Tag | Content |
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EnhancerAtlas ID | HS183-05094 | Organism | Homo sapiens | Tissue/cell | T47D-MTVL | Coordinate | chr5:848770-850490 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr5:849585-849606 | GGAGGAGCAGGGGGAGGAGCG | + | 7.64 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 4 | Chromosome | Start | End |
chr5 | 848919 | 848970 | chr5 | 849832 | 850073 | chr5 | 849958 | 850059 | chr5 | 850098 | 850231 |
| | Number: 1 | ID | Chromosome | Start | End |
GH05I000849 | chr5 | 849704 | 850515 |
| Enhancer Sequence | GTCACCTGGC ATGTCAAGGA AGAACCTGGC CCAGGGCCTG GTCAGCCTGG CACGAGGCGT 60 CCCCGTGAGG CCCAAGGGCC CAGAAGAGGC GTGGCCGCTG GTCAGCCCTG CTCACCCAGC 120 CCTGCACACG TGAGCCCAGC TCACCCAGGC CTGGCCCTGC TCACACAGCC CTGCACACCC 180 AGCCCTGCAC AACTGAGCCC TGTTCGCCTG GCCCTGCTCA CCTGGGCGTG CTCACCTGGG 240 CCTGCACACC CAGCCCTGCA CAGCCAGCCC TGCACAGCCA GCCCTGCACA CCCAGCCCTG 300 CTCACCCGAG CCCAGCTCAC CCATGCCCGG CCCTGCTCAC ATGGCCCTGC TCATCCAGTC 360 TTGCACACAC GGCCCTATAC ACCCGGCCCT TCACACATGG CCCTGCACAC ACAGCCCTGC 420 TCACCCAGAT CTAGAGGAGA TGAGTCCACC CGTCGGCCCT GCACACACAG CCCTGCTTAC 480 CCAGGCCTAG AGAAGATGAG GCTACCCATT GGCCCTGCAT ACACAGCCCT GTGCCAGTCG 540 GGGACCGGGA AGGCTGCCCC CGTGCCCCTT TTGGTTCATC CCTGTTGGAC ACAGGGCAAA 600 TCCCCCACAG AATGTACCGC ACCCCCAGAG GCTCAGTCAG CCCAGCCAAG CACAGTGACC 660 CCAAAACCCT TTACAGCTTG AGGGACAGAG CAGGGCCACA GGAGGGACAT CCCAGGTATA 720 AACACAGCCG GATGCAGCCC CAAAGGCCCT GGAGGAGCCT GGGTTCTTTC ATACCAGAGA 780 CCCCTGAGCA CTGGGAGAGA AGACAGCCTC AGACAGGAGG AGCAGGGGGA GGAGCGAGGG 840 AGCTGCACAA CCTACCCGCT CCCTGTAGAC CCCAGACAGC TCACTCAGGG ACCCTCTCCC 900 CGAGAATAGC TCAGGGAAAC CCCCCTCAGA CTCCCTCAGG GCCCCTCCGG ACTCTCTCGG 960 GGACTCCAGA CTCTCTCGAG GACCCCAGAC TCACTCAGGG ACCCTGGGCC TCTTTCTTGG 1020 GCCCTCTGGG CTCAGAGCCT GGCTGCGGGG GCACTGGGGA GAGGATCCTT GTCCCCTGGA 1080 GCCAGGAGAA GCTGGGCTCC CCGTGCCTGG GACGTCAGCT CCCGCCCTCA GATCCTGGCT 1140 CCCTCCTCCT CTCACCCTGG GACAAACACA GACTCTCCAT GGCAACCAAA TAGAAGGGGT 1200 GGAGTGCGGG GCCCTCCAGT CACCCTGCCT GGCCCCTGGA CCGCCTTCTA GCCAGGAGTT 1260 CAGGGTTGAC AGCCATCTCC GCAGGGCAGC CCAGAGGCCC TCGCAGTGTG GCCTAAGCTT 1320 GGCATGGAAA CGCAGGCTGC CGACCTGCGG GGCATGGCGC TGTTCCTCCT TGGCACCAGG 1380 GGCAAGGAGA AAGGTGCTGG CCATGTGCAA AATGCTGCGC AGGGATTTTA GCGGAAGGCT 1440 GCCAGCAGGG CGGGTCCTGC GCCACGCCAG GGGGCTGCTG TCCCTCCTGA CAGATTCCCT 1500 CTCCGGAGCC CCCTCAGCCA ACGCTGTCCT GTCCTGACCC TAAGCAGGGG CTGCACAGAG 1560 CATGAGTGGC CACTGGGCCC ACCTGCAGGC TCAGGGGACA TAGTCTGGCC CAGGGCAGGT 1620 GACTGGTGCC ACCGGGCAGC CATGGCCCAG ACCCCACAGC CAGGTCCATC GCAAGTTCCT 1680 CCAGGAACCC CTCCCGCTTA GACCATGCCA CGATGAAAAG 1720
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