Variant report

Variant	rs2967892
Chromosome Location	chr19:23448435-23448436
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr19:23439080..23441693-chr19:23448189..23450377,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000269837	Chromatin interaction

Extended variants
information (count: 47 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs10405424	0.81[ASN][1000 genomes]
rs10410902	0.81[ASN][1000 genomes]
rs10420886	0.81[ASN][1000 genomes]
rs10421850	0.81[ASN][1000 genomes]
rs17569085	0.86[ASN][1000 genomes]
rs2053247	0.81[ASN][1000 genomes]
rs2362132	0.81[ASN][1000 genomes]
rs2560729	0.81[ASN][1000 genomes]
rs2560730	0.83[ASN][1000 genomes]
rs293897	0.83[ASN][1000 genomes]
rs295356	0.81[ASN][1000 genomes]
rs295357	0.81[ASN][1000 genomes]
rs295358	0.82[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs295359	0.83[ASN][1000 genomes]
rs295360	0.83[ASN][1000 genomes]
rs295361	0.83[ASN][1000 genomes]
rs295363	0.83[ASN][1000 genomes]
rs295364	0.83[ASN][1000 genomes]
rs295365	0.82[ASN][1000 genomes]
rs295366	0.82[ASN][1000 genomes]
rs295424	0.86[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs295426	0.84[ASN][1000 genomes]
rs295427	0.84[ASN][1000 genomes]
rs518603	0.83[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs560926	0.85[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs7254300	0.81[ASN][1000 genomes]
rs772196	0.80[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:20 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv34470	chr19:22922549-23659458	ZNF genes & repeats Flanking Active TSS Active TSS Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	80 gene(s)	inside rSNPs	diseases
2	esv34907	chr19:22922549-23683097	Weak transcription ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Active TSS Enhancers Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	80 gene(s)	inside rSNPs	diseases
3	nsv9686	chr19:22989454-23653750	Weak transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	76 gene(s)	inside rSNPs	diseases
4	nsv817826	chr19:23000745-23620632	Active TSS Strong transcription ZNF genes & repeats Weak transcription Bivalent/Poised TSS Genic enhancers Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	75 gene(s)	inside rSNPs	diseases
5	esv3693269	chr19:23000745-23652839	Weak transcription Active TSS Strong transcription Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	76 gene(s)	inside rSNPs	diseases
6	esv2758491	chr19:23071299-23940467	ZNF genes & repeats Bivalent/Poised TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	87 gene(s)	inside rSNPs	diseases
7	nsv1065157	chr19:23091826-23812323	Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Enhancers Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	83 gene(s)	inside rSNPs	diseases
8	nsv543959	chr19:23091826-23812323	Active TSS Weak transcription Strong transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	83 gene(s)	inside rSNPs	diseases
9	esv3424935	chr19:23111817-23495542	Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	48 gene(s)	inside rSNPs	diseases
10	esv3429878	chr19:23246650-23590744	Strong transcription ZNF genes & repeats Weak transcription Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	52 gene(s)	inside rSNPs	diseases
11	esv3410568	chr19:23246670-23590714	Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	52 gene(s)	inside rSNPs	diseases
12	esv3433243	chr19:23249108-23585814	Strong transcription Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	44 gene(s)	inside rSNPs	diseases
13	esv3387823	chr19:23265885-23590028	ZNF genes & repeats Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	47 gene(s)	inside rSNPs	diseases
14	esv3321838	chr19:23303462-23482478	Strong transcription Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
15	nsv833789	chr19:23329463-23487797	Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
16	esv3440847	chr19:23361380-23481908	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
17	esv3446056	chr19:23361400-23481878	Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers Genic enhancers Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
18	nsv579033	chr19:23387788-23461424	Active TSS Strong transcription ZNF genes & repeats Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
19	nsv579034	chr19:23387788-23610784	ZNF genes & repeats Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
20	nsv833790	chr19:23405972-23557520	ZNF genes & repeats Active TSS Weak transcription Flanking Active TSS Genic enhancers Strong transcription Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	25 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	chr19:23433200-23455000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
2	chr19:23433200-23456200	Weak transcription	Small Intestine	intestine
3	chr19:23433400-23450400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
4	chr19:23433400-23455400	Weak transcription	Stomach Mucosa	stomach
5	chr19:23433400-23455800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr19:23433400-23456000	Weak transcription	Osteobl	bone
7	chr19:23433600-23449400	Weak transcription	Fetal Intestine Small	intestine
8	chr19:23433600-23453800	Weak transcription	Fetal Brain Male	brain
9	chr19:23433600-23455000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
10	chr19:23433600-23455600	Weak transcription	Psoas Muscle	Psoas
11	chr19:23433600-23455600	Weak transcription	NHDF-Ad	bronchial
12	chr19:23433600-23455800	Weak transcription	Muscle Satellite Cultured Cells	--
13	chr19:23433600-23455800	Weak transcription	Right Atrium	heart
14	chr19:23433600-23455800	Weak transcription	NH-A	brain
15	chr19:23437600-23455600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr19:23438600-23450200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr19:23438600-23455000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr19:23441400-23451400	Strong transcription	Fetal Stomach	stomach
19	chr19:23441400-23452400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr19:23441400-23454800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chr19:23441400-23455200	Strong transcription	HUES48 Cell Line	embryonic stem cell
22	chr19:23441400-23455200	Strong transcription	HUES64 Cell Line	embryonic stem cell
23	chr19:23441600-23454600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
24	chr19:23442000-23455800	Weak transcription	Colonic Mucosa	Colon
25	chr19:23442200-23455600	Weak transcription	NHLF	lung
26	chr19:23442800-23450400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr19:23442800-23453800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
28	chr19:23442800-23455400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
29	chr19:23442800-23456000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
30	chr19:23443000-23455600	Weak transcription	Fetal Heart	heart
31	chr19:23443000-23455800	Weak transcription	HMEC	breast
32	chr19:23443200-23448800	Weak transcription	Monocytes-CD14+_RO01746	blood
33	chr19:23443200-23455400	Weak transcription	Primary hematopoietic stem cells	blood
34	chr19:23443200-23455400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
35	chr19:23443200-23455600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr19:23443200-23455600	Weak transcription	NHEK	skin
37	chr19:23443200-23455800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr19:23443200-23455800	Weak transcription	Right Ventricle	heart
39	chr19:23443200-23456000	Weak transcription	HSMMtube	muscle
40	chr19:23443800-23448600	Weak transcription	Primary T helper cells PMA-I stimulated	--
41	chr19:23443800-23449800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
42	chr19:23443800-23450400	Weak transcription	Primary monocytes fromperipheralblood	blood
43	chr19:23444200-23449200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr19:23444200-23449200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
45	chr19:23444200-23450200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
46	chr19:23444200-23455600	Weak transcription	Fetal Kidney	kidney
47	chr19:23444200-23455600	Weak transcription	Pancreatic Islets	Pancreatic Islet
48	chr19:23444400-23449000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr19:23444400-23449400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr19:23444400-23449600	Weak transcription	Aorta	Aorta

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