Tag | Content |
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EnhancerAtlas ID | HS023-17509 |
Organism | Homo sapiens |
Tissue/cell | CD8+ |
Coordinate | chr22:50319210-50320900 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
REST | MA0138.2 | chr22:50319535-50319556 | GAAGCTGCCCAGGGTGCCGCA | - | 6.05 | ZNF263 | MA0528.1 | chr22:50320479-50320500 | CCCCCCGTCCCCTCATTCTCC | - | 6.06 | ZNF263 | MA0528.1 | chr22:50320489-50320510 | CCTCATTCTCCTCCCTCCCCC | - | 6.17 | ZNF263 | MA0528.1 | chr22:50320243-50320264 | CCTCTTGCCCCTCCCTCCCCC | - | 6.26 | ZNF263 | MA0528.1 | chr22:50320309-50320330 | CCTCTTGCCCCTCCCTCCCCC | - | 6.26 | ZNF263 | MA0528.1 | chr22:50320342-50320363 | CCTCTTGCCCCTCCCTCCCCC | - | 6.26 | ZNF263 | MA0528.1 | chr22:50320363-50320384 | CCTCTTGCCCCTCCCTCCCCC | - | 6.26 | ZNF263 | MA0528.1 | chr22:50320396-50320417 | CCTCTTGCCCCTCCCTCCCCC | - | 6.26 | ZNF263 | MA0528.1 | chr22:50320429-50320450 | CCTCTTGCCCCTCCCTCCCCC | - | 6.26 | ZNF263 | MA0528.1 | chr22:50320462-50320483 | CCTCTTGCCCCTCCCTCCCCC | - | 6.26 | ZNF263 | MA0528.1 | chr22:50320353-50320374 | TCCCTCCCCCCCTCTTGCCCC | - | 6.27 | ZNF263 | MA0528.1 | chr22:50320471-50320492 | CCTCCCTCCCCCCCGTCCCCT | - | 6.53 | ZNF263 | MA0528.1 | chr22:50320497-50320518 | TCCTCCCTCCCCCCCACCCTC | - | 6.56 | ZNF263 | MA0528.1 | chr22:50320359-50320380 | CCCCCCTCTTGCCCCTCCCTC | - | 6.98 |
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| Number of super-enhancer constituents: 15 | ID | Coordinate | Tissue/cell |
SE_10530 | chr22:50318034-50320296 | CD19_Primary | SE_11301 | chr22:50316692-50320874 | CD20 | SE_12420 | chr22:50318500-50320256 | CD3 | SE_17545 | chr22:50317098-50320327 | CD4p_CD25-_CD45RAp_Naive | SE_17909 | chr22:50316945-50320773 | CD4p_CD25-_CD45ROp_Memory | SE_23738 | chr22:50319429-50319982 | Colon_Crypt_2 | SE_24687 | chr22:50319477-50319997 | Colon_Crypt_3 | SE_26808 | chr22:50319426-50320067 | Esophagus | SE_31381 | chr22:50319263-50319902 | Gastric | SE_50117 | chr22:50318781-50320236 | Sigmoid_Colon | SE_52469 | chr22:50318810-50320296 | Small_Intestine | SE_53398 | chr22:50318743-50320264 | Spleen | SE_61206 | chr22:50315437-50364432 | HBL1 | SE_61985 | chr22:50315627-50364432 | Toledo | SE_62450 | chr22:50318672-50364388 | Tonsil |
