Variant report

Variant	rs2079228
Chromosome Location	chr11:17832029-17832030
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:17802523..17804116-chr11:17831830..17833743,2	MCF-7	breast:
2	chr11:17823576..17826889-chr11:17829759..17833137,3	MCF-7	breast:

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs1005711	0.84[ASN][1000 genomes]
rs2237949	0.85[ASN][1000 genomes]
rs4756919	0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4756921	0.85[EUR][1000 genomes]
rs7109364	0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7932302	0.81[EUR][1000 genomes]
rs7948134	0.86[EUR][1000 genomes];0.82[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	nsv832078	chr11:17780503-17953521	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases
2	nsv1043973	chr11:17781560-17869896	Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	1 gene(s)	inside rSNPs	diseases
3	nsv949248	chr11:17791822-18692687	Weak transcription Flanking Active TSS Strong transcription Enhancers Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	156 gene(s)	inside rSNPs	diseases
4	nsv897026	chr11:17823296-18084878	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:17802800-17832400	Weak transcription	Stomach Smooth Muscle	stomach
2	chr11:17806000-17837800	Weak transcription	Primary B cells from peripheral blood	blood
3	chr11:17806800-17867400	Weak transcription	Primary B cells from cord blood	blood
4	chr11:17808200-17861400	Weak transcription	Thymus	Thymus
5	chr11:17808800-17834600	Weak transcription	Aorta	Aorta
6	chr11:17809000-17833200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr11:17815600-17841400	Weak transcription	HepG2	liver
8	chr11:17818600-17843200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr11:17820800-17832600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr11:17825400-17843400	Weak transcription	Lung	lung
11	chr11:17825600-17832400	Weak transcription	Brain Substantia Nigra	brain
12	chr11:17826000-17832400	Weak transcription	Brain Cingulate Gyrus	brain
13	chr11:17826600-17832200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr11:17829000-17832400	Weak transcription	Fetal Brain Male	brain
15	chr11:17829200-17832200	Weak transcription	Fetal Stomach	stomach
16	chr11:17829200-17832400	Weak transcription	Brain Anterior Caudate	brain
17	chr11:17829200-17833400	Weak transcription	Rectal Mucosa Donor 31	rectum
18	chr11:17829400-17832200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
19	chr11:17829400-17832200	Weak transcription	Brain Angular Gyrus	brain
20	chr11:17829400-17833400	Weak transcription	Gastric	stomach
21	chr11:17829400-17833600	Weak transcription	Fetal Intestine Large	intestine
22	chr11:17829600-17832400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr11:17829600-17832600	Weak transcription	Fetal Brain Female	brain
24	chr11:17829800-17832200	Weak transcription	Cortex derived primary cultured neurospheres	brain
25	chr11:17829800-17833400	Weak transcription	Fetal Intestine Small	intestine
26	chr11:17831000-17836200	Enhancers	Skeletal Muscle Male	skeletal muscle
27	chr11:17831200-17834400	Enhancers	Brain Hippocampus Middle	brain
28	chr11:17831200-17837000	Enhancers	Breast Myoepithelial Primary Cells	Breast
29	chr11:17831200-17849400	Weak transcription	Primary T cells fromperipheralblood	blood
30	chr11:17831400-17833000	Enhancers	HSMMtube	muscle
31	chr11:17831400-17834400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
32	chr11:17831600-17832600	Enhancers	Right Ventricle	heart
33	chr11:17831600-17833200	Enhancers	Right Atrium	heart
34	chr11:17831600-17834000	Weak transcription	Duodenum Mucosa	Duodenum
35	chr11:17831600-17835600	Enhancers	Fetal Muscle Leg	muscle
36	chr11:17831600-17836400	Enhancers	Skeletal Muscle Female	skeletal muscle
37	chr11:17831800-17832600	Enhancers	Esophagus	oesophagus
38	chr11:17831800-17833600	Enhancers	HMEC	breast
39	chr11:17831800-17833800	Enhancers	Fetal Heart	heart
40	chr11:17831800-17834600	Enhancers	Fetal Muscle Trunk	muscle
41	chr11:17831800-17835600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr11:17831800-17835600	Enhancers	Left Ventricle	heart
43	chr11:17832000-17833000	Weak transcription	Adipose Nuclei	Adipose
44	chr11:17832000-17833000	Weak transcription	Psoas Muscle	Psoas
45	chr11:17832000-17833600	Weak transcription	Fetal Kidney	kidney
46	chr11:17832000-17833600	Enhancers	NHEK	skin
47	chr11:17832000-17834600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr11:17832000-17834600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
49	chr11:17832000-17834800	Enhancers	Brain Inferior Temporal Lobe	brain
50	chr11:17832000-17849600	Weak transcription	Primary T cells from cord blood	blood

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