Variant report

Variant	rs6792734
Chromosome Location	chr3:150168336-150168337
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr3:150161430..150164240-chr3:150167006..150169731,3	K562	blood:
2	chr3:150125330..150128900-chr3:150162907..150168897,9	MCF-7	breast:
3	chr3:150168054..150172807-chr3:150173642..150176262,4	MCF-7	breast:
4	chr3:149955639..149959111-chr3:150165929..150170127,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000196428	Chromatin interaction
ENSG00000244541	Chromatin interaction

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

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs10513373	0.82[ASN][1000 genomes]
rs10513374	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10935800	0.81[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11711035	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11719977	0.84[AFR][1000 genomes];0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12638309	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12639090	0.96[ASN][1000 genomes]
rs13081231	0.98[ASN][1000 genomes]
rs13099758	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs13321876	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs16862627	0.82[ASN][1000 genomes]
rs16862644	0.82[ASN][1000 genomes]
rs4423794	0.81[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs4681203	0.98[ASN][1000 genomes]
rs4681204	0.82[ASN][1000 genomes]
rs4681205	0.82[ASN][1000 genomes]
rs4681206	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4681207	0.82[ASN][1000 genomes]
rs4681616	0.82[ASN][1000 genomes]
rs4681617	0.82[ASN][1000 genomes]
rs4681618	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs58628422	0.98[ASN][1000 genomes]
rs59793956	0.80[ASN][1000 genomes]
rs67319423	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6762432	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6784048	0.98[ASN][1000 genomes]
rs6795124	0.94[AMR][1000 genomes];0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs73165707	0.82[ASN][1000 genomes]
rs7427177	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7626725	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7651353	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7651989	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs9784335	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9826729	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9865031	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9882777	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[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	nsv877645	chr3:150103135-150212698	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	48 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:113 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:150132400-150175000	Weak transcription	Primary T cells fromperipheralblood	blood
2	chr3:150132400-150175000	Weak transcription	Placenta	Placenta
3	chr3:150134600-150174800	Weak transcription	Dnd41	blood
4	chr3:150135000-150175600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
5	chr3:150137200-150176200	Weak transcription	HepG2	liver
6	chr3:150140000-150171800	Weak transcription	Skeletal Muscle Male	skeletal muscle
7	chr3:150140000-150176200	Weak transcription	Fetal Stomach	stomach
8	chr3:150141400-150175200	Weak transcription	GM12878-XiMat	blood
9	chr3:150144200-150179000	Weak transcription	Aorta	Aorta
10	chr3:150149600-150176000	Weak transcription	Fetal Brain Female	brain
11	chr3:150151400-150171200	Weak transcription	Brain Anterior Caudate	brain
12	chr3:150151400-150171600	Weak transcription	Rectal Mucosa Donor 29	rectum
13	chr3:150152200-150168800	Weak transcription	Brain Inferior Temporal Lobe	brain
14	chr3:150152200-150171200	Weak transcription	Sigmoid Colon	Sigmoid Colon
15	chr3:150153000-150175600	Weak transcription	Right Ventricle	heart
16	chr3:150153600-150178200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
17	chr3:150153800-150176000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
18	chr3:150154000-150175800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
19	chr3:150154200-150176000	Weak transcription	H1 Cell Line	embryonic stem cell
20	chr3:150157800-150173000	Weak transcription	Brain Hippocampus Middle	brain
21	chr3:150158600-150178200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
22	chr3:150159800-150171600	Weak transcription	Brain Substantia Nigra	brain
23	chr3:150159800-150175600	Weak transcription	Thymus	Thymus
24	chr3:150159800-150176200	Weak transcription	Spleen	Spleen
25	chr3:150160200-150175800	Weak transcription	Fetal Muscle Trunk	muscle
26	chr3:150160400-150174800	Weak transcription	Primary B cells from peripheral blood	blood
27	chr3:150160600-150176200	Weak transcription	Esophagus	oesophagus
28	chr3:150160600-150178000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
29	chr3:150160800-150175200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
30	chr3:150160800-150175200	Weak transcription	Fetal Thymus	thymus
31	chr3:150160800-150175800	Weak transcription	Fetal Muscle Leg	muscle
32	chr3:150160800-150176200	Weak transcription	Fetal Kidney	kidney
33	chr3:150160800-150176200	Weak transcription	Gastric	stomach
34	chr3:150161200-150174800	Weak transcription	Duodenum Mucosa	Duodenum
35	chr3:150161400-150168600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
36	chr3:150162000-150168600	Weak transcription	Primary monocytes fromperipheralblood	blood
37	chr3:150162000-150168800	Weak transcription	Rectal Mucosa Donor 31	rectum
38	chr3:150162200-150175000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
39	chr3:150162400-150174600	Weak transcription	Primary hematopoietic stem cells	blood
40	chr3:150162400-150174800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr3:150162600-150168400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr3:150164400-150169600	Enhancers	Hela-S3	cervix
43	chr3:150164400-150169600	Enhancers	Osteobl	bone
44	chr3:150164600-150169200	Enhancers	NHEK	skin
45	chr3:150164600-150169600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr3:150164800-150169400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr3:150164800-150169600	Enhancers	HSMMtube	muscle
48	chr3:150164800-150169600	Enhancers	NHLF	lung
49	chr3:150165000-150169000	Enhancers	HMEC	breast
50	chr3:150165200-150169400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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