Tag | Content |
---|
EnhancerAtlas ID | HS105-10086 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr10:69523170-69524560 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HINFP | MA0131.2 | chr10:69523612-69523624 | CCACGTCCGCGG | + | 6.32 | NRF1 | MA0506.1 | chr10:69523394-69523405 | TGCGCATGCGC | - | 6.32 | ZNF263 | MA0528.1 | chr10:69523747-69523768 | GGGGGCGGGCGGGGGGGGGGA | + | 6.33 |
|
| 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 |
GH10I067763 | chr10 | 69522820 | 69525406 |
|
Enhancer Sequence | GTCTCAAGAA AAGTTACACA CCTTATCAAG TGGAGTCACA ACATAGAGGC TTCCAAAGGT 60 CGAGTTGCCT TCCTGCCTTA TTATGAAATG TACCATTATG AGAAGGGCAG TGGGGTTTCC 120 ATGAACACTC CTAGAAACTT CAACTAGTAA AAGGCCTTCT GTTACTTTTC TCAAATTGCC 180 CATCGACAGA AGTTGGCGCT TCTGTGGCGC TACGTGACAA GGGCTGCGCA TGCGCTCTGG 240 GATCAGCCAG GCCCACCCGC GGCACAACCC CAGGCCTCAG TGCCGTCAGG TGGGCTAAGA 300 CAGAACAGAC CTCGGTTCTC AGGGCTTTAA CGAAATAACG CGGGTAAAGC ACCTAGGGCA 360 GAAGCCACAC AGAACACCAG AAGGCATTAA TGGCATTTAA AGGTATTGAA TGCAGACTAA 420 TGCGCAGAAC TTGGTTCTCA GACCACGTCC GCGGCCACCC CTCTCCTGAG AGAGCAGAGA 480 GCACACTTGC AGCCTGACAT CTCCCAGTTG AGCTCGGCAA TGAAGGGATC ACTGGGGATT 540 TAAAAAATGG GAGACGGCTG CTTGGGCAGA AGCCCGAGGG GGCGGGCGGG GGGGGGGAAG 600 GGACGAGCCC ACAGGCAGCA TCCCGACACC TCACACTTCC TGCCTCAATG CACAGAAGAA 660 AGTGTTCTGA AGGCGACGCC CCCAGTCTTG GCGGGAAACG CCGCGGAAGA CGCTTCTCTC 720 GCAGAAATGC CAAATTTTCG GGAGCGCGGG CTCGCAGCAC GTAACAGAAC AGATCTTTTT 780 GTTTCACGGC CCTCTCGTAG ACCTAATAAG CGCGAGGGCG AAAACCAGGT CAGCGACCAG 840 AAGCCAGGCA AGGTTGCGAT TTTCGGAGCA CAGCGAAGGG GAGAGTTTCT AAGTTCTGAA 900 TGTACCTCTA TTTAGGGTGG TTTCTATTAT TTCTTCGCGT CTACCCTGTA GTTGCCGCAC 960 CCTGAGCCCT CAGCCCCGCC GCTTCGCACG GAGCGGAGCT CAGAGGGTGC GCGCTCCGCC 1020 CTTTCGCGGG CCTGGCATGA GCGCAGTGGT TGTTACACTA AAGTGTCTCC GCCTGTCGAA 1080 TATTCTCGTG GCAGCGATGG CCGAGTGGTT AAGGCGTTGG ACTTGAAATC CAATGGGGTC 1140 TCCCCGCGCA GGTTCGAACC CTGCTCGCTG CGGAAGCGGG TGCTCTTATT TTTTCTATTT 1200 TTTTAAATAA ACACCTTCAA ATGAAAACTT TTACTCTTCT CTGTATTTTC AATGCCTGTC 1260 AGCTAAATGG CGCGCCTACG GAGTGGTTTT ATACGCTGTA GAAAAGCGAA TAAATGTCAG 1320 TGCTGCAAAC ATGTACTGTT TACACCAAGA GGAAAATCCT TCCACTGTCC TAAAAGGCAA 1380 GGTAACTCTT 1390
|