Tag | Content |
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EnhancerAtlas ID | HS105-46513 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr2:181901690-181902930 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NKX2-5 | MA0063.2 | chr2:181902606-181902616 | ACCACTTGAG | + | 6.02 | TFAP2A | MA0003.3 | chr2:181902047-181902058 | AGCCTCAGGCA | + | 6.32 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr2 | 181902007 | 181902210 | chr2 | 181901731 | 181901965 |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I181036 | chr2 | 181901007 | 181903386 |
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Enhancer Sequence | AGACTTACTG TATTGAACCT TGATTGTGAC CTCACATCAT CCATAGTTAT GCATTGTATA 60 ATGACATTTT GATGAACAAC AGTCCTCATA TATAATGGTG GTTCCAGAAG ATTATGATAG 120 AGCTGAAAAA TTCCTGTCAC CTAATTGAGG TTGTAGTCAT CGTAGCATCG TCAGACAGTG 180 CATTACTCAC ATGTTTGTGG TGATGCTGGT GGAAACAAAC TTGTGCTGCC AGCAAATATA 240 ATTATATGTA GTACATACTT GATAATAAAC AACTGTGTTC CTGGTTTATG TATTTACTGT 300 ACTTTTTATT GTTATTTTAG AGTGTACTCC TTATTTTTTT AAAGTTAACT CTAAAACAGC 360 CTCAGGCAGT TCTTTCAGGA GGTATTGCAG GAGAAGGCAT TGTTATAGGA GATGACAGCT 420 CTATGTGTAT GTTATTGCTC ATGAGGACCC TACAGTGGAA CAGGATGTGG CGGTGGAAGA 480 CAGTAGTGAT ATATATGCTC CTGAGCCTGT GTGAGCCTAG GCTAATGTGT ATGTTTGTGT 540 CTTAGTTTTT ACAAAAAAAG TTTAAAAAAT TAAATAAAAT AACTTTTAAA AATAAAAAAG 600 CTTATAGACA AATACAAAGG AAAATATTTT TGTACAGCTA TACACTGTGT TTGTGTTTTA 660 AGCTCAGTGT TACTACAGAA GAATCAGAAA GTTAAAAAAA AATTTTAAGT TGACATAGTA 720 AAAAAGTTAC AGCCAGGCTC ACACCTGTAA TGCCAGCACT TTTAGGAGGT TAAGGGGGGA 780 GGATTATTTG AGGCCAGAAG TTTGAGGCCA GCCTGGGCAA TATAGCAAGA CACCATCTCT 840 ACAAAAAATT TAAAAATTAG CGGGCATGGT GGCATATGCC TGTAGTCCCA GGTGCTTGGG 900 AGGCTGAGGT GGGAGGACCA CTTGAGCCCA GGAGTTCAAG ATTGCAGTGA ACTATGATCA 960 TACCACTGCA CTCTGGTCTG AGTGACAAAG TCAGATCTTG TCTCTAAGCA CAAAATAAAA 1020 GTTATAGTAA GCTAAAGTTA ATTTATTATT GTGGAAGAAA AGTATTTTTG TATAAATTTA 1080 GTATAGCCTA AGTGTTTATA AAGCCTGCAG TAGTGCACAG ATACATCCTA CGCCTTCACT 1140 ACTCACCCCT GACTCACCCA GACCAACTTC CAGTCCTGAA AGCTCCATTG TGGTAAGTGC 1200 CCAATACAAG TGTACCACTT TTTATCTTTT ATATCATTTT 1240
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