| Tag | Content |
|---|
EnhancerAtlas ID | HS050-28225 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr17:26834640-26835620 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF5 | MA0599.1 | chr17:26835035-26835045 | GCCCCGCCCC | + | 6.02 | | ZNF263 | MA0528.1 | chr17:26835450-26835471 | CTTCCTTTCCCCCCATCCCCC | - | 6.3 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_27527 | chr17:26832548-26835764 | Esophagus |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr17 | 26834682 | 26834872 | | chr17 | 26834954 | 26835432 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH17I028507 | chr17 | 26834669 | 26835419 |
|
Enhancer Sequence | AAGTCTTTAC TGCTGCAGGG TCCAGCTCTG CTTGCCCGGT AGCCTTCTTC CTCCCGCACT 60
GAGGAACACT AGTTCCTCGG ATCCGAGGGC GGCGTTGCAC TGCAGTCCTG TCCCCACCGG 120
GCTTGGCTCA GAACCTTTTA CCATCTTGCT CATTCCCTGA CCACAAGACA CAGGCAGTAC 180
AAGGGCACCC CGAGTGGATG GGGGAAGGGG CAGGGCCTCC TATCCTGGTC CCTTTCTCTT 240
GTGGCTCTGT GAGGGGTCCA GGGTGAGCCA GGCAGGGACA GAGCCAGGCT GAGTCCTGGA 300
GAGGGGCAGA CGGGGTGAGG GCTGCCCCAG GTTGGGGATC CTCAAAGGCG AAGGAGCCAC 360
AGGGAGAGGC GCATGTCCTC CCGGCTCCCC GCCCAGCCCC GCCCCGCCCG CGCTGCCTGT 420
GCGAGCTCAG CTCCCGGCTC CAGGGCCTGC CGAGGCACGC TGCACCCCCA GGCCCGGCGC 480
CTCACTCACT CCCAGAGCCA GAAACCTGTT CTCCCGGGAA TGCCAGGGAG TTCTCAGAGG 540
ACTTTATTTC CCAGGGGCTC AGGGAGCCCC AGAATCTTCT GGACCAGTGG GTCCTGGGAA 600
ACTAGAGAAA AATTAGGGGG CTTAGGACCC CTCCCTGCTC CCCAGCTTTG TCTCATCCAC 660
GCACTGACGC CACATTGCCT CCAACCAACA GCCGTCTTCA CCGTGAGAAG GCTTCATCGC 720
GAGAAGGCTT AGGAAAGTTA AAGACAAGGG GGAAAGCCCA CTGGTGACAT GCACCTTCTG 780
TCATGTGCCA TCCGTTGCCT CAGGGAAAGC CTTCCTTTCC CCCCATCCCC CAGACAGTCC 840
CATCTGGCCT CTAAGAAAGC AACATATCGC CTCTTTCCTT GGACTCTTCA CCTTCTCTAG 900
CTAGGAAGTC CTTCCTGATG TCTAACCTCT CCCTTTCTGG CTTGAGTTGA CACCTGGTCT 960
TCATGGACCA GCAGAACCCC 980
|
