Tag | Content |
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EnhancerAtlas ID | HS098-27471 | Organism | Homo sapiens | Tissue/cell | HSMM | Coordinate | chr19:18373690-18375170 | 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 | GACAGAGTCC TCCTCAGCTC TGTCTTGACG GTTGCCTGGG ACACCTCAAT CAGATTCACA 60 GAGCTCTTGC CTAAGGAGAA CTTGTGGATC TCAGCCTCTG AGCCCCAGTG AACACGCAAG 120 GTCAAGCAGT TAGACACTGA GCTGTGTTGG AAACTGGGCA CTTTCTCCGA GGCTGGAGTG 180 GGCCGGTAGG GGAAGTGTAG GGTCATGTAC CTATAGCCGG TTTCAGTCTC TTGCGTATCC 240 TTAAACCTCT GGAGTGTCCC CATGGACTCC GGAGGAAAAA CAGACTTCAC CGCAAGGTCC 300 CCTTCTAAAC TGCTTTCCCG TGACTCATCT ATCTTGTTGA CGGCAGGCAG GCTGGCCACA 360 GACATAGTGG AAAGGCTGAG GGAACTAGAA CTTTGCAGAG AGCTTTCGGA ATTGTTCTCC 420 TGACTGTAGG TCACAAAGCC CTGGGAGAAG CTCCTGGCCA GGTCACCGTC TCGATCCTGT 480 GGCAAACCAC CTACTGGCTC ACCGAGGATG GATGGCTGGT GGTCTGTTGC TAGCTTCTGG 540 GGGCAGAGCA GGGCAGACAC AGAACCCTGT GTTCGATTCC TCCCCTGTCC ACAGACAGAT 600 GTCTTGGGAC GAACTTGAGC CAATGCACTG CCGGGGGAAG CTTGAAACAG ACCATGAGTC 660 TTGGATGCCT GAGTTTTGGT CACCATGGTG ACCTGCAAGG GACTTGGGGC CCCCTTGTCT 720 ATCACCTCCC TAGTACCCGG GGGGGCCTGT TTGCGATTTG GGGGCTGATA CCTCCTCCCC 780 AGGCTCTCCC TGGAAGCCCT GGATGCCTGC TGCTGGCCTC TGGCCACTAA GGGTTGGTAG 840 AGACCACGAT GTACCCCTGA GGACTGACAC CAAGGCAGGC CCCCACAGGT GAGGTAAGGC 900 TGGTGAACAT GGGCAGCCCT CCCACCACCC ACGCTGCAAG GAAGCCTACC CGAGGCCACC 960 CTGCCCTCCC TGGTCGATAG ATAAGAGGCC ACCCTGCTGA CCACATGTGG CCTGTGGCAG 1020 CTCGGGGCTG TGCCATAGAT CACAGAGGGC TGGTTCATGC TTGGGCCCAC ACAGTTGGCA 1080 ATGAGAGGCT GCCACAGACT CGGGGGTGGC TGCATGTGGG ACAGCTTGAG CAAACTGGGG 1140 CCCTCCCCAC TCCCCTCGGG GTTAAAATCT GATGCCAATG TGCCAGGCTC CAGGGTCGGG 1200 CATGCTTCTT CCTTTTGGAA CTTGGGGCTC AAATCCAGGT TTGAGGAGAA GTCCCTGCTG 1260 GACTCCATCA TCTCCCGGGA CAGCATGGGA TACAGGCCAG TGATCAGGGG ACCCTGGTGA 1320 ATGCTGGTGA TGACGCTACC CATCACCGAG GCTCCCACAG TGACCACAGA TAAGCAGGGT 1380 GACCCCCACA AGATGGCCCC ATCAATCCCC CATCTCCTCC AAGGGCCCGG CAGGTTGGCC 1440 CATGGTGAAA CAACCCCAGA TCCCAACCTG GGAATCCCTG 1480
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