| Tag | Content |
|---|
EnhancerAtlas ID | HS134-03373 |
Organism | Homo sapiens |
Tissue/cell | Mesendoderm |
Coordinate | chr1:159753120-159754270 |
Target genes | | Number: 12 | Name | Ensembl ID |
|
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RREB1 | MA0073.1 | chr1:159753749-159753769 | CCCCCATCCACCCCTCCCCC | + | 6.32 | | ZNF263 | MA0528.1 | chr1:159753748-159753769 | TCCCCCATCCACCCCTCCCCC | - | 6.86 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | TTCTGCAATA GCAGGCTGAA TAAGATAGAA ATTCACCATA AAATATGTGA GTTCCTGTAC 60
GTACCTGTAT GAGTTCTGTT AGATCTGGAG GCCGCACAGT GGAATGAGAC ATAATTCCTG 120
CTCTCAGGAG CTCAGCCTGC TGGAGAAGAT GGGCACAGAT AGAGTCCACC ACAGACAATG 180
GATGCTATTG TAGACATGCA TTCCAGTTCC AGTGGAGACA TAGAAGAGTG GGGAGTCAAG 240
GGTTCCCCTG TAGATCTCAT CTTTTGTATC ATAGACCAGA GACAGGCCTA GCCAACTGGT 300
CCTCCTTTCT GCTGCTTTCC CCCTTCCACC ACTAACCACC CAGTTCATCC CTGTCCAACT 360
CAACCTTAAA CAAGAGATAT CAGCTGAAGT CTTGCCAATC TAAGGCCATA AGATGCCCTC 420
TCCCCAGTTT AACTTTATTT GTCAAATCTG AGTGATCAGT TCCTTCAAGC TTAGTCTCCA 480
CCTAGCCTAC TCAAGTGAGG ATGTCTCCCA AAGAGAAGAA ACCCACACAT TCCAGGCATT 540
CCAGCTGCAA CAGAGGAATG AGAATGCAAA TAGAGGATGC ACTGAAACCC TTACCCTCCT 600
GTCACCAAAA GTTCTGTCTA CCCTGCTCTC CCCCATCCAC CCCTCCCCCA ATAGTATGGC 660
CCCATTCTGT TTCTGATGCA AACCAGAACA TCTTCCAAAG GGGTGTGTGT GTATTTTCAT 720
GTGAAGGGAG TAGGGCATGA AGGGTGTGAA TGGGCCACTT CCTGAACCTC TCCCCTCCAG 780
TCGGAGGGCT TACCAGGATG GAGAGAGAGA GAGAGAGGTG TGAGGCATGA AGCTTCCCCA 840
AGTTCGTGTC TCCACTCTGA TCCTCACCTG CTAGGCCATA CAACCAATCC TTGCCCTTTC 900
TGCCTCTGTT CCTGTGTCAC TCCATCCTCC CCACATCTCT GCACTGTGGA AGAGGAATAT 960
GCCCTTCCCT TCCTCCCAAG GCTCCTGCAA GGGAAACAAA ATTTTGCTAA CCCCATTAAA 1020
GCCCTGTGTA CTGCCTCCAT CCCCATAATT TAAGCAAGTC TCCTCTGCCT CAAGAGTTCC 1080
TTAGGGAAAT ACACGTATAA TTAAGTGCTT AAGGAAACTG CTTTTTAAAT AATAAGAGTT 1140
GGCTTGAAAT 1150
|
