Tag | Content |
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EnhancerAtlas ID | HS064-03950 |
Organism | Homo sapiens |
Tissue/cell | GM18507 |
Coordinate | chr13:45941470-45942520 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFAT5 | MA0606.1 | chr13:45942407-45942417 | AATGGAAAAT | - | 6.02 | NFATC1 | MA0624.1 | chr13:45942407-45942417 | AATGGAAAAT | - | 6.02 | NFATC3 | MA0625.1 | chr13:45942407-45942417 | AATGGAAAAT | - | 6.02 | Nr2f6(var.2) | MA0728.1 | chr13:45942203-45942218 | TGAACTCCTGACCTC | - | 6.22 |
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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 |
GH13I045366 | chr13 | 45940916 | 45943622 |
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Enhancer Sequence | ATGAGGACAA GGACATTTTA TTATCATGGG ATTATGGGGA CAAATGATTG CTGAAATCAT 60 AATTAGCTTT CTGGCGGGGG AAGATAGTAA GGTAGAAAGA GGAGAAATGG GTGTAATCAA 120 AGGAAGTGGC AGAGAGAGAT TAAAAAAAAA AAACAGGAAA TGAGAACAAG AATATGACTA 180 ACAATGCCTG AGCCCCACCC ACCCATCCTC AGAGTGGACT CCCTCTCTCA AAGGCTTGTG 240 GGCACCTGCC CCCGAGCTGA CTCACCCTGT TCAGTCATCA CAGCTCACTG CAGTGATGAA 300 GGCTCAGGTG ATCCTTTCAC ATCAGCCTCT CCAGTAGCTG GGACTAAAGG CATGTGCCAC 360 CATACCTGGC TAATTTTTTG TTTTTGTTTT TGTTTTGAGA TGGAGTCTTG CTCTGTCACC 420 CAGGCTGCAG TGCAGTGGCA TGATCTAGGC TCACTGCAAC CTCCACCACC TGGATTCAAG 480 CAATTCTCTG CCTCAGCTTC CTGAGTAGCT GGGACTACAG GTGCCTGCCA TGACGCCCAG 540 CTAATTTTTT TGTGTATTTA GTAGAGATGG GGTTTCACCA TGTTAGCCAG GATGGTCTCG 600 ATCTCCTGAT CTCGTGATCC ACCTGCCTCA GCCTCCCAAA GTACTGGGAT TACAGGTGTG 660 AGCCACCGTG CCCGGCCGTA TTTTTTGTAT TTTTAGTAGA GACAGGGTTT CACTATCTTG 720 GCTAGGCTGG TCTTGAACTC CTGACCTCAA GTGATCCACC CACCTCGGCC TCCCAAAGTT 780 CTGGGATTAC AGGCATGAGC CACTGTGCCC AGCCACCCGT CACCTGCTAG TGTAGACAAA 840 TGAATAAACT TAGACAAGCA CATGGGCTCC CTCTATACCA GCCTAGACTT TGACACTGAA 900 ACTCCATGAG TCTGGGCCAC TTCCTGCCAC AAGTGTGAAT GGAAAATAAA TCATTTTCCA 960 AGGAACCCAA AATCACTAAG CCAAGGAGTC AAGCTGAGAA CTTTCAGGCA AACCTGCCCC 1020 CCATTTTATT TCCTAAATAA GAGAGCTACA 1050
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