Variant report

Variant	rs6432195
Chromosome Location	chr2:11590579-11590580
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr2:11582548..11585072-chr2:11589512..11591069,2	K562	blood:
2	chr2:11587382..11589670-chr2:11589924..11591433,2	MCF-7	breast:
3	chr2:11585540..11588575-chr2:11588932..11591157,3	K562	blood:

Extended variants
information (count: 62 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:60)

rs_ID	r²[population]
rs10186511	0.82[ASN][1000 genomes]
rs10192676	0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10803737	0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10929741	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10929742	0.83[ASN][1000 genomes]
rs10929745	0.87[AFR][1000 genomes];0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10929746	0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10929747	0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10929748	0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10929749	0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11680919	0.82[ASN][1000 genomes]
rs11685543	0.80[ASN][1000 genomes]
rs11686138	0.83[ASN][1000 genomes]
rs11687178	0.83[ASN][1000 genomes]
rs11694857	0.83[ASN][1000 genomes]
rs12472962	0.83[ASN][1000 genomes]
rs12611958	0.83[ASN][1000 genomes]
rs12615317	0.83[ASN][1000 genomes]
rs12988106	0.80[ASN][1000 genomes]
rs13028340	0.87[EUR][1000 genomes]
rs13395890	0.81[ASN][1000 genomes]
rs1369500	0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1369501	0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1369502	0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1369503	0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs34075853	0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs35047869	0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs35160324	0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs35306821	0.82[ASN][1000 genomes]
rs35606161	0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs35727311	0.83[ASN][1000 genomes]
rs35734540	0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs35818376	0.80[ASN][1000 genomes]
rs35973068	0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4292073	0.83[ASN][1000 genomes]
rs4491705	1.00[ASN][1000 genomes]
rs4553788	0.83[ASN][1000 genomes]
rs60323348	0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs60819231	0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs61016299	0.83[ASN][1000 genomes]
rs6432193	0.83[ASN][1000 genomes]
rs6432196	0.82[ASN][1000 genomes]
rs6432197	0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6432198	0.87[AFR][1000 genomes];0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6432201	0.85[EUR][1000 genomes]
rs6705284	0.87[AFR][1000 genomes];0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6714698	0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6719876	0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6724082	0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6724463	0.87[AFR][1000 genomes];0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6729114	0.83[ASN][1000 genomes]
rs6743597	0.84[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs6751915	0.83[ASN][1000 genomes]
rs6753836	0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7425786	0.82[ASN][1000 genomes]
rs7556984	0.82[ASN][1000 genomes]
rs7565965	0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7577942	0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7584175	0.83[ASN][1000 genomes]
rs9789694	0.83[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	nsv1010506	chr2:11430965-12057286	Enhancers Strong transcription Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	88 gene(s)	inside rSNPs	diseases
2	nsv535585	chr2:11430965-12057286	Enhancers Flanking Active TSS Bivalent/Poised TSS Weak transcription ZNF genes & repeats Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	88 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	chr2:11575800-11597000	Weak transcription	Fetal Heart	heart
2	chr2:11577600-11603800	Weak transcription	Colonic Mucosa	Colon
3	chr2:11578600-11594000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
4	chr2:11579000-11604800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
5	chr2:11579200-11594000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr2:11579800-11590600	Strong transcription	Primary T cells from cord blood	blood
7	chr2:11580000-11593800	Strong transcription	Duodenum Smooth Muscle	Duodenum
8	chr2:11580200-11604000	Weak transcription	Fetal Brain Male	brain
9	chr2:11580400-11591800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
10	chr2:11580400-11596000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
11	chr2:11580600-11594000	Strong transcription	Placenta	Placenta
12	chr2:11581000-11596400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
13	chr2:11581200-11597000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
14	chr2:11581800-11593600	Strong transcription	Fetal Muscle Trunk	muscle
15	chr2:11581800-11596400	Strong transcription	Liver	Liver
16	chr2:11582600-11594400	Strong transcription	NH-A	brain
17	chr2:11582800-11595600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
18	chr2:11583000-11590800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
19	chr2:11583000-11594000	Strong transcription	K562	blood
20	chr2:11583600-11594400	Strong transcription	Duodenum Mucosa	Duodenum
21	chr2:11583800-11594200	Strong transcription	Osteobl	bone
22	chr2:11583800-11596800	Strong transcription	Muscle Satellite Cultured Cells	--
23	chr2:11583800-11597600	Strong transcription	HepG2	liver
24	chr2:11584000-11593400	Strong transcription	Skeletal Muscle Female	skeletal muscle
25	chr2:11584200-11593800	Strong transcription	HSMM	muscle
26	chr2:11584200-11596000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
27	chr2:11584200-11597000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
28	chr2:11584400-11593800	Strong transcription	Primary monocytes fromperipheralblood	blood
29	chr2:11584400-11594200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
30	chr2:11584400-11596400	Strong transcription	Monocytes-CD14+_RO01746	blood
31	chr2:11584400-11598800	Strong transcription	A549	lung
32	chr2:11584400-11599600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr2:11585000-11596200	Strong transcription	HUES6 Cell Line	embryonic stem cell
34	chr2:11585000-11596800	Strong transcription	HUES64 Cell Line	embryonic stem cell
35	chr2:11585000-11597600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr2:11585200-11590800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr2:11585200-11590800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
38	chr2:11585200-11597200	Strong transcription	Dnd41	blood
39	chr2:11585400-11592400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
40	chr2:11586000-11591800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
41	chr2:11586400-11593800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
42	chr2:11586400-11593800	Strong transcription	Fetal Thymus	thymus
43	chr2:11586400-11594000	Strong transcription	Cortex derived primary cultured neurospheres	brain
44	chr2:11586400-11594400	Strong transcription	HUVEC	blood vessel
45	chr2:11586400-11595400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr2:11586400-11596800	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr2:11586400-11598600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr2:11586600-11591600	Strong transcription	Fetal Stomach	stomach
49	chr2:11586600-11593400	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
50	chr2:11586600-11593400	Strong transcription	Brain Hippocampus Middle	brain

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