Variant report

Variant	rs41270187
Chromosome Location	chr1:228878871-228878872
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr1:228871721..228874007-chr1:228877352..228880161,2	MCF-7	breast:
2	chr1:228872086..228874934-chr1:228877939..228879672,2	MCF-7	breast:
3	chr1:228878069..228881022-chr1:228881765..228883502,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000116574	Chromatin interaction

Extended variants
information (count: 28 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs1062060	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11578216	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11580020	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11583565	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11587994	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs17352654	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs17352829	0.81[ASN][1000 genomes]
rs3738073	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs41270189	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs41271473	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4391638	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4641285	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4993975	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs55730631	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs55956922	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs56221905	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs61825705	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6665334	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6701241	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs72751907	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs72751929	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.87[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1013051	chr1:228786702-228903706	Genic enhancers Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
2	nsv997801	chr1:228786702-228975127	Enhancers Weak transcription Bivalent/Poised TSS Genic enhancers Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
3	nsv870365	chr1:228788356-229267904	Enhancers Active TSS Flanking Active TSS Weak transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
4	nsv998255	chr1:228791784-228919202	Enhancers Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
5	nsv549299	chr1:228793246-229455876	Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Strong transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
6	nsv468316	chr1:228854703-228919202	Flanking Active TSS Strong transcription Enhancers Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
7	nsv549300	chr1:228854703-228919202	Active TSS Enhancers Bivalent/Poised TSS Weak transcription Bivalent Enhancer Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:84 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:228872400-228880200	Weak transcription	Left Ventricle	heart
2	chr1:228872600-228880600	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr1:228872600-228881200	Weak transcription	Esophagus	oesophagus
4	chr1:228872600-228884400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
5	chr1:228873200-228879000	Weak transcription	Ovary	ovary
6	chr1:228873200-228884800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr1:228873400-228879000	Weak transcription	Small Intestine	intestine
8	chr1:228873600-228879000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
9	chr1:228873600-228879000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr1:228873800-228879000	Weak transcription	H1 Cell Line	embryonic stem cell
11	chr1:228873800-228879000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr1:228873800-228879000	Weak transcription	Primary T helper cells PMA-I stimulated	--
13	chr1:228873800-228880200	Weak transcription	Thymus	Thymus
14	chr1:228873800-228882800	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr1:228873800-228884200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr1:228873800-228884200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
17	chr1:228874000-228879200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
18	chr1:228874000-228879400	Weak transcription	HUES48 Cell Line	embryonic stem cell
19	chr1:228874000-228881800	Genic enhancers	Liver	Liver
20	chr1:228874200-228880400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
21	chr1:228874400-228884000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
22	chr1:228874600-228879000	Weak transcription	Primary T helper cells fromperipheralblood	blood
23	chr1:228874600-228879800	Weak transcription	A549	lung
24	chr1:228875000-228881000	Strong transcription	Rectal Mucosa Donor 29	rectum
25	chr1:228875000-228884200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
26	chr1:228875400-228879400	Transcr. at gene 5' and 3'	Brain Hippocampus Middle	brain
27	chr1:228875400-228879400	Genic enhancers	Gastric	stomach
28	chr1:228875600-228883200	Strong transcription	Duodenum Mucosa	Duodenum
29	chr1:228875800-228881000	Strong transcription	Sigmoid Colon	Sigmoid Colon
30	chr1:228875800-228884000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
31	chr1:228876200-228883200	Strong transcription	Primary neutrophils fromperipheralblood	blood
32	chr1:228876600-228882600	Strong transcription	Placenta	Placenta
33	chr1:228876600-228883400	Strong transcription	Fetal Intestine Small	intestine
34	chr1:228876800-228884800	Weak transcription	Fetal Brain Male	brain
35	chr1:228877000-228879000	Weak transcription	Stomach Mucosa	stomach
36	chr1:228877000-228883200	Strong transcription	Fetal Muscle Trunk	muscle
37	chr1:228877000-228884800	Weak transcription	Fetal Kidney	kidney
38	chr1:228877200-228879000	Enhancers	Brain Inferior Temporal Lobe	brain
39	chr1:228877200-228879000	Weak transcription	Placenta Amnion	Placenta Amnion
40	chr1:228877200-228880200	Strong transcription	Fetal Thymus	thymus
41	chr1:228877200-228880800	Strong transcription	Fetal Intestine Large	intestine
42	chr1:228877200-228883600	Strong transcription	Fetal Stomach	stomach
43	chr1:228877200-228889600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr1:228877400-228883800	Strong transcription	Fetal Brain Female	brain
45	chr1:228877600-228881200	Strong transcription	Colon Smooth Muscle	Colon
46	chr1:228877600-228881600	Strong transcription	Duodenum Smooth Muscle	Duodenum
47	chr1:228877600-228883600	Strong transcription	Fetal Muscle Leg	muscle
48	chr1:228877800-228879000	Transcr. at gene 5' and 3'	Brain Substantia Nigra	brain
49	chr1:228877800-228881000	Strong transcription	Skeletal Muscle Male	skeletal muscle
50	chr1:228877800-228881200	Strong transcription	Primary T cells from cord blood	blood

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