Tag | Content |
---|
EnhancerAtlas ID | HS026-31478 | Organism | Homo sapiens | Tissue/cell | CNCC | Coordinate | chr7:99827970-99829390 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr7:99828057-99828072 | TGAACTCCTGACCTC | - | 6.22 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TGGAGCTACA GGCATGTGTC ACCATGCCCA GGTAATTTTT GTATTTTTGG TAGAGATGGG 60 GTTTCACCAT GTTGACCAGG ATGGTCTTGA ACTCCTGACC TCAGGTGATC TGCCTGCCTC 120 AGCCTCACAA AGTGCTGGGA TTGTAGATGT GAACCACTGT GCCTGGCCAA AATGCTAATA 180 TTTTGGCAGC ACTTTGGGAG GTCAAGGCAG GTGGATCACT TGAGTTCAGG AGTTTGAGAC 240 CAGCCTGGTC AACATGGTGA AACCAAACCC CACCTCTACT AAAAATACAA AAAAATTAGC 300 CGGGCATGGT GGTGGGTGCC TATAATCCCA GCTACTCAGA AGGCTGAGGC AGGAGAATCG 360 CTTGAACCTG GGAGGTGGAG GTTGCAGTGA GCCAAGATCA CGCCACTGCA CTCCAGCCTG 420 GGTGACAGAG TGAGACTCTG TCTCAAAAAA AAAAAAGAAA AGAAAAAAGA GAAAAAACAA 480 ATCCACTCAA TTTTTTTTTT CTTGGGCAAT AATAGATTTC CAAGCAGCCT AGTTTGCTGA 540 CCAGGAAACG CACCCTGGAA TGGAAGCCCT TACCCTGAAG TCACAGAGGT AAGGCTGGCT 600 GGCTGGCTAG CCTCCGGCCT TGCTGGGCTA ATTGAAACCT GCTTTCCCAG TGGTCCCTGT 660 GTTCCTCAGT GCTGCGCCTG TGGCTGGGAA AGGCTCAGGG AGGGGCAGGG CAAGGCAGTT 720 TCAAAAGTCA CAAGGCTCTG GGGAATGGCA GAGTCGAGGG ATTGCGGGCA ATTCCTTCCC 780 TGGGCCAGCC GAGGGTCTCA GCCTGGGCCC AAGGACCTCT ATATGAAGAG AGCTTACTCA 840 CCCCCAGGAA TTTCCTACTT CACTCCTTGT TCCCTCTCCT GCACACACAC ACACACACAC 900 ACACCCCAGG AGACTCTACC CCAACTCAGC CCTAACCCAG CCGAACAACC TTCAGTGGCT 960 CCCCAGTGCC TGAAGAATAT GATCCAAACT TTCCCTGCCT ACCTCTGTCT TCCCCTTTTT 1020 TACGTGCTGG ACCTGGCCCT TGCTTCTGCT CCTGTACTTT CTCATTCAGC TCTCCTCTGA 1080 CATGTTTTCT TCCTTCCCCA CAAGGCCAGC AAAAATATCA CCTCCTCCAG GAAGTCCTCC 1140 ATGACCACGT GAGCTCACCA GGAACTTCTG CTTTTGAGCC CCCAGAAAGA GCCATGCTGC 1200 AGAAGTCTCC CCATGCTGCT TCTAACCCAA ATAAAGTACA GGAGAGGAGT TCAGGAAAAA 1260 GTCTAGAGCC AGGCACAGCA GTACACGCCT CTACTCTCAG CTACTCGGGA GGCTGAGGTG 1320 GGAGGATTGC TTGAACCCAG GAGTCTGAGG CTGCTATGCA CTATGATCAC ACCTGTGATT 1380 AGCCACTGTA CTCCAGCCTG GGCAACATAG CAAGAACCTG 1420
|
| |
|
|
|