Tag | Content |
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EnhancerAtlas ID | HS184-06874 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr11:125743640-125745270 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr5a2 | MA0505.1 | chr11:125745009-125745024 | AAGTTCAAGGACATG | + | 6.22 | ZNF263 | MA0528.1 | chr11:125744544-125744565 | TTCTCCCTCTACCCTTCCTCT | - | 6.06 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH11I125874 | chr11 | 125744521 | 125744670 |
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Enhancer Sequence | ACTTGGTCCA ACTAAATCCC TAGGCCCTAT GTAAATCAGA TACTGCCTCC TCAAGCCCTC 60 TATAAAACCA GCCGCTTCCC ACCGCAACCC GGGAGATCCC TTCGGAACCC CCTCCCTCTG 120 CACAGGGGAG CTTTCCTCTT GTTTCTTTCA CCTATTAAAC TTTCTGCTCT TAAACCCATT 180 CCCTGTGTGC CCACATCTTT GTTCTCCTTA GCGCGAGACA ACGAACCTCA GTTATTTCCC 240 CAGACAGACA ACACCACTTC ATTGTGGGGA CTCGCCCAGG ATCAGAATCA GAACAGAAGG 300 TATATTCATC AGAGGGGTGA GTACAGGCGC AGAACTTAAC TTTCAACTCT GTCCTTTCAT 360 TTGGAGGCTC TCGGCCTCCA TCTTAAGTTC AAACAATGGG CATCCTATAG CCACCTAAAT 420 GCTAATAGGG CGGCCGCCAT GCGGGAAGTC TCAGATGTTA GGCTTGCTTG GGAGAACATG 480 GAGAACTTCT CAATACTCAC GGATCATTGG GAATGTTGGC CATGCTTCTC GAACCAGTTT 540 TCTCTCACGG AGGACCTAGC CGTCGCGTGG GGCTAGAAAA GGTCCTGAAG CAACTGAAGA 600 TTTCTCGCCA GGACTACACC CTGGTGTTAT CTGAAGGCTT CTGGACTGAC CCCACCTCCA 660 ACTGCCCGGC TGGGTGTCCG CAACAGGATC TACAGCTGTC CTATCGCAAA ATTTCCTCAT 720 TTCCTATCCG CAAAGGCCAT GTCTCCTATC CTCTCTGTGT ATGCAGTGTT TGAGAATTTT 780 TACAGTTCAG GAAAATAGTC CTGTTAGGAA AGATTAGCGA ATGCCATAGT AACTGAGAAT 840 ATAGCACAAG GGAATGCTGT TTTCTGTCAT TTTCTAGGAG CAAAGAGCCC TTCTCAATAA 900 GCATTTCTCC CTCTACCCTT CCTCTGGGAA GCGCACGGTA TTTCTAGGTC AACGTCGCCA 960 CCTAGTGGAA TAGGAATCCT CTCCATGAGG CACAGCGTTG GTCCATTGCT GTAACACTCT 1020 AGCCTCCCAA TTCTCCTCCC TTTTTGCACC CCTATACTAG AGACCAGGCT TTATGCCCCT 1080 TCTGTGAATG CGAAAACACT GCCTTCAACA ATTAGGAGTA AAATGTCCTC CAAAGCCAAA 1140 TTTTAGTTCT GATACTGTCC CATCAGCAGG AAAACAGCCA TTAGGTCCCT ACGTTCTTTT 1200 AAGGCACACA TTCTGCCCCC AGTTAAAACA GTACTTAATT AGTAAGGAGA TTTTAAATCC 1260 AGAAGTTCAC CAGAACCATT CTCTAAGGGT AAACCATTCT CTAAACACCT GAGATTGGGT 1320 AATTTAGAAA GAAAAGAGGT TTATTTAGCT CATGGTTCTG CAGGCTTGGA AGTTCAAGGA 1380 CATGGCCACC CTGGCTTCTG GTGAGGGTGT CATAACATGG CAGACAAGGT CAAAAGAGAA 1440 GAGAACAGGT ACAAAGAGAG AAAACCTGAA GAGCATCTGG GCTTTATAAC AACCCACTCT 1500 TATGGGAACT AATCCATTCC TGTGTTGCCA GAGTGAGAAT GCAAAGCCAT TTCATGAGGG 1560 ATCCACCCCC AAAACCCAAA CACTTCCCAC TAGGTCCCAC AGCCCAACAT CACCACATAG 1620 GGGATCAAAT 1630
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