Tag | Content |
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EnhancerAtlas ID | HS091-27504 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr2:128081820-128083300 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NR2C2 | MA0504.1 | chr2:128083156-128083171 | GGGGGTCAGAGGTGG | + | 6.04 |
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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 | TAAAGAAAAA ACATCACATT AAGTTTACAG AAAGAACGTA AGACATTAAA AAGAAAATCT 60 TTGAGCAATA TCTATATCTA TCTGTGCCTC TCTGTATGTG TTTGTGTAAA GGAGCTCACT 120 TTGAAAGGTT AGCATACCTA AAAAAGAAAA ACTACACTTA CTTGGTACAT GTAGGCAAAG 180 AGCATGACTT AAAATTAACC TTACAGTACA GTGGAAGAAT GACGTATTTT GGAATCATTA 240 GGTGTTTCTA AGCACTGTGT TTCAATCCAA GCTCTGCCAC TTAACTATGT AACCTTGGCA 300 AATCACCCTT CTGCATCAAC AAAAAAGATA ATTTCCAACT ATTCAAGTGT ACATAAGTAA 360 GGTATCCAGG ATAGTGTTTT GCAAATGGTA AGTACTCAAA TATATAGCTT TCTCGTTACT 420 ACTTCCCTGA ATTTCTTAAA TGTCTACCTT AAGATAGACA TTGACACAGA CAGAAATTTC 480 ATATACATGG ATAAAAGAAA CTTAAATGTG CATTCCCACG CAATATTAGT TATTTTTTTC 540 AGAATTTGCT TTCATAAAGC AATTCCAGAG AGGATTACCA AGAATACTGT CCTATTGAGA 600 CCAGGAGGGG GAGCACGTGT AACAAAAAAT TCACATTTTG CAACTTTATC CTGCTCATAT 660 TCCTGAACAG CTTTTTCACA AAAGTACTTA AATTTTTGCC TACATGTACC AATGTGACAC 720 AGTGGGCTAC AATTTCCAAG AATTTAAATT ATTTCTAATC TGGTGCCAGA ATGAACATAA 780 TCCTGAACAG GTGAAATAAC TCAGGAAATT TCCAAAACCA AACATATTAA TGTAAAAGTT 840 GATAGCACTT TTCATAAACA CAGTTTTAAA AGTAAATGTA CATAAATTCT AAATTTGATT 900 TGCCTTCAAA CACACAATTT TGACAAGCAG GAATACTCAA ACTATTATAA TCAGATTTCC 960 TTTTAACTAA CAAAGATACT GAGTCCCATG AGGTAAAGGG ATTTATCCAC ACTGTGCAAA 1020 AATTCATCTG CCGTCATCAT ACACAAGTAC CAATTCTATT CCTCTGAATG TAGCACAAAA 1080 AAGTTACTGA TAATTCAACA TTCTATCTGT ATGAATATTT ACTCATATCT ATTAAAAAAG 1140 AAAACTACAG TAAGCTGAGC ATGGTGGCTC ATGTGTGTAA TCCCAGCGCT TTAGGAGACC 1200 AAGGCAGGAG GTTCGCTTGA GCCCAGGAGT TCAAGATCAG CCTGGGTAAC AAAGTGAGAC 1260 CCCCATCTCT ACAAATAATA CAAACAAAAT AGCCAGATGT GGTATTAATA GCAAATGCCT 1320 TTGGTCCTAG TTCCTCGGGG GTCAGAGGTG GGAGGACTGA TGGAGCCAAG GAGGTCAAGG 1380 CTGCAGTAAG CCGCATTCAC GCCACTGCGC TCCAGCCTGG GTGACAGCAA AACTCTGTCT 1440 CAAATAAACA AATAAACCCT CCAAAAACTA CGATAAACAT 1480
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