Variant report

Variant	rs10186867
Chromosome Location	chr2:38803855-38803856
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr2:38803779..38806486-chr2:38953077..38954678,2	MCF-7	breast:
2	chr2:38800582..38805538-chr2:38967531..38972325,7	K562	blood:
3	chr2:38801102..38805914-chr2:38807147..38811065,7	MCF-7	breast:
4	chr2:38802059..38810352-chr2:38974835..38979723,14	K562	blood:

Variant related genes	Relation type
ENSG00000115875	Chromatin interaction
ENSG00000152147	Chromatin interaction

Extended variants
information (count: 24 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs10166466	0.84[AFR][1000 genomes]
rs10192837	0.95[AFR][1000 genomes]
rs10197071	0.95[AFR][1000 genomes]
rs10198949	0.89[AFR][1000 genomes]
rs10204707	0.89[AFR][1000 genomes]
rs10204840	1.00[AFR][1000 genomes]
rs13388732	1.00[YRI][hapmap];1.00[AFR][1000 genomes]
rs13391054	1.00[YRI][hapmap];0.84[AFR][1000 genomes]
rs13391755	1.00[AFR][1000 genomes]
rs13392719	1.00[YRI][hapmap];1.00[AFR][1000 genomes]
rs13401946	1.00[YRI][hapmap];0.89[AFR][1000 genomes]
rs13404643	1.00[YRI][hapmap];0.89[AFR][1000 genomes]
rs13413591	1.00[AFR][1000 genomes]
rs13423067	1.00[AFR][1000 genomes]
rs13424641	1.00[AFR][1000 genomes]
rs13427158	0.89[AFR][1000 genomes]
rs17022981	0.89[AFR][1000 genomes]
rs17022992	0.89[AFR][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	nsv916059	chr2:38332341-39119398	Weak transcription Flanking Active TSS Enhancers Genic enhancers Strong transcription Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	143 gene(s)	inside rSNPs	diseases
2	nsv9646	chr2:38358311-39082189	Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	141 gene(s)	inside rSNPs	diseases
3	nsv873881	chr2:38745624-38877636	Enhancers Flanking Active TSS Active TSS Strong transcription Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
4	nsv581482	chr2:38799820-38858669	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription Active TSS 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	17 gene(s)	inside rSNPs	diseases
5	nsv581483	chr2:38799820-38862223	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
6	nsv581484	chr2:38799820-38874177	Flanking Active TSS Active TSS Enhancers Weak transcription Genic enhancers Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:120 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:38763600-38809600	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr2:38768200-38812800	Weak transcription	Psoas Muscle	Psoas
3	chr2:38775800-38821800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr2:38777000-38807200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
5	chr2:38779000-38818200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr2:38779400-38821800	Weak transcription	Right Ventricle	heart
7	chr2:38779600-38807400	Weak transcription	Fetal Heart	heart
8	chr2:38779600-38812800	Weak transcription	Aorta	Aorta
9	chr2:38781200-38827600	Weak transcription	Esophagus	oesophagus
10	chr2:38782400-38819000	Strong transcription	Fetal Thymus	thymus
11	chr2:38783800-38827800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr2:38785000-38827600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr2:38786000-38827600	Weak transcription	Colonic Mucosa	Colon
14	chr2:38786400-38806200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr2:38786400-38818800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr2:38786600-38819000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr2:38787200-38805600	Strong transcription	HUES6 Cell Line	embryonic stem cell
18	chr2:38787200-38806200	Strong transcription	HUES64 Cell Line	embryonic stem cell
19	chr2:38787200-38807000	Strong transcription	HUES48 Cell Line	embryonic stem cell
20	chr2:38787200-38807000	Strong transcription	iPS-20b Cell Line	embryonic stem cell
21	chr2:38787400-38804400	Strong transcription	Placenta	Placenta
22	chr2:38787400-38806400	Strong transcription	Dnd41	blood
23	chr2:38790800-38807000	Strong transcription	iPS-18 Cell Line	embryonic stem cell
24	chr2:38791200-38805200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
25	chr2:38792600-38810200	Strong transcription	K562	blood
26	chr2:38795200-38807200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
27	chr2:38795200-38808400	Weak transcription	Left Ventricle	heart
28	chr2:38795200-38808400	Weak transcription	Lung	lung
29	chr2:38795200-38808400	Weak transcription	Ovary	ovary
30	chr2:38795200-38809200	Weak transcription	Fetal Intestine Small	intestine
31	chr2:38795200-38809200	Weak transcription	Fetal Stomach	stomach
32	chr2:38795200-38814800	Weak transcription	Gastric	stomach
33	chr2:38795400-38808200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
34	chr2:38795600-38804400	Weak transcription	Brain Inferior Temporal Lobe	brain
35	chr2:38795600-38808400	Weak transcription	Brain Cingulate Gyrus	brain
36	chr2:38796200-38808200	Weak transcription	H9 Cell Line	embryonic stem cell
37	chr2:38796400-38804200	Weak transcription	Fetal Brain Male	brain
38	chr2:38796400-38808400	Weak transcription	Brain Angular Gyrus	brain
39	chr2:38796400-38812800	Weak transcription	Small Intestine	intestine
40	chr2:38796600-38808600	Weak transcription	Brain Hippocampus Middle	brain
41	chr2:38797000-38806000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
42	chr2:38798000-38808000	Weak transcription	Colon Smooth Muscle	Colon
43	chr2:38798000-38818000	Weak transcription	Stomach Mucosa	stomach
44	chr2:38798000-38827600	Weak transcription	Spleen	Spleen
45	chr2:38798200-38804400	Weak transcription	Primary T cells from cord blood	blood
46	chr2:38798200-38808000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
47	chr2:38798200-38808400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
48	chr2:38798200-38808400	Weak transcription	Pancreas	Pancrea
49	chr2:38798200-38812800	Weak transcription	Fetal Muscle Leg	muscle
50	chr2:38798200-38812800	Weak transcription	Thymus	Thymus

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