Tag | Content |
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EnhancerAtlas ID | HS060-14698 | Organism | Homo sapiens | Tissue/cell | GM12891 | Coordinate | chr17:38149500-38151200 | SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
| TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr17:38150312-38150333 | CCCTCCTCCTTTTTCTGCTTT | - | 6.02 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CCACCCATAT GACCTCACTT TACCATAATT ACCTCTTTAA AGGCCCTGTG TCCAAATAGA 60 GTCCCATTCT GAGGTACTGG GGTTTAGGTC TCTAACATGA ACTTGAGGGG GATGCAGTTT 120 AGCCCATAAC ACTAACTCTG ACCCCTCTCA CGAGCATCAG GCCTGCAGAT CCAGCTCCCC 180 CTCCCACTCC CCATGTCTCT CTCTACAGCG TGTCCCAAAG AGATCCCTCC TGGCCCCCTT 240 ACCATTCCTT CCTCCTGCTT TCCCGATCCA GATCAGGGCC TTGGGATCAT CTCTGACTCT 300 CCCCCATCCT CCTTCCCATC ACTTGGTCGT CTGTTGAATT GTCTGCACAT CTTCTGTGTT 360 TGCCTGTTCC TTCATATTGC CAGTGCCATG GTTTGAGCCA CTAACATTCC CAGACACTTC 420 TGCCTGGTCA TCTTCCTCTC CAGCAGCCCA GCTTACATTC ACTTGCCTTA CTAAGCAGAG 480 CTCCAGCTCT GTCCTTCCCT TGCCTGGGAA GCTTCCATTG CTCCCCACTG CTGTAGGGTA 540 TCATAACGGT CTTGTGAGGT AGACAGGCTA GGTATTGTTA TTGTTATTTG GTAGTTTTAG 600 AGATGAGGAA CTAAGGACCC AGTTGCTCAG TGTTTCCTAG CTAGTGAATA GAGACTAGAC 660 ACCAAGTGTT CTACGTGCAG ACTTTATACT GCTCAGCCTG GCACACAAAA TGGCAATGGC 720 ATAGTCCCCA GACTGCGGTC CCAACTGTCT CTTTCCTAAC AGCTCCCCAG GCACCCACAC 780 TTTTCTGCCT CTTTTTCAAT CTGTACCCTT GACCCTCCTC CTTTTTCTGC TTTGTCAGAC 840 TCCTTAAGGC ACTTCATAAA TTAACCATTT CCAGGGATTT CCCCTCACAC ATGAGTTATT 900 CCAGTGGACA GGGCAGCCTC ATGGGTGCCT GTGGAGGGTG AAGGGTCTGC CTGGCCGTAG 960 GTGTGATCAC ACACTCCCGT TGTAACCCCT GTCTCCTGTG ACACTTGCTG CCCCACGATT 1020 TAGCTGCTTT GTGTTCCGTG CCTCCTGTTT GCTGGTGAAC TCCTGAGTTG GGGGGCGTCA 1080 TTCCCTCCAC TGTAGTTCTT CCGCGATGCT GACTCCACCC ACGGTCAGCA CCACTCGGAA 1140 ATACTTCACA GTCCTGTAGA GGAAGACAGG TCCAGGTTTC CAGTTACCCT TCTATGTCTG 1200 GATACTCTGC TCATTCACTG AAGCCAGGCC CCTTCCTGCA CTTATGCCTC TACCCAGATA 1260 ATGAGTTCTA CCCACTGATG ACCTCCTCTC CTCTAGTAAC AGTCCGCCTC CCTAATGAGC 1320 ATCTCTGGCT GACACACGTT CCGTTCTCCA GGCCTGTGAG CCCTGGTCCC TCGCTGTTGC 1380 TGAGCCACAG CACCCGCCCT TCTGGCCTCA CTTTAGAGCA CTGTCATTTC AGAGCAGACT 1440 ACGCGCGGGG TGGCCAGGTG AAATGCAGCT GACGGCTCTG CGACCAAATG TGACCAAAGG 1500 GCCACATTCC CAGCACCCGG CTCCAAAGGC AGAGCTTGGA TTCTATGCCC AGCACAGGTT 1560 TTCAGGGCTT CCTCCTCTCT CTGGGCCTAA ACAGTGATCC CTTTCCCTGT TTCCCACTAC 1620 ATCTGGCAGA ATTTAGGCCA CATTTCATTT TCTTCTTCCG CCCATGGGGC TCCCTGCCCA 1680 CTGTGTTCCC CTGTCACTCT 1700
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