Tag | Content |
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EnhancerAtlas ID | HS059-00446 |
Organism | Homo sapiens |
Tissue/cell | GM12878 |
Coordinate | chr1:15944300-15945730 |
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) |
ELK1 | MA0028.2 | chr1:15944819-15944829 | CACTTCCGGT | - | 6.02 | ELK4 | MA0076.2 | chr1:15944818-15944829 | GCACTTCCGGT | + | 6.02 | ERG | MA0474.2 | chr1:15944819-15944829 | CACTTCCGGT | - | 6.02 | ETS1 | MA0098.3 | chr1:15944819-15944829 | CACTTCCGGT | - | 6.02 | FEV | MA0156.2 | chr1:15944819-15944829 | CACTTCCGGT | - | 6.02 | FLI1 | MA0475.2 | chr1:15944819-15944829 | CACTTCCGGT | - | 6.02 | Foxd3 | MA0041.1 | chr1:15944952-15944964 | GTTTGTTTGTTT | + | 6.32 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_27568 | chr1:15942659-15947022 | Esophagus | SE_48498 | chr1:15942770-15947153 | Psoas_Muscle | SE_51348 | chr1:15942521-15949842 | Skeletal_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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Enhancer Sequence | CAGGTACGCC GGGCAGCGAG CCGGGCCTGC CCCGGAGCTA AGCCCTCCCC GCCTCGGGGC 60 CTCACTCCCT CCCTTTGCTA CTGGTGAAGA ATTGGGGGCT GGGGGGAGCA AGGATAGCCA 120 TTCTCAGGTC ACCCCCGCAT CCGGAAAGGA GCTGGGGAGC TGGCATCAGT AGCTGCCCTC 180 ACACACTCCG AGCATGGGGT GGGGTACGAG GAGAGGGAGC GGAGAACCTG ACCGCAGACG 240 CACCCACTGC AGCGTGAGGG GCGCGTGGAC TGTTGAGCAG CGCTAACCCT CCCCACCTTT 300 GGCTCTTTGG CCCTTCCCTG TTTCTAATCC CGAGTGTAGG ATATCGTTGT GGACCTCAGA 360 AGCAGCCCTG GGTTTGCTAG GATTCATACA TCCTGCAAAC CAGAAATACC AGTTTGGATC 420 ACTGTGGTAG ATAGATGTTC CTCTGCTTTT TTTTTTTTTT TTTTCTGGAG AGGGTTTCTG 480 CTTAAATATA CGCAGTTTAC CTTTAAATGC ACAGATTTGC ACTTCCGGTG AAAGAAAAAG 540 TTTAAGACTT GCACTACCTC ATTTTGGGGT CTTTGGAAAT GCTCTTTACC CACCACATGC 600 GTTTCTGGTT AAATTCTTTT GAAAAACAGT ACCTATTGGT TCAACTCAAG CTGTTTGTTT 660 GTTTCGGTTC TACCCTGGTA GTAAGCCAGA AGGCCCTTTT TCTTTCAGGT CACAGTTCAG 720 AGTTTGGGTC AGTTCAAAGC TCAATGCTTT AAAAGGATAT TTGCTTGGAA ACGGCCTAGT 780 ATCAGTGCTG TTTGGTGGTT TCATTTCCCT ACTCAGCTTG CTGGAAAGAA GTTCAGCCTC 840 TCATATTTTA ACTAAGCAAA GTAATTCTCA AAATGCTTTG GGGCTGCCCC TAGTCTTTAT 900 CAAACAGAAT CGGTGACACT AACGCTGTAA ACTTTACACT AAAACACTTA GATCATGACT 960 TAATAAATTT AGCCTGGAGG AAATAGTCTA AACATTAAGA AAATTATAGA GGTCTCCCAA 1020 GTCTCCATCA AGTAAATCTT GATTTTCTAC TGCAGTTATG AAATAGTTTA CAAAACGATT 1080 GCCCAACTGC AGCTTGTTCT GCTGTCTTAT GGTAAACACG TGTCAATACT TTGTTCAGAA 1140 GTATGATTCC TTTACACAAT GTGAACTTTA GAACCTTGGC ATAAAGCTGT TCAGAAAGAA 1200 TTTAAAAAGT TAATCCACAA AAGCTCAGGA ACCAGTTCTG TCAGTGAATG CCTCATGTGG 1260 AGAACTAGGA AAGGACTGTT TAAATAGAGA AAATAAACTC TTCAATTTTT TTTCTTTTTT 1320 TGTTTTTGTT TTTGAGACGG AGTCTTGCTC TGTCGCCCAT GCTGGAGTGC AGTGGTGCGT 1380 TCTCGACTCA CTGCAACCCC AGTCTCCCGG GTTCAAGCGA TTCTCCTGCC 1430
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