Variant report

Variant	rs9426929
Chromosome Location	chr1:155693399-155693400
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	chr1:155691136..155693112-chr1:155693289..155696050,2	K562	blood:

Variant related genes	Relation type
ENSG00000132676	Chromatin interaction

Extended variants
information (count: 55 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:45)

rs_ID	r²[population]
rs10908468	0.84[EUR][1000 genomes]
rs1094462	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs11803678	0.87[AFR][1000 genomes];0.90[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs13374129	0.95[EUR][1000 genomes]
rs1624846	0.82[AFR][1000 genomes];0.90[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs16837037	0.95[EUR][1000 genomes]
rs171167	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs17377506	0.84[EUR][1000 genomes]
rs1749417	0.84[AMR][1000 genomes]
rs1749421	0.82[AFR][1000 genomes];0.90[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs1765284	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1962247	1.00[EUR][1000 genomes]
rs2477541	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2686255	0.82[AFR][1000 genomes];0.90[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs28574887	0.95[EUR][1000 genomes]
rs2985708	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs348206	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs35044707	0.95[EUR][1000 genomes]
rs41264969	1.00[EUR][1000 genomes]
rs4253908	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4612618	0.95[EUR][1000 genomes]
rs4933	1.00[EUR][1000 genomes]
rs4971086	0.87[EUR][1000 genomes]
rs4971087	0.87[EUR][1000 genomes]
rs543854	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs548809	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs552778	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56758819	0.95[EUR][1000 genomes]
rs59706606	0.88[AFR][1000 genomes];0.90[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs59791187	0.95[EUR][1000 genomes]
rs61258690	0.90[EUR][1000 genomes]
rs621181	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs682020	0.90[AFR][1000 genomes];0.90[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs708612	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs73001021	0.95[EUR][1000 genomes]
rs7525057	0.95[EUR][1000 genomes]
rs7535158	0.95[EUR][1000 genomes]
rs822016	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs822018	0.81[AFR][1000 genomes];0.90[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs822019	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs822020	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs822022	0.82[AFR][1000 genomes];0.90[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs822026	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs822523	0.82[AMR][1000 genomes]
rs9427223	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv529709	chr1:155154933-155757219	Strong transcription Weak transcription Flanking Active TSS Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	450 gene(s)	inside rSNPs	diseases
2	esv33869	chr1:155223283-155917961	Flanking Active TSS Strong transcription Weak transcription Active TSS Bivalent/Poised TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	187 gene(s)	inside rSNPs	diseases
3	nsv1002390	chr1:155553423-155706930	Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
4	nsv428246	chr1:155558197-155785831	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
5	esv3381327	chr1:155582853-155718436	Enhancers Flanking Active TSS Strong transcription Weak transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
6	esv3436971	chr1:155618172-155733386	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
7	esv3338099	chr1:155618190-155733359	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
8	esv3423892	chr1:155664084-155901487	Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
9	nsv3065	chr1:155682768-155727524	Strong transcription Weak transcription Genic enhancers Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases
10	esv3412069	chr1:155693117-155693821	Strong transcription Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:124 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:155660200-155698800	Weak transcription	NHLF	lung
2	chr1:155660400-155706200	Weak transcription	Colonic Mucosa	Colon
3	chr1:155661600-155707800	Weak transcription	HUVEC	blood vessel
4	chr1:155663200-155701000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr1:155665200-155708000	Weak transcription	Placenta Amnion	Placenta Amnion
6	chr1:155665400-155695000	Weak transcription	Pancreas	Pancrea
7	chr1:155665400-155699000	Weak transcription	Right Ventricle	heart
8	chr1:155665600-155707200	Weak transcription	Psoas Muscle	Psoas
9	chr1:155665800-155707000	Weak transcription	Small Intestine	intestine
10	chr1:155669200-155702200	Weak transcription	Gastric	stomach
11	chr1:155672800-155698800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
12	chr1:155673200-155695000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
13	chr1:155673800-155707800	Weak transcription	Aorta	Aorta
14	chr1:155676000-155695000	Weak transcription	Skeletal Muscle Male	skeletal muscle
15	chr1:155676400-155695400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr1:155676400-155698600	Weak transcription	Stomach Mucosa	stomach
17	chr1:155676400-155706200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
18	chr1:155677400-155705200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr1:155679400-155710400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
20	chr1:155679800-155695200	Weak transcription	Fetal Brain Female	brain
21	chr1:155679800-155704200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
22	chr1:155681600-155696800	Weak transcription	Rectal Smooth Muscle	rectum
23	chr1:155681600-155707800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
24	chr1:155681800-155693600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr1:155682800-155697200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr1:155683000-155703200	Weak transcription	Spleen	Spleen
27	chr1:155683200-155695200	Weak transcription	Primary neutrophils fromperipheralblood	blood
28	chr1:155683200-155715000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr1:155683400-155699200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
30	chr1:155683400-155707800	Weak transcription	Fetal Heart	heart
31	chr1:155683800-155709000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
32	chr1:155683800-155715000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr1:155684000-155700000	Weak transcription	Rectal Mucosa Donor 31	rectum
34	chr1:155684000-155707800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
35	chr1:155685200-155704800	Strong transcription	Fetal Thymus	thymus
36	chr1:155685400-155698200	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr1:155686000-155695000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
38	chr1:155686200-155698800	Weak transcription	Fetal Kidney	kidney
39	chr1:155686600-155697600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr1:155686800-155697600	Strong transcription	Fetal Intestine Large	intestine
41	chr1:155687200-155694800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
42	chr1:155687200-155695200	Weak transcription	HSMM	muscle
43	chr1:155687200-155715000	Weak transcription	Esophagus	oesophagus
44	chr1:155687400-155694800	Weak transcription	Colon Smooth Muscle	Colon
45	chr1:155687400-155697000	Weak transcription	Primary B cells from cord blood	blood
46	chr1:155687600-155699200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
47	chr1:155688400-155705000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
48	chr1:155688400-155711200	Strong transcription	Fetal Muscle Leg	muscle
49	chr1:155688600-155695000	Strong transcription	Fetal Intestine Small	intestine
50	chr1:155688800-155710800	Strong transcription	Fetal Stomach	stomach

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