Tag | Content |
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EnhancerAtlas ID | HS146-03004 |
Organism | Homo sapiens |
Tissue/cell | NHDF |
Coordinate | chr11:94690590-94692020 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ESR2 | MA0258.2 | chr11:94691303-94691318 | GGGTCAGGGTGGCCT | + | 6 | Foxq1 | MA0040.1 | chr11:94691280-94691291 | TATTGTTTATT | + | 6.62 | Sox6 | MA0515.1 | chr11:94690736-94690746 | CCATTGTTTT | + | 6.02 |
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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 |
GH11I094958 | chr11 | 94691205 | 94691775 |
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Enhancer Sequence | TCTAAATCTA AAAGGATTTT GTTGTTTCCT TATTCACTGA ATCTATCAGC CTTGCTTGGC 60 CTTGTGCTTG ACAGTAGCAA CCTATTTTCT AGCAAATTGT TGGTAAATTT TCCTGACACT 120 ATTTACTAAA TAGTTCATTC TCTTTTCCAT TGTTTTTCTT ATTTCTTCTC CTTTTAGAAT 180 TTTTTTTCCT ATGTACTAAA TTATTTTGTA GCTGTGCTAG TATCTGACCT TTTATTATGG 240 TCCATTTTTC CTTCATCTCT TTATTCTGGG GACAGAACCA CACTAATTTT TGTACATTTA 300 TAATGCATTT AAAAATTGGT AGAGAAAACC CCTCTCATTA TTCTTGCTTG CAAGATTTTT 360 TTTTTCTGGA TGTTCTTACA AATTTATTCT AATGAAAAAT TCTAAAAGAA TTTGGTCAAA 420 ACACCAATTA CATGGGTTAA AAAATATCCC AACCCATTTC GTAATTTCTT TTGGATAGAG 480 AACTGGTATC TTTATACCAC TGAGTCTTCT CATCCAGACA TATGTATTCC TCCACATTTA 540 TTAAAGTCTT ATTTAATGCC CCACAAGAGA GTACTGGCAT TTTCTTCAAA GAGGTCCTGT 600 ACATTTCGTC TTCAGTTTAT GCCTATGCAT TTTACATTCT CTGTAGCTAT CATGAATGGG 660 ATTGTCTGTC CATTATATTT CCTAAATGGT TATTGTTTAT TACAGGGATG GTGGGGTCAG 720 GGTGGCCTAG CAGGAGGCAC AAAGCCAGCT CAGGAACTGG GGCATCTGTG GGGCCTGCTG 780 CCACAGGGAA CATGCTTGGA TGCTCTGCAA GCTTTGCCAT GTCTGCTATC CCAGTTTTCT 840 TCTCGTTAGC AGCTTCTTCC TCCCTTGTGA CTTGTTTGAA GTAAACTCTT CAAGAGAGTG 900 ACTCACCTCC CAGTTCTTAC TGAAAATACT CTCTGGAAAT AGGCCTCTGA GACCAAGAGT 960 TAGACTTTGA AGGTGTGAGT GCAGAGGAAA TCTCAAGATG CATTAGAATT CTCTTCTCTG 1020 AAAAAGTCAA AATATTATTT AAGCCCCCAC CCCTCTTTCC CCCTTTCTTG GGCTCCAGCA 1080 CATACAGAGA TGGCTGAGCT CCCAGAAAGC TGCTTCCAAT TAGTCTAGGA CTTTTAGGAG 1140 CCATTTCTCT GCCTCTTTCT GAAAAGGGAG GCTGTTTGAG ACCACCCTAG AGAGGAAACC 1200 TGGCAGACGC CTCTCTCAGG AGTGTGAACA CAACAGGTTT CTTCCTTCTC CTCTCACCTC 1260 CTAAAGTGCC TCTGAGAGCT AGGTCAGGTG AGAGAGAACA GGACATTTTA AAAAATACAA 1320 AACTCCTAAA AGGGCCCTGC ATAAAGATTT CAGGAACATA GATGTATGTG GAGGCTCTGT 1380 GGGAGTGTAA TTTAGGAAAG ATGCTGGTGA CACATCTACA ACATCACCAC 1430
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