Tag | Content |
---|
EnhancerAtlas ID | HS029-05547 | Organism | Homo sapiens | Tissue/cell | CUTLL1 | Coordinate | chr16:23605970-23607440 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6 | MA0677.1 | chr16:23606891-23606905 | TTGGTCAAAGGTCA | + | 6.16 | Zfx | MA0146.2 | chr16:23606052-23606066 | CCCGCCTCGGCCTC | + | 6.01 | Zfx | MA0146.2 | chr16:23606333-23606347 | GAGGCCGAGGCGGG | - | 6.01 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CCTAATTTCT GTATTTTTTG TAGAGACGGG GTTCCACCAT GTTGCCTAGG AGGGTCTCAA 60 ACTCCTGGGC TCAAGCGATT CGCCCGCCTC GGCCTCCCAA AGTGCTGGGA TTACAGGCGT 120 GAGCCACCAC GCCTGGCCAG ACACACTTAT TTTTCACACT AACATGCAGT CAAGGTTGAA 180 ACCACTATTA CCTGAAGTCT ATGACTTTGA AAAGGGGTTT CATAACTTGA CCTTGGGAGT 240 CTATCCTACC TTAAGACGGT TATTTTTATT CCCAACTGCA CTTCAGAGTC ATCTGGAGAA 300 CTTAGAAAAC AACAAAAAAA AGGCAGGGCG CGGTGGTTCA CGCCTGTAAT CCCAGCACTT 360 TGGGAGGCCG AGGCGGGTGG ATTGCGAGGT CGGGAGTTCA AGACCAACCT GGCCAATATG 420 ATGAAACCCC GTCTCCACTA AAAATACAAA ACTTAGCCGG GCATGGTGGC GGGCGCCTGT 480 AGTCCCAAAT ACTCGGGGGG GCTGAGGGAG GAGAATTGCT TGAACCTGAG AGGCGGAGGT 540 TGCCGTTAGC CGGAGGTTGC AGTGAGCTGA GATCACGCCA CTGCATTACA GCCTGGGTGA 600 CAGAGCGAGA CTCTGTCTCA AAAACAACAA CAACAACACC GAAATCACTG CCTCCCGGCG 660 TTTCAGCCTC ACGCAGATTT CATCAGCTCA AGCTATATAC TACAGGTACA GTCGTTCCTT 720 GGTATTTGCG CAGATTGGTT CCAGGACCCC CGACTATACC CAAATCCCCG CACACTCACG 780 TCCCGCAGTC AGCCTTGCAG AATCCGCTTA TAGGAAGAGC CTGCCCTCCT TATACGCGGG 840 GCGGCACATC CCGTAAATAC TGGTCGCGTT TGGTTGAAAA AAAATCCGCA TATAAGTGGA 900 CCCGCGCAAT TCAAATCCTT ATTGGTCAAA GGTCACTTGG CTTGTTTCCT AGAATTACTT 960 CCAGGAGTCC TGGACACAGG CAGAAGGTGC TGCAGGGAAG AGTAAGGACA GAACTGCAGA 1020 GAGAAAACCG CTCTGGAGAA GGCTGTAGGC CAGTGTGGCT GCCTCTTTGC ATGCTGCTTT 1080 CACTACAATA CGGTGACCGC TATTTTGAGA CCGTACGAGG TGCTCTAGCC GCATTAACTC 1140 ATCTAATCCT CATTGCTACT CCGCAAGGTA GAGACCAGGA TCCCAATTTT GCAGGTGAGT 1200 GTGAGCCAGG CTAGGAGACT TGTCCAAAGT TTCGGTAAGC GGCAGCCCAG CAGTGCTGGA 1260 CTCGAGTCAG TGCTCTTGCT CGTTATTACG AGGTCACCCG GCCTCCCGTC AGGGGTCAAC 1320 TAAACACCTT TAGGCAGCGG GGCTGCGGAG CGAGCCGGCT GCCCCCCGGG TCACCCCTGC 1380 CTGCAGCTGG CGCGCCCCGG ATGCCCGGCC CCCACCCCCA CCGGGCCCAA TCCCTGACCC 1440 TTGCCAAGCG GCAGCAAAGT CACCACGAGT 1470
|
| |
|
|
|