Variant report

Variant	rs4603103
Chromosome Location	chr1:165705788-165705789
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	chr1:165699676..165701483-chr1:165703927..165706866,2	K562	blood:

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs10800153	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10800154	0.98[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs10800155	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10918274	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs12133745	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12691499	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12691500	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1547725	0.82[AMR][1000 genomes]
rs2790049	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2790052	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2790053	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2814463	0.83[ASN][1000 genomes]
rs2814471	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28504591	0.87[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs4233408	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4537525	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4656460	0.82[AMR][1000 genomes]
rs4656461	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4657471	0.81[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4657472	0.82[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs4657474	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4657475	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4657476	0.81[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4657477	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6426936	0.86[AMR][1000 genomes]
rs6660601	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6662839	0.81[AFR][1000 genomes];0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6668108	0.81[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6668885	0.86[EUR][1000 genomes]
rs6696454	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs71628393	0.83[ASN][1000 genomes]
rs7518099	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7524755	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7528177	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7555523	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2756102	chr1:165652342-165877342	Weak transcription Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
2	nsv1011720	chr1:165669589-165802516	Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers Genic enhancers Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:119 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:165685200-165721600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr1:165687600-165706000	Weak transcription	HepG2	liver
3	chr1:165687600-165709800	Weak transcription	HUES48 Cell Line	embryonic stem cell
4	chr1:165687600-165709800	Weak transcription	HUVEC	blood vessel
5	chr1:165687600-165737600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
6	chr1:165687800-165707000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr1:165687800-165709800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
8	chr1:165690200-165710800	Weak transcription	Pancreatic Islets	Pancreatic Islet
9	chr1:165691000-165710000	Weak transcription	Fetal Kidney	kidney
10	chr1:165693400-165709600	Weak transcription	Colon Smooth Muscle	Colon
11	chr1:165693800-165706000	Weak transcription	Sigmoid Colon	Sigmoid Colon
12	chr1:165694000-165706000	Weak transcription	Rectal Smooth Muscle	rectum
13	chr1:165694000-165708600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
14	chr1:165694000-165709800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
15	chr1:165694000-165709800	Weak transcription	Brain Substantia Nigra	brain
16	chr1:165694000-165711800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
17	chr1:165694200-165709800	Weak transcription	Colonic Mucosa	Colon
18	chr1:165694200-165709800	Weak transcription	Pancreas	Pancrea
19	chr1:165694200-165709800	Weak transcription	Spleen	Spleen
20	chr1:165694200-165710000	Weak transcription	NHEK	skin
21	chr1:165694200-165721600	Weak transcription	Aorta	Aorta
22	chr1:165694200-165721600	Weak transcription	Esophagus	oesophagus
23	chr1:165694400-165705800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
24	chr1:165694400-165721600	Strong transcription	Primary T helper cells fromperipheralblood	blood
25	chr1:165694600-165709800	Weak transcription	Placenta Amnion	Placenta Amnion
26	chr1:165694600-165711000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr1:165694600-165711000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
28	chr1:165694600-165736800	Strong transcription	Monocytes-CD14+_RO01746	blood
29	chr1:165694800-165709800	Weak transcription	Small Intestine	intestine
30	chr1:165695600-165708600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr1:165695600-165709800	Weak transcription	Brain Angular Gyrus	brain
32	chr1:165695800-165712000	Weak transcription	Psoas Muscle	Psoas
33	chr1:165696000-165709800	Weak transcription	HUES6 Cell Line	embryonic stem cell
34	chr1:165696000-165721600	Weak transcription	Gastric	stomach
35	chr1:165696400-165709200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
36	chr1:165696600-165706800	Weak transcription	Fetal Heart	heart
37	chr1:165696800-165709800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
38	chr1:165696800-165709800	Weak transcription	Brain Germinal Matrix	brain
39	chr1:165696800-165709800	Weak transcription	NHLF	lung
40	chr1:165697200-165709800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
41	chr1:165697200-165710400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
42	chr1:165697400-165706000	Weak transcription	Fetal Brain Female	brain
43	chr1:165697400-165708400	Weak transcription	Brain Hippocampus Middle	brain
44	chr1:165697400-165709000	Weak transcription	Stomach Smooth Muscle	stomach
45	chr1:165697400-165709600	Weak transcription	Brain Cingulate Gyrus	brain
46	chr1:165697400-165709800	Weak transcription	HUES64 Cell Line	embryonic stem cell
47	chr1:165697400-165709800	Weak transcription	Brain Inferior Temporal Lobe	brain
48	chr1:165697400-165709800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
49	chr1:165697400-165709800	Weak transcription	Skeletal Muscle Female	skeletal muscle
50	chr1:165697400-165709800	Weak transcription	HMEC	breast

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