| Tag | Content |
|---|
EnhancerAtlas ID | HS062-01731 |
Organism | Homo sapiens |
Tissue/cell | GM18486 |
Coordinate | chr10:4891210-4892710 |
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 | TGTGCAGGGA TGTGTAGAAA CCTTCTAGCT TGGCCTCAAG AGAGGACTTT GCTGCGGGTG 60
TCACCAAAAC GAAAAGACAT GACTGGTGCA AGAGCTTCAT GGGAGCCTCG CCCTAGTGGG 120
GGTAGGATTG AGGGTGGGGT GTCATGGTTT GACCAAATTT CCAGGGAGAG TTTAATCAGA 180
AGACTGTTTA CAAAGGACTG AGGAAATGGG AGAGTCTCTT GACCTTCCTA CGATCAGGCC 240
CTGTCCACCA CCATGGACCT TTAATTTTTC CATGTTCGTG ACTCCTTATC ATTCATTAGC 300
TGTGTGACTT TGTGCAAATT ACTTAACCTT TTAAACCTTT AAACTCTTTG TCACTGTCTA 360
CCTAGAGGTG TTAGGATTCA GTGGCATAGT GCCATGCAGC AGGTGACACA GTCATCTGCA 420
TGTAGCACTC TTGTGAACAC ATGCGTGTGT AGGTGTGTGA CTTGTATTTT ATCTCCCACA 480
GAGTCAAAAA TCTAACTGCT ATTTTGTGAA TTTTCCTTGT CACTTATACT TAAACCATTG 540
TTCATTGACC TTAAAAGTAG AGAGTAGAAT GGTGGTTACC AGAGGCTGGG GAGGGCAGGG 600
GTGGATGGCT GATGAGGAGA GGTTGGTCAG CAAGGACACA GTTGCAGTTG GGAGGAATGA 660
GTCTCAGCGC TCCATTGCAC AGTAGCGTGA GTTGGTTAAC AGTAATACGT CAGGTGTCTC 720
ACGATAGCTG GCCAATGAGG ATCCACTACG TTATTTGCAT TTCATGGATT TACTTCCAGC 780
CGGCATGAAA ACTGAGTGAA GCTGGCCACC AGGTGGCGCT GGGAAGCACT TAATGGTCCA 840
GTGCATCTGC GGCTCTTAAC AGGAGATGGC AGCCTTTTAC TGTCTTTGAT TTTAAGACCT 900
CTTCAACTTT GTACAATCAC AGTGAGGAAG GAAACAATGG ATAGCAAAAA TAGGCAAACA 960
CTGGGCAACT GCAAAGCTTA AAAAGTTTCA CAGAAGTTAC GCAGCCTCGT TCTTGAGCAG 1020
TATTTCCCAG TTCCCTTTTC AGATGGTAAT TGATAACCCG GCCCCTCTTG TCTGTTCATT 1080
CTGAGTGGAG CTGACAAGCC CTCCCCTTCT TTGGTTCCCT GCTTTTCTCT AGGGAATGTG 1140
ACTTCTGTGT AAGTTCTTCC CCACTCTGGG GCCTGGAGAC CAAGGTCCAC AGAGGAGGTG 1200
TAAACGTGTG CCCTTAAGGG ACCCTCTGCG TCAAATGATT GTGGGCATCT CTCCTGACTT 1260
TAAGACTGGG AGATACTCAG ATACTCGTTT CAGTAGCTGC TTCTCCTCAT TGGCACTTTC 1320
GTATTTTATT TGAATGGAAA ATCCAAGGAT AAGTGGTAAT CAAAGGCTTA AAAAGCTGGA 1380
AACAGATTCG GGAGGTGTGG ATGGGCATCA AATGGGCATC AAGGAGCAAG AGACCTTGGG 1440
GAGGATGGCA GGGCCTCGCT GACTGATGGC AGTTTATGTT TGATTGTTTT GAGAAACTGC 1500
|
