Tag | Content |
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EnhancerAtlas ID | HS104-05327 |
Organism | Homo sapiens |
Tissue/cell | HUVEC |
Coordinate | chr1:209576700-209578060 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr1:209577762-209577783 | CTCTCTACCTTCTCCTCCCTC | - | 6.52 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_26692 | chr1:209576752-209577680 | Esophagus | SE_33755 | chr1:209574939-209586916 | HCC1954 | SE_35814 | chr1:209576085-209580538 | HMEC | SE_64219 | chr1:209576613-209580286 | NHEK |
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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 |
GH01I209403 | chr1 | 209576601 | 209580287 |
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Enhancer Sequence | GATCACGCCA TTGCATTCCA GCCTGGGCGA CAGAGTGAGA ATCCGTCTCA AAAAAAAAAA 60 AAAAAAAAAA AAAGATCTGG GAACACAGGG TTTATCTCCT TCAACTGTGA ACTGCGGAGC 120 AACTGTGCCC TTTTTGAGCA TCATGGGGTC TCCAGCTCAC CACTGAACCC CCTAGGGCTT 180 GTGTCACTCA TTTAAGAGGC AGACCTGCCC TTGTCACAGT ACACTGGAGA CACTTTGGAG 240 AGCACTGGCA ATGCCAGTGA GCTTGAGCCT AAAAGCGGCC AAGACTTTCA CTTGAATCAT 300 TTGGGGAGTG AAGATGGGGA GCAGGGATGG TGCCAACGCC AGCGGCTGAT GCTGAGATGC 360 AGCAGAATTA GCAGTCTCCC CTTGAGAAGG CTACAGAGAA CACAGAACAC TCGAGGGAGA 420 GGCAGGTGCA GATGAAAAGG CAGAGGGAGT GAAGTGGTCA AGGAAGAGTC TGAGGCTACG 480 AATGAGTTTA TTCACCATGG ACATTCCAGA GGACAGACAT AAAACTGTTG GTAGGAGCTG 540 GGCCAGGCAA GGGGAAGCAC AGGGTGATGG CACAGGATCG GAAATCACCT GGGGAAACAT 600 TTCAGGTGTA AGCGTCTAAT GAGAAGTCTC AAAAATGTCA AGCTAATTAC TCTTGGGAGC 660 AACCTGGTGG TTGGGTTGGA GTCACTGACC TGGACCCTGG GCACCCAAAT TGCCTTGGCA 720 CAGAGACCTT TCCAGGACAG CTCAGGCATA CCTAAGAATC ACCTTAATAC CAGGTCACCG 780 GGAAGTGAGT CAGGCTAAAT TTCAAATCCT CTTCCTCTGC TCTGTCCGTG AGTCACAGAA 840 GATCAATAGG AGGAATCTCA GTCAGATTCG ACACTGGTTA TCCCAAGCAA GAGCCCTTTT 900 TATAGCATTC TTACAACAAT GAATTTAGTC ACCTTGCGGG CCACACAATT CGCTGACAAC 960 AAGGGGAGAG AGGAGCAGAA AGGGAAGATG CCAAAAACAT GCTATGTCTA TTTCAAAATT 1020 TCCCCCTAAT TTGGCTCAAG GTGCAGGAGA AAGGAGTAGA AACTCTCTAC CTTCTCCTCC 1080 CTCACCACAT AGATTCCAAC TCCATCAATC TAAAACTCTT AGCAATACAT TTCCAACAAA 1140 CTAGTATGTA TTAAATGGAC TGTTGTGTAT AGGCTGAAAA AGCTGATCAC CATATTAAAG 1200 GGCTAATTTG AAGTAAATTG TGTTCCAGAT TCTAAAAACC CAACTTGTAA ACTCCAGCAC 1260 ACAGCTCATC AGTAGGGTGA AGGCTGCCTA TATACTAAAA CCAAATTTCT GAAAGCATAT 1320 AAAAGTTTCA GCTTGTTTTG TTCAGGAACA CTATCAATCA 1360
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