| Tag | Content |
|---|
EnhancerAtlas ID | HS176-13569 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr15:42120390-42121650 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr15:42120825-42120843 | TCTCTCTTCCCTCCTTCC | - | 6.02 | | EWSR1-FLI1 | MA0149.1 | chr15:42120829-42120847 | TCTTCCCTCCTTCCTTCT | - | 6.77 | | Spz1 | MA0111.1 | chr15:42120655-42120666 | GCTGTTACCCT | - | 6.62 | | ZNF263 | MA0528.1 | chr15:42120825-42120846 | TCTCTCTTCCCTCCTTCCTTC | - | 6.75 | | ZNF263 | MA0528.1 | chr15:42120821-42120842 | TCTTTCTCTCTTCCCTCCTTC | - | 7.45 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_27389 | chr15:42119324-42127945 | Esophagus |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | GTGGCTCTCC CACAGGCTGC GGCGATTTCC GAACACGGGA GGGGCCCTGG GATGCCGCTG 60
ACACCGGGGG CTCGGAACCT CGTGTGTGCG ACTGCCCTGA GGCCCCGCTC GGGTTGCTCT 120
TCTGTGGCAA CCTGCTTCCC TTCTCCCGTG TTCGCGCGCT CCCGCGGCTT CCTGGGTGAT 180
TCTGTTCACG TTGTTCCCAA GGCCCGGTGC CGTCTTGACC GTGGTCGCGG CGAAGCCCTG 240
TGTTTCCTAC AGTCTTGAGC AGCTTGCTGT TACCCTTGTT GAAAGCTCAT CGAAGGCACA 300
CAGCTGGTGG TCGGATTCCT CCCCCACGCG CCCCACCTCC GACCTCAACT CCCTTGTCGC 360
ACTTTGGGAG GATTGCAGGC TGACCAAATG GTCCCTGGCT CTTCCCCTGC TTGGTTTTTA 420
TTCCTTTTCT TTCTTTCTCT CTTCCCTCCT TCCTTCTTTT TTCTATTTTT AAATGATTTC 480
TTACCACTGA ACAGCAACAC AGGCTCATGT GTATGTGATG GGTATGTAAT ATACAGTGGT 540
ACGCAATGTA AATGAAGCAA GGTTTCCTCC CAGCCCCAGT TTGCATTCTT ACAGAAAGAT 600
TGTTTATATC CGTGCACACA CGACTTTTTA CCCTTTTTTT GTACAAATAG TAGCCTGCTA 660
AACACACTCT TCTGCACCGT GTATCTTGGA GATCATTTCA CATTCCTCTA CCTCAGTCTT 720
TTTCACGTCT GTGTGCTAGT GCTGTATTCA CTTAGTCATT TAGGTCATGT CCAATCCGTT 780
GTTTTCAATA ATGCTGCAAC GAATACTTTG AGGATTGATT TAACAAATAC TTATTCAGCA 840
TCTCTGTGTG CCAGGCTCTG TTCAGTGTGT TTGAGATACA TCACTGAACA AAACAAATCT 900
GTCTTTTACA GTCTATGTCC TGTTACATTC TAAGTGAGAA CGTGGACAAT CAACCACAGG 960
TGTACTGAAT GAGTACATTG TAGAGTAGAA GAAGTAGGTT AGAAGGTAAG TGCAGGCAAA 1020
GCCCTCTTTG GGAGTATGCC TGATGTGTTT AGGAAACAGT GAAGAAGCCA GTCTGCAGGA 1080
GCAGCGTCTT CTGCGCATGT GTGAGTATGT TTGTTGGTTA AATACTTTAT ATTTTTTGAG 1140
ACAGGGTCTT ACTCTGTCAC ACAGGCTGGA GTGCAGTGGC ACGATCATAG CTCGCTGCAC 1200
CTCGACCTCC CAGGTTCAAG AGATCCTCCT GCTTCAGCAC CTGGGAGTAG CTGAGACTAC 1260
|
