Tag | Content |
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EnhancerAtlas ID | HS104-23138 |
Organism | Homo sapiens |
Tissue/cell | HUVEC |
Coordinate | chr16:50644970-50646270 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr16:50645094-50645115 | TCCCCCTCTCCCATCTCCCTC | - | 6.09 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_01851 | chr16:50645998-50648683 | Aorta | SE_26977 | chr16:50641523-50649046 | Esophagus | SE_54751 | chr16:50640080-50652062 | Stomach_Smooth_Muscle |
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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: 2 | ID | Chromosome | Start | End |
GH16I050609 | chr16 | 50643146 | 50645132 | GH16I050611 | chr16 | 50645312 | 50645924 |
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Enhancer Sequence | GCAGGACTCC AGGTAGTCGC AGCCTGCGGC TTGGGCCCCA CGGGGAGAAT GGGTGGCCAG 60 GCCACGTTCC CCTGCATGGC CTCCAGGAGT CACTGTGTCT GAGGGTGCTG CAGCCACTGC 120 TTCATCCCCC TCTCCCATCT CCCTCTCTCC AGGTCCCCCC TGCCTCTCAC CTGGTGAACG 180 CTGCCCCCGC CCAGCTTCTT GGCTATCTCT GTGTCTCATC TCTGGGCCTT TGCTCGTTGT 240 CTCTCCGCAT CCTCAAGTGC CTGGTTTCTA TTTCTCCACT CTCCGGCATC TTTAGGAAGG 300 CTGCTCTGCA GCTTCCCTAA AGGAGATGCT CAGAGCCACT GAAGTCAGGC AGCCCCTCCT 360 CCTCGGGACC AGGCCCAGGC CTCCCAGCTT CCAGGGCAGG CCTTGCTTTG GCCCTGCTGC 420 CCTCTCCCCA CTGGCCTGGC GTGCGCATGT GGCAGCCCGT GGGGTGGTCT CTGCTTCCTC 480 AGCCCAAGGG TGGATGTGCC TGGAGTTGGT GGTTCTGCCC AGCAGGGAGC AGTGTTAAGA 540 CTGAGGCCTG GTGGGGGCTG AGCAGCACTC GGGGAGCTCG GGGCCTGTTC AGCTCTGCAA 600 TGGTCCCTAA CTTTGCCTTC CTCATCTCTC CTCCCTTGAT TCTGACTTCC TGTGAATTCG 660 CAGCTCAGAC CCCATTCCAG CCTGGCTTAC CCACACTCAC TGTGTGACCT TGGGTGAGTC 720 ACTTCCCTGT GGCTCAACTT CCTCACTGGG TTCCTTGTAG CACTTCTTTG CCAGGGTTAT 780 TGTGAAGACA ATGAGGTGAT GGATGTAGGT CGCAAGGGTG GCCCTGGTAC AGAGTAAGTG 840 CCCAGCACAC TTGAGCTGCC ATGATTCTTG TTTCCTGGGT TCAGTTTTCT TGAAGAGGTG 900 TCAGCCCGTG TTTATAATCA TTTACCTAGC CCAGATCAAA GAGGACCTCT TTGCAAAGCT 960 TCTTTAATCC TGTTAGAATC TCCAAAGGCC TCCCCGTACT CCTGGTGCCT GGAGTAGGGT 1020 CTGGCATGCT GTATGTGCTC AATAAATAAA CACTCACTGA AGAAGGAAAG TCAATACCCT 1080 GTAGTCACTG AAAGCAGGTG ACCTCTCCCT CTGCCTCACT GAAAGCAGGT GACCCCTCCC 1140 TCCGGCCTCT CAGGCAGGAC CTGTGTACCT GTGTTGGGGC CTGGGCCAGT CTGTCCAGGC 1200 TCCCAGGGGT CAGATGTTGG GCAAAGGAAC TTGGGAGGCC TGTACTTCCT TTCATCTGTA 1260 GTTGGAAAAC TGAAGCCCAG AGAGGGAAGT GACCTGTCCA 1300
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