Tag | Content |
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EnhancerAtlas ID | HS105-33799 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr17:32633200-32634630 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr17:32634204-32634225 | GGAGGAGAGAGAGAAAGGGCA | + | 6.25 | ZNF263 | MA0528.1 | chr17:32634201-32634222 | AAAGGAGGAGAGAGAGAAAGG | + | 6.88 |
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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 |
GH17I034306 | chr17 | 32633368 | 32634890 |
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Enhancer Sequence | ATTGATACTC AGAAGACCCT CTGGCACTCA GCAAGGCTTG GGCAGGAGGC GGTGGAAAAT 60 GGTAAATGCT GTATGTCTCT ATGTTGAAGA AGTTCTCAGG CTGTTTTTCC TCCAATTCCC 120 ATAGCATGAA CCTGTAAACT CAAAGAATTG GAGATGTTGG GGCCTCTAAT AGAGCAGTTT 180 CCAGTAGGGA CCAGCAACCA GACAGGAATG CATTGCACAT CTTTGAGCAT TGCATCCTCA 240 GCTCTTTCTT TAGGCTGTGT GTCAGGTAAA TCTGTGCAAA TCATTTTTTC TTCCATGAAA 300 CCCAGCTTAC CTTTTGCACT AGACTGATGG TTTCCAAACT GAGTATGAAT CAGAATCACC 360 AGGACTACCC CTGAAAATGC AGATTTCCTG GCCTTATCCC AAGATTCTGA GTCAGGACAT 420 TGGGTTGTGG AACAGTGCCC CCATCAGGAT TTCAACCAGT TTTCCTGGGG ATACAGAGGT 480 ATAGCTCAGT ATAGCACTGG AACACCAATG CTCTCTGAGG TTCCTTTGTT CTCTCACATT 540 TGAGTTCGGA CCCCACGGCT TTGAACTTGC ATGGCAGTCT TTGGAATGAC CTGCCCAAGT 600 CCTGTGTGGC CTCTCACTTC TTCTCCAGTC CTGGATTGCC ATAAACCAGC TGTGCGACCT 660 GCTGTGACTT CATCTCTCCC TCTTAGTGTC TCTTTCCATT ACTTCTATGA CTTTTGTGAT 720 CTCTGAATAA ATCTGAGATG AAGATGAAGA ATGTAGCCAT TCTCCAGAAC TTGCGATTTG 780 CAGAACATTC TTCTACCTGA CCCTGCTATG TTCCTTGGGA ATCACTTAAG ACAGAGAACA 840 GCTTCCATTG CAGGAGATTT GTTTCTTTTC CAATGCTAAT TGATCCCTGT CTTCTACTAG 900 CTTATGGTCT AGACCATGGT CTCACCATTC ACCACCTCCT AAATTATGAG CACGTTTTTG 960 CATCCGCTTT AGATAATGGC TAACTAGGAA GGAGTTAGAG AAAAGGAGGA GAGAGAGAAA 1020 GGGCAGAATG GCCACCTCCC CAGGGAATGC ATTCTGGCTG CTGGAACAAA CAACTGCAGG 1080 AATTGGGCAG TCTTAAGTTT CATTTTAGTT TTTCACGCTA AGGTTTTTGA AATCCACATT 1140 AAAACCAAAA CCAAAGGAAG GGAAATTGCA AAACACAGGG ACTTTCCAAC TGCAGGCTCT 1200 GAACCATCTG CAGAACATGA GCATGGTGTC TCTGGGTATG TGTCATACCT GGGATCTTTC 1260 TCCTATTCTT TCTGGGGTCC AGAGCATCCT GCACCTCTGG CTGATGTGAA GATCCTGGGG 1320 TCTCTTGCTT CCCTGTTTCC GGGAGACTCT TTTTATTTCC TTATTTACAG CACAGGCATT 1380 CCTGAAGGTC CATCTCTATC ACATGTCTTC ATCTGAATGC ATGAAGACAA 1430
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