Variant report

Variant	rs10099784
Chromosome Location	chr8:121629752-121629753
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:121628159..121631762-chr8:121633780..121636360,3	K562	blood:

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs10089944	1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs10102980	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10103010	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10104248	0.90[ASN][1000 genomes]
rs10104255	0.90[ASN][1000 genomes]
rs10108821	1.00[CHB][hapmap];0.90[JPT][hapmap];0.90[ASN][1000 genomes]
rs10109195	1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs10113166	1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs12155872	0.81[YRI][hapmap]
rs4259452	0.81[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4329308	1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs4338145	1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs4409430	0.91[CHB][hapmap]
rs4448320	0.80[ASN][1000 genomes]
rs4514023	0.90[ASN][1000 genomes]
rs4514024	1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs4556123	0.89[CHB][hapmap]
rs4610796	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs55646138	0.96[ASN][1000 genomes]
rs55704534	0.90[ASN][1000 genomes]
rs57622256	0.80[ASN][1000 genomes]
rs58181006	0.80[ASN][1000 genomes]
rs58929354	0.80[ASN][1000 genomes]
rs60307797	0.81[ASN][1000 genomes]
rs6469936	0.91[CHB][hapmap]
rs6999024	0.91[CHB][hapmap]
rs7010052	0.88[CHB][hapmap]
rs7017780	1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs72680599	0.99[ASN][1000 genomes]
rs73708912	0.99[ASN][1000 genomes]
rs7812594	1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs7814782	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7824154	0.96[ASN][1000 genomes]
rs7824846	0.91[CHB][hapmap]
rs7827232	0.80[ASN][1000 genomes]
rs7827807	0.91[CHB][hapmap];0.80[ASN][1000 genomes]
rs7835353	1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs7845125	0.91[CHB][hapmap]
rs7845469	0.91[CHB][hapmap];0.80[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	nsv891421	chr8:121292407-121653902	Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
2	nsv612113	chr8:121616345-121635396	Enhancers Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:49 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:121587800-121640600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
2	chr8:121588200-121642400	Weak transcription	Primary T cells fromperipheralblood	blood
3	chr8:121588600-121636600	Weak transcription	Primary B cells from cord blood	blood
4	chr8:121605800-121644400	Weak transcription	Gastric	stomach
5	chr8:121607600-121643000	Weak transcription	Fetal Intestine Large	intestine
6	chr8:121609600-121641000	Weak transcription	Lung	lung
7	chr8:121610800-121629800	Weak transcription	Primary hematopoietic stem cells	blood
8	chr8:121613200-121668000	Weak transcription	Pancreas	Pancrea
9	chr8:121613400-121637200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr8:121616000-121637200	Weak transcription	HSMM	muscle
11	chr8:121616600-121639000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
12	chr8:121618200-121634000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr8:121618400-121637200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr8:121619000-121633400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr8:121621600-121630200	Strong transcription	Liver	Liver
16	chr8:121621800-121644400	Weak transcription	Spleen	Spleen
17	chr8:121623000-121635000	Weak transcription	Duodenum Smooth Muscle	Duodenum
18	chr8:121623400-121637400	Weak transcription	H1 Cell Line	embryonic stem cell
19	chr8:121623400-121647600	Weak transcription	Fetal Intestine Small	intestine
20	chr8:121624400-121637200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
21	chr8:121625000-121642200	Weak transcription	Primary T helper cells fromperipheralblood	blood
22	chr8:121625000-121643600	Weak transcription	Primary T helper cells PMA-I stimulated	--
23	chr8:121625400-121636600	Strong transcription	HepG2	liver
24	chr8:121625600-121645400	Strong transcription	Monocytes-CD14+_RO01746	blood
25	chr8:121626200-121630200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr8:121626200-121630800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr8:121627000-121640400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
28	chr8:121627400-121630000	Enhancers	Cortex derived primary cultured neurospheres	brain
29	chr8:121627600-121635000	Weak transcription	Psoas Muscle	Psoas
30	chr8:121627600-121637200	Weak transcription	HSMMtube	muscle
31	chr8:121627800-121631800	Weak transcription	Skeletal Muscle Female	skeletal muscle
32	chr8:121627800-121635000	Weak transcription	Right Atrium	heart
33	chr8:121627800-121635200	Weak transcription	Aorta	Aorta
34	chr8:121627800-121637400	Weak transcription	H9 Cell Line	embryonic stem cell
35	chr8:121628200-121635000	Weak transcription	HUES48 Cell Line	embryonic stem cell
36	chr8:121628400-121635000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
37	chr8:121628400-121639600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
38	chr8:121628600-121673200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
39	chr8:121628800-121630200	Strong transcription	Primary monocytes fromperipheralblood	blood
40	chr8:121628800-121631000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
41	chr8:121629000-121630200	Strong transcription	Fetal Muscle Leg	muscle
42	chr8:121629200-121630200	Strong transcription	Primary T cells from cord blood	blood
43	chr8:121629200-121631400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr8:121629200-121643600	Weak transcription	Primary B cells from peripheral blood	blood
45	chr8:121629400-121630600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr8:121629400-121634000	Weak transcription	Left Ventricle	heart
47	chr8:121629400-121642600	Weak transcription	Fetal Muscle Trunk	muscle
48	chr8:121629400-121645200	Weak transcription	Fetal Stomach	stomach
49	chr8:121629600-121637000	Weak transcription	NHLF	lung

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