Tag | Content |
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EnhancerAtlas ID | HS065-02607 | Organism | Homo sapiens | Tissue/cell | GM18508 | Coordinate | chr19:18373470-18374980 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ESR2 | MA0258.2 | chr19:18374117-18374132 | AGGTCACAAAGCCCT | + | 6.3 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| | Number: 2 | ID | Chromosome | Start | End |
GH19I018262 | chr19 | 18373661 | 18373810 | GH19I018263 | chr19 | 18373901 | 18374050 |
| Enhancer Sequence | CCTTGGGGTC ACCCAATTAC CCATAGATGG GCAGGTTAGC CTTGGGGATA CCTTACTGGA 60 TGCTATATGC TGGGATAGGC TTGGGGCCAG CCTACTGAAC CCTGATGCCT GGCCTAGGTT 120 TGGGGCTACC CTACTGGCCA GTGTAGCCTG GGACACAATT GGGGCCAAGC TCTTGGCCAC 180 AGATGGTGGC TTATATGCAG TGGAGACCAC AGTACCTAAA GACAGAGTCC TCCTCAGCTC 240 TGTCTTGACG GTTGCCTGGG ACACCTCAAT CAGATTCACA GAGCTCTTGC CTAAGGAGAA 300 CTTGTGGATC TCAGCCTCTG AGCCCCAGTG AACACGCAAG GTCAAGCAGT TAGACACTGA 360 GCTGTGTTGG AAACTGGGCA CTTTCTCCGA GGCTGGAGTG GGCCGGTAGG GGAAGTGTAG 420 GGTCATGTAC CTATAGCCGG TTTCAGTCTC TTGCGTATCC TTAAACCTCT GGAGTGTCCC 480 CATGGACTCC GGAGGAAAAA CAGACTTCAC CGCAAGGTCC CCTTCTAAAC TGCTTTCCCG 540 TGACTCATCT ATCTTGTTGA CGGCAGGCAG GCTGGCCACA GACATAGTGG AAAGGCTGAG 600 GGAACTAGAA CTTTGCAGAG AGCTTTCGGA ATTGTTCTCC TGACTGTAGG TCACAAAGCC 660 CTGGGAGAAG CTCCTGGCCA GGTCACCGTC TCGATCCTGT GGCAAACCAC CTACTGGCTC 720 ACCGAGGATG GATGGCTGGT GGTCTGTTGC TAGCTTCTGG GGGCAGAGCA GGGCAGACAC 780 AGAACCCTGT GTTCGATTCC TCCCCTGTCC ACAGACAGAT GTCTTGGGAC GAACTTGAGC 840 CAATGCACTG CCGGGGGAAG CTTGAAACAG ACCATGAGTC TTGGATGCCT GAGTTTTGGT 900 CACCATGGTG ACCTGCAAGG GACTTGGGGC CCCCTTGTCT ATCACCTCCC TAGTACCCGG 960 GGGGGCCTGT TTGCGATTTG GGGGCTGATA CCTCCTCCCC AGGCTCTCCC TGGAAGCCCT 1020 GGATGCCTGC TGCTGGCCTC TGGCCACTAA GGGTTGGTAG AGACCACGAT GTACCCCTGA 1080 GGACTGACAC CAAGGCAGGC CCCCACAGGT GAGGTAAGGC TGGTGAACAT GGGCAGCCCT 1140 CCCACCACCC ACGCTGCAAG GAAGCCTACC CGAGGCCACC CTGCCCTCCC TGGTCGATAG 1200 ATAAGAGGCC ACCCTGCTGA CCACATGTGG CCTGTGGCAG CTCGGGGCTG TGCCATAGAT 1260 CACAGAGGGC TGGTTCATGC TTGGGCCCAC ACAGTTGGCA ATGAGAGGCT GCCACAGACT 1320 CGGGGGTGGC TGCATGTGGG ACAGCTTGAG CAAACTGGGG CCCTCCCCAC TCCCCTCGGG 1380 GTTAAAATCT GATGCCAATG TGCCAGGCTC CAGGGTCGGG CATGCTTCTT CCTTTTGGAA 1440 CTTGGGGCTC AAATCCAGGT TTGAGGAGAA GTCCCTGCTG GACTCCATCA TCTCCCGGGA 1500 CAGCATGGGA 1510
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