Tag | Content |
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EnhancerAtlas ID | HS091-24410 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr19:47798920-47799810 |
Target genes | Number: 16 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr19:47799557-47799576 | TCTCCACAAGGGGGCGCCA | + | 7.2 | EWSR1-FLI1 | MA0149.1 | chr19:47799734-47799752 | ATTTCCCTCCCTCCTTCC | - | 6.4 | EWSR1-FLI1 | MA0149.1 | chr19:47799786-47799804 | CCTCCCTCCCTTCCTTCT | - | 6.71 | EWSR1-FLI1 | MA0149.1 | chr19:47799770-47799788 | CCTCCCTTCCTCCCTCCC | - | 6.88 | EWSR1-FLI1 | MA0149.1 | chr19:47799766-47799784 | CCTCCCTCCCTTCCTCCC | - | 6.92 | EWSR1-FLI1 | MA0149.1 | chr19:47799762-47799780 | CCTCCCTCCCTCCCTTCC | - | 7.08 | EWSR1-FLI1 | MA0149.1 | chr19:47799782-47799800 | CCTCCCTCCCTCCCTTCC | - | 7.08 | EWSR1-FLI1 | MA0149.1 | chr19:47799754-47799772 | CCTTCCTCCCTCCCTCCC | - | 7.28 | EWSR1-FLI1 | MA0149.1 | chr19:47799774-47799792 | CCTTCCTCCCTCCCTCCC | - | 7.28 | EWSR1-FLI1 | MA0149.1 | chr19:47799738-47799756 | CCCTCCCTCCTTCCTTCC | - | 7.97 | EWSR1-FLI1 | MA0149.1 | chr19:47799750-47799768 | CCTTCCTTCCTCCCTCCC | - | 8.32 | EWSR1-FLI1 | MA0149.1 | chr19:47799746-47799764 | CCTTCCTTCCTTCCTCCC | - | 9.47 | EWSR1-FLI1 | MA0149.1 | chr19:47799742-47799760 | CCCTCCTTCCTTCCTTCC | - | 9.72 | ZNF263 | MA0528.1 | chr19:47799761-47799782 | CCCTCCCTCCCTCCCTTCCTC | - | 6.54 | ZNF263 | MA0528.1 | chr19:47799749-47799770 | TCCTTCCTTCCTCCCTCCCTC | - | 6.86 | ZNF263 | MA0528.1 | chr19:47799738-47799759 | CCCTCCCTCCTTCCTTCCTTC | - | 6.96 | ZNF263 | MA0528.1 | chr19:47799745-47799766 | TCCTTCCTTCCTTCCTCCCTC | - | 7.08 | ZNF263 | MA0528.1 | chr19:47799785-47799806 | CCCTCCCTCCCTTCCTTCTCT | - | 7.11 | ZNF263 | MA0528.1 | chr19:47799757-47799778 | TCCTCCCTCCCTCCCTCCCTT | - | 7.14 | ZNF263 | MA0528.1 | chr19:47799777-47799798 | TCCTCCCTCCCTCCCTCCCTT | - | 7.14 | ZNF263 | MA0528.1 | chr19:47799773-47799794 | CCCTTCCTCCCTCCCTCCCTC | - | 7.19 | ZNF263 | MA0528.1 | chr19:47799753-47799774 | TCCTTCCTCCCTCCCTCCCTC | - | 7.29 | ZNF263 | MA0528.1 | chr19:47799782-47799803 | CCTCCCTCCCTCCCTTCCTTC | - | 7.38 | ZNF263 | MA0528.1 | chr19:47799769-47799790 | CCCTCCCTTCCTCCCTCCCTC | - | 7.5 | ZNF263 | MA0528.1 | chr19:47799742-47799763 | CCCTCCTTCCTTCCTTCCTCC | - | 7.75 | ZNF263 | MA0528.1 | chr19:47799762-47799783 | CCTCCCTCCCTCCCTTCCTCC | - | 7.9 | ZNF263 | MA0528.1 | chr19:47799765-47799786 | CCCTCCCTCCCTTCCTCCCTC | - | 8.23 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 2 | ID | Chromosome | Start | End |
GH19I047295 | chr19 | 47799241 | 47799390 | GH19I047296 | chr19 | 47799481 | 47799670 |
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Enhancer Sequence | TTCTAGACCA CCCTGGGCAA CATGGCAAAA CCCTGTCTCT ACTAAAAATA CAAAAATTAG 60 CCAGGCATGG TGGCACACGC CTGTAAACCC AGCTACTCGG GAGGCTGAGG CAGGAGAGTC 120 GTTTGAATCC GGGAGGTGGA GGCTGCAGTG AGCCGAGATT GCACCACTGC ACTCCAGCCT 180 GGGTGACAGA GCAAGACTCT GTCTAGAAAA AAAAAAAAAG AATACAAATT GCTTATTTCC 240 AAGAAAACAT CTCTGCCGTG CTTTCAGATT TTCAGCTGAT TACAAATCAC GCACCCATGA 300 TCAAATCCAA CAAGAGATAG ACCCCCTGCC ATAAAGGAAG AAGGCTGGCT GGGTGTAGTG 360 GCTTATGACT GCAATCCCAG TGCTTTGGGA GGCTGAGGCA GGAGGATCTC CGAGGCCAGC 420 AGTTCAAGAC CAGCTTGAGC AATATAGCGA GACACCCCCT CATCTCTCCA ATAATAATAA 480 AAAAAATCAG CCAGGCATGG TGGCGCGTGC CTGTAGTCCA ATCTACTCGG GAGGCTGAAG 540 TGGGAAGATT GCTCCAGGAG TTCGAGTCTG CAGTTGGCTG AGATCTCGCC ACTGCACTCC 600 AGCCAGGGCG GTAGAGCCAA ACCTTGTCTC AATAAAATCT CCACAAGGGG GCGCCATCTA 660 CATGATGATA GCAGGAAGGG AACCGGCCAG TGTCTCCTGG TGACGTACTC ATTCAGCGCT 720 TCTTATACCT TAAAGGTGAC CAGGAATCAC CTGGGGGTCT TGTTAAAATG CAGGTTCTAA 780 TTCAGCAGGG CTGGAGCAGG ACCACAGCTC TTGCATTTCC CTCCCTCCTT CCTTCCTTCC 840 TCCCTCCCTC CCTCCCTTCC TCCCTCCCTC CCTCCCTTCC TTCTCTTTCT 890
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