Tag | Content |
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EnhancerAtlas ID | HS187-13855 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr2:113847380-113848170 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFYA | MA0060.3 | chr2:113848033-113848044 | TCTGATTGGCC | - | 6.02 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I113090 | chr2 | 113847761 | 113847860 |
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Enhancer Sequence | ATTAATGCTT GCTAGAATAA ATAGCTCTAC TGAATAGCAG ATGGAGGAAA GCACACTGGG 60 CTTTGCAAAT CATCACTGTG ATGCATGTAA TTTTGCAGCA CTGCCAGGGT TTCTCACAGC 120 AACTCATTCC CATTGTGGCC CCTTAGGGAA AGCTGTGACC AGTGCAAGAT CTCTCCTACC 180 TGCATGACCT CAGGGCCAGC AACAGACAAT TGCAACTCCT GCCCACAGAC TCCATGGGTC 240 AGGGAACCAC TGGAAAGCAA AGCAGACACT TGCTGTATCA GGGTTGGAGG AAGCCTTTGA 300 GGCCCTTTGC ATGCAGCTCA GAGAGGAATG GCATTCTCAG GTTGAGCAAA GGGAAGTGGC 360 TAGCACTTCA GACATGACAC TCATTGAAGC TTGGAGGAGA CTTTTTTAGG GCAAAGAAAG 420 GGAAGTTTTA TTTCACTCAT GGTTAGTAAA CATAAGACAT GTACATTCTT AATACATCTC 480 CAAATAACAT TAGAGGAAGA CCAGGAACAA TGCTGAGGGG ATAGAGCTAT AACCGACTGG 540 GGTGAGAAGT GGGGGCATTT GGGAAGGGTG AGAAGTGGGG GCATTTGGGA AAGAGTCCTC 600 ATTCCAAGTG GCCTCAAGGT CAGTATCTGG GCTCCTGTGA TTCTCTCTGA TGCTCTGATT 660 GGCCACTGCA TTGGAAATGC CACTCAGGCT CAGATTGGTG CCCTCCTTGT GTGTTTTTTC 720 TTTATCACAT ATCCTACAGT CCACTTTCCT GATTCTCTCC TAACATGTGC CTCTTCTTGA 780 GATCAAGAGG 790
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