Variant report

Variant	rs34667799
Chromosome Location	chr11:48053497-48053498
allele	-/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr11:48026525..48028849-chr11:48051139..48053523,2	MCF-7	breast:
2	chr11:48051913..48054330-chr11:48054555..48057402,3	MCF-7	breast:
3	chr11:48041770..48044575-chr11:48053476..48055088,2	MCF-7	breast:
4	chr11:48002002..48003604-chr11:48052430..48054818,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000149177	Chromatin interaction

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

Variant overlapped rSNPs/rCNVs (count:17 , 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

No data

Chromatin state (count:113 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:48035600-48056600	Weak transcription	HSMM	muscle
2	chr11:48046400-48056600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr11:48046400-48058200	Enhancers	Primary monocytes fromperipheralblood	blood
4	chr11:48046600-48059600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr11:48047000-48057800	Weak transcription	NHLF	lung
6	chr11:48047400-48073400	Weak transcription	HSMMtube	muscle
7	chr11:48047400-48073800	Weak transcription	Left Ventricle	heart
8	chr11:48047600-48055600	Weak transcription	Pancreatic Islets	Pancreatic Islet
9	chr11:48047800-48055000	Weak transcription	Stomach Smooth Muscle	stomach
10	chr11:48048000-48056600	Weak transcription	Pancreas	Pancrea
11	chr11:48048000-48057200	Weak transcription	Placenta Amnion	Placenta Amnion
12	chr11:48049000-48058600	Genic enhancers	A549	lung
13	chr11:48049400-48056600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
14	chr11:48049600-48054200	Enhancers	Primary T helper cells PMA-I stimulated	--
15	chr11:48049800-48054400	Enhancers	Stomach Mucosa	stomach
16	chr11:48050200-48068200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr11:48050400-48053800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr11:48050400-48053800	Enhancers	Sigmoid Colon	Sigmoid Colon
19	chr11:48050400-48054000	Enhancers	Skeletal Muscle Female	skeletal muscle
20	chr11:48050400-48055400	Enhancers	Placenta	Placenta
21	chr11:48050400-48058000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr11:48050600-48053800	Enhancers	HUES64 Cell Line	embryonic stem cell
23	chr11:48050600-48053800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr11:48050600-48053800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
25	chr11:48050800-48053800	Enhancers	iPS-20b Cell Line	embryonic stem cell
26	chr11:48050800-48055000	Weak transcription	Rectal Smooth Muscle	rectum
27	chr11:48050800-48056800	Weak transcription	Small Intestine	intestine
28	chr11:48050800-48058000	Enhancers	Adipose Nuclei	Adipose
29	chr11:48050800-48058600	Enhancers	Brain Anterior Caudate	brain
30	chr11:48050800-48073000	Weak transcription	Esophagus	oesophagus
31	chr11:48051000-48054000	Enhancers	Brain Angular Gyrus	brain
32	chr11:48051000-48056600	Weak transcription	Brain Germinal Matrix	brain
33	chr11:48051000-48057200	Weak transcription	Fetal Heart	heart
34	chr11:48051200-48053800	Enhancers	Skeletal Muscle Male	skeletal muscle
35	chr11:48051200-48055200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
36	chr11:48051600-48054000	Enhancers	Rectal Mucosa Donor 29	rectum
37	chr11:48051600-48057600	Weak transcription	Fetal Lung	lung
38	chr11:48051600-48071200	Weak transcription	Fetal Intestine Large	intestine
39	chr11:48051600-48073800	Weak transcription	Aorta	Aorta
40	chr11:48051800-48053600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr11:48051800-48057200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr11:48051800-48057200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
43	chr11:48051800-48057200	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
44	chr11:48051800-48057400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
45	chr11:48051800-48058600	Enhancers	Primary T cells fromperipheralblood	blood
46	chr11:48052000-48056200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
47	chr11:48052000-48056600	Weak transcription	Muscle Satellite Cultured Cells	--
48	chr11:48052000-48057000	Strong transcription	Fetal Intestine Small	intestine
49	chr11:48052200-48053600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr11:48052200-48054000	Enhancers	Brain Inferior Temporal Lobe	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links