Variant report

Variant	rs35313553
Chromosome Location	chr4:110371285-110371286
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 52 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:49)

rs_ID	r²[population]
rs10016533	0.97[EUR][1000 genomes]
rs10025781	0.93[EUR][1000 genomes]
rs10452150	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13110999	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13122093	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13132816	0.93[EUR][1000 genomes]
rs13133491	0.93[EUR][1000 genomes]
rs13140373	0.93[EUR][1000 genomes]
rs13151464	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13151516	0.93[EUR][1000 genomes]
rs15821	0.84[AFR][1000 genomes];0.93[EUR][1000 genomes]
rs33911248	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs34132975	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs34133579	0.84[AFR][1000 genomes];0.93[EUR][1000 genomes]
rs34320670	1.00[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs34368920	0.82[EUR][1000 genomes]
rs34473874	0.85[EUR][1000 genomes]
rs34502105	0.93[EUR][1000 genomes]
rs34660885	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs34710885	0.84[AFR][1000 genomes];0.93[EUR][1000 genomes]
rs34727629	0.84[AFR][1000 genomes];0.93[EUR][1000 genomes]
rs34813537	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs34851707	0.93[EUR][1000 genomes]
rs34861128	0.90[EUR][1000 genomes]
rs34953524	0.84[AFR][1000 genomes];0.93[EUR][1000 genomes]
rs35199349	0.93[EUR][1000 genomes]
rs35273490	0.81[EUR][1000 genomes]
rs35329136	0.93[EUR][1000 genomes]
rs35450490	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs35598950	0.93[EUR][1000 genomes]
rs35699695	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs35829490	0.83[AFR][1000 genomes];0.90[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs35865655	0.84[EUR][1000 genomes]
rs35866656	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs35950484	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs36102563	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs41277037	0.93[EUR][1000 genomes]
rs6533427	0.81[EUR][1000 genomes]
rs6533434	0.82[EUR][1000 genomes]
rs66493839	0.93[EUR][1000 genomes]
rs67066117	0.89[EUR][1000 genomes]
rs67727505	0.83[AFR][1000 genomes];0.90[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs67923759	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6828719	0.84[EUR][1000 genomes]
rs6834685	0.82[EUR][1000 genomes]
rs71603034	0.92[EUR][1000 genomes]
rs71603035	0.84[EUR][1000 genomes]
rs72672698	0.84[EUR][1000 genomes]
rs7694710	0.92[EUR][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	nsv461613	chr4:109922064-110593460	Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Strong transcription Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
2	nsv595129	chr4:109922064-110593460	Strong transcription Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
3	esv3349784	chr4:110348873-110723163	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	35 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:110358000-110372000	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr4:110358000-110384000	Weak transcription	Fetal Brain Male	brain
3	chr4:110358000-110384200	Weak transcription	Colonic Mucosa	Colon
4	chr4:110358600-110378600	Weak transcription	Brain Cingulate Gyrus	brain
5	chr4:110360400-110384200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
6	chr4:110363000-110384200	Weak transcription	Esophagus	oesophagus
7	chr4:110363600-110372000	Weak transcription	K562	blood
8	chr4:110363600-110383600	Weak transcription	Pancreas	Pancrea
9	chr4:110363600-110383600	Weak transcription	NHDF-Ad	bronchial
10	chr4:110363600-110384200	Weak transcription	Rectal Smooth Muscle	rectum
11	chr4:110363600-110384200	Weak transcription	Hela-S3	cervix
12	chr4:110363600-110398400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr4:110364600-110384200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
14	chr4:110365000-110372000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
15	chr4:110365000-110383400	Weak transcription	Fetal Heart	heart
16	chr4:110365000-110384000	Weak transcription	Placenta Amnion	Placenta Amnion
17	chr4:110365200-110384200	Weak transcription	Aorta	Aorta
18	chr4:110366000-110391400	Weak transcription	Small Intestine	intestine
19	chr4:110367200-110373600	Strong transcription	NHEK	skin
20	chr4:110367200-110373800	Strong transcription	HSMM	muscle
21	chr4:110367400-110383600	Weak transcription	HUVEC	blood vessel
22	chr4:110367600-110372000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr4:110367600-110372400	Weak transcription	Psoas Muscle	Psoas
24	chr4:110367600-110373400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
25	chr4:110367600-110374200	Weak transcription	Gastric	stomach
26	chr4:110367600-110375000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr4:110367600-110375600	Weak transcription	Brain Substantia Nigra	brain
28	chr4:110367600-110376800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr4:110367600-110383200	Weak transcription	Right Ventricle	heart
30	chr4:110367600-110383800	Weak transcription	NHLF	lung
31	chr4:110367600-110384000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
32	chr4:110367600-110384200	Weak transcription	H1 Cell Line	embryonic stem cell
33	chr4:110367600-110384200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr4:110367600-110384200	Weak transcription	Brain Germinal Matrix	brain
35	chr4:110367800-110372000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
36	chr4:110367800-110373400	Weak transcription	HUES48 Cell Line	embryonic stem cell
37	chr4:110367800-110375000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr4:110367800-110377400	Weak transcription	Pancreatic Islets	Pancreatic Islet
39	chr4:110367800-110380800	Weak transcription	Brain Angular Gyrus	brain
40	chr4:110367800-110383800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
41	chr4:110367800-110383800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
42	chr4:110367800-110384200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
43	chr4:110367800-110384200	Weak transcription	Fetal Kidney	kidney
44	chr4:110367800-110384200	Weak transcription	Osteobl	bone
45	chr4:110368000-110372600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr4:110368000-110374000	Weak transcription	Placenta	Placenta
47	chr4:110368000-110383400	Weak transcription	HMEC	breast
48	chr4:110368000-110383600	Weak transcription	HepG2	liver
49	chr4:110368000-110384200	Weak transcription	Muscle Satellite Cultured Cells	--
50	chr4:110368600-110383600	Weak transcription	Primary T killer memory cells from peripheral blood	blood

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