Variant report

Variant	rs6801203
Chromosome Location	chr3:46459432-46459433
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:46448370..46452594-chr3:46456008..46460093,7	K562	blood:
2	chr3:46457920..46459873-chr3:46460241..46461934,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000121797	Chromatin interaction
ENSG00000223552	Chromatin interaction

Extended variants
information (count: 45 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs11574431	1.00[EUR][1000 genomes]
rs11574437	0.95[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs11574439	0.96[AFR][1000 genomes]
rs11574440	1.00[EUR][1000 genomes]
rs11574441	0.97[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs11575814	1.00[EUR][1000 genomes]
rs11575817	1.00[EUR][1000 genomes]
rs11575818	1.00[EUR][1000 genomes]
rs11575822	1.00[EUR][1000 genomes]
rs13327723	1.00[EUR][1000 genomes]
rs17141003	1.00[EUR][1000 genomes]
rs17141076	1.00[EUR][1000 genomes]
rs17842821	1.00[EUR][1000 genomes]
rs17842822	1.00[EUR][1000 genomes]
rs2373253	1.00[EUR][1000 genomes]
rs3136536	1.00[EUR][1000 genomes]
rs3176763	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs3181037	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs35212534	0.97[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs3918370	1.00[EUR][1000 genomes]
rs41495153	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs55951695	1.00[EUR][1000 genomes]
rs56062522	1.00[EUR][1000 genomes]
rs57509359	1.00[EUR][1000 genomes]
rs57761566	1.00[EUR][1000 genomes]
rs58966767	1.00[EUR][1000 genomes]
rs59998539	1.00[EUR][1000 genomes]
rs60350631	1.00[EUR][1000 genomes]
rs61737000	1.00[EUR][1000 genomes]
rs6441969	1.00[EUR][1000 genomes]
rs6776013	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6798819	1.00[EUR][1000 genomes]
rs723577	1.00[EUR][1000 genomes]
rs73831107	1.00[EUR][1000 genomes]
rs7611447	1.00[EUR][1000 genomes]
rs7614209	1.00[EUR][1000 genomes]
rs7638702	1.00[EUR][1000 genomes]
rs7640084	1.00[EUR][1000 genomes]
rs7640708	1.00[EUR][1000 genomes]
rs7650273	1.00[EUR][1000 genomes]
rs7652954	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9282632	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv876734	chr3:45725031-46468467	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
2	esv3323840	chr3:46352348-46497196	Strong transcription Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
3	esv3389382	chr3:46352798-46496696	Enhancers ZNF genes & repeats Weak transcription Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:24 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:46438800-46459800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr3:46448600-46460000	Weak transcription	Gastric	stomach
3	chr3:46455800-46496800	Strong transcription	Primary neutrophils fromperipheralblood	blood
4	chr3:46456600-46469400	Weak transcription	Right Atrium	heart
5	chr3:46457400-46459600	Enhancers	Left Ventricle	heart
6	chr3:46458200-46463400	Weak transcription	Primary B cells from cord blood	blood
7	chr3:46458400-46460600	Enhancers	iPS-20b Cell Line	embryonic stem cell
8	chr3:46458400-46464000	Weak transcription	Rectal Mucosa Donor 31	rectum
9	chr3:46458600-46463800	Weak transcription	K562	blood
10	chr3:46458600-46469400	Weak transcription	Duodenum Mucosa	Duodenum
11	chr3:46458800-46461400	Enhancers	Fetal Heart	heart
12	chr3:46459000-46465600	Strong transcription	Spleen	Spleen
13	chr3:46459200-46459600	Weak transcription	Fetal Intestine Large	intestine
14	chr3:46459200-46460000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
15	chr3:46459200-46460000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr3:46459200-46460400	Enhancers	H9 Cell Line	embryonic stem cell
17	chr3:46459200-46460400	Enhancers	HUES6 Cell Line	embryonic stem cell
18	chr3:46459200-46460600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
19	chr3:46459400-46460200	Enhancers	Right Ventricle	heart
20	chr3:46459400-46460600	Enhancers	H1 Cell Line	embryonic stem cell
21	chr3:46459400-46463800	Weak transcription	Lung	lung
22	chr3:46459400-46465000	Weak transcription	Skeletal Muscle Female	skeletal muscle
23	chr3:46459400-46468600	Weak transcription	Fetal Intestine Small	intestine
24	chr3:46459400-46491600	Weak transcription	Skeletal Muscle Male	skeletal muscle

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links