| Tag | Content |
|---|
EnhancerAtlas ID | HS175-02014 |
Organism | Homo sapiens |
Tissue/cell | SK-N-MC |
Coordinate | chr1:159851640-159852900 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr1:159852039-159852057 | CTTTCTTCCTTTCCTTCC | - | 6.06 | | EWSR1-FLI1 | MA0149.1 | chr1:159852030-159852048 | CCCTTCTCCCTTTCTTCC | - | 6.13 | | ZNF263 | MA0528.1 | chr1:159852021-159852042 | TCCTTTTCCCCCTTCTCCCTT | - | 6.02 | | ZNF263 | MA0528.1 | chr1:159852018-159852039 | CGCTCCTTTTCCCCCTTCTCC | - | 6.33 | | ZNF263 | MA0528.1 | chr1:159852030-159852051 | CCCTTCTCCCTTTCTTCCTTT | - | 6.37 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_09609 | chr1:159849306-159853172 | CD14 | | SE_27216 | chr1:159851194-159853009 | Esophagus | | SE_34829 | chr1:159848784-159853407 | HeLa |
|
| | 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 |
| GH01I159881 | chr1 | 159851078 | 159852772 |
|
Enhancer Sequence | AATCAATCTC AGACTCCTTA AGTTCTTCTA TTGATTAACT CACCCCACCT CCCACACTGT 60
TTCCAGCTCC CTCCATTTCT CCAAAGACTA AATCCCTCCC TGGCCTTCCA GGTCTTCCTC 120
AGCCCAGCTG CTGCCCTGAT TCATCTAACC AAGGTAACTC TCCCTGTGTG TCTTCCTGTA 180
GTGCTGGCTC TCTGCCAGCT TGGCTCACTG CCCAGTTCAA GGCTTCTTCC TTCAGGAAGG 240
CTTCTGAACC AGAGCGGTAT GGCAACTCTC TGCCTCTGAG GTCCATGTGG TGCGTGAGTC 300
ACAGACATTC CCTCTCTCTC TCACCATACT CATTTCTTTG CTCACTCCAC TTTTCCCTTT 360
CTGCCCCTCC AACTCTCTCG CTCCTTTTCC CCCTTCTCCC TTTCTTCCTT TCCTTCCTAA 420
CTGCTTCTCA CTGATTTTAG GCCTGCTATT TGTATCCCAG ACATCATTTA ATCTCACTGG 480
CCCTCAAAGC TAAAGATGCT GTTGATTTCT GATGTATGAC ATACATACAA TCATGTATTT 540
ATTTACTTCT TTCCCTATTT ATTTACTTTT TGGATTGTTG TTTTTGTTGG CTCATTTCAA 600
TTCCAAGACA CCAAAGGACT TTCCCTGTTT CTTTTGAAGC CCTTCCAAAG CAACCCCAGA 660
TAAATTCCCT TCACTCTTTC CCCCTTTGTT AGCAAGGTGG GAAACGCTGC CCTTCGTACC 720
ACCATGAGAT GATACAGTAG GTCTAAAGCT GGGAAGGCAC AGGTTTCCTT GCTAAAGTTG 780
CCCAATAATA CTTCCTGGAG ACTCAGGGAG TGCCTGTTAG AAGGACATTA AAAGGATAAT 840
GACACAACAT CAACATAATG GTGCTGACTC ATGGACTCCT AGAACTTCCT CAGTGAGCCC 900
ACTAATTCCC ACTCCCCACA TCTAGTTGGA TTTTCCTGCC CTCACTTCTC ACCCACTACC 960
TTGCATATTT GCCCCATAAC TTTCCTTCTT GGCCCTTTCC CACTCTCTCT CCCCTGAGCC 1020
AGGAAATGGA GTAACTTGGC CAGGTCTCTC ATTGCCTTCA CCCTGCTATT CTCCTTCTCA 1080
TGCAGTTCAC AGAGCTGTGT GCCCCTTCAG TTTCCCAACT ACCCAGGTGA TCTTCATTGC 1140
ACTTCTCTAG CAGCTCCTCA CACTGCAGAT GTGATGAGAA GGCTTCATAA TTACAAGTCT 1200
GCCCACCTGC AGCACTCTTC ACGTCCCCCT GTCACTCACC ACCATCAAAT GCACTAGCTG 1260
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