Tag | Content |
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EnhancerAtlas ID | HS023-05348 |
Organism | Homo sapiens |
Tissue/cell | CD8+ |
Coordinate | chr12:6735350-6738060 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EGR3 | MA0732.1 | chr12:6735958-6735973 | AACCGCCCCCGCAAC | + | 6.07 | EGR3 | MA0732.1 | chr12:6737012-6737027 | CCCCGCCCACGCTCT | + | 6.09 | EWSR1-FLI1 | MA0149.1 | chr12:6737607-6737625 | CTTTCCTTCCTTCCTTCC | - | 10.53 | EWSR1-FLI1 | MA0149.1 | chr12:6737611-6737629 | CCTTCCTTCCTTCCTTCC | - | 10.83 | EWSR1-FLI1 | MA0149.1 | chr12:6737599-6737617 | CTTTCTTTCTTTCCTTCC | - | 6.95 | EWSR1-FLI1 | MA0149.1 | chr12:6737615-6737633 | CCTTCCTTCCTTCCTTTT | - | 7.95 | EWSR1-FLI1 | MA0149.1 | chr12:6737603-6737621 | CTTTCTTTCCTTCCTTCC | - | 8.46 | IRF9 | MA0653.1 | chr12:6737822-6737837 | AGTTTCACTTTTGTT | - | 6.15 | RREB1 | MA0073.1 | chr12:6737001-6737021 | CCCCCAACTACCCCCGCCCA | + | 6.46 | ZNF263 | MA0528.1 | chr12:6737599-6737620 | CTTTCTTTCTTTCCTTCCTTC | - | 6.02 | ZNF263 | MA0528.1 | chr12:6737603-6737624 | CTTTCTTTCCTTCCTTCCTTC | - | 6.03 | ZNF263 | MA0528.1 | chr12:6737611-6737632 | CCTTCCTTCCTTCCTTCCTTT | - | 6.16 | ZNF263 | MA0528.1 | chr12:6737607-6737628 | CTTTCCTTCCTTCCTTCCTTC | - | 6.48 |
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| Number of super-enhancer constituents: 10 | ID | Coordinate | Tissue/cell |
SE_07176 | chr12:6735348-6736378 | Brain_Hippocampus_Middle_150 | SE_11453 | chr12:6734943-6738138 | CD20 | SE_21167 | chr12:6735446-6736603 | CD8_Memory_7pool | SE_23036 | chr12:6735642-6737842 | CD8_primiary | SE_28237 | chr12:6735430-6736246 | Fetal_Intestine | SE_29410 | chr12:6735350-6736378 | Fetal_Intestine_Large | SE_39678 | chr12:6735278-6736563 | Jurkat | SE_39678 | chr12:6736843-6737199 | Jurkat | SE_40114 | chr12:6735427-6736087 | K562 | SE_62049 | chr12:6711664-6754706 | Toledo |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr12 | 6736600 | 6737000 | chr12 | 6737000 | 6737200 | chr12 | 6736052 | 6736200 |
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| Number: 1 | ID | Chromosome | Start | End |
GH12I006626 | chr12 | 6735440 | 6737714 |
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Enhancer Sequence | CGCTTGAACC CAGGAGGCAG ACAGAGGTTG CAGTGAGCTA AGATCGCGCC ACTGCACTCC 60 AGCCTGGGCA ACAGAGCAAG ACTCCATCTC AAAAAAAGAA AAAATTTTTT CATAGAAACG 120 GGGTCTGACT GTGTTGCCCA GGCTGGTCTT AAACTCAGGC TCAAGCAATC CTTTTGCCCT 180 GGGCTCTGTA AGTCCTAGGA TTACAGGCAT GAGCCACTGT ACCTGGCCAC AAGTTTTTCT 240 TGTATTTGGT TTTGTTCTCC TTCCAACCAC CACCATCAGC AGTTTGAGAC TTGTAAGAGA 300 TATAGTAAAA CAGTTAAAGG GAATAAAGAA ATACTTCCTC TGCAAAATAC CAGTCTCAAC 360 AATGAAAATA ATACCAAATG AGACTTAAAC ATGCTGAAAA GCAAGTAAAA CCAGGCTCAT 420 TTCTGATACA CTCCCCTGCT