Tag | Content |
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EnhancerAtlas ID | HS091-24199 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr19:43966000-43967270 |
Target genes | Number: 15 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFAT5 | MA0606.1 | chr19:43966320-43966330 | ATTTTCCATT | + | 6.02 | NFATC1 | MA0624.1 | chr19:43966320-43966330 | ATTTTCCATT | + | 6.02 | NFATC3 | MA0625.1 | chr19:43966320-43966330 | ATTTTCCATT | + | 6.02 | Sox3 | MA0514.1 | chr19:43966376-43966386 | AAAACAAAGG | - | 6.02 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_17644 | chr19:43966063-43969257 | CD4p_CD25-_CD45RAp_Naive | SE_26835 | chr19:43964356-43970776 | Esophagus |
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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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Enhancer Sequence | TGCAGGAAGG AGACACAGAT AGGTCAGTGG CTGGAGGGAG AGAGGTTGAC ATGGCCAGAA 60 CAAAACTTAG AGGCATCAGA CAAGAACAGA GAACCTGACC GGGCGTGGTG GCTCACGCCT 120 GTAATCCCAG CACTTTGGGA AGCCGAGGCA GGTGGATCAC TGGGCAACAG AGTGAGACTC 180 TGTCTTGCAA AAAAAAAAAA GAACAGAGAA CCCCCAAAAT GAGACAGAAA GTCTCTGCAT 240 CCATTAATCC CAAAATCTCA ACTCAGGTCC TACTATGAGA AACAGACAGA CTCACTGTCT 300 TTGGCACATG GTGGATTAAC ATTTTCCATT GTGCTTTGAA TGGAAATGTG TGTAGGCTGA 360 ACCAAAAGTA GGGTTTAAAA CAAAGGCTTA GACTGAGATA CAAGACCTCT CACAAGACCA 420 CAGTGCAGAA CAAACTTCCT CTACAACCCT CTCACCATTA TCCCCTTAGC CTTCACCCTG 480 GCTTTTACCT CCCCATCAGA ATTTACTCTT AGAGTCAGAG TTACATCTCC ACACCAGGCT 540 CAGTGGTTCA CGGCTGTAAT CCCAGCACTC TGGGAGACCT AGGCAGGGGG ATCTCTTAGC 600 CCAAGAGTTC AATACCAGCC TGGGTAACAT GGCAAGACCC CACTGTTACC AAAAATAAAA 660 GGAACCAGTC GTGGCGGTGC ACCCTGTAGT CCCAGCTACT TGGGAGGCTG AGGCGGGAGG 720 ACTGCTTGAG CCCAAGAGGT AGAGGCTGCA GTGAGCTATG ATTGCGCCAC TACACTCCAG 780 GCTAGGCGAT AGAGCAAGAT GCTGTCTTTA AAAAAAAATA GTAATAATAA AATAAAAAAG 840 AACTACATCT TCCATAGCAT AACTGGCAGG GGATGGGATT TGAAGAACTT CATTTTCCAT 900 GGTTACATTT CTCAATAGTC TGGGACAGGC GGGGGACCCC TTGAGTTTTA AGGGCTAAGA 960 ACTAGAGATT CCCCGCAGTG CCTGGGCAGA AGCTTAGAGG CTTAAATACC TCTTAAGTAC 1020 CTGGCAGCCC TCTATGGAAA TGCATTTCCC TCCAAAACAC TCTGGGACAA AGCATCACTA 1080 TCCCCACACT ATTAATATGT TGGGGGAAGG GACTGCATTT TCCATGATGC CCTACGATAC 1140 AAGCACCTAG GCCCCACGAT TCCCAGAATG CGTCGCAGGT TAAGGAAACG CTTTGGGTAA 1200 AGGGCTCCCT ACCGCCCAGG GTGCTTCAGA AGGGCTACCA CAACTCCCGT AGGTCCCGTG 1260 CTCCGGGGCT 1270
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