| Tag | Content |
|---|
EnhancerAtlas ID | HS062-10388 |
Organism | Homo sapiens |
Tissue/cell | GM18486 |
Coordinate | chr20:57978010-57979510 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| PPARG | MA0066.1 | chr20:57978142-57978162 | CATGGGTCACTGTCACCCAT | - | 6.02 | | PPARG | MA0066.1 | chr20:57978143-57978163 | ATGGGTCACTGTCACCCATT | + | 7.69 |
|
| | 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 |
| GH20I059402 | chr20 | 57977448 | 57982019 |
|
Enhancer Sequence | TAGTTTATTG CTTTTTCCCA CCAGCAGAAA TATCTCCTAC CTTAACCCCT TACAGGGGCT 60
GGGGACCTGC ACGCACTCGC CCTGCAAATC TGAAAACCCG GCGCTCTCCC TCCTGCTCTT 120
TAGAAAAAGG GGCATGGGTC ACTGTCACCC ATTTTCTTAT CACGAGAAGA GAGTGCCTGT 180
GTTATTCTCT CTTTAGCTAG GAGAGCTCTC TGTCTTTGTC ACACGCACCC CCTTTCCATG 240
TCTGAAAAGG GTGTTTGTGT CACTGTCTGG GCCCAATGTC ACTGTCCATT TACTCTGCAC 300
CCTGGGCAGG CAGTGCCTTT CACTAGGAAA GAAGGAAGTT TCTCCCACTG CTCCGTCCCC 360
AGGGTCCTCT CAGGGACCTT CCCCCTGTCC CCGCACCTAG TCCAGGTGGG AACCGGTCTC 420
CCCTTGCAGG GAGGCGCTCT GTCTTCTCCC GGGCCTGGAT ACACAGGTGT CGCAGCAGGA 480
GTTCAATGTA CCCCGTGACG CCCTCGCGGC CAGACGCCCC TGCCCAGAAA GAGGGGACCC 540
TCCACTTCAC TGAACCCAGC CCGTGCCAGG CCCCCGAGGA CACCGGGCCA CAGTCTCCTA 600
GGATGCTCCC AGGCCTGGAG CGGGGCAGGG TATCTCGGTG CCAGGCAAGT TGGTCCCCAA 660
CGAGCCACCC CAGCGGGGGT CCCTCCTCCA GTCCCCTGAA TCCCTTGTCT CTGGGACCAC 720
GTCTCATCTA GGCTCAATCA GGGGCGATGA CAACAACCAT GACTTTGCCC CAGGAACCTG 780
AGTGGGGGGC ACGGGGCCCG AGGAAGAAGG GGCCAGCGGG CTGTTCCCCA CGCTGCACCC 840
CCACTCTGGC GCAGCGAAGT CTGCAGATCT CTGGGCCCCG GCGCTGCCGA AGCCTCCCCC 900
ACGCGCCGCG CTCACTCGCT GCACAACAGC GCCACCACGA GGCCGCGGGC GGAACTGCCG 960
GCAGCACAGC GGTCGCACCC CCCGGGCCCC CCGCCGGCTG TGCGGATCCC GAATCCCTGC 1020
TTGGCTCGGA GCTGCCAGGT CTAAGCCGAC CCTCAGAGAC GCACGCCCCT GACCCACTGG 1080
GCAGCTGTGG TGTCTTTGTA TACAATGTTC CCTTCCTTTC TCCTCTTCTC GTAGATGTTC 1140
AGATTCCAAG GGACTTTTCC AGAAGCTTCC AGAAAACTTT CCTTTTAGGG GCCCAAGAGA 1200
CCTTGATTTC AGGGACACAG TGAACCCCAC TTAGGACCCC AAGAAAAGGG ACTTGTCTCC 1260
AATCTCCTGT CCTAGAATGT GCAGACTTAG GGGGCTCTCC TGTACTCCTG GGTCCCGCAC 1320
ATCTGTCCAG CCCCGCCTCG TTCACCAGAG GCAGCAGAGA CAGGCTGAGC ACACAGACGT 1380
GGGCTCAACT CTCTGCCCAT CCACTCACTG TCTGGGGAAC TTGAACAACT CACGTTGCCT 1440
TTCTGTGCCT CAGTTTCCCC ATCTGGAACT GGTCTAAAAG AACACCCCCC GGTAGAGCTT 1500
|
