Tag | Content |
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EnhancerAtlas ID | HS050-36125 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr2:39797390-39798880 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
LHX2 | MA0700.1 | chr2:39798249-39798259 | ACTAATTAAC | + | 6.02 | NFIL3 | MA0025.1 | chr2:39797457-39797468 | AGGTTACATAA | - | 6.14 | RORA(var.2) | MA0072.1 | chr2:39798507-39798521 | CTGACCTACTTTCT | - | 6.02 |
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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: 1 | ID | Chromosome | Start | End |
GH02I039567 | chr2 | 39794271 | 39799254 |
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Enhancer Sequence | TCTTCACAAC TTTTGATGTA GATGCTTCCT TTACTTTCAT CTACAGATGG GGGACTCAGG 60 CCAAGAAAGG TTACATAATT TGCCCCAAAT CACAGAGAAG CTTATGGATC AAAGATCAGA 120 ACCTAGGAGG TCTGACTTCC AAATCCAAAC TTGAACTGCT GCGCCCACTG GCTAGAGATA 180 AGTCAACAGT TGAAATGAAC AGGCTAATTG TTTCCCCCTC AAAGCACTGG AAAAAGGAAA 240 CAGCAGCTAT TTGGAATGAG ATTTTTGCAT CCTGGTCTGC TAAAGATCAT GGTCCTGAAA 300 AACAGAGCAT GGTATCTGAG AAATTAGTGT TCTTAGTTTA TAGAAGGGCC CCTCCCTGTT 360 CTATAGGACT AGCTAAAGGG TGGTAGAACC AGATTGAGCG TTAGAGCATT CTCCATCCCC 420 TACACCTCTC TTTCCATTTT GGGTAACTTG AGGACATTCT CCACACTCCC TGCAAGATCT 480 GTAAAGTACT TTAGGTGCTG TTAGCAAGGT TCAGAGGGTC ACTACCAGCT GATCCCACTG 540 CTTCTCACTG TTGGCCTGAA AAACAATTCC ATTTAGATCT GGATTGCCTA AAAGTTTGTG 600 TGTGTGTGTA AAGGGTGTAG AAGGATTACT ACTAGACACG ATTCTTCTCT TTTTTTAGAA 660 AGAATAATTT GAAATACAAA CAAAATAAGG CTGTGGGGTC TTATTCCCAG CAGCTGGCAG 720 ACTTTCACTT AATTAAACTA CCGTGATTGC TTTATTCATA TATTTTGCTT GCCCCCATTC 780 TCTTCCTCTC TGACTCCTTA TAAAAACAAT ACTATTTCAT GAAGGGAGAA ATTAAATGCT 840 GTTAGTCTTT AAGACCAACA CTAATTAACA GCATTTATTT TTACTGTGAT TGCCTACGTG 900 AAAGTATGCA AAAGTAAATT TATATTCTGA GAATGTGGTT GCTTTGGTCT GAAGCGGTAA 960 AGGGAATTAA CTGTTCCTGG GAACTCATCA TTCTTTGCTT GAAATTCTCC AGAGAGCAGT 1020 GAAACACCAG TGCCAGGGGC AGAATATAGA AACAAGGGCC GAATGCTGTG GCCAATTGAG 1080 CTGCCAGCCA CCAGTATGAT CATTCTCAAA TCCAGGTCTG ACCTACTTTC TCTCCTGTTG 1140 CAAAACCTGA GATGGATCTC CTGCCTGCTG GGTCAAGGTG AAGCTCCTCA GCCTGGCATT 1200 TAAAACATTT TGCAGTCTGG CTCCCTCTCT CTCCAGCCTT ATCTCCCTGT ACTCACCACT 1260 GCATGCCAAT GCTCCGATTG TAGCCCTGCC CCTCATCATT CTTTTTACAT CTCTGTGGCT 1320 TTTTGGAAAT GACTCCCTTT TGTTTTAAGG CCTTCCACAC CCACCACACC CGTGCTACCT 1380 GGTGAGTCTT GTCATCCTTT AAATTGAAGG TTGGAGCTTG CCTTTTCTGT GCAGCCTGTC 1440 TGAACTCCCC CGGCAAAGTT AGTTTCTCCC TCCCCTGTGC TCCCACACTA 1490
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