| Tag | Content |
|---|
EnhancerAtlas ID | HS180-04313 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr1:207174980-207175620 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ELF5 | MA0136.2 | chr1:207175391-207175402 | AACTTCCGGGT | - | 6.14 | | TFAP2A | MA0003.3 | chr1:207175303-207175314 | TGCCTGAGGCA | - | 6.02 |
|
| | Number of super-enhancer constituents: 8 | ID | Coordinate | Tissue/cell |
| SE_26663 | chr1:207174076-207177334 | Esophagus | | SE_27711 | chr1:207174549-207176229 | Fetal_Intestine | | SE_31518 | chr1:207174225-207175679 | Gastric | | SE_33873 | chr1:207174470-207177225 | HCC1954 | | SE_34694 | chr1:207175413-207177474 | HeLa | | SE_57640 | chr1:207174392-207175686 | VACO_503 | | SE_57951 | chr1:207174806-207175106 | VACO_9m | | SE_57951 | chr1:207175382-207175652 | VACO_9m |
|
| | 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 |
| GH01I207001 | chr1 | 207174816 | 207177209 |
|
Enhancer Sequence | TGCCTGTGCT GGGTGTTTGC CATCAGCCAT TTTTCCCTCT GATTTTATCA CTTCCAATAT 60
AGGTATGTGC ATTAATGTAG GTATGTGCAT TCTTAGAGAT TCATTCCTTT GGCTTACACT 120
AACGACTTTT CTTACACAAA AGACCTCAGT GAACCTTGGG AGAGAAGGCA GTTCTTGGGG 180
AGGAGAAAGA TTGAGACTGG GAAGGCACAT GTAGCTGCTT TGTATTCTAC CCTCTGGTTG 240
GCCTTAGTGC CCTCTTTTTG CTTGGTCTCT GGGCACTGAA TCCTTCTAGG AATCTTCTTA 300
GTTTTAGGCA CTGGTTTTAA TCCTGCCTGA GGCAGTTGCA ACCACCTTTT CTGAGCTAAC 360
AACAATCTCC ACCCCCTTAC CTAGGAAGCA CCTGCAACTT TAGTCAGATG GAACTTCCGG 420
GTGTCTCACC TGGGAGAGAG AGCTATGTAG CCCTTAGGAG GAGTTCAGTG TTGTTAACCT 480
AGTGCAGCAG AATTGTGAGC GGGGCTGAGC CTCTGCCTCA GCCTCAACTC CATTGGGGCT 540
GCGGACAGGA GGGAAAATTG GGGGTGGGGA ACTCAGCCTT GCTTGTTGGA GCACTATTTT 600
CTAGTTAAAG AGTTCTCAGG GCTTTGATGG CCACAGATGA 640
|
