Tag | Content |
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EnhancerAtlas ID | HS102-06442 |
Organism | Homo sapiens |
Tissue/cell | HuCCT1 |
Coordinate | chr12:121340220-121341640 |
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: 1 | ID | Coordinate | Tissue/cell |
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: 1 | Chromosome | Start | End |
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Enhancer Sequence | ATTACCCATT TCTTAGATGT TTCTCTAGGA TAATTATAAT TAATGTAGTA AGATCTGTGG 60 CACTTCACAG TTTGCCAAGT GCTTTCTAAA TGTACTCACT TAATCCTTAC AGGCTGTGGA 120 AAAGGTAATT CCCTCTATTT TATAGGTAAG GAAAAAGGAC CGAAGAACTC ACTACCATGT 180 CGTATCAACA AAGCAAGTTG GTGGCAAACC GGACCTCCGA AATAGGTCTT CCAACTCCAC 240 ACGGCATGCT CGTCCCATTC TATTATGCTC TTTTCTAAGA AGGGAATGTC TACAGTTCTG 300 TCCCAAACCA CATTTGCTTC AAGAGTAAAC CATCTTCAAA CCATTTCTCT AAATTGCAAT 360 CAGGTCCCCC ACTCCTACGA TCATGCCATT TCTTGCTTCC TCACTCTCCA GCTATGACTT 420 CCTTCTCACT ACCCGATTTC CACTCTTCAT GGATACTGCC ATCATTCCTT CAACCCGTCC 480 TGCAAATATC CCACCTCTAC ATGCTAAAGG GAGACCCCTC ATGTTCCTTC CCCCAAACCC 540 TGGCACTCCC TTCTCCGGAT ATGTAGGTTG TCACCCCATA AACTACACAG TAGCTTCTCG 600 CTTCTCGGCC CTTAACGAGC TACTTACTAA CTTTAAAAGC CCCACAGAAA TGAACTTAAC 660 TTGCAGGTCC TCCACCTCCA CACTTGGCCC TGGGCGCCAT TCCTCTGAAA ATAATAGTAC 720 CAACCCTTAC AAAGACTCTG CCCATGCCCC ACTGTCACCA ACGAATTCCT TTTCCAGAAG 780 GAAAAGGAAA CAGGTTCTTC AGGCTCCTCT TCCAACCTCT TCACCAGTGA CTCCCCTCCA 840 AGGTTCGTGG ACTCTACCCC CGCAGTTTTC CTCCCCTCAC TCCCGGGCCT CTGCCCACCT 900 CACCAACTCT CCCTGCGCTC CCTGTCCCAG AGCCAAGCGG CGGCCGCTCC ACTCTCCCAA 960 CTTAGAAGTT CTGCCTCTAT CACCTGTTCT CACTAGAGCT TCCTCTCAGC CCAGCGGCCC 1020 ACCTTTGCCC TGGCCTGCCT CTCTCCACCC CTTCGAGTCC TCCTGCCCAG GAAACACCCC 1080 CACGAGTCAG TTCCGGGGTG CCTGTCGGAT TCAACTTCCC ATCCGTGGGA TTCCCACCCC 1140 CGGGGTCATG CTCCCCTTCT CCATCACCTG CTCCGCCCAT AGCCAGATGA CATCCGCCGC 1200 TGCCTCCTCC TCCATTCCCC TTCTCGGACG CCAGGTCCCC GGCCACTCAC CGCCCTCCGT 1260 GCGCGCCAGC CGCCCCCTCC GGTGGGGAAG AGGGGGGCGT GCACCCCAAC CCGCGCCCCC 1320 CCCCCACGAC ACGCACCTGT TCTTCCTCCT CTTCCCCTCG GCGGGCCGCG CCGGCGCCCC 1380 GACCCCCACC CTTGCCGCCT CCCGGCCTCC CGGAGCCCCG 1420
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