| Tag | Content |
|---|
EnhancerAtlas ID | HS191-15489 |
Organism | Homo sapiens |
Tissue/cell | Trophoblast |
Coordinate | chr17:2277550-2278780 |
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 | TAACAGAAAA TGTAAGTTGA AGTAAGTTAA ATATAACTGG CTGGGTGTGA TGGCTCATGC 60
CTGTAATTCC AACACTTTGG GAGGCAGAGG TGGGAGGATT GCTTCAGTTC AAGAGTTTGA 120
GACCAGCCTG GGTAACATGG CGAAACCCTG TCTTTACAAA AAATGCAAAC CTTTGCCGCA 180
TGTGTTGGGG TGCGCCTGTA GTCCCAGCTT CTCGGGAGGC TGAGGTGGGG GGACCACCTG 240
AGCCATGGAG GTTGAGGCTG CAGTGAGCCG TGATACCACC ACTGTACTCT AGCCTGGGCC 300
ATAGAGTGAG ACACCCTGCC TCAGAAATAA AATAAAAAAA AAGAAATAGA ACAAACAAGG 360
CACATTGTCA TTTCCCACGT GCTTTGTTCT TAATCCCCTA TCCAGGAACA CATTCTCCCT 420
CTCTCTGGCT TTGGGTTTTG TAAAAATCTG TCTGTGCCAG TGCCCAGCTG CTGAGCTCAT 480
GGACAGCAGT AGCTCCTCGC TGGCGTATTA GATTGCCACA GAACCGTGGC CTTACCCAGC 540
ACTTCATGCT TCCTGCCCAA AGTAGAAACT ACTTTTAGCA TTGCTTTCCC TACGTGGTGA 600
AAACAGAGAG AGAAAAATCC CAAACAGTCT CTGTATGTGT CTCTTCTTTT CCTCGTGCCT 660
TGTCCATGGT GGTGGACTGT ATCTAGGAGG CAGAATGTTT GCTTTTCCTT CCTACATCTC 720
CCCACCTTGC CTGAGGGCTA ATGGAACTGA CTAGGTGCTT GCTACAGAAC GTTCCTGTCT 780
TGTCCTGCTG AACACTCAGT ACTGAAAATA AGGCAAAACT TGTTTTTCCT AAAACCTCTA 840
GGCTTCTCTC CACCCAGCCA CACCAAAACA CTAAGGCCAT TCTCCCGGTC TCATGACTTC 900
AGGCGTTTCT AGAATGAGAC TGAGTTCAAA CTGGCCATTG AGCGTTCAGC CCCCTGGCTC 960
CCCTACTTCC CTTCAGTAGC CACAGGAAGA CCTGGGGCTG TTCCTTCAAG CAGGGCTGAA 1020
GACGTGTCTT CATGTTTGGC CAGAGGCTTG TTTCTCTCCG CCTGGCTGGC TGGGTCAGAA 1080
GCTGGCTTGG TGCCCCGTGG CCACAGTGTT GGAGGCTGTG GTGGGAGAGG GGGTGTGAAG 1140
AGTTTTGCAT TCCAGCTCCC TTCTGGCCCG AGGAGGCGGT GGGCTGCGGG AAGGTGCTGG 1200
AGTGCAGGTG GAGCCGCCCT GTGTTCACCC 1230
|
