| Tag | Content |
|---|
EnhancerAtlas ID | HS060-27641 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr5:79963280-79964850 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF4G | MA0484.1 | chr5:79964311-79964326 | AGTGTCCAAAGTCCA | + | 6.18 | | NFYB | MA0502.1 | chr5:79964052-79964067 | CTGATTGGTTCATGG | - | 6.92 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr5 | 79964166 | 79964596 | | chr5 | 79963294 | 79963390 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH05I080667 | chr5 | 79963672 | 79964863 |
|
Enhancer Sequence | GTTTTTACTT GGGCCTGCTG GGCTCATTCC TCCCACTCGG CCTGGCAGGC TGTGCTTGGC 60
TTTTGCTTTT GGCCTGAATC TCGCAGCTGC CAAGGGTGAG CCAGGAGTGG AGTGGTGAGG 120
GTGAGGGGTG TGTGAGCAGG TGACCATGGG GTCTGGCCCC TGTGCACTGC CAGGCATGCT 180
GGCTTCGGCA GGGTGGGCAG CTCCAGGTGC CAGCGTGAGT GAGGGCTGGA CCAGGCGTAC 240
CACAAACAGC TTCCACAGCT GGCACCAGGG AACACAGTGG CGCCCAGAAG CTTGGAGATT 300
CCAGGAACTG CAGAGCCCCA GAGAGGGTGT CATAGACCTG GCTTAGGAGC CCCTAGGTCT 360
GAGCTCCCCA GAGGTCCACA GCTCTTCTCT CCTGTCTTCT CTCCTTCTTG TTGCTGCAAT 420
GTGGCAAGCA AGAGATGGGT TTCAGGCCTG TTTGTGTTAC AGCTCTTTTA GCCCTGCCAT 480
TCGGTGGGTC CCAGGTTCTT GTCCTGCTTC CAGGAAGAAT GAAGTATGTG GACGAGTGGA 540
GGGTGAGCAA GGCAAAGAGG GGCTTCCTTG AGTGACAGAA CATTGAGGGG AGACCCGCAG 600
TGGGTGCTTC TTTCTGCAGG CAGGGCATCC CATCAAGTGA GAAGTGATGA GCCTTCAGCC 660
GAGAGGGGAC CCTGGAGTGG GTAGCTCCTC TCCGCAGGCA GGTTGTCTGC TTGTCTCTTC 720
AAGTTTGGCC GAGTCTGGGG ATTTGTATGG GCTTGAGAGG AGGAAGTGTG TGCTGATTGG 780
TTCATGGGCT GCCATGGGCG GGCTCAGAAA ACACCGTAAG TTCTAATTCT GGTTCGTCAG 840
CCTGGCCCCC AGGCTTCAGG CTGTTCCTGG CTTGAAGGTG GGGCTTCACC CGGACCTGAC 900
CCTTTCTGCT CAGGAGCCTG TCTGCCTCCT GCCGTCATCC ATGGCACCCA GGCTGTTTGT 960
GCCATGGGGC ACCTGCAGGA CAGCTCTGAG CTGCCCTCAG CCCTCTCCTT GGCCTCCTTC 1020
CCATGTTCAT CAGTGTCCAA AGTCCAGAGG GGGCCGAGGC AGCAGGGGGC TGGCATGTTA 1080
GCACTGCCCT GAGCATGTGC ACACCCAGCC AGGTTGCAAC AGTTCCTAGG CTTGGCCTTA 1140
ACTTTGAGAT CAGAGTGGGT GCTGGGAGCT GGGAGAGGCC AGGCAGTCGG AGCAGGTACT 1200
TCTGAGCCTG CAGAGGGAGG GGGAATTCCC TTTCTGGGCC CTTGAGATTG CAGAGATGCC 1260
CGGGTCCACA GCCACAGCTT GGGTGGCTGT GGCTGCAGCT GCACCCAGGA GGGTGGGGCT 1320
CCTGCCTGCT CCCAGCCCCC AAGAGCACAG GGATGCCCAG GTTTGCAGCC ACAACTGGGC 1380
AGCCACAGCT GTGCCCAGGG AGCGTGAGGC TCTCACCCTG CCAACTCAGA AGGGGGCGAG 1440
GCTTCTTCCA CCCATTTCTG GCTCCTGTCG GTTCTGTGGA GCATGCAGCC CTGGCTGCGC 1500
CTCTCCTACT GCAGCTGGCG TTACGGCAGT GGCTGCTCCA GATGGGCTGC CATTGCCATC 1560
ATAATGACCT 1570
|
