Variant report

Variant	rs73526907
Chromosome Location	chr19:18947384-18947385
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr19:18882889..18885685-chr19:18945828..18948339,2	MCF-7	breast:
2	chr19:18549229..18551891-chr19:18947314..18949690,2	K562	blood:
3	chr19:18893741..18897746-chr19:18945981..18952333,7	K562	blood:
4	chr19:18682558..18684067-chr19:18947357..18950283,2	K562	blood:
5	chr19:18895462..18897674-chr19:18946976..18949711,3	K562	blood:
6	chr19:18630141..18633061-chr19:18945412..18948320,2	MCF-7	breast:
7	chr19:18682709..18684257-chr19:18945521..18948229,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000221983	Chromatin interaction
ENSG00000105656	Chromatin interaction

Extended variants
information (count: 27 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs10410987	0.86[AFR][1000 genomes];0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11673194	0.91[AFR][1000 genomes];0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2005695	0.91[AFR][1000 genomes];0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2018392	0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4808161	0.81[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4808163	0.93[EUR][1000 genomes]
rs4808164	0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4808859	0.85[ASN][1000 genomes]
rs4808866	0.81[AFR][1000 genomes];0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4808868	0.93[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4808869	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4808870	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs57870078	0.84[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7250661	0.97[AFR][1000 genomes];0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7252523	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7252796	0.86[ASN][1000 genomes]
rs7257086	0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs73526909	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs757114	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs886298	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv911293	chr19:18872917-19050957	Flanking Active TSS Genic enhancers Strong transcription Active TSS Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
2	nsv911294	chr19:18872917-19093619	Active TSS Weak transcription Strong transcription Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
3	nsv833777	chr19:18875936-19031076	Weak transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
4	nsv911297	chr19:18928480-19077385	Enhancers Strong transcription Flanking Bivalent TSS/Enh Weak transcription Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Genic enhancers Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
5	nsv911298	chr19:18928480-19093619	Weak transcription Transcr. at gene 5' and 3' Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
6	nsv911299	chr19:18939954-18984843	Active TSS Genic enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
7	nsv911300	chr19:18944025-19093619	Genic enhancers Weak transcription Flanking Bivalent TSS/Enh Strong transcription Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:18944600-18948400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr19:18945000-18947400	Enhancers	Primary T killer memory cells from peripheral blood	blood
3	chr19:18945200-18948000	Weak transcription	Brain Inferior Temporal Lobe	brain
4	chr19:18945200-18948200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr19:18945200-18948200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
6	chr19:18945200-18948200	Weak transcription	Placenta Amnion	Placenta Amnion
7	chr19:18945200-18948400	Enhancers	Skeletal Muscle Female	skeletal muscle
8	chr19:18945200-18948800	Transcr. at gene 5' and 3'	GM12878-XiMat	blood
9	chr19:18945200-18949200	Strong transcription	Fetal Muscle Trunk	muscle
10	chr19:18945200-18951600	Genic enhancers	Fetal Adrenal Gland	Adrenal Gland
11	chr19:18945200-18952200	Genic enhancers	Primary T cells fromperipheralblood	blood
12	chr19:18945200-18956600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
13	chr19:18945400-18948200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
14	chr19:18945400-18948200	Enhancers	Adipose Nuclei	Adipose
15	chr19:18945400-18948800	Genic enhancers	Primary T helper naive cells fromperipheralblood	blood
16	chr19:18945400-18950600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
17	chr19:18945400-18952600	Genic enhancers	Primary T regulatory cells fromperipheralblood	blood
18	chr19:18945600-18947400	Genic enhancers	Primary mononuclear cells fromperipheralblood	Blood
19	chr19:18945600-18947400	Genic enhancers	Fetal Brain Female	brain
20	chr19:18945600-18947400	Enhancers	Pancreatic Islets	Pancreatic Islet
21	chr19:18945600-18947400	Genic enhancers	K562	blood
22	chr19:18945600-18947600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr19:18945600-18948200	Weak transcription	Ovary	ovary
24	chr19:18945600-18948200	Weak transcription	Rectal Smooth Muscle	rectum
25	chr19:18945600-18948200	Weak transcription	HUVEC	blood vessel
26	chr19:18945600-18948200	Weak transcription	NHDF-Ad	bronchial
27	chr19:18945600-18948400	Weak transcription	Fetal Lung	lung
28	chr19:18945600-18948600	Genic enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr19:18945600-18948600	Strong transcription	NHLF	lung
30	chr19:18945600-18948600	Strong transcription	Osteobl	bone
31	chr19:18945600-18948800	Genic enhancers	Breast Myoepithelial Primary Cells	Breast
32	chr19:18945600-18948800	Strong transcription	HSMM	muscle
33	chr19:18945600-18949200	Genic enhancers	Primary T helper cells fromperipheralblood	blood
34	chr19:18945600-18949400	Strong transcription	HUES6 Cell Line	embryonic stem cell
35	chr19:18945600-18949800	Genic enhancers	HepG2	liver
36	chr19:18945600-18950200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr19:18945600-18950200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr19:18945600-18950200	Strong transcription	Fetal Muscle Leg	muscle
39	chr19:18945600-18950200	Weak transcription	HSMMtube	muscle
40	chr19:18945600-18950400	Genic enhancers	Duodenum Mucosa	Duodenum
41	chr19:18945600-18950400	Strong transcription	Fetal Stomach	stomach
42	chr19:18945600-18950600	Enhancers	Skeletal Muscle Male	skeletal muscle
43	chr19:18945600-18953200	Weak transcription	Aorta	Aorta
44	chr19:18945800-18947600	Genic enhancers	Primary B cells from peripheral blood	blood
45	chr19:18945800-18948200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
46	chr19:18945800-18948200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr19:18945800-18948400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr19:18945800-18948800	Strong transcription	Primary hematopoietic stem cells	blood
49	chr19:18945800-18948800	Genic enhancers	Primary T helper 17 cells PMA-I stimulated	--
50	chr19:18945800-18948800	Genic enhancers	Rectal Mucosa Donor 29	rectum

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