| Tag | Content |
|---|
EnhancerAtlas ID | HS103-02175 | Organism | Homo sapiens | Tissue/cell | HUES64 | Coordinate | chr1:228858660-228859980 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MAFG | MA0659.1 | chr1:228859942-228859963 | TATTTGCTGAATGAGCAAATC | - | 6.26 | | MAFG | MA0659.1 | chr1:228859942-228859963 | TATTTGCTGAATGAGCAAATC | + | 6.32 | | MAFK | MA0496.2 | chr1:228859943-228859962 | ATTTGCTGAATGAGCAAAT | + | 6.66 | | MAFK | MA0496.2 | chr1:228859943-228859962 | ATTTGCTGAATGAGCAAAT | - | 6.87 | | POU2F2 | MA0507.1 | chr1:228859341-228859354 | TGCATTTGCATAT | + | 7.22 | | POU2F2 | MA0507.1 | chr1:228859203-228859216 | ATATGCAAATGCA | - | 7.22 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CCCGGCCCCG GCCTTCTCTT ATACATGTAA ACTCAAGACC CAATGCTCCA GGTAGATCAT 60
GCTGCGTCTA CCTTAAAGGC ATATTCAAAA CCCAACCTCT TTGCACCACC GCCTCTGCTA 120
CTCCTGGTCC CAGCCCCTCT CCCCATTCCC CTCTCCCTAG TTATCTCTTT CTATCTGGCA 180
GCCTGAGTTA GATGATGCTA CTACTCAGCT CTATTTGATA CCACTCCGAT GAGTGGAGGA 240
ACACCAGTGT TCTTGGTCCT CATGCCAGTT TCGATAAAAT GACATGAACA CTCTTGGAGT 300
GGTTTTAAGG AGTGGAGGGT TTAATAGGCA AGAAAGAAGG AAGACAGAAG GAAGAAGTAC 360
AGAGACAGAG GGAGGGGGCT CCAAAGCCAG GAGAGGAGAC CCCAAGTGGG GTGGAAACCA 420
GCCAGGTATA TACAGAGGCT GGAGGAAGCA GTGTCTGATT TGCATAGGGC TCAGGGTTGG 480
TTTGACCCGG CATGTCATTC ACGCAGCCCC TGAAGAAACT AGCCCTCCTC CCCTAGTCTT 540
TTAATATGCA AATGCAGGGC ACCATGATGT TCTACACACG TGAGGATATG TGGGGGTGGC 600
CATGTTGCCA GGCACATGTG GGGCAAGGGC AAGGAGGCTG TGGGAATTGC CATGTTTGGG 660
TGGACCCAGT TTCTAATGGC CTGCATTTGC ATATCAAAGG TTGCCGTCAG GCTCTAAGAG 720
CTAAGAGCCG GGGCTTTACG AGTGGGGCCT TTACAAAAAA GGTCTTTGGA GCTGCCGTAA 780
AAGAAATGAA AACTTTTCCT TTCTGCCTGA AATAATTTCT TAATAACTCC TACCACATAT 840
TCCAATGGCT CCCAGGCTTC TGCAGAATTT ACACCATCTT TACGTTGACC TACATGTATT 900
TTTGCCTTTT TTCCTTTCTT CTATGGCCTC ACCTCCTGCC TTAGGTTCAC TAGGCTCCTT 960
GCTGCTTCTC CAACACGGAG ACAGTCAATT GCTGTTTTTG CCCTTGATGG TCCATTTGCC 1020
TGGAACGCTG TTTCTTAGAC ATCCACGGGA CTTGCTCTCT TACATCTTTC AAAGTCTTTG 1080
CTCAAATATG GCCTGCATGA GGCCTTCCAT GTGCACCTTC CTGCCTGTTT TTTTTCGTCT 1140
CTGTGACAGT CATCCTGGAA CATGTTACAT CATTTATTTA TTTTGAGTGT TGCACTGAAA 1200
CATCAGCTTC GTGGAGTGTC TGTGTGCTCA CTGACGTATC CCCAACTACT CTCGGCCTCA 1260
CATGTAGTGG GTGCTTAATA AATATTTGCT GAATGAGCAA ATCAATGCAA ATCCTGCTAC 1320
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