| Tag | Content |
|---|
EnhancerAtlas ID | HS048-22479 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr2:241898940-241900290 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxa2 | MA0047.2 | chr2:241900223-241900235 | TGTTTACATTGG | + | 6.62 | | PLAG1 | MA0163.1 | chr2:241900002-241900016 | GGGGCCCACGGGGA | + | 6.72 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_65735 | chr2:241899187-241900671 | 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 |
| GH02I240959 | chr2 | 241898516 | 241903712 |
|
Enhancer Sequence | GGGGGTGCCA GGAGGAAAGA GAGGCTGTAC CACAGAGAAG GGAAGAGTAG TCCCTGGGAC 60
TAGGAAGAGG CAAACAGCCA TAGGGGCATG GGACAAGGGG CCCTCACACC ACGCACTAAG 120
CCAAGCCCAG GCTCTCAGGG CAGATGAAAT GGTGCCTGGC CCAGGCCATT GGCTAAGGGA 180
AGCTGACACC AGTTTTCAGG GGAAAGAAGG CATCATTTCT AAGCCTCCTG AAGGGGTGAG 240
TTTGACTTCA GGGTGAAAGT GGGCCTGGCT GAGTCAGGTG GACTTGGCTG GGTCACGGTG 300
CCAGCTGAGT GGGAAGGGAG CTCCCTGGAG GCTGCCGTGG GTCCCGACGC GGCTCCTGCT 360
GCCCTGCTTG TCCTGGGAAG GTGCACAGCA CACCTGCCAG CTCCCAGGGC ACTGGAGGGG 420
CACACCTGCC GCTGGGAGGG CCAGCATGTG AAAGGGTGGC CAGAGCCACG CAGCCAAAGG 480
CTCCAGGAGT CCAGCCGGCC CCCTCGTTCC ACGCACAGTT AAGAAAGTGG AGTCAGGAAG 540
GGCCTGACTC TGGAGGCACT GGGGCAGCTG TCGCCTCCCA AAGCCTTCCC GAGAGACAGG 600
CATGACCTGG GGCGAAGGGG AATTCGGACC CTTGGCCAAG AGGCCCATCG AGCCATCCAC 660
TGAGGCACGG GGAGGCCCTA GACAAGCTGG GCTCTGCCCA CACAGCAGGA GGCGCGGACT 720
TCACTGGGCT GGACACTAAG GTCGGGGGAG GCTGGATTTG GGGCAGCAGG CAAGAAAATA 780
AGTGGGTTAG TGGAGATTTC GGGGTGTGCC TGGGCCTGGC CAAGGGCCCG AGGTTGACAC 840
GGAGGCCCCC AGGAGCCACA TGATGGTGAC GTGGGGTGGG GGACAGTCTT GGGCAGGGGG 900
CAAGAGTGGC CAGGGCTAGG CTCACCTGGG CTCAGCGGGC AGGCAGATTG GAGAGGCATT 960
TCTGAGGGGG GTTGGCAGGA CGGGGGGACG CCTGTGTGTG GCAAGGGCAG GAGGGCACGC 1020
GGATCTGGGC TAGAGGAGGG GAGGGTCAGC TGGAGCCCCA GCGGGGCCCA CGGGGACGGG 1080
GCGACCTCGC ACACTCCCTG GGCTGCTTGC CAAGGCTGGA GGCTGCGCAG CTGACCTGGT 1140
GCTGGAGCGA GCGGCTGGCG CACACCACGC CCCAGAGGCC GGGCCGGCCG GCAGGGGAGA 1200
GTGAGAAGAG GGGCTCAGCC CTCCCCAAGC ACCCCCGAGA GGCAGGCTGA GAGAGGAAGA 1260
GAACATGATT TAACATGACC GGCTGTTTAC ATTGGCCCCA AGGAGAAAGG TCTCCTTTCA 1320
ACAGATTTCA AAGTCAGGCC CGGTCAGCGA 1350
|
