| Tag | Content |
|---|
EnhancerAtlas ID | HS113-18498 |
Organism | Homo sapiens |
Tissue/cell | Keratinocyte |
Coordinate | chr2:1050440-1051890 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFAT5 | MA0606.1 | chr2:1051498-1051508 | ATTTTCCATT | + | 6.02 | | NFATC1 | MA0624.1 | chr2:1051498-1051508 | ATTTTCCATT | + | 6.02 | | NFATC3 | MA0625.1 | chr2:1051498-1051508 | ATTTTCCATT | + | 6.02 |
|
| | 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 |
| GH02I001053 | chr2 | 1049462 | 1051935 |
|
Enhancer Sequence | TGTATTTTTG GATTTTCAAA GAGGTACATT TTCAAATGAA AAATCTAAAT TGGGAAAATG 60
AAGAAAGTAA AACAGAATAA TGTAATTGTA ATTAGGGTCT ACTATTAAGC ATTTGAAATA 120
CATGAGATGA AAATTAGCCA TTTTAGAAGT TAAAAATATT GCCAGGGTGA TGGCTTTTTT 180
TGTTTTGTTT TTGTTTTTGT TTTTTTTTCC CTATTGATTC CTTTGGTCTT TATTTCATTC 240
AGAAAACAAT TGCCTCTCAC CTCCTCTATC CAGCCTGCGT CAGGTACTGC TGTGTGAGTC 300
TATAAATGCT GTTACCTCCT CTGTGCAGCC CACGTCAGGT ACTGCTGTGT GTTGCTATAA 360
ATGCTGTTAA CTCTGCATTC ACATTGTAGA CGTGGCCCTG ACTGCAGGGA GCCAAGAGAG 420
AAGTGGCTTC ATGTCATGGG CAGCGAAACA GGGGCTGTGT GAGAGGAGTG GGAATGTGAG 480
CTTGCCCCGG CCCAGGCCAT CTGCCTGACT GTGCAGTTCA TGGCTTGGGG CCGCTCTGCT 540
CGGGGCTTCT TTCTGTAAGT TTTTCATTTT GTGTAGGTGA CTTTTTCCAG TGCTGTTGCC 600
TAGAGTGGGT ACCGTTTTCT GATGAGCCCA CACAGAAAGA ATGCATTTCC TCTCACTGGA 660
GGCTCACGAC CTGCCTTGTG TCTGATGACC CACACAGAAA GAATGCATTT CCACCCACTG 720
TGGAGGCTCA CAACCTGCCT TGTGTGGGTC AGGATTTTTC ATGGACGTCA CTAGATCAGT 780
GTGCTGAATG CCCATCGAGA CAAAAATACT AATTTTGAGT CAGTGTGATG CCAGAAATGT 840
TTTTATCAAG TAGCAGGTAC AACTATTTAT CAGTTTTAAT ATGAAAATGT TAGTCATTCA 900
TAGAGATCAA ACCATGTTGC AGAAATTCAG ATTTGGAAGA AACCCGGAAC AGTAATTGAT 960
CTTATCCATT CTCCTAGGGT TATCATGAAG GATTTAACAG TGTGAACATT TCCATTTTCT 1020
AAGGTGACCG TGCCTTTATT TTGATGGCTC TGAATTGTAT TTTCCATTCA GTTGCAGCAC 1080
CAGCCCTCCC TTGATGTGCA GAATGAGCAG GTGTCTTTAG GAGTGAGGCT GGGGCACGAC 1140
TGAATGCAAA TTAGCCCTTG CCCAGACAGA AGACAGTCTC ATCTCACCAG CGGTATTTCC 1200
TGGAGGGTCT GATCTGTCCT GGACATGCGG TGGGTCGCGG GGACTGCAGC TTCATCTCTC 1260
AGACGGCTCC TTGTCCCCAC TGTTTCAGAG TGGACACAGG GAGAAGGGGT GAGGCAGCTG 1320
GGACCCAGGC GGCTCCTCTG GCTCCCATCT TGGTGGGAAG CTGGTCCACA CCACCAAGAG 1380
CACGGGGAGG ACTCCCTGCG GATGGGCTCC AGCTTCATTC TGAAGGAAGG AGTTGAATAA 1440
GTTAAGGAAA 1450
|
