Variant report

Variant	rs599777
Chromosome Location	chr8:103931938-103931939
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr8:103931524..103933304-chr8:104018085..104019856,2	K562	blood:
2	chr8:103875028..103877482-chr8:103931087..103934755,3	MCF-7	breast:
3	chr8:103926652..103929593-chr8:103930931..103933539,2	K562	blood:
4	chr8:103874124..103877156-chr8:103929505..103932868,5	K562	blood:
5	chr8:103874124..103876322-chr8:103930861..103932524,2	K562	blood:
6	chr8:103874643..103877584-chr8:103931125..103934060,5	MCF-7	breast:

Variant related genes	Relation type
ENSG00000253320	Chromatin interaction
ENSG00000155096	Chromatin interaction

Extended variants
information (count: 48 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:46)

rs_ID	r²[population]
rs10104704	0.85[ASN][1000 genomes]
rs10808382	0.80[JPT][hapmap]
rs1138	0.96[CHB][hapmap];0.81[JPT][hapmap];0.81[ASN][1000 genomes]
rs1714399	0.85[ASN][1000 genomes]
rs1806299	1.00[CHB][hapmap];0.81[JPT][hapmap];0.85[ASN][1000 genomes]
rs1961102	1.00[CHB][hapmap];0.95[JPT][hapmap];0.99[ASN][1000 genomes]
rs1991927	0.96[CHB][hapmap];0.81[JPT][hapmap]
rs2117313	0.96[CHB][hapmap];0.80[JPT][hapmap]
rs2304346	0.96[CHB][hapmap];0.81[JPT][hapmap]
rs2436857	0.81[JPT][hapmap]
rs2458280	0.83[ASN][1000 genomes]
rs2570940	0.95[CHB][hapmap]
rs2570944	0.83[ASN][1000 genomes]
rs2570946	0.81[ASN][1000 genomes]
rs2570948	0.83[ASN][1000 genomes]
rs2679741	0.96[CHB][hapmap];0.81[JPT][hapmap];0.83[ASN][1000 genomes]
rs2679744	0.83[ASN][1000 genomes]
rs2679746	0.96[CHB][hapmap];0.81[JPT][hapmap]
rs2679748	0.96[CHB][hapmap];0.81[JPT][hapmap]
rs2679758	0.96[CHB][hapmap];0.81[JPT][hapmap];0.81[ASN][1000 genomes]
rs2679759	1.00[CHB][hapmap];0.83[ASN][1000 genomes]
rs2916558	0.96[CHB][hapmap];0.81[JPT][hapmap]
rs2916560	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs3018949	0.90[ASN][1000 genomes]
rs491770	0.85[ASN][1000 genomes]
rs492770	0.85[ASN][1000 genomes]
rs520393	0.90[ASN][1000 genomes]
rs522547	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs551241	0.85[ASN][1000 genomes]
rs560038	0.90[ASN][1000 genomes]
rs601588	1.00[CHB][hapmap];0.80[JPT][hapmap];0.85[ASN][1000 genomes]
rs606335	0.86[ASN][1000 genomes]
rs608236	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];1.00[YRI][hapmap];0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs613049	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs613559	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs642004	0.83[ASN][1000 genomes]
rs644299	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs647313	0.85[ASN][1000 genomes]
rs650987	0.90[ASN][1000 genomes]
rs657000	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs666830	0.90[ASN][1000 genomes]
rs667927	1.00[CHB][hapmap];0.85[ASN][1000 genomes]
rs676498	0.82[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs7833202	1.00[CHB][hapmap];0.81[JPT][hapmap]
rs892485	0.96[CHB][hapmap];0.81[JPT][hapmap]
rs892486	0.96[CHB][hapmap];0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv33118	chr8:103358567-104068172	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	145 gene(s)	inside rSNPs	diseases
2	nsv891246	chr8:103928940-103967694	Weak transcription Active TSS Enhancers ZNF genes & repeats Flanking Active TSS Genic enhancers Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:63 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:103923000-103932000	Weak transcription	Duodenum Smooth Muscle	Duodenum
