| Tag | Content |
|---|
EnhancerAtlas ID | HS184-20853 | Organism | Homo sapiens | Tissue/cell | T47D | Coordinate | chr3:124901610-124902700 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr5a2 | MA0505.1 | chr3:124901642-124901657 | CCTGGCCTTGGCCTT | - | 6.14 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | AAGTTCTGGG ATTACAGGCG TGAGCCACCG CGCCTGGCCT TGGCCTTGTC CCCATTTTTG 60
TAAAAACAAG CAAGCACTTC AAAAATCCAT AAATACATGT GTATAAGCCG AGGGAAATGT 120
TCCAAAAGAG AACACTGGGA TCACCTCAAG GGTGTGGGGG AAAGCTCTTT ATTTTCATTG 180
TCTCCAATGT GTTAACTGAC TACAATGAAT ATCATTATGT AACTGTCAAA GAATTTTATT 240
AAAAAATACA AGCAAACATA TTAAAAGTAC CCTTATGTTT ACGCAAAAAC TAAATCAGGG 300
TATATCATCA CCCTGTCTGC CCAGGTTTAG GGAAGCAGCC CAGGACTCAA GGCCTTCGTC 360
CACACACTCA GCAACTGCCC AGCCTTCCCT AGAGCAATCC AGCCACCCCA GAGGCGGTAC 420
CCCTTCCAAC CTGAATGCTG CTTTTCCTTG GAAAACATTC CTGGTGGTTT GTTTAATGTG 480
TAAATGTCTT AAGGGTTTGT TATACGTTAA ACGTATTCTA TTTCCTCCTA AATCTTAGAC 540
CAGGCATTCC TTTTCTTTTT CATTCTCCAC AGAGAAAAGC CTAATTCCTT CTCACAAGAC 600
ACAGTGGGTG TTGCTCACCA TTTTAAAGAG AGAAGGTGGC CTATTTTCAG GGTGTAATGC 660
TTCCATTCCA AGGTAATTCT TTTAGCAAAA TTGCACCTTG ACAATCACAG GCATTTTCCT 720
TCCACCTTAC CTGGAGGACC AGCGCTGCCC CTCAACACCC CTCCCCTTCT GACACAAACT 780
TCCAGGTTTA AGGTTAAAGA GTTGGTGGAT TAACACATAT GTCCTGAATA TGCGTTAACA 840
CCCATAACAA AAACTCCAGG CCTATATCAG GTCCATAAAA ACTTTCCAGT CATTCATTGT 900
TTTTATACAG AGTCCAGCAC AAAGCATGTG AGCCACTAAT GAACGTTCTT CCACGTGTCA 960
GCACAGGCTG AAGCTAGACA TTTTGGTGTT CAGGGTAAAC AGTCACCAAG AACCCTCAGG 1020
CCCACACAGG TAAGTGGAGC AGGGAGTGAG GGGAGTCTGT AGTCCATCGT CTCCTCCCCT 1080
GACAAAGAGT 1090
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