Variant report

Variant	rs2019561
Chromosome Location	chr12:122250617-122250618
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:10)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:122249312..122252163-chr12:122325172..122327877,3	K562	blood:
2	chr12:122148543..122152154-chr12:122247522..122251412,4	MCF-7	breast:
3	chr12:122248304..122251064-chr12:132568953..132570962,2	MCF-7	breast:
4	chr12:122248762..122251835-chr12:122331420..122334118,3	MCF-7	breast:
5	chr12:122250365..122256158-chr12:122324216..122328328,5	MCF-7	breast:
6	chr12:122247695..122252163-chr12:122325172..122328033,7	K562	blood:
7	chr12:122232209..122233866-chr12:122249576..122251017,11	MCF-7	breast:
8	chr12:122248283..122252969-chr12:122325592..122328736,7	MCF-7	breast:
9	chr12:122220378..122221895-chr12:122249646..122252036,2	K562	blood:
10	chr12:122138274..122140885-chr12:122248656..122250859,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000188735	Chromatin interaction
ENSG00000139725	Chromatin interaction
ENSG00000185684	Chromatin interaction
ENSG00000110801	Chromatin interaction
ENSG00000256950	Chromatin interaction

Extended variants
information (count: 45 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs1004390	0.92[EUR][1000 genomes]
rs11043202	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11043203	1.00[CEU][hapmap];1.00[CHB][hapmap];0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11043207	1.00[CEU][hapmap];0.81[EUR][1000 genomes]
rs1168663	0.89[EUR][1000 genomes]
rs1168664	0.93[EUR][1000 genomes]
rs1168665	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1168666	1.00[CEU][hapmap];0.94[EUR][1000 genomes]
rs1168668	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1168669	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1168671	1.00[CEU][hapmap];0.93[EUR][1000 genomes]
rs1168672	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1168673	1.00[CEU][hapmap];0.93[EUR][1000 genomes]
rs12307227	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12313997	0.89[ASN][1000 genomes]
rs12314801	0.89[ASN][1000 genomes]
rs12820413	0.82[ASN][1000 genomes]
rs12823194	0.85[EUR][1000 genomes]
rs1667578	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs1667579	0.93[EUR][1000 genomes]
rs1795965	0.81[AFR][1000 genomes];0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1795966	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs2019562	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2122266	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2707057	0.82[ASN][1000 genomes]
rs2707066	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2707067	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs712852	1.00[CEU][hapmap];0.89[EUR][1000 genomes]
rs7957564	0.92[EUR][1000 genomes]
rs7974348	1.00[CEU][hapmap];0.93[EUR][1000 genomes]
rs895951	1.00[CEU][hapmap];1.00[CHB][hapmap];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs895952	0.83[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs895953	1.00[CEU][hapmap];1.00[CHB][hapmap];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs895954	1.00[CEU][hapmap];0.85[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs895957	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs921286	1.00[CEU][hapmap];1.00[CHB][hapmap];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs921287	1.00[CEU][hapmap];1.00[CHB][hapmap];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs921288	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs930665	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv529868	chr12:121956483-122944265	Flanking Active TSS Enhancers Weak transcription Active TSS Genic enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	173 gene(s)	inside rSNPs	diseases
2	nsv899566	chr12:122167095-122265106	Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	97 gene(s)	inside rSNPs	diseases
3	nsv899567	chr12:122203680-122281575	Enhancers Genic enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	97 gene(s)	inside rSNPs	diseases
4	nsv984477	chr12:122226309-122271532	Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	95 gene(s)	inside rSNPs	diseases
5	nsv911	chr12:122234524-122279425	Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Strong transcription Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	87 gene(s)	inside rSNPs	diseases
