| Tag | Content |
|---|
EnhancerAtlas ID | HS170-03855 | Organism | Homo sapiens | Tissue/cell | RS4-11 | Coordinate | chr8:139847280-139848400 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr8:139848297-139848312 | GAGGTCAGGAGGTCA | + | 7.19 | | RARA | MA0729.1 | chr8:139848297-139848315 | GAGGTCAGGAGGTCAAGA | + | 6.22 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GGGAAGGCGC TCCGGGAGGA AGCTACCAGG TAGAGGCCTG CTCTGGCCTG CGATGGTCTG 60
GGAAGGGGGT TCTGAGCAGG GCAAGGTTGC TCTGGGATTG AAACCCTGCA CTTTTTGGAT 120
TGGACCGTTC CCTGCCCTTT GCCATCCTGA GGTTGTCAAG TTCTTGGAAA ATGACTAAGA 180
GCTGCCATTA TGTCATTTTT AAATAGCATT TCACACACAG GCTATTTAAT GGAATTCATG 240
ATATAATTGT TAAATGATAT TGGGTCCTAA AGATGCGAAC AGTATTCAGA AGCTTCATTA 300
TAGATGGAAA AAGCACCCCT CCAAACCGTG CTTGTTTACA CACACTAGTG TGAGTGATTC 360
AGCATCTCTG GAGACGGTTG GTTTGTGGGA GGGAACAGGC ACCCACAGTC CCACAACTGA 420
GGTCCCCTGT GGTGCATGGG TTGATCCAGC TGAGAGGCTG CCACTAGGCA CAGGCTGAGT 480
GAGGCCAGCT TTCCTGACCC GCCAGCTGCT TGAAGACAGG GCCCAGCTTG CTGAGTTCGC 540
CACCCTATCC CCCTCAGGAC CTGCAGGGCT GGCCCACAGT GCAGATTTGT CAAACTGAAC 600
ATAGGGCCTC ACTCTGAGCT GTAACGCAGC CTTGGTCCCT GGTAGAGACT GTGTGGGGGA 660
GAGAACACCC AGCACGTGGA CCAGATACCC AGATACTCCT GACTGAAGTC CTACAAATGA 720
GCTGTGTGGC CTTGAGTACG AGCCTCAACC TCTCTGGGCT TATTTCTTCT GCAGTTTTGT 780
AAAATTGGGA TAATAATAAC AGTGTAGTAG ACAAGTAAGG GCTATGATAA CAATTTACAT 840
GCAAATCCCT GTTCCCACAC TTTCTCTCCC TGCCAGCTCT CAGGTAATTT ACTCAACCTC 900
TCTGGACCTC ATGTCTTCAT CCACCAAATG GGACATTAAG AATAACCAGT CAGCCAAGCA 960
CAATGGCTCA CGCCTGTAAT CCCAGCACTT TGGAAGGCCA AGGTAGGTGG ATCACTTGAG 1020
GTCAGGAGGT CAAGACCAGC CTGGCCAACA TGGTGAGACC CTGTCTTTAC TAAAAATATA 1080
AAAATTAGCC AGGGGTGGTA GTGGGTTCCT ATAATCTCAG 1120
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