Tag | Content |
---|
EnhancerAtlas ID | HS197-02356 |
Organism | Homo sapiens |
Tissue/cell | ZR75-30 |
Coordinate | chr10:5653660-5654810 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
JUN(var.2) | MA0489.1 | chr10:5654039-5654053 | ATGACTCACCTCTC | - | 6 | ZNF263 | MA0528.1 | chr10:5654402-5654423 | TGTCCCCTTCCCTCCTCCCCC | - | 6.49 |
|
| Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
SE_01811 | chr10:5653648-5654888 | Aorta | SE_26546 | chr10:5653647-5654862 | Esophagus | SE_33798 | chr10:5653626-5654785 | HCC1954 | SE_35816 | chr10:5650375-5654335 | HMEC | SE_55779 | chr10:5650994-5654889 | 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 |
GH10I005611 | chr10 | 5653921 | 5654170 |
|
Enhancer Sequence | TGGCCAGGAT GGTCTCAATC TCTTGACCTC GTGATCCGCC CACCTCAGCC TCCCAAAGTA 60 CTGGGATTAC AGGTGTGAGC CACCACACTT GGCCTCTAGT GCAGGGGCTA CCAGGTGACC 120 AGAGTTTTTA TTCTTGGTCA CTTTAGCACA AAAATAGAGA AAAGTGGCCT CAGTGAACCT 180 TATCTGTACC TCATTTCATC CTTGCAGACA TCCCCAGGCT CTGCAGGACC AGCGAGTGAG 240 AGGAACCACG CACATACCTG GCAACAGCAG TCTGGGGTTG GTGTGCCCGT CTGTAATGGC 300 TGCATGTGGT ACATTTGATT CTATGAGCGC GTGTCTAATG TGAGTTTCAG GAAGGCGACA 360 GCTGTGCCAT GAAGAATGGA TGACTCACCT CTCTGCACCA GCCTCGCCAG CATGCAGGCC 420 TGTGTGGTGC CGTCCAGAGC CCAGGGCTCA GCATGAATGA GGAACGCACG TACCTGAAGT 480 CGGGTTCCCA TTCCAGCCCT TCCCCATCCA GCTTCTACTG ACTTCCAACC ACTGCGAAGA 540 GAAACGTGTT GTCTCTGGCT AATTCCCTCT CTCGACCTTC TTAAGCAAAC CTCCAGGAAA 600 GGCTGCAGAA GGGGACCTGT GAGGTTTGCA GATGGCATCA GAAGGCTGAG AGACAAGTGT 660 CCTCCAGCCT CACCAGCAAG ATTTCCTGTG CCCTTCCCAT CTCCACTTCC CCACCCTGCA 720 GGCTCCCTGC AGGCAACCTT TCTGTCCCCT TCCCTCCTCC CCCACTATGT TTTCCTGCCC 780 CTTATTCATC ATTCACTGGA CATTCTGAGC ACCCATCTTG GCTAGATTTC AAGGCACTGA 840 GGATTCAAAA GGAGAGTCAG GCATTGCCCC TGCCCTCAAG GTGAAAGCTG GAGCTCAGCT 900 GGGAGAAAAG AACCTGCCTT CAAGTGACAT CAAAAGTTGC AGGGGTGGCC AGGCATGGCG 960 GTTCATGCCT GTAAATCCCA GCACCTTGGG AGGCAAGGCG GGAGGATCAG TTGAGCCCAA 1020 GAATTCAGGA GCAGCCTGGA CAACATGGCA AAACCTTGTC TTTAGAAAAA AATACAAAAC 1080 AAAAACAAAC CAAAAAAATA AAGCCAGGCA CGGTGGCACA CGCCTGTAGT CTCAGCTACT 1140 TGGGAGGCTC 1150
|