| Tag | Content |
|---|
EnhancerAtlas ID | HS101-21837 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr19:42440100-42441210 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESR1 | MA0112.3 | chr19:42440789-42440806 | CAGGTCTCGGTGACCCT | + | 6.08 | | ESR1 | MA0112.3 | chr19:42440789-42440806 | CAGGTCTCGGTGACCCT | - | 6.6 | | ESR2 | MA0258.2 | chr19:42440790-42440805 | AGGTCTCGGTGACCC | - | 6.51 | | RREB1 | MA0073.1 | chr19:42440583-42440603 | GTGGGGGTGGTGTCTGGGGG | - | 6.22 | | RREB1 | MA0073.1 | chr19:42440244-42440264 | GGGTGGGGGTGGGGGTGGGG | - | 6.27 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_60313 | chr19:42431637-42456169 | Ly4 | | SE_60575 | chr19:42431108-42443012 | DHL6 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr19 | 42440713 | 42441005 | | chr19 | 42440101 | 42440390 | | chr19 | 42440218 | 42441178 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH19I041934 | chr19 | 42438484 | 42441127 |
|
Enhancer Sequence | ATGTTTTGCT TTCGCCCAAA TTGAAACATT AAACAACACG GGACGAGAAG AGGCGGCCGC 60
AAATCACTCA TGAAAGATTC ATCTTCTCCC AGGCAGCCGC CACCGCCCGC CTCCAAGGCT 120
GCCCGCCCCA GCCGGGAAGC CTCAGGGTGG GGGTGGGGGT GGGGCAGCAC CCCTGCTCAC 180
TCTGGGGAGC CCCAGCCCTA GTGGTCTGGG GAAGTTCTTC CCACTGTCTC GCCTCAATCC 240
TACAGGTGGT CTCAGAGACT AGAACCCTGG ATCCCTCGGC CTTCCCTGGA CAGCATGACC 300
TTAGCCCTGT CCCTGTCCCT CTCTGGCTGG GGAATCCTTG CCCTCTCTGG GGTCCATCTC 360
TCCAGTTACC TTCCTGGACC AGCCTGGACC TTTGGGACAT GGAAGGGGCT GCTCAGAGTT 420
GGGGGATGAG GTCTGGGAGC CTCCTCCCCG TGCAGTGGGG CTTTCTGGGT TCTTGATCCA 480
AGAGTGGGGG TGGTGTCTGG GGGCTGAGTC AGAGGGAGGT GGCCGCTGTG TCAGGATCAG 540
TGCAAATGGG CAGACAGGGA GTGTGTTCCC TGCCACTTGG GAGCTCAGTG TGTCTCTGTG 600
TCTGCCTGCA TATATGACTG TGTATCTTCT GTCTCGCTCT GCCCATGTTG GTGTAACTTG 660
CTTTGCGATT GTCCCTGTGT CACTACACTC AGGTCTCGGT GACCCTGCGT GTGACGGTAA 720
CTCTGTGGGC TTGTGGGTAT GTCTGTCTGC CTGTCTGGCA CTTTCTGTAT GTGCGTCCTG 780
TGGGCAGCAT TTTTGTGTGG TGTGTGTCTG TATCAGTGTG ACTTTTGGGG TGTGGCTGTG 840
TGTGACTCCC TGTGTGTAAG TCTGTGGATG ACTGTGTGCC GTGTCTGTCT GTCTGTCTGT 900
GTGTTGCCTG CTCTGGGTCT GTCTGCAGGT CTGTGTTGAA CTATTTCTGT GTCTGGGTCT 960
CTTTTCTGCA TCCGCATGTC CCTGTGTCTC TTTCAGCCTC TGTCTCTGTC TCTGCCTGAG 1020
GGGGCACCTG CTGGGGCCAC TAGAGGAAGG CCTGGGTGCG GAGAAGCTGG GGAGAGAGGA 1080
GGCAAGAAAG ACGGAGAGAC AGGACAGCGG 1110
|
