Tag | Content |
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EnhancerAtlas ID | HS080-09034 |
Organism | Homo sapiens |
Tissue/cell | H9 |
Coordinate | chr12:119714680-119715480 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXP1 | MA0481.2 | chr12:119715321-119715333 | TTCTGTTTACAT | - | 6.92 | FOXP2 | MA0593.1 | chr12:119715322-119715333 | TCTGTTTACAT | - | 6.02 | SCRT1 | MA0743.1 | chr12:119715023-119715038 | GTGCAACAGGTAGCA | + | 6.09 | SCRT2 | MA0744.1 | chr12:119715023-119715036 | GTGCAACAGGTAG | + | 6.09 | ZNF263 | MA0528.1 | chr12:119714804-119714825 | GGTGGAGGGTGTGCAGGAAGA | + | 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 | CAGAGCACCA ACTAACTCTC AGAACTATGC CAAACATGGG GGATGAGAAG ACAATATGAT 60 ACGATACACT CCCTGCCTTC AGTGATGTCA TTGAGACCTA TGATGTGGTC TATCAGGGTC 120 AGGGGGTGGA GGGTGTGCAG GAAGAACAAG ATGGAAACGA AGAATTCCAG TCCTGCATAT 180 ACCCAGGAAG CTACCATGGA AGGCACACAT TACATAGATG TCATCCATAT ACAGAGATTT 240 GGTTATTTTA AGATTAACCC TTTCTTGTCT GGAGTTAGCT AAGAGAAAGT CAGGGATGGG 300 AGACAAGGCT GCTAAGTTTG GAAAAAGAAT GTCTCCCTGA TGTGTGCAAC AGGTAGCACA 360 GGACACTGGG AACAGGGGGA TGTACTGGAG GGAACCAAGA GGGAAAAATC GGAGTTGCAG 420 GGCTATGTGT TTTTCTCAGC AGCCTTTACA GCCCCAGATG ACAGCCTCTG CAGTCATTGT 480 CTATGGCCCC TCTACAGCCC TCTTGGAACC TTCAGAGCTC AGCAGATGCA TAGACCTTCA 540 GCTGATTAGC CTCAGAGGTG ACTGGGCGGC TCCAAGAGGC TAGAAGCAAA GAAAGAGCAG 600 CGAGTGTGGA GGTGGATGGG TCTAATTATG CAGGAGCCAT TTTCTGTTTA CATAAAAATA 660 CCTTGAGTAA TCAGTGGTGA TGAGCAAGAG GAGGAAAGAG CCTGCCTGAG AGTCTGAGGA 720 TGTTATGATC AATTAAATAC CATCTTTCCA AATGTTTGCA GAGGGGAATT TTAAGATGGA 780 ACTGATTTTA ATTTGACAAA 800
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