Variant report

Variant	rs6833514
Chromosome Location	chr4:79495309-79495310
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr4:79494956..79497942-chr4:79518671..79521873,3	K562	blood:
2	chr4:79494191..79497379-chr4:79578006..79580422,3	K562	blood:
3	chr4:79473071..79475678-chr4:79493342..79496132,3	K562	blood:
4	chr4:79488302..79490787-chr4:79493222..79497094,3	K562	blood:

Variant related genes	Relation type
ENSG00000138772	Chromatin interaction

Extended variants
information (count: 27 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10003947	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11098257	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12509033	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12641838	0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12642521	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs13126934	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1472365	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1587223	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1874486	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1874487	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1874488	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1995062	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2867462	0.96[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs3805174	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs3805175	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4466067	0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6533804	0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6851992	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7654600	0.94[AMR][1000 genomes];0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7656476	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7679218	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7682502	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7683399	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7683582	0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs867677	0.95[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs950699	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1009633	chr4:78887573-79652236	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:51 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:79474400-79527200	Weak transcription	Spleen	Spleen
2	chr4:79481800-79521000	Weak transcription	Right Ventricle	heart
3	chr4:79482800-79505000	Weak transcription	Fetal Lung	lung
4	chr4:79483000-79530000	Weak transcription	H9 Cell Line	embryonic stem cell
5	chr4:79488400-79505800	Weak transcription	Lung	lung
6	chr4:79488400-79508000	Weak transcription	Gastric	stomach
7	chr4:79488400-79523600	Weak transcription	Esophagus	oesophagus
8	chr4:79488400-79527400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr4:79488600-79512200	Weak transcription	Rectal Mucosa Donor 29	rectum
10	chr4:79489200-79502800	Weak transcription	Rectal Mucosa Donor 31	rectum
11	chr4:79489200-79504400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr4:79489800-79513600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr4:79490000-79523400	Weak transcription	Colon Smooth Muscle	Colon
14	chr4:79490600-79505800	Weak transcription	Stomach Mucosa	stomach
15	chr4:79490600-79521000	Weak transcription	Fetal Heart	heart
16	chr4:79490800-79495400	Weak transcription	HUES64 Cell Line	embryonic stem cell
17	chr4:79490800-79499400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
18	chr4:79490800-79532600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr4:79491000-79500200	Weak transcription	Stomach Smooth Muscle	stomach
20	chr4:79491000-79501800	Weak transcription	Fetal Stomach	stomach
21	chr4:79491000-79505600	Weak transcription	Placenta	Placenta
22	chr4:79491000-79506000	Weak transcription	Pancreas	Pancrea
23	chr4:79491000-79506000	Weak transcription	Sigmoid Colon	Sigmoid Colon
24	chr4:79491000-79507000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
25	chr4:79491000-79508000	Weak transcription	Adipose Nuclei	Adipose
26	chr4:79491000-79510200	Weak transcription	Skeletal Muscle Male	skeletal muscle
27	chr4:79491000-79512200	Weak transcription	Rectal Smooth Muscle	rectum
28	chr4:79491000-79529600	Weak transcription	Aorta	Aorta
29	chr4:79491200-79505800	Strong transcription	NHEK	skin
30	chr4:79491200-79507600	Weak transcription	HUES48 Cell Line	embryonic stem cell
31	chr4:79491200-79535400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
32	chr4:79491400-79507600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
33	chr4:79491600-79497000	Strong transcription	Fetal Intestine Large	intestine
34	chr4:79491600-79500200	Weak transcription	Placenta Amnion	Placenta Amnion
35	chr4:79491600-79504800	Weak transcription	Duodenum Smooth Muscle	Duodenum
36	chr4:79491600-79512000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr4:79491800-79499200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr4:79491800-79502000	Strong transcription	Primary neutrophils fromperipheralblood	blood
39	chr4:79491800-79533200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr4:79491800-79542600	Weak transcription	NH-A	brain
41	chr4:79492000-79531600	Strong transcription	HMEC	breast
42	chr4:79492200-79495800	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr4:79492200-79496200	Strong transcription	HUVEC	blood vessel
44	chr4:79493200-79499400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
45	chr4:79493400-79496000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
46	chr4:79493400-79500200	Weak transcription	Hela-S3	cervix
47	chr4:79494400-79495800	Strong transcription	Fetal Intestine Small	intestine
48	chr4:79494600-79496000	Strong transcription	HUES6 Cell Line	embryonic stem cell
49	chr4:79494600-79496200	Strong transcription	A549	lung
50	chr4:79494800-79495600	Strong transcription	Left Ventricle	heart

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