Variant report

Variant	rs35123416
Chromosome Location	chr4:56887194-56887195
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:56883307..56884980-chr4:56885984..56888736,2	K562	blood:

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

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs11133419	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11724411	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11726419	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11731842	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11732545	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11734217	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11934142	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11937929	0.91[AFR][1000 genomes];0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11945709	0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12642567	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12645491	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs13121634	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs13127483	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs13129197	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2290014	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs28507080	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs28610174	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs3214045	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs35003282	0.88[AFR][1000 genomes];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs35814086	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3806749	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4499751	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs59511278	0.89[ASN][1000 genomes]
rs62308565	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs62308614	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs62308617	0.89[ASN][1000 genomes]
rs62308621	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6814923	0.90[EUR][1000 genomes]
rs6815354	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6823178	0.89[ASN][1000 genomes]
rs6830668	0.90[EUR][1000 genomes]
rs6849999	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7670026	0.88[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9312668	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2755990	chr4:56317136-57143037	Strong transcription Weak transcription Flanking Bivalent TSS/Enh Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	40 gene(s)	inside rSNPs	diseases
2	nsv1005845	chr4:56522075-56980357	Active TSS Bivalent Enhancer Weak transcription Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
3	nsv427681	chr4:56651921-56908209	Strong transcription ZNF genes & repeats Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:121 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:56816200-56887800	Weak transcription	Gastric	stomach
2	chr4:56816400-56890800	Weak transcription	Colon Smooth Muscle	Colon
3	chr4:56816600-56890600	Weak transcription	Brain Hippocampus Middle	brain
4	chr4:56816600-56896400	Weak transcription	Fetal Heart	heart
5	chr4:56819000-56897400	Weak transcription	HSMMtube	muscle
6	chr4:56819200-56890600	Weak transcription	NHLF	lung
7	chr4:56820600-56892400	Weak transcription	Hela-S3	cervix
8	chr4:56823600-56893800	Weak transcription	HMEC	breast
9	chr4:56829600-56890600	Weak transcription	A549	lung
10	chr4:56835400-56904800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr4:56837200-56905000	Weak transcription	Brain Substantia Nigra	brain
12	chr4:56839800-56896600	Weak transcription	Brain Angular Gyrus	brain
13	chr4:56842800-56890800	Weak transcription	Osteobl	bone
14	chr4:56844200-56891000	Weak transcription	Colonic Mucosa	Colon
15	chr4:56847200-56891000	Weak transcription	Right Ventricle	heart
16	chr4:56852600-56890600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr4:56856200-56892600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
18	chr4:56856400-56889200	Strong transcription	Primary monocytes fromperipheralblood	blood
19	chr4:56857600-56897400	Strong transcription	Fetal Thymus	thymus
20	chr4:56857600-56898200	Strong transcription	Dnd41	blood
21	chr4:56857600-56898200	Strong transcription	Monocytes-CD14+_RO01746	blood
22	chr4:56858200-56889200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr4:56859600-56889200	Strong transcription	Primary T cells from cord blood	blood
24	chr4:56861200-56889400	Strong transcription	Primary T helper cells fromperipheralblood	blood
25	chr4:56863200-56892600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
26	chr4:56864600-56894200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
27	chr4:56864800-56892200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
28	chr4:56865400-56894400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
29	chr4:56866200-56895000	Weak transcription	Lung	lung
30	chr4:56866800-56890600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr4:56866800-56890600	Weak transcription	Skeletal Muscle Female	skeletal muscle
32	chr4:56866800-56891000	Weak transcription	Esophagus	oesophagus
33	chr4:56866800-56896000	Weak transcription	Small Intestine	intestine
34	chr4:56867000-56895000	Weak transcription	Psoas Muscle	Psoas
35	chr4:56867200-56892200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
36	chr4:56869000-56891200	Weak transcription	Fetal Brain Male	brain
37	chr4:56872200-56889400	Strong transcription	Primary T cells fromperipheralblood	blood
38	chr4:56872200-56893200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr4:56872200-56904800	Weak transcription	HepG2	liver
40	chr4:56873400-56897000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
41	chr4:56874400-56887800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
42	chr4:56874800-56890600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
43	chr4:56875400-56889800	Strong transcription	Primary B cells from cord blood	blood
44	chr4:56875600-56887600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr4:56876400-56887800	Strong transcription	Duodenum Mucosa	Duodenum
46	chr4:56876600-56895400	Weak transcription	Brain Anterior Caudate	brain
47	chr4:56876800-56887800	Weak transcription	Fetal Brain Female	brain
48	chr4:56879000-56892800	Weak transcription	NHEK	skin
49	chr4:56879200-56890600	Weak transcription	Stomach Smooth Muscle	stomach
50	chr4:56879200-56893400	Weak transcription	Placenta Amnion	Placenta Amnion

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