Tag | Content |
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EnhancerAtlas ID | HS091-44430 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr7:99028750-99030900 |
Target genes | Number: 20 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NKX2-5 | MA0063.2 | chr7:99029141-99029151 | ACCACTTGAG | + | 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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Enhancer Sequence | TTTTTTTCTT TTTTTTTGAG ATGGAGTCTT ACTCTGTCGC CAGGCTAGAG TGCAGTGGCG 60 TGATCTCGGC TCACTACGAC CTCCCTCCAC TTCCTGGGTT CAAGTGATTC CCTTGCCTCA 120 GCCTCCTGAG TAGCTGGGAC TACAGGTACG TGCCACCACG CCCAGCTAAA TTTTGTATTT 180 TTAGTAGAGA CAGGGTTTCA CCATGTTGGC CAGGATGGTC TCAATCTCTT GACCTCGTGA 240 TCCGCCCACT TTGGGCTCCC AAAATGGTGG GATTACAGGT GTGAGCCACC GCACCTGGCC 300 AAAAATAATA GTTTTTTAAA ATAGATGTAA TGGGCTGGGT GCGGTGGCTC ACGCCTGTAA 360 TTCTAGCACT TTGGGAGGCC AAGGCGGGTG GACCACTTGA GGTCAAGAGA CCAGCCTGGC 420 CAACATGGTG AAATGCTGTC TCTACTAAAA ATACAAACAA AATGAGCCAG GCATGGTGGC 480 ATGTGCGCCT GTAGTCCCAG CTACTCGGGA GGCTGAGGTA TGAGAACTGC TCGAGCCCAG 540 GAGGCGGAGG TTCCAGTGAG CCGAGGTCGC ACCACTGCAC TCCAGCCTGG GCGACAGAGC 600 GAGACTCTGT CTCCAAAAAA AAAGGACTGT AGGAAAAAGA AAGAGAGATC AGACTGTTAC 660 TGTGTCTATG TAGAAAGAAG TAGACACAAG AAACTCCATT TTGTTCTGTA CTAAGAGAAA 720 TTCTTCTGCC TTGAGATGCT GTTAAACTGT AACCCTAGCC CCAACCCTGT GCTTGCAGAG 780 ACATGAGCTG TGTTGACTCA AGGTTTAATG GATTTAGGGC TGTGCAGGGT GTGCTTTGTT 840 AAAAAAGTGC TTGAAGGCAG TAGGCTTGAT AAAAGTCATC GCCATTCTCC AATCTCGAGT 900 ACCCAGGGAC ACAATACACT GCGGAAGGCC GCAGGGACCT CTGCCCAGGA AAGCCAGGTA 960 TTGTCCAAGG TTTCTCCCCA TGTGATAGCC TGAGATATGG CCTCGTGGGA AGGGAAAGAC 1020 CTGACTGTCT CCCAGCCTGT CCCCCAGCCC GACGCCCATA AAGGGTCTGT GCTGAGGAGG 1080 GTTAGTGAAA GAGGAAGGCC TCTTTGCAGT TGAGATAAGA GGAAGGCATC TGTCTCCTGC 1140 TCGTCCCTGG GAATGGAATG TCTTGGGTGT AAAACCAGAT TGTGTGTTCT ATTTACTGAG 1200 ATAGGCGAAA ACCGCCTCAG GGCTGGAGGT GGGACCTGCT GGAGACAATA CTGCTCTTTG 1260 ATGCACGAGA TGTTGTGTAG GTGCACATCA AAGCACAGCA CCCTTCCTTA AACTTATTTA 1320 TGACACAGAG ACCTTTGCTC ACATATTTTC CTGCTGACCC TCTCCCCATT ACCCTATCGT 1380 CCTGCCACAT CCCCCTCTCC GAGATGGTAG AGATAGTGAT CAATAAATAC TGAGGGAACT 1440 CAAGAGACCA GTGCCTGCGC AGCGCAGGTC CTCCGTATGC GCAGGTCCTC CGTATGCGGG 1500 ATGCTGAGCG TATGCTGAGC ACCGGTCCCA GGGGACCACT GTTCTTTCTC TATACTTTGT 1560 CTCTGTGTCT TATTTCTTTT CTCAGTCTCT CGTCCCACCT GACGAGAAAC GCCCACAGGT 1620 GTGGAGGGGC TGGCCCCCTT CAGAGGAGCA GATGCGGTGG CTGGGCTGTG ACCTGTAATC 1680 CCAGCACTTT GGGAGGCTGA GGCGGATGGC CAGGGGTTAG AGACCAGCCT AGACAAAGCA 1740 GCACAATCCC ACCTCTACAA AAAACTTAAA AATTAGCCAG ATATGGTGCT ACACACCTGT 1800 GCTCACAGCT ACTGGCGAGG CTGAGGCAGG AGGAACTCTT GAGCCAAGGA GTTGGAGGCT 1860 GCAGTGAGCT ATGACTGCAC TCCAGCCTAG GTGACAGAGT GAGGCTCCCT CTGTTTTTTT 1920 TTGAAGGGAA AAGAAAGGGA ACATGGGGAC CGCCACAGTC CAGGCAGGTG CTAAAGGGCT 1980 TTCCATGTCA TCTCGTTTAT CACCCACAAT CACCACCATT TTAAGGAGAT GACTCTGAGG 2040 CCAGGGAGGT GAAGTCACCT GCCCAGTGTA AAGCACTAGC AAGTGGCACA CTTGGGATCC 2100 GCCCCCAGCT TTTCAGAGCC TCACCCCGGC TGCCCTGCGC CCACATGCAC 2150
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