CCATGCTCCT TTGCTCCATT CACACCAAAC TAATACTAAT 480 TGTGGACATA CCTTATGTTT TCAGGACTCT GCCTTTGTAT GTGGTGTTTC TTCAACTTGG 540 AATGCCCTGC CTCCCGTTCT CCAACTGGCA AGCCTAGTAT TTTCTCAGGA CTCTGCAAAG 600 CCTTCCCTAA CCGCCCCCGC AACACAAGGC GGATGTGGTA CCCTCACTTG TGCCTCCGCA 660 ACAGTGCGCA GGTTTATCAG AGCTCTCCCC ATGCATGGTA GTCAGCTGTT CCTGGTCTGC 720 CCCTCCCATT AGACTGTGAA CTCTTAGAGG GAGGGGCTGT GGACCATGGC TTATTCATCT 780 TTGTGTATTC TCAGCACCTA CCTCTGTAAA TGTTAAAAAT AATAGGTATC ATTTACTGAT 840 CATCACCATA TTTTAATTTC TATACATAAT ATCTAACATA GATACATTAT TTCACTTCCT 900 CATTGTCCAA CTGAAATGTA TAAAGTGGGT TATTTGAAGT GGGTTATTAA AAATAACCAC 960 TTCCAAAAGT GGTGACATAA ACTCATCTTT CACACATACA CATAAATATG CCTCCTTGAA 1020 TCACTTGAAC CCAAGAGGCG GAGGTTGCAG TGAACGAAGA TCATGCCACT GCACTACAGT 1080 TTGGGCAACA GAGTGAGACT CCGTCTAAAT AAAAATAAGT AAATAGACCG GGAATGGTGG 1140 CTCACGCCTG TAATCCCAGC ACTTTGGGAG GCCGAGGCAG GCGTATCACG AGGCCAGGAG 1200 TTCGAGACCA GCCTGGCCAA CATGGTGAAA CCTCGTCTCT ACTAAAAATA CAAACAATTA 1260 GCCGGGCGAG GTGGCAGGTG CCTGTAATCC CAACTACTCG GGAGGCTGAG GCAGGAGAAT 1320 TGCTTGAACC CAAGGGGCGG AGGTTGCAGT GAGCAGAGAT CGTGCCACTG CACTCCAGCT 1380 TGAGTGACAA AAGCGAAACT CCATCTCAAA AAAATAAATA AACCTCCTTA AAATTCCCCC 1440 TTAAGTGCAT ACGTAAGCAC TTAGTTTGCT GTTTTGAGCC CCTCAATCGT TTTATGTATA 1500 TTTGTTCTAT TTCCCCAACT AGATGGTAAG CTCCTAGGGT GGGAGCGCAC CTTGCAGACA 1560 CATTTCACTC TCTGCATTTA GCAGGTCCTG AGCGATACTC ATTGGCTGCT TAACAGGAAA 1620 TCCACCCTCC CCACCTCCTA CACCCATCCC GCCCCCAACT ACCCCCGCCC ACGCTCTAAT 1680 CCTGTGATAA TAGCTCTTGT ATCAATCTTG TCCAAATGTA TAACTCAGTA AAAGACCACT 1740 TCCCTTAAAA GACCTGTTTG GAAACAGCTT GCAAACAAGA TTTCAATAAC AGTTTACACT 1800 ATGATTACAG TATCACTTGA TCATTCTTTT CTTTTTCTTT TTTCTTTTTT TTTTTGAGAC 1860 AGAGTCTTGC TCTGTCGTCC GGGCTGGAGT GCAGTGGCTC AATCTGGGCT CACTGCAAGC 1920 TCTGCCTCCC GGGTTCACGC CATTCTCCTG CCTCAGCCTC CCGAGTAGCT GGGACTACAG 1980 GCACCTGCCA CCTCACCCGG CTAATTTTTT GTATTTTTAG TAGAGCTGGG GTTTCACTGT 2040 ATTAGCCAGG ATGGTCTCTA TCTCCTGACC TCGTGATCTG CCCGCCTTGG CCTCTCAAAG 2100 AGCTGGGATT ACAGGCGTGA GCCACCGCGC CAGGCCCACT TGATCATTCT TAACCATTAC 2160 TTGGAGAACC AGTAGATCCT TCCAATTAGA AAGCATATAC TAGACACTGA ATGAGTGGAT 2220 GGATGATTTT CAAAGAACCT CAAGTCTGTC TTTCTTTCTT TCCTTCCTTC CTTCCTTCCT 2280 TTTCTTTTTT GAGATGGAGT TTCGCATGCT CTGTCACCCA GGCTGCAGTG AAGTGGCAGA 2340 ATCTCGGCTC ACTGCAACCT CCGCCTCCCG GGTTCAAGTG ATTCTCCTGC TTCAGCCTCC 2400 TGAATAGCTG AGATTACAGG CGCTCACCAC CACGCCCAGC TAATTTCTTT TTTTTTTTTT 2460 TTTTTGAGAT GGAGTTTCAC TTTTGTTGCC CAGACTGGAG TGCAATGGCA CGATCTCCGC 2520 TCACCGCAAC CTCTGCCTCC CAGGTTCAAG CGATTCTCCT GCCTCAGCCT CCTTAGTAGC 2580 TGGGATTACA GGCATGTGCC ACCACGCCCA GCTAATTTTG TATTTTTAGT AGAGATGGGG 2640 TTTCTCCATG TTGGTCAGGC TGGTCTCGAA CTCCCAACCT CAGGTGATCT GCCCGCCTCA 2700 GCCTCCAAAA 2710
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