Tag | Content |
---|
EnhancerAtlas ID | HS026-00686 | Organism | Homo sapiens | Tissue/cell | CNCC | Coordinate | chr1:27396610-27398390 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NR2C2 | MA0504.1 | chr1:27396717-27396732 | GGAGGGCAGGGGTCA | + | 6.26 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| | Number: 2 | ID | Chromosome | Start | End |
GH01I027071 | chr1 | 27396941 | 27397090 | GH01I027070 | chr1 | 27397346 | 27397995 |
| Enhancer Sequence | ATTCTGTGTC CTCATGTAAC TCTTAAGAAA ATCAGGAGTC CATTCCGAAC CCTTGGGTGA 60 ACTGAAGGCA GGTGGAGATC AGGGGACTTG GGGGAGGCAG TGAGGGTGGA GGGCAGGGGT 120 CAAGCACCCA GGGCCTCAGG TCATCTGTGT CCATCCCCTG AGGCAGGCTC TGGGCAGCCC 180 TCCCTGAGGA GGTAGCCCTG TCCCCAGGGC CCTGGATGGT GAGGATGACC CAGCCTTCGT 240 AACCCTGCCC TCACACACAG CGCTCACTCC AAAGCTTGCT GGAATCATCT GAGGCTACCA 300 GTGTCTACAG CACATCGAGC TACCCTTATG GAGCCTGGGA CCAGCCCCAG GAAGCCAATC 360 TCAGCTCAGG AGCCAGGATT TTAGTGCAAA GCTGCGCCCC CTTCTGTAAA CCATGGTTCT 420 CCTGAGAAAC AGCTCATGCC TTTGGTAAGC TCCTGGGCCC TGGGGAGATG GAACACCTGA 480 CTTGCGGCAC CTGGGGACCA TGTGACCAGA GCTGAGCACT GTCTGACCTT GCCACAAAGT 540 CAGGTGTGCC CAACGGTTTC TGTCATCAAG GGGAGAAAGT ACACGTGGGT GAGGGCTGAG 600 CGCAGGCATG TCCTGAAGCC CAGCTGAGCC TCTCAGCAGG CAGCTCCTTC CCCAGAGTCC 660 CTTCTCCAGC TTCCCAAAGC CCCTGCGTCC GCCCATACCT TGGGCACAGG TCCCTAAGAC 720 CAACTGAACA CTCGAGCATG AGCCAGGCAG ACAGCCTGGG TGGATGCCAG CAGAAAGATT 780 GGTGAAGACT GGATCTCCTG GGCAGAAGCG GTGACAGGCA CATGGCGTCC AGTGTGAGGC 840 TGGAGGCATC AGGGAGCACA GGGATGCAAG CCCCTCTACG TTCTCCCTTG TCATGGCTGG 900 GTGTGAGAAT GACCTTAGGC AATGGGGTGG GGCATGAATA TTTTGAGCTT GTGCCAGCTG 960 TGTGGTGGAG CGTGGGCCTG TACGGAGGCA CTGCACTCCC ATCTCCCTCG GCTCCCAACT 1020 CCCTCCGTGG GAAGCTGAGT TCAGGCACTG CCCCTCCTGT ATGGACAGGG AGCCACTGGT 1080 CCCAGCTTGC TGGTTGCCAG GCAACCCAGG ATGAGCCTTC GAGGTCATTC CTCAGACAAC 1140 TCTGAGCTCT CTCCACAGCC TGGGAACAGA TGGTTCCGCA GCAGCCAGCC CCAGCCTGAA 1200 ATGAGTTGCG GAGGCACTGC TGCCTGTCTC CACCAGCAAG AGGGAGGAGA GGCCCTTCCC 1260 GTGCCTGCAG CAGTCCAGGG TAGATGCAAG CAGAAAGACT GGTGAAGACT GGAGCTCCTG 1320 GGCAGAAGCA CTGACAGGCA CGTGGGGTCC TGTATGAAGA GCTGCACTTT GTGTGAAAGG 1380 AAAGGTGGCC CAAGGTCTGG CTCTACTTCA GCCGGGGCAG TGGCTGGTGG TCTTGCCGGG 1440 TGGGCCAGTC TTGGGAGGGG GTGATGGGGA AGTTGGTGAA ACAGAGGCAC TGGGTCAGCA 1500 ACTATGTGGT GGGACTCTCA GAAACGGCCC AGATTACAAG AGAATGCTTG ACCCGAGTGA 1560 CTGTTTACCA AAGCCCTCCC CCTCAAAAGA GGCTTTTAAC AGTCAGGTGA CACCTGTGGG 1620 TGTCACCATC TTCCCTTTCT CTATTATTAG GACCTGGACA AAATTCAAGA AGATGTCCCA 1680 ACCACATGTA GCCTTACCTT TGATACTTCC AATTGCAATG AGACTTAAAT TTTAGAATAA 1740 GAGATACACG CTGGGCGCGG TGGCTCACGT CTGTAATCCC 1780
|
| |
|
|
|