Variant report

Variant	rs11204895
Chromosome Location	chr1:151795497-151795498
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr1:151786405..151788283-chr1:151795067..151797465,2	MCF-7	breast:
2	chr1:151762692..151764712-chr1:151794747..151796682,2	MCF-7	breast:
3	chr1:151789315..151792282-chr1:151793123..151796667,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000203288	Chromatin interaction
ENSG00000182134	Chromatin interaction
ENSG00000143365	Chromatin interaction

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs12036145	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12144914	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6587620	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6693413	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7531041	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7540027	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7540034	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7540530	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[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	nsv516369	chr1:151780177-151820324	Weak transcription Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Enhancers Active TSS Genic enhancers Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
2	esv1804657	chr1:151784152-151825756	Bivalent Enhancer Active TSS Strong transcription Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
3	nsv1008033	chr1:151785029-151843154	Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Weak transcription Enhancers Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
4	nsv160848	chr1:151789609-151796769	Weak transcription Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Strong transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:55 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:151778600-151802400	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr1:151787400-151800000	Weak transcription	Spleen	Spleen
3	chr1:151788200-151796800	Transcr. at gene 5' and 3'	Fetal Thymus	thymus
4	chr1:151790000-151799000	Transcr. at gene 5' and 3'	Primary T helper 17 cells PMA-I stimulated	--
5	chr1:151790200-151801600	Weak transcription	Right Atrium	heart
6	chr1:151791000-151800600	Weak transcription	Rectal Mucosa Donor 29	rectum
7	chr1:151791600-151795600	Enhancers	Liver	Liver
8	chr1:151792000-151796000	Flanking Active TSS	Dnd41	blood
9	chr1:151793000-151800600	Weak transcription	Lung	lung
10	chr1:151793400-151800200	Weak transcription	Gastric	stomach
11	chr1:151793600-151800800	Weak transcription	Stomach Mucosa	stomach
12	chr1:151793600-151801000	Weak transcription	Rectal Mucosa Donor 31	rectum
13	chr1:151793800-151797600	Weak transcription	Adipose Nuclei	Adipose
14	chr1:151793800-151797600	Weak transcription	Psoas Muscle	Psoas
15	chr1:151793800-151797600	Weak transcription	Right Ventricle	heart
16	chr1:151794000-151798200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr1:151794000-151798400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
18	chr1:151794000-151798600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
19	chr1:151794200-151796200	Weak transcription	Skeletal Muscle Female	skeletal muscle
20	chr1:151794400-151795800	Enhancers	iPS-15b Cell Line	embryonic stem cell
21	chr1:151794400-151797400	Genic enhancers	Skeletal Muscle Male	skeletal muscle
22	chr1:151794600-151796000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr1:151794600-151797800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
24	chr1:151794600-151798800	Weak transcription	Hela-S3	cervix
25	chr1:151794800-151795600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
26	chr1:151794800-151796000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr1:151794800-151797000	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
28	chr1:151794800-151798200	Active TSS	Primary T helper cells PMA-I stimulated	--
29	chr1:151795000-151796000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
30	chr1:151795000-151796000	Enhancers	HUES6 Cell Line	embryonic stem cell
31	chr1:151795000-151796000	Genic enhancers	Pancreas	Pancrea
32	chr1:151795000-151796200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr1:151795000-151797800	Transcr. at gene 5' and 3'	Thymus	Thymus
34	chr1:151795000-151798600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
35	chr1:151795200-151795600	Active TSS	Primary T helper memory cells from peripheral blood 1	blood
36	chr1:151795200-151796000	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr1:151795200-151796000	Active TSS	Duodenum Mucosa	Duodenum
38	chr1:151795200-151796400	Weak transcription	Primary T cells from cord blood	blood
39	chr1:151795200-151796600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
40	chr1:151795200-151799800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
41	chr1:151795400-151795600	Active TSS	Primary T cells fromperipheralblood	blood
42	chr1:151795400-151795800	Active TSS	Primary T regulatory cells fromperipheralblood	blood
43	chr1:151795400-151796200	Genic enhancers	Breast Myoepithelial Primary Cells	Breast
44	chr1:151795400-151796400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
45	chr1:151795400-151796600	Weak transcription	Primary hematopoietic stem cells	blood
46	chr1:151795400-151796800	Active TSS	Primary Natural Killer cells fromperipheralblood	blood
47	chr1:151795400-151797000	Active TSS	Primary T helper cells fromperipheralblood	blood
48	chr1:151795400-151797000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
49	chr1:151795400-151797600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
50	chr1:151795400-151797800	Weak transcription	H1 Cell Line	embryonic stem cell

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