Tag | Content |
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EnhancerAtlas ID | HS095-15272 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr19:43507210-43508700 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXP1 | MA0481.2 | chr19:43507334-43507346 | GAGTAAACAGAA | + | 6.27 | ZNF263 | MA0528.1 | chr19:43507904-43507925 | GAAGGAGAAGATGGGTGAGGG | + | 6.03 |
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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 |
GH19I043003 | chr19 | 43507901 | 43508050 |
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Enhancer Sequence | AAAAGGTGCC ACCCTGGACA TCCAGAGTGG GGAGATGTTT TCCAGTCAGG GTCCAGGCAG 60 GCCAGCTGGA GACGAAGCTG ATTAGTGGGG AAGCTTAACT TCCAGGAGTG GAAGAATTTA 120 GGAGGAGTAA ACAGAATGCA CAACATACTG TAAACATTCC TTTACCCAAC AGTAGGAATA 180 CTCAGAGTGG GTGTGTCTTC CGTGGCAATC ATTATCTCCT GGGAATCTAA GAATGTGTCC 240 TAGAGTCAAA TGGCTTTGAT GTAAGCCAAA CCCAGAAATG GGCTTCAGGG CTGCCTTGCA 300 CATAGCATTC ATTCATCTTG AAAAAGGAAA GCATTCATCT TGCTAAAGGA ATCCCCTCTT 360 CTGGCCCAGA CCATTATTTT TGTTTTTTTA CTATCCTAAT TTTAAGATGT AAGGAGAAAG 420 ACTGAAGAAC AAAATAATGA AGTACATGAA TGAAATAACA GGGTAGAATT GAGACTGGTA 480 TGTGTAAGTT AAGAGAAATT GTGTATAAAT TTTGTGTGAA CAGAAAATTG ATTTCTTGTT 540 GCAAACAGAC CTCTCTACAT AAATAATACC TCCTGCCTTG AGTGGATAGC AGACCTCATC 600 ACAAGAACAT TCCAGCAGAG TCATGAGAGA ATGGGTAGTG TGGCTTCTTT AATTGGCAGG 660 TTAGACTGAG TAAGTTACTG AAGAGAAAGA AGTTGAAGGA GAAGATGGGT GAGGGCAAGA 720 AAAATGGGAA GGTGAAAGGA AAGGACTGAA AGGAATGTTT ACCAAGGGCT CATCAGGTAC 780 CAGGCTCTGT GACTAATGTC TTACACATGT TAATTTACTC TTCCACTGTC ATTTTCTGAT 840 GCGGTAAGAG TCAGTCTTAC ACTACAGGTG AGGAAAGAGG CTGAGGGAGG TCAAATGAGT 900 GGCCCAGGGT CATCCAGCCA CTTCATAGCA GAGCTAGTGT GTTTCACTGT GGTTTGTGCA 960 GACAGAAAAG TGAGACATGG AAGGAAGGCA AAACATTTTT GTTGTGGGTG ATGTTTATGA 1020 AAGTGACCCA TATGAGGCAG AATAATGGCC TCTTAAAAAT GTCCACATCC GGGCCGGGTG 1080 CAGGGGCTCT CACCTGTAAT CCCAGCCTTT GGAAGGCTGA TACGGGTGGA TCATGAGGTC 1140 AGGGGTTCGA AACCAGCCTG GCCAACATGG TGAAACCCCA TTTCTACTAA AAATGCAAAA 1200 ATTGGCTGGG CGTGGTGGCA CATGCCTCTA ATGCCAGCTA CTTGGGAGGC TGAGGCAGGA 1260 AAGTCATTTG AACCTGCAAG GGGGAGATTG CAGTGAGCCC AGATTGTGCC ACTGCACTCC 1320 AGCTGGGGCA ACATGAGGGA AACTCTGTCT CAAAAAAAAA AAAATCCACA TTCTAACTCT 1380 TGGAACACAT GCATTTACTT TTCTTGGCAA AAACACTGTA CAAAGGTGAT GAAGTTGAGT 1440 ATCTTGAGAT GGAAAGCTTA TTCTGGCTTA TCTATGTGGC TCCCAGTGTC 1490
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