| Tag | Content |
|---|
EnhancerAtlas ID | HS098-58944 | Organism | Homo sapiens | Tissue/cell | HSMM | Coordinate | chr9:133029910-133031400 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr9:133030495-133030516 | CCCACCTCCCACCCCTGCTCT | - | 6.06 |
| | | 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 |
| GH09I130268 | chr9 | 133030437 | 133031790 |
| Enhancer Sequence | TGGGAAGACA TAGTTCTACG TAGGCTTCAG GCTGAGTTTG TGGTCTAGGG GCTTGGAGGC 60
CCCTCTGCTT CCAGGAGTTC TGGGCACCAC AGGGTTTTGC AGCTCAAAGC TCAGAAGCCA 120
AGGCTCTAGA CAAAGATTTC TAGGAACATC AGATGGACAG CTTCTATCTT GGAGTCAGGG 180
GGCAACCAAG CTGGGGGTTG TGAGGAGGTG GGCTGTGAAG TGTGTTCTGG CACTTAAGCT 240
GGAACACAGG TCACCCTCCG TCTCCCCAGC TCTCTCACCC ACTTTCTGAA TTGTTCTGGG 300
GCTTCCGAAG ACATCACACT GAAGGAGCTT AGAGATCGTT GAATCTACCC CTTTATCTTA 360
CAGTTGGAAA AACTGAGGCT CAGGACACTG ATGAGACTTT CCCAAGGCCA CCTGCCAGGG 420
TGGCGTCATT CCTGAATCAT AACCCACATT TGTCTCTGAA ATATGTGGCT CCAGTGGCCC 480
AGCAGGATAG CAGCCTTTCA GAGCCAGATG TCGTGTCCTG AAGCCCAGAC CAGGGTTCCT 540
GAGACTGTCC TCGCTGCCCC ATTTGTGGCC ATGAGCCTCA GGAAGCCCAC CTCCCACCCC 600
TGCTCTTCCC TCTCCTCTCT GGGCACTGAG CTGGTGGGCA GTTCTCCAGC CTTCACCAGG 660
CTCAGCCCCC TCACTCCATC CTCTATGAAA CAAAAATCCA GTTCTCCATC CTGGTTCCCC 720
AAATTAGCTT CCGAGTGACA CCCCCAGGTT CAGACGTCGG GGAGACTTCA GCACCATGGA 780
GCCCTTGATC TGTGTAGAGC CCAGGGAGGC TCACAGTGTA AAGGGGCATG GTTCATTCCA 840
CGGGGCTGGT AGCCCTCTGG GACAGGCCAG GTGGGGAGTA GAAAGTGACA TGTGGTGGCT 900
CAGGTGCCAA CTCCTGGCCA TGGGCCAGTA AGCAAGGAAG GGGGCTAAGG AAAGACCCCC 960
CCCTGAGGAA GCAGCCTGTG AGTAGGGCCT GAAGAACATC AGTGAATGTT TACTGGGTTT 1020
TGGCCGTTTG CCTGGCAGAT GCCAGGTGCT GGGAACACAG CAGGGAGAGA GGACTCCCTG 1080
GGGCATGTGG AGCTGGCTGG GTAAGGACCG GGGGATGGAC AGGAGGGCTG ATGTGGAGGG 1140
ACAGGTGTGT GTGGGAGCTG GGTGTGCACG GGAGGAGTGG AGCGGGAAAG TGGGGAAGGG 1200
CAAGATTGGA CACAGCCGTG AGTGCAGGGC CGATTGATGC CTTGGCGGAC TTGGATTTCC 1260
TTTTCCTTCT ATGGGCTGTG AACAGCCACC GAGGGCTTCT GAGCAGCAGT TTGGAACTGT 1320
GATTTAGGCC TGGCTGTGCC TTTTGAATCA GCAAATAGAA TCCCCTTTGG TGGAAGAGGA 1380
ACTTGAGAAA CGGGTTGTAG CTGTTTGTTC CAGCTCCCAG AGCTGCACAG CGGGAGGGTT 1440
TTCTTAAAGT AAGCCCCTCT CCTAAACCCC AAGAGGCGGG TGCGGGGCAA 1490
|
| |
|
|
|
