| Tag | Content |
|---|
EnhancerAtlas ID | HS188-09497 | Organism | Homo sapiens | Tissue/cell | Th2 | Coordinate | chr3:182941980-182943180 | 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 | AGGTGGGAAA AAATTAGAAT AAATTAATCA GGCAGCATTT TTCAGTAAGT GGACAGGATG 60
ATACAGTTTA TTCATTCATT CAACAAGCCA GAGTATTCTA ATGTGTAAGG AATTGGGGGT 120
GTACAGTAAG TAATCTTATG TTGGGATGTG TGTGTGATGG AGAGATAAAC AGAAGGCTTT 180
AAACAACCAT AACTACCAGA CATAGATAGG CACAGAGTGC TCTGGGAGCA TCTACAAGGG 240
CTATTGGTAA ATACATAAGT AGACTCACAA ACAGGAATTG GTTTTTATCT TTATCATTCT 300
TTTCCTGCCC TTTGTCCAGG ACATCGACAT CTCCCCACAA CAGGTCTGCA ATGAGTAGTA 360
AAACTGACAG AAAAGAGGCT GGTGTTTGAT GGTCCCCCTC TCTTCTCTCT CCACCCTCTC 420
CTTGTGGTCA TCGTGACACC AACCCTGCAA AGAAGCCCAA GAAACAACCA AAAGATGGAA 480
ACATGCCAGA GGGGAGATGT GGTAGATCGG GCAACCAATA CGGAGCTCAG TCATTTGGGC 540
AACCCTCAAA GTGACAGGCT CCGCCTCAAA CATCACTTTC AACCTGCAGC ACAAGACTCT 600
GAGACAGGAA ATGTTATGTG ACTGTTTCGG AGCTAGAGAG CAAGGAGGAC TCAACGTGCT 660
GTTCAACCTG TATTCTCATG GTATCAAAGA CGCTGAGAGG TGGGCACATA TCTGCCAATC 720
TCCCGGAGAG AAAGCACACT CCAAGCCTCT GGCGTCAGCT TGCCAGCTTC ACTCGCTCTA 780
TCAGGGAGCC TGGCCCACAG CGGCTGTGCT GGCCACAGAT CCCATGCCAT TCTGGTGGAG 840
AAGCCCATGT AGCCACCTCC TTGCAGAAGT CTGTGTCCCT GTCCTCCTGC TCAGCCCAAC 900
TCTGGATTTC CTTCATGTCA ACACAGATGA TTCCTTCCCT CTCAGCTTCA ATGATGCCTG 960
TTCTACTCCC AAATACATTG CTATAGTGGA TGACTTCCAT TTCTGTAGCT CTTTCTTTCT 1020
CCCAATAGGT TGTAAGTGGT CATTTCAGCA TAGGAACTAC AGCAACCGTC CTTTGCTATT 1080
CCCTCCAGGA AAAAAATGGC ACACACATTT AAGACAGATG GCCCTTGAAA AATGTTCAGA 1140
CTGGTTAAGG AGCTAGAATA ATAACTCAGA GCTTAACAAT ATAGTATTGA CCTAAATTGC 1200
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