| Tag | Content |
|---|
EnhancerAtlas ID | HS098-05977 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr10:4891710-4893030 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr10:4892012-4892031 | TGGCCACCAGGTGGCGCTG | + | 9.86 | | NFAT5 | MA0606.1 | chr10:4892542-4892552 | AATGGAAAAT | - | 6.02 | | NFATC1 | MA0624.1 | chr10:4892542-4892552 | AATGGAAAAT | - | 6.02 | | NFATC3 | MA0625.1 | chr10:4892542-4892552 | AATGGAAAAT | - | 6.02 |
|
| | 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 |
| GH10I004847 | chr10 | 4889313 | 4893281 |
|
Enhancer Sequence | ATTTTGTGAA TTTTCCTTGT CACTTATACT TAAACCATTG TTCATTGACC TTAAAAGTAG 60
AGAGTAGAAT GGTGGTTACC AGAGGCTGGG GAGGGCAGGG GTGGATGGCT GATGAGGAGA 120
GGTTGGTCAG CAAGGACACA GTTGCAGTTG GGAGGAATGA GTCTCAGCGC TCCATTGCAC 180
AGTAGCGTGA GTTGGTTAAC AGTAATACGT CAGGTGTCTC ACGATAGCTG GCCAATGAGG 240
ATCCACTACG TTATTTGCAT TTCATGGATT TACTTCCAGC CGGCATGAAA ACTGAGTGAA 300
GCTGGCCACC AGGTGGCGCT GGGAAGCACT TAATGGTCCA GTGCATCTGC GGCTCTTAAC 360
AGGAGATGGC AGCCTTTTAC TGTCTTTGAT TTTAAGACCT CTTCAACTTT GTACAATCAC 420
AGTGAGGAAG GAAACAATGG ATAGCAAAAA TAGGCAAACA CTGGGCAACT GCAAAGCTTA 480
AAAAGTTTCA CAGAAGTTAC GCAGCCTCGT TCTTGAGCAG TATTTCCCAG TTCCCTTTTC 540
AGATGGTAAT TGATAACCCG GCCCCTCTTG TCTGTTCATT CTGAGTGGAG CTGACAAGCC 600
CTCCCCTTCT TTGGTTCCCT GCTTTTCTCT AGGGAATGTG ACTTCTGTGT AAGTTCTTCC 660
CCACTCTGGG GCCTGGAGAC CAAGGTCCAC AGAGGAGGTG TAAACGTGTG CCCTTAAGGG 720
ACCCTCTGCG TCAAATGATT GTGGGCATCT CTCCTGACTT TAAGACTGGG AGATACTCAG 780
ATACTCGTTT CAGTAGCTGC TTCTCCTCAT TGGCACTTTC GTATTTTATT TGAATGGAAA 840
ATCCAAGGAT AAGTGGTAAT CAAAGGCTTA AAAAGCTGGA AACAGATTCG GGAGGTGTGG 900
ATGGGCATCA AATGGGCATC AAGGAGCAAG AGACCTTGGG GAGGATGGCA GGGCCTCGCT 960
GACTGATGGC AGTTTATGTT TGATTGTTTT GAGAAACTGC CAACTGTTTC CCAAAGTGCA 1020
CAGGCTTACA GTCGCATCAG CAATGTGCGA GGTTCCGGTT TCTCCACACC CTCGCCAGCA 1080
TTAGTTTTGG TCTGCCCCTG TTGTTGTTAC AGCTGTTTTA GTGGGTGTTC AATGGTGTCT 1140
CATTGTGGAT TTCATTACAA TTCCTTACTG CCTAATGATC TGAGCATCTT TTCATGTGCT 1200
TATTGGCCAT TTGTATGTCT TTGGTGAAAT CCCCCATGGC ATTCCTATGA GTTCACTGTG 1260
GGTGCCGCAG GGTGACTATG TGCACAATCT TGGAACTGTG CATTTAGACA CTATTTATTA 1320
|
