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EnhancerAtlas ID | HS176-18932 | Organism | Homo sapiens | Tissue/cell | SK-N-SH | Coordinate | chr19:33662740-33663250 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
JUN(var.2) | MA0489.1 | chr19:33663023-33663037 | ATGACTCATCTATT | - | 6.04 | MEF2C | MA0497.1 | chr19:33662840-33662855 | AGCTATTTTTGTATT | - | 6 | Nr2f6(var.2) | MA0728.1 | chr19:33662897-33662912 | TGAACTCCTGACCTC | - | 6.22 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GCGATCTTGG CTCACTGCAA CCTCCGCCTC CTGGGTTCAA GTGATTCTCC TGCCTCAGCC 60 TCCCAAGTAG CTGGGACTAC AGGTGCACGC CACTGTGCCC AGCTATTTTT GTATTTTTAG 120 TAGAGACGGG GTTTCACCAT ATTGGTCAGG CTGGTCTTGA ACTCCTGACC TCACCCACCT 180 TGGCCTCTCA AAGTGGTCGG ATTACAGGCA TGAGCCACCG CGCCTGGCCA TACAGAATAG 240 TTTTACTATT CATCCCTCCT CCTCTTCCCT ATAATCCTGG GCAATGACTC ATCTATTTAT 300 ATTCTTCAGT TTTGCCTTTT CCAGAATGTC ATATGGTTGG AATTATACTC TGTAGCCTCT 360 TCAGGTTGGC TTCTATGGCA TAACAATGTG CATTGAAGGT TCCTCTGTCT TTTTGTGCCT 420 TGACAGCCCA TGTCTTTTGA TTGTTGAATG ACATTCCTTT GTATGGATGT ACCACAGCCT 480 GTTTTGTGAC CGCTGGTTTG CTATTTGTTT 510
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