Tag | Content |
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EnhancerAtlas ID | HS023-06170 |
Organism | Homo sapiens |
Tissue/cell | CD8+ |
Coordinate | chr12:96633130-96637700 |
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) |
EWSR1-FLI1 | MA0149.1 | chr12:96637050-96637068 | CATTACCTCCTTCCTTCC | - | 6.79 | Nfe2l2 | MA0150.2 | chr12:96636500-96636515 | TGCTGAGTCACTGGG | - | 6.54 | Nr2f6(var.2) | MA0728.1 | chr12:96637284-96637299 | GAGGTCAGGAGTTCA | + | 6.22 | REST | MA0138.2 | chr12:96636486-96636507 | GCAGATGTCCCCGGTGCTGAG | - | 6.39 |
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| Number of super-enhancer constituents: 24 | ID | Coordinate | Tissue/cell |
SE_00497 | chr12:96629631-96637525 | Adipose_Nuclei | SE_10023 | chr12:96634142-96637312 | CD14 | SE_13801 | chr12:96634933-96637221 | CD34_Primary_RO01536 | SE_18022 | chr12:96628675-96638734 | CD4p_CD25-_CD45ROp_Memory | SE_18611 | chr12:96633891-96637257 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19232 | chr12:96634012-96637403 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_25927 | chr12:96626332-96637389 | Duodenum_Smooth_Muscle | SE_26883 | chr12:96633056-96634989 | Esophagus | SE_26883 | chr12:96635064-96636891 | Esophagus | SE_30111 | chr12:96633035-96634612 | Fetal_Muscle | SE_30111 | chr12:96634997-96636656 | Fetal_Muscle | SE_37329 | chr12:96634716-96636973 | HSMMtube | SE_37993 | chr12:96626748-96637313 | HUVEC | SE_41167 | chr12:96633042-96636892 | Left_Ventricle | SE_42845 | chr12:96629756-96636922 | Lung | SE_44155 | chr12:96626477-96637379 | NHDF-Ad | SE_44822 | chr12:96626570-96637232 | NHLF | SE_45717 | chr12:96626406-96637373 | Osteoblasts | SE_49103 | chr12:96633052-96633955 | Right_Atrium | SE_49103 | chr12:96634117-96634976 | Right_Atrium | SE_49103 | chr12:96635140-96636961 | Right_Atrium | SE_54807 | chr12:96626336-96637253 | Stomach_Smooth_Muscle | SE_63930 | chr12:96635115-96635780 | HSMM | SE_64664 | chr12:96635262-96636494 | NHEK |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr12 | 96634891 | 96635110 | chr12 | 96635574 | 96636027 | chr12 | 96636403 | 96636783 |
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| Number: 1 | ID | Chromosome | Start | End |
GH12I096232 | chr12 | 96626732 | 96637366 |
