Variant report

Variant	rs56206629
Chromosome Location	chr9:95627310-95627311
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr9:95622406..95624700-chr9:95624887..95627823,2	MCF-7	breast:
2	chr9:95622113..95625066-chr9:95625770..95628383,4	K562	blood:
3	chr9:95616347..95619799-chr9:95626429..95628758,3	K562	blood:
4	chr9:95614976..95617847-chr9:95627258..95628901,2	K562	blood:

Variant related genes	Relation type
ENSG00000127081	Chromatin interaction

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs10435920	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10992485	0.91[EUR][1000 genomes]
rs10992502	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10992527	0.80[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs4076631	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs72741015	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7854940	0.83[EUR][1000 genomes];0.93[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	nsv831654	chr9:95542920-95720961	ZNF genes & repeats Flanking Active TSS Active TSS Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
2	nsv893574	chr9:95580376-95688099	Active TSS Weak transcription Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:95609000-95639800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr9:95611200-95632800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr9:95616200-95639800	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr9:95616400-95632800	Weak transcription	Gastric	stomach
5	chr9:95616400-95639800	Weak transcription	Small Intestine	intestine
6	chr9:95616600-95639600	Weak transcription	Placenta Amnion	Placenta Amnion
7	chr9:95618200-95630200	Weak transcription	Right Ventricle	heart
8	chr9:95618200-95639800	Weak transcription	Colonic Mucosa	Colon
9	chr9:95618400-95637600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
10	chr9:95618400-95638600	Weak transcription	K562	blood
11	chr9:95618600-95630400	Weak transcription	Skeletal Muscle Male	skeletal muscle
12	chr9:95618600-95630800	Weak transcription	Psoas Muscle	Psoas
13	chr9:95618600-95638000	Weak transcription	Brain Anterior Caudate	brain
14	chr9:95619600-95638600	Weak transcription	Brain Angular Gyrus	brain
15	chr9:95619800-95630200	Weak transcription	HepG2	liver
16	chr9:95620000-95630000	Weak transcription	HUVEC	blood vessel
17	chr9:95622400-95629800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
18	chr9:95622400-95630000	Weak transcription	HUES48 Cell Line	embryonic stem cell
19	chr9:95622400-95630000	Weak transcription	Muscle Satellite Cultured Cells	--
20	chr9:95622400-95630200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
21	chr9:95622400-95630800	Weak transcription	Skeletal Muscle Female	skeletal muscle
22	chr9:95622400-95631600	Weak transcription	Osteobl	bone
23	chr9:95622400-95632800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
24	chr9:95622400-95632800	Weak transcription	Thymus	Thymus
25	chr9:95622400-95635200	Weak transcription	Colon Smooth Muscle	Colon
26	chr9:95622400-95637600	Weak transcription	Brain Inferior Temporal Lobe	brain
27	chr9:95622400-95637800	Weak transcription	Hela-S3	cervix
28	chr9:95622400-95638000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr9:95622400-95638000	Weak transcription	Pancreatic Islets	Pancreatic Islet
30	chr9:95622400-95638600	Weak transcription	HMEC	breast
31	chr9:95622400-95638600	Weak transcription	NHDF-Ad	bronchial
32	chr9:95622400-95638800	Weak transcription	NHLF	lung
33	chr9:95622600-95627400	Weak transcription	Fetal Intestine Small	intestine
34	chr9:95622600-95627800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
35	chr9:95622600-95628000	Weak transcription	Lung	lung
36	chr9:95622600-95629000	Weak transcription	HUES6 Cell Line	embryonic stem cell
37	chr9:95622600-95629000	Weak transcription	HUES64 Cell Line	embryonic stem cell
38	chr9:95622600-95629000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
39	chr9:95622600-95629000	Weak transcription	Brain Germinal Matrix	brain
40	chr9:95622600-95629200	Weak transcription	A549	lung
41	chr9:95622600-95629800	Weak transcription	Rectal Mucosa Donor 31	rectum
42	chr9:95622600-95630000	Weak transcription	Primary monocytes fromperipheralblood	blood
43	chr9:95622600-95630000	Weak transcription	Primary neutrophils fromperipheralblood	blood
44	chr9:95622600-95630000	Weak transcription	Cortex derived primary cultured neurospheres	brain
45	chr9:95622600-95630200	Weak transcription	Brain Cingulate Gyrus	brain
46	chr9:95622600-95630200	Weak transcription	Placenta	Placenta
47	chr9:95622600-95630200	Weak transcription	NHEK	skin
48	chr9:95622600-95631600	Weak transcription	Fetal Lung	lung
49	chr9:95622600-95632600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
50	chr9:95622600-95632800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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