Tag | Content |
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EnhancerAtlas ID | HS110-00923 |
Organism | Homo sapiens |
Tissue/cell | KATO3 |
Coordinate | chr12:26392290-26394450 |
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) |
LMX1B | MA0703.2 | chr12:26393315-26393326 | GATTTAATTAA | + | 6.02 | NFYB | MA0502.1 | chr12:26392297-26392312 | ATGTCAGCCAATCAG | + | 6.03 | RARA(var.2) | MA0730.1 | chr12:26392894-26392911 | AGTTCATCTATAGGTCA | + | 6.14 | TFAP4 | MA0691.1 | chr12:26393015-26393025 | AACAGCTGAT | + | 6.02 | ZNF263 | MA0528.1 | chr12:26393459-26393480 | AGAGGAGCAGGAGAAAGAGAG | + | 6.79 | ZNF263 | MA0528.1 | chr12:26393462-26393483 | GGAGCAGGAGAAAGAGAGGGG | + | 7.22 |
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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 |
GH12I026238 | chr12 | 26391098 | 26393585 |
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Enhancer Sequence | GGAGGACATG TCAGCCAATC AGCAGGAAAG ATGCTCATTT CTTGTTGAAA AAGTCCCAAA 60 TTGTAACTTA ACAGGGTGAT CTCTCTCTCA CTCTCTCTCT CTCTTTTTTT TTTTAATTTC 120 CAGAATGTGT TTTTCCCCTA GAGTCCTTGA GCACAGACCT GCGGTTTTCT CTCTCCTGGT 180 TTTACAGTCT ATCTGCCTCA AGCCAAGAGA CTTGGCTCTG CTCCCCCCTG ACTCAGAGTC 240 TCGGCTGGTA GCTGAACCCA GGAAGCCCTG GCCCCACGTC TCTCCCTGGA ACCACCAGAC 300 CACACAGCCT CCTGTGCTCA ACCCTTTGGC TGGGTGTCCT GCCTCCTCTT TGTTTGGAAA 360 GAGATGTCTT ACGTAACTCC ACAACCTTCT AAAGGCTCCA TTGTCTTCCA CTTGGGAGAG 420 CTCAAAACAA CCCATTAGTG ACTTATGACT TATCACAAAG AGAATCTATT GCCCACATAT 480 CCACAGCCCC CATGGAGCTA GCCTCACCTA TCTTACTTAG ATCAATAATC AACAATGAGA 540 CTTAATGACT TGTGGTCTTT GGGAAATTAT AAGTTCAGTA CAAGGTGCAG GAAATACAAA 600 GGCTAGTTCA TCTATAGGTC ACGGTACTTC GCCCAGGCAG CACATGAAAG TCATTTGTAA 660 TTCAAGATTG AGACAGGCAT AAACAATTCT GATCTGATTA TTCTTTTACT AATCTGATTT 720 TGATAAACAG CTGATGAAAA TGGAAGGTGT CTGGTCATCA GAGGAGAGAT ACTCAGGCAG 780 TGAAATAAGT TTTCCTTATC TCACTGGATA GGGATTTATT TCAAGGCTCC TATTAATAGC 840 CCCTAATGCC AAGAACTGTG ATCGCTGCCC TGGACTGCAA GAGCCTTCTG AGCAAAATGA 900 CAGAAACCCA TTGGGTAGGG CATTCTCCTT CATTTTTATT TTCTATAAGT CTCTGATTAG 960 CCCTGTTGGG AATTCTAGTA ATTATTTTAA GCTGGCACCT TTAGGAAAAA AAATATATCT 1020 CTTAGGATTT AATTAAAAAT GAAAAGAACC TCTGCATGAT GTTGCCAAGG AGCTTTCACT 1080 GTTTAAGGTG GGGTGTAGAC CAGGAAGAAT AAAACACTCT GCACTAGGTG ACATTTCCAT 1140 CTGGTTCTGC TGCCAGAGCA GCCCTGGGGA GAGGAGCAGG AGAAAGAGAG GGGACAGCCT 1200 GCTCCAGCCT GCTCTCTCCT CCCCATGGAC CTCATGGTCT TTCAAGGATC CTGCAAGTCC 1260 TTTGCTTCTT TCTTTCTGCA GCAGACATTT TCTCATCTGG GACCAGCTAT GTGACTTGTT 1320 TCAGGTGGAG GCACATTTCT TTCCCTGCTC AGTGACATGT GAGTCCTCGA CAAGCTTTCA 1380 GAAGGGATTC CTGAACTTGG TGAGGCACAG CCCTCTCCAA CTGCCTTGTG GAGCATCCCT 1440 GGGCAGCATG CAGAGGAGAG GTGAGAGGCT GCCTACCCGT GCTGTGGCTG TCCCTCCCAC 1500 CTCCCTTAAA GCCTCCACGT CAGGCGCCAG TCCACCAGGT TCACTGCGTG CATCTTTGGA 1560 CAGCAGTTGC AAAACTGAGA GTTCCAGAAA TTGTGCTACA CTCAGTTTTG TGTATACATG 1620 TGGCTCAGGT CTCATCATCT TCAGCTCATC ACATTTCAAA ATGCTGAGAG TAGAAAGCGT 1680 TTCTCATTCT GGCTTTAAAA GAGAGATTTC CCCAAGGATC ACACCTCTTC AGTCTTTGGG 1740 CCCAAGCTTC TTGAAGGAGC TACTTGCCTA CTTTACAGGG CAAAATTTTA GAACACATAA 1800 TTTGAAAACC CCACCAACTT TAATGTGAAA AAAAAAAAAT CAATTCCTTT TGATTTATTA 1860 TCCCCAGGAG ACAAGGTGAA GTTCAAGTCC ACCTCAGATA AGAAAATGAA ATTGCTTCCG 1920 TTTTATGTGA ATACAATCTG CATCCAAAAT GGGTGGGGCT ACCTATACTG CAAGGACAAG 1980 AACTCAAAAG GCAGTGCTCG AAATGCTCAT GGAAGTGTCA TTACAAATCC ATTTTCTTTT 2040 TCAACACTAA CTGACTAGGA ATAATTTAGA ATAGACATTA GGATGAAAGT CCTAACTATG 2100 AATCTGTAAG AAATGGAAGA AATTACCAAG GGATCTTTGT ATAAGCCCTA TTTCTGCAGT 2160
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