Tag | Content |
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EnhancerAtlas ID | HS034-04828 |
Organism | Homo sapiens |
Tissue/cell | ECC-1 |
Coordinate | chr11:12071820-12073090 |
SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
PBX1 | MA0070.1 | chr11:12072038-12072050 | ACATCAATCAAA | + | 6.74 | POU2F2 | MA0507.1 | chr11:12071926-12071939 | ACATGCAAATGCA | - | 6.37 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_45624 | chr11:12071554-12072746 | Osteoblasts | SE_47453 | chr11:12071688-12074097 | Panc1 | SE_48611 | chr11:12071643-12073023 | Right_Atrium |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr11 | 12072475 | 12072833 | chr11 | 12071899 | 12072430 |
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| Number: 1 | ID | Chromosome | Start | End |
GH11I012050 | chr11 | 12072181 | 12073469 |
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Enhancer Sequence | ACACAGTCAC ATTCACATGC CTGTACACAT AAACACATAT AAGGACACAC ATATAAGCCC 60 CCCAACTTAC TCTTCATGCT AATCATACCC AGAGACCCTT AAGGATACAT GCAAATGCAT 120 ATGTACGGGC ACACATCAAT ACGTATGTGT ATATACACGT GTTCTTCCTC AGCCCAGCCT 180 CTCCTTTTAG GCCTGGAGCT GGGGCTGACA TTGGGTTTAC ATCAATCAAA GCCACTAGGA 240 AACGTCTATC CTGCCTGGGC CCAGAGTCCA TTTCTGACAG AGGCTTCTCC AGGCTTTACT 300 TGTAAACGCT ATTTATTTTG GAAAGCAACT TCTCTGTTTT CAAATAAAAC GTTGGGACAT 360 GCAGTATTGG ATTTCCCTGA TCTGACATTG ACCTAGAAAA ATGTGCTGGC AGGAACAGAA 420 AATGCGATGC CCCACTGTGC TGGCAGGCAC AAGAGTTTCC CTCCTCTTGG CTTTGATTGC 480 AAAGGTTAAG ATGCAAGTGA GAGAGCGCAG TTCCCCCTCC CTGCCTGAGC AGCACTCTCC 540 CTGCAGAGCT GGAGGGAACT GGGGGCCATG TTTAGGGGCT TCCTGCAGGT TTTGGTGCTT 600 GTGGTCTTAG GGGCATGCTT CTGGGTGGGG AGCTTATCAC AGAGGGGCAG CTTGTCACAG 660 GGCTGGTGGC CGAGGCCAGC ATGTAGAGAG CAAACAGCTC CAGGATGTGC AAAATATGAA 720 TAGGGCCCAG CTATGGGGGT CCCCACGGTT GTCATCAGTG AAAAGGGCAA AGCAACTTGA 780 GCTCTGGGTG AGGTTTGAAG CCAGTTCCTG TCCCTTGGGG AAGAGGTTTC CTGGAGGCAG 840 ACCTGCCAGG TCCAGCTTCA GGTGAAGGTC ATGGCCTGCT GCCATCTGCA GCGGCCTGGG 900 CACCAGTTGC AACGGTTAGG GGCAGAAGCT GGGAGCAAGG GCTGAGGCAG GAGCCCCACA 960 TCATGGTGGG AACCCAGACA CCTGTGGTCT GCTTGCGGGG GTGGGCCCTG GTCTAATTAG 1020 CAAAGGAGGC TCAAAAAGCA ATACACAATT CATTGCCCCA GCTGAGCCAC AGAATCTCTC 1080 AGAGTTCCTC AGCTGCTCCA GTGACTTAAT TCTGTGCCTG TTAATTCTGT TCCTATTCCA 1140 CCCACATCCC TTATGGCCTC TCTGAGGATG AAATGAGATC AGAAATGTAA CATGCTCAGC 1200 CAGGGCCGGA TGCATAATAG GTAGGCTCGG TAAACGTGAG AGCAAATCCC AGCTTCACCA 1260 CTCACTAGCT 1270
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