| Tag | Content |
|---|
EnhancerAtlas ID | HS081-01727 |
Organism | Homo sapiens |
Tissue/cell | HACAT |
Coordinate | chr1:207174970-207175550 |
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 | CCTGAACTGT TGCCTGTGCT GGGTGTTTGC CATCAGCCAT TTTTCCCTCT GATTTTATCA 60
CTTCCAATAT AGGTATGTGC ATTAATGTAG GTATGTGCAT TCTTAGAGAT TCATTCCTTT 120
GGCTTACACT AACGACTTTT CTTACACAAA AGACCTCAGT GAACCTTGGG AGAGAAGGCA 180
GTTCTTGGGG AGGAGAAAGA TTGAGACTGG GAAGGCACAT GTAGCTGCTT TGTATTCTAC 240
CCTCTGGTTG GCCTTAGTGC CCTCTTTTTG CTTGGTCTCT GGGCACTGAA TCCTTCTAGG 300
AATCTTCTTA GTTTTAGGCA CTGGTTTTAA TCCTGCCTGA GGCAGTTGCA ACCACCTTTT 360
CTGAGCTAAC AACAATCTCC ACCCCCTTAC CTAGGAAGCA CCTGCAACTT TAGTCAGATG 420
GAACTTCCGG GTGTCTCACC TGGGAGAGAG AGCTATGTAG CCCTTAGGAG GAGTTCAGTG 480
TTGTTAACCT AGTGCAGCAG AATTGTGAGC GGGGCTGAGC CTCTGCCTCA GCCTCAACTC 540
CATTGGGGCT GCGGACAGGA GGGAAAATTG GGGGTGGGGA 580
|
