Tag | Content |
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EnhancerAtlas ID | HS189-00034 |
Organism | Homo sapiens |
Tissue/cell | Thymus |
Coordinate | chr1:26081050-26082440 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ESR2 | MA0258.2 | chr1:26081736-26081751 | GGGCCAGCCTGACCT | - | 6.33 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_55546 | chr1:26080998-26082556 | Thymus | SE_65420 | chr1:26079704-26081956 | Pancreatic_islets |
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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: 2 | ID | Chromosome | Start | End |
GH01I025754 | chr1 | 26080874 | 26081893 | GH01I025755 | chr1 | 26082403 | 26088335 |
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Enhancer Sequence | GAGAAATCCC AGTCTCGATG CCAGGGTTGA CTCCTCAGAG CTGGACTCCT GGATCTCTGC 60 TCAGATCCCT CTTCCATAAA CACTGATCCT GGAGAGACAC AGCCAGCTGT CATGAAGCCC 120 AGACACACAC ACACTGTCCT CTGGCTCCCC CTCCCCGGGT CTGGGGTAGG ACATCATTGG 180 GGGCATCCCT TCCTCTTCTG TCCCCAGCCC TTCCCTAGGT CTCTCAGAGC AGGGACCTGA 240 TCTGACACGA ATCCTGACAT TTGTGATTAA GGAAGCGCGT TTGCTTTTAG GCTGTTTGCC 300 TGCTGTCCGT GCCGTGTGCG CATGTACATT CATGTATATT TCCTGGCAAC ATCCGCCTTT 360 TTGTTCTTGG TAAGAAAGTC TGTTGCTAAA AATGCCTGGC TCAGAGAGTG GCAGGGCTGT 420 ATGGGCCCAT GTGGCACTGA GTTTGCTCTT CGGAGGGGGC CTCCTGGCAG GAGCTGGGCT 480 ACTGTTGTTG CACCTGCCCC CGGCAGGGCT CGCTGTGGGC AGCCCCAACA GGAGGGGGAA 540 GAACGTGGGC CCTTCAGGAG AGTAGGTAAC CAGCCCTGCC CTACTCGTCA GGGTGGGAAG 600 GACCCTGAGG AGAGGCCGTT CCCTGGCAGG TGTGAGCTGC ACCTCCTCAC TGGTGTCTGC 660 ACAGACCGGC CTGGGAGACT GAGGCAGGGC CAGCCTGACC TGGGACCTTC AGGGACACTG 720 GACTGCCTGG GAGAGTGACG GTGGCCTGTG CAAGGACCTC TGCAGCCAAG CTGGTCTTTT 780 TCACTCATGC TCTCTCACAC ACATGCAGAC ACTCTCCTGC CACCCTTATA GATCATAAAG 840 GCCTGGATAC ACAAGCTGGC CTTTGTCACA GACATGCTGG CATCCATACA TGGGCACACA 900 CATTCACAAA CGAATATCCA TTTACACATG CATGCTCCCG CCACACACAA ATAGACATGT 960 CTTCACAATT GCAAACGTCT GGTGAGAAGT CACTGTGTGT CAGGCATCAC GTGAGCACGT 1020 GACATGGATT GTCTTTTCAA CCTCACAGCA ACCACAGGGA CTCCATTTTA CCGGTAAAGA 1080 AACTGAGGCT CAGAGAGGTG AGGTAACTTG CCTGAGGTCA CACAGCAGCA AAGCAAACTT 1140 AATTAGAATC CAGGTCTGTC TACCTCCAAA GTTGATGATT ACACCATACT CATGAGTGTA 1200 CCTGCCTAGA AGCTACAGCC AGGGTGGGAA GGGGCATTGT GGAGCAGCCC CTCCTGCCAG 1260 GAGAGAGAAC ACAGGCTATG GGCCCACTTG CACTTGAAAG GCTGGGAGAG GAGATCAGAG 1320 CTTCCTGCTG GCCCATTGGC TCACAGGGCT GAGCAGAGGC CCTCCTGGTC TCTGGGATGC 1380 TGCCCAGAGC 1390
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