Variant report

Variant	rs5030174
Chromosome Location	chr11:32449098-32449099
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr11:32447031..32449133-chr11:32603580..32605616,2	K562	blood:
2	chr11:32420914..32422943-chr11:32448387..32450097,2	K562	blood:
3	chr11:32413863..32417759-chr11:32446575..32449998,5	K562	blood:

Variant related genes	Relation type
ENSG00000184937	Chromatin interaction
ENSG00000149100	Chromatin interaction

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

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs12272493	1.00[ASN][1000 genomes]
rs17749506	1.00[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs3899020	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4078090	1.00[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs5030198	1.00[AFR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs5030199	1.00[AFR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs5030212	1.00[AFR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs5030225	1.00[AFR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs5030242	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs5030244	1.00[AFR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs5030247	1.00[AFR][1000 genomes];0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs5030263	1.00[AFR][1000 genomes];0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs5030265	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs5030267	1.00[AFR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72893503	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72893539	1.00[AFR][1000 genomes];0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72893546	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72893548	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72905032	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72905039	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72905047	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72905081	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72905083	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs72905088	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72906988	1.00[AFR][1000 genomes];0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs72908924	1.00[AFR][1000 genomes];0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs72908926	1.00[AFR][1000 genomes];0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs72908928	1.00[AFR][1000 genomes];0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs72908989	1.00[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs72909438	1.00[AFR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72909441	1.00[AFR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72909473	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72909474	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72909477	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72909479	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72909480	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][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	nsv832108	chr11:32395937-32560583	Bivalent/Poised TSS Enhancers Bivalent Enhancer Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Weak transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
2	nsv1038188	chr11:32410305-32449799	Bivalent Enhancer Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
3	nsv1044547	chr11:32435753-32465233	Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
4	esv2753303	chr11:32447324-32494924	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
5	nsv1051559	chr11:32447347-32465233	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Weak transcription Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:59 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:32447600-32449200	Bivalent Enhancer	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr11:32447600-32449200	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr11:32447600-32449800	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
4	chr11:32447600-32450000	Bivalent Enhancer	Fetal Heart	heart
5	chr11:32447800-32449800	Bivalent Enhancer	Fetal Brain Male	brain
6	chr11:32447800-32450000	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
7	chr11:32448000-32449600	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
8	chr11:32448000-32450000	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
9	chr11:32448000-32450000	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 1	blood
10	chr11:32448200-32449200	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
11	chr11:32448200-32449200	Flanking Bivalent TSS/Enh	Brain Germinal Matrix	brain
12	chr11:32448200-32449600	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
13	chr11:32448200-32449600	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
14	chr11:32448200-32449800	Bivalent Enhancer	Placenta Amnion	Placenta Amnion
15	chr11:32448200-32450000	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
16	chr11:32448400-32449200	Flanking Active TSS	Primary hematopoietic stem cells	blood
17	chr11:32448400-32449200	Flanking Bivalent TSS/Enh	Thymus	Thymus
18	chr11:32448400-32449600	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
19	chr11:32448400-32449600	Enhancers	Pancreas	Pancrea
20	chr11:32448600-32449200	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
21	chr11:32448600-32449200	Bivalent Enhancer	Brain Anterior Caudate	brain
22	chr11:32448600-32449200	Bivalent Enhancer	Lung	lung
23	chr11:32448600-32449400	Bivalent Enhancer	Fetal Stomach	stomach
24	chr11:32448600-32449800	Bivalent/Poised TSS	Primary T cells from cord blood	blood
25	chr11:32448600-32449800	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
26	chr11:32448600-32450200	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr11:32448600-32450400	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
28	chr11:32448800-32449200	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
29	chr11:32448800-32449200	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
30	chr11:32448800-32449200	Bivalent Enhancer	Adipose Nuclei	Adipose
31	chr11:32448800-32449200	Bivalent Enhancer	Brain Hippocampus Middle	brain
32	chr11:32448800-32449200	Enhancers	Gastric	stomach
33	chr11:32448800-32449200	Bivalent Enhancer	Left Ventricle	heart
34	chr11:32448800-32449600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
35	chr11:32448800-32449600	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr11:32448800-32449800	Bivalent Enhancer	Fetal Muscle Leg	muscle
37	chr11:32448800-32450000	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr11:32448800-32450200	ZNF genes & repeats	Spleen	Spleen
39	chr11:32448800-32450400	Bivalent Enhancer	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr11:32448800-32450600	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
41	chr11:32448800-32454800	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
42	chr11:32449000-32449200	Flanking Bivalent TSS/Enh	ES-WA7 Cell Line	embryonic stem cell
43	chr11:32449000-32449200	Flanking Bivalent TSS/Enh	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr11:32449000-32449200	Flanking Bivalent TSS/Enh	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr11:32449000-32449200	Bivalent Enhancer	Aorta	Aorta
46	chr11:32449000-32449200	Bivalent/Poised TSS	Fetal Brain Female	brain
47	chr11:32449000-32449200	Flanking Bivalent TSS/Enh	Fetal Kidney	kidney
48	chr11:32449000-32449200	Flanking Active TSS	Right Atrium	heart
49	chr11:32449000-32449200	Transcr. at gene 5' and 3'	K562	blood
50	chr11:32449000-32449400	Bivalent Enhancer	iPS DF 6.9 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links