Variant report

Variant	rs17217765
Chromosome Location	chr2:47637147-47637148
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:47635783..47639666-chr2:47641286..47645571,5	K562	blood:

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs17217912	0.92[AMR][1000 genomes];0.80[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs17224213	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs17224311	0.81[AFR][1000 genomes];0.92[AMR][1000 genomes];0.82[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1863332	0.90[ASN][1000 genomes]
rs34519172	0.87[AMR][1000 genomes];0.82[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs36225899	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs3963351	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4952887	0.96[ASN][1000 genomes]
rs4952888	0.87[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs58011858	0.89[ASN][1000 genomes]
rs61348463	0.97[EUR][1000 genomes]
rs61493074	0.95[EUR][1000 genomes]
rs62139708	0.89[ASN][1000 genomes]
rs7558107	0.95[EUR][1000 genomes]
rs7572133	0.92[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv817517	chr2:46819371-47715140	Enhancers Weak transcription Genic enhancers Bivalent Enhancer Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	152 gene(s)	inside rSNPs	diseases
2	nsv1004828	chr2:47056849-47814482	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	144 gene(s)	inside rSNPs	diseases
3	nsv531348	chr2:47433147-47827310	Flanking Bivalent TSS/Enh Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
4	nsv999576	chr2:47506116-47773960	Weak transcription Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	43 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:124 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:47631200-47642000	Weak transcription	Aorta	Aorta
2	chr2:47631400-47657400	Weak transcription	HSMMtube	muscle
3	chr2:47631400-47697000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
4	chr2:47631400-47714400	Weak transcription	Right Ventricle	heart
5	chr2:47631600-47637200	Weak transcription	Adipose Nuclei	Adipose
6	chr2:47631600-47637400	Weak transcription	Sigmoid Colon	Sigmoid Colon
7	chr2:47631600-47638600	Weak transcription	Gastric	stomach
8	chr2:47631600-47639400	Weak transcription	Liver	Liver
9	chr2:47631600-47657400	Weak transcription	Skeletal Muscle Female	skeletal muscle
10	chr2:47631800-47637200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr2:47631800-47637200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr2:47631800-47637200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr2:47631800-47637200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
14	chr2:47631800-47637200	Weak transcription	Brain Anterior Caudate	brain
15	chr2:47631800-47637200	Weak transcription	Duodenum Mucosa	Duodenum
16	chr2:47631800-47637200	Weak transcription	Rectal Mucosa Donor 29	rectum
17	chr2:47631800-47637200	Weak transcription	Monocytes-CD14+_RO01746	blood
18	chr2:47631800-47637400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
19	chr2:47631800-47637400	Weak transcription	Stomach Smooth Muscle	stomach
20	chr2:47631800-47638000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr2:47631800-47638200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr2:47631800-47638200	Weak transcription	Placenta Amnion	Placenta Amnion
23	chr2:47631800-47638400	Weak transcription	Duodenum Smooth Muscle	Duodenum
24	chr2:47631800-47638600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
25	chr2:47631800-47638600	Weak transcription	Placenta	Placenta
26	chr2:47631800-47638800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
27	chr2:47631800-47638800	Weak transcription	Brain Cingulate Gyrus	brain
28	chr2:47631800-47638800	Weak transcription	Ovary	ovary
29	chr2:47631800-47638800	Weak transcription	Skeletal Muscle Male	skeletal muscle
30	chr2:47631800-47639000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
31	chr2:47631800-47639000	Weak transcription	Rectal Mucosa Donor 31	rectum
32	chr2:47631800-47639200	Weak transcription	Fetal Kidney	kidney
33	chr2:47631800-47639200	Weak transcription	Left Ventricle	heart
34	chr2:47631800-47639600	Weak transcription	HUVEC	blood vessel
35	chr2:47631800-47640400	Weak transcription	Brain Substantia Nigra	brain
36	chr2:47631800-47640800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr2:47631800-47640800	Weak transcription	NH-A	brain
38	chr2:47631800-47641000	Weak transcription	HMEC	breast
39	chr2:47631800-47642000	Weak transcription	Colon Smooth Muscle	Colon
40	chr2:47631800-47642000	Weak transcription	Spleen	Spleen
41	chr2:47631800-47642600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr2:47631800-47643000	Weak transcription	NHDF-Ad	bronchial
43	chr2:47631800-47643200	Weak transcription	HSMM	muscle
44	chr2:47631800-47643400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr2:47631800-47643400	Weak transcription	Fetal Heart	heart
46	chr2:47631800-47643800	Weak transcription	Osteobl	bone
47	chr2:47631800-47646000	Weak transcription	Brain Inferior Temporal Lobe	brain
48	chr2:47631800-47647400	Weak transcription	Primary monocytes fromperipheralblood	blood
49	chr2:47631800-47649000	Weak transcription	Muscle Satellite Cultured Cells	--
50	chr2:47631800-47649200	Weak transcription	NHEK	skin

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