Tag | Content |
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EnhancerAtlas ID | HS105-75301 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr7:121076320-121077200 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ESR1 | MA0112.3 | chr7:121077065-121077082 | AAGGTCAAGAAGACCCT | + | 6.03 | Myod1 | MA0499.1 | chr7:121076476-121076489 | TGCAGCTGTCACC | + | 6.5 | Myog | MA0500.1 | chr7:121076475-121076486 | CTGCAGCTGTC | - | 6.62 | POU2F2 | MA0507.1 | chr7:121076984-121076997 | ATATGCAAATGAA | - | 7.82 | Pou2f3 | MA0627.1 | chr7:121076982-121076998 | TAATATGCAAATGAAG | + | 6.37 | Pou2f3 | MA0627.1 | chr7:121076900-121076916 | TCTGATTTGCATAGGA | - | 6.37 | Tcf12 | MA0521.1 | chr7:121076475-121076486 | CTGCAGCTGTC | - | 6.14 |
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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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| Number: 1 | ID | Chromosome | Start | End |
GH07I121436 | chr7 | 121076861 | 121077010 |
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Enhancer Sequence | TTTAATCCAA ATAATTAGCT GGTGACATAA TCCATGTGTT ATTGGAAAGA AAGCACACTC 60 CCTTTCCACT GCCATACTTC CATGTCTTCC TGTTCTCCTG TTACTCATAA TTCCTGCTCC 120 TCTTCATTAT TAACTCCTAT TTATGCTCTG GATTCCTGCA GCTGTCACCT TTGCCCTGCA 180 CATGGCCACT GCTCTCCTAC CTGCATTCAG CAAAGCACCA CTAACACTGG GCTCTTAGGC 240 AGGTAATAGA TACCTGCCTA AGGTTTGAGA ATAATAGAGA CATAGGAAAA TTCATTCATC 300 CCATTTAGTA AATAGTTTTT AACACCTATC ATTGATACAG CTCCAATGAG TGGAGGAACA 360 ACAGGTTCTT CGTCTGGAGT CGAATTAGAT AAAACGACAT GGACAGACAT GGAGTGGTTT 420 TAAGGAGCGG AGAGTTTAAT AGGCAAGAAA GAAGGAAGAA GGCAGAAGGA AGAAGCTCCC 480 CCGTACAGAG AGGGAGCCGT GCTCCAAAGT AGAGAGAGGG AACCAACCCC AAGTGCGATG 540 GATACCAGCC AGATATATGC AGAGGCTGGA GGAAGCGGTG TCTGATTTGC ATAGGACTCA 600 GGGGATTGGT TTGACCAGGC ATGTCATTCA TGTAACCCAT GAAAAAGCTG GCCCTCCCAC 660 CCTAATATGC AAATGAAGGG CGCCATGATG TTCTACACAC GTGGGGATAT GTGGGGGTGG 720 CCATGTTACC AGGAACATGT GGGGCAAGGT CAAGAAGACC CTGGGAATCA CTATGTTTGG 780 GTGGACCCAG TTTCTAATGG CCTGTTTTTG CATATCAAAG GTTGCCAGCC TGGCTCTAAG 840 AGCAGGGGCT TTACAGGAAA CTTTTCTGGA GATGCTTTTT 880
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