Variant report

Variant	rs56260092
Chromosome Location	chr2:111491106-111491107
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 108 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:103)

rs_ID	r²[population]
rs13421709	0.86[ASN][1000 genomes]
rs13426054	0.83[ASN][1000 genomes]
rs17041539	0.82[EUR][1000 genomes]
rs17041553	0.82[EUR][1000 genomes]
rs17041554	0.82[EUR][1000 genomes]
rs17041555	0.82[EUR][1000 genomes]
rs17041561	0.82[EUR][1000 genomes]
rs28452164	1.00[EUR][1000 genomes]
rs34026418	0.82[EUR][1000 genomes]
rs3817265	0.82[EUR][1000 genomes]
rs4255970	1.00[EUR][1000 genomes]
rs55682108	1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs55780486	0.82[EUR][1000 genomes]
rs55849112	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs55857945	1.00[EUR][1000 genomes]
rs55875504	1.00[EUR][1000 genomes]
rs55875530	1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs55927063	1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs56010803	0.82[EUR][1000 genomes]
rs56031628	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs56062220	1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs56110941	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56146538	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56165253	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56169320	0.82[EUR][1000 genomes]
rs56177778	1.00[EUR][1000 genomes]
rs56181028	1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs56202720	0.86[ASN][1000 genomes]
rs56238325	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs56272335	1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs56281800	0.82[EUR][1000 genomes]
rs56289191	1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs56320021	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs57101781	0.82[EUR][1000 genomes]
rs57318054	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs57847126	0.82[EUR][1000 genomes]
rs57862073	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58054304	1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs58569659	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs58588523	1.00[EUR][1000 genomes]
rs59258102	1.00[EUR][1000 genomes]
rs59413237	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs60185821	0.82[EUR][1000 genomes]
rs60357733	1.00[EUR][1000 genomes]
rs61124407	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61376946	0.82[EUR][1000 genomes]
rs61637608	0.82[AFR][1000 genomes];0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs66616139	1.00[EUR][1000 genomes]
rs68130860	0.83[ASN][1000 genomes]
rs72828836	0.88[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs72828838	0.88[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs72828843	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs72828844	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs72828845	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs72828846	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs72828847	0.83[ASN][1000 genomes]
rs72828848	0.85[ASN][1000 genomes]
rs72828849	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72828850	1.00[ASN][1000 genomes]
rs72828851	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72828852	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72828854	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs72828856	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs72828857	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs72828859	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs72828861	1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs72830976	1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs72830979	1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs72830980	1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs72830982	1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs72830984	1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs72830985	1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs72830986	1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs72830989	1.00[EUR][1000 genomes]
rs72830990	0.82[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs72830993	1.00[EUR][1000 genomes]
rs72830995	0.92[EUR][1000 genomes]
rs72830997	1.00[EUR][1000 genomes]
rs72831000	1.00[EUR][1000 genomes]
rs72832803	1.00[EUR][1000 genomes]
rs72832804	1.00[EUR][1000 genomes]
rs72832809	1.00[EUR][1000 genomes]
rs72832810	1.00[EUR][1000 genomes]
rs72832813	1.00[EUR][1000 genomes]
rs72832815	1.00[EUR][1000 genomes]
rs72832816	1.00[EUR][1000 genomes]
rs72832817	1.00[EUR][1000 genomes]
rs72832818	1.00[EUR][1000 genomes]
rs72832820	0.82[EUR][1000 genomes]
rs72832821	0.82[EUR][1000 genomes]
rs72832822	0.82[EUR][1000 genomes]
rs72832824	0.82[EUR][1000 genomes]
rs72832826	0.82[EUR][1000 genomes]
rs72832828	0.82[EUR][1000 genomes]
rs72832837	0.82[EUR][1000 genomes]
rs72832838	0.82[EUR][1000 genomes]
rs72832839	0.82[EUR][1000 genomes]
rs72832841	0.82[EUR][1000 genomes]
rs72832842	0.82[EUR][1000 genomes]
