Variant report

Variant	rs61860883
Chromosome Location	chr10:43876786-43876787
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr10:43872190..43874613-chr10:43876662..43879551,2	MCF-7	breast:
2	chr10:43871509..43873780-chr10:43874816..43877105,2	K562	blood:
3	chr10:43803844..43805693-chr10:43875587..43878080,2	K562	blood:

Extended variants
information (count: 44 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:38)

rs_ID	r²[population]
rs11548184	1.00[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs11814130	1.00[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs11817218	1.00[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs11817723	1.00[AFR][1000 genomes];0.80[EUR][1000 genomes]
rs11819010	1.00[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs12569974	1.00[AFR][1000 genomes];0.97[EUR][1000 genomes]
rs12570067	1.00[AFR][1000 genomes]
rs12571047	1.00[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs12571447	0.85[EUR][1000 genomes]
rs12571906	0.85[EUR][1000 genomes]
rs12572226	1.00[AFR][1000 genomes];0.80[EUR][1000 genomes]
rs12572292	1.00[AFR][1000 genomes];0.97[EUR][1000 genomes]
rs41307500	1.00[AFR][1000 genomes];0.94[EUR][1000 genomes]
rs57862979	0.83[EUR][1000 genomes]
rs61858960	1.00[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs61858962	1.00[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs61858963	1.00[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs61858964	1.00[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs61858965	1.00[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs61858966	0.85[EUR][1000 genomes]
rs61858967	1.00[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs61858989	1.00[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs61858996	0.82[EUR][1000 genomes]
rs61858997	1.00[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs61858998	1.00[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs61858999	1.00[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs61859003	0.80[EUR][1000 genomes]
rs61859005	1.00[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs61859006	1.00[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs61859048	0.80[EUR][1000 genomes]
rs61859049	0.83[EUR][1000 genomes]
rs61859050	0.83[EUR][1000 genomes]
rs61859051	0.83[EUR][1000 genomes]
rs61860882	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs61860885	1.00[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs61860886	1.00[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs61860887	1.00[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs61860890	1.00[AFR][1000 genomes];0.85[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv430159	chr10:43291894-43946294	Flanking Active TSS Enhancers Active TSS Strong transcription Weak transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	92 gene(s)	inside rSNPs	diseases
2	nsv1043661	chr10:43626619-43890162	Bivalent Enhancer Active TSS Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
3	nsv540574	chr10:43626619-43890162	Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription Genic enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
4	nsv895087	chr10:43783339-43982390	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	73 gene(s)	inside rSNPs	diseases
5	nsv831842	chr10:43846541-43987501	Strong transcription Flanking Active TSS Active TSS Weak transcription Enhancers Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	69 gene(s)	inside rSNPs	diseases
6	nsv895088	chr10:43871999-44003101	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	67 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:51 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:43858600-43891000	Weak transcription	Right Atrium	heart
2	chr10:43869000-43880400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr10:43869200-43882000	Weak transcription	Left Ventricle	heart
4	chr10:43869400-43880200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr10:43869800-43878600	Weak transcription	A549	lung
6	chr10:43870000-43881200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
7	chr10:43870000-43882000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
8	chr10:43870200-43881000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
9	chr10:43870200-43882000	Weak transcription	Brain Cingulate Gyrus	brain
10	chr10:43870200-43882000	Weak transcription	Brain Substantia Nigra	brain
11	chr10:43870400-43880000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
12	chr10:43870400-43881000	Weak transcription	Primary T helper cells PMA-I stimulated	--
13	chr10:43870400-43881600	Weak transcription	Brain Inferior Temporal Lobe	brain
14	chr10:43870400-43882000	Weak transcription	Brain Angular Gyrus	brain
15	chr10:43871000-43880400	Weak transcription	Brain Anterior Caudate	brain
16	chr10:43871200-43881600	Weak transcription	Brain Hippocampus Middle	brain
17	chr10:43871400-43880800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
18	chr10:43871600-43880000	Weak transcription	Fetal Muscle Leg	muscle
19	chr10:43871800-43879600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
20	chr10:43872200-43880200	Weak transcription	Lung	lung
21	chr10:43872600-43881000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
22	chr10:43873200-43878400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr10:43873200-43880200	Weak transcription	Gastric	stomach
24	chr10:43873200-43880600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr10:43873200-43881200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
26	chr10:43873200-43890200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
27	chr10:43873400-43878600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr10:43873400-43880800	Weak transcription	HUES64 Cell Line	embryonic stem cell
29	chr10:43873400-43881000	Weak transcription	H1 Cell Line	embryonic stem cell
30	chr10:43873400-43881000	Weak transcription	HUES48 Cell Line	embryonic stem cell
31	chr10:43873400-43881000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
32	chr10:43873400-43881200	Weak transcription	HUES6 Cell Line	embryonic stem cell
33	chr10:43873400-43881400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
34	chr10:43873400-43881800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
35	chr10:43873400-43882000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr10:43873400-43891000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
37	chr10:43873600-43878600	Weak transcription	Fetal Intestine Small	intestine
38	chr10:43873600-43878800	Weak transcription	Fetal Intestine Large	intestine
39	chr10:43873800-43878600	Weak transcription	Placenta	Placenta
40	chr10:43873800-43881000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
41	chr10:43873800-43881000	Weak transcription	Placenta Amnion	Placenta Amnion
42	chr10:43873800-43882000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr10:43873800-43882000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr10:43874400-43882400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
45	chr10:43874600-43878600	Weak transcription	HepG2	liver
46	chr10:43876000-43879600	Weak transcription	Fetal Stomach	stomach
47	chr10:43876000-43881800	Weak transcription	Colon Smooth Muscle	Colon
48	chr10:43876200-43877000	Enhancers	K562	blood
49	chr10:43876200-43880000	Weak transcription	Fetal Muscle Trunk	muscle
50	chr10:43876600-43880200	Weak transcription	Dnd41	blood

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