Tag | Content |
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EnhancerAtlas ID | HS047-00012 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr1:999040-1000010 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr1:999343-999362 | GGCCGCCACCTGGTGGCCG | - | 8.19 | FOSL2 | MA0478.1 | chr1:999173-999184 | GGGTGACTCAG | + | 6.02 | JUNB | MA0490.1 | chr1:999173-999184 | GGGTGACTCAG | + | 6.02 |
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| Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
SE_24070 | chr1:999416-999769 | Colon_Crypt_2 | SE_24817 | chr1:999005-1000308 | Colon_Crypt_3 | SE_27529 | chr1:999243-999870 | Esophagus | SE_34539 | chr1:997968-1000257 | HCT-116 | SE_58139 | chr1:999418-999667 | VACO_9m | SE_65935 | chr1:996609-1000366 | Pancreatic_islets |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I001061 | chr1 | 996971 | 1001049 |
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Enhancer Sequence | ATGTGTGTGT GTGTGTGTGT GCGTGTGCCT GCATCCTGAG GGACGGCGTC TGCTAAGCAC 60 TGGTTCAGGG CACAGGGTCC TGCACCTGCC TCCCTCAGGC CTCCTTCCTT CAGGTCTCAG 120 GCACTGGAGT CCAGGGTGAC TCAGGGAAGC CGGTGCCTCC CCTGGCCCCA TCCCTGCCCT 180 CCTGGCTGGT ACCCTGGGCT GAGCTGGTTC CTCCAGCCTC AGTTTCCCCA CTGCAGCGGG 240 CTGCATCTGC AGAGAAGGAG ACCTGGTCTG GGGAGGCCCC TGGCCCCTCC TTGCTGAGGA 300 CCAGGCCGCC ACCTGGTGGC CGCCCGCCCC TGCAGCGCCC GCCTGCCTCC TGCCGGCTCC 360 TGGGTGGGGC GAGGGCCAGA AAGGCGAGCA GAGCAGCTCT GGGGCCCGGG TGGTGGTGCT 420 GCCTGGACCC CCAAGGTCTG CGTATGTCTC GCTAAGCCTT CTGCCCTATC CGTGTGGGTC 480 TCTCCCCCTC ACCTGGCCAG GCCGTGGCCT CCAGCCTCAC CTGTGCTCGC CTGTGCCTGG 540 CCCAGGTGGT ACCACGGGCG CCTGTCTGGC AAGGAGGCTG AGAAGCTGCT GCTGCAGAAG 600 GGGCATCCGG GCAGCTTCCT GGTGCACATG AGTCAGAGCG ATCCTGGGGG CTTCCCGCTG 660 TCAGCGCTGA CGCAAGGGTG GGACGAGGCG CAGGGCTCAG GCCGCCAGCC ACAGGTCACG 720 CACATCATGA CTCACTCCCA GGTGGGAGGG GGCGGCGAGC TGGGGCGGCC TCTGGGAAGG 780 GCGGGCGGCC TTGGCCAGGC CCCTCACCGC CACCCCCACG GCCGGATGAG AAGTGGGAGA 840 CGGGGAGCGT TTTGACACCC TCGGAGACCC GGTGTAGCAG GAAGAGCCCA TTGATGGGGA 900 AGGTGGGGGC GGTTGTGCAC CTCAAGCAGG TAAAAGCCCC TCCACAGGCA CCAGGGCCGT 960 GGGCACAGCC 970
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