| Tag | Content |
|---|
EnhancerAtlas ID | HS087-05928 | Organism | Homo sapiens | Tissue/cell | HEK293T | Coordinate | chr13:73425060-73426910 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF4G | MA0484.1 | chr13:73425595-73425610 | TGGACTTTGGACACT | - | 6.18 | | NFYB | MA0502.1 | chr13:73425883-73425898 | CTATGGACCAATCAG | + | 6.7 | | NHLH1 | MA0048.2 | chr13:73425375-73425385 | CGCAGCTGCG | + | 6.02 | | NHLH1 | MA0048.2 | chr13:73425375-73425385 | CGCAGCTGCG | - | 6.02 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TTTCTTTTCT TTTCAATAAG AGTTATCTAT ACTCCAGCAT TTCTGAAGAA ACTATTTTAT 60
TTCTGGCTTA TCAACTATTT TACTGACAAA TCTCTAATGG TTGACATTTT TAAAATTTTA 120
AATTTGTTGT TAATATTGAT GGCAGCAGCG GCCCATCTGG AGCAGCTGTT GTAAAGATGC 180
CAGCTGCAGT GGGGGAGGCG CGTCCAGGGC TGCATGCTCC ACTGAGCCAG CAGGAGCCGG 240
AAACAGGCAG AAACCCAGAC CCCTTCCGAG TTGGAGGGGC GGGAGCCCTC CCAGGCGCAG 300
CTGCAGTGGC CCAGTCGCAG CTGCGGACCC AGGCATTCCC TCACTATCTT CGGCCTAGGG 360
AGCCCCCTTC CCCCACGGGT TCAGAAATGC CTGTTCCCGC TGCCTGACCT CTCCCTACTC 420
CCAGCACCCA CTCTGATTTC AGAGCAAAGT TGAGGCCAAG CCTGGGCACT GTTGCAGGTG 480
TGCCCGCTCT TGGGGCATTG CTGACACCCC AGCCCCCTGC CACCTCGGCC TCCTCTGGAC 540
TTTGGACACT GACAAGCACG GAAGGGAGGC TGGCCAAAGT GGGGGATGAG GGTGTCTTGG 600
TGCAGGCCTG CAGGTGCCCT TTGGCACTCC AGGCTGGGCG CCAGGTTACA GCTGGTTGAT 660
GGCGGCAGGA GGCAGGCTGG CTTCTGGGCG GAAAGGGGTG GGTCCCTGGT GAAGCCCCAC 720
CCTCAAGCCA GGGATAGCCT GGAGCATGGG AGCTGCGCCA CCAGTTTCAC AGAACGGAGT 780
GAGAACTTAC AGTACTTTTT TCCTCTGGCC CACCCATTGC CACCTATGGA CCAATCAGCA 840
TATACTTCCT CCCCACTGAA GCCCACAAAA ACCCCAGACT CTGGCAGACC TCTGGACGAT 900
CTGCCTGCAG AGAGGAGCTA CCAACTGTGG GTCTCCTCTC AGCTGAGAGC TGAGCAGATG 960
TAGAGACAAC CTGCCTGCAG AGAGAATCTA CCCACTGTGG GTCTCCTCTC AGCCAAGAGC 1020
TGAGCAGACA GTGGGATGGC CTGCCTGCAG TTAGGAGCTA CCCATTCCAG ATCTCTTGAG 1080
AGCTGTACTG CTGCTCAGGG AAGCACCTCT TTGTCTTATT CATGCTCCGG TTGTCTGTGT 1140
ACTTCATTCT TCCTGGACAC AGGATGAGAA CTTGGGACCT GCTTAATGGT GGGACTGAAA 1200
GAGCTGTAAC ACAAAAAGAG CTGAAACATG CCCCTCACTC GCCACATTGC AACAAGGAGA 1260
GAATTGCTGC AGCCCTTTGG GGAGCCCAGA CCTAGGAGCT CCCTGAGCAA GGGCTCTGAC 1320
ACCTGTTTGG GGCTCTGCAG TTCCTGGCAT CTCCAAGCTT CCGGACACCA CTGCATTCCC 1380
CGGTGCCAGC AGTGGAAGCT GCTTTCAGTA TGCCTGTCCA GTCGCAGCCT CACAGGAAGC 1440
CTGGAGCCGC CTACCCCACG GCAGCCGGTG TGCCCTGCTG TGTGCAGTGG TTGAACCCTG 1500
TACTCACTGA CTTGCTCACG CACCCCTTGC TCACACACCC CTTGCTGCTC TGCACTTGGC 1560
TTGCCCTCAG CAGGTGTGAG ATCCCGGCCA GTATAGCTTG AGCCGAGTAC AGCCTGTGAG 1620
GCCGAGTGGG TGGAACAAGC CCAGTGGGCC TGAGCATAAC TCGGGCAAAG GCGCCACTGG 1680
CCACAAAGGT TTCCAGCTGA CAAAGTGACG CCCCAAGGAT CCTGTGACAG CACCACCATG 1740
CAAAAGACTA GATTGAGTAC TGGTACAGCA AATATGACTA CTAAGCATTT CTATCCAATA 1800
TTCAATAGAT AGGTTTATTC AAACTTTATG GCTTTCATGA CTCCCTACTC 1850
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