Tag | Content |
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EnhancerAtlas ID | HS091-19037 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr17:16216930-16219120 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr17:16219012-16219033 | TCTTTCTTTCTTTTTTTTTTT | + | 6.25 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_28022 | chr17:16216124-16217657 | Fetal_Intestine | SE_28895 | chr17:16216081-16217967 | Fetal_Intestine_Large |
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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 |
GH17I016312 | chr17 | 16216254 | 16217805 |
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Enhancer Sequence | ATGATTCTCC GGGTGATGGA TGTGGGGGAG GGTTTGTTTA TTTGATTAGG GCTCATGGTT 60 TAAAGTCTAA AGCACTTTCC CACTTGTTAT CTGAGCCCAT GAAACTCACT GCTGGCTTAT 120 CTTCTAGCCC TTTTTGGCCA TGTTGCTCAC TGCATCTCAC CATGTCCTCT CGCTGAGAAA 180 TCTCTCTCAA GTCCTAGTAC GAATGCTCGT CTCCTAAACA GCTGAATTCT TTTTTATACA 240 CTGAATACTG CGAATGGGGT AATTGACTTT ATTCATCTCT TTTCTGTGGC CACAGGAAGC 300 TTGAGGGCCA AATTTGCAAG CCCTGTGGCA CTGGACAAGA CTTTAAGGAA TGAGTGCTGT 360 CAATCAGTGT GCCTCCACCT TCACCATCTT CTTCCCCTTA CTCTCACTTC CGTCATGTGT 420 TTTATACAAC TCTCAAATCT TTCTTGGAGA AGGAGGATAT ACATACATAA TATGAAATGT 480 GTTTGTTCTT CACAGTCACC CGATTTTACT GATATTTATT TGCATTTTAC CAATAAAAAG 540 AAAATGCAAG CTCAAAGGTA TTGAGTGACA TAGAGTCATA CAAACATAGA TGTGTTTCCT 600 GTCCCCTAGC AAAGTGCTTC TCCTGGGCCC CTGATCAGTG GTGTGGCAGG CCTGTCCCAG 660 CTACTGAGGA AGGAAAGAAG CAACTTGAAG GGAAGGACTT ATTTAATAAC CTTCTTCTAA 720 ACATGCTTAA CACTCAGACT GAAGCAATGC AATATGTAAA GTTGGAAATG ACCTCACCAA 780 CCATTAAGTC CAATCACTGG GAAGTGGTTT GCCCAGCACC ACAAGGTTAA ACTATGGCAG 840 AGGCAGAATT CAGGAATCCT AGTTCTCCAT TCATTATTCT GTCAGATGTA TGTGAAGACC 900 AATCCAAACT GAAGACCCTC CTTGTCCTTA AATTTTACAT CACTTGGTGG AAGATGCTAG 960 AATTTTACCC ACATACTCTT TCTAGGCAGA TTTCCCTGTT TCCTTGACTA TGGAATGAGG 1020 GGAGGCTAGA CTGTTCTCCC TGTAAAGACT ATTCGGTTCC TGGTCCAGCC AGCAGCCACA 1080 GCTTTAGAAG AGACATGCTC CTAGTCGCAT TAGGTCCCTT CAAATTCAGG AAAGAAACAT 1140 TCCCTGGTTA CAGTCTGAAA TACAAATTTT TTTGATGATA TATGGAAAAA TGAGGCAGCC 1200 CCAGAGTGGT CTTTCCAACC ACATGGTTAC TCTGAGGCCT TGAGCTTCCA AGACTAGCAT 1260 GGACAGCAAG CCCCATGGAG AACTGGAAAA ATGGTCCCAC CTCATTCTGG ATGCACACTG 1320 AGCCTGGTGA TTTCTCTCCG AGAATTTACA CTGCACCAGA GAAAGGATCA GGTCAGGTCT 1380 ATTGCAAACA AAGAGTACCT CAACAGGCAG GGGGCTGGGG CACTTGAGAT TGAGTCACCT 1440 GGTCCCATTC CTGGTCCAGT CACCACTGAA GTGGAGAAAA TAGAGAAGGC GTCATTCTGG 1500 GCAGAGAAAG AACCCAAGGG GACAACTCTG TGTAGATAGA ACTGCCTGGG GCCATTTTCC 1560 TCAGAAGAGG CTGGAGTGCC ACAGGCTCTC AGCACGAAGG AGGGCCACTG TGCTTCAGAT 1620 AAAACAATTC ATGGACATGC CACCAATCTG CCACAACCTT TTTCCCCACA GTCATCTCTT 1680 GCCTGCTAAA TTCGTTAGAC TCACGTTAGT CCTCAGCCAC CTTGAACCTT CTGTGGCATC 1740 TGGCCCTGCC TGTCCCTCAC TGCAATGCTG CTTTGACTTA TATGGCACCA GCTTGCCCTC 1800 CTCACTCTGG CCTTTCTGGC TACTTCTCAT TCTCTTCCCG GCTTCCCTCC CACCAGTGGC 1860 CCCTTGGTCC CCCTGTCCCC AGGGCTCACT CCCCAGTCCT CCTCAGCACA GCTTCTCCTG 1920 TGGCTTTAAG GGCTATAAGC TCTACTTCCA GACAGCGCCT CTAGCTCACT GCTTTCCCTG 1980 GACATCAGAA TATCCACAGG GCTTTGCCCA GAGTACAGGA CAAGCCACTT CATTCTCAGG 2040 ATCCCAGAAA GTTTTTTCAG TCTTTTCTTT TCTTTCTTTC TTTCTTTCTT TCTTTTTTTT 2100 TTTTTTTTTT TTTTTTTGAG ACAGAGTCTC GCTCTGTCAC CCAGGCTGGT GTGCAGTGGC 2160 GTGATCTCAG CTCACTGCAG CCTCCGCCTC 2190
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