Tag | Content |
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EnhancerAtlas ID | HS113-14383 |
Organism | Homo sapiens |
Tissue/cell | Keratinocyte |
Coordinate | chr16:70642080-70643270 |
Target genes | Number: 12 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr16:70642250-70642265 | TGAACTCCTGACCTC | - | 6.22 | Nr2f6(var.2) | MA0728.1 | chr16:70643200-70643215 | TGAACTCCTGACCTC | - | 6.22 | SP3 | MA0746.2 | chr16:70643132-70643145 | CACCACGCCCACC | + | 6.48 | SP8 | MA0747.1 | chr16:70643133-70643145 | ACCACGCCCACC | + | 6.32 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_29256 | chr16:70641988-70643157 | Fetal_Intestine_Large | SE_54230 | chr16:70642379-70642888 | Spleen |
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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 |
GH16I070608 | chr16 | 70641989 | 70643157 |
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Enhancer Sequence | GAGGGCAGTG GTGTGCTCTC GGCTCACTGC AACCTCTGAC TCCCGGGTTT AAGCCATTCT 60 CCTGCCTTAG CCTCATTTGT AGCTGGGATT ACAGGCATGC ACCACCATGC CCAGCTAATT 120 TTTGTATTTT TAGTAGGGTC AGTGTTTCAC CATGTTGGCA AGGCTGGTCT TGAACTCCTG 180 ACCTCAGCTG ATCCACCCGC CTTGGCCTCC CAAAGTGCTG GGATTATGGC TTGAGCCACC 240 ACGACCGGCC TTGATTTTCA AATATTAAAC TAATTTTTCG TTCCTGAAAT TGCATATGGG 300 ATTAGGAGAT TAGGATACAG GGATCTAGGT GCCCCCAGCA CATGGTGGGT CTGGTTCCCC 360 AGTAAAACCC AGTTTTGGGC CTGGTCATCT GGTAGAGGGA GGGAGGAGGC ACAGATCAAG 420 GGTGGGGAGA GGGCTGACCT CCAGACACTA TAGCCTCTGC CGCCAACTCT GAGCAGCACA 480 GGTGAGTCAG CCCAGGTGAG CCTTAGGCCA AGGCCGTGCA GGCGACTGCT TCCCACAGCA 540 GGTTCAGGTG GGGCAGGCTC TGCTGCCTCT CTCTCTTGCC TGGAGAGGCA CCTGGGGCTC 600 ATCATGGGTT CAGTGTGCAG ACTTGCACCT CAGCCTCACG CCTCAGTCTC TGCATCTGGG 660 AAGCTGGGAA GCAGAGCTGG CCCCAGGGAA AGCTCAGGCA GCGAGGAAGG CGGGGTGTGG 720 GGGCGGGTGT TGCCACTCAG ACCTGGTTCC AATTGTGCTT CCCTTCTCTG TAAAATGGGG 780 GTAATCATGC CTTCCTTCCA TGTGATATGA GCTGATGGTG ACAAGCCACT TAAATACATG 840 AGAGGAAAGC ATAATTCTTT TATTTTTTAT TTTTATTTAT TTTTTAAAAA TTATGTTTAT 900 TTATTATTAT TATTTTTTGA GATGGAATCT TGCTCCGTCG CCCAGGCTGA AGTGCAGTGG 960 TGCGATCTCA GCTCACTGCA ACCTCCGCCT CCCCGGTTCA AGCAATTCTC CCTGCCTCAG 1020 CCTTCCATGT AGCTGGGATT TCAGGTGTGT GCCACCACGC CCACCTAATT TTTGCATATT 1080 TAGTAGAGAC GGGGTTTCGC CATGTTGGCC AGGATGGTCT TGAACTCCTG ACCTCAGGTG 1140 ATCTGCCCGC TTCTGCTTCC CAAAGTGCTG GGATTACAGG TGTGAGCCAC 1190
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