Tag | Content |
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EnhancerAtlas ID | HS060-12112 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr16:630970-632240 |
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) |
GLI2 | MA0734.2 | chr16:632122-632137 | CTTCGTGGGTGGCCA | - | 6.2 | Nr2f6(var.2) | MA0728.1 | chr16:631982-631997 | TGAACTCCTGACCTC | - | 6.22 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_47572 | chr16:629808-631480 | Pancreas | SE_47572 | chr16:632080-633270 | Pancreas |
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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 | GGGTAAGTGC TGCGTATTGG GCAGCTGGCC CTGGGTAGGT GGAGGGGAAC CACACCTGTG 60 GGCCCTGCAG AAGCAAGGAC AGCATGGGCC ACTGTGCCTC CAGCCTGGAA GCCGTGGTAT 120 GCATGCGCAA GCGGGCAGGG AGGACAGGGC CTCCTAGTCC CAGAGGTCTG CAGGACCAGC 180 TGCCTCCAGG GAGGTGGAGA GAGACTCAGA GACTCACCTG CCGCGCAGGT TCAGAACCCT 240 GGAGACCTGA GGCCACAGGC CTTTGTTCTT CTGCCTTGGG ATTTTCTGGG CTTGGGAGTC 300 TGAACTGCAG GCCAGGGGCC AAGCGCGGCA AAGTCAGAGG CACTAGGAGC CAGCAGGGCG 360 GCCACCATCC AGTAAGTGCC CCGTCCGCTG TGCCGGAAAA CCCCGTCCAC TCAACAGCAC 420 AGCCTGCGCC CGTCCCTCAC TGGGGCTCTT CCCTGCTTGC CGGACACCTG GCTTCTTTCA 480 GTGGAGTCTG CAGGAGGCTT TTTTTTTTTT GAGACGGAGT CTCACTTTGT CGCCCAGGCT 540 GGAGTGCAAT GGCGCAATCT CGGCTCACTG TAATCTCTGC CTCCTGGGTT CAAGCGATTC 600 TCCTGCCTCA GCCTCCCGAG TAGCTAGGAT TACAGGTGTG TGCCACCACG CCCAGCTAAT 660 TTTTTGTATT TTAGTAGAGA TGGGGGTTTC ACCATTTTGG CCACGCTGGT CTCGAACTCC 720 TGACCTCGTG ATCCTCCCAC CTCAGCCTCC CAAAGTGCTG GGATTACAGG CACGAGCCAC 780 CGTGCCCGGC TTTTTTTTTT TTTTTTTTTT GAGATGGAGT CTTGCTCTTT TTGCCCAGGC 840 TGGAGTGCAA TGGTGTGATC TCAGCTCACT GCAACCTTCG CCTCCCTGGT TGAAGCGATT 900 CTCCTGCCTC AGCCTCCCAA GTAGCTGAGA TTACAGGCAC ACGCCATCAC ACCCGGCTAA 960 TTTTTGTATT TTTAGTACGT ATGGGGTTTC ACCATGTTGG CCAGGCTGGT CTTGAACTCC 1020 TGACCTCATG ATCCGCCCAC CTCCCAAAAT GCTGGGATTA CAGGCGTGAG CCACCGTGCC 1080 TGGCTGCAGG AGGCTTTGAT GCCGGCCTGG CAGCCAGCTC CAGGAGTTGG GCGACGGAGG 1140 GGGCGGGGAG AGCTTCGTGG GTGGCCACGG CCAGCAGCAC CCGGGTGCCC CTCAGAGAGG 1200 AAGGTACCTG CAGCCTCTGC TCATGTGTGG GGCCAGCCCC CACGCGTCCC CTCGTCAGCC 1260 GCTTGCTATC 1270
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