Tag | Content |
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EnhancerAtlas ID | HS052-35660 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr7:107232740-107234150 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MEF2A | MA0052.3 | chr7:107233527-107233539 | GCTAAAAATAAA | + | 6.04 | MEF2C | MA0497.1 | chr7:107233525-107233540 | CTGCTAAAAATAAAA | + | 6.01 | NEUROD2 | MA0668.1 | chr7:107232997-107233007 | ACCATATGGC | - | 6.02 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr7 | 107233593 | 107233997 | chr7 | 107233533 | 107233880 |
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| Number: 2 | ID | Chromosome | Start | End |
GH07I107593 | chr7 | 107233466 | 107233590 | GH07I107591 | chr7 | 107232401 | 107233374 |
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Enhancer Sequence | CCAAAGATGA TATACAAATG ATCAACAAGC ACATGAAAAG ATGTTCAACA GCATTAGCTA 60 TCAGAGAAAT GCAAATAAAA ACCACAAAGA AATGCCACTT TACACCCACT AGGATGACTA 120 TAATCAAAAA TATAATAACA AGTGTTGCTG AGGATATGGA GAAATTGGAA CCAACATACA 180 CTGCTTGTGG GAATGTAAAG TAGTACAGCT GCTTTGGAAT ACAGTTTGGC AGTTCCTCAA 240 AAATTAAACA TAGAGTTACC ATATGGCCCA GCAGTTCATC TCTTAGGTAT GTACCAAGAG 300 AAATGAAAGC ACATGTCGAT ATAAAACTTG CACATGAATG TTCGTAGCAG CGTTATTCAT 360 AATAGCCGGA AGGTGGAAAC AGCTCAATGC CATCAACCAA TGAATAGATA AACCAAATGT 420 TACCACATTC ATACAATGGA ATATTATTCA GCCATAAAAG TAATGAAGTA CTGACACATA 480 CTACAGTGCA GACGAACTTT GAAAGCATTA TGCTAAGTGA AGGAAGCCAG ACACAAAAGA 540 GCAGATAGTA TATGATTCAG TTTATATGAA ATGTCTAGAA CAGGTAGTTC TGTAGAGACA 600 GAAAGCAGAT TGCTGGTCAC CAGGAGCTGA GGGATGTGTA TAGATTTTCT TTGTGGGGTG 660 ACCAAAATGT TCTGAAATTA GATAGTGGTA ATGGTTATAC AACTTTGTGA ATATACTAAA 720 AACTACTGAA TTATACATTT TAAAGAGGTA AATTTTTATG GTATGTGAAT TACATCTCAA 780 TAAAGCTGCT AAAAATAAAA TAGTAGTCAA AAAGGCCCCA GTTTTCTAAC TGGAGTCTCC 840 TTGTGTGGCA ATAACTCTTA CCCAAGACTT CTGTTGGTCG CATGAAAGGG GAGCATTCAA 900 ACTTGTTCAT ATACTTCCAC TGGCTTTTGA GACCTTATAA GGCAGATGCC TTCCCTAGTA 960 CATACAAGAA TCCAGGAACT AAGAATGCAC TCAATGTAGA CCCTTATAAG CTGATATCTA 1020 TTTTCCACTG GAAAGAAGTG GTTCCCCTGC ATCTGAGACT TCCCAGAACT GAAAGCATCA 1080 AAGGAGCAGC TATCTGAACC TTTCCAGTAG CAGCTGCTAT GCACTAGTCG GAGGAGTGTA 1140 TGCCACCACA GATCAAATCC CATGTTAACA AACTTATGCC AGTGGAAATT TCAGTATAAC 1200 CAAATATTTT GAAAATCTCA ATCATTTAAA GTAATAATAT GTAATAAAAT GCTAGTGTAG 1260 TAAGAGAAAT GGGATAGTCT CTTGGAATTG ATTGTAATGG GATATGACAT CTGTCATTGT 1320 CAATAGGCTG AATTTTAGTC ATCTTAGAGA CAGAAAATGT AAAGGATAAT AGTTTGCAGT 1380 GTAGTTAGAG ATGAGAAACA ATAAAATGAT 1410
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