Variant report

Variant	rs34427316
Chromosome Location	chr8:126186427-126186428
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr8:126184359..126187803-chr8:126204598..126207522,3	K562	blood:
2	chr8:126183828..126186606-chr8:126190098..126191640,2	MCF-7	breast:
3	chr8:126184530..126188708-chr8:126189850..126192758,4	MCF-7	breast:
4	chr8:126184387..126187013-chr8:126442001..126443979,2	MCF-7	breast:
5	chr1:875400..877590-chr8:126185955..126188744,2	K562	blood:

Variant related genes	Relation type
ENSG00000187634	Chromatin interaction
ENSG00000173334	Chromatin interaction

Extended variants
information (count: 53 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:49)

rs_ID	r²[population]
rs12675943	0.84[EUR][1000 genomes]
rs13253942	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13254947	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13259062	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13262348	0.81[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs13264500	1.00[AFR][1000 genomes];0.94[EUR][1000 genomes]
rs13267325	1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13273034	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13273231	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13273421	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13277490	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16900452	1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17310558	1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17401283	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2384882	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34110249	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34246020	1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs34298715	1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34448805	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34461511	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34694976	0.81[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs34737949	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs34903473	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35033076	1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35140299	1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs35215140	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35336507	0.86[EUR][1000 genomes]
rs35401436	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35475899	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35564243	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35774093	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35822368	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs35861494	1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs35955519	0.86[EUR][1000 genomes]
rs35991395	1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs36081564	1.00[ASN][1000 genomes]
rs3923300	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4360308	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4477044	1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4601329	1.00[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs4871570	0.81[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs56135036	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs66561774	1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs66826725	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs66929016	0.92[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs71516763	0.92[ASN][1000 genomes]
rs71516769	1.00[AMR][1000 genomes];0.86[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs72720550	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72720569	0.88[EUR][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	nsv891434	chr8:125630655-126324432	Strong transcription Enhancers Weak transcription Active TSS Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	80 gene(s)	inside rSNPs	diseases
2	nsv949614	chr8:126063646-126376699	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
3	nsv917158	chr8:126101990-126255266	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	19 gene(s)	inside rSNPs	diseases
4	nsv1034798	chr8:126179383-126241525	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Strong transcription Active TSS	Chromatin interactive region	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:100 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:126118000-126191800	Weak transcription	Thymus	Thymus
2	chr8:126137600-126213600	Weak transcription	Fetal Stomach	stomach
3	chr8:126138000-126191000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
4	chr8:126138000-126197800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
5	chr8:126138200-126200400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr8:126138400-126200200	Weak transcription	Primary T cells fromperipheralblood	blood
7	chr8:126142600-126231400	Weak transcription	Stomach Smooth Muscle	stomach
8	chr8:126143000-126193200	Weak transcription	Left Ventricle	heart
9	chr8:126143200-126186800	Weak transcription	Adipose Nuclei	Adipose
10	chr8:126156600-126199800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
11	chr8:126158200-126186600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
12	chr8:126160600-126187400	Weak transcription	Gastric	stomach
13	chr8:126162200-126186600	Weak transcription	Colon Smooth Muscle	Colon
14	chr8:126163200-126193200	Weak transcription	Ovary	ovary
15	chr8:126164800-126186800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr8:126166000-126200200	Weak transcription	Dnd41	blood
17	chr8:126167000-126187000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
18	chr8:126167000-126200400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
19	chr8:126169800-126187200	Weak transcription	Colonic Mucosa	Colon
20	chr8:126170600-126200600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
21	chr8:126171000-126199200	Weak transcription	Primary T helper cells fromperipheralblood	blood
22	chr8:126172000-126187000	Weak transcription	Primary hematopoietic stem cells	blood
23	chr8:126172000-126201000	Weak transcription	Fetal Thymus	thymus
24	chr8:126172800-126186600	Weak transcription	Brain Angular Gyrus	brain
25	chr8:126173000-126186800	Weak transcription	Brain Cingulate Gyrus	brain
26	chr8:126173400-126187000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr8:126175800-126186600	Weak transcription	Hela-S3	cervix
28	chr8:126176200-126200400	Weak transcription	Primary B cells from peripheral blood	blood
29	chr8:126176600-126186600	Weak transcription	K562	blood
30	chr8:126179200-126194400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
31	chr8:126179200-126195800	Weak transcription	Esophagus	oesophagus
32	chr8:126179400-126187200	Weak transcription	Primary T helper cells PMA-I stimulated	--
33	chr8:126179400-126208800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
34	chr8:126179800-126193800	Weak transcription	Pancreas	Pancrea
35	chr8:126180000-126186600	Weak transcription	GM12878-XiMat	blood
36	chr8:126181200-126187400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
37	chr8:126181200-126188200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
38	chr8:126181800-126186800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
39	chr8:126181800-126200600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
40	chr8:126182000-126217600	Weak transcription	Fetal Kidney	kidney
41	chr8:126182200-126186800	Weak transcription	Duodenum Smooth Muscle	Duodenum
42	chr8:126182400-126186600	Weak transcription	Primary monocytes fromperipheralblood	blood
43	chr8:126182400-126186800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr8:126182400-126187000	Weak transcription	Right Atrium	heart
45	chr8:126182400-126201000	Weak transcription	HepG2	liver
46	chr8:126183400-126186600	Weak transcription	Small Intestine	intestine
47	chr8:126183800-126187000	Weak transcription	Psoas Muscle	Psoas
48	chr8:126184000-126200400	Weak transcription	Primary T cells from cord blood	blood
49	chr8:126184200-126187200	Weak transcription	Skeletal Muscle Male	skeletal muscle
50	chr8:126184600-126187400	Weak transcription	HUES48 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links