| Tag | Content |
|---|
EnhancerAtlas ID | HS118-18112 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr8:22266010-22267450 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxd3 | MA0041.1 | chr8:22266899-22266911 | GTTTGTTTGTTT | + | 6.32 | | Nr2f6(var.2) | MA0728.1 | chr8:22266417-22266432 | TGACCTTTTGGCCTG | - | 6.32 | | RARA | MA0729.1 | chr8:22266414-22266432 | CCTTGACCTTTTGGCCTG | - | 6.92 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_65369 | chr8:22267172-22268100 | Pancreatic_islets |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH08I022409 | chr8 | 22267230 | 22270169 |
|
Enhancer Sequence | TGAGCCAGGC CAGGAAGGCA GGAGCCCATC TCCCATCTCG CCCGCGTCTC ACAAGGACCC 60
CTGGGCTGAG CTGCTGCTGC TCCTCACTGA ATGCCTCACC AGTGATGACC AGGATGAGGT 120
TGTCGGTGTC AGGAGCGGGA GCGATGATTG GATGGATAAT TTTTGTATTT TGCAAGGATG 180
GCCTAGCACA TTGTCAGACT CCTGGGCCGT AGCTGGCGAA TGTTCAGAGC GTTGGACTTC 240
TTGAGCGGCC TATGGATCCC TTTTTGGTCT GCTTTTTGTT TCATGTTGAA CCACGGGGGC 300
CCAACCCTTT GGCTTTTTTA ATCTTTTTTT TTTTTTTTTC TGAGATAGGA TGTCGCTCTG 360
TCTCCGAGGC TGGAGTCCAG TGGTGCAATC ATAGCTCACT GCAGCCTTGA CCTTTTGGCC 420
TGAAGTGACC CTCCTGCCTC AGCCTCCTGA GTAGCTGGGA CTACAGGCGT GCACCGCCAT 480
GCCCAGCTAA TTTTTAAATT TTTTGTAGAG ACACGGTCTC ACTATGTTAC CCAGGCTGGT 540
CTCAAACTCC TGGGCTCAAG TGATCCTCCT GCCTCGGCCT CCCAAAGTGC TGGGATCACA 600
GGCATGAGCC ACCATACCTG GCCTACTTTG GTTTTATAGT TTTTCCTTTA AGACCTCCCG 660
GAGGCTGCAC TTGGCCCCTG AATCCTTCTT CCCCTCCCTA TCCCGGTATC CCTGATCCAG 720
CCACAGTGGG CTTGCCACGA GCTGTGAGTG TACACCCTGA TAGCCCTAAG CCCCATAGGG 780
CCGGCGTGTG CTGCCTGAGT GTCGGCACCC GGAATATACT GTCTGTGTTA CTGCAAGTCC 840
CTGTTTTCTG CTGTCGTTAT TTACTTGTAT GGCTTTTTTT GTTTTTTTTG TTTGTTTGTT 900
TTGAGACAGA CTTTCGCTCT TGTTGCCCAG GCTGAAGTGC GGTGGTGCAA TCTCGGCTCA 960
CTGCAACCTC CGCCTCCTGG GTTCAAGCGA TTCTCCTGCC TCAGCCTCCT GAGTAGCTGG 1020
GATTTCAGGC ACGCGCCACC ACGCCCAGCT AATTTTTTGT ATTTAGTAGA GATGGGGTTT 1080
CACCATGTTA GTCAGGCCGG TCTCGAACTC CTGACCTCAG GTGATCCACC TTCCTCAGCC 1140
TCCCAAAGTG CTGGGATTAT AGGCTTGCGC CACCGCACCT GGCCTACTTG TATGGTTTTT 1200
AGGCTTCCAT TGCTGTTTGC ATCCGTCTCT CCATGGAAAA GGTGTTTCTC TTGGATAGCA 1260
ATTTTGATAG TTTCCCTAGG CTTCTCCGCA GCATCTGGTG AGAGATGGAC TCAGCAAATG 1320
TTTACTGATG GGTTGGTGGA TCTCAGTCTG CCCCATCACA CCTGAATTCA GAACAGGGCC 1380
GCCCCAGGCA GCAGGAGTGT CCCCACCCTC AGTAATAGAG GCCCTCGTCT GTTCTTGTTC 1440
|
