Tag | Content |
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EnhancerAtlas ID | HS074-10245 |
Organism | Homo sapiens |
Tissue/cell | GM19239 |
Coordinate | chr22:43147140-43149300 |
Target genes | Number: 10 | Name | Ensembl ID |
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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) |
Nr2f6(var.2) | MA0728.1 | chr22:43147693-43147708 | TGAACTCCTGACCTT | - | 6.04 | Nr2f6(var.2) | MA0728.1 | chr22:43147839-43147854 | TGAACTCCTGACCTC | - | 6.22 | Zfx | MA0146.2 | chr22:43147440-43147454 | CCCGCCTAGGCCTC | + | 6.24 |
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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 |
GH22I042751 | chr22 | 43147605 | 43149690 |
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Enhancer Sequence | CACTCCGCAG GCTGAGGCAG GAGAATCAGG CAGGGAGGTT GCAGTGAGCC GAGATGGCAG 60 CAGTATAGTC CAGCTTCGGC TCGGCATGAG AGGGAGACCG TGGAAAGAGA GGGAGAGGGA 120 GACCATGGGG AGAGGGAGAC CATGAGGAGA GGGAGAGGGA CAGGGACAGG GACAGGGAGA 180 GGGAGAGCTA CTCCCTGTGT TTGATTCCCC TCCAAGAGCC CTAATTTTCA TCTTTTAATA 240 GAAACGGGGT TTCACCATGT TGGCCAGGCT GGTCTCGAAC TCCTGAACTC AGGTGATCTG 300 CCCGCCTAGG CCTCCCAAAG TGCTGGGATT ACAGGCGCAT GACACCATGC CCAGCTAATT 360 TTTGTATTTT TAGTAGAGTC AGTTTCACCA TGTTGGCCAG GCTGGTCTCG AACCCCTGAC 420 CTCAAGTGAT CCACCCGCCT CGGCTTCCCA AAGTGCTGGG ATTACAGGCG TGAGCCACCG 480 TGCCCGGCTA CGCCCTGCTG ATTTTTGTAT TTTTAACAGA GATGGGGTTT CACCATGTTG 540 GCCGTGCTGG TCTTGAACTC CTGACCTTGT GATCCGCCTG CCTCTGCCTC CCAAAGTGCT 600 GGTATTACAG GCATGAGCCA CCGCGCCTGG CCACGCCTGG CTAATTTCTT TTGTAATTTT 660 AGTAGAGACA TGGTTTCACC ATGTTGGTCA GGCTGGTCTT GAACTCCTGA CCTCAAGTGA 720 TCTGCCCGCC TTGGCCTCCC AAAGTGCTGG GATTACAAGC ATGAACTACT GTGCCTGGCC 780 CCAAGCCCTT CTTCTTAACC CCAGTGGACT GGGACCCGAA GAAGGCCTCC ACGCCCCACG 840 TTTCCTGTTA GGAAACTGTG AGACTTCGTA TCTGCCCATG GAACACCCCC ACCCCAGATG 900 CTGAAACACA GTGCAAGGCC AGGTGACGAG GGGTGGGGGC CTGTCCCAGC CGTGTCCTCA 960 GATGGCCCTG AAACCTAGCC AGTCTGTGGG AGACCTCAGG GTGGGGGGCC GCCCTGCAGG 1020 GCCGCTGCCC CGGGATTGCC TCTGACTTCC TTTCACGCCC CTGTTCAAGC TGCCTTGACC 1080 TGTTATTTGA AATAAAGCAA AACAATCTGG AGCTAGGACG AGTTCCCAAA TCAACTTACA 1140 AGTGGTTCCC CCAGGAAAGC AGGACAAAGG ACCGTGCTGC GCAGGGTGGG GTCAGCCTTT 1200 TGGGAGCTGA GAGAGGACTT AGAATTATCC CTTGAGTCAT GGACACAGGT GACAGGCATC 1260 CCCCACAGCT CTCGGATAGC ACTAACAGGC CACATCTGTG CCTGGGTGCC CATGGGGAGC 1320 AGAAGGAGGG GCGGAAAGGC CAGGGCCAGG CTGGAAGGGG AAGTGAGGAG AGGGGTGGAC 1380 GCCGTGAAGG CTCCCCCAAC CCCGTGGTCC TCCTCCTTGA CATTTCCCAA GCCCCCTCCC 1440 TGCTGTCCAG CTGGGGGGGT CAGCTAAGGC AAGTCCCCAG GAAGTGACCT GGGCAGATCC 1500 TCTGCCGGAC TCCAAAGGCT GGCTCTGGAA AGGGAGCTTC CTGGCATGCG AGGGACCCAT 1560 GGGAAAGAGG TATTGGGGAG AGGGCACCCC GGATCAGCTC AGCCACCTCG TTCAGTGGCA 1620 GCACCTGTCC CGAGAGGCAG ACGAGGCTGT GGACTCCAAC AGGCCTGGTT AGCATCTTTC 1680 AGCTGCTCAT TCTTTGTGAG ACTGTGGGCT GTTCAGAGCC TCAGTTTCCT CGTCTGTAAA 1740 CTAGGAAGAG TAATCATCCT TCCCTCCCAG GCTTGGGGTG ACACACTGGT TACTGGGGGC 1800 TGTGCAGGGA GGGGGTCTCT CCCAATCCCC CTCCAGCTGT GAGGGCTGTG GTTCTGGGAA 1860 CCTGCAGCCT CCTCCTGTCA CCCTCCCAGG ACCCAGGACA AGCTGTCTGT GTCCACTGAG 1920 CTTCGGCCTT AACCAAATTA CTCCAGTTCT GGCAAAGTCC CTCTGCAAAC GCACAAGACC 1980 AGCAGATTAA AAATCAGCCA CAGCCCCATG ACGCATGGCT CGGGGGTTCT GGACTGAAGG 2040 GGATTTTTCA GGTTTTTTTT TTCTTTACAT TTTTTTTTTT TTTAAAGACG GGATCTCATT 2100 CTGTCTCACA GACTGGAGTG CAGTGGTGCG ATCTCAGCTC ACTGCAACCT CTGCTTCCCG 2160
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