| Tag | Content |
|---|
EnhancerAtlas ID | HS127-28148 | Organism | Homo sapiens | Tissue/cell | Macrophage | Coordinate | chr7:2732810-2734330 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr7:2732940-2732955 | TGAACTCCTGACCTC | - | 6.22 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr7 | 2733557 | 2733913 | | chr7 | 2732841 | 2734150 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH07I002693 | chr7 | 2733557 | 2734035 |
| Enhancer Sequence | CCGCAACCTC CGCCTCCCGA GTTTAAGCAA TTCTTCTGAG TAGCTGGGAT TACAGGCATG 60
CGCCACCACG CCCAGCTAAT ATTGTATTTT TAGGAGAGAT GGGGTTTCTC CATGTTGGTC 120
AGGCTGGTCT TGAACTCCTG ACCTCAGGTG ATTGCCCGCC TCCCAAGGTG CTGGGATTAC 180
AGGTGTGAGC CACCGTGCCT GGTTGGTGGG ATTGTTGTTG TTGGACACAG GGTCTTGCTG 240
TCATCCAGGC TGGAGTGCAG TGGTGCGATC ACAGCTCACT GCAGCCTTGG ACTCCTGGGC 300
TGGAGACTTC CTCCGACCTC AGCCTCTCGA GTAACTAGGA CCACAGATGT GTGCCACCAC 360
ACCCAGCTAA TTTTTGTTTT GTTTTGTTTT GTTTTTTGAC ACGGAGTCTT GCTCTGTGGC 420
CCAGACTGGA GTGCAGTGGC GCGATCTCCG CTCACTGCAA GCTCCGCCTC CCGGGTTCAC 480
TCCATTCTCC AGCCTCAGCC TCCAGAGTAG CTAGGACTAT AGGCGCCCGC CACCACGCCT 540
GGCTAATTTT TTGTATTTTT AGTAGAGACA GGGTTTCACC GTGTTAGCCA GGATTGTCTT 600
GATCTCCTGA CCTCCTGATC CGCTCGCCTC GGCCTCCCAA AGTGCTGAGA ATGCAGGCAT 660
GGGCCACTGC AGCCAGCCAG CCTTTTCTTT TTCCAACAGG ACCTGTCACC TTCTAACCTA 720
CCTTCTATGC TATTTACTTA GCACTTTTGC CACCTGCCTT CCTGCTGGAG CACCTAACTC 780
CATGGGGCCA GGGACCTCTG TTTTGTCCAC TCATGTTGGA AAACCCCCAG CACAGGGCCC 840
AGCACCCAGG AAGCCCTTGG CAGCTAATGT CACTGTCATG AGTCCGCTGA ACTGGGCCAC 900
AGGGTGCCTG ATGCAACACC GTTCCTGGGC GTGTCTGTGA GGGTGCTCGA GATGACATTA 960
GGATTAGGAC AGTGGGTTCA GGAAGGTGGA CTGCCCTCCC CAAGTGGCTG GGCACCTTCC 1020
AATCCCTCCA GACCCTGAAT AGAACAGACG GCAGAGGGAG GAGGAGTTCA CCCCTCATTT 1080
CCTGCCTCGC CGCTGGAGCT GGGACATGTC ATCCTCTCTT GCCCCGGGAC TGGATGTCCA 1140
CCATCGGCTG CCCTGGTTCT CAGGCCTTCG GACATGAGCT GAGTTTGAAT CACGCCTTGG 1200
GCTTCCCTGG GTCTCTGGCT TGTAGGCAGC ACACTGTAGG ACTTCTCAGC TTCTGAGGCC 1260
TGTGAGCCAA TTCTCATAAT AAATCCTTAT TTTATTTTCA TAGAGTAGAG ATGAGGTCTA 1320
TGTTGCCCAG GCTGGCCTTG GCCGCCCCTG CTCAAGTGAT CCTTCTGCCT CCCGAAGTAC 1380
TGGGATTACA GGTGTGAGCC ACCGTACCTG GTCATAATCC TATAAATATA CATGTGAGAT 1440
TATATTACAT TAATATATTA TCGTATATAT TAAAATCTCA TATATATAAT ATATATTTTA 1500
TTTATTTTTT TTTTGAGATG 1520
|
| |
|
|
|
