Tag | Content |
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EnhancerAtlas ID | HS177-04614 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH_RA |
Coordinate | chr11:111999050-111999990 |
Target genes | Number: 15 | Name | Ensembl ID |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Tcf12 | MA0521.1 | chr11:111999705-111999716 | CAGCAGCTGTT | - | 6.32 |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH11I112128 | chr11 | 111998729 | 112000881 |
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Enhancer Sequence | GAGACACTCG GTCTAAAAAA AAAAAAAGAA AAAAAAATTA GTTTGTCTTC TTCTACCTAA 60 GGGTGAAAAT AACATGTGAG CTTCAAGATT CAATGCATGG CTTCCAACCC TGATGGGCTA 120 GCTGGAGAGT GGTGGAGTGA GAAGACAAGG TGGCAGACCC AAGGTGGATT GTCAGATGGC 180 AGAGATGGGA AGACACCAGG AAACCAGGCT CATATTTTCA TGGAACCACT GGCTGCTGAA 240 GCCTGTGACT TTGGCAGGCA GCCCAGGGTG AATCACTACT TAGATGAATG AGGAGATTCT 300 GCTTTGTCCC TGACACTTCA AATTGTTATT CCTTCCTTAA GCAATTTATG GGCACTCCCA 360 TAGACTCTCT AGCCTTTGGA GCCTTTGCAT TAGGAGCTTG ATTTATGGAT ATCTGTATAG 420 TTACAGGAAA TAATGTCGTA TAAAAGGCAT TTAATATGGA GGGGCTTTAT GACCCCTTGC 480 TTGGGTGTAA CCATCCCTGT CAGGGTGCCA GGAGAGAAGG GTGGAGCCTT TTTGGATGCT 540 GGGAAGTGAG GGTGTGAGGT GTTATCCAGG TGGGAAAGGC ATGCTGAGAG GGAGGGCCCC 600 TGTGTGGTTC TGAACACTGT GCTCCATCCA CACAGCCCTC CTCGGGGGCT GGGTGCAGCA 660 GCTGTTGGAG TTCTTTCTTC ACAGTAAATA TTTAACCACG TAAGATGCCC AGGCTACCAG 720 CCACTGCTAA GTGACAGGCA AAATCCTAAG CCACAGATGT TGCCCTCTGG CTCTCAGCTC 780 AGAGAGCTGA GGCTGTTGAC TGGAGTCCTC AGAACTTCAG AGAGCTTGGA AGTTTGTGCA 840 TTTCATCAAC TGACTTGCTT TGTCTGCCAG AAAGCATTAA GCCTCAGAAT TTATACCTTC 900 CCTTCTTCAT TCATTTGTGT ATATTCATAC ATTGAGCACC 940
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