Tag | Content |
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EnhancerAtlas ID | HS023-06398 |
Organism | Homo sapiens |
Tissue/cell | CD8+ |
Coordinate | chr12:121339510-121341640 |
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) |
ZNF740 | MA0753.2 | chr12:121341532-121341545 | GCGCCCCCCCCCC | + | 6.1 | ZNF740 | MA0753.2 | chr12:121341534-121341547 | GCCCCCCCCCCAC | + | 6.29 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_27043 | chr12:121339452-121340105 | Esophagus | SE_27043 | chr12:121340195-121348599 | Esophagus |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr12 | 121340361 | 121341175 | chr12 | 121339600 | 121340000 |
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Enhancer Sequence | GGGCTAAGCT CCCCGATTTC AAGGAGTTTC TTTGCCTGTA AAGCAAACAG AGCTGACATT 60 GAAGGAAGTA TTTTAGTAGA ATAAATTTGT AAATTGTCAA ACTTCACAAA GTAATCCCTC 120 CTTAATAGAG CCAACTAATG TCAGAGAGAG GTCGTGTGTG TCCAACCTAC CTAGTAAAAC 180 ATTTTCATTT TCCCCATTTC TTGACCACTG AGTTTTCTAT TCTTTCAACC ATCCAGGGCC 240 TCTGTACAGC ACAGTAAAAA CAGCAAAGCA GCCATTAGGA CTCTCAGGGC CACAGCCATT 300 AGGGCCAGAG TATGAGAAGC TCAAGATGAG TAACCACAAG GCATGACAGA AACACCTTTA 360 CCTTCATTTC TTACTCTGTC CAGAAGGAAG CTGAAATTGT AATCTTGTGT TCCCTACGAC 420 CTGCTACTGA AAGGCAGCTG TCACGCAAAA CTATGAAATT AGCTTAAACC TCTTTTTAGA 480 GCACGTGTTC ACCAAGATTT TAATTCTTCC TTTAGGGTTA CTTTGTCTCT CAGTTACCTT 540 CTTCTTGAGA TTGCACATAC ATCAATGAAG TTCTCTTAAG AATTATCATC TTCAATCCCC 600 AACTCCCTTT CTCTTATGTG AAGACTCAAT GAGTTACTGA CTTATAACCT CTAACACTAT 660 AAATAATCCA CTCAAAGTCT TCTACCTAAA ACCATTCCTT ATTTTCTGAT ATTACCCATT 720 TCTTAGATGT TTCTCTAGGA TAATTATAAT TAATGTAGTA AGATCTGTGG CACTTCACAG 780 TTTGCCAAGT GCTTTCTAAA TGTACTCACT TAATCCTTAC AGGCTGTGGA AAAGGTAATT 840 CCCTCTATTT TATAGGTAAG GAAAAAGGAC CGAAGAACTC ACTACCATGT CGTATCAACA 900 AAGCAAGTTG GTGGCAAACC GGACCTCCGA AATAGGTCTT CCAACTCCAC ACGGCATGCT 960 CGTCCCATTC TATTATGCTC TTTTCTAAGA AGGGAATGTC TACAGTTCTG TCCCAAACCA 1020 CATTTGCTTC AAGAGTAAAC CATCTTCAAA CCATTTCTCT AAATTGCAAT CAGGTCCCCC 1080 ACTCCTACGA TCATGCCATT TCTTGCTTCC TCACTCTCCA GCTATGACTT CCTTCTCACT 1140 ACCCGATTTC CACTCTTCAT GGATACTGCC ATCATTCCTT CAACCCGTCC TGCAAATATC 1200 CCACCTCTAC ATGCTAAAGG GAGACCCCTC ATGTTCCTTC CCCCAAACCC TGGCACTCCC 1260 TTCTCCGGAT ATGTAGGTTG TCACCCCATA AACTACACAG TAGCTTCTCG CTTCTCGGCC 1320 CTTAACGAGC TACTTACTAA CTTTAAAAGC CCCACAGAAA TGAACTTAAC TTGCAGGTCC 1380 TCCACCTCCA CACTTGGCCC TGGGCGCCAT TCCTCTGAAA ATAATAGTAC CAACCCTTAC 1440 AAAGACTCTG CCCATGCCCC ACTGTCACCA ACGAATTCCT TTTCCAGAAG GAAAAGGAAA 1500 CAGGTTCTTC AGGCTCCTCT TCCAACCTCT TCACCAGTGA CTCCCCTCCA AGGTTCGTGG 1560 ACTCTACCCC CGCAGTTTTC CTCCCCTCAC TCCCGGGCCT CTGCCCACCT CACCAACTCT 1620 CCCTGCGCTC CCTGTCCCAG AGCCAAGCGG CGGCCGCTCC ACTCTCCCAA CTTAGAAGTT 1680 CTGCCTCTAT CACCTGTTCT CACTAGAGCT TCCTCTCAGC CCAGCGGCCC ACCTTTGCCC 1740 TGGCCTGCCT CTCTCCACCC CTTCGAGTCC TCCTGCCCAG GAAACACCCC CACGAGTCAG 1800 TTCCGGGGTG CCTGTCGGAT TCAACTTCCC ATCCGTGGGA TTCCCACCCC CGGGGTCATG 1860 CTCCCCTTCT CCATCACCTG CTCCGCCCAT AGCCAGATGA CATCCGCCGC TGCCTCCTCC 1920 TCCATTCCCC TTCTCGGACG CCAGGTCCCC GGCCACTCAC CGCCCTCCGT GCGCGCCAGC 1980 CGCCCCCTCC GGTGGGGAAG AGGGGGGCGT GCACCCCAAC CCGCGCCCCC CCCCCACGAC 2040 ACGCACCTGT TCTTCCTCCT CTTCCCCTCG GCGGGCCGCG CCGGCGCCCC GACCCCCACC 2100 CTTGCCGCCT CCCGGCCTCC CGGAGCCCCG 2130
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