Tag | Content |
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EnhancerAtlas ID | HS050-05717 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr1:209977940-209979290 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RREB1 | MA0073.1 | chr1:209978709-209978729 | CCCCAGAGCAACCACACCCC | + | 6.16 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_27309 | chr1:209977673-209980487 | Esophagus | SE_27823 | chr1:209977468-209983975 | Fetal_Intestine | SE_35823 | chr1:209974126-209984775 | HMEC | SE_64223 | chr1:209974556-209984573 | NHEK |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 209978699 | 209978810 | chr1 | 209979142 | 209979287 |
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Enhancer Sequence | ATGTAAGGCC TGTGTCTCTA ACAGGTACTT AAACAGCCAA AGGACAATGA TGCTAACCTA 60 TCTATTCCCC TCACAGTGAG CATAGAGGAG GGACACTTTC AGCCTCCTCC GAGCATAACT 120 GTCCTCTCCC ATACCCCTAT TCTAGGGAGC AGGTCCTCCA TAAACACCCT CATTGCCACC 180 TCCATAGCTC CTCCCCAGAC TAGTTTCCAG GGGCACTGCC ACACAAAAGC CGAGATTTGG 240 CCGTCAGTGG TTTTGCTCAG GTTAAAACAC ACGCCATTTC TCGCAGACAA TTCTTAGCAG 300 TCCCAGCTCT TCCCTTTCTC CTGAAAGAAA TGAAATGCCA TCGTCTAAGT TCCGTTCCTC 360 AGGCTTCCCT GTTTAGCCCT GCTTAGGGGT AAACTGCAGG CCTCTAGTCA AAATGCCCAC 420 ACCCTTCCCT TCTGCTGGAT GGAAGCTGGG GGATGGCGAA TGGGAGTTAC AAGGTATTGA 480 GTGCCACTGT CATACATCAT ACACACGTCT CATCCTAAAC CACACTCCTG GGTCAACACC 540 AGCTTTCACC AATCCCACCC AAGCGCCTTC CTCTCTCTAT CCATCTCTTT TCCCTGACTT 600 CCACTCTTGA CATCCACCAA GAGAACAGGT TGGAACAGGA TGACCCCTTT ACCACAAAGC 660 AGGCTCCCTG TAAAGAGTGA CACCTCAGGC CTCCTTTCCA AGTCAGGCCT GGGAGACTTT 720 CCCCATTCTC CACACCACCC TCCAGCCCCT TCGGGCAAAG AGGGCCCACC CCCAGAGCAA 780 CCACACCCCA GCGCCACCCT CCCCAGCACC TAGCTCCGCT CCTTGGAAAT CCAAGGTTGT 840 CTCCCAGGCC CAGGGCGAAG GGCCTAACTG TGCCAAACAG ACTCAGGGAG GGAAGACAAA 900 CCGCCAATGC TCCAAAGCTC CTGGCCACCC TCACTCCAGT TTCCCAAAAC GCCCACTAGG 960 ATCAAGGACC TGCGGACCTG GGAAGTCCCC TCTCTGGGAC ACAGGGGCCA GCCGCAAGTT 1020 GGTAAGACTG AAGGGGGCGC GGTGCTTTAG CTCTACCGGA TAGTGGGGTT GTTGACGGCC 1080 GAGAGCAGTG CCCTCCGCTT CGGCGGTGGG GGTAGGGAGA GTAGACACAA GTGTAGATTC 1140 GAGAGGGGCC TAGCGCTACA GAACTGAGGC CGCCCCAAAG CTATCTGGAA AAGGGCGACA 1200 GGCACCCAGC CCCAGTGGGT ACCCACCCCA AACACACAGA TGCCCCCAAG CAAGTTCTCT 1260 CACCCCCTAC AAACTCCGGG GATGGGTCCT ACCCCACCCA CGGGGGAGCC TCTCCTCCCT 1320 CAAGCTGGTC CCCAGAAGTT GGCGTACCCA 1350
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