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Enhancer Sequence | AAGTGTTAGC AATGTCGTGT CCCCTGAAGT AGCTACGTGG TATTCCATTG TATGGCTCTC 60 CCAATATTTA ACCTACCCCC AGGTGGTGGA CAGTTGGATA TAACCTCACT GTCCAGGGGG 120 ACCTTGGCTT CTCCATCTCT GCAATGGGAT AACAGTGCCC ATCCTGCAAG GCAGCTGTGT 180 GTGCTCAGCA TGCAGCTGGC CCTCATAAAT GCTGGCTTCT TTCCTTGTCC TTTCTCTGTA 240 CTGGTTCCTT TCACGTAGGG TATCTACCAC GATAAAATGA GTGTGCCCCA AATAAATGCA 300 TTGTCTCGTG TGTCTGCTCA GCACCTGAAC AGGTTCCTGC CTCGGGTCTT GCTGACAAGT 360 GCGCAGGGCC AGCAGCTTCC CGTTGGCCTC TCCCAGGAAC CCTGAGCAGA GGCCTGAGCC 420 CAAGCAGACG CTGCAAGGCT GCTCTTCTCC CTCCCAGTCT GGGCAGCATG GTTTCTGCTC 480 TGAGAAGCCG CCGGGAGCAG TTGAGATGAG CTGGGTGCCT GGTTAGTGTC TGCACCACCT 540 TTCGGGGCCT GACATGTGGC GTCTCGCCTG TAGGCTGCGG CCAGCATCTA AGCGGAGCAC 600 TTGGATCTAG CAGTTATTCA CATCTGCGGC TCCGTGTGTC CCCCTCCTAG AACCTCCCCA 660 CAACCCCCAA ATTAATTGGA TTGTGTAAGG TTTTCGTCAC AGTGGATGTC AAGTGCTGGC 720 CGTGTTAGGC ACAATATAAT ATAAGCCTTG TATCTATTTC TTGTCTGAAC CTAACTAAAT 780 AAAAACATCA TGTTTCCCTG CTCAGTTGAG ATATGTAAAC CAGATGTAAT TCTGCCTGCT 840 GTGCAACTGA TCATGTTACC CAGAACTTTG GACAAAGCTA GCAGAATATG CGCAGCCTTC 900 TGTGAGGGTT AATTTTGTCT ATTAAATTGT CATTAGGGCT GACACAGGGT GATATTTATG 960 TTTTGTTCTG TTTTTGCTTA AATGGGAGTG TAAAAATGAT GATAATACTA ATAGCTAGTA 1020 TATGTTATGG GGCTTGTCAT GCGTGGATGC ATCGGGCGTT CTGATAGAAG CTGTATATGG 1080 ATGTCTCATT CAGTCCCATG AGGCAGATGG ATCAGTCCCC ATTTTATACA TGAGAAGCTG 1140 AGGCATTGAA CTCAGGCAGT GACTCTGGAG CCTCTCCTTT TAATCCCTGC AGCAGTCTTT 1200 GTGATAGGGT CAAGTGGGTA TTTATTGGAA AGGTCCCCTG CTCTGTCCCC CTTACCCAGT 1260 GCAGGGGTTA AGAAGGGCCT GTTTGTTAGG AAAAGTCTTC AGCACAACCG ATCCTGCTTG 1320 CTTACTGAGC TGCTGACATT CTCAGTTTTG AGAACGAGGT AGGAGAGTTG CAGAATCAGA 1380 GGGCAGGAGC GCTGTGTTTC CAGGGTGCCC TGAAATGGCA GAGGATCCAG GGGCCAGACC 1440 AGAATGACGA GGAACTCGCC ACAGGCCTGG CTCCTCGCGG GGAGGAAAAC GGAAGATCAG 1500 ATAACAAGAC TAAGCACGTG AACTCCAGAT GCATAACCTT GGATCAAAAT TGGGGTGCCA 1560 GACCAGAGTG GGTGGACAGA CACATGCAGC AAATATTTGC CACGTAAATG GATGGGTGAA 1620 ATTATGGCTC ATTAAGCTCT CACGGGAGGT GTGAGGTTGT ATGTAGCATG TGGAGTTTGC 1680 ATATGGCCTC TAATATCTGC CTGGGAGTTT TCAGTTTAAA AATGCCAGCA AAGAAGAACA 1740 AGCAGGTATA TGTATGGGAT ACACCCACAG GGAGCTTTAA CCAGCCTAAG AATGAGCCGT 1800 GGAAAATTGT GTCTTTCATG CCTGTGGCTT TATGCCTGGG TCAGTTCTCC TTATAGTTGG 1860 TAATTCATTC AACAAACATT TAATTAACTC ATTTAAATAT AATCCTAATA ACATCATCAA 1920 GAAGGTAAAT CTAATTCCAT ATGCATCTTT TCATTACCTA GCACTGCATA TGCTTTTTTT 1980 AAATTACAAA ACTTATCGAA ATATTTCTCA TCTATCTACT ATTTGAGATT ATTTACACAG 2040 ACTCCTTCCT CTTCAAAGGG CACAGTGGAG CGTTTGTGTG TGTGTGTGTG TGTGTGTGTG 2100 TGTGTGTACA TATGTAAACA CACTGTGGAC AGCCATACCT TTTCTTATAG GTAGGTATGC 2160 CTGTAACCTG TCAGGGTAAC AGACAGCACT GAAATGGAAA TGGAAATATG ACCTGCTCTC 2220 TTGGCATTTT CTATGCAGTT AAAGTGAAAT AATTGAGGGA TCCTGTCACG AGATCCTGTC 2280 ATGGGCTGCT GTCATGGGAT GCCTTGGTCC CCAGAGGTGG CTGGTGAGTT GGGAAGGGTT 2340 CTTCTGCACA GGTCTGCCCG GAATCCTGTC CCAAAGGGAC GACTTGCCCT TTAGGCTACT 2400 ACTGCATTCT CAAAATGGCA