Variant report

Variant	rs134655
Chromosome Location	chr22:29487725-29487726
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr22:29486627..29489970-chr22:29658706..29660641,3	K562	blood:
2	chr22:29486742..29489044-chr22:29491221..29492780,2	K562	blood:

Variant related genes	Relation type
ENSG00000100263	Chromatin interaction

Extended variants
information (count: 42 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs126077	0.82[EUR][1000 genomes]
rs134566	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs134570	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs134580	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs134581	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs134583	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs134585	0.80[AMR][1000 genomes];0.85[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs134587	0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs134589	0.80[AMR][1000 genomes];0.88[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs134590	0.80[AMR][1000 genomes];0.88[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs134591	0.80[AMR][1000 genomes];0.88[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs134593	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs134597	0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs134611	0.97[ASN][1000 genomes]
rs134614	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs134615	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs134618	0.81[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs134627	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs134642	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs134646	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs134647	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs134649	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs134651	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs134652	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs134661	0.97[ASN][1000 genomes]
rs134662	0.97[ASN][1000 genomes]
rs134665	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs134678	0.82[EUR][1000 genomes]
rs134679	0.81[EUR][1000 genomes]
rs134680	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs134683	0.81[EUR][1000 genomes]
rs134684	0.81[EUR][1000 genomes]
rs134686	0.81[EUR][1000 genomes]
rs134688	0.81[EUR][1000 genomes]
rs134689	0.81[EUR][1000 genomes]
rs134690	0.81[EUR][1000 genomes]
rs134691	0.82[EUR][1000 genomes]
rs1978046	0.82[EUR][1000 genomes]
rs2049937	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2049938	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs5752870	0.82[AMR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv531586	chr22:29252132-29902266	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	46 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:54 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:29471400-29488000	Weak transcription	Right Ventricle	heart
2	chr22:29472400-29489000	Weak transcription	Fetal Intestine Small	intestine
3	chr22:29475000-29489200	Weak transcription	Fetal Intestine Large	intestine
4	chr22:29475600-29491000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr22:29475600-29505600	Weak transcription	Spleen	Spleen
6	chr22:29476400-29487800	Weak transcription	Brain Hippocampus Middle	brain
7	chr22:29476400-29489600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr22:29476600-29489400	Weak transcription	Psoas Muscle	Psoas
9	chr22:29476600-29491000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
10	chr22:29476800-29494800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr22:29478800-29489600	Weak transcription	Dnd41	blood
12	chr22:29478800-29490200	Weak transcription	Thymus	Thymus
13	chr22:29478800-29498200	Weak transcription	Brain Germinal Matrix	brain
14	chr22:29479600-29489200	Weak transcription	Fetal Kidney	kidney
15	chr22:29480400-29488000	Weak transcription	Fetal Thymus	thymus
16	chr22:29480600-29489600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr22:29480600-29498000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
18	chr22:29480800-29492400	Weak transcription	HUES6 Cell Line	embryonic stem cell
19	chr22:29483400-29550200	Weak transcription	Rectal Smooth Muscle	rectum
20	chr22:29485800-29492200	Weak transcription	K562	blood
21	chr22:29486000-29487800	Weak transcription	Left Ventricle	heart
22	chr22:29486000-29487800	Weak transcription	Lung	lung
23	chr22:29486000-29487800	Weak transcription	Pancreas	Pancrea
24	chr22:29486000-29487800	Weak transcription	Right Atrium	heart
25	chr22:29486000-29488000	Weak transcription	Gastric	stomach
26	chr22:29486000-29488000	Weak transcription	Skeletal Muscle Male	skeletal muscle
27	chr22:29486000-29489600	Weak transcription	Brain Angular Gyrus	brain
28	chr22:29486000-29489600	Weak transcription	Esophagus	oesophagus
29	chr22:29486000-29491000	Weak transcription	Colonic Mucosa	Colon
30	chr22:29486000-29492600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
31	chr22:29486200-29490800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr22:29486200-29491000	Weak transcription	Fetal Brain Female	brain
33	chr22:29486400-29487800	Weak transcription	Liver	Liver
34	chr22:29486400-29488000	Weak transcription	Duodenum Mucosa	Duodenum
35	chr22:29486400-29488000	Weak transcription	Rectal Mucosa Donor 31	rectum
36	chr22:29486400-29488200	Weak transcription	Stomach Mucosa	stomach
37	chr22:29486400-29488200	Weak transcription	HepG2	liver
38	chr22:29486400-29489400	Weak transcription	Brain Cingulate Gyrus	brain
39	chr22:29486600-29494800	Weak transcription	NHEK	skin
40	chr22:29486600-29519000	Weak transcription	Fetal Brain Male	brain
41	chr22:29487000-29489400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr22:29487200-29489000	Enhancers	Fetal Muscle Trunk	muscle
43	chr22:29487200-29490200	Enhancers	Fetal Muscle Leg	muscle
44	chr22:29487400-29489200	Enhancers	NHDF-Ad	bronchial
45	chr22:29487400-29489600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
46	chr22:29487600-29487800	Enhancers	Pancreatic Islets	Pancreatic Islet
47	chr22:29487600-29488400	Enhancers	Brain Anterior Caudate	brain
48	chr22:29487600-29488800	Enhancers	NHLF	lung
49	chr22:29487600-29489400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr22:29487600-29489800	Enhancers	Rectal Mucosa Donor 29	rectum

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