Variant report

Variant	rs7893144
Chromosome Location	chr10:98607167-98607168
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr10:98607034..98609759-chr10:98615492..98617827,2	MCF-7	breast:
2	chr10:98606102..98610299-chr10:98611284..98615817,4	MCF-7	breast:
3	chr10:98605679..98608625-chr10:98610602..98614600,4	K562	blood:

Extended variants
information (count: 61 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:57)

rs_ID	r²[population]
rs11188937	0.80[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11188939	0.83[ASN][1000 genomes]
rs11188940	0.80[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11188947	0.80[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11188954	0.83[ASN][1000 genomes]
rs11188955	0.83[ASN][1000 genomes]
rs11188956	0.83[ASN][1000 genomes]
rs11188959	0.83[ASN][1000 genomes]
rs11188967	0.83[ASN][1000 genomes]
rs12242330	0.83[ASN][1000 genomes]
rs12243551	0.83[ASN][1000 genomes]
rs12246067	0.80[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12247344	0.83[ASN][1000 genomes]
rs12249381	0.83[ASN][1000 genomes]
rs12249427	0.83[ASN][1000 genomes]
rs12249891	0.80[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12252424	0.83[ASN][1000 genomes]
rs12252435	0.80[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12256424	0.80[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12257413	0.83[ASN][1000 genomes]
rs12258355	0.83[ASN][1000 genomes]
rs12258469	0.83[ASN][1000 genomes]
rs12259265	0.80[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12261278	0.80[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12261881	0.80[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12262784	0.80[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12263331	0.83[ASN][1000 genomes]
rs12265242	0.83[ASN][1000 genomes]
rs12266068	0.80[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12266185	0.80[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12267926	0.80[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12268216	0.83[ASN][1000 genomes]
rs12268272	0.83[ASN][1000 genomes]
rs13376965	0.83[ASN][1000 genomes]
rs17112175	0.83[ASN][1000 genomes]
rs17112190	0.83[ASN][1000 genomes]
rs2104785	0.80[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs28439735	0.83[ASN][1000 genomes]
rs28758432	0.83[ASN][1000 genomes]
rs4394767	0.83[ASN][1000 genomes]
rs56867696	0.83[ASN][1000 genomes]
rs57716318	0.80[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs58376960	0.83[ASN][1000 genomes]
rs59751908	0.83[ASN][1000 genomes]
rs59938221	0.83[ASN][1000 genomes]
rs59999388	0.83[ASN][1000 genomes]
rs60576681	0.83[ASN][1000 genomes]
rs7072273	0.83[ASN][1000 genomes]
rs7082316	0.83[ASN][1000 genomes]
rs7085822	0.83[ASN][1000 genomes]
rs7085851	0.83[ASN][1000 genomes]
rs7893564	0.83[ASN][1000 genomes]
rs7894418	0.80[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7910221	0.80[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7918085	0.80[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7921193	0.80[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7921216	0.80[EUR][1000 genomes];0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv532232	chr10:98360775-99141797	Enhancers Strong transcription Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
2	nsv895910	chr10:98386483-98640994	ZNF genes & repeats Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	21 gene(s)	inside rSNPs	diseases
3	nsv1053801	chr10:98506832-98610101	Flanking Active TSS Weak transcription Enhancers Genic enhancers ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	19 gene(s)	inside rSNPs	diseases
4	nsv825532	chr10:98567434-98618034	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	17 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:112 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:98593800-98624200	Weak transcription	Colonic Mucosa	Colon
2	chr10:98594200-98610200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr10:98594200-98610800	Weak transcription	Fetal Thymus	thymus
4	chr10:98594200-98639400	Weak transcription	Thymus	Thymus
5	chr10:98594400-98618800	Weak transcription	Fetal Stomach	stomach
6	chr10:98595800-98610400	Weak transcription	Aorta	Aorta
7	chr10:98596000-98610400	Weak transcription	Rectal Smooth Muscle	rectum
8	chr10:98596200-98610400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
9	chr10:98596200-98616200	Weak transcription	Brain Germinal Matrix	brain
10	chr10:98596400-98613000	Weak transcription	Fetal Muscle Leg	muscle
11	chr10:98596400-98616200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr10:98596600-98607400	Weak transcription	Stomach Smooth Muscle	stomach
13	chr10:98596600-98616000	Weak transcription	Gastric	stomach
14	chr10:98597600-98610400	Weak transcription	Fetal Heart	heart
15	chr10:98597600-98618000	Weak transcription	Dnd41	blood
16	chr10:98600200-98624000	Weak transcription	Fetal Brain Male	brain
17	chr10:98601000-98607400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr10:98601000-98609800	Weak transcription	NHDF-Ad	bronchial
19	chr10:98601000-98610000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
20	chr10:98601000-98610400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr10:98601000-98610600	Weak transcription	GM12878-XiMat	blood
22	chr10:98601000-98612800	Weak transcription	Psoas Muscle	Psoas
23	chr10:98601200-98610000	Weak transcription	NH-A	brain
24	chr10:98601200-98610200	Weak transcription	HSMM	muscle
25	chr10:98601400-98610400	Weak transcription	Primary B cells from cord blood	blood
26	chr10:98602200-98621200	Weak transcription	Fetal Muscle Trunk	muscle
27	chr10:98602600-98610200	Weak transcription	Small Intestine	intestine
28	chr10:98603000-98610600	Weak transcription	Rectal Mucosa Donor 29	rectum
29	chr10:98603000-98617200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
30	chr10:98603000-98618200	Weak transcription	Fetal Kidney	kidney
31	chr10:98603200-98610200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
32	chr10:98603200-98610200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr10:98603200-98610200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
34	chr10:98603200-98610400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
35	chr10:98603200-98610400	Weak transcription	Placenta	Placenta
36	chr10:98603200-98611000	Weak transcription	Duodenum Mucosa	Duodenum
37	chr10:98603200-98612000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
38	chr10:98603200-98615400	Weak transcription	Spleen	Spleen
39	chr10:98603200-98616000	Weak transcription	Lung	lung
40	chr10:98603200-98617600	Weak transcription	Fetal Intestine Large	intestine
41	chr10:98603200-98618200	Weak transcription	Sigmoid Colon	Sigmoid Colon
42	chr10:98603200-98619600	Weak transcription	Rectal Mucosa Donor 31	rectum
43	chr10:98603200-98620000	Weak transcription	Hela-S3	cervix
44	chr10:98603200-98621400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr10:98603400-98607600	Enhancers	HepG2	liver
46	chr10:98603600-98609800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
47	chr10:98604400-98610400	Weak transcription	Duodenum Smooth Muscle	Duodenum
48	chr10:98604600-98623400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
49	chr10:98604800-98609600	Weak transcription	A549	lung
50	chr10:98604800-98610000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland

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