Variant report

Variant	rs7068656
Chromosome Location	chr10:97021164-97021165
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:97007670..97009998-chr10:97020607..97023208,2	K562	blood:
2	chr10:97007090..97010166-chr10:97019600..97021879,3	MCF-7	breast:
3	chr10:97019128..97021944-chr10:97028081..97030163,2	MCF-7	breast:
4	chr10:97017870..97021906-chr10:97048495..97052362,4	MCF-7	breast:
5	chr10:96990145..96991863-chr10:97020383..97022213,2	MCF-7	breast:
6	chr10:97019690..97021827-chr10:97044842..97047086,2	MCF-7	breast:
7	chr10:97018988..97023049-chr10:97048311..97051430,5	MCF-7	breast:
8	chr10:97010783..97013765-chr10:97019245..97021501,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000234026	Chromatin interaction
ENSG00000107438	Chromatin interaction

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

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

rs_ID	r²[population]
rs11188253	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11188254	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11596920	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11597364	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12768190	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2026679	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2296962	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2296963	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2296964	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34566882	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4917682	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4918907	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6583987	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7067902	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7079728	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7087560	0.90[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7095761	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7101278	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7895650	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7910388	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7923547	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[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	nsv497859	chr10:96058024-97027747	Strong transcription Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
2	nsv529726	chr10:96632494-97106315	Strong transcription Enhancers Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
3	esv15160	chr10:96942869-97074756	Bivalent Enhancer Active TSS Strong transcription Enhancers Weak transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:98 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:96991000-97024000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr10:96998400-97030200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
3	chr10:97000400-97024400	Weak transcription	Fetal Kidney	kidney
4	chr10:97007000-97026400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
5	chr10:97009200-97028200	Weak transcription	Fetal Muscle Trunk	muscle
6	chr10:97015400-97022000	Strong transcription	Primary B cells from peripheral blood	blood
7	chr10:97016200-97022200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr10:97016200-97023000	Strong transcription	Sigmoid Colon	Sigmoid Colon
9	chr10:97016400-97023000	Strong transcription	HUES48 Cell Line	embryonic stem cell
10	chr10:97016400-97026200	Weak transcription	Pancreatic Islets	Pancreatic Islet
11	chr10:97016800-97036000	Weak transcription	Primary hematopoietic stem cells	blood
12	chr10:97017200-97024400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr10:97017400-97022000	Strong transcription	iPS-15b Cell Line	embryonic stem cell
14	chr10:97017600-97022200	Strong transcription	Primary B cells from cord blood	blood
15	chr10:97018000-97024000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr10:97018800-97023800	Strong transcription	H9 Cell Line	embryonic stem cell
17	chr10:97018800-97030000	Weak transcription	Thymus	Thymus
18	chr10:97019200-97023400	Genic enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr10:97019200-97023600	Genic enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr10:97019200-97024800	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr10:97019400-97021400	Genic enhancers	Duodenum Mucosa	Duodenum
22	chr10:97019400-97026400	Genic enhancers	Breast Myoepithelial Primary Cells	Breast
23	chr10:97019600-97024800	Genic enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr10:97019800-97021600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr10:97019800-97022000	Genic enhancers	NHDF-Ad	bronchial
26	chr10:97019800-97023600	Genic enhancers	Placenta Amnion	Placenta Amnion
27	chr10:97019800-97023800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
28	chr10:97020000-97021400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr10:97020000-97021600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr10:97020000-97022000	Enhancers	NHLF	lung
31	chr10:97020000-97022400	Enhancers	Fetal Heart	heart
32	chr10:97020000-97024000	Genic enhancers	Left Ventricle	heart
33	chr10:97020000-97026600	Genic enhancers	Fetal Intestine Large	intestine
34	chr10:97020200-97021200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr10:97020200-97021200	Genic enhancers	Rectal Mucosa Donor 31	rectum
36	chr10:97020200-97021200	Flanking Active TSS	A549	lung
37	chr10:97020200-97021400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr10:97020200-97021400	Enhancers	Cortex derived primary cultured neurospheres	brain
39	chr10:97020200-97021400	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr10:97020200-97021400	Genic enhancers	Adipose Nuclei	Adipose
41	chr10:97020200-97021400	Genic enhancers	Fetal Stomach	stomach
42	chr10:97020200-97021400	Genic enhancers	Stomach Mucosa	stomach
43	chr10:97020200-97021400	Genic enhancers	K562	blood
44	chr10:97020200-97021600	Enhancers	Psoas Muscle	Psoas
45	chr10:97020200-97022600	Genic enhancers	Right Ventricle	heart
46	chr10:97020200-97023000	Weak transcription	Aorta	Aorta
47	chr10:97020200-97024200	Genic enhancers	Lung	lung
48	chr10:97020200-97024600	Genic enhancers	Skeletal Muscle Male	skeletal muscle
49	chr10:97020200-97025000	Genic enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr10:97020200-97026600	Genic enhancers	Fetal Intestine Small	intestine

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