Tag | Content |
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EnhancerAtlas ID | HS153-00199 |
Organism | Homo sapiens |
Tissue/cell | Osteobl |
Coordinate | chr1:27321100-27321840 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Six3 | MA0631.1 | chr1:27321807-27321824 | CCAGGTGATACCCTTTA | - | 6.36 |
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| Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
SE_26796 | chr1:27320100-27322233 | Esophagus | SE_31795 | chr1:27319283-27327051 | Gastric | SE_34461 | chr1:27319108-27326655 | HCT-116 | SE_36077 | chr1:27320120-27329970 | HMEC | SE_47963 | chr1:27320102-27321641 | Pancreas | SE_49333 | chr1:27319936-27322236 | Right_Atrium | SE_65116 | chr1:27320938-27323497 | 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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Enhancer Sequence | GAGGTGCGGT CTTAGCGGCT GGTGCGTTCG AGGGTCGGTC ATGGCGTGTG GGGGGCTGGT 60 CCAGGGCCCG GGAACTCCCT TCCCTGGAGC TTCTGGCGTC TGCTGGGTCC CTAGTAAAGC 120 TGCCACTTTC TGTTGCCGCC TCTCCCGACC ATCTGGAGAG TGAGAGGTGG TAGCATCAAG 180 TCTCCATTAT AAGAGTTGGA CTCTTGAGGG GGCTCAGATC CCAGGAACGG GTTGGCGGCA 240 AACTTTTACC ACTTGGAACC TGCCGCACGG ATGCAGCACC CCCCATCCTC ACCCCCACTT 300 GCGTGGCCTT TCCCGGGCCC CTCGGAGCTG TGAGCAGTCT TGCCCTTGAG GATGCTGCTT 360 CCTGGCGCCG CCCAGCTCCG TGCCTTCGGG AGGACAGAAT AATGAGGCCC CAGGATGGGG 420 TGGAGGCTGG CACAGGGCTG TACCACTGAA TTCCCCCTCT AGGCCTGTTT CACCTTTGGG 480 GAGACGGAAT CCCAGAGAGG TTTAGGATTT GTTCTCTTCA TACTTAGGCC CTTCTTCTTC 540 TAGGAGACAG CTTTTCTTAT GCCGTCATGC AGGTTCGCAA AAATTACAGC CTGACTCACA 600 TAACCAGGAC AGGATGTCTG GCACCTGCTC ACCCAGGGAT CCTTACATAG CAGAACCTAG 660 AGGCTTAACT CCCAACCTGT TACTAAGATG GCTCGGCCAG GTTGGAACCA GGTGATACCC 720 TTTAACAGGC CCCAAGGGGG 740
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