Tag | Content |
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EnhancerAtlas ID | HS104-41844 |
Organism | Homo sapiens |
Tissue/cell | HUVEC |
Coordinate | chr3:126720510-126721900 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Klf1 | MA0493.1 | chr3:126721847-126721858 | TGGGTGTGGCC | - | 6.62 | MEOX1 | MA0661.1 | chr3:126721598-126721608 | GCTAATTAAC | + | 6.02 | NR2C2 | MA0504.1 | chr3:126721751-126721766 | TGGCCTCTGCCCCCG | - | 6.03 | ZEB1 | MA0103.3 | chr3:126720561-126720572 | GCGCAGGTGCG | - | 6.32 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_01881 | chr3:126710278-126723275 | Aorta | SE_68930 | chr3:126718954-126724302 | H9 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH03I126998 | chr3 | 126717520 | 126723428 |
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Enhancer Sequence | CCCACTCCCT GGTGGCTGTC TTAAGCCGCT GGCTTGGATG TGTGGTTGGC TGCGCAGGTG 60 CGGTGATTGC TGTGGGCCTG GCCACCCTGG GTCCCCCTGC TCCCGCCTGG CACACCTGGC 120 CTGGTTCTCA TATAATCCTC AGAACAACTC TGTCTGAGGG AGGCAGAGAG AGGTTTGGAC 180 CCAGGCACTG TGGCCCAGAG GCTGGTCCTG GCTGGCATCC GCCTGGGTCT GAGTACCTGC 240 CTCTGGCCAC TGACCCAGAG CAAAGCAGGG GGTTTGTGGT GCTGGCATCC TAAGCGTCCG 300 TCGGGCAGGC CTTGGGCCAG TGGTCATCTT AAACAAGGAC TCCTACTCCT GCTGTGGCTG 360 CAGGGCAGGC AGGCACGGGT GCACTTGGTG CGGGTGTGGG TGCAGTCCAG GCCCCACCGG 420 CAGGGGTGCT GGGCGGCCGT GGCCTGGTTG CTCCTGGGCC GCCCGCTGTC CCTGCATCTC 480 TCCTCCCAGA GGCCGTGGGC CATGGCCCTG CAGCCAGTGC AGCTGGGCCC ATCCTGGCCG 540 CCTCTTCCCC TGCCCAGCTT TGGGCTCCAC TCTTCCGGGT CTGGTTTGAC TTAAGCCTGC 600 TTGGTGGCGA GGCAGCTGAG CGGATGTGGG GGGTGGCCGG CGGCGCTCAG GAATGCGGCC 660 CTCCCCCTCT CCCAGCCGAC AGCCTCTTTG GCTCAGAAAC ACAGCGCCCC ACCCTGGCTG 720 GCCGCCCTCA GCCCAGGCCT GATGGATCGG ACTCCAACCA GGGCTTTCGC TGGGCCCTGC 780 TGCCCTGGAC CTGCCCTGCT CTGTAACCGT GAGGAGTGAG GACACAGAGG AGGGGTACTG 840 AGTCTGGGCC TAGGCCCCTG CCCTGAGGTG GAAGTGGAGA GGTAGAGCGG GAGCAGGAGT 900 GGGTCAGGCT GGGGGAAGCA GGCCACAGCC CGCAGCCTGA GAGCCTACCC TGGACTCAGA 960 GCTGGGCAGA CACGCCCCAA GAGTCCCATC TCTGGAAAGC CCCGTGGGTC TCTCTGTTAA 1020 TTAAATACAT TTGTTTGGTA AAAGCAACTA AAAATACTTG CAGCATCGTG AGCTGCGGAG 1080 AAGAGCTGGC TAATTAACGC CTGGTTTGTT TGGGATCTGG AATACATTTC CATGCCGATG 1140 AGACGCCCAC CCTCCTCCAC TGCCTTGCCA GGATGCCCCC ACCCCTAGGA CACCCCATTC 1200 TGGAGTCTCC TGGTCCACTG CCCTAGACTT CCTGTGAGCC CTGGCCTCTG CCCCCGACAA 1260 CCAACATCCC TCCTTCAAAA GCCCAGCCTG GCCCCAGGGA TGGCTAGGCA CCCGTGGGAC 1320 TCCTGTAGCC TTCACCCTGG GTGTGGCCAT GCTGCTCCGT GGTGGGTGCT GGGCTGTGGT 1380 TGTCTCCAGG 1390
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