| Tag | Content |
|---|
EnhancerAtlas ID | HS070-00962 | Organism | Homo sapiens | Tissue/cell | GM19099 | Coordinate | chr21:30494040-30495020 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SNAI2 | MA0745.2 | chr21:30494373-30494383 | TGCACCTGTT | - | 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 |
| GH21I029121 | chr21 | 30493772 | 30495252 |
| Enhancer Sequence | CCTTAACATT GAAGCTTATT TGAGAAATGT CTGAAGGGTA CTTAGGCTAC ATCTCGTAGG 60
CCTTCTGATT TTAAGAGGCT TGTATTCATG GATAAATGTA GCTGTGGTTG GGGAAAAAAG 120
AGAGAGACCA ACATTTATGA ACACCAGGCA CTCAGCACTT TCCTCACAAT GTGTTCTTGC 180
TGCATGAAGA CCAAGGATGT CACAGGCACT AGTCAAATTT GAGTTGCAAA GCAGGCCACA 240
GAGGGAAAGT CCTGCAAGTA CTCAGTCATC AGCATGGGGA GGAGGAACTC AAACCAAGTG 300
TACACTACAG AATGTGTCCC ATGTTCATGT TTGTGCACCT GTTTGGTTTC TGGAAAGTGC 360
TCCCTCATGT TAAATTTATG TAGTTAAGTT GTAAAACAGG AAATCTTCCT TGACCCTTTG 420
CAGGATTTGT GAAAGGGGTG GCTTGTTTAC TGAGCCCGCA GCACTCAATC CCTTACGGGA 480
TGGGGAACAT GCAGGTAAGT GGGTGCGGGG GCCAGGATGA GTGCTTCTGG GTGTCAGCGG 540
GAGCAGAACT TTGTGCGGCC CTGTGACAGC ATCTGGGGGG GTACCCGTGA CCCCTGGAGC 600
CCTGAGGGCA TGTATTACAC TGCAGTTTTT TAGCTTTGCT GTTCACGGAT GGCTTAAGTG 660
TTTAACAGCT CAATGTGACA GCCCTCTGTA TCCTGAGCTC TCATTCAGTG TCCAGGAAGA 720
ATCAGGTTGC ACGAACGAAT TGAAGATGGT AAATTGTGGG CGATTTTATT GCCAATGAAA 780
CTGGCTTTTA GTGGAATGGA GAGCTGGAAA GGGGATGGAG CGGGAACGTG GTCTTCCCCT 840
GGAGTTTGGC CATCCACTGC CAAACTCTTC TTCGAGGCCC TGCCGTCAAG CCGTCCCTCT 900
TAAGTTAAGC TGCTTCTCAC CAACGTCTAG CTGCTGCTGC TTTTCTCTAC TTCTCTGCCG 960
CTCTGCTGCC AGTGGCGGCT 980
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