Tag | Content |
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EnhancerAtlas ID | HS091-42809 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr6:160225670-160227010 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr6:160225914-160225935 | AAAAAGAAAAAGAAACTGACT | - | 6.93 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr6 | 160225965 | 160226045 | chr6 | 160226924 | 160227000 | chr6 | 160226295 | 160226365 |
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| Number: 1 | ID | Chromosome | Start | End |
GH06I159805 | chr6 | 160226199 | 160228999 |
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Enhancer Sequence | TATGGCCTGT TTCTCCAGGT GCCTTTTTGT TTCCTTGTTG CTGTTGTCTG CATTTCCCGT 60 GGGCGGGCGT GCCGTTTCCA GGAGTGTGGT GACCTCCATC CATGCTTGGC GGGGATGGCT 120 TCAGCTGCCT GTGCAGCTGG CGCTGCTCTC CCTGTGCCCC AACTGAGAAT GGCTTTCACC 180 TGTCTCCATC ATGTTCCACT CCCTAATGAA CCTCTCACTG CGTTGAGTGT GAGTTTCAGT 240 GTTTAAAAAG AAAAAGAAAC TGACTCCTAA TTTGGAACTC AAAGAAACAA GAATTCCATT 300 CCAGTGCTAG AGGGGAAGAA ATCGTTCTGT TGGACTTGCT GTGAGATGTT ATGTTGATCC 360 CCCATGTGAT CTTCTGAGGG ATTTTTCAAG GATATCTCTC GGGCAACCTT GACTGTGCCA 420 ATCATACTGG GCACTGACTT CAGATGTGTG CCTTGGTTAG GCTGTGTCTG CCCTGCTGTG 480 CCTGACCCTG CTCCCCTAGG CCGGGACCTC TGCCTTTTTA CTTTGGCTGT CTGTGCCAGC 540 CCCAGTCTCC AAAACCTCGT ATTCCTGTAG AGCTGGGGTC AGGAGTGACC ACAGCGAGAG 600 CAACAGCATT GTGGGTAGAC GGACCGGGGG CCTTGGGGCT GGTACCCTCA CCTGGAGCCA 660 AGTGCTATCA GCTAGGTGTG GGTTTGAACA AGGTATGGAA GCTCTTTGCC TTTATCAGGA 720 AGGGGGAGAT TAAATGAACA TCTGAAATGC GATGAGTGAT GATCTCTTCC AGATAATTCT 780 GTTATGTTGG AGGAATTTTT GTCTCTTTGT ATTTTTCCTG CTGGTTTTCA TATAAAAATG 840 TAGCTTTTTG TAAGGGAAAA ACAAGTTGAA TTTTTAACCT TCTTTCATTT TCAAGAGTTG 900 GAGAAAGGCC TTTCCTTATC TCAAAATGAT GTTAGGTTCT GTTTCTGATG CAAGAGGCAA 960 TGTGTTTACC AAAGTCCTTG TCTTTTCCTG ATTATCCCAG ATAGAGACTT TATCACCCCT 1020 GAAAGCTGAA TAAAGAAGAC GGTCCTGATA GCAATGCTTG GTATTGGCTA GATACCAATA 1080 GCTTTTCCTC CATACATCCT AGTGAAGCAG GAGGGGATTG AATATATGCC TGGATCCTAT 1140 GGAAGGTTGT GGGCTATTCT TCCAATTGTT TGGCTTCCTA TTGCATAAGA GCCTCAGAGA 1200 AGAAATCGTC TTCTTTTGGT ACATTTTCTT TGTATATTGC AACATGAAAA CCAGAGGGTT 1260 CAGAAACTGC TCTCATGTTA ACATAGTCTT GCGGTTCTGA AGTGTTTTTC TCTGACATGT 1320 TCACTTTCAT GCGCCCATTT 1340
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