| Tag | Content |
|---|
EnhancerAtlas ID | HS093-01332 |
Organism | Homo sapiens |
Tissue/cell | HL-60 |
Coordinate | chr1:90222910-90223920 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF4G | MA0484.1 | chr1:90223491-90223506 | CAGGGACAAAGTTCA | + | 6.12 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I089755 | chr1 | 90221267 | 90225158 |
|
Enhancer Sequence | CTTCGTATTT AAGAGACCAT TGCTCGGCAC AACATGGCAG CTAATATTTA AAACAAATGG 60
TAAAGAGGAA AGGCAATCAT TTCCTCACTA AATGAAAAAG GAGATATGAA TCTGAGGAAC 120
ACAATCCGGC ACTGATTGAA AGTAAATTAC CAGTTGATTA GACGGCTGTA AATTCAGGGA 180
GAGAAGCCTC AACCGGCAGC TGGATTTTGT AAGGAAGAGG GCAATTAGAG AGGGCACAGG 240
CGAGGCAGAG CACAGAGAGG GCTCTGCACA GAGCAGACAG GGCAGCTTTG CAACACTAGG 300
ATTACAAAGG CAGGAAGGGG TTTGTAGGAA GTGTTCTGTG GATGGAGCCT GCAAGAAAGG 360
GGAGCTCCCC ACTCCCACTC GCCCTGCCCC ACCTCCCTAG TGAGCAGGAA GAGGTTAAAC 420
TGCCAGTTCC CTGTCTAGCA GCAGTTAGGA CGGGTGTTTG TTATTGCAAC ACAGGAAGTA 480
TCACGATTTC TCTTCCTTTT TCAGGCTGTA CTCAATCTAG AAGCTTTTTG CTTCCTATCA 540
AAAGCCAGGG ACTTGAAAAC TACTCAGGTC CCTGCAGCCC ACAGGGACAA AGTTCATGCA 600
GATTTCAGTG GGAGATGCCA TCTCCGGATA GCAACTGGGG CCAGTTTTTG CAGATGGCAA 660
GCGCTTAAAG ATGCAAGCCT CCATGATTAC CACGAACTGA GAAATCTCTG CAATTAGCAG 720
GAGTGTAACT GGAAAACCAA GGGCTCCTCT GTGCCTTACC AAAAGACATT CCCTCTTCCT 780
CTGGCAAGTT GAAGAAGATA ATTTGGCCAG CCTAGGAGGA AGTGATTGAT TGAGACAGAA 840
ATGGTGGAGA GAAGGATGAC TGTGATTTTT ACTTTGGTGA TGGGCATGAA CATAACAAAG 900
AACAGATGGT GGATGCCTTA GTCCCACTGG TGTTATCAAT TCCGTAGCCC TGAGCCCTGC 960
CCTGCTACAG GCTTATGTAA TTCTCAAGCA TGTGCTCTCA TGGCCCAAGG 1010
|
