Variant report

Variant	rs865710
Chromosome Location	chr3:143194056-143194057
allele	G/T
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:

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs1525007	0.85[AFR][1000 genomes];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1525009	0.85[AFR][1000 genomes];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1723033	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2140765	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs66623546	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs708484	0.85[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73144723	1.00[ASN][1000 genomes]
rs838599	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs838602	0.80[EUR][1000 genomes]
rs838613	0.85[AFR][1000 genomes];0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs838616	0.85[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs838618	0.85[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs838620	0.85[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs838622	0.85[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs838623	0.85[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs838627	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs838630	0.85[AFR][1000 genomes];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs838634	0.85[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs838635	0.85[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs838636	0.85[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs838637	0.85[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs838643	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs838644	0.85[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs838646	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs838648	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs838649	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs9289661	0.85[AFR][1000 genomes];0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[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	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
4	esv32611	chr3:143191298-143195462	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:37 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:143159600-143200800	Weak transcription	Esophagus	oesophagus
2	chr3:143163400-143196800	Weak transcription	Stomach Smooth Muscle	stomach
3	chr3:143163800-143196400	Weak transcription	Fetal Stomach	stomach
4	chr3:143163800-143203400	Weak transcription	Ovary	ovary
5	chr3:143174400-143220400	Weak transcription	Fetal Lung	lung
6	chr3:143176800-143220400	Weak transcription	Brain Cingulate Gyrus	brain
7	chr3:143177200-143200800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr3:143177800-143204400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
9	chr3:143178000-143203200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
10	chr3:143179400-143220400	Weak transcription	Brain Substantia Nigra	brain
11	chr3:143179800-143213400	Weak transcription	Primary T helper cells PMA-I stimulated	--
12	chr3:143180200-143200600	Weak transcription	Aorta	Aorta
13	chr3:143184200-143196800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr3:143184200-143198600	Weak transcription	Colonic Mucosa	Colon
15	chr3:143185800-143213800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
16	chr3:143186000-143201200	Weak transcription	Adipose Nuclei	Adipose
17	chr3:143186000-143215600	Weak transcription	Primary T helper cells fromperipheralblood	blood
18	chr3:143186000-143223000	Weak transcription	Primary T cells fromperipheralblood	blood
19	chr3:143186400-143204400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
20	chr3:143191200-143196400	Weak transcription	HUES48 Cell Line	embryonic stem cell
21	chr3:143191200-143196400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
22	chr3:143191200-143196800	Weak transcription	Dnd41	blood
23	chr3:143191200-143197000	Weak transcription	HUES64 Cell Line	embryonic stem cell
24	chr3:143191200-143197000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr3:143191200-143211000	Weak transcription	Primary T cells from cord blood	blood
26	chr3:143191400-143196400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
27	chr3:143191400-143196600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
28	chr3:143191400-143231000	Weak transcription	Primary B cells from cord blood	blood
29	chr3:143191600-143197000	Weak transcription	H1 Cell Line	embryonic stem cell
30	chr3:143191800-143196200	Weak transcription	HUES6 Cell Line	embryonic stem cell
31	chr3:143192200-143196400	Weak transcription	K562	blood
32	chr3:143192400-143196200	Weak transcription	Primary B cells from peripheral blood	blood
33	chr3:143192400-143211400	Weak transcription	Monocytes-CD14+_RO01746	blood
34	chr3:143192400-143215200	Weak transcription	Primary monocytes fromperipheralblood	blood
35	chr3:143193200-143196400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
36	chr3:143193600-143198800	Weak transcription	Duodenum Mucosa	Duodenum
37	chr3:143193800-143198800	Weak transcription	Fetal Intestine Large	intestine

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