Variant report

Variant	rs72885545
Chromosome Location	chr2:172687191-172687192
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr2:172679219..172682051-chr2:172683706..172687568,3	K562	blood:
2	chr2:172673517..172675266-chr2:172684577..172687349,2	K562	blood:
3	chr2:172679219..172682051-chr2:172684647..172687568,2	K562	blood:

Extended variants
information (count: 34 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs12053046	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12614709	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12619041	0.94[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs12620126	0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12622772	0.96[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs12622895	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17581361	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs17581439	0.82[AFR][1000 genomes];0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs17615262	0.86[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2176465	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3736499	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3765166	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3765167	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3770448	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3770449	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3770455	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs3821093	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs55864623	0.85[EUR][1000 genomes]
rs55957712	0.90[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs56275355	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs57718990	0.91[AMR][1000 genomes];0.80[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs57775770	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58540694	0.84[ASN][1000 genomes]
rs62182370	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs62182372	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs62182373	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs62182374	0.82[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62182392	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs72881938	1.00[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs72885532	0.97[AFR][1000 genomes];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs72889848	0.87[AMR][1000 genomes]
rs7584258	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[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	nsv834457	chr2:172564939-172770901	Strong transcription Genic enhancers Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
2	nsv583611	chr2:172683481-172750257	Strong transcription Weak transcription Active TSS Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:116 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:172603000-172688400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
2	chr2:172642400-172688400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
3	chr2:172643600-172687800	Weak transcription	Hela-S3	cervix
4	chr2:172645400-172687200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr2:172648200-172687400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
6	chr2:172648200-172687400	Weak transcription	Colonic Mucosa	Colon
7	chr2:172648400-172687600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
8	chr2:172648800-172687400	Weak transcription	Esophagus	oesophagus
9	chr2:172649000-172687400	Weak transcription	Gastric	stomach
10	chr2:172650400-172687400	Weak transcription	Duodenum Mucosa	Duodenum
11	chr2:172650400-172687600	Weak transcription	Lung	lung
12	chr2:172653000-172687400	Weak transcription	Fetal Heart	heart
13	chr2:172655400-172687400	Weak transcription	A549	lung
14	chr2:172655600-172687400	Weak transcription	NH-A	brain
15	chr2:172655800-172687400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr2:172657600-172687400	Weak transcription	Muscle Satellite Cultured Cells	--
17	chr2:172663600-172687400	Weak transcription	Fetal Brain Male	brain
18	chr2:172664200-172687400	Weak transcription	K562	blood
19	chr2:172664400-172687400	Weak transcription	HUVEC	blood vessel
20	chr2:172664600-172687400	Weak transcription	NHEK	skin
21	chr2:172664800-172687600	Weak transcription	HMEC	breast
22	chr2:172665200-172689600	Weak transcription	Small Intestine	intestine
23	chr2:172666200-172689600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
24	chr2:172667000-172687400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
25	chr2:172667800-172687200	Weak transcription	Rectal Smooth Muscle	rectum
26	chr2:172667800-172687400	Weak transcription	NHLF	lung
27	chr2:172668200-172687400	Weak transcription	Fetal Kidney	kidney
28	chr2:172670200-172687400	Weak transcription	HSMMtube	muscle
29	chr2:172675400-172688400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
30	chr2:172679400-172687400	Weak transcription	Primary neutrophils fromperipheralblood	blood
31	chr2:172680800-172687200	Weak transcription	Osteobl	bone
32	chr2:172680800-172687400	Weak transcription	Placenta	Placenta
33	chr2:172680800-172688800	Weak transcription	Psoas Muscle	Psoas
34	chr2:172681000-172695000	Weak transcription	Pancreas	Pancrea
35	chr2:172681200-172687400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr2:172681600-172687400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
37	chr2:172681600-172687400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr2:172681800-172687400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr2:172681800-172687400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
40	chr2:172681800-172687600	Strong transcription	Monocytes-CD14+_RO01746	blood
41	chr2:172681800-172693800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
42	chr2:172682000-172687400	Strong transcription	Primary monocytes fromperipheralblood	blood
43	chr2:172682000-172694000	Strong transcription	Primary T cells fromperipheralblood	blood
44	chr2:172682400-172687400	Weak transcription	Brain Substantia Nigra	brain
45	chr2:172682400-172687400	Weak transcription	NHDF-Ad	bronchial
46	chr2:172682400-172687600	Weak transcription	Brain Angular Gyrus	brain
47	chr2:172682600-172687600	Strong transcription	Fetal Muscle Leg	muscle
48	chr2:172683400-172687200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr2:172683400-172687400	Weak transcription	HepG2	liver
50	chr2:172683400-172693800	Strong transcription	Stomach Smooth Muscle	stomach

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