Tag | Content |
---|
EnhancerAtlas ID | HS118-02221 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr10:33796590-33797840 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr10:33796872-33796890 | TCTTCTTTCCTCCCTCCC | - | 6.04 | HNF4G | MA0484.1 | chr10:33796934-33796949 | TGCACTTTGCACTCT | - | 6.24 | ZNF263 | MA0528.1 | chr10:33796878-33796899 | TTCCTCCCTCCCTCCTTCTCT | - | 6.09 | ZNF263 | MA0528.1 | chr10:33796867-33796888 | TCTCCTCTTCTTTCCTCCCTC | - | 6.23 | ZNF263 | MA0528.1 | chr10:33796871-33796892 | CTCTTCTTTCCTCCCTCCCTC | - | 6.58 | ZNF263 | MA0528.1 | chr10:33796875-33796896 | TCTTTCCTCCCTCCCTCCTTC | - | 7.79 |
|
| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_35768 | chr10:33795923-33799671 | HepG2 |
|
| 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 |
GH10I033506 | chr10 | 33795426 | 33799611 |
|
Enhancer Sequence | CAACCTCCAC CTCCCAAGTT CAAGTGATCC TCCTACCTGA GCCTCCAGAG TAGCTGAGCC 60 TCCAGAGTAG CTGGGAGTAC AGGCATGCGC CACCACGCCT GGCTAACTTT TGTATTTTTA 120 ATAGTGACGG GGATTCACCA TGTTGGCCAG GCTAGTCTTG AACTACTGAC CTGAGGTGAT 180 TCACCTGCCT TGGCCTCCCA AATTTCTGGG ATTACAGGCG TGAGCCACTG TGTCTGGCCT 240 GGACTAGGGA AATCTTAATT GCTCTGAGAA AATGCAATCT CCTCTTCTTT CCTCCCTCCC 300 TCCTTCTCTG TCTTTTACTC TCTCTTCTCT CCCCGTGAGA GAGCTGCACT TTGCACTCTT 360 TCTTAAGCCA CCGATCTTCT CAATGGACTC AGAATTTTGA CAGCTTTTAC AGTAGGGAAC 420 CCTACCACAG CACGGACCTT GATACCTCTT TGAACAGGCG AAGGTCAAGG CAAAACACAG 480 AGTGAAAGCT TCAATAAATA TTTCAAAACA CACTCTTGCC ACATCACCTT TCGCTTATTT 540 TTACAATATG CTGCACGCTT ACTCACTCTC ACACTCACAA ACATAACTGC ACAAACATCA 600 TTTCCCATTC TTTTGATGTT TAAATACTTT CCTTCTCCTA TCAGATGAAG TTTATATTAT 660 CTAGGCTTTG TCTCTGACAA TTCTGATGTT GTTGTTATGG AAATATGTCA AGACATTTCT 720 TTGTAAAAAT TCCCAATGAG GCTGGGCACA GTGGCTCACA CTTGTAATCC CACCACTTTG 780 GGAAGCTGAG GTAGGAGGAT CACTTGAGTC CAGGAATCAA GACCAGCCTG GGCAACATTG 840 TAAGACCCCA TCTTTACAAA TAATAGTAAT AATAATTAGC TGGGCATGGA GTGCATGCCT 900 GTAGTCCCAG CTACCCAGGA GGCTGAGGTG GGAGGATGGC TTGAGCTTGG GAAGTTGAGG 960 GTGCAGTGAG CTGTGATCAT GCCACTGTGC TCTAGCCCAG GTGACACAGT GAGATTCTAT 1020 CTAAAAAAAA TTTTCCAATA AACTTTACAT TATAGTGATG CCCCTGTGGT TGTGGGCAAT 1080 GTATAAATGA TTTGACTAAT TTTTTCCCAT ATGTCAATTC AACCCTCAAT ATTTTCCAAA 1140 TTTATCTTAG AATTTATATT TAAATTTATG AATTATCTTG AAAGACCTGA TTGTTTGGAA 1200 TCTACCCTCA TCTATTCTAC TTATTTGAAT CTTTAGAAAG ATTATTAAAG 1250
|