Variant report

Variant	rs56822355
Chromosome Location	chr1:185529260-185529261
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:185139306..185139973-chr1:185528908..185529803,2	MCF-7	breast:
2	chr1:185284911..185288305-chr1:185527011..185530807,5	MCF-7	breast:
3	chr1:185528036..185530199-chr1:185540176..185542231,2	MCF-7	breast:
4	chr1:185284990..185287378-chr1:185527957..185530692,5	MCF-7	breast:
5	chr1:185523762..185526492-chr1:185528261..185529807,2	MCF-7	breast:
6	chr1:185207686..185208214-chr1:185529005..185529598,2	MCF-7	breast:
7	chr1:185518755..185520867-chr1:185527549..185529971,2	K562	blood:
8	chr1:185528755..185530819-chr1:185535016..185536527,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000116679	Chromatin interaction
ENSG00000273004	Chromatin interaction

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs10911754	0.93[AFR][1000 genomes];0.95[AMR][1000 genomes];0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10911755	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10911756	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11576129	0.85[EUR][1000 genomes]
rs11576884	0.81[EUR][1000 genomes]
rs11581960	0.81[EUR][1000 genomes]
rs11583193	0.81[EUR][1000 genomes]
rs11586588	1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11586605	0.87[EUR][1000 genomes]
rs12029108	0.92[EUR][1000 genomes]
rs12048982	0.81[EUR][1000 genomes]
rs12402146	0.81[EUR][1000 genomes]
rs12402607	0.81[EUR][1000 genomes]
rs1321998	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1321999	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2295792	0.92[EUR][1000 genomes]
rs28776539	0.81[EUR][1000 genomes]
rs35495151	0.83[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs41453048	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs56164019	0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs57836721	0.96[AFR][1000 genomes];0.89[AMR][1000 genomes];0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs58678353	0.94[AFR][1000 genomes];0.95[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs58848006	0.99[AFR][1000 genomes];0.95[AMR][1000 genomes];0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6701720	0.82[ASN][1000 genomes]
rs72726098	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs72727706	1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs72727712	0.92[EUR][1000 genomes]
rs72727717	0.81[EUR][1000 genomes]
rs74132957	0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7518777	0.81[EUR][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	nsv548398	chr1:185136458-186003094	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	69 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:64 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:185521000-185533800	Weak transcription	Placenta	Placenta
2	chr1:185525400-185536000	Weak transcription	Stomach Mucosa	stomach
3	chr1:185526400-185533800	Weak transcription	Osteobl	bone
4	chr1:185526600-185530600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr1:185527600-185530400	Enhancers	Rectal Mucosa Donor 31	rectum
6	chr1:185527800-185529400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr1:185527800-185530000	Weak transcription	Left Ventricle	heart
8	chr1:185527800-185532400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
9	chr1:185528000-185536000	Weak transcription	Fetal Kidney	kidney
10	chr1:185528200-185531800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
11	chr1:185528400-185529400	Enhancers	Fetal Heart	heart
12	chr1:185528400-185530600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
13	chr1:185528400-185530600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
14	chr1:185528400-185530600	Enhancers	Primary T killer memory cells from peripheral blood	blood
15	chr1:185528400-185530800	Enhancers	Monocytes-CD14+_RO01746	blood
16	chr1:185528400-185531000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
17	chr1:185528400-185531200	Enhancers	Primary hematopoietic stem cells	blood
18	chr1:185528400-185531800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr1:185528400-185532400	Enhancers	Primary T helper cells fromperipheralblood	blood
20	chr1:185528600-185529600	Enhancers	Rectal Mucosa Donor 29	rectum
21	chr1:185528600-185529800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr1:185528600-185530800	Enhancers	Primary T helper naive cells from peripheral blood	blood
23	chr1:185528600-185530800	Enhancers	GM12878-XiMat	blood
24	chr1:185528600-185531000	Enhancers	Primary monocytes fromperipheralblood	blood
25	chr1:185528600-185531200	Enhancers	Primary T cells fromperipheralblood	blood
26	chr1:185528600-185531400	Enhancers	Primary hematopoietic stem cells short term culture	blood
27	chr1:185528600-185533000	Enhancers	Primary T cells from cord blood	blood
28	chr1:185528600-185539800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
29	chr1:185528800-185529400	Enhancers	iPS-15b Cell Line	embryonic stem cell
30	chr1:185528800-185529400	Enhancers	Adipose Nuclei	Adipose
31	chr1:185528800-185529400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
32	chr1:185528800-185529400	Enhancers	Fetal Intestine Small	intestine
33	chr1:185528800-185529400	Enhancers	Pancreas	Pancrea
34	chr1:185528800-185529400	Enhancers	Sigmoid Colon	Sigmoid Colon
35	chr1:185528800-185529600	Enhancers	Fetal Intestine Large	intestine
36	chr1:185528800-185530000	Enhancers	Brain Substantia Nigra	brain
37	chr1:185528800-185530400	Enhancers	Primary B cells from cord blood	blood
38	chr1:185528800-185530800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr1:185528800-185530800	Enhancers	Spleen	Spleen
40	chr1:185528800-185531000	Enhancers	Primary B cells from peripheral blood	blood
41	chr1:185528800-185531200	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
42	chr1:185528800-185531600	Enhancers	Fetal Thymus	thymus
43	chr1:185528800-185531800	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
44	chr1:185528800-185531800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
45	chr1:185528800-185531800	Enhancers	Thymus	Thymus
46	chr1:185528800-185532800	Enhancers	Primary T helper cells PMA-I stimulated	--
47	chr1:185529000-185529400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr1:185529000-185529400	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
49	chr1:185529000-185529400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
50	chr1:185529000-185529400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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