Variant report

Variant	rs56371666
Chromosome Location	chr1:179294425-179294426
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:179279773..179281355-chr1:179292902..179294753,2	K562	blood:

Extended variants
information (count: 34 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs10798655	0.84[ASN][1000 genomes]
rs12725375	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12749666	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2050450	0.91[ASN][1000 genomes]
rs2050451	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2152318	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2247061	0.94[ASN][1000 genomes]
rs2248979	0.83[AFR][1000 genomes];0.95[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2250352	0.87[AFR][1000 genomes];0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2250477	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2254214	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2254580	0.91[ASN][1000 genomes]
rs2254623	0.94[AFR][1000 genomes];0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2257089	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2257100	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2484440	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2484443	0.81[AFR][1000 genomes];0.89[AMR][1000 genomes];0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2484446	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2492777	0.92[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2492778	0.97[AFR][1000 genomes];0.94[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2493116	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2493117	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2493118	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2493119	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2783391	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2783392	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2783393	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs404818	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs433722	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4652364	0.93[AFR][1000 genomes];0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs61824366	0.93[AFR][1000 genomes];0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6425530	0.90[AMR][1000 genomes];0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7523431	0.94[AFR][1000 genomes];0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][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	nsv1005278	chr1:179197645-179371395	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region miRNA target site	16 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:98 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:179263800-179304600	Weak transcription	Lung	lung
2	chr1:179263800-179306400	Weak transcription	Gastric	stomach
3	chr1:179264600-179304600	Weak transcription	Right Ventricle	heart
4	chr1:179264600-179310200	Weak transcription	Brain Substantia Nigra	brain
5	chr1:179264600-179314000	Weak transcription	Brain Angular Gyrus	brain
6	chr1:179264600-179314000	Weak transcription	Brain Inferior Temporal Lobe	brain
7	chr1:179264800-179313800	Weak transcription	Brain Hippocampus Middle	brain
8	chr1:179264800-179313800	Weak transcription	Fetal Brain Female	brain
9	chr1:179264800-179334200	Weak transcription	Colon Smooth Muscle	Colon
10	chr1:179266400-179322800	Weak transcription	Small Intestine	intestine
11	chr1:179268400-179312000	Weak transcription	Fetal Thymus	thymus
12	chr1:179272600-179313800	Weak transcription	Brain Anterior Caudate	brain
13	chr1:179273000-179311600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
14	chr1:179273200-179294600	Weak transcription	Placenta	Placenta
15	chr1:179274600-179302400	Weak transcription	Left Ventricle	heart
16	chr1:179274600-179304400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
17	chr1:179274600-179306000	Weak transcription	Stomach Smooth Muscle	stomach
18	chr1:179275600-179311600	Weak transcription	HUVEC	blood vessel
19	chr1:179276400-179306200	Weak transcription	Fetal Muscle Trunk	muscle
20	chr1:179276600-179304800	Weak transcription	Pancreas	Pancrea
21	chr1:179276800-179295200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
22	chr1:179277600-179296400	Weak transcription	Rectal Mucosa Donor 31	rectum
23	chr1:179280400-179296200	Weak transcription	NH-A	brain
24	chr1:179280400-179314000	Weak transcription	NHLF	lung
25	chr1:179280600-179299000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr1:179281200-179300200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr1:179282000-179313000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
28	chr1:179282200-179295200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
29	chr1:179282400-179304200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr1:179282400-179313800	Weak transcription	HSMMtube	muscle
31	chr1:179283200-179298800	Weak transcription	HepG2	liver
32	chr1:179283200-179308600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr1:179286400-179313800	Weak transcription	Psoas Muscle	Psoas
34	chr1:179287200-179294800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
35	chr1:179287200-179297200	Weak transcription	Spleen	Spleen
36	chr1:179287400-179304400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
37	chr1:179287600-179299000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
38	chr1:179289000-179299200	Weak transcription	Fetal Stomach	stomach
39	chr1:179290000-179297800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
40	chr1:179290200-179297800	Strong transcription	Primary T cells fromperipheralblood	blood
41	chr1:179290200-179297800	Weak transcription	Fetal Intestine Small	intestine
42	chr1:179290200-179300000	Strong transcription	Primary T cells from cord blood	blood
43	chr1:179290200-179300200	Strong transcription	Hela-S3	cervix
44	chr1:179290400-179310000	Weak transcription	Aorta	Aorta
45	chr1:179290600-179298200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
46	chr1:179290600-179298600	Weak transcription	Primary hematopoietic stem cells	blood
47	chr1:179290600-179304200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
48	chr1:179290600-179308800	Weak transcription	Fetal Muscle Leg	muscle
49	chr1:179290800-179298600	Weak transcription	A549	lung
50	chr1:179290800-179298800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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