Tag | Content |
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EnhancerAtlas ID | HS023-17397 |
Organism | Homo sapiens |
Tissue/cell | CD8+ |
Coordinate | chr22:42792500-42793860 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr22:42792531-42792552 | AGAGGGAAAGTGAGAGTGAGA | - | 6.27 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_33430 | chr22:42791776-42794477 | H2171 | SE_65474 | chr22:42792500-42793395 | Pancreatic_islets |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr22 | 42792596 | 42792990 | chr22 | 42793400 | 42793800 |
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| Number: 1 | ID | Chromosome | Start | End |
GH22I042396 | chr22 | 42792110 | 42794306 |
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Enhancer Sequence | ATATATATCT CACATATGTG TATGCTGGGG GAGAGGGAAA GTGAGAGTGA GAGGGAGAGA 60 GAGAAATATT TTCATCTAAC AGTTGACACC AGAATCCCTG GTAGGGAAAA TACCACTATG 120 AGATGCTGGG AGACAGGAGA GAGTATGAGG AAGTCTCCGG CCACGTGCAA AACCGTGGCT 180 GACAGAAACT CCCCAGGATG GGGAAGCTGA AAGCCCTTTG AGAACCATCA CATTCCACTT 240 GGAACTGTTG GCACTGCCCC ACAGGGACAT TTCCTTGGCC TCGCTGCCAC CCGCCCCATC 300 CTCAGCAGAC AAGGCTGTAT CCTGGGCGTC CTCTGTGTGG TGTTCTGTGG CGTTATTAGG 360 GTGAGTCAAT GTTGTGGGAA CAGAAACGAC AGCACGTACG AGCAGAACCC AAGCACCATC 420 GCAGCCAGGG GGCGTGCACC TGGGGGGCGT GCACCTGGGG AGCGTGCACC TGGGAACCTG 480 CAGGGCCCCA GAAGGGCTGT GTGCCTTCCA GGCGTGGAGT GGGGAGCCCA CCTGGCGGTG 540 CCAGATCTCA CGAGATGGGG ACCCCAGCTG GCACTGGGTG GCATTTCTTC TTCCCTTGCT 600 CTACTTGGAG CATATGTTGT TCGTGGAGCC GAAAGGAACG TAGCAAAAAG AGTGTTCCCA 660 GCCCTCCCCG GCCCCAGCCG CTGGGCAGAG GGCTGCATGC TGGCTGGCTG GCCAGGCTGG 720 GGCAGCCTGG CCTCCTCGGC CCCTACGCTG CACCCACCTT CCACTTCCTG GAGATGCACC 780 CACATCTCCA GGAAAATTGT TTCAGAAAAT GCCTACAACA CAGCAGAGAG TGGAACAAAC 840 AGGGTCCCAA CGCATGTCTG CGCTGTGATT GTGACCATGT AAGATAATAT CTGCATGTGC 900 CAGGAGGGGA GAGAGCAAAT CATTACAAAT CACTGATGTG TTAAGGGCGT GGGATGGCGC 960 CTGACCTCTT CCTCTTTTTG TGATTTTTGT TGTTTATACA ATAAAAACAG GAGGAAGTGG 1020 TAAGAGCTGT TTGGTCAGAT GAAGGAGCTT TCTTCATTCT TCGCCAACTT GTGCCGTCAC 1080 TACCCCTTGT CCCAGAATGA GGATCCATGC CAAGGAGGGG AACAGGGCAT GGGGGGCACC 1140 TGACATTCGT ATGCCTTCCA GGAGCCCTGC ACGTGTCATC TCTTTTCAGC TTCAGAGAAA 1200 TTCCATGAGG TAAGAATTGT TATCCCCATT TTATAGATGA GGAACTTGAG GCTAGGAGAG 1260 TCCACACAGC TGGTACAAGA CTGAGCCAGA CAGACCCTGG TACAAGACAG ACTCTGCCTA 1320 AGGCCTGAAA GAGGTGGAGG GAGCCGGGGG CCCCGGGACT 1360
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