Variant report

Variant	rs10076610
Chromosome Location	chr5:17258046-17258047
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr5:17255104..17256658-chr5:17257028..17259986,2	MCF-7	breast:
2	chr5:17224192..17226114-chr5:17256791..17258663,2	MCF-7	breast:
3	chr5:17216171..17217892-chr5:17257911..17259730,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000215196	Chromatin interaction
ENSG00000176788	Chromatin interaction

Extended variants
information (count: 5 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:2)

rs_ID	r²[population]
rs10068662	1.00[AMR][1000 genomes]
rs9312949	1.00[AMR][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	nsv880277	chr5:16829442-17316288	Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
2	nsv830218	chr5:17093162-17290045	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Strong transcription Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
3	nsv1029959	chr5:17133214-17455995	Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Strong transcription 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:67 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:17229800-17261600	Weak transcription	Fetal Stomach	stomach
2	chr5:17232000-17259200	Weak transcription	Fetal Muscle Leg	muscle
3	chr5:17232800-17260000	Weak transcription	Fetal Kidney	kidney
4	chr5:17232800-17278800	Weak transcription	H9 Cell Line	embryonic stem cell
5	chr5:17242800-17275000	Weak transcription	Cortex derived primary cultured neurospheres	brain
6	chr5:17244800-17274600	Weak transcription	Ovary	ovary
7	chr5:17249400-17275200	Weak transcription	Aorta	Aorta
8	chr5:17252800-17260800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr5:17252800-17271200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr5:17253200-17258200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr5:17254200-17259600	Genic enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr5:17254400-17259000	Genic enhancers	Osteobl	bone
13	chr5:17255000-17259200	Enhancers	HUVEC	blood vessel
14	chr5:17255000-17259200	Enhancers	NHDF-Ad	bronchial
15	chr5:17255200-17259400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr5:17255600-17258400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
17	chr5:17255600-17259200	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr5:17255600-17260800	Enhancers	Fetal Brain Male	brain
19	chr5:17256000-17258200	Enhancers	Primary monocytes fromperipheralblood	blood
20	chr5:17256000-17258800	Enhancers	Muscle Satellite Cultured Cells	--
21	chr5:17256000-17261400	Weak transcription	Fetal Lung	lung
22	chr5:17256200-17259000	Weak transcription	H1 Cell Line	embryonic stem cell
23	chr5:17256200-17259200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr5:17256200-17279800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
25	chr5:17256400-17260200	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
26	chr5:17256400-17274600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr5:17256600-17275200	Weak transcription	Placenta	Placenta
28	chr5:17257000-17258400	Enhancers	Rectal Mucosa Donor 31	rectum
29	chr5:17257000-17259000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr5:17257200-17258400	Genic enhancers	Primary B cells from peripheral blood	blood
31	chr5:17257600-17258200	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr5:17257600-17258200	Genic enhancers	HUES64 Cell Line	embryonic stem cell
33	chr5:17257600-17258200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
34	chr5:17257600-17258200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr5:17257600-17258200	Genic enhancers	NH-A	brain
36	chr5:17257600-17258400	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
37	chr5:17257600-17258400	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr5:17257600-17258800	Genic enhancers	Hela-S3	cervix
39	chr5:17257600-17259000	Genic enhancers	HUES48 Cell Line	embryonic stem cell
40	chr5:17257600-17259000	Genic enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr5:17257600-17259000	Genic enhancers	NHEK	skin
42	chr5:17257600-17259200	Genic enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr5:17257600-17259200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
44	chr5:17257600-17259400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
45	chr5:17257600-17259800	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
46	chr5:17257600-17259800	ZNF genes & repeats	A549	lung
47	chr5:17257600-17260600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr5:17257600-17260800	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr5:17257800-17258200	Enhancers	Sigmoid Colon	Sigmoid Colon
50	chr5:17257800-17258400	Genic enhancers	HSMM	muscle

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