| Tag | Content |
|---|
EnhancerAtlas ID | HS118-15720 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr5:179278990-179280350 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXP1 | MA0481.2 | chr5:179279338-179279350 | AAGTAAACAGTA | + | 6.18 | | Foxa2 | MA0047.2 | chr5:179279335-179279347 | CCTAAGTAAACA | - | 7.22 | | Nr2f6(var.2) | MA0728.1 | chr5:179279064-179279079 | GAGGTCAGGAGTTCA | + | 6.22 | | ZNF263 | MA0528.1 | chr5:179279696-179279717 | GAAGGAGAGGAAAGATGAGAG | + | 6.07 |
|
| | 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 |
| GH05I179852 | chr5 | 179279263 | 179280597 |
|
Enhancer Sequence | AATAAAAAAT ATCAGGTGAA GGCACTCACC AACATTATGA AATGTTTTTG TCTACGGAGG 60
CAGGTGGATC ATTTGAGGTC AGGAGTTCAA GACCAGCCTG GCCAACATGG TGAAACCCCG 120
TCTCTATTAA ACATACAAAA AACAAATTAG CTGGGTGTGG TGGCATGCAT CTGTAGTCCC 180
AGATACTCAG GAGGCTGAGG CAGGAAAACT GCTTAAACCC GGGAGGCGAA GGTTGCAGTG 240
AGCCGAGATT GCGCCACTGC ACTCCAGCCT GCATGACAGA GAGAGACTCC ATGTCAAAAA 300
AAAAAAAAAC CCCAAAAAAC AGCAATTTAA CTTTTAGGAC TTTGTCCTAA GTAAACAGTA 360
AACAGCTGGT CACGTGGATA AAGAGGTTTT TGTGAAAAGC TTCACGGTAG AGTTGTGCAT 420
AACAGTCAAA AGGGAAATCA ACCTAAATGC CCAACAAGGT TGGGCCAGTT CCTTACTCAC 480
TCCACAAACA CCGAGCACTG TGCTAGGTGC TGCGGATACA CCAGCAAATA AAAAGCCTCT 540
GTTCTCACGG AACTTACAGC CTTAGATGGA CAATCCGTGC ATAAACACAT GACTATGTAA 600
CTTCCATAGG ATACTGAGAA GAGGGAGGGG AACTCCACAG TGAGCACAAA GGCCTGAAGA 660
GGGAGCAAAT TTGGGTTTAA GGTCAGAAAG AAAGCACATG GCTGTAGAAG GAGAGGAAAG 720
ATGAGAGGTG AAGGGAGAGG TGGCACTGGG GCTGGAGCAG GAAAAGAGCA AGTTCAGTAA 780
GGCAAAGGAT GCAGGACAGT TTGGGGTCCT AGAGTTCAGG AGGGGCAATA CGGATGGACT 840
GAAAAGACGT ACTGAATGCC AGCTGCAAAC AGCTGGATGA GAGCATTTAC AGCCTGCCCC 900
TGCCTGCCTC CACTTCCTGA GCCCACTATC CCACACCTCC ACCTCCACCA ACGGCCTCTG 960
CCCTTCCCCG GCTGCCCTGA TTCCTCTGTC ATCTTCTCAC AGTCCCCAGT GCTTTCCTTT 1020
CCTTGTGCTC AGCCGAGTTT TAAATTATGC AGATGCATGT GTGCATTAGT TTCTCTTCCC 1080
CTTCCACACA AGTGCATCTG TGAGGGCAAG AATGACAATG GGCTTACTTT CCACTGTTCC 1140
CCTTGTGCTT GGCACACAGA AAGTACTCAA GAAATACTTG CTGAATGAAG AATCAAATGG 1200
CAGTACCTTT CCAGATTCTG CTCCATCCAT TTCACTTCCT GAAGGAACAG GAAGCTCGGA 1260
AGCAGGAGCT CCGTGTCTGG GGAACTCTGT TTGAGAGAGG ATGATCCCAG CTGTGGCATG 1320
CTGGGACTCC CTGGAAGGGC TCGCTGCAGG CCTGCGCCCC 1360
|
