| Tag | Content |
|---|
EnhancerAtlas ID | HS150-07074 | Organism | Homo sapiens | Tissue/cell | NT2-D1 | Coordinate | chr21:46449230-46450370 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| PAX5 | MA0014.3 | chr21:46449815-46449827 | GAGCGTGACCCT | + | 6.92 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr21 | 46449400 | 46450000 | | chr21 | 46450000 | 46450194 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH21I045029 | chr21 | 46449179 | 46454770 |
| Enhancer Sequence | GGGTTACGGT GTGGACATCT TGAGGGGTCA CCATTCAGCC CACTCCAGAG GGGTCCATTG 60
AGCTGGGTCC TCTGCAGGGC TGTGGCCTGT GCTGGGTGGA GACAGTCCTG GGGTGCTGGA 120
GGCAAGCGGG GCTTCACTCA GGGCTGTATC TGGCTGCCTC CGAATCGCAA CAGAAGCTCA 180
ACAAGCCTGG AGCTCCCTCA GGGGGCTCAG TGGCCTCTGA GACCTCCCAT CTTCCATTTT 240
CCCCTAGAGC TGGCCATGCC TGGGGACTCT GACCATGGGC CCCAGAGAGC GCTGCTCCCC 300
TTTGGCCAGC GACAGGGTGG CCAGGCCCAG GATCTGGAGG GAGAAAGCTG CTGGCCTTCT 360
CCAGGGTGCA GCCTGGAGCT TCCCTGCTCT TCTGCAGCTG TGCTCAGCTA CGCTCCAGGG 420
CTGCGCTGAT TTCCGCTGTC AGTGACTTAA GCCAGCGTCC ACGGCCAATC AGCACAGCAC 480
TTCTGCCTGC TGCCTGCTGG GTTCAGACCA GGCTGGGTCT GGTCCCTGAC GGAGGATGCA 540
GTTCTCATCC TTCAAGCACA AGCCTACAGG CAGCCCCTTG TCACCGAGCG TGACCCTGCC 600
TCAAGGCCTC CTCCTCCCTC TCTTGAGTGA GTGGAGCAGA GCTGGCCGTG GCCTCCCTGC 660
CTCCGCTGAG CCCACCACCA GTGGGTTTTG TTCGGGGCTA ATGAGGCGCG GGAAAGGCGG 720
AAGGTGCCGG CGTGACAGCT CAGAAGATGG AACTAATGAG ACCTTGTTGC TGGACAAAGG 780
TGGCATTCAG GGTGTCCTTT TGGCCTCGGC CCCCGACTCC CAAACGGGCC CCTCTAATCA 840
CAGATGGTTC CCGGACCTGT CCCAGCAAAG GGTCCTGAAG CCCCGGCTTT GCTGTGCAGA 900
GGCTCCTCCC AACCTGGGTT TAGCCAGGCG CCTCCTCGCC TGCCCCACCC CCTGCATCTG 960
GTCACCTCAC CCCTCCAGGC GCAGTTTTGA TGGAGAAAAC CAGACGCTGT GGGAGCCCAG 1020
GCCGGCGTCT GAAGTCCGAG GTTCCAGGGG CCACAGAGCC CCGGCCTGGA CTCACAGGGG 1080
AACTCCCTCA CGGCAGGTGG GCCTCCTGGG TCTTTGTCTT CCTCATCAAT TGGCAATAGC 1140
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