Variant report

Variant	rs4670536
Chromosome Location	chr2:33668852-33668853
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 6 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:2)

rs_ID	r²[population]
rs4670537	0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs62147116	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1005435	chr2:33136117-33747159	Weak transcription Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	22 gene(s)	inside rSNPs	diseases
2	nsv535624	chr2:33136117-33747159	Weak transcription Enhancers Genic enhancers Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	22 gene(s)	inside rSNPs	diseases
3	esv2762447	chr2:33643724-33674484	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv517737	chr2:33664350-33676440	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:33662800-33670200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
2	chr2:33663200-33671400	Weak transcription	Right Ventricle	heart
3	chr2:33663600-33670200	Weak transcription	Fetal Muscle Leg	muscle
4	chr2:33665000-33669000	Weak transcription	Left Ventricle	heart
5	chr2:33665000-33670000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr2:33665200-33670000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr2:33667400-33671400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr2:33667600-33669600	Enhancers	Skeletal Muscle Female	skeletal muscle
9	chr2:33667800-33669800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
10	chr2:33667800-33670000	Enhancers	Skeletal Muscle Male	skeletal muscle
11	chr2:33668000-33670400	Enhancers	Adipose Nuclei	Adipose
12	chr2:33668400-33673200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr2:33668600-33670000	Weak transcription	Brain Hippocampus Middle	brain
14	chr2:33668600-33670200	Enhancers	Psoas Muscle	Psoas
15	chr2:33668800-33669000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr2:33668800-33669200	Weak transcription	Fetal Heart	heart
17	chr2:33668800-33685200	Weak transcription	HUVEC	blood vessel

Quick Search:

Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

what's new

Quick links