Tag | Content |
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EnhancerAtlas ID | HS098-24181 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr17:43778030-43779500 |
SNPs | Number: 1 | 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 | chr17:43779008-43779029 | TCCTCCACACCCCCTTCCCTC | - | 6.03 | ZNF263 | MA0528.1 | chr17:43778996-43779017 | TTTCCTTCCCTCTCCTCCACA | - | 6.04 | ZNF263 | MA0528.1 | chr17:43779017-43779038 | CCCCCTTCCCTCTCCTCCCCA | - | 7.06 |
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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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Enhancer Sequence | ATCAGCCTGT AAAAAGTTCC CAGCTTTGGC AAAGGTAATT ACCAGCCTAG GTGGCTGGGC 60 CAGGTCGGGA CATGGGGGGA GGTGAAGCTG TCATTTCCAA TTCACCAGCC TCCATTTGCT 120 GTTTGGTCAA GAGGTTCAAA TGAAAAGGTT AATTAAGAAT CAGAGGATTT GCTCATCAGG 180 TTAAGTCATG TATACACAGC ACAAAGGGCA TGTCTATACA TGATAACTGC TTTTAAAGAA 240 ACCAATTCAA TTCAGCATGC ATTTGTTGAC ACACTCACCT CCCCCACCCC CAACACACTT 300 ACAACCTCTC GGGGTTAGGT GTGTGCTAGC CTCTTTGTTT GTTACAGGGG ATATGATAGC 360 CGGTGAGGTA TGGGTACTTG CTTGGGATAT ATGGCTCCCT CTGCAATGGA GATCAGCCCA 420 CAAATGTGGG GGCTCCAGTC AAACTAGCTA CTTGCCTACT GTGTGTCCCT TGGGCAAATA 480 ACTCTCTGTC TTGGAGGAGG TTAGAGTAGA TCTGCAATTC CTAGTCATAA TAGTCTGCGG 540 ATTGGGGAAA AGGAGATGCA ATAGAACCAT TCTGGACAAC TTTTAAAAAT ATACTCCCTA 600 CAGGAATTCT GATAGTTGCC CTTCTCCCAA TTTCATCCAA GTCTCTTGGT ACATGTAGTG 660 GATGCTGTAG AATGTCAACC TGGTCCCTCC TTCAGGATTG AGGTCCTCAC TTCTCCAGTT 720 GCAGCTAGGA GTATTGACAG ATGATGTCTC TCAGCTAGGT CCCTCTCTAG GAATTGCCTC 780 AGCCAAGGAG AGCCAAGTTC ACTTCCTTGG GGCAGCCTGC ATCAAACTGT GGATGTGGGG 840 GTGTAAATAC CCATTCCTTT TGCTTCAGGA CAGGACAACT TAGAAGGCCA TCCTAGCTCC 900 AGAACTCCCG GTAGGCTTGG CTGGGACCCT TCATCCCAGC TCAGTTTCTC TCTCTGCCTA 960 ATCCCATTTC CTTCCCTCTC CTCCACACCC CCTTCCCTCT CCTCCCCACC CCAAGTTGTT 1020 GATGCCAAAA GCAACCTCAA TAAATTTCCT GCATGAAAAT ATCCATTTCA GAGTCTGTTT 1080 CCCAGGAAAC CCAACCCAAG GCAGCACACA CAAAAAATTG AGACTCACCA GATCCAATGA 1140 TCGGCAGGAG CCGTTCATCC ATTCAGCAAA CGAGTGTTTG GCACCTATGT TAACTCTAGC 1200 CCTAGAAGAC GTCCTGGGTG AGGAAAGATT CCAAGTGGGC CTCAAAGAGT GGGCAGAGTG 1260 TGGAAGGAGG AGGAGAGGCA ATGAATTTAG TGGAATCATT GTGTGTTTTG GAGTGCACAC 1320 GTGGAGTGAC CAACTAGATG TCTGAAATTA TCCTGGAGTG CCGAATTACT AATTCCAGCT 1380 CTGGAGTGTC CCTATCTGAC CTTTAGTGGG TGCAGGATTA TTGCCTGTGG AAAATTCTGT 1440 CTTGCTTCTG CCATGTGTTA TGTCCCAATG 1470
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