Tag | Content |
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EnhancerAtlas ID | HS091-34330 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr3:52861210-52863130 |
Target genes | Number: 10 | Name | Ensembl ID |
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SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr3:52862932-52862950 | GGATGGAGGGAAGGACGG | + | 6.77 | Gfi1b | MA0483.1 | chr3:52862512-52862523 | AAATCACAGCT | + | 6.14 | POU4F2 | MA0683.1 | chr3:52861346-52861362 | GCCATTTATTATGCAC | - | 6.27 | STAT3 | MA0144.2 | chr3:52862484-52862495 | TTTCTGGGAAG | + | 6.02 | ZEB1 | MA0103.3 | chr3:52861551-52861562 | CCCACCTGCCC | + | 6.14 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr3 | 52861523 | 52861815 | chr3 | 52861600 | 52861905 | chr3 | 52861903 | 52862098 |
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| Number: 1 | ID | Chromosome | Start | End |
GH03I052827 | chr3 | 52861961 | 52862090 |
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Enhancer Sequence | ATCCTGGGGG CAGAAGGGTG GGAGTTGTTG AGAGCCTGGT GGCAGGGGCC CATTCCACTC 60 CTGCCTCCTC CAGAGAGCCT TTCTGGACTC GGTGTGCCTC TTGACACAGT GACTCCCATC 120 TTTGCCTGAG CCCAGTGCCA TTTATTATGC ACCTACCGCA TACAGGACCC TGTGCAGGGC 180 ACTCTGCAAA GTGCTCCAGG CCTCTAGCTC CCGGAGGTGT GTACAGTAAC AGTAAGCATT 240 CATTTTATAG AAGGGACGAA GGGGAGGCTG CAGAGGGGCA GGGCCGGGCT AAATCCTGCC 300 TTCTCTCCAC CTGTCCAGTC TGGCCGAAGC TGGCCCACAT TCCCACCTGC CCCTTCCATT 360 TCACGGACTG TTCCAGGGGA ACTAGTTCAT CACCAGCAAG AGCTCTCTGA GTCACACTTG 420 TTCCCAGCCC TGCGTGCAGC CGTGTGGGGC CAGGACTGAG GAGGAAGCAG ACGTAGGGCT 480 GGAGGCTCTG AGCACTTTCC CCCTACAGCA GTCTCCCCGC TCCCTCCCAC AAGAGGCAGG 540 CACCCTATAG GGAGGCTGGC ATATCTGGAA GGAGGTTTTG GACAACTGGT GGACGGGACT 600 CCTGGGTGTG TGGACACACT CCTAGCAGCC ATCCTTTGGG GGCTGAGAAA GAATGGCCCA 660 GGCCATTTCT CAGGGAGGAA AACGACTTTT TCAGAGCCTC CTTGTGGGGT GTGTAGGGAT 720 GTGCCTGGTC AACTTCATGT GGTAGTGTGT GGCAGTGGGC AGGAGGGGGA GCAGCCAGGA 780 TGTCAGGACT ACGCGTCCCT CCTGCCTGAC CTTCCTGGTT ATAATTTAAC TCTAGCCCGG 840 GATGGGGCTG GTGAGTGGGC AGTGGCACTC CTCCCCCTGG GTAGGCAGTG CTTCATCTCT 900 CCAGATGGCC AGCTGGGGCT CCTGGCCAGG TCAGGGAGCA GGGAACCTGC TCTCTGCTCC 960 CCTAACTCAT GCAGCAACAG GTTCTGGGTC TAGAGAAGGC AAGTGACAGT CTTGGGCTCT 1020 CAGCAGATGC CACGGGCCTG GACCTGGCAA CTGCTGACCC TGGCACCCAT GTCGAAGGCT 1080 GACACAGCCC GTGGGGCTTG CACTGCAAGC TGGGCAGCAT AGGCCCGGGC TCTGGGTTAG 1140 GAAAAGTAGA GGCTGCGGTG GAGTGGGGGA TGCTTGGCGC CTGAGGGAGG AGACTAGCCC 1200 CCACTGCAGT TTTCCAGAGG CCACAGTGTG GGACCCCACA TGAGACACTC CCTCTCTGCC 1260 CCACCATCGC CCTGTTTCTG GGAAGAGTCT TGCCCTTGTC CTAAATCACA GCTTTTCCTG 1320 GCAGCAAGGG ACAGGCGGCA TCCTGGTGCA TTTAGTAAAC ATTGGAAACT GAGTTGGGAA 1380 GGGTAGGGGA GGGTGGCAGA GGACAAAGTG AGGACCATCC TTGGCTCATA GAATTCAGAG 1440 AAACCTCAGG CATCTCTCAC GCAGCCTGAG CAAAAATGTC CTCTGCAGGA TCCCAGCTGG 1500 GGCAGACCTA GGAGAATCCT CCTCAAGCCA CTCTCCACTG TGAGGAAGCC AAGGGTCTAG 1560 AAGGTTTTCT GTACTTTGAG CTGGAATGTG CATTTTGGTG ACTCCCTCTT GCCTGGTCTG 1620 GCCTCAGGAG GCCTCAAGTC TGTGCTCCTC AAAGGCAAAG TCACAAAGAT TCTGTGGTTC 1680 TCTGCCTAAC ACCTGGACAG CACTTAGGGA TGATGAATGG CTGGATGGAG GGAAGGACGG 1740 GGGCATCTTT GAGAATAAGT CCTTTGGCAA GCCCCTGTTC CTGTGTGGCC CCAGGTGCAG 1800 GGTGTACTCC TGAAGATGTA CACCCTGGCA TGCCTTACTT CAAGAAGAGG GTTTGCTGGC 1860 ACAGAGCGAT GGAGTCATAG CACTGGGGGG TGTGGAGAGG GGAGGAGGGT GGGAAGGCAC 1920
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