Tag | Content |
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EnhancerAtlas ID | HS187-13987 | Organism | Homo sapiens | Tissue/cell | Th1 | Coordinate | chr2:137068140-137069310 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NR2C2 | MA0504.1 | chr2:137068542-137068557 | CGAGGGCAGAGGTGA | + | 6.08 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | AGCAGAGTTA TATGTGAGGG GAAATCCACT GTGGGATCTT TCAGTTCTTA AAACACACAC 60 TAAGAGATGC CGTGCTCACT GGGCATTGCC AATGGGTTCA GTCACATTTT GGAATGATTT 120 CTGCAATTAG TACTAAAATG AAGGAGGACA GATTCTAGTT TTGAAAATTA AGGCAGGAGA 180 AGCTTGGATA AGAAATCTTT ACTTGCTTTT ATTTCTCATT TATCATCAAG TCCCAGCTTT 240 CCCAGGAAGT TATTGAACCT TGCTGGTTTC ACTAACTTAA AAAAAAAAAA GCTGCTCTTC 300 TTTTGCCCAC AGAGTGAGCT GCTGGTAGCT GAGATCGGGG TCGCCAGCAT GGTGACTTTC 360 AGAGACTAGC CAGATTGGTT CATAAACAGA TTCCCTGAGT GGCGAGGGCA GAGGTGAGGA 420 CAGACAATGA AGATGGGGAG TGTAAGCGCG AAGCCGGAAC ATCTCTTGGA GACAGCAATG 480 GGTAACAGGG AAGCAACACA TCTGACTTGG TGTTTAAGAA AGGTTAAGCA ATGATGCTAC 540 TCGTATCAGA CTATTAGTCC CTAGAGAAGA CCTCAAGAGA TGCACGTTTA AAGTTTCCAT 600 AAACCCCAGA TGATAAATCT TCTTGTCTTT CTTCCCAACT TTCAAAAATG GCGCTTATTA 660 CTCAAGAAAA ACCACAACGC TTTGAGCTGG CACTAGTTAG CTCAATTGAA GGTCAGATTT 720 TGCATAGAAG ATTCAGAGAC AGGAAATTTA TTGGCGTAAA AGCCATCAAG AGGGTATTGA 780 AACAATACCA TCCTTTCCAC AATCTTCACA CCAAGATGTG CTGTGTCATC TGTGGGTGTC 840 TTTCTGGATG ATTTGCTTGT AAAAATGACT ACAGCACCTC TGCATTGCCA GGGAGACTCT 900 GTTGTGAAAT TCCATGGAAT GAAAGAAAAG GGGAAATTTT GCTGTGTAGC CTGGAGTCCA 960 TTCTCAGTTA GGAAGGAGGA GGAGGAAGCT GCTGGTCTGA TGGATGAGTC TGTACTGTGA 1020 CCTCCACAGT TAAACAAAAT AAAGTACTGG TTTCTTCTCT CATTAGGAGT GGTGTCAAAG 1080 CTGTCCGAAA GAAAACACTG CTATCCTTCC ACGCACTTTA GTAAACAGAT CTTTGGGACA 1140 ACATCTTCAC AATGTGCTTT TTACAATTTA 1170
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