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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: 1 | ID | Chromosome | Start | End |
GH22I049924 | chr22 | 50318289 | 50320259 |
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Enhancer Sequence | TGGCACGGCT GCCCTCCACA CAGGCTGCCC TCCCCTGGGC CGCAGGGCTT GCACGTAGAC 60 TGGCTGCTTG GTCTGAAATC CACACAGATG GTGGCCTTGA GATGGTGAGA GGGGGATTCC 120 CGGAAGACAG GTGCATGACA TCTCTGTGTG GGCACGCTTG CGCGAGAGGT ACTGGCTTCC 180 TGAGGATGAA GCCCCAGGTT CACAGCTCAA ACGGAAGTTC AGGCGATGAA GGGGGAAGTC 240 TCTGAAGCTC AGACCTCAGC GGGCGATGAG CAGAGGAGCA GACGCAGGAG AAGAGGCAGC 300 TAAAGAGCTG GAAAAGTCAT CCGGGGAAGC TGCCCAGGGT GCCGCAGAGA CAGGGACAGG 360 CAGGAAGTGG TGGAGGGCAA GCGGGTCCCC CACACCTGTT TCCTGGGGCT ACCTTACCAA 420 GAACCAGGAA CTTAGGGCTC CAGCAACAGA AATGTGCCGC TCACAGGAGC CAGAAGTCAG 480 AGGCCCAGAC GCAAGCAGGC TGCTTCCTTG GGAGGCTGGG TGGGCGCGTC TGTTCCGGGC 540 CTCTGTCCTC GCCTGGGGAT GCCACCTGCT CCCCGTGTCT TCACGTGGTC TCCATGCGGG 600 TGTCTGTCTC TGTCCAAACC TCCCCTCTTT GTAAGGACAC CAGTCACTAA TGCCCTCATG 660 TTAACCTGGC CAGTGGTAAA GACCCTATTT CCAAACAAGG TCACAATCAC AGGTACTGGG 720 AGTAAAGACT TCAGCGTGTT TTGGGGGACA TAAATCTGCC CGTGACAGTC CTCACAGAAG 780 TCTAGAATAT AGAGAGTGGG AAAGAAGCAG TGTTCAAGGA GATATTGGCT AAGGGTTTTT 840 CAGAATGAAT AAGGCACGAT TCAGATTCCA GAAGCTGTTT CCTGAGCAGG ACAAATAAAA 900 GCAATTCCAC ATCTAGAAGC ATCGTAGTAA ACAGCAACAG CAAGACAGAA CTGAGGGGTT 960 AGCAGAGACG GACAGGCCAG AAGACAAGGC TGCCTGCTAC CCCCTCGGTC CCCTCTGCCC 1020 TGGGCTGGCC CTGCCTCTTG CCCCTCCCTC CCCCCACCCT CGGTCCCCTC TTGCCCCTCC 1080 CTCCCACCAC CCTGGGTCCC CTCTTGCCCC TCCCTCCCCC CACCCCGGGT CCCCTCTTGC 1140 CCCTCCCTCC CCCCCTCTTG CCCCTCCCTC CCCCCACCCC GGGTCCCCTC TTGCCCCTCC 1200 CTCCCCCCAC CCCGGGTCCC CTCTTGCCCC TCCCTCCCCC CACCCCGGGT CCCCTCTTGC 1260 CCCTCCCTCC CCCCCGTCCC CTCATTCTCC TCCCTCCCCC CCACCCTCGG TCCCCTCTTG 1320 CCCCTCCCTC CCCGTACCAC CCTCAGTCCC CTCTTTCTCC TACCTCCCCC ACCCTCGGTC 1380 CCCTCTTTCT CCTCCCGCCA CAACCATTGT TCAGGCTCCC ATTCTGCCAG GCCGCAAGGA 1440 ACCCCTTGCC GCTCCCAACT CTGCATCCTC CACACCCACG GCAGCGTGGG GGCTCTGAAA 1500 TGCCGTCTGC CTCATCTCTC ATCTGCTTTG TGGGAAACGG GGGTCTCCGA GCTGCCCTTG 1560 GATGGCTGCG TCCGGGGCTT TGAGCCAGGA CTGGACGGGC AGGCCCTGCA CATGCGCTGC 1620 TGTCCTGGGA AAGGCCTCAT CCCCAGGGCC CTTTGTGCTC AGCCTTGACG ACCTATGCTT 1680 GTTTTCTGAC 1690
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