Tag | Content |
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EnhancerAtlas ID | HS091-29604 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr2:242533840-242535550 |
Target genes | Number: 28 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HES2 | MA0616.2 | chr2:242534917-242534927 | GGCACGTGCC | + | 6.02 | HES2 | MA0616.2 | chr2:242534917-242534927 | GGCACGTGCC | - | 6.02 | Nr2f6(var.2) | MA0728.1 | chr2:242534836-242534851 | AAGGTCAGGAGTTCA | + | 6.04 | RREB1 | MA0073.1 | chr2:242534181-242534201 | CCCCAAATCAAAAACAAACA | + | 6.22 | RUNX1 | MA0002.2 | chr2:242534380-242534391 | AAACCACAGAA | - | 6.32 |
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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 | CTACAAATAA AGTAGCCGTG CTCATTAGGT GGCTCATGCC TGTAATCCCA GCATCTTGGG 60 AGGCCCAGGT GGGTATACTG CTTGAGTTCA GGAGTTCAAG ACCTGCCTGG GCAATGTGGC 120 AAGACCCCAT CTCTACTAAA AATACAAAAA ACAAAACAAA ACAAAACAAC AACAACAACA 180 ACAAAAACCG GGCATGCTGG TGCATACCTG TGGCCCCAGC TACTTGGGAG GGCGAGGTGG 240 GAGGATCGCT CAAGCCTGGG AGCCAGAAGT TGCAGCGAGC CAAGATCTTG CTACTGTATT 300 CCAGCCTAGG TGATGGAATG AGACCCTCTC TTAAAGAAAA ACCCCAAATC AAAAACAAAC 360 AAAAAAATGA GCCAGGTGTG GTGGTGCGCA TTCGCAGTCC CAGCTACTGA GGAGGCTGAG 420 GTGGGAGGAT CACCTGAGTC CAGGGGGGTT GAGGCTGCAG TGAGTTATGA TTGTGCCACA 480 GAAGATAAAT GTTCTGAAAT TAACTGTAGT GATGGGTACA CAGTGCTGTG AACATACTAA 540 AAACCACAGA ATTGCACACT GTGAGCGATC TGAATAGTAT GTGAAGATCT TTTTTTTTCT 600 TTTCTGATAA CAGAGTCTCG CTCGGTCGCC AGGCTGGAGT GCAGTGGCGC CATCTCAGCT 660 CATTGCAACC TCTGCCTCCC AGGTTCAAGC GATTCTCCTG CCTCAGCCTC CTCAGTAGCT 720 GGGATTACAG GTGCCTGTCA CCACGCCTGG CTAATTTTTT TGTATTCTTA GTAGAGATGG 780 GGTTTCACCA TGTTGTCCAG GCTGGTCTCG AATTCCTGAC CTCAGGCGAT ATGCCCACCT 840 TGGCCTCCTA CAGAGCTGGG ATTACAGGCG TGAGCCACCG CACTCAGCCC TGCATTATAT 900 CTTTAAAGAG CTGTTAAAAA TACATGAGAC AGCCGGGTGC AGTGGCTCAC ATCTGTAATC 960 CTGGCACATT GGGAGGCTGA GCTGGGCGGA TCACCTAAGG TCAGGAGTTC AAGACCAGCC 1020 TGACCACCAT GGAGAAACCC CATCTTTAAT AAAAATATTA AATTAGCCCA GCATGATGGC 1080 ACGTGCCTGT AATCCCAGCT ACTCGGGAGG CTGAGGCAGG AGAATCGCTT GAACCCAGGA 1140 GGCAGAGGTT GCGATGAGCT GAGATGGCGC CACTGCACTC CAGCCTGGGC AACAAGAGCG 1200 AAACTCTGTC TCAAAAAAAA AAAAGAAGAA GAAATACATG AGACATGCTG AGTGACAGGT 1260 ATATGGCAAA CAAACATGGA CACAAACAAG GCAGCAGCAG TCACTCCCCA GCTTCCACCA 1320 CCAGCTCCCC GTACCGAGGC AACTGTGCCT CCCTCTACCA GCAGAGGGTG ACATGAGAAT 1380 CTGGGCCTCA GCTGTGCCCA GACACTGGGA GCAAGAACCA GGCAGAGGCT GCTGTAAGAC 1440 CAGCCCCGGA ACGACCCTGG GCACTGAGGT TCTGAAGGGC TTCCCTAGTT GGGACATTTC 1500 ACTCCTGTCG CTACAATGCG ATGCTGGGCA ATGGAGCGCG TCCCGTGGGC TGCACGTGGA 1560 AAGGATGCTG GAAGCTCACA CCTGTTTCCT CCAGACTCTG CCCCGTGCCC TGCCCTGTGC 1620 TGACCGTGCT CCATGTCCTT CCGCTGTAAT AAGTCAGCTC CTGCCACGTC CTATGAGGCC 1680 TCCCAGTGAA CCTGGCTGGG GGTGGTCCAA 1710
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