Tag | Content |
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EnhancerAtlas ID | HS088-16272 |
Organism | Homo sapiens |
Tissue/cell | HeLa-S3 |
Coordinate | chr14:24564060-24565770 |
Target genes | Number: 39 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr14:24564193-24564211 | GGAGGGAGGCAAGCAAGG | + | 6.32 | GLI2 | MA0734.2 | chr14:24564412-24564427 | CCTTGTGGGTGGTCT | - | 6.48 | KLF4 | MA0039.3 | chr14:24564458-24564469 | AGAGGGTGTGG | - | 6.02 | NFYA | MA0060.3 | chr14:24564949-24564960 | GGCCAATCAGA | + | 6.02 | USF1 | MA0093.2 | chr14:24564833-24564844 | GGTCACGTGGT | - | 6.32 | USF2 | MA0526.2 | chr14:24564830-24564846 | CGGGGTCACGTGGTCC | + | 7.77 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_28386 | chr14:24559518-24566199 | Fetal_Intestine | SE_29515 | chr14:24559630-24566262 | Fetal_Intestine_Large |
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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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Enhancer Sequence | GAGCCCCGGG AGACTAAGCT CAGAGCCCCC TAAAGAAGGT GGAAGGTTAA ATATCCATTC 60 CCGGCCTCTC CCGGACTGGA AGGACTGGAA CCTGGCGGGA AGTCCAGAGC AGCCCGAGGG 120 ACCTGGGCCC AGGGGAGGGA GGCAAGCAAG GTGGGAGGAG GGCGCCAAGT TGCCTTCGTT 180 TCTTACATAG CTGGCTTCTT CCTCCGTCCA GGCCTGGAGC CCCCAGGCTC GTCCTGTTTG 240 TCTGCCTGTC CTCTTAGTCT CCTATTTATT CTCTGAGGCC TCTCTTCTCA GCTTTTGTCC 300 CAGAGTCGGA AGTGACCCAC ATCTGTCGCA CAGCCCGTTC CACTTGGGCA GCCCTTGTGG 360 GTGGTCTCTG AAGGAAACGT CCCACTTAGA GGGCTGCAAG AGGGTGTGGG GGCTTCACAA 420 GAGATAACGT GAGCCAGGCT CCAGGGAGAG AGAGGCTGTC CTCAAGACTG TGTGCTTGAA 480 AACTGATGCT CACGGAGAAC TTCCCTCTGA GGCAGGAACA GACCCAGGTC CCAGTAGCCC 540 TCCTCCCCTG CCCCTGGGGC CACACTGATC ATCTATCCTG CTTTAGCGGA AACCACCCCA 600 GCTTCTACCC CAGACAGACT CAAGCTCCCG TATCCATGCT CTGAGCTTTC TTCCTTCCCC 660 AGGCTAACAC CCTCTGAGTC TGAGCTGCCA GCAAGCTGCT GTTCCACCCT CCCACCAACA 720 CCAAAGCTCT CTAGGCATGT GGCCTCTAGG AAGAAGAGCC AGGGGAAGCA CGGGGTCACG 780 TGGTCCTGGG TGTGGGGGCA GTTTCTGATG GGCGAGGCCT TGATAGAGGA GGAGAGTAAC 840 ATCCCCTTCA TGGTCTTTGC TCTCTCGGGT TTACTCCACC TTGAGTCCAG GCCAATCAGA 900 GCAGACGTTG CTTCTCTGTC TCCCAGGGCC ATGAGAGGAC AGACAACAGG ACGCTGACCT 960 CCTGAGAATT AAGCCCATGA ACCCCAGCCA GTGACACTCA TTCCCCAGTG GTCAACCTTC 1020 CGCAGAGTTC AGAAATACTT ACCCGAGGGC AACATTTTAT GCAACCATTG TTGGTCCAAG 1080 TGGGCAGCAG CAGATCAGGG CCTGGAAGCC CAGCATCCAG TCACCTATTC TCTGTGCAAG 1140 AGCCCTCATC TAGAAACCTG GCACTGGAAA GACTGTGACC TTTGCTTGGG GCTTTCATAG 1200 TCTTACAGCA TACACACCAG AAGGAAAGAA TAAACACAGC TGCCATTTTA ATTTATAAAA 1260 AACTATACTT GAAAATGGAA ATAAAATGGA TGAGGCTTCA AATACCAGAC ATATGAAATT 1320 GTCACCTGGG CCCAACTTCT TGTCTTGACA CTTGGGCCAA AGGCCCCTAC TCATTTCTTT 1380 TTTTTTTTTT TTTTTTTTTT TTTTTGAGAC AGAGTCTTGC TCTGTCGCCC AGGTTGGAGT 1440 GCAGTGTCCC GATCTCGGCT CACTGCAACC TCCACCTCCC GGGTTCAAGC GATTCTCCTG 1500 CCTCAGCCTC CTGAGTAGCT GGGACTAGAG GCACACGCCA CCACATCCGG CTAATTTTTA 1560 TATTTTTAGT AGATGGGGTT TCACCATGTT GCCCAGTATG GTCTTGATCT CCTGACCTCA 1620 TGATCCACCT GCCTCAGCCT CCCAAAGTGC TGGGATTACA GGCATGAGCC ACCGTGCCCA 1680 GCCATCTCCC TACTTATTTC TAAACGTTGA 1710
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