Tag | Content |
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EnhancerAtlas ID | HS095-12025 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr17:2277790-2278780 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
REST | MA0138.2 | chr17:2278205-2278226 | TGCCTTGTCCATGGTGGTGGA | - | 6.13 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_26563 | chr17:2277614-2279017 | Esophagus | SE_37443 | chr17:2277226-2278709 | HSMMtube | SE_65320 | chr17:2278414-2279145 | Pancreatic_islets |
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| 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 |
GH17I002374 | chr17 | 2277558 | 2279506 |
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Enhancer Sequence | AGCCATGGAG GTTGAGGCTG CAGTGAGCCG TGATACCACC ACTGTACTCT AGCCTGGGCC 60 ATAGAGTGAG ACACCCTGCC TCAGAAATAA AATAAAAAAA AAGAAATAGA ACAAACAAGG 120 CACATTGTCA TTTCCCACGT GCTTTGTTCT TAATCCCCTA TCCAGGAACA CATTCTCCCT 180 CTCTCTGGCT TTGGGTTTTG TAAAAATCTG TCTGTGCCAG TGCCCAGCTG CTGAGCTCAT 240 GGACAGCAGT AGCTCCTCGC TGGCGTATTA GATTGCCACA GAACCGTGGC CTTACCCAGC 300 ACTTCATGCT TCCTGCCCAA AGTAGAAACT ACTTTTAGCA TTGCTTTCCC TACGTGGTGA 360 AAACAGAGAG AGAAAAATCC CAAACAGTCT CTGTATGTGT CTCTTCTTTT CCTCGTGCCT 420 TGTCCATGGT GGTGGACTGT ATCTAGGAGG CAGAATGTTT GCTTTTCCTT CCTACATCTC 480 CCCACCTTGC CTGAGGGCTA ATGGAACTGA CTAGGTGCTT GCTACAGAAC GTTCCTGTCT 540 TGTCCTGCTG AACACTCAGT ACTGAAAATA AGGCAAAACT TGTTTTTCCT AAAACCTCTA 600 GGCTTCTCTC CACCCAGCCA CACCAAAACA CTAAGGCCAT TCTCCCGGTC TCATGACTTC 660 AGGCGTTTCT AGAATGAGAC TGAGTTCAAA CTGGCCATTG AGCGTTCAGC CCCCTGGCTC 720 CCCTACTTCC CTTCAGTAGC CACAGGAAGA CCTGGGGCTG TTCCTTCAAG CAGGGCTGAA 780 GACGTGTCTT CATGTTTGGC CAGAGGCTTG TTTCTCTCCG CCTGGCTGGC TGGGTCAGAA 840 GCTGGCTTGG TGCCCCGTGG CCACAGTGTT GGAGGCTGTG GTGGGAGAGG GGGTGTGAAG 900 AGTTTTGCAT TCCAGCTCCC TTCTGGCCCG AGGAGGCGGT GGGCTGCGGG AAGGTGCTGG 960 AGTGCAGGTG GAGCCGCCCT GTGTTCACCC 990
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