Variant report

Variant	rs7843780
Chromosome Location	chr8:118925828-118925829
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:118924992..118927722-chr8:118950419..118952468,2	MCF-7	breast:

Extended variants
information (count: 56 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:47)

rs_ID	r²[population]
rs11562671	1.00[CEU][hapmap]
rs11562687	1.00[CEU][hapmap]
rs11562703	1.00[CEU][hapmap]
rs11562737	1.00[CEU][hapmap]
rs11562774	1.00[CEU][hapmap]
rs11562775	1.00[CEU][hapmap]
rs11562776	1.00[CEU][hapmap]
rs11562821	1.00[CEU][hapmap]
rs11562822	1.00[CEU][hapmap]
rs11562823	1.00[CEU][hapmap]
rs17430645	1.00[CEU][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17430666	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17430673	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17430721	1.00[CEU][hapmap]
rs17430755	1.00[CEU][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17430819	1.00[CEU][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17430930	1.00[CEU][hapmap]
rs17430965	1.00[CEU][hapmap]
rs17431152	1.00[CEU][hapmap]
rs17431166	1.00[CEU][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17431208	1.00[CEU][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17431215	1.00[CEU][hapmap]
rs17431249	1.00[CEU][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17431429	1.00[AMR][1000 genomes]
rs17453105	1.00[CEU][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17453112	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17453133	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17453344	1.00[CEU][hapmap]
rs17453357	1.00[CEU][hapmap]
rs17453448	1.00[CEU][hapmap]
rs17453560	1.00[CEU][hapmap]
rs17453567	1.00[CEU][hapmap]
rs17453602	1.00[CEU][hapmap]
rs17453651	1.00[CEU][hapmap]
rs17453784	1.00[AMR][1000 genomes]
rs17475946	1.00[CEU][hapmap]
rs17476226	1.00[CEU][hapmap]
rs17476233	1.00[CEU][hapmap]
rs17476254	1.00[CEU][hapmap]
rs17476296	1.00[CEU][hapmap]
rs28357283	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28357284	1.00[CEU][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs56660440	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60412456	1.00[ASN][1000 genomes]
rs7843728	1.00[CEU][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7844054	1.00[CEU][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7844255	1.00[CEU][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1019636	chr8:118598433-118946091	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv539734	chr8:118598433-118946091	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv933516	chr8:118764605-119009093	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv1030459	chr8:118840179-119155835	Weak transcription Flanking Active TSS Enhancers Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
5	nsv831440	chr8:118871930-119052269	Weak transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv891411	chr8:118891896-118942698	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
7	nsv1032355	chr8:118896733-119003223	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Strong transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
8	nsv465785	chr8:118901928-118970300	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
9	nsv612046	chr8:118901928-118970300	Weak transcription Enhancers Genic enhancers ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:42 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:118919000-118926800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr8:118919200-118933200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr8:118921200-118926400	Enhancers	NHDF-Ad	bronchial
4	chr8:118921200-118926600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr8:118921600-118926400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr8:118921800-118926400	Enhancers	NHLF	lung
7	chr8:118922400-118926400	Enhancers	Breast Myoepithelial Primary Cells	Breast
8	chr8:118922800-118932800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr8:118922800-118934800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr8:118923000-118926600	Enhancers	Muscle Satellite Cultured Cells	--
11	chr8:118923200-118926400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr8:118923200-118926400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr8:118923200-118933000	Weak transcription	Stomach Smooth Muscle	stomach
14	chr8:118923600-118926800	Enhancers	Osteobl	bone
15	chr8:118923800-118930000	Weak transcription	Pancreas	Pancrea
16	chr8:118923800-118933800	Weak transcription	Fetal Stomach	stomach
17	chr8:118924000-118932800	Weak transcription	Ovary	ovary
18	chr8:118924000-118933000	Weak transcription	Lung	lung
19	chr8:118924800-118926400	Enhancers	HSMM	muscle
20	chr8:118924800-118926600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
21	chr8:118925000-118926400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr8:118925000-118927000	Weak transcription	Liver	Liver
23	chr8:118925000-118927800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr8:118925400-118926000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr8:118925400-118926000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr8:118925400-118926000	Enhancers	Rectal Smooth Muscle	rectum
27	chr8:118925400-118926000	Enhancers	HSMMtube	muscle
28	chr8:118925400-118926400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr8:118925400-118926400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
30	chr8:118925400-118926400	Enhancers	HMEC	breast
31	chr8:118925600-118926200	Enhancers	Colon Smooth Muscle	Colon
32	chr8:118925600-118926400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr8:118925600-118926400	Enhancers	NH-A	brain
34	chr8:118925800-118926000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr8:118925800-118926000	ZNF genes & repeats	Duodenum Mucosa	Duodenum
36	chr8:118925800-118926000	Enhancers	Duodenum Smooth Muscle	Duodenum
37	chr8:118925800-118926000	Enhancers	Small Intestine	intestine
38	chr8:118925800-118926200	Weak transcription	Aorta	Aorta
39	chr8:118925800-118926400	Enhancers	A549	lung
40	chr8:118925800-118926400	Enhancers	NHEK	skin
41	chr8:118925800-118926600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
42	chr8:118925800-118926600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin

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