Tag | Content |
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EnhancerAtlas ID | HS092-14681 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr13:50285450-50286420 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ESRRB | MA0141.3 | chr13:50285804-50285815 | TCAAGGTCAAA | + | 6.14 | Esrra | MA0592.2 | chr13:50285803-50285814 | TTCAAGGTCAA | + | 6.14 | NFAT5 | MA0606.1 | chr13:50286345-50286355 | AATGGAAAAT | - | 6.02 | NFATC1 | MA0624.1 | chr13:50286345-50286355 | AATGGAAAAT | - | 6.02 | NFATC3 | MA0625.1 | chr13:50286345-50286355 | AATGGAAAAT | - | 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 |
GH13I049710 | chr13 | 50284944 | 50286358 |
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Enhancer Sequence | TAATTCTCCC TGCCCTCACA AATTAGCTAC CTAATAATCC CACAGAAAAA CACTATTTAC 60 AAGAATGAGG CCAACACACC ATACTGTTTC AAGTTCAGAA GAGAACAGAA AGGTCATCTA 120 TTTACTCTAC TGGTTTTCCA ACATATTTAG CAATACAATT TTTCAGGCTA CTAAAGTAAA 180 CCAATAAAAG AAATGACTTG GCACTTTAAC TTCATCTGGG GAAAAAACTG TTTGAAAATC 240 TCCTGAAATG TGTCCCCAAC TGAAGTATAA ACCTGGAGTA TAAACCATGC CCTAGGCCTA 300 TCCTAACTTT GCAACTACAT AGAAGAAAAC AGGCTTAGCG ATCTGGTGAT TCATTCAAGG 360 TCAAAGATCT TGTATGTGGC ATTGCTTGGT GTCGTCACAG AGGAATATAA GCACTGGTTG 420 TAGCTTATGC AAAATCAAGA TGTTTCCTAT TAGGTCATCC AAATTGAAGA CATCACATCT 480 TTTTGCCCTA AAATAATAGC AGGCACCTGA ATTCACATAC CCTTCAAAAA AGGATATAGA 540 TGAATAAATA AAATAGAACT ACACATATAA CCCACACCCC TTCAGCATTA CTAAGAGTCA 600 GAGAACACTA AAAATTTCCA TTATCTGTAA GAGGAGAAAA AATTAAATTC TAGCTTTTGT 660 CTGGACCTCT TGCCTCAAGA CTGTGTAAAA GAGAGGACAG AAGCTGGGCC TAAGAGCTGA 720 GCCCACCTAC CAGCCCATTT CCCACTCTGG AAGTGAGGAG GCCTCCCTGC TGGAGGTGTC 780 TGCAGATGCT GGGTCTGAGA ACAAAGTCTG GCTACTGCCC ACCCTGGCAG TAACAGTAAC 840 TAGATTTACC TAGAAACAGG GGTCTCAAAG CATAACACCA ATATGTGTAG GCTACAATGG 900 AAAATAACCC TTCATACCAA GATCCAGGAA ATTCTCAAAA GAGAAAAGAC AGTCAACAGA 960 TGCCAATATT 970
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