Tag | Content |
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EnhancerAtlas ID | HS050-46209 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr3:18767050-18767770 |
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) |
CEBPB | MA0466.2 | chr3:18767503-18767513 | ATTGCGCAAT | + | 6.02 | CEBPB | MA0466.2 | chr3:18767503-18767513 | ATTGCGCAAT | - | 6.02 | RUNX1 | MA0002.2 | chr3:18767198-18767209 | TTCTGTGGTTT | + | 6.32 | ZNF263 | MA0528.1 | chr3:18767238-18767259 | GGAGGCGGAGGGGAAAGGAGG | + | 7.03 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_18730 | chr3:18763374-18769766 | CD4p_CD25-_Il17-_PMAstim_Th | SE_20677 | chr3:18763711-18769948 | CD56 | SE_22750 | chr3:18763516-18769686 | CD8_primiary |
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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 |
GH03I018722 | chr3 | 18763866 | 18769778 |
|
Enhancer Sequence | GCCTTCAGGT GGATGAACAC TTTCATAGGC AAGTAAAATA GATTGTTACA CCTGACTTAT 60 TTACACAAAG TAAAAAATAG GTTACAGCCT TTTAATTTAA GCTGATCAAC TTTATTATTT 120 CTCTTTGGAT GAAAGCATGT GCAATGTTTT CTGTGGTTTG GGTGTAATTT CCTGCCAGAG 180 GGGGATGTGG AGGCGGAGGG GAAAGGAGGG GTTGCTGAGT TTTGCCATCA AATTCTTAAG 240 TCCAGCTGCT CTCTTTTAAG TGTCAATGAC CTTACTCTAT AGCATCCAGA CTGGTCAAGG 300 TCCCTATAAT GAGAAAACCA AATTACAGGT ATGTAATTTT CACAGTTTTC TGCCGGGATC 360 TCCAAGTTGG TGACAAATTG ATATACTACT GTCTGTACGG AAGACTGCTT TCAGAAAACA 420 GGCCACTCTC AGTTGAAACA CTATGCCTGA AGGATTGCGC AATTTTAAAC TTCCGAGATA 480 TAAAAAACAT CCTTCACCCA AGTCTCTTGT AGAATGTTGA ACTATAGAGC ATATTGTTTA 540 AGCTTGGAAA GCCCTGCCAG AACAACAAGA TGTGAGAAAA ATCTTCAGGC ACCAGGAACA 600 AGGAGATCAT GGAAAAGCAA CTAACAATGG GAAGATAACG TATGTCATGG GACTAGAATC 660 TCAAATTGTG AATTTTGTTA TACATTCCTC TGCCAAACTT TTAGACATTC ACAGTTAGTC 720
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