Variant report

Variant	rs2658555
Chromosome Location	chr11:18511006-18511007
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs1857908	1.00[AMR][1000 genomes]
rs2658556	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2658560	1.00[YRI][hapmap];0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2698570	1.00[AMR][1000 genomes]
rs4150669	1.00[AMR][1000 genomes]
rs4635056	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4757670	1.00[YRI][hapmap];0.92[AFR][1000 genomes]
rs7107188	1.00[AMR][1000 genomes]
rs895531	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	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
2	nsv553633	chr11:18311701-19058451	Weak transcription Strong transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	144 gene(s)	inside rSNPs	diseases
3	nsv1047049	chr11:18359702-18520008	Enhancers Active TSS Weak transcription Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
4	nsv540955	chr11:18359702-18520008	Enhancers Genic enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
5	nsv1038015	chr11:18435855-18558211	Strong transcription Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
6	nsv1042155	chr11:18435855-18697576	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	72 gene(s)	inside rSNPs	diseases
7	nsv467719	chr11:18447611-18542227	Weak transcription Strong transcription Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
8	nsv553634	chr11:18447611-18542227	Strong transcription Weak transcription Enhancers Flanking Bivalent TSS/Enh Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:18483600-18526200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr11:18496000-18515200	Strong transcription	Fetal Muscle Trunk	muscle
3	chr11:18496200-18513200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
4	chr11:18496200-18513400	Strong transcription	Fetal Muscle Leg	muscle
5	chr11:18496200-18538000	Strong transcription	Primary neutrophils fromperipheralblood	blood
6	chr11:18496200-18541200	Strong transcription	Monocytes-CD14+_RO01746	blood
7	chr11:18496400-18542000	Strong transcription	Primary T cells fromperipheralblood	blood
8	chr11:18496600-18540600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr11:18496600-18541000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
10	chr11:18497000-18511600	Strong transcription	Duodenum Mucosa	Duodenum
11	chr11:18497000-18513200	Strong transcription	Duodenum Smooth Muscle	Duodenum
12	chr11:18497200-18513200	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr11:18497600-18513200	Strong transcription	Cortex derived primary cultured neurospheres	brain
14	chr11:18497800-18512200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr11:18498400-18512200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr11:18498800-18513600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
17	chr11:18499400-18513400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr11:18500000-18547000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
19	chr11:18503000-18512200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr11:18503200-18512200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
21	chr11:18503200-18516200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr11:18503800-18512400	Weak transcription	Psoas Muscle	Psoas
23	chr11:18504000-18540600	Weak transcription	Pancreatic Islets	Pancreatic Islet
24	chr11:18504200-18512200	Weak transcription	Placenta Amnion	Placenta Amnion
25	chr11:18504200-18522800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
26	chr11:18504400-18511800	Weak transcription	K562	blood
27	chr11:18504600-18511200	Weak transcription	Brain Inferior Temporal Lobe	brain
28	chr11:18504600-18511600	Weak transcription	H9 Cell Line	embryonic stem cell
29	chr11:18504600-18512200	Weak transcription	NHLF	lung
30	chr11:18504600-18513000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
31	chr11:18504600-18523400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
32	chr11:18504600-18523400	Weak transcription	Small Intestine	intestine
33	chr11:18504600-18523600	Weak transcription	HMEC	breast
34	chr11:18505000-18511200	Weak transcription	H1 Cell Line	embryonic stem cell
35	chr11:18505000-18511600	Weak transcription	Aorta	Aorta
36	chr11:18505000-18512200	Weak transcription	Colon Smooth Muscle	Colon
37	chr11:18505200-18512200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
38	chr11:18505200-18531800	Weak transcription	Fetal Brain Male	brain
39	chr11:18505600-18511600	Weak transcription	Fetal Heart	heart
40	chr11:18505600-18511800	Weak transcription	Gastric	stomach
41	chr11:18505800-18511400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
42	chr11:18505800-18511600	Weak transcription	A549	lung
43	chr11:18505800-18511800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
44	chr11:18505800-18511800	Weak transcription	Rectal Smooth Muscle	rectum
45	chr11:18505800-18512200	Weak transcription	Pancreas	Pancrea
46	chr11:18505800-18512200	Weak transcription	Stomach Mucosa	stomach
47	chr11:18506000-18511200	Weak transcription	Brain Anterior Caudate	brain
48	chr11:18506000-18511600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr11:18506000-18511600	Weak transcription	Brain Substantia Nigra	brain
50	chr11:18506000-18519200	Weak transcription	Primary T killer memory cells from peripheral blood	blood

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