Tag | Content |
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EnhancerAtlas ID | HS184-10089 | Organism | Homo sapiens | Tissue/cell | T47D | Coordinate | chr14:65433350-65434240 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr14:65433746-65433767 | CCCTCACCATCTCCCACCTCC | - | 6.1 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| | Number: 1 | ID | Chromosome | Start | End |
GH14I064966 | chr14 | 65433404 | 65434321 |
| Enhancer Sequence | TCTTCACAAC AACCTTTAAG AAAGACTCTG TTACCATCTT CAATTTACAG ATGCAGAAAC 60 GAAGCACAAA GATGTCATCA AAGTGTCTGA AGGTCACAGG GCCAGTAAGG CCATGGGAAA 120 TGTGCATGTT AATCTGGGCT CTTTCCATTC TGCTCATTGC TTCTCACCTT CCCTTCCTTT 180 CTAGGTACCA GGGGAACAGA GTAGGTAGAG ACTGGTCTCA GGCTGCCTGA AGGCTGACAC 240 AGACCCAGCC CTGACCCTCT CACAACGTCA CACTGCATTT GCCCCCAGCT CCTCTCAGTC 300 TAGAAACCTG CAAACCCCAG GATCCTAGTG TCTAAGCACA GGCCCCAGTG TCTGTTAGGT 360 CACCCCATTC CAGGCTTGGA TCTAGCCCCA CCCCCTCCCT CACCATCTCC CACCTCCTCA 420 GTCAAAAGCA AAGTCAAGAC AGGCAGCCAA GCCAGTCCCA GCAGAACTCC TTGAGAAAGG 480 TGACATAGCA GCAGCAACCC AGCCTGAGAA AGTGCCCTGA AGCCACAGCA GCCCAACCTG 540 TCCAACCAGA TCACCCTCCT CCTCACCCAG AAGGAGTGTA GCCTGGAGGG TGGCTTTCAA 600 AACAAAAGGT CCAGGGACTA GGTGACAGGT CTACTCAGGG AAGACTAAGG ATGGGAGGGA 660 GAAAACCAAC TCCTGAGGGA GTGAGGTAGC TCACGCCTAT AATCCCAGCA TTTTGGAAGG 720 CTGAGGCTGG TGGATCACGA GTCCAGGAGT TCGAGACCAG CCTGGTCAAC ATAGTGAAAC 780 CCCATCTCTA CAAAACGTAC AAACATTAGC TGAATGTGGT GGCATGCACC TGTAGTCCCA 840 GCTACTTGAG AGGCTGAGGT GGGAGGATTG CGTTTAGGAG ATCGAGGCTG 890
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