| Tag | Content |
|---|
EnhancerAtlas ID | HS091-49812 | Organism | Homo sapiens | Tissue/cell | HepG2 | Coordinate | chrX:117973740-117975380 | Target genes | | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chrX:117974531-117974546 | TGAACTCCTGACCTC | - | 6.22 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TTGGCCCTTC CCGCAATGCA ACAAAGGAGG GACTTTGTCC CAGCCTTTCC CCTAGCCAGG 60
AGAGGTGCTG TTAAATCCCT TTGTGCCTCC CCACCGGCCT TGGAGAGATG AGATTTCCCC 120
TGTAGTACCC CAGGGGACGG GCCGACGGGA TGGACTTTGT ATCTTTTGGC TGATCTGGCC 180
GGACATCCTT GCCCAATAAG CACTTACCCA GTTGCCCACC CTCCAAAAAA AGGAGAAAAT 240
CAAATCAGTA ATTTGATCGA TCATTTTCAT AGATATGCTG TAATAGAACA ATTCACCTGG 300
TTGTGAACTG GGCTGGGGAG TTTCAAGACG TGAGTTTGTT AACTGACTAG TTTCTTGCTT 360
GGTGTAGAGG CCTTAGGCAC TCTCACACTT AAACCAGCAG AAAGGCCAGG GAGTATCTAG 420
ACTACACACT GGGGTCACTC AACTGGAAAC ACGTTGTACA CCTCAAGACA TCGTACAATT 480
TCTCAGACTG AGATGCTGGC TGTGATGTCT ATGCAGCACA GCCCCAAGTC CCAACTGACA 540
GAAATGTCTC AGAAACTTAA TTCACCACGG TCTTTTTTTT TTTTTTTTTG AGACAGAGTC 600
TTGCTCTGTC GCCCAGGCTG GAGTGCAATG GCGCGATCTC GGCTCACTGC AACCTCTGTC 660
TCCTGGGTTC AAGCAATTCT CCCGCCTCAG CCTCCTGAGT AGCTGGGATT ACAGGCGCCC 720
GCCACGACAC CCGGCTAGTT TTTGTATTTT TTAGTAGATA TGGGGTTTCA CCATGTTCGC 780
CAGGCTAGTC TTGAACTCCT GACCTCAAGT AATCCGCCCA TCTTGGCCTC TCAAAGTGCT 840
GGGATTACAG GCGTGAGCCA CATGCCTGGC CTCACCACGG TTTTATTTTT GTTTTTGTTT 900
TTTTTTGTTT TTGTTTTTGT TTTTTCTTGA GACGGTCTCA CTCTGTCGCC CAGGCTGGAG 960
TGCAGTGGCA CGATCTCGGC TCACTGCAAC CTCTGCCTCC TGGGTTCAAT CAGTTCTCCT 1020
GTCTCCAACT CCCGAGTAGC TGGAATTACA GGCATGCCAC CACCATGCCC AGCTAATTTT 1080
TGTATTTTTA GTAGAGACGG GGTTTCACCA TGTTGGCTAG GCTGGTCTCG AACTCCTGAC 1140
CACAGGTGAT CTACCCGCCT TGGCCTCCCA AAGTGCTGGG ATTACAGGCG TGAACCACTA 1200
CCAGCAGCCT CACCACAGTT CTTAATAGAA GTAGTCTATT TGAGGAAAAA CAGTTAATTT 1260
ATAAAGAAAC TGAATAATGT AATAAATTGA GGAATTTTTT CCCAGCCTTG TACTTTTTAT 1320
ACCATCAAAT CCACTGACTT TAAGTGTACA GTTTAAAAAA TAAATTTAGC CAGGAGCGGT 1380
AGTGCACACC TGTAGTCCCA GCTACTTGGG GGCTGAGGTG GGAGGATCAC TTGAGCCAGG 1440
GAGGTTGAGG CTGCAGTGAG CTGTGATTGT GCCACTGCAC TCCAGTCTGG GTGACAGAGC 1500
AAGACCCTGT CTCAAAACTA AACAAATAAA TAAAAATAAA TTTATGGAGT TGTGCAACCA 1560
TCACCACAAT ACAGTTTTAG GACATTTTCC CTATCCCCCA CGAATTCCCA GAAGCAGTTT 1620
GCAGTTAATC TCCTCTCTCA 1640
|
| |
|
|
|
