Tag | Content |
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EnhancerAtlas ID | HS091-27205 | Organism | Homo sapiens | Tissue/cell | HepG2 | Coordinate | chr2:110883250-110885030 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EGR4 | MA0733.1 | chr2:110883831-110883847 | GAATGCGTGGGTGGAA | - | 6 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CACGAACTCT AAAGAGCAAA CAGAAATATT ATGTTAGTCC AAGTAGTAAC AAGTCCTTGC 60 AACACTTATG CAAATTTACT CTGTAAATAA ACTTATGGAC AGGGTTAAAA ATGCTGTACA 120 GATTCTATAC AAGCAAGAAG TGAATCTGTA ATTAGGAATC TATTGCAAAT GACCCAGCAC 180 CAGAATGACC AGGCAGATGT ATCTGTGAAA AATGCCGTAG AAGCCCATGA TAATTATAAA 240 TCAAAACTAA CTTAAGAATA GAATCAGCGA AACACTAACA CATCCATGAA AACTATACAA 300 CCACAGCACC TGAATAATAA AATAGTATTA AGCTTTCCAA GTAAGACAGT AATGAAAATA 360 GAAAACACTG CCAAATACCA AACTTTTCTA CAATTCTCTC TGTCATGATG ATGACAATGG 420 TCAGAATGAG ACAGACTGAA GTACAATTTT GTGAGTAAAT ATTTCTAATC TGTCCACAGG 480 GCTTCACAGA AATTTCCTCA AATAAATAAA AACCCCAGAG TTCAATTAGT CCCACAGAAG 540 TATGAATTTA AGACTTTCAC TGTGCCATTT CCTGGCAAAC TGAATGCGTG GGTGGAATAT 600 GACCAGTCTC ACGGCTGCCT GTTCCAGGGT CTGGGTTCTG TGCATGTCAG TAGATATCCT 660 CCTGTTGGCA CCTGATATCA TGAGTAACCT GAAAGCATCA GACCTTTCTC AGCAGGGAGG 720 CCCTGGGATG AACATAACAT ATGGCACCAA TAAAGAGATT CTCCATAAAA TAAATGATGC 780 ATTGATAGAG CGTTTCTCAG CAGGAGATAA CAGACTATGC CACTCATGAG AACATTTTGG 840 AATGTTCATA CCTATTACCA CGTGAGGGGA CTATGGTCCT CCACCCTATT AACTGCTGTG 900 CTATGGGTCC TTAGGAGTTT GAAGAGGACC CTTACAGAAC CAGAGTGTTT TACTAAACAG 960 GCCAAGTGCC ATTCTTCTTA TTATTAAAAT GTCATCCACA AACTGAACTG TGCTAGGTAA 1020 GTAAACTCTA GGAGGCTCAC ATGCTGTACA TTTTAAATTT TATTCAGTTG GTGCAAAAGT 1080 AATTGTGGTT TTTGCTACTA CTTTTATGGC AAAAACCACA GTTCTCTTGC ACCAACCTAA 1140 TAATATGGTT TAACGTGAGT ATCACTTAGC AAATGTAGAC TTAGTGTCTG GTAAAATTTG 1200 TCTATTTTTG TTAGTTACAT GTCAATGTCC CACCTTATTT TTCATTCAGC CACCAGCAAA 1260 TAGTAGGATG TTTCACTTAG AGTAACTCAT TTGGGAATAG CAAACGTGTT AAAGGTCACT 1320 ATTACCTCAC CAAGATCCAC TTCCTTTCTT CTGGAACAAA AAGAAGACTA TACCTCCTTT 1380 GAAGTTAAAT GGACCGTGTG ACTGGTTTTG GCCAATGCAA TGTGAGCAGA AGTGGCCCAG 1440 GCCCCTTTGA AGCAAAGGCA GTGAAAGCCC AAGAACAATT CTCCATTCTC CCTCTTCTGC 1500 AGGGAAACTG GCAACAGAGG CAGCTACTTG TTCCAGATGG TGCTGTGAGA CAGTAGAGGC 1560 TCCACCAGCC TGTACCCTTG GGTGACTGTG GAGCAGCATC TTCCACTGAT CCATGCTGGA 1620 TACATACCAT GGGTAAGAAA TAAACCTGTG CTAACCACCA CAGCACAGCC AAGCTTCTCC 1680 TAAGTAATAC ACTATGCCAC GGAGAGAAGA AGGCTCATGG GTGTAGAAAC AACCACCACT 1740 TTCTTTTTTA AAATTATCAT AACACAAATA ATTCAATGTG 1780
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