Tag | Content |
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EnhancerAtlas ID | HS091-32912 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr22:31974440-31976250 |
Target genes | Number: 11 | 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) |
Zfx | MA0146.2 | chr22:31975544-31975558 | CCCGCCTCGGCCTC | + | 6.01 |
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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 |
GH22I031579 | chr22 | 31975941 | 31976090 |
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Enhancer Sequence | AAGAGCCCTG CATCCTGGCA CGGGTCCGCT TGGCAGCCTT GCTTGGGTAT CCACTCTTGG 60 GGGACCCTGA CCCCTATCAC CTTCATTAAA TGCAGTCAGC TATGGGTGAG TTTTGGTCAT 120 GAAGCCCTCC TTTCATTGTG GGTGTCCTTC TTTTCATTTT GGATTACAGG TGCTAATGTT 180 GTAGGGTCAG AGGGGTATGG AGCTGTAAAG GAACCTCAGA GATTATTTAG TCCTGAGCTT 240 TTTTTACATG GTAAAACCCC TTTTGAGTGG CGGAAGCCTC ACCTATAAAA TAGGTCAAAG 300 TAGCCATGCT GTGGTTGAAG CACGTCAGGG AGTCCGTCCC TGTTCTACCT GCTACTCTTC 360 CCTTCCCTTG CTACACGAGG TGGTCTTCAT ATGTTTTCAG GAGCCTCTGG GGCTCCACAA 420 AGCACAGTAC GAAAACCCCT AATCCAGTCT GATATCTTCA CTTCTGTCTC AGAAAATTGA 480 AGCCTAAGGC ATGGGGAAGT ATGGGCAAAT CAGCTTTGCT TAGCCAATTT GTGAGGCATT 540 ATTATTATTT TTTAGAGATG CGGTCTCACT ATGTTGTCCA GGCTAGATTC AAACTTCTGG 600 GCTCAAGCAA TCCTCCCACC TCAGCCTCCT GAGTAGCTGG GACTATAGGC ATGTGCCACC 660 AGGCCCAGTG TTGAGGCATT AGTATTATTA TCATTACTAT TATTATTAGA GATAGGGTCT 720 CCTCTGTCAC CCAGGCTGGA GTGCAGTGTT AAAATCATAG CTTGCTGCAG CCTTGAACTC 780 CTGGACTCAA GTGATCCTTC CACTTCAGCC TCCCAAGCAG CTGGGACCAC AGGCACATGC 840 CACCATGCCC AACTAATTTT TTAGATTTTT TTTTTTTTTG AGACAGAGTC TCGCTCTGTC 900 ACCCAGCCTG GAGTGCAGTG GTGCTATCTT GGCTCACTGC AAGCTCTGCC TCCGGGGTTC 960 ACGCCATTCT CCTGCCTCAG CCTCCCGAGT AGCTGGGACT ACAGGTGCCT GCCACCACAC 1020 CCAGCTAATT TTTTGTATGT TTAATAGAGA CGGGGTTTCA CCATGTTAGC CAAGATGGTC 1080 TCGATCTCCT GACCTCGTGA TCCGCCCGCC TCGGCCTCCC AAAGTGCTGG GATTACAGGC 1140 GTGAGCCACC ACGCCCGGCC TAATTTTTTA GTTTTTTTAT ACAGACGGAG TCTCCTTCTG 1200 TTGGCCAGGC TGGTCTTGAA CTCCTGTGCT CAAGCAGTCC TCCTGCCTCA GCATCCTAAA 1260 GTGTTGGGAT TACAGGTGTG AGCCACTGCA CCTGGCCTTT TAGGCATTAT TGATGGAGCT 1320 GGATCCAGGT CCATCCTGGC CCAACTCCAA CCCTTCCTTT CACTAAAGAT TCCTTCTTCC 1380 ATTTTAGCAG CACTGCATTT ATAATCATAC AAATGTATGC ACTGAGCCCA CATGGTAAAA 1440 AAACAAAAAC CACCACAGAC AAAAAGTCTG TCTTCTCCTG AGAGGCAACA GTTGATGTTT 1500 ACCTTGGTCT GTAGAATTGT CATGTGGGTC ATGGGGTTCT TTCCTGGTGT GGGTGTGTTT 1560 GTTCTTGTGC AGTATAGATG GACAGCAGGG AGGGTTCAGC AAATATTTAT TAAGTGCCTG 1620 CTGTGCAGGC TGGCTTGTGT TAGGCTCCCA GTTGAATCTC AAAGCAGAGA AACACTCAGG 1680 GAGATGGAAC AGCTACAAGA AGCTGTGACC AAGCTTCTCC CCGCTGATTT GAGGCACTGT 1740 TTGCCTTCCT CTACTCTTAG TTTACAGACT CTACTGATCC CAGTCCTTGT AATCAGTTGT 1800 GTCCTTTCTT 1810
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