| Tag | Content |
|---|
EnhancerAtlas ID | HS091-20187 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr17:47109340-47110650 |
Target genes | | Number: 12 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr17:47109695-47109714 | TGGCGCCATCTAGTGATAA | - | 6.24 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_67981 | chr17:47049476-47113351 | TC32 | | SE_68412 | chr17:47048796-47109684 | TC71 |
|
| | 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 |
| GH17I049031 | chr17 | 47108993 | 47110190 |
|
Enhancer Sequence | TGGGCTGGGA AGTGGGGCTG GGTGCGGTGG GGGGGGGTTC TGTGAAGGGT GGTGTGAGCC 60
TGGTCCCACT TTTTCCTCAG GGGGGTCTAG GCAGGCTGGG TCCCCATCCA GGGTTCTGAT 120
ATTAGCCCAA GCCAAACCTA GAATCTTCCA TAAAAGGTTT CTTCAGGGGG TCTCCTTCAT 180
GTCCATTGTT TCAGGGATCT CAAAGGCTCA GAAACATCAA GATTGATAGC AAAAATACAT 240
AGAAGGGAGG GCTCCAAAGC CCTCCCAGAT AAGTGGGAAA TCCCTTGCAG AGAAAATGTC 300
CCCTGCTGAT AGGTCTCTGG TTGCTCCAGG ACCTTAGAGT CCTTTGCCGT GTTCATGGCG 360
CCATCTAGTG ATAATGAGGG GGAACTTCGG GGTTCAAAAA AGATTCCTCA ACCTTGGGAT 420
GCTGGGACAT TTTATTGCAG TGATGGTCGT AAACCTAGCT GGTGATAGTT GTGGGGTCCT 480
TTTAGTCCCA TCGCACCCAC AATTTTAGCT CCTAGCCCTT TGATTGAGCA ATTATGCGTC 540
TCACTCACTG TTACAGACAG ACTATACATT TTGCGCATTA CTCATTTATA TTAATATCCG 600
AGCCCGTTAT AGGCTTTTGC CACATTTTGC TTTGGGCTTT CTTGCTTCTT AACATGCCGC 660
CTTCTCCAAT CTAATAATAC TATGTAAAAT CCTACCTCTT CTTCAAATAC CTACCATTTT 720
CTTTTAGATA CCTCCTGGGC TCAGAATTTT CTAGAGGTTC CTACTGCCCC TTGTGGCCAC 780
TAGGGTTTGG CTTTAAAGCT CATGTCAACA GTTGTTCATT CTCTCCTGCC TATTGTTGCT 840
GTGTTCTTGT TTTTTGGAGA CAAGTCTCAC TCTGCCACCC AGGCTGGAGT GCAGTGGCAT 900
GATATCTGCT CACTGCAACC TCAACCTCCT GGGCTCAAGC AATCCTCCCA CCTCAGCCTC 960
CCAAGTAGGT GGGACTACAG ACATGCACCA TTATGCCTGG TTCATTTTTG TATTTTTTTG 1020
TAGAGACGAG GTTTCACCAT GTTGCCCAAG CTGGTCTCGA ACGGCTCAAG TGATCCGCTT 1080
GCCTTGGCCT CCCAAAGTGC TGGGATTACA AGCTTCAGCC ACCTCGCCTG CCCTTTGTTA 1140
CCTCGTTAAC ATTTCTGGGC TTTTTATTTA TTTATTTATT ATTTTGAGAC TGAGTCTTAC 1200
TCTGTCGTAC AGGAGGCTGG AGTGCAGTGG TGCAATCTTG GCTCACTGCA ACCTGCGCCT 1260
CCTGGATTCA AGCAATTCTT GTGCCTCAGC CTCCTGAGTA GCTGGGACTA 1310
|
