| Tag | Content |
|---|
EnhancerAtlas ID | HS187-17966 | Organism | Homo sapiens | Tissue/cell | Th1 | Coordinate | chr3:182942060-182942960 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr3:182942374-182942395 | CCCCTCTCTTCTCTCTCCACC | - | 6.29 |
| | | 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 |
| GH03I183222 | chr3 | 182939770 | 182946156 |
| Enhancer Sequence | CAACAAGCCA GAGTATTCTA ATGTGTAAGG AATTGGGGGT GTACAGTAAG TAATCTTATG 60
TTGGGATGTG TGTGTGATGG AGAGATAAAC AGAAGGCTTT AAACAACCAT AACTACCAGA 120
CATAGATAGG CACAGAGTGC TCTGGGAGCA TCTACAAGGG CTATTGGTAA ATACATAAGT 180
AGACTCACAA ACAGGAATTG GTTTTTATCT TTATCATTCT TTTCCTGCCC TTTGTCCAGG 240
ACATCGACAT CTCCCCACAA CAGGTCTGCA ATGAGTAGTA AAACTGACAG AAAAGAGGCT 300
GGTGTTTGAT GGTCCCCCTC TCTTCTCTCT CCACCCTCTC CTTGTGGTCA TCGTGACACC 360
AACCCTGCAA AGAAGCCCAA GAAACAACCA AAAGATGGAA ACATGCCAGA GGGGAGATGT 420
GGTAGATCGG GCAACCAATA CGGAGCTCAG TCATTTGGGC AACCCTCAAA GTGACAGGCT 480
CCGCCTCAAA CATCACTTTC AACCTGCAGC ACAAGACTCT GAGACAGGAA ATGTTATGTG 540
ACTGTTTCGG AGCTAGAGAG CAAGGAGGAC TCAACGTGCT GTTCAACCTG TATTCTCATG 600
GTATCAAAGA CGCTGAGAGG TGGGCACATA TCTGCCAATC TCCCGGAGAG AAAGCACACT 660
CCAAGCCTCT GGCGTCAGCT TGCCAGCTTC ACTCGCTCTA TCAGGGAGCC TGGCCCACAG 720
CGGCTGTGCT GGCCACAGAT CCCATGCCAT TCTGGTGGAG AAGCCCATGT AGCCACCTCC 780
TTGCAGAAGT CTGTGTCCCT GTCCTCCTGC TCAGCCCAAC TCTGGATTTC CTTCATGTCA 840
ACACAGATGA TTCCTTCCCT CTCAGCTTCA ATGATGCCTG TTCTACTCCC AAATACATTG 900
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