| Tag | Content |
|---|
EnhancerAtlas ID | HS020-17917 |
Organism | Homo sapiens |
Tissue/cell | CD34+ |
Coordinate | chr16:89969290-89970520 |
Target genes | | Number: 20 | 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) |
| Nr2f6(var.2) | MA0728.1 | chr16:89969997-89970012 | GAGGTCAAGAGTTCA | + | 7.64 | | RARA | MA0729.1 | chr16:89969997-89970015 | GAGGTCAAGAGTTCAAGA | + | 6.45 |
|
| | 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 |
| GH16I089903 | chr16 | 89970330 | 89971828 |
|
Enhancer Sequence | GTTCTGTGGG TTTCCAGGGC TCTGTCTGGG CCCCGAGGAG GCCCACGGCG TGGGGTTGGG 60
CAGCTTCTAG CACAGGCAGA AACGTGCCCC CCAGAGGGGC CTGGCCAGGC CTCAGTCTGC 120
TCGCTGACCC CAAAAGTTTC GTCCCCTGTG TCTAAGAAGC ACCTTTGTCC TCCTCTGGGG 180
CTGCATGCAG CTGGCCATAT GCTCCACCAG TGCAGCCGTG TCTGGAAACG CGGCTGGGAG 240
GCCCTGTCCT TTGTGGCAGA GCTGTGCTGC TGTGTCACAG GCTGTAGCGT CAGCACCTCC 300
CTTGAAGGCA GGTGGGCTGC CAAGAAGCCG CTGCCACTTA CCCCAGAACA CTGGAGATCA 360
CTGCAGGCTC TGCCCTCGGG GCCCGTTCCC CTACATGGCG GCCTCTGCCC TCAACCTGCA 420
GTGCTGGCTC TTCCACTGGG CACAGGTGGC CTCCGCTCCC ACCAGCCTGC CATGGGGTCC 480
AGTCTTTGTG ATTAAAACAT CCAACCGGCC GGGCACGGTG GCTCACGCCT GTAATCCCAG 540
CACTTTGGGA GGCCGAGGCA GGAGGATCGC TTGAGCATAG GAGTTCGAGA CCAGCCTGGT 600
CAACACGGTG AAACCCTTTC TCTACCAAAA ATATAAAAAT TAGCCGGGTG TGGTGGCGGA 660
CGCCTGTAAT CCCAGCACTT TCGGAGGCTG AGGCAGGTGG ATCACCTGAG GTCAAGAGTT 720
CAAGACCAGC CTGGCCAGCA TGGTGAAACC CTGTCTCTAC TAAACATACA AAAATTAACC 780
GGGGCGTGGT AGTGTGCGCC TGTGATCCCA GCTACTCGGG AGGCTGAGGC AGGAGAATCG 840
CTTGAGCCTG GGAGGTGGAG GTTGCAGTGA GCCGAGATTT CGCCAACGCA CTCCAGCCTG 900
AGCAACAGAG TGAGACCCTG TCTCAGAAAA ACAAAAAAAA ACCCAACCCC ATGTGTGTGG 960
AGGGTGGTGG GTGAGTCTTC CCTTGGATGC AAATGGGGGC CCTGGCAGCC TCCTTGGGGC 1020
TGGTGTGAAG GAGACCCCCA GCCTCAGACC CTGGGCACGC CAGCAGCAGC AACTCAGAAT 1080
ACCACCCGGA AGCAAGCCGC TGGCCCTGCA GACTCTCCAC CTTAGAACAG CTGTGTCTGT 1140
GACAAGGACC TCGCTGTGTC CCTTACTGCC TTGGGGGCTA GGAGTGGCTG GGGTGTGTGC 1200
TGAGGGCCCC CACAGAGCCT CCGCTTCCCC 1230
|
