Variant report

Variant	rs838635
Chromosome Location	chr3:143197079-143197080
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	chr3:143193715..143198774-chr3:143199748..143204167,7	K562	blood:
2	chr3:143196850..143198555-chr3:143200057..143202935,2	K562	blood:

Extended variants
information (count: 32 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs1097938	1.00[YRI][hapmap]
rs1525007	1.00[AFR][1000 genomes];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1525009	1.00[AFR][1000 genomes];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1723033	1.00[CEU][hapmap];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2140765	1.00[CEU][hapmap];0.91[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs66623546	0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs708484	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73144723	1.00[ASN][1000 genomes]
rs838599	1.00[CEU][hapmap];0.91[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs838602	0.81[EUR][1000 genomes]
rs838613	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs838616	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs838618	0.95[CEU][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs838620	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs838622	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs838623	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs838627	1.00[CEU][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs838630	1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs838634	1.00[CEU][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs838636	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs838637	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs838643	1.00[CEU][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs838644	1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs838646	1.00[CEU][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs838648	1.00[CEU][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs838649	1.00[CEU][hapmap];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs865710	0.85[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9289661	1.00[AFR][1000 genomes];0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs940636	0.81[CEU][hapmap]

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	nsv949288	chr3:142793323-143585882	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
2	esv2757894	chr3:142992697-143285979	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
3	esv2759184	chr3:142992697-143285979	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:47 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:143159600-143200800	Weak transcription	Esophagus	oesophagus
2	chr3:143163800-143203400	Weak transcription	Ovary	ovary
3	chr3:143174400-143220400	Weak transcription	Fetal Lung	lung
4	chr3:143176800-143220400	Weak transcription	Brain Cingulate Gyrus	brain
5	chr3:143177200-143200800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr3:143177800-143204400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
7	chr3:143178000-143203200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
8	chr3:143179400-143220400	Weak transcription	Brain Substantia Nigra	brain
9	chr3:143179800-143213400	Weak transcription	Primary T helper cells PMA-I stimulated	--
10	chr3:143180200-143200600	Weak transcription	Aorta	Aorta
11	chr3:143184200-143198600	Weak transcription	Colonic Mucosa	Colon
12	chr3:143185800-143213800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
13	chr3:143186000-143201200	Weak transcription	Adipose Nuclei	Adipose
14	chr3:143186000-143215600	Weak transcription	Primary T helper cells fromperipheralblood	blood
15	chr3:143186000-143223000	Weak transcription	Primary T cells fromperipheralblood	blood
16	chr3:143186400-143204400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
17	chr3:143191200-143211000	Weak transcription	Primary T cells from cord blood	blood
18	chr3:143191400-143231000	Weak transcription	Primary B cells from cord blood	blood
19	chr3:143192400-143211400	Weak transcription	Monocytes-CD14+_RO01746	blood
20	chr3:143192400-143215200	Weak transcription	Primary monocytes fromperipheralblood	blood
21	chr3:143193600-143198800	Weak transcription	Duodenum Mucosa	Duodenum
22	chr3:143193800-143198800	Weak transcription	Fetal Intestine Large	intestine
23	chr3:143195000-143197400	Weak transcription	Liver	Liver
24	chr3:143195200-143198600	Weak transcription	Thymus	Thymus
25	chr3:143196200-143197600	Enhancers	HUES6 Cell Line	embryonic stem cell
26	chr3:143196200-143198000	Enhancers	Primary B cells from peripheral blood	blood
27	chr3:143196400-143197200	Enhancers	iPS-15b Cell Line	embryonic stem cell
28	chr3:143196400-143197200	Enhancers	K562	blood
29	chr3:143196400-143197400	Enhancers	iPS-18 Cell Line	embryonic stem cell
30	chr3:143196400-143197400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
31	chr3:143196400-143197400	Strong transcription	Fetal Stomach	stomach
32	chr3:143196400-143197600	Enhancers	Primary hematopoietic stem cells short term culture	blood
33	chr3:143196600-143197600	Enhancers	ES-I3 Cell Line	embryonic stem cell
34	chr3:143196600-143200200	Enhancers	Rectal Mucosa Donor 31	rectum
35	chr3:143196600-143203800	Weak transcription	HUES48 Cell Line	embryonic stem cell
36	chr3:143196800-143197200	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
37	chr3:143196800-143197400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr3:143196800-143197400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr3:143196800-143197400	Enhancers	Fetal Thymus	thymus
40	chr3:143196800-143197400	Enhancers	Dnd41	blood
41	chr3:143197000-143197400	Enhancers	H1 Cell Line	embryonic stem cell
42	chr3:143197000-143197400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr3:143197000-143197400	Enhancers	HUES64 Cell Line	embryonic stem cell
44	chr3:143197000-143197400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr3:143197000-143197400	Active TSS	Hela-S3	cervix
46	chr3:143197000-143198800	Weak transcription	Sigmoid Colon	Sigmoid Colon
47	chr3:143197000-143202800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin

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