| Tag | Content |
|---|
EnhancerAtlas ID | HS060-26105 | Organism | Homo sapiens | Tissue/cell | GM12891 | Coordinate | chr4:25971740-25972890 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| POU4F2 | MA0683.1 | chr4:25971809-25971825 | GTCATTAAATATGCTT | - | 6.58 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH04I025969 | chr4 | 25971301 | 25973159 |
| Enhancer Sequence | GGATTGTCCT ACATATGCTG CTTTTTATAA CCTGCATTTT TTTTAACCTA CCACTGAACA 60
TTTTTCCGTG TCATTAAATA TGCTTCTACC ATCCTCATTT TGGTGTCAGC CTCGTCTTCC 120
GATGCGGGGC TTCCTGCCTG GCTGAGCTGC CTTCTCAACC CTCCCCTCCC CAGGACACTC 180
AGCTGTGAAA GGCGCTGATT TGCACAGGTG GATCTAATGA GCTCATCTCG CTTCCCCCTA 240
CACATTTCAG TTGATCCGAG GCCCAGGGCT GCCAAGTGGG GCCCGGGCTG TCTGTGGTAG 300
TGGGAGCTTC CCCAACAGCC GTAGACTCTC CGGGGAAATC ACCAGTCAGC TCTCTACAGC 360
TTCCTCATTC CCCACATGCC ATCTGCAGCT CAGGACACCG GAAACTCAAA TCATCAAAAA 420
CCGGAGCTGG AAGCTCCCTT AGGAAGCTGC TCCAGCTCCT CCAGCCCCTC AAAAACCAGG 480
CTGAGAGAGG GGAAGTGGCC CATCCACACT CAGCCAGGGA GTCGGTGGCA ACGCCAAGAC 540
TCAAGTTGTG TGCCTTTAAC CAAGCCCGGT CTCTTCTTGC CACCACCCCA ATGCCTGTCA 600
GGAGCTGGGG TTTTCCTTCT CCACCCATCA GCCCTGCAGG GTGAAGTCTC CATGGCATTC 660
CTGAGCCCCA GGATGAGCCT GCCAACTTAA TAGCCCTAGC CCAAGGCTTG ACCTTGGGGA 720
AGGTAACTGC CCCACCAGCC TCCTCTGGAT CAAGTCCCAG TTTCACATCC CGGGACATGG 780
TGCGGTTAGA ACAGCTGCCT TTCTGACTCT CTGAGGTGGC TGAGTAAACA TTCCCACAAC 840
ATCAGGTCTT CCTGCCACTG GGGCCTATGT TGGTGAAGTG CGCTGGGCTT TGGAGACTGT 900
CACTAGCCGC TGAGACTCTG CTTCAGACCT CCAGGCTCTC AGTCCATGGA GCAGATTCTG 960
GTGGCTGGAG CAAGACCAGG AGTCTGGGAC AGCCCTGCCC TTCCAGTGGG CAGTCACTTG 1020
GAGATGCCCT CAGGGCTAGC CTGGAGCCCA CGTGAGGAGT CTGGTTACCA GGGGAACCTG 1080
AAGGAGACTT TGCCTCCATG GTGATTAAAG GAGTCAGGCC CAGAGTGTGC CTTGGGAAGC 1140
AGTTCTTCCA 1150
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