Tag | Content |
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EnhancerAtlas ID | HS184-27035 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr6:152084470-152085820 |
SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr6:152085460-152085481 | GGAAGAAGAAGGAGAGGGGAG | + | 6.09 | ZNF263 | MA0528.1 | chr6:152085461-152085482 | GAAGAAGAAGGAGAGGGGAGA | + | 6.22 |
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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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| Number: 1 | ID | Chromosome | Start | End |
GH06I151763 | chr6 | 152084325 | 152086286 |
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Enhancer Sequence | CACTTTGCTG CATTCTTGTG TGCATTCTTT TCTCCCACGT TGGAAAGAAA TATGCATATT 60 GAGCGATTCC AACCCCCAAA GGCAAAAATT ACTAGCCAGT GTTGAAAATG AAAGCAAGGA 120 ATTTTTTGGT TATTGTTGCT GTAACTTTTT GATGTGCGTA CATATGTGCG TCTTTTTTTT 180 CCCCCTAGGG GTGGAATGGG GTGGTGTTAG TCAGGGATTA CTGACAGGAC GGTGTTGCCT 240 ACTGTGTTGG AGAGACTAAG ACTGGGGAAA GATTCTCCAA GGCTGGGAAA TGCAGACGTC 300 CAGTCTTGGA AAACAGTTTG TCGTTGGTCG TTATGTCAGA AGAGGAGTGT ATTCCTGGAA 360 GAAGGCCCAC AAAATATACC CAGAGCCCAG GTGCCTTTCT AAGACGAATC AACATTCACT 420 CACAAGTTCA GCTAATATAT GACAGAAATA CAAGAATGAA CAAGACTCCT GACTTAAGCT 480 TACAGCTGAT GGGAAACTTG GGAACTGGAC AGAGAATTAA AATACAACGT GGTTAGGTAC 540 AACTTACCTG CGCCAGAGGA GTGACGGAAG GCCTTGGACG GGGAGTGATG CCTGGAGGAT 600 GACAGGGCGA CAGGTAAGTT AGGGGGCTGG GAAGGGGAAG GGCGGCCCTG TGGGTAAAGG 660 GAAGGAGGTT AAAGTCAGCA GGGAAACAGG CAGTTCCCTG TTGCTGGAGC AAAGCGCGGG 720 GGTGTGGCTC TCCTGTCTCT GGCTTTGCTG TCAACAGGCG AGATTGGCAA GTAGGGCGAC 780 CAACCGGCCT GGTTTGCTCG GGACCGGGGT TTCCTGGAAG GTGGGACTTT CAATGCTAAA 840 ACTGGGACAG TCCTGGGCAA ACAAATCAGT ACGGTTGGCC ACCCTATCTT TGTGTGGGCA 900 TCTGCTAACT GAGTCATGGG CCTGTCTGGT TTATTTATTT ATTTTTTTTC TGCCTGAGTA 960 ACAGAAGAAT GTGTTAAACA TATGGAGTAT GGAAGAAGAA GGAGAGGGGA GATAGGATTT 1020 TTATGTTATA GATTGGAAGA AGACATCCTT GATGAAGGAG ATGTTTTTAC TTTGGAGAAG 1080 GACTGCCTCA GCCGCGAAAG ACCAAGGGGT GGCACCACAG GGAGAAGTCT GCACTGCGCT 1140 TGTCAGGACG GCCAGTGGGG GGCTGCTGAG CGCAGGGAGT CAGTCCTCGC AATGAAGATA 1200 TAGTCTCGGG GAGATAATGC TGGAAATCGA TGGAAGAAGT GGAACAGGAC ACAAATTTAG 1260 TGGAATTTCT TTACAATGTG TGCTTCTTGT CACCAGTTCG TTAACCATGA TAAAAACGGT 1320 TATGTTGTTA CATTCATCAA GATCCAAATT 1350
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