Variant report

Variant	rs73464862
Chromosome Location	chr11:48070620-48070621
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr11:48001276..48003972-chr11:48068984..48071526,3	MCF-7	breast:
2	chr11:48068334..48069860-chr11:48070016..48072544,2	MCF-7	breast:
3	chr11:48069835..48071887-chr11:48083817..48085807,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000149177	Chromatin interaction

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:1)

rs_ID	r²[population]
rs73464824	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:19 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1052397	chr11:47675470-48594256	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	97 gene(s)	inside rSNPs	diseases
2	nsv530620	chr11:47765455-48664555	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	93 gene(s)	inside rSNPs	diseases
3	nsv1036992	chr11:47794621-48666024	Strong transcription Flanking Active TSS Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
4	nsv1036451	chr11:47902321-48616646	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers Flanking Active TSS Active TSS 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 miRNA target site	26 gene(s)	inside rSNPs	diseases
5	nsv541037	chr11:47902321-48616646	Enhancers Strong transcription Genic enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
6	nsv1047490	chr11:47916708-48388686	Enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent/Poised TSS Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
7	nsv1044266	chr11:47929586-48276132	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Strong transcription Genic enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
8	nsv541038	chr11:47929586-48276132	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
9	nsv1053145	chr11:47967902-48086950	Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
10	nsv870381	chr11:47989434-48142648	Enhancers Bivalent Enhancer Weak transcription Bivalent/Poised TSS Flanking Active TSS Strong transcription Genic enhancers Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
11	esv3396029	chr11:47993857-48241494	Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
12	nsv897327	chr11:48004369-48911660	ZNF genes & repeats Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
13	nsv869124	chr11:48014539-48783113	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
14	nsv1051805	chr11:48016488-48378048	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
15	nsv428573	chr11:48032457-48152344	Genic enhancers Weak transcription ZNF genes & repeats Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
16	nsv897328	chr11:48043053-48901553	Strong transcription Enhancers Genic enhancers ZNF genes & repeats Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
17	nsv897329	chr11:48052676-48319974	Enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
18	nsv1048554	chr11:48062861-48388686	Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region miRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
19	nsv1038210	chr11:48068862-48388686	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA miRNA target site	13 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:95 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:48047400-48073400	Weak transcription	HSMMtube	muscle
2	chr11:48047400-48073800	Weak transcription	Left Ventricle	heart
3	chr11:48050800-48073000	Weak transcription	Esophagus	oesophagus
4	chr11:48051600-48071200	Weak transcription	Fetal Intestine Large	intestine
5	chr11:48051600-48073800	Weak transcription	Aorta	Aorta
6	chr11:48053800-48073400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
7	chr11:48058000-48073400	Weak transcription	K562	blood
8	chr11:48058600-48072000	Weak transcription	Fetal Kidney	kidney
9	chr11:48060000-48073000	Weak transcription	Hela-S3	cervix
10	chr11:48060000-48073200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr11:48062600-48073400	Weak transcription	Gastric	stomach
12	chr11:48064400-48073200	Weak transcription	NHLF	lung
13	chr11:48064600-48073400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr11:48065000-48071600	Genic enhancers	A549	lung
15	chr11:48065600-48076000	Weak transcription	Rectal Mucosa Donor 31	rectum
16	chr11:48065800-48074200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr11:48066000-48071800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr11:48066000-48073000	Weak transcription	Duodenum Mucosa	Duodenum
19	chr11:48066000-48073800	Weak transcription	Colonic Mucosa	Colon
20	chr11:48066000-48073800	Weak transcription	Right Atrium	heart
21	chr11:48066000-48074000	Weak transcription	Fetal Muscle Leg	muscle
22	chr11:48066000-48075600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr11:48066000-48076800	Weak transcription	Thymus	Thymus
24	chr11:48066200-48071600	Weak transcription	HUES64 Cell Line	embryonic stem cell
25	chr11:48066200-48071800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
26	chr11:48066200-48072000	Weak transcription	Liver	Liver
27	chr11:48066200-48072400	Weak transcription	Fetal Thymus	thymus
28	chr11:48066200-48073000	Weak transcription	Sigmoid Colon	Sigmoid Colon
29	chr11:48066200-48073800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
30	chr11:48066400-48071800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
31	chr11:48066400-48073400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr11:48066400-48073800	Weak transcription	Lung	lung
33	chr11:48066600-48073400	Weak transcription	H9 Cell Line	embryonic stem cell
34	chr11:48067000-48072800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
35	chr11:48067000-48073800	Weak transcription	Skeletal Muscle Female	skeletal muscle
36	chr11:48067200-48071400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
37	chr11:48067200-48071400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
38	chr11:48067400-48071600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
39	chr11:48067600-48071200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
40	chr11:48067600-48071600	Weak transcription	Primary T cells from cord blood	blood
41	chr11:48068200-48071200	Enhancers	Primary neutrophils fromperipheralblood	blood
42	chr11:48068200-48071600	Weak transcription	Primary T helper cells PMA-I stimulated	--
43	chr11:48068600-48071200	Enhancers	Placenta Amnion	Placenta Amnion
44	chr11:48068600-48072000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr11:48068800-48071000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr11:48068800-48071400	Enhancers	Brain Anterior Caudate	brain
47	chr11:48068800-48074000	Weak transcription	Right Ventricle	heart
48	chr11:48068800-48074600	Enhancers	Placenta	Placenta
49	chr11:48069000-48071000	Enhancers	Brain Substantia Nigra	brain
50	chr11:48069000-48071200	Weak transcription	Primary T killer memory cells from peripheral blood	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links