| Tag | Content |
|---|
EnhancerAtlas ID | HS184-31690 | Organism | Homo sapiens | Tissue/cell | T47D | Coordinate | chr9:131955720-131956750 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESR1 | MA0112.3 | chr9:131956134-131956151 | CAGGTCACACTGACCCA | + | 6.35 | | ESR1 | MA0112.3 | chr9:131956134-131956151 | CAGGTCACACTGACCCA | - | 6.84 | | ESR2 | MA0258.2 | chr9:131956135-131956150 | AGGTCACACTGACCC | - | 6.36 | | ESR2 | MA0258.2 | chr9:131956135-131956150 | AGGTCACACTGACCC | + | 7.6 | | SP2 | MA0516.2 | chr9:131955992-131956009 | GTGGGGGTGGGACTTAC | - | 6.31 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TTTGCATTTT AAAAGTGATC TGGGAGATGC GGAAAGACTA TTTGGCCACA ACGAACTTTT 60
CACAAATCAA ATGATCCTCC CCAGCTTCTT GTACGGGCAG TTTCCTGGTC TGCACAGCCA 120
TGGCCTCAGT GCTGCGGCCC CATTAGTAGT TTGGTACACC TGGTTGAGAG CGCGGCTCTG 180
CCAGTGACTA GTGTGGAATA ACAGTCACCA GGGTTTGCTG GGTTCTCACC TGCTGCTAAG 240
CGCTCCCATC TCATCGCCTT CATGGCTCTG CTGTGGGGGT GGGACTTACA CTCCCCCATT 300
TTCCAGGGAA GGAAACCGAG ATTTGCACAG GCTAAGCCAG TGCTTCTCAG ACCTGGCTGT 360
GCCTCAGAAT CACAGCAGGG CTTGTTCATG ACACAGAGTC TCAGGAGGGA GGGCCAGGTC 420
ACACTGACCC AAACTTGAGT CTAATCCGCA CTTCCCTCTT GTCCTCCCTG TCACCTAGCA 480
CTTCCTGCCT CCCAGGGGCA GCTGGGGGTT CTCTGAGTTC CAGAAAGAGG GAGACATGGG 540
AACAGGTGAG GACGCAGGGG ACAGAGCTGC CTCACGTGCC ATGCTGGGGC CCCTCGAGAG 600
TACCCACCTC ATTCCCTGCT CTCCCTGAGG TGCCCTGAGA CCCGACTGAG CCTCAGCCAG 660
CCTCTTGTCT CCTCTCTCAA CATCCAGGGT GGCGAGACTC CAGCCTCCCT CTCTCCGTCC 720
CTCCCCAAGC CCTGCCTGTG CCATGCCCTG AGGAAGACTC TGGAGGAGTG CATGGTCTTA 780
TGGGGGAGAC AGTGTCTCGG GTGAGCTGCC TCTACAGTCA GCCTTTCCCC ACACTCAGAG 840
GAGAGCACCC AGGAGCCAAC TCTCAGCCCT CCTGTGGGTT CTTTGTGCCT AGAATACAAT 900
CCCCTCTCTG TTCCCAACCC TTCAAACTCT CCCCTTCCAA AGCTGCTTCC TCCAGGAAGC 960
CTTCCTTGAT CTCCCCGTTA GAACCATCCA CTGTTCTTTG TCCCTGTGAC TGTGAACATC 1020
TCTGCTTAGC 1030
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