Tag | Content |
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EnhancerAtlas ID | HS103-04975 |
Organism | Homo sapiens |
Tissue/cell | HUES64 |
Coordinate | chr11:132274980-132276450 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
GLI2 | MA0734.2 | chr11:132275683-132275698 | CGCCCACCCACCCCG | + | 6.1 | RREB1 | MA0073.1 | chr11:132276001-132276021 | TGTGTGTGTGTGGTGTGTGT | - | 6.16 |
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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 |
GH11I132405 | chr11 | 132275361 | 132276035 |
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Enhancer Sequence | CAGCTTCTGA CTCCTGGGCT CAAGTGATCC TCCTGCCTCA ACCTTCTGAG TAGTCAGGAA 60 CACAGGGGTG TTAGTTTTTA ATTTTTTGTA GAGATGGGGT CTCACTATGT TGCCTAGACT 120 GGTCTTGAAC TCCTGGCCCC GAGCAATCCT CCTGCCTTAG CCTCCCAAAT AGCTGGAATT 180 ACAAGTGTAA GCCATGCCAC CCGGCTTCAT TCCATTTTTT AAACAATTAT ATCTCCCCAT 240 TGAGAATGTG AAAAATGAGA TATGTGGCAG GGCTAGGGAA ACAAAGGGTT AAGTACCTTC 300 TTCTTCAACA GTGTGCTCTG GGGATGAGAA GAACCCTGGT CAATAAACAG ATATATTGAC 360 TTGTTATTAT TTAAAGTTGT TTAACCAGGT AGAGATAAAC GAAAGCTTTC AGCAGCTGAA 420 CTATCACACA AATCACAATT AAGGTGGCAT ATGTGTTTGG AAGACGTAAA ATCAATTCCC 480 GTGAAGATAA TGTTTTAGTC TCTATTTGAA CTTGAAAACA GAAGTAAATT TTCAGTAGCA 540 ACAGCTGGTC TTGTTCCATC CAGGAGGCTC TCTATTAACT GTATAAGAAG GGCCTTTATT 600 ACCTCTTCTA ATGGTTTTCC TCTATGGTTT TGTCTTCATC AAAAAGGCCC AGTTGATTGT 660 TGTGTTGCTG TTTACTGATG TGGCACAGAG GACGGCAGCT GGGCGCCCAC CCACCCCGGT 720 GTTGGGCCCT CCCTCCCCTG AGTGCTGTTT ATTGTTTATG GAGGGAGAAC AATGGATCCT 780 GGGAACAACT GGTCAGGCTG GGTAGGGGAG GGAGGGGAAC TTGCCCTCTT TCTCAGCTTT 840 GCTCCTCCAG GTAGCCTTCC CTGAGCTGCA CTGGTGGGGA GGTGTGTGTT TAGGCAAAGG 900 AGGGCATTTG AGCAAAGTAG TCTTTGTGAT GTAATCACCC CCCCCAAGTT TCCAGCAGTG 960 GGAGTGACCT CTAAAGACTA CTCACCATTT CAGGTTTTAG TCATGCAAAT TTGTGCGTGT 1020 GTGTGTGTGT GTGGTGTGTG TCACACGTGT GTGTTGTCCT TCCAATTCTA TCCTATACTC 1080 CCAGAGGCAG GGACCACATT TTATGCCACT CCATTCTTTA CCAGGCTGAG TGTGGTGCTG 1140 GCACAAAGCA GATGCTCAGG GAAAGGAGGC TGTGGCACTG GGAATCCACT GGATATAAGC 1200 CACCTCCTGG TTGAGTTAGT CGTGCAGTCT CTCTCTCTTT CTTTCTTTCT TTCTCTCTTT 1260 CTCTCTTTCT CTCTCTCTGT CTCTCTTTCT TTCTCTCTCT CTCTCTCTTT CTTTCTTTCT 1320 TTCTGACAGA GTTTTGCTGT CACCCAGCTT GGAGTGCAGT AGTGCAATCT CGGCTCACTG 1380 CAACCTCCGC CTCCTGGGTT CAAGTGATTC TCCAGCCTCA GCCTCCCGAG TAGCTGGGAC 1440 TACTGCAGGT GCCTGCCACC ATTCCTGGCT 1470
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