Tag | Content |
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EnhancerAtlas ID | HS145-00044 | Organism | Homo sapiens | Tissue/cell | NHBE | Coordinate | chr1:3381220-3382710 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Myog | MA0500.1 | chr1:3382676-3382687 | GACAGCTGCGG | + | 6.32 | PLAG1 | MA0163.1 | chr1:3382001-3382015 | GAGGCCGAAGGGGG | + | 6.33 | ZNF263 | MA0528.1 | chr1:3382475-3382496 | TTCAACCCTTCCTCCTCCTCC | - | 6.46 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TCAGTGAAGG ACGAGGGCGG GGGCAGGTGC TGTGTGACCC AGATGAGTTC CTGAACCTTC 60 CTGAGCCTTG GCTTCCCCAT GTGGAAGCAA AGATCACAGC CGCCCTCTGG GCATCCTCTG 120 GGCAGTGTCC ACGGAAGGTG TGTGCCAGAG CGTCTTCTTC ACTGGTTGCC GTCCCAGCTG 180 CCTCCTCAGG CCCAGCTCCT GCCCAGACTG GGAGTGGCAG TGCCAGCCTC AGGAGACGCC 240 AAGACCACCT GTCAGAATGT CCCATGGGCG TCCACTGCAG GCCGATGGTG GCTGAGGTGG 300 GGTCCCCCAT GTCCCCAGCA CCAGCCACTG TCCTCGGTCA CAGCTCTCTC TTGTGCCTAC 360 CTGAGACGCC CAGGACTCAG AAATGCCTCA GCACCTCTGC CGCAGGCCCC TGCACCCCAG 420 CAGCTGGAAG GGCCCCAGCA CTCTCTACAC CCACCAGGCC CAGGCCCATG GGGCTCCGTT 480 CATTCATTCA CTGTTTATTT CATGCAGTCA GCAGACACTT CTGGGCACCT GCCACATGCT 540 TGGTGCTGGG GTTCCAAAGT GAGCCCACGG GCATGGGCCT GGTTCTCAGA GGGCCTCCAG 600 CGCAGGGAGA ATGCCGAGGG CTGGGCTGAG GGCAGCTCGG GGGTGCTGGG AGCACAGAGG 660 AGGGGGCTCC CCATGGCCTC GGGTCAGGGT AGGGTCCCGG AGGAAGGAGG GTTAGCGCAG 720 AGGCAGACAG GAGGAGAGGA CGGAGTCGGG GTGGGGGAGG CAACAGCTCC AGCCAGACCT 780 GGAGGCCGAA GGGGGGCTGG GGGAGTCCTT GAGGTGGGGT GCGGGGCACG GGGCTGAGGG 840 TGCCAGGCCA GGTACAGCTG GGAGCACCAC ACACTCCCAA CCAGTAAGGG GAGTTTACAG 900 GCCCCAACTC GTTCCGAGAA ATCAGCCCCT TTCCTTCCGG GAACCAGCAT ACCTGTGGCG 960 TCAGGAAAGT GTGGTGTCCC AGCCGAGGAG GGTGGGCTCC GAGTCGGGCA CCTGAGCGTG 1020 GGGGCTTCCC AGGAGCCCAG CCCTCCCGTC ACTTCTGCCA TCCCGGCCTC CTGCTGGGGC 1080 CCCCAGACCC ATGCTTGGGG CTGGACACTG GCCAATCCTT GCTCGTCTGT CCCACCAGGT 1140 CCTAGTCCCC AGGGGCCTGT GTCCTGCCCC ACTGTCCCTT CACAGCCCTC TCCCAACCTC 1200 ACCTGCCCTG CCACGGGCCT GCTCGAAACT CTTCTGAGCG TCCCCTCACG ATGAGTTCAA 1260 CCCTTCCTCC TCCTCCAAGC AGCCCTCAGT CACGTGTCCT GCCTGCTCTG AGCCCTCCTC 1320 CCACCTCTCT TGGCCTCTGC TTGGCGGCCG TGAGGCCCTG TGGAGCTGAC ATCTATTGGG 1380 CACAGCTTCG CATGTGGAGC CGAGAGGTCT CTGGGGTCCC AGGGCAGAAT CGCCGTGGGC 1440 AACACCTGCC CCGGCTGACA GCTGCGGTTT CTGTGTCTCT CTTTTGTGCA 1490
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