ACTTGGACGG GGTGAGGGAT TAATTTTGGT ATCTGGTCCT 2460 CCTCTTTTGC CTGGAACTGC CACTGGGCTC TGTTTGAAGG GGATGTTGCT TTTTCCTCTC 2520 ACTAAAATTG GTCCCATCCT TGCTGCCCGT AACCTCACAT GGAATGCCTG CCGGGCAAAG 2580 AGGCAGCCCT TTTGCAAATA CGTATTTAAT GGGAAATTAC AAAGAGACTG GTCCCACCCA 2640 TGTAAGAGGG AAGCGGATGT GTGTAACACT CTAAAACCAC GCTGGAGATG CACTCAGCTC 2700 CACCCGACAC AGACCAGCAT CGCTCAGGTT ACCAGGCAAC TGTGAGCAAC AAATACTTGT 2760 GAGTCTGGGA TTGAAGGGGG TGGAAACCCG ACTTTTTCTA AATATCCTCA TCACTTACCA 2820 TAATAAGAGC CCTTACCCAA GTGTGCTTGT GTCCCGGGCT GCCTAAGTTG GCCTGAATCT 2880 TGTGTCACCC TTCATAGTAG CCAAGACCTC AGGAGTCAGA TTGCCTGGGT ACCATCTGTT 2940 CTCTCCAGGT ACAAGCTTCC AACAGTGTAT AATTTATACT TTCCGAGCCT CAGCTTGCTT 3000 ATCTCCAAAA TGGGGATAAT AATCATTCCA TTCTCTAAGA GGATTGAGTG AGTTGATGGT 3060 TGACAGGTTC TTAGAAGATA GCCTGACAAA TAATACGTGC TCAGCACATA CTAGCTTGTA 3120 TTATTCCTGA CACTGAGTCT TCTCAGCAAA CTCTTGGAAG GAAACTTCCC TCTGGAAGCC 3180 ACAGAGAGAT CTTCAAACAT ACATGGCGCT GCTTCTGGGG GCAGCCCTGG AAGATAAGGA 3240 AGAAGGGGCT GTCAGTGCAG CTGCAGGGAC ACACGTCCTC TGAGCCCAGG TTGTTCCTAA 3300 TCCTCCAGCC GTGGGCACCG CTGTGGGGGG CTTTCCTTAC CAGCTCCCCT CGTCTAGCAG 3360 ATGTCCCCGG TGCTGAGTCA CTGGGCTGCA CTGCTCTGAC CCACTTACTG TACCCGACCC 3420 TGCCCTCTTC CCTCCCAGTT CCACTCTTTA GCCTTCGACC CTGGCAGGTT TCCAGGTAGC 3480 CAGATCGAAT CCGTCTTTCC CATTGGTCTC TAGAGAAGCA TGACCTGCCT CGGTTCTTTC 3540 CAATGGCTGT CACTTCCTCC TTTTGGCCAG CTAGTAAATT GTCTCCATCC CCGTCACTGC 3600 GTAACCTTTC CCCAGAAAAC TCTTGGTGTC CTCTCTGCTC CCCCAGCAGA GGCAGCAGCT 3660 ACTGAAGGGC CCTTCCCAGT GTCTCCCTTT TTACATTCTG AGTAGGGTTA TGACAGTTGC 3720 TTCTAGCTAT AGAAAGTTCC CACTGTCTTC CACTTAAACA CGTAAAATAC TTAAGATTCT 3780 TATATGTTCT TTTCTTTAAA AACCAGCTTC ATTAAGATAA AATTCACATA CCATACAATT 3840 CACCCATTTA CCATATACAG TTCAGTGGCT CTGAGTATAG AGTTCTGCAC CCATCACCGT 3900 GACCCACTTT AGAACATTTT CATTACCTCC TTCCTTCCAC CCCTCTCAGC CCTAGGTAAC 3960 CATGCTCTAC TTTCTGGTTT TTTGTATAGA TATCATGATT CTGGACATTT CATATAAATG 4020 GAATCATATG TGACCTTTAT CATGTAATAT CTGGCTGCTT TCACTTTGCA GTGAATCATA 4080 GAATAGAATA TTCTATTCTA TGGCTCATGC CTATAATCCC AGCACTTTGG GAGGCTGAGG 4140 CGGGCAGATC ACCTGAGGTC AGGAGTTCAA GACCAGCCTG GCCAACATGG TGAAACCCCG 4200 TCTCTATAAA AATTAGGCAG GGCGTGGTGG CTCACGCCTG TAATCCCAGC ACTTTGGGAG 4260 GCCGAGGCAA GGCAGATCAC GAGGTCAGGA GATCGAGACC ATCCTGACTT ACACGGTGAA 4320 ACCCCATCTC TACTAAAAAA AATTAGCCAG GCATGGTGGC GGGCGCCTGT AGTCCCAGCT 4380 ACTCAGAGGC TGAGGCAGGA GAATGGCGTG AATCAGGGAG GCGGAGCTTG CAGTGAGCCG 4440 AGATCACACC ACTGCACTCT AGCCTGGGCA ACAGAGCGAG ACTCCATCTC AAAAAAAAAA 4500 AAAATTAGCT GGGCATGATG GTGGGTGCCT GTAATTCCAG CTGCTTGGGA GGCTGGGGCA 4560 GAAGAATCGC 4570
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