Tag | Content |
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EnhancerAtlas ID | HS050-57972 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr6:30488580-30489460 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFKB1 | MA0105.4 | chr6:30488779-30488792 | AGGGGATTTCCCT | + | 6.15 | NFKB1 | MA0105.4 | chr6:30488779-30488792 | AGGGGATTTCCCT | - | 6.1 | REL | MA0101.1 | chr6:30488780-30488790 | GGGGATTTCC | + | 6.02 | ZNF740 | MA0753.2 | chr6:30488993-30489006 | GTTGGGGGGGTGG | - | 6.07 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_62602 | chr6:30456364-30512797 | Tonsil |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr6 | 30489226 | 30489361 | chr6 | 30488979 | 30489409 |
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| Number: 1 | ID | Chromosome | Start | End |
GH06I030519 | chr6 | 30487651 | 30489450 |
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Enhancer Sequence | TTAAAAGCAT CTTGCTGGAA TAGGAACAGC TCCGGTCTGC AGCTCTCAGC AAGACCAACA 60 CAGAAGATGG GTGATTTCTG CATTTCCAGC TGAGGTACCT GGTTCATCTC ATTGGGACTA 120 GTTGGACAGT GGGTGCAGCC CATGGAGGGC GAGCCAAAGC AGGGCAGGGC ATCGCCTCAC 180 CTGGGAAGTG CAAGGGGTCA GGGGATTTCC CTTTCCTAGC CAAGGGAAGC CGTGACAGAC 240 TGTACCTGGA GGAACAGTAC ACTCCTGCCC AAATACTGGG CTTTTCCCAT GGTCTTCACA 300 ACTGACAGAC CAGGAGATTC CCTCCCGTGC CTGGCTCGGT GGGGCTCATG CCCATGGATC 360 CTTGCTTACT GCCAGTGCAG CAGTCTTAAG ATTGGCCTGG CATGCTGCAG CTTGTTGGGG 420 GGGTGGGAGG GCGTCCGCCA TTCCTGAGGC TTGAGTAGGC AGTTTTATGC TCACAGTGTA 480 AACAGGCCGG GAAGCTTGAA CTGGGTGGAG CCCACTGCAG CTCAGCAAGG CCTACTGCCT 540 CTCTAGATTC CACCTCTGTG GGCAGGGCAT GTCAGAACAA AAGGCAGCAG ACAGCTTTGG 600 CAGACCTAAA CGCCCCTGTC TGACAGTTCT GAAGAGAGCA GTGGTTCTCC CAGCATGGCA 660 TTTGAGCTCC GAAAATGGAC AGACTGCCTC CTCAAGTCGG TCCTTGACCC CCGTGTACCC 720 TGACTGGGAG ACACCTCCCA GTAGGGGCCA ACAGACACCT CACACAGGCA GGTGCCCCTC 780 TGGAACAAAG CTTCCAGAGG AAGGATCAGG CAGCAATATT TGCTGTTCTG CAGCCTCCGC 840 TAGTGATATC CAGGCAAACA GGGTCTGGAG TGGACCTCCA 880
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