Tag | Content |
---|
EnhancerAtlas ID | HS105-72379 | Organism | Homo sapiens | Tissue/cell | IMR90 | Coordinate | chr7:5671460-5672880 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
PAX5 | MA0014.3 | chr7:5671497-5671509 | AAGGTCACGCTC | - | 6.04 |
| | 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 |
GH07I005632 | chr7 | 5671918 | 5679948 |
| Enhancer Sequence | ACACTTCACT GTCAAGCCCA CTCAGATTCC ATTGTAGAAG GTCACGCTCT GCCCCCACGA 60 GGTCCTGCTG CCTTGTACGG ATTGCTTAGC TCACACCCCC TTCTCCACGC CACGGGAGGC 120 TGGCAAGGAT TTCATAAGAG GACCCTGAGG CTCAGAAGAT GCAGAGAGTG GCTGGACCAC 180 CAAGGTGGGC AGTGTGCTGA GGCCAGGGCA GGAGGTCTGG ACTTGTAGGT TCCAAGGATG 240 GCCGGCAGTT CTCAACTCTG CATGGCTCAG GCTGGGTTGC TGGGCTCACC CTGGACAGCG 300 GTCTATAGAG GTTCACCTGA ACCTATTTGA GATCTGAGTT CCTGTTCATG CCATTTGCCC 360 TGGCCAGTGG GGGCAGGAGG GGCTGCTGGC TGCATCTTTA CTCGCTGCCA CAGATCCATG 420 ACAGACCATG GTGCATCCCC TCGAGGGCTG CAGTCTCTGT GCCTCATCCT TGGTTTCTGG 480 CACAGGCCTT AAGAAGGACC CAGCTGGCCT GAATGAGTTC TGTCTCTGCT CTCCTTCTGG 540 CCCCTCCTAA TCCCAGTGAA AACTTTCAAA TGAATTCTCA GCACAGCTCC TTTCTGATGA 600 GCAAGGCCAG GCTGAGGTGA GAGGGAGTGG ATGCTGATCA GCGACCAAGG TGTCCCTGGA 660 TCAGCAAGGG CTCAAAAGAA CAAGCGTAAT GATGTGTCAG GCCAGGGTAG AAGTTAGCCC 720 TCCAATCACC TGATGTCAGG GGTTCGAGAC CAGCCTGGCC AACATGGCGA AACCCCATCT 780 CTACTAAAAA TACAAAAATT AGCCAGGCGT GGTGGTGGGT GCCTGTAATT CCAGCTACTT 840 GGGAGGCTGA GGCAGCAGAA TCGCTTGAAC CCGGGAGGCA CAGGTTGCAG TGAGCCAAGA 900 TCACGCGACT GCATTCCAGC CTGGGCGACA AGAGCAAAAC TCCATCTCCA AAAAACAAAA 960 CGAAGCCCTC CAGTGCCCCA TCGCTACTCC AGAAGGTGTA CCTATGGATC ACAGTGGGAT 1020 CCAATGAGTA CCATGACGAA GCACACGAAT GGCACCACAG TGGGCAGTGC ACCCCAAATG 1080 CAGTGTCAAG GACAAAGGGT CAAAGCAGAG AGTGAAACGG GAGTCTCACC CACCCAGCGG 1140 AACTGGAAGA GCACTTTCTG TTTTTTTTGA GACAGAGTCG TGCTCTATCG CCCAGGCTGG 1200 AGTGCAGTGG TGCGATCTCT GCTCACTGCA ACCTCCGCCT CCCGGGTTCA AGTGATTCTC 1260 CTGCCTCAGC CTCCCAAGCA GCTGGGAGTA CAGGCGTCCG CCCCATGCCC AGCTAATTTT 1320 TGTAGTTTTA GTAGAGACGG GGTTTCACCA TATTGGCCAG GCTGGTCTCG AACTCCTGAC 1380 CTTGTGATCC ACCCGCCTTG GCCTCCCGAA GTGCTGGGCT 1420
|
| |
|
|
|