Variant report

Variant	rs4834705
Chromosome Location	chr4:119733323-119733324
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr4:119708422..119711280-chr4:119731156..119733832,2	K562	blood:
2	chr4:119733285..119736755-chr4:119749936..119754070,3	K562	blood:
3	chr4:119732984..119735511-chr4:119760384..119762746,2	K562	blood:
4	chr4:119728433..119730857-chr4:119731911..119734285,2	K562	blood:

Extended variants
information (count: 28 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs1019696	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11098453	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11098459	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11098460	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12512594	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12643205	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs13112913	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13139244	0.94[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1365549	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1365550	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1365551	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1962840	0.89[AFR][1000 genomes];0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2303512	0.97[AMR][1000 genomes];0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2389688	0.85[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs34057511	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs35934778	0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs36096663	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3775839	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3775840	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4833592	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4833593	0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4834704	0.93[AMR][1000 genomes];0.87[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs4834706	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6811006	0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6817084	0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7375858	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.86[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	nsv519017	chr4:118828807-119771481	Strong transcription Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
2	esv3355840	chr4:119296640-119774737	Strong transcription Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS 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 target site	20 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:119703800-119738200	Strong transcription	Placenta	Placenta
2	chr4:119704200-119740000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr4:119704800-119735200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr4:119705200-119748200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
5	chr4:119712400-119739000	Strong transcription	Fetal Muscle Leg	muscle
6	chr4:119713800-119739600	Strong transcription	Fetal Muscle Trunk	muscle
7	chr4:119714000-119738200	Strong transcription	Duodenum Mucosa	Duodenum
8	chr4:119714000-119739000	Strong transcription	HSMM	muscle
9	chr4:119714000-119739200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
10	chr4:119714400-119740200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr4:119714600-119737800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr4:119715200-119733800	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr4:119715800-119734200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr4:119716200-119736000	Weak transcription	A549	lung
15	chr4:119716200-119738000	Strong transcription	Rectal Mucosa Donor 29	rectum
16	chr4:119716400-119737200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr4:119716800-119738600	Strong transcription	GM12878-XiMat	blood
18	chr4:119717600-119737600	Strong transcription	Fetal Intestine Large	intestine
19	chr4:119718200-119735000	Weak transcription	Brain Anterior Caudate	brain
20	chr4:119718200-119739600	Weak transcription	Brain Germinal Matrix	brain
21	chr4:119718400-119734800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr4:119718400-119756000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
23	chr4:119718600-119734200	Weak transcription	Fetal Brain Female	brain
24	chr4:119718600-119736200	Weak transcription	Brain Cingulate Gyrus	brain
25	chr4:119718600-119744200	Weak transcription	Hela-S3	cervix
26	chr4:119718600-119753600	Weak transcription	Fetal Heart	heart
27	chr4:119719000-119756200	Weak transcription	Fetal Brain Male	brain
28	chr4:119719600-119737000	Strong transcription	Duodenum Smooth Muscle	Duodenum
29	chr4:119720600-119738200	Strong transcription	NH-A	brain
30	chr4:119722600-119737600	Strong transcription	HUVEC	blood vessel
31	chr4:119722800-119738600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
32	chr4:119723000-119738000	Strong transcription	Rectal Mucosa Donor 31	rectum
33	chr4:119723200-119738600	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr4:119723600-119738800	Strong transcription	Dnd41	blood
35	chr4:119724000-119737600	Strong transcription	Primary T helper cells fromperipheralblood	blood
36	chr4:119724000-119748200	Weak transcription	Psoas Muscle	Psoas
37	chr4:119724600-119737400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr4:119724600-119738200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr4:119724800-119735000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
40	chr4:119725000-119737400	Strong transcription	Placenta Amnion	Placenta Amnion
41	chr4:119725400-119737200	Strong transcription	Stomach Smooth Muscle	stomach
42	chr4:119725400-119738600	Strong transcription	HUES6 Cell Line	embryonic stem cell
43	chr4:119725400-119738600	Strong transcription	iPS-18 Cell Line	embryonic stem cell
44	chr4:119725400-119739000	Strong transcription	HUES64 Cell Line	embryonic stem cell
45	chr4:119725600-119738600	Strong transcription	HUES48 Cell Line	embryonic stem cell
46	chr4:119725600-119738800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
47	chr4:119725800-119736600	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr4:119725800-119737200	Strong transcription	Primary T helper cells PMA-I stimulated	--
49	chr4:119725800-119737400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
50	chr4:119725800-119737600	Strong transcription	Fetal Stomach	stomach

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