6	nsv916686	chr12:122240149-122714056	Enhancers Strong transcription Weak transcription Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	89 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:122243800-122251600	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr12:122247200-122251400	Transcr. at gene 5' and 3'	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr12:122247800-122252000	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr12:122248200-122250800	Transcr. at gene 5' and 3'	Dnd41	blood
5	chr12:122248600-122250800	Transcr. at gene 5' and 3'	Primary mononuclear cells fromperipheralblood	Blood
6	chr12:122248600-122251400	Transcr. at gene 5' and 3'	Fetal Thymus	thymus
7	chr12:122248800-122250800	Transcr. at gene 5' and 3'	Skeletal Muscle Male	skeletal muscle
8	chr12:122248800-122251000	Transcr. at gene 5' and 3'	NHEK	skin
9	chr12:122248800-122251200	Transcr. at gene 5' and 3'	Primary T cells fromperipheralblood	blood
10	chr12:122248800-122251200	Transcr. at gene 5' and 3'	Primary hematopoietic stem cells short term culture	blood
11	chr12:122248800-122251200	Transcr. at gene 5' and 3'	NHLF	lung
12	chr12:122248800-122251600	Transcr. at gene 5' and 3'	Primary T regulatory cells fromperipheralblood	blood
13	chr12:122249000-122250800	Active TSS	H9 Cell Line	embryonic stem cell
14	chr12:122249000-122250800	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
15	chr12:122249000-122250800	Transcr. at gene 5' and 3'	Primary T helper naive cells fromperipheralblood	blood
16	chr12:122249000-122250800	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
17	chr12:122249000-122251000	Transcr. at gene 5' and 3'	Thymus	Thymus
18	chr12:122249000-122251000	Flanking Active TSS	HepG2	liver
19	chr12:122249200-122250800	Active TSS	ES-WA7 Cell Line	embryonic stem cell
20	chr12:122249200-122250800	Transcr. at gene 5' and 3'	Fetal Muscle Leg	muscle
21	chr12:122249200-122251000	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
22	chr12:122249200-122251000	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
23	chr12:122249200-122251200	Flanking Active TSS	Brain Hippocampus Middle	brain
24	chr12:122249200-122251200	Transcr. at gene 5' and 3'	Fetal Intestine Small	intestine
25	chr12:122249200-122251400	Active TSS	iPS-15b Cell Line	embryonic stem cell
26	chr12:122249200-122251400	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr12:122249200-122251400	Flanking Active TSS	Stomach Smooth Muscle	stomach
28	chr12:122249400-122250800	Transcr. at gene 5' and 3'	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr12:122249400-122250800	Transcr. at gene 5' and 3'	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr12:122249400-122250800	Transcr. at gene 5' and 3'	Breast Myoepithelial Primary Cells	Breast
31	chr12:122249400-122250800	Flanking Active TSS	Primary B cells from cord blood	blood
32	chr12:122249400-122250800	Flanking Active TSS	Liver	Liver
33	chr12:122249400-122250800	Transcr. at gene 5' and 3'	Fetal Muscle Trunk	muscle
34	chr12:122249400-122250800	Flanking Active TSS	HUVEC	blood vessel
35	chr12:122249400-122251000	Transcr. at gene 5' and 3'	IMR90 fetal lung fibroblasts Cell Line	lung
36	chr12:122249400-122251000	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
37	chr12:122249400-122251000	Flanking Active TSS	Adipose Nuclei	Adipose
38	chr12:122249400-122251200	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
39	chr12:122249400-122252000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
40	chr12:122249600-122250800	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
41	chr12:122249600-122250800	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
42	chr12:122249600-122250800	Flanking Active TSS	Placenta	Placenta
43	chr12:122249600-122251000	Active TSS	HUES64 Cell Line	embryonic stem cell
44	chr12:122249600-122251000	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
45	chr12:122249600-122251000	Transcr. at gene 5' and 3'	Fetal Stomach	stomach
46	chr12:122249600-122251000	Flanking Active TSS	HMEC	breast
47	chr12:122249600-122251200	Active TSS	Pancreatic Islets	Pancreatic Islet
48	chr12:122249600-122251200	Active TSS	Small Intestine	intestine
49	chr12:122249600-122251400	Active TSS	ES-I3 Cell Line	embryonic stem cell
50	chr12:122249800-122250800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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