Tag | Content |
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EnhancerAtlas ID | HS040-19294 | Organism | Homo sapiens | Tissue/cell | Esophagus | Coordinate | chr2:23907410-23908150 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NR2C2 | MA0504.1 | chr2:23908056-23908071 | TGCCCTCTGCCCTGG | - | 6.01 | ZNF263 | MA0528.1 | chr2:23907530-23907551 | CTCTCCTCCTCCTCCTCCTCC | - | 10.75 | ZNF263 | MA0528.1 | chr2:23907533-23907554 | TCCTCCTCCTCCTCCTCCTCC | - | 12.34 | ZNF263 | MA0528.1 | chr2:23907536-23907557 | TCCTCCTCCTCCTCCTCCTCC | - | 12.34 | ZNF263 | MA0528.1 | chr2:23907527-23907548 | CATCTCTCCTCCTCCTCCTCC | - | 7.61 | ZNF263 | MA0528.1 | chr2:23907539-23907560 | TCCTCCTCCTCCTCCTCCCCA | - | 8.68 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TGCCTTCCTT CCAGCTGTGG TCGGGTCTGT TCCTTTGTAG GACGCTTTTG TGTCGCTTTT 60 CTCTTCCCCT CTCTTGCAGG TTCCTGAAGC GTGACTCCCT GTCACAGAGC CAGTAGCCAT 120 CTCTCCTCCT CCTCCTCCTC CTCCTCCCCA GTACCCTCTC ACACACAGCC TCAGAGCAGC 180 CACTGCGCCC AGCACCCGCC CCCACCCACA GCTTTGCTGT CACCAGCTTT GCTGGTCACC 240 AGGGGCCTCT GCCAGCAGTA GACAACACCG TGCCCCACCC CTGAGATCCC AGGTTCTCAG 300 TGGCTCACAA GCTGTCCCTG AGATTAGGGG GGACTGTAGG CTCCATTTTA AGGGATCACT 360 ACACACTGCC CCCACCGGGC CAGAGCAGGA TCCCCAGTGC CATCGTCCCT GCTGTCGGTG 420 GTGACTAATG CCAGGAAAGC GCATCGGCCA GGCTGTCCCT GCTGAGGAGC ACAAGGTGCC 480 CCCGGGGCTG CTTTTCCCCA GCCCAAGTAG GGGAGAAGAG ACTTGTAGCA ATGCCTGGGC 540 CACACTGCAT GTCTGATCCT TGTGCAGTGA GCCTAAACCG GCGCTGTGGA GCATAGACCA 600 GGTGTGTCCT AAACACGGTC TCTCTCAACC CTTGCTCCCT CCCTCCTGCC CTCTGCCCTG 660 GCTATTTCTA CCTGAATGAG TCTTATTGGT GCATGAGCAT CTTTTTTTTT TTCCTCCATT 720 ATGTTGATTT TTTAATTTGT 740
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