Variant report

Variant	rs2006196
Chromosome Location	chr6:26358143-26358144
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Variant related genes	Relation type
RNU6-1259P	TF binding region
ENSG00000252399	Chromatin interaction
ENSG00000186470	Chromatin interaction
ENSG00000184825	Chromatin interaction
ENSG00000197903	Chromatin interaction
ENSG00000215979	Chromatin interaction

Extended variants
information (count: 22 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs11966630	0.89[ASN][1000 genomes]
rs16891666	0.89[ASN][1000 genomes]
rs1804836	0.89[ASN][1000 genomes]
rs2393650	0.82[ASN][1000 genomes]
rs3757141	0.80[AFR][1000 genomes];0.89[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs3846841	0.89[ASN][1000 genomes]
rs3885849	0.89[ASN][1000 genomes]
rs4712988	0.89[ASN][1000 genomes]
rs59121933	0.89[ASN][1000 genomes]
rs6901118	0.89[ASN][1000 genomes]
rs72500814	0.89[ASN][1000 genomes]
rs7356980	0.89[ASN][1000 genomes]
rs9461247	0.89[ASN][1000 genomes]
rs9467749	0.89[ASN][1000 genomes]
rs9467753	0.89[ASN][1000 genomes]
rs9467755	0.89[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1029920	chr6:25638507-26585842	Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Enhancers Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Active TSS Genic enhancers Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	1215 gene(s)	inside rSNPs	diseases
2	nsv538162	chr6:25638507-26585842	Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	1215 gene(s)	inside rSNPs	diseases
3	nsv1023453	chr6:25853830-26528250	Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	1201 gene(s)	inside rSNPs	diseases
4	nsv482729	chr6:26291011-26470898	Weak transcription Active TSS Flanking Active TSS Enhancers Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
5	nsv5230	chr6:26321593-26361531	Weak transcription Bivalent Enhancer Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
6	nsv482836	chr6:26352883-26520964	Enhancers Flanking Active TSS Strong transcription Active TSS Genic enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:26352600-26364200	Weak transcription	NHEK	skin
2	chr6:26352800-26364000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr6:26353000-26364200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr6:26355000-26361200	Weak transcription	Duodenum Mucosa	Duodenum
5	chr6:26355400-26364200	Weak transcription	Fetal Intestine Small	intestine
6	chr6:26355600-26358800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
7	chr6:26356000-26358200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr6:26356200-26365400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr6:26356400-26358400	Weak transcription	Thymus	Thymus
10	chr6:26356400-26364400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr6:26356600-26359000	Weak transcription	Fetal Thymus	thymus
12	chr6:26356600-26360800	Weak transcription	HepG2	liver
13	chr6:26357400-26361600	Weak transcription	K562	blood
14	chr6:26358000-26359400	Enhancers	Primary T cells fromperipheralblood	blood

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

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