Tag | Content |
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EnhancerAtlas ID | HS091-10824 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr12:110405300-110406400 |
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) |
IRF1 | MA0050.2 | chr12:110406038-110406059 | CTGTACTTTCAGTTTTTGTTT | + | 7.63 | LMX1B | MA0703.2 | chr12:110406215-110406226 | ATTTTAATTAA | + | 6.62 | Lhx3 | MA0135.1 | chr12:110406219-110406232 | TAATTAATTAACT | + | 6.64 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_11241 | chr12:110404286-110406554 | CD20 | SE_18587 | chr12:110404438-110406569 | CD4p_CD25-_Il17-_PMAstim_Th |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH12I109966 | chr12 | 110404086 | 110406890 |
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Enhancer Sequence | TTTGTGATCT GAAACAGAAA CCAAGTCAAA GTTTTGTTCA TAGAAATGTT GATAAGATCT 60 GTAAAGGAAC ATCACCATTA TTTCCTCAAA CTAAGTTTTG CGATTAGTAT TTGTGCATAA 120 TGACGAGTCA TGTTGCTAGA CTAGCTAAAA ATTCCTGAAG ACCCAGCTAG TAGTAAGGCT 180 CATAGCCTTG TTTTTTTCTG GTACAAAGGT CCAGGCATCA TTTAGCAGAA ACCTATGCTC 240 ACCCCAATCA CGACGATTAG TTTGCCCTCA GTGTAACTGA CGATCTTTGG CCATGGAAAG 300 TGTGCTGAGG GAGCTGAATC AGCTCACAGC AGGTGTCCAT CAGCCCACGG TGTGGGACAG 360 TGGATGAGCT CTAGGTCTTG CTCAAATGAA TCTATTAGTA TAAAACAGCT AGGGCTGGGA 420 CAGGTGGCCT TTGCAGATCC AGACAGGGAC TCCATCTGCA AGGAAGCTTA CTGACTCAGC 480 CCTAATCTAG CTCCTGGAGA ACACTGATCC ATGTGCCAAT GAATAACGCC ACTATCAGCA 540 CTCCTATGTA GGTTTTTCTT TAACATAAGT CTATCTTTCT TCTGGGTAAA GACCCAGGAG 600 TAGAAATGCT GGGTTATATG GTAAATGTAT GTTTAACTTG GTAAGAAACT GCCAGACCTT 660 TTCCCTTGAG TAGCGCTATC ACTTTGTTTT CCAAACAGCA ATGTGAGAGT TACAGTTGCT 720 TCCTGTCTTT CCCAGCACCT GTACTTTCAG TTTTTGTTTT TAAAAGTTTA ATCATTCTAA 780 TAGGTATGCT GTGGCATCTC ATTGTGCTAA TGACTAATCA TGCCACGCTT GTCTTCATGT 840 GATTTTTTTT TTTGCCATCC CATATCTTGT CTTTGCCCAG TTTTTATTGG GTTGTTTTCT 900 TACTGTTGAG TTTTAATTTT AATTAATTAA CTTATTTATT TATTTGAGAC AGAGTTTCAC 960 TCTTGTTGCC CAGGCTGGAG TGCAATGGCG CAATCTCGGC TCACCGCAAC CTCCGCCTCC 1020 TGGGTTCAAG CGATTCTTCT GCCTCAGCTT CCTGAGTAGC TGGGATTACA GGCATGCGCC 1080 ACCACGCCCA ACTAATTTTG 1100
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