| Tag | Content |
|---|
EnhancerAtlas ID | HS197-08586 |
Organism | Homo sapiens |
Tissue/cell | ZR75-30 |
Coordinate | chr17:2277150-2278780 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| REST | MA0138.2 | chr17:2278205-2278226 | TGCCTTGTCCATGGTGGTGGA | - | 6.13 |
|
| | 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 |
|
| | 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 |
|
Enhancer Sequence | GACAAGCTGA ATGTCTCTGG GCAAGCACTT CCCGTCTCTG GGTCTCAGTT TCCCCTCTCC 60
ACCCATATCC TCTGACTGCA GAGGCTTCCT GAGATCTGTG GGCCTGAGAA TAGGGGAGCC 120
CGTAGAGCAG CCCCATTGGT GTCGACTGGC GAGATCCTTC CTCCCCGCGA TGTTGCCTGT 180
CACTGTACAG AACTGACTAT GGCAGGCTTG TTCGGAGCAC GGGAGGGTAG CTCTTTCTGG 240
CATCACTCCT GCCTTTTGAA CAGCAAGTTC TAAACTGTGA CTGCCTGGCC CAACCAACAC 300
TGATAAGTTT CAATTTTAAG GACGCTTTAT TAATTTTTCT TTAAAATTGC CTCTTTAGAT 360
AATGTGTATT CTTGTTACTT TACTAAATCC TTACCAACAT TAACAGAAAA TGTAAGTTGA 420
AGTAAGTTAA ATATAACTGG CTGGGTGTGA TGGCTCATGC CTGTAATTCC AACACTTTGG 480
GAGGCAGAGG TGGGAGGATT GCTTCAGTTC AAGAGTTTGA GACCAGCCTG GGTAACATGG 540
CGAAACCCTG TCTTTACAAA AAATGCAAAC CTTTGCCGCA TGTGTTGGGG TGCGCCTGTA 600
GTCCCAGCTT CTCGGGAGGC TGAGGTGGGG GGACCACCTG AGCCATGGAG GTTGAGGCTG 660
CAGTGAGCCG TGATACCACC ACTGTACTCT AGCCTGGGCC ATAGAGTGAG ACACCCTGCC 720
TCAGAAATAA AATAAAAAAA AAGAAATAGA ACAAACAAGG CACATTGTCA TTTCCCACGT 780
GCTTTGTTCT TAATCCCCTA TCCAGGAACA CATTCTCCCT CTCTCTGGCT TTGGGTTTTG 840
TAAAAATCTG TCTGTGCCAG TGCCCAGCTG CTGAGCTCAT GGACAGCAGT AGCTCCTCGC 900
TGGCGTATTA GATTGCCACA GAACCGTGGC CTTACCCAGC ACTTCATGCT TCCTGCCCAA 960
AGTAGAAACT ACTTTTAGCA TTGCTTTCCC TACGTGGTGA AAACAGAGAG AGAAAAATCC 1020
CAAACAGTCT CTGTATGTGT CTCTTCTTTT CCTCGTGCCT TGTCCATGGT GGTGGACTGT 1080
ATCTAGGAGG CAGAATGTTT GCTTTTCCTT CCTACATCTC CCCACCTTGC CTGAGGGCTA 1140
ATGGAACTGA CTAGGTGCTT GCTACAGAAC GTTCCTGTCT TGTCCTGCTG AACACTCAGT 1200
ACTGAAAATA AGGCAAAACT TGTTTTTCCT AAAACCTCTA GGCTTCTCTC CACCCAGCCA 1260
CACCAAAACA CTAAGGCCAT TCTCCCGGTC TCATGACTTC AGGCGTTTCT AGAATGAGAC 1320
TGAGTTCAAA CTGGCCATTG AGCGTTCAGC CCCCTGGCTC CCCTACTTCC CTTCAGTAGC 1380
CACAGGAAGA CCTGGGGCTG TTCCTTCAAG CAGGGCTGAA GACGTGTCTT CATGTTTGGC 1440
CAGAGGCTTG TTTCTCTCCG CCTGGCTGGC TGGGTCAGAA GCTGGCTTGG TGCCCCGTGG 1500
CCACAGTGTT GGAGGCTGTG GTGGGAGAGG GGGTGTGAAG AGTTTTGCAT TCCAGCTCCC 1560
TTCTGGCCCG AGGAGGCGGT GGGCTGCGGG AAGGTGCTGG AGTGCAGGTG GAGCCGCCCT 1620
GTGTTCACCC 1630
|
