Tag | Content |
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EnhancerAtlas ID | HS060-37323 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chrX:152156140-152157360 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chrX:152156764-152156785 | CCCTTCCTCTCCCCCTCCCCA | - | 6.73 |
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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 |
GH0XI152988 | chrX | 152156945 | 152158488 |
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Enhancer Sequence | GGCAGCCACC CATTCCCAGC ATTGGCTCTG AGGCTGCTTT GGGGGAGCCT GGCTATCATC 60 TGAGCCATGG GGATGGCCGG AGGCTCTGTG CTCCAGAACA GCCGGAGGAA GTGTGTGGAC 120 ACAGACTGAG TGAGCCCCGG GAGACCCTCG CCACGTCCAA GTCAATGATC CCGTCCCCTC 180 CCCACACATG TGCAGGGAGG GGCCTATCAC TTGTCCCAGT TCTGTCGCCC ACAGACTCTG 240 GGCTAGTTAA ATGGCTGATC GAGGACTACC CTCCATTTGT GGCGAGCTCC CTGGCCTGTT 300 GGGAGAGAGA GCCAGTCCCA GGAGGGCTCA GGAGGGCGGG TTCCAGGATC CTCAGGCCCC 360 CACCAAGAAC TGCCCCTCTG GCCACAGTGC TGAAGGAGGG GTGTCTGGAT TAGCAGCGCC 420 GTCCATCCTG AGGGAGCCCT CCTCAGGCAG CATCCAGGGC TCAGAGGGCC TCGGGGATGC 480 AGGACAGAAA GGGGTCACTC CCCAGGGCCA TCTAGGCTTC CTGCTCATGG CCCACTGCCT 540 GCTCCCAGGA CACAGGAGTA GAGCGCCTCC CAGTACACTG GGAAGGGAGC AGGACAGGAC 600 CCAGGATGAA GTGCAGCTCC CCCGCCCTTC CTCTCCCCCT CCCCAAGACA TGAGCACTTG 660 GGATCCCTTT CTCGCCCACA CTCTGTCCCC TTGGCCATCA CACACACACT GTCCCCAAAC 720 ATCCCTCAGT GGCTAGGCCA AGGCTGGCCA CCTGCGGGCT GATCTGGGAG GATGGGCACA 780 CACCAGCCCC TACCCCACCC CGAGTCCTGC ACACAGCTCT TCACAGGGCC TCTGACTGCC 840 TGTCCAGGCC CTCCTGGGGC TCTTCTCTGA CCTCGGTTGC TGGCCTTGGT TGCACACGTG 900 GCCTCTCTGA CCCTTCCGGA AGCCTTGAGC CACACCCCTA CAGTGCTGCC AGGGATCAGG 960 GGCCTGGGAC CCACCTGCTG CCCCTTGCCC AGCCTTCAAT GTCCAAGTCA CTTATTCCTG 1020 AGGACACCTG GAGTGCCTTT GGTACCCAGC CAGTCACTGC TCATGACCAC CAGCATCCTG 1080 TTGCCAGGCT CCATGCAGCC CAAGGCACCC CACAGGCCCT CATAGACCCT GCCCCACACA 1140 CACCTCGATG TCAGCCTGGC CACTGTGGCC CCATCCCCAG CAGACCACCT CCCACCCCAG 1200 TTTCACACAG CAGAGGCAAG 1220
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