Tag | Content |
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EnhancerAtlas ID | HS003-22830 | Organism | Homo sapiens | Tissue/cell | A549 | Coordinate | chr19:18373410-18375170 | 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 | CACCACAGAT GGCTGTGCTG GTCTTGGTGT CACTCTATTA GGCACAGAGG AGTGTGGTAG 60 CCTTGGGGTC ACCCAATTAC CCATAGATGG GCAGGTTAGC CTTGGGGATA CCTTACTGGA 120 TGCTATATGC TGGGATAGGC TTGGGGCCAG CCTACTGAAC CCTGATGCCT GGCCTAGGTT 180 TGGGGCTACC CTACTGGCCA GTGTAGCCTG GGACACAATT GGGGCCAAGC TCTTGGCCAC 240 AGATGGTGGC TTATATGCAG TGGAGACCAC AGTACCTAAA GACAGAGTCC TCCTCAGCTC 300 TGTCTTGACG GTTGCCTGGG ACACCTCAAT CAGATTCACA GAGCTCTTGC CTAAGGAGAA 360 CTTGTGGATC TCAGCCTCTG AGCCCCAGTG AACACGCAAG GTCAAGCAGT TAGACACTGA 420 GCTGTGTTGG AAACTGGGCA CTTTCTCCGA GGCTGGAGTG GGCCGGTAGG GGAAGTGTAG 480 GGTCATGTAC CTATAGCCGG TTTCAGTCTC TTGCGTATCC TTAAACCTCT GGAGTGTCCC 540 CATGGACTCC GGAGGAAAAA CAGACTTCAC CGCAAGGTCC CCTTCTAAAC TGCTTTCCCG 600 TGACTCATCT ATCTTGTTGA CGGCAGGCAG GCTGGCCACA GACATAGTGG AAAGGCTGAG 660 GGAACTAGAA CTTTGCAGAG AGCTTTCGGA ATTGTTCTCC TGACTGTAGG TCACAAAGCC 720 CTGGGAGAAG CTCCTGGCCA GGTCACCGTC TCGATCCTGT GGCAAACCAC CTACTGGCTC 780 ACCGAGGATG GATGGCTGGT GGTCTGTTGC TAGCTTCTGG GGGCAGAGCA GGGCAGACAC 840 AGAACCCTGT GTTCGATTCC TCCCCTGTCC ACAGACAGAT GTCTTGGGAC GAACTTGAGC 900 CAATGCACTG CCGGGGGAAG CTTGAAACAG ACCATGAGTC TTGGATGCCT GAGTTTTGGT 960 CACCATGGTG ACCTGCAAGG GACTTGGGGC CCCCTTGTCT ATCACCTCCC TAGTACCCGG 1020 GGGGGCCTGT TTGCGATTTG GGGGCTGATA CCTCCTCCCC AGGCTCTCCC TGGAAGCCCT 1080 GGATGCCTGC TGCTGGCCTC TGGCCACTAA GGGTTGGTAG AGACCACGAT GTACCCCTGA 1140 GGACTGACAC CAAGGCAGGC CCCCACAGGT GAGGTAAGGC TGGTGAACAT GGGCAGCCCT 1200 CCCACCACCC ACGCTGCAAG GAAGCCTACC CGAGGCCACC CTGCCCTCCC TGGTCGATAG 1260 ATAAGAGGCC ACCCTGCTGA CCACATGTGG CCTGTGGCAG CTCGGGGCTG TGCCATAGAT 1320 CACAGAGGGC TGGTTCATGC TTGGGCCCAC ACAGTTGGCA ATGAGAGGCT GCCACAGACT 1380 CGGGGGTGGC TGCATGTGGG ACAGCTTGAG CAAACTGGGG CCCTCCCCAC TCCCCTCGGG 1440 GTTAAAATCT GATGCCAATG TGCCAGGCTC CAGGGTCGGG CATGCTTCTT CCTTTTGGAA 1500 CTTGGGGCTC AAATCCAGGT TTGAGGAGAA GTCCCTGCTG GACTCCATCA TCTCCCGGGA 1560 CAGCATGGGA TACAGGCCAG TGATCAGGGG ACCCTGGTGA ATGCTGGTGA TGACGCTACC 1620 CATCACCGAG GCTCCCACAG TGACCACAGA TAAGCAGGGT GACCCCCACA AGATGGCCCC 1680 ATCAATCCCC CATCTCCTCC AAGGGCCCGG CAGGTTGGCC CATGGTGAAA CAACCCCAGA 1740 TCCCAACCTG GGAATCCCTG 1760
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