rs72832843	0.82[EUR][1000 genomes]
rs72832846	0.82[EUR][1000 genomes]
rs977406	0.82[EUR][1000 genomes]
rs981196	0.82[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv874838	chr2:111376870-112046226	Weak transcription Strong transcription ZNF genes & repeats Active TSS Enhancers Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
2	nsv874839	chr2:111400934-111868010	Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv1008758	chr2:111415136-111626467	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv535890	chr2:111415136-111626467	Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	nsv997829	chr2:111486961-111780537	Enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:53 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:111489000-111491200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
2	chr2:111489600-111491200	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr2:111489600-111491400	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr2:111489600-111491600	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
5	chr2:111489600-111491800	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
6	chr2:111489800-111491200	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
7	chr2:111489800-111491200	Active TSS	Pancreatic Islets	Pancreatic Islet
8	chr2:111489800-111491200	Flanking Bivalent TSS/Enh	Placenta	Placenta
9	chr2:111489800-111491400	Bivalent Enhancer	Primary B cells from peripheral blood	blood
10	chr2:111489800-111491600	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
11	chr2:111490000-111491200	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
12	chr2:111490000-111491200	Flanking Bivalent TSS/Enh	Primary T regulatory cells fromperipheralblood	blood
13	chr2:111490000-111491200	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr2:111490000-111491400	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
15	chr2:111490200-111491200	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells	blood
16	chr2:111490400-111491200	Flanking Bivalent TSS/Enh	Primary neutrophils fromperipheralblood	blood
17	chr2:111490600-111491200	Bivalent Enhancer	Primary T helper naive cells from peripheral blood	blood
18	chr2:111490600-111491200	Bivalent Enhancer	Primary T killer naive cells fromperipheralblood	blood
19	chr2:111490600-111491200	Bivalent Enhancer	Brain Angular Gyrus	brain
20	chr2:111490600-111491200	Bivalent Enhancer	Duodenum Smooth Muscle	Duodenum
21	chr2:111490600-111491200	Enhancers	Ovary	ovary
22	chr2:111490600-111491200	Bivalent Enhancer	Rectal Mucosa Donor 29	rectum
23	chr2:111490600-111491200	Bivalent Enhancer	Spleen	Spleen
24	chr2:111490600-111491200	Bivalent/Poised TSS	GM12878-XiMat	blood
25	chr2:111490600-111491400	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
26	chr2:111490600-111491400	Flanking Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
27	chr2:111490600-111491400	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
28	chr2:111490800-111491200	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
29	chr2:111490800-111491200	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
30	chr2:111490800-111491200	Bivalent Enhancer	Primary T helper naive cells fromperipheralblood	blood
31	chr2:111490800-111491200	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
32	chr2:111490800-111491200	Bivalent Enhancer	Fetal Intestine Small	intestine
33	chr2:111490800-111491200	Bivalent Enhancer	Fetal Stomach	stomach
34	chr2:111490800-111491400	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 2	blood
35	chr2:111490800-111491400	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
36	chr2:111491000-111491200	Flanking Bivalent TSS/Enh	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
37	chr2:111491000-111491200	Bivalent/Poised TSS	Primary B cells from cord blood	blood
38	chr2:111491000-111491200	Flanking Bivalent TSS/Enh	Primary T killer memory cells from peripheral blood	blood
39	chr2:111491000-111491200	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr2:111491000-111491200	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr2:111491000-111491200	Flanking Bivalent TSS/Enh	Brain Hippocampus Middle	brain
42	chr2:111491000-111491200	Bivalent Enhancer	Brain Substantia Nigra	brain
43	chr2:111491000-111491200	Bivalent Enhancer	Small Intestine	intestine
44	chr2:111491000-111491200	Bivalent Enhancer	Stomach Mucosa	stomach
45	chr2:111491000-111491200	Bivalent/Poised TSS	HMEC	breast
46	chr2:111491000-111491200	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
47	chr2:111491000-111491400	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
48	chr2:111491000-111491400	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
49	chr2:111491000-111491400	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr2:111491000-111491400	Bivalent Enhancer	Ganglion Eminence derived primary cultured neurospheres	brain

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