Tag | Content |
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EnhancerAtlas ID | HS105-23017 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr13:102050120-102051360 |
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) |
FOXC1 | MA0032.2 | chr13:102050141-102050152 | ATATTTACATA | - | 6.62 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr13 | 102050160 | 102050487 | chr13 | 102050613 | 102050878 | chr13 | 102050913 | 102051095 |
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| Number: 1 | ID | Chromosome | Start | End |
GH13I101397 | chr13 | 102049721 | 102052168 |
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Enhancer Sequence | CAGTTATTTA TAGATAACTT TATATTTACA TACAAATATA AAACAGGCTA AGTGGAAAGA 60 GAAGAGAGGT ACATTCTGTC TGTGGTGGAA ATAAGCCTTT CAGAGGAGGA TGCCAGAGGT 120 GACATCTCAT CCAGTCCTAA TGGATGAGGA GGATTTGACT CATCAGAGGA GCTGGGAAAG 180 GGTCACTGGG GCCAGGGAGC AGTACGAGCA GGGAAAGCAA TGTGAACAAT CCAGAGAGCC 240 TAGAGGAGTA GGAGGCTGCT GATGGGGCTC AAGTGGACAG TGTGCTGACA CAGGAAAGGA 300 GCAGTTGCTG GACAGGTTAG GTCCTGAATG AAAAGAAGCA GGAATGTCAC ACTAACGTAT 360 TTTAATTTGC AATGAAGGTA ATAGGGATGC TTCCATGATT ATAAAGCAGA AGCGTGATGT 420 GAATAAAAAT AGAAATATAG AAAGAAATGT GAGCAGGCAG GGAAAGTAAC CTGGAGGGCA 480 GATTAGAGGA AGAGAGACTG GGAAGGACAG CAAAGAGTCC AAGCAGATCA TGTGTGTATC 540 ATGGTTGGGG GAAGGACAAG CACTGCAAGA GGGAACAGGC CATTTCCTTT TGTTACTTCA 600 GCATCAACCA TGAGATGAGT AAGAAGTTGA TCCTGCTTGG TTTTGCAGAG CTGAGATTCC 660 AGCACTCATG GATATGCATG CCTGTCAGGC TTAGTTCTGG TTACTATGCT TTCTGGCACA 720 CAGTCGTGCC TGGCCTAGCA GTTCTTCTCA AATCCTCATC AACTTAATTA GGCGGTGAAG 780 GTGACAAAGT TCTTCAGAGA TACCATCCAT TATCTCATTG ACCTTTTACT CAAATTTTGC 840 AAATCAGAAG GAGACCTTTA ATTCCAAACA TGTGCATATT GTCTCACGGA TTCAGGAACG 900 TTGACAACAA GTAAAGGAGG TTCATTCAGA ACAGGTTGCT CATCTTGGAC CCCAGCTTTG 960 GATCAGCCTA AGAAGTGGTA TCATCTCTAC ACCATGTGAC TCTGAGGACA GGGTGCACAG 1020 CGTGGGGAGG GGAGGGGATC AGACTACCCA GTGCATCTTC CTATGTGAGT AACTCATAGC 1080 GACATCTCAC TATTTCATTG GATTGTTCTC TACTTCCAGA CTCTGAACCT CATCCATATT 1140 CTACTGCAGC TCAGATATTT CGAAGCCAAA GGTACATGAT ATTTGAATTT GTCAATCACA 1200 TTTATCTCAC ATCCACATAT GCTTCTCCAT ACTCAAAGAA 1240
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