Tag | Content |
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EnhancerAtlas ID | HS073-05756 |
Organism | Homo sapiens |
Tissue/cell | GM19238 |
Coordinate | chr17:1245420-1246870 |
Target genes | Number: 16 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Zfx | MA0146.2 | chr17:1246702-1246716 | CCCGCCTCGGCCTC | + | 6.01 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr17 | 1246149 | 1246291 | chr17 | 1245425 | 1246508 |
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| Number: 1 | ID | Chromosome | Start | End |
GH17I001342 | chr17 | 1245487 | 1246153 |
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Enhancer Sequence | ATAAAACAAC ACAGGGCTTG GTTTTCCTGA TCCAGGTTGG ATCTGGGAGC ATTCCCATTT 60 CCTCTCACAG TGCTCACAAA GGCTTCCTTT AATGACACAC TCTAGGATTT CACCAGTTTT 120 CCATGAACTA TTACTTGTTA CAATTTTCAA AAGAACACAG GGGTCACACC TTTATCCCGC 180 TTTTTCAGCA AGCCTCACTC TCCTCTATTG TCCTAGGATC AGGAAGCAGC TAATTTGGGG 240 TCTCATTTAT AAGGCTCAAG GCATTTGTCT GGGACAGAAG CCAATTAATG TCTCCATTTA 300 TCCCACCAGT TTCCCCTTTC AGTGATGGAA GTTCATCCCC ATCTTCCTAT AGGACCGAAA 360 TTTAACTTTG CAGACGTGCT GTTCTGAGGA CCCACCCGGA ACAGAGCATG TACACAAACC 420 CACTTACTGT CGCTTCTAAC ATTGTAGGAA GCCTTTGGGT TTTCCAAGGC AGCAAAGTAC 480 TGAGATTTGT AATTAAAAAC ACATATTAGC TACATTCAAG TTGTAACTAA CTAAAAACTT 540 CTACTTAAGT CGACTGATCC TCAAAGTAAG ACTCAAATCA AAACCAGAAA AGTTTGGGGG 600 CAATTCCCTT TCCAGCCCAC AAATACAGGA ACTGGGAGTG ACACCGTCCT CACAGGGCTA 660 CGGCACCTTT CTGCAGCTTC CCTGGCTCCC TTTCAATTTT TTTTTTTTTT TTTTTTTTTT 720 GAGACGGAGT TCTGCTCTTA TTGCCCAGAT TAGAGTGCAG TGGCGCGATC TTGGCTCACT 780 GCAAGCTCCG CCTTCCAGTT TCCAGCGATT GTCCTGCCTC AGGCCTCCCA AGTCACTGGA 840 TGTTAATTAC ACCCAGCAAG GTCGCCCGCC ACCACGCCTG GCTAATTTTT TTGTATTTTT 900 AGTAGAGACA GGGTTTCCCC ATGTTGTCCA GGCTGGTCTC TTAACTGCTG ACCTCGTGAT 960 CCACCCACCA CGGCCTCCGA AAGTGCTGGG ATTACAGGCG TGAGCCACCG CACCCGGCCT 1020 TTCAATTTTT GATAAGGATC TTTCCTTTTT TTTTTTTTTG AGACAGTCTC ACTCTGTCGC 1080 CCAGGCTGGA GTGCAGTAGC GTGATCTCGG CTCACTGCAA CCTCTGCCTC CCGGGTTCAA 1140 GCGATTCTCC TGCCTCAGCC TCCCGAGTAG CTGGGAGTAC AGGCGTGCGC CACCATGCCT 1200 GGCTAATTTT TTGTACTTTT AGTAGAGACG GAGTTTCACC GTGTTAGCCA GGATGGTCTC 1260 AATCTCCTGA CCTCGTGATC CGCCCGCCTC GGCCTCTCAA ATTGCAGGGA TTACAGGTGT 1320 GAGCCACCGC ACCCAGCCGA GTGGTTTCTT TAAACTCTGC AACAGACTTG ACGAATTCCT 1380 TGGATTTTGA CCTTTAAGTG TAGCAGGTGT GCTGGAAACA GAGCAAATCA ACTTGAAAGC 1440 TTCTTGGAGG 1450
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