2	chr8:103923200-103935800	Weak transcription	Fetal Lung	lung
3	chr8:103923400-103932000	Weak transcription	HUES64 Cell Line	embryonic stem cell
4	chr8:103926000-103932000	Weak transcription	Small Intestine	intestine
5	chr8:103926000-103932600	Weak transcription	Skeletal Muscle Female	skeletal muscle
6	chr8:103926400-103932600	Weak transcription	Fetal Muscle Leg	muscle
7	chr8:103926400-103937400	Weak transcription	Lung	lung
8	chr8:103926600-103936600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr8:103926800-103932600	Weak transcription	NHDF-Ad	bronchial
10	chr8:103927800-103939800	Weak transcription	H9 Cell Line	embryonic stem cell
11	chr8:103927800-103941600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr8:103928800-103933400	Enhancers	A549	lung
13	chr8:103929200-103933600	Enhancers	Fetal Heart	heart
14	chr8:103929200-103934800	Enhancers	Liver	Liver
15	chr8:103929400-103932200	Enhancers	Breast Myoepithelial Primary Cells	Breast
16	chr8:103929400-103933000	Enhancers	Pancreas	Pancrea
17	chr8:103929400-103934600	Enhancers	Adipose Nuclei	Adipose
18	chr8:103929600-103934600	Enhancers	Duodenum Mucosa	Duodenum
19	chr8:103929800-103932600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr8:103929800-103932800	Enhancers	Brain Anterior Caudate	brain
21	chr8:103929800-103933000	Enhancers	Fetal Brain Male	brain
22	chr8:103929800-103934200	Enhancers	Hela-S3	cervix
23	chr8:103930000-103932200	Weak transcription	Fetal Intestine Small	intestine
24	chr8:103930000-103932400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
25	chr8:103930000-103938000	Weak transcription	Gastric	stomach
26	chr8:103930200-103932400	Weak transcription	Skeletal Muscle Male	skeletal muscle
27	chr8:103930200-103932600	Weak transcription	Psoas Muscle	Psoas
28	chr8:103930800-103932000	Enhancers	Brain Hippocampus Middle	brain
29	chr8:103930800-103932800	Enhancers	ES-I3 Cell Line	embryonic stem cell
30	chr8:103930800-103932800	Enhancers	Cortex derived primary cultured neurospheres	brain
31	chr8:103931000-103932000	Enhancers	Primary monocytes fromperipheralblood	blood
32	chr8:103931000-103932000	Enhancers	Muscle Satellite Cultured Cells	--
33	chr8:103931000-103932400	Enhancers	Aorta	Aorta
34	chr8:103931000-103932600	Enhancers	Brain Cingulate Gyrus	brain
35	chr8:103931000-103932800	Enhancers	H1 Cell Line	embryonic stem cell
36	chr8:103931000-103932800	Enhancers	HUES6 Cell Line	embryonic stem cell
37	chr8:103931000-103932800	Enhancers	Brain Angular Gyrus	brain
38	chr8:103931000-103933000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
39	chr8:103931000-103933400	Enhancers	HUES48 Cell Line	embryonic stem cell
40	chr8:103931000-103935000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr8:103931200-103932400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
42	chr8:103931200-103932800	Enhancers	iPS-20b Cell Line	embryonic stem cell
43	chr8:103931200-103933000	Enhancers	Right Atrium	heart
44	chr8:103931200-103933200	Enhancers	Ovary	ovary
45	chr8:103931200-103933400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
46	chr8:103931200-103936800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr8:103931400-103932600	Enhancers	Right Ventricle	heart
48	chr8:103931400-103936800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr8:103931600-103932000	Enhancers	iPS-18 Cell Line	embryonic stem cell
50	chr8:103931600-103933000	Enhancers	ES-WA7 Cell Line	embryonic stem cell

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