Variant report

Variant	rs11672257
Chromosome Location	chr19:38439362-38439363
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr19:38434369..38435997-chr19:38437453..38439918,2	MCF-7	breast:
2	chr19:38438618..38442193-chr19:38444314..38446890,3	MCF-7	breast:
3	chr19:38395717..38398405-chr19:38438245..38443084,4	MCF-7	breast:
4	chr19:38396361..38399135-chr19:38437232..38439468,2	K562	blood:

Variant related genes	Relation type
ENSG00000105738	Chromatin interaction
ENSG00000171804	Chromatin interaction

Extended variants
information (count: 24 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs11083442	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs11665869	0.84[AMR][1000 genomes]
rs11666497	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11667246	0.84[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11668748	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs11672440	1.00[CEU][hapmap];0.90[JPT][hapmap];1.00[YRI][hapmap]
rs11672673	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11672724	0.86[CEU][hapmap];0.84[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1807157	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2382624	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs241952	0.94[CEU][hapmap]
rs241955	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs56672492	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs59616348	0.87[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs705496	1.00[YRI][hapmap]
rs73025630	0.84[AMR][1000 genomes]
rs73027418	0.84[AMR][1000 genomes]
rs73029180	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs73031215	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs73034929	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs73034946	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949296	chr19:38034722-38763140	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
2	nsv1061106	chr19:38400149-38448723	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv544001	chr19:38400149-38448723	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:78 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:38399600-38441200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr19:38423200-38443000	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr19:38423600-38444400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
4	chr19:38424800-38444000	Weak transcription	NHDF-Ad	bronchial
5	chr19:38425000-38441000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr19:38425000-38454000	Weak transcription	HSMMtube	muscle
7	chr19:38426400-38444000	Weak transcription	Muscle Satellite Cultured Cells	--
8	chr19:38426600-38442600	Weak transcription	HMEC	breast
9	chr19:38426600-38448200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
10	chr19:38426600-38450800	Weak transcription	Ovary	ovary
11	chr19:38426800-38439400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
12	chr19:38426800-38441000	Weak transcription	Primary monocytes fromperipheralblood	blood
13	chr19:38426800-38443800	Weak transcription	HUES48 Cell Line	embryonic stem cell
14	chr19:38427000-38439400	Weak transcription	Lung	lung
15	chr19:38427000-38441000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr19:38427000-38441000	Weak transcription	Brain Germinal Matrix	brain
17	chr19:38427000-38441200	Weak transcription	Adipose Nuclei	Adipose
18	chr19:38427000-38441200	Weak transcription	Left Ventricle	heart
19	chr19:38427000-38444000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr19:38427000-38444000	Weak transcription	Fetal Brain Female	brain
21	chr19:38427200-38443800	Weak transcription	NHEK	skin
22	chr19:38427200-38444200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr19:38427400-38443600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr19:38427600-38443600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
25	chr19:38428000-38441000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
26	chr19:38428600-38443400	Weak transcription	Fetal Stomach	stomach
27	chr19:38429200-38443800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
28	chr19:38429400-38441400	Weak transcription	Primary hematopoietic stem cells	blood
29	chr19:38429800-38442600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
30	chr19:38430600-38444000	Weak transcription	HSMM	muscle
31	chr19:38430600-38453600	Weak transcription	Aorta	Aorta
32	chr19:38432000-38440800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
33	chr19:38432400-38443200	Weak transcription	Stomach Smooth Muscle	stomach
34	chr19:38432600-38439600	Weak transcription	NH-A	brain
35	chr19:38432600-38441200	Weak transcription	Esophagus	oesophagus
36	chr19:38432600-38442600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr19:38432600-38443400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr19:38432800-38439600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr19:38432800-38443800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr19:38433000-38444000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr19:38433200-38439400	Genic enhancers	Fetal Intestine Small	intestine
42	chr19:38434000-38447800	Weak transcription	Hela-S3	cervix
43	chr19:38434200-38443000	Weak transcription	Right Atrium	heart
44	chr19:38434400-38440800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr19:38434400-38441000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr19:38434400-38441200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
47	chr19:38434400-38444200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr19:38434400-38451800	Weak transcription	Primary T cells from cord blood	blood
49	chr19:38435200-38444000	Weak transcription	Colonic Mucosa	Colon
50	chr19:38436000-38439600	Weak transcription	Rectal Mucosa Donor 29	rectum

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