| Tag | Content |
|---|
EnhancerAtlas ID | HS176-28857 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr4:40992330-40993450 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr4:40992535-40992553 | GGGAGGAAGGCAGGGAGA | + | 6.29 | | EWSR1-FLI1 | MA0149.1 | chr4:40992531-40992549 | GAAAGGGAGGAAGGCAGG | + | 7.52 | | IRF1 | MA0050.2 | chr4:40993017-40993038 | ACTGAGTTTCATTTTTTTTTT | + | 6.66 | | ONECUT1 | MA0679.1 | chr4:40993368-40993382 | GGTATTGATTTTTA | - | 6.13 | | ONECUT3 | MA0757.1 | chr4:40993368-40993382 | GGTATTGATTTTTA | - | 6.15 | | ZNF263 | MA0528.1 | chr4:40992921-40992942 | GGAGGAAAAAGAAAGGAAGGA | + | 6.17 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_56719 | chr4:40990895-40998540 | u87 |
|
| | 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 |
| GH04I040989 | chr4 | 40991617 | 40997548 |
|
Enhancer Sequence | CCTCTTGTCT CTCTCTCTCT TTCTCTCTCC AGCTGTTGTT GGACATCAGA AGAATATTCC 60
AGTTGTATCC GGTGTCTACC GTGAAAAAAA GTGTTCTTTT TTGCAAAAGT GCCAGAAAGG 120
AGTGGTGAGA TTCATCCCAA GCCAATCATT TCTCATGAAA GACACTGTGC CATAACCGCT 180
TTTCACACAC ACAAGAAAGG AGAAAGGGAG GAAGGCAGGG AGAAACTCAG CAAACAGCTC 240
AGGATTTCCA CAGCCTACCA TTCCAAACCT TTCGCACTTC CAGAAGGCTT CTTGATGGAG 300
TTGTGGCAAG CTCATGGGGG AAATGCTTCA CCCCAACGTA ACCCAGACCA AATATGCCAT 360
TGCACAGGAA GTGGGTGCTG AGTCCAAGTG TGTCCATATG AGCAAAGTAA CACAGATTAA 420
ACAGTGATTC ATTTCATACC AAACTGCATC CATCATTTTA AAAACTGTGT CATCATCCTA 480
CTCCAAACTG TATGTGGCAT CTTCTCTTCC TCTTCTGCCA AGCAGAGCAA AGACTCTAGG 540
TTACAGCTCA TGAAGGTGTA AATTGGGTTG ATATGCTCTA TGGAGGCAAA TGGAGGAAAA 600
AGAAAGGAAG GAAACCCTGA ATGGGGGTTG GGGGCAGGGA GGGGTAAGAT TTACTCTGCT 660
AACTACATAG ATTTCTGGTC ATTTTGGACT GAGTTTCATT TTTTTTTTTT TTGGAGGCAA 720
GGTTTCACTC TGTTGCCCAG GTTGCAGGGC AGTGGTGCAA TCTTGGCTCA CTGCAACTTT 780
CGTCTCAGCC TCCTGAGTAG CTGGAACTAC AGATGTGTGC CACTACGCAT GGCTAATTTT 840
GTTGTGTGTG TGTGTGTTTT GCTTTTTTTT TTTTTTTTTT TTTTGTAGAA ATGAGATCTC 900
ACCATTTTGC CCAGGCTGGT CTCGAACTCC TGGGCTCAAG AAATCTGCCT GCCTTGGCCT 960
CCCAAAGTGC TAGGATTACA GGTGTGAGCC ACCGTGCCTT GCTGGGTTTT GATTTTTAAA 1020
TTTTTTATTT TGCTTCCTGG TATTGATTTT TAAAAGTCCC CTGGAAAATG CCTTGCATTT 1080
AAAAACCCTC ACACCCCTTA CGATAACCTA TTCTGTCCCT 1120
|
