Tag | Content |
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EnhancerAtlas ID | HS050-50323 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr4:3496210-3497210 |
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) |
KLF5 | MA0599.1 | chr4:3496827-3496837 | GCCCCGCCCC | + | 6.02 | SP1 | MA0079.4 | chr4:3496824-3496839 | CAAGCCCCGCCCCTC | + | 6.34 | SP2 | MA0516.2 | chr4:3496823-3496840 | ACAAGCCCCGCCCCTCT | + | 6.94 | SP4 | MA0685.1 | chr4:3496824-3496841 | CAAGCCCCGCCCCTCTC | + | 6.6 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_37486 | chr4:3492383-3497475 | HSMMtube | SE_40841 | chr4:3495357-3497003 | Left_Ventricle |
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| Number: 1 | ID | Chromosome | Start | End |
GH04I003491 | chr4 | 3493028 | 3499818 |
|
Enhancer Sequence | CACCTTGTCC TAGTCCGTTG CCCAGCCCTC TCCGCCTCCT CGCCCACCCT CCACGTGGGG 60 CCTCTGCCTG GATGCGAAGT CCCCGGGCCC GGCTTCCCTG GCCTTTATCT CAGAGAGTGC 120 GAGAGGCCTC ATCTGTCTTG TGAGCCTTGG GCCTGAATGC TGTGGTGTGC GGAGAGGCAG 180 CTCCGGGCAG CCCCCGGGCT GGGATGTGCA TGTGTGGTGT GTGCACGTGT GGCACATTCC 240 TGGGTGTGTC CTGGAGACCA CAGTGGGGTC TGCAGTAGTC CCTCAGGCAT GGGGCTCCTC 300 AGGTCCCGGT GAGGGCGGAC CTCAGGAGGG GGCTGGCTCT GAGCCCAGGG CCCCTGCCCT 360 GCCTGTCTCC CCTACATGGG GCCGAGTTCC AGGCTTGTCT CAGTCACCCC TGCACATCTG 420 TGTGGGTGCC TGCCTGCCCC CTCACCCGCC ACCCTGTTGT GGGTGCCTGC CTGTCCCTTT 480 GCCTGCCACC CTGTCAGGGA CTGACTCTGA GCGGGGAGTT CTGGAGGGCT TCTGCAGCAG 540 TGCCTGGTGA GCAAGCGTGG GCTTTGGGGA CTGAGTTTGG GCCACATCCA CTACCTGCTG 600 GCTGGGTGAC CCTACAAGCC CCGCCCCTCT CTGAGCCTCA GTTTCCTCTT GCAAACGGGA 660 TGACAGACCC CGCCTCACTG GGCTGCACTG AGGGTCTGAT GAGGTCACTC TTCAGGCGCT 720 CAATAGCTGC CCGTCACCAT TACCCCTGCT GCTGTCACCT CCGGAGGTGG CCGCGCCAGT 780 CTTGTTGCAG GACGAGTGAG GCTGTGGCTC CTTTGCTGGG GAGCCAGGCC CTTCCCGCTA 840 GTCTTCATCA TCCACGCTCA GCCCTCTGTG TTCCCACGGG TCGCCTGCCC AAGGCTAGTG 900 GGGGCAAGGT CCCTCTGATG GGACCAGACT GAAGCACCCC ACAGCGGTGG CCTGGAGTCA 960 TGGGGCCTCT TGCCTGGCGG GGCTGGGCCC CTGGACAGCC 1000
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