0001t0006g0050a0001c0002t0001g0154 | 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 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(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 | a0001c0001t0001g0020a0001c0001t0002g0001a0001c0001t0002g0002others(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 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0139others(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 | a0001c0001t0002g0058a0001c0001t0002g0065a0001c0001t0002g0074others(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 | a0001c0001t0004g0104a0001c0001t0004g0105 | 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 | a0001c0002t0001g0265a0001c0002t0001g0266a0001c0002t0001g0267 | 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 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0139others(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 | a0001c0001t0001g0270a0001c0001t0001g0275a0001c0001t0001g0276others(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 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0139others(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 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0139others(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 | ||||||
| chr1:40746786
|
G | A | 1 | a0001c0001t0001g0110 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.106-748G>A | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 2/9 | chr1 | 40746786 | ||||||
| chr1:40746935
|
A | G | 2 | a0001c0001t0004g0104a0001c0001t0004g0105 | 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 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0139others(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 | a0001c0001t0001g0232a0001c0002t0001g0234a0001c0002t0001g0239others(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 | 282 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(279): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): 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 | a0001c0001t0001g0290a0001c0001t0002g0024a0001c0001t0002g0086others(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 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0139others(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 | a0001c0001t0001g0020a0001c0001t0002g0001a0001c0001t0002g0002others(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 | a0001c0001t0001g0013a0001c0001t0001g0148a0001c0001t0001g0269others(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 | a0001c0001t0003g0138a0001c0001t0003g0271a0001c0001t0003g0279others(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 | a0001c0001t0002g0043a0001c0001t0002g0044a0001c0001t0002g0071others(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 | a0001c0002t0001g0193a0001c0002t0001g0194a0001c0002t0001g0195others(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 | a0001c0002t0001g0213a0001c0002t0001g0242a0001c0002t0001g0244others(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 | a0001c0002t0001g0134a0001c0002t0001g0135 | 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 | a0001c0001t0001g0292a0001c0001t0001g0294a0001c0001t0007g0293 | 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 | a0001c0001t0002g0016a0001c0001t0002g0018a0001c0001t0002g0019others(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 | a0001c0001t0010g0107a0001c0002t0001g0193a0001c0002t0001g0194others(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 | a0001c0001t0001g0020a0001c0001t0002g0001a0001c0001t0002g0002others(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 | a0001c0003t0001g0100a0001c0003t0001g0101a0001c0003t0001g0102 | 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 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141others(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 | a0001c0002t0001g0193a0001c0002t0001g0194a0001c0002t0001g0195others(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 | a0001c0002t0001g0185a0001c0002t0001g0186 | 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 | a0001c0001t0001g0111a0001c0001t0001g0270a0001c0001t0001g0272others(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 | a0001c0001t0001g0020a0001c0001t0002g0001a0001c0001t0002g0002others(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 | a0001c0002t0001g0206a0001c0002t0001g0221a0001c0002t0001g0226 | 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 | a0001c0001t0001g0232a0001c0001t0001g0246a0001c0001t0001g0251others(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 | a0001c0003t0001g0100a0001c0003t0001g0101a0001c0003t0001g0102 | 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 | a0001c0001t0001g0272a0001c0001t0005g0318a0001c0001t0010g0107 | 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 | a0001c0001t0001g0232a0001c0001t0001g0246a0001c0001t0001g0251others(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 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0121others(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 | a0001c0001t0002g0004a0001c0001t0002g0091 | 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 | a0001c0002t0001g0181a0001c0002t0001g0183 | 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 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141others(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 | a0001c0001t0001g0020a0001c0001t0002g0001a0001c0001t0002g0002others(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 | a0001c0001t0001g0232a0001c0001t0001g0246a0001c0001t0001g0251others(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 | a0001c0002t0001g0093a0001c0002t0001g0255a0001c0002t0001g0286 | 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 | a0001c0001t0001g0020a0001c0001t0002g0001a0001c0001t0002g0002others(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 | a0001c0001t0004g0104a0001c0001t0004g0105 | 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 | a0001c0001t0001g0020a0001c0001t0002g0001a0001c0001t0002g0002others(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 | a0001c0003t0001g0100a0001c0003t0001g0101a0001c0003t0001g0102 | 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 | a0001c0001t0001g0020a0001c0001t0002g0001a0001c0001t0002g0002others(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 | a0001c0003t0001g0100a0001c0003t0001g0101a0001c0003t0001g0102 | 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 | a0001c0001t0001g0232a0001c0001t0001g0246a0001c0001t0001g0251others(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 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(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 | a0001c0003t0001g0100a0001c0003t0001g0101a0001c0003t0001g0102 | 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 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141others(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 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0025 | 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 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141others(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 | a0001c0001t0002g0032a0001c0001t0002g0036a0001c0001t0002g0053others(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 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141others(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 | a0001c0002t0001g0213a0001c0002t0001g0242a0001c0002t0001g0244others(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 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141others(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 | a0001c0001t0002g0061a0001c0001t0002g0085 | 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 | a0001c0001t0002g0028a0001c0001t0002g0029a0001c0001t0002g0031others(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 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0139others(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 | a0001c0001t0002g0030a0001c0001t0002g0032a0001c0001t0002g0036others(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 | a0001c0002t0001g0197a0001c0002t0001g0198 | 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 | a0001c0003t0001g0100a0001c0003t0001g0101a0001c0003t0001g0102 | 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 | a0001c0003t0001g0100a0001c0003t0001g0101a0001c0003t0001g0102 | 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 | a0001c0003t0001g0100a0001c0003t0001g0101a0001c0003t0001g0102 | 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 | a0001c0003t0001g0100a0001c0003t0001g0101a0001c0003t0001g0102 | 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 | a0001c0001t0001g0020a0001c0001t0002g0001a0001c0001t0002g0002others(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 | a0001c0001t0001g0020a0001c0001t0002g0001a0001c0001t0002g0002others(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 | a0001c0001t0001g0269a0001c0001t0001g0274a0001c0001t0001g0281others(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 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0139others(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 | a0001c0003t0001g0100a0001c0003t0001g0101a0001c0003t0001g0102 | 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 | a0001c0003t0001g0100a0001c0003t0001g0101a0001c0003t0001g0102 | 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 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0139others(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 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0035 | 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 | a0001c0001t0001g0013a0001c0001t0001g0269a0001c0001t0001g0270others(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 | a0001c0002t0001g0207a0001c0002t0001g0215a0001c0002t0001g0233others(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 | a0001c0003t0001g0100a0001c0003t0001g0101a0001c0003t0001g0102 | 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 | a0001c0001t0001g0232a0001c0001t0001g0246a0001c0001t0001g0251others(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 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(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 | a0001c0001t0001g0020a0001c0001t0002g0001a0001c0001t0002g0002others(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 | a0001c0001t0010g0107a0001c0002t0001g0240 | 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 | a0001c0001t0001g0020a0001c0001t0001g0232a0001c0001t0001g0246others(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 | a0001c0001t0001g0232a0001c0001t0001g0246a0001c0001t0001g0251others(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 | a0001c0001t0001g0020a0001c0001t0002g0001a0001c0001t0002g0002others(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 | a0001c0003t0001g0100a0001c0003t0001g0101a0001c0003t0001g0102 | 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 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141others(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 | a0001c0001t0001g0020a0001c0001t0002g0001a0001c0001t0002g0002others(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 | a0001c0001t0001g0013a0001c0001t0001g0287a0001c0001t0001g0288others(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 | a0001c0001t0001g0020a0001c0001t0001g0246a0001c0001t0001g0251others(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 | a0001c0001t0001g0013a0001c0001t0001g0269a0001c0001t0001g0270others(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 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141others(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 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0119others(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 | a0001c0001t0002g0043a0001c0001t0002g0044a0001c0001t0002g0071others(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 | a0001c0001t0001g0270a0001c0001t0001g0272a0001c0001t0001g0273others(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 | a0001c0002t0001g0132a0001c0002t0001g0149a0001c0002t0001g0151others(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 | a0001c0001t0001g0020a0001c0001t0002g0001a0001c0001t0002g0002others(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 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(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 | a0001c0003t0001g0100a0001c0003t0001g0101a0001c0003t0001g0102 | 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 | a0001c0003t0001g0100a0001c0003t0001g0101a0001c0003t0001g0102 | 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 | a0001c0001t0004g0104a0001c0001t0004g0105 | 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 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0139others(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 | a0001c0001t0002g0078a0001c0001t0002g0087 | 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 | a0001c0001t0001g0292a0001c0001t0001g0294a0001c0001t0007g0293 | 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 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0139others(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 | a0001c0001t0001g0020a0001c0001t0002g0001a0001c0001t0002g0002others(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 | a0001c0001t0004g0104a0001c0001t0004g0105 | 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 | a0001c0001t0001g0282a0001c0001t0010g0107 | 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 | a0001c0001t0001g0020a0001c0001t0002g0001a0001c0001t0002g0002others(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 | a0001c0001t0001g0269a0001c0001t0001g0274a0001c0001t0001g0281others(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 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0139others(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 | a0001c0002t0001g0132a0001c0002t0001g0149a0001c0002t0001g0151others(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 | a0001c0002t0001g0161a0001c0002t0001g0179 | 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 | a0001c0003t0001g0100a0001c0003t0001g0101a0001c0003t0001g0102 | 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 | a0001c0001t0002g0001a0001c0001t0002g0033a0001c0001t0002g0034others(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 | a0001c0001t0002g0080a0001c0002t0001g0179 | 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 | a0001c0001t0001g0020a0001c0001t0002g0001a0001c0001t0002g0002others(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 | a0001c0001t0001g0020a0001c0001t0002g0001a0001c0001t0002g0002others(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 | a0001c0001t0001g0020a0001c0001t0002g0001a0001c0001t0002g0002others(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 | a0001c0001t0001g0020a0001c0001t0002g0001a0001c0001t0002g0002others(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 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0139others(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 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0139others(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 | a0001c0002t0001g0200a0001c0002t0001g0201a0001c0002t0001g0203others(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 | a0001c0001t0002g0003a0001c0001t0002g0048 | 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 | a0001c0001t0001g0020a0001c0001t0002g0001a0001c0001t0002g0002others(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 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0026others(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 | a0001c0001t0001g0020a0001c0001t0002g0001a0001c0001t0002g0002others(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 | 27 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(24): Show | 31 | HG01069.hp1 HG01071.hp1 HG01168.hp2 others(28): 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 | a0001c0001t0001g0020a0001c0001t0002g0001a0001c0001t0002g0002others(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 | a0001c0001t0001g0020a0001c0001t0002g0001a0001c0001t0002g0002others(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 | 27 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(24): Show | 31 | HG01069.hp1 HG01071.hp1 HG01168.hp2 others(28): Show |
intron_variant | MODIFIER | c.828+839C>T | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 8/9 | chr1 | 40767542 | ||||||
| chr1:40767555
|
G | A | 258 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(255): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(269): 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 | ||||||
| chr1:40767761
|
A | G | 317 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(314): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.828+1058A>G | NFYC | ENSG00000066136.21 | transcript | ENST00000447388.8 | protein_coding | 8/9 | chr1 | 40767761 | ||||||
| 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 | a0001c0001t0001g0020a0001c0001t0002g0001a0001c0001t0002g0002others(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 | a0001c0002t0001g0234a0001c0002t0001g0248a0001c0002t0001g0305 | 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 | a0001c0001t0001g0013a0001c0001t0001g0269a0001c0001t0001g0270others(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 | 258 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(255): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(269): 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 | a0001c0001t0001g0010a0001c0001t0001g0119a0001c0001t0001g0125others(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 | 314 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(311): Show | 328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): 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 | a0001c0001t0001g0013a0001c0001t0001g0139a0001c0001t0001g0140others(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 | a0001c0001t0002g0005a0001c0001t0002g0026a0001c0001t0002g0056 | 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 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141others(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 |