Variant report

Variant	rs6919467
Chromosome Location	chr6:13422651-13422652
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:13421809..13424895-chr6:13440143..13443244,3	MCF-7	breast:

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:5)

rs_ID	r²[population]
rs6904847	0.91[AFR][1000 genomes]
rs6916302	0.91[AFR][1000 genomes]
rs6934350	1.00[AFR][1000 genomes]
rs7739234	1.00[AFR][1000 genomes]
rs7752876	1.00[AFR][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	nsv532021	chr6:13232627-13805381	Active TSS Genic enhancers Strong transcription Enhancers Flanking Active TSS Weak 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 miRNA target site	74 gene(s)	inside rSNPs	diseases
2	nsv1028533	chr6:13239059-13484814	Enhancers Strong transcription Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers 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 target site	23 gene(s)	inside rSNPs	diseases
3	nsv538136	chr6:13239059-13484814	Strong transcription Weak transcription Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
4	nsv1033620	chr6:13419730-13571788	Weak transcription Enhancers Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:102 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:13408800-13423000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr6:13411600-13424200	Enhancers	Right Ventricle	heart
3	chr6:13417200-13424200	Enhancers	Brain Angular Gyrus	brain
4	chr6:13417600-13424000	Enhancers	Brain Cingulate Gyrus	brain
5	chr6:13417800-13424000	Enhancers	Adipose Nuclei	Adipose
6	chr6:13417800-13424200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
7	chr6:13417800-13424200	Enhancers	Left Ventricle	heart
8	chr6:13417800-13424600	Enhancers	Right Atrium	heart
9	chr6:13417800-13424800	Enhancers	Brain Inferior Temporal Lobe	brain
10	chr6:13417800-13427000	Enhancers	Psoas Muscle	Psoas
11	chr6:13418800-13422800	Enhancers	Fetal Heart	heart
12	chr6:13419200-13424200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr6:13419200-13428200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
14	chr6:13419400-13424000	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
15	chr6:13419400-13429800	Enhancers	Fetal Lung	lung
16	chr6:13419600-13424200	Enhancers	HUES6 Cell Line	embryonic stem cell
17	chr6:13419800-13422800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr6:13419800-13422800	Enhancers	Fetal Muscle Trunk	muscle
19	chr6:13420000-13423000	Enhancers	Breast Myoepithelial Primary Cells	Breast
20	chr6:13420000-13424000	Enhancers	Brain Substantia Nigra	brain
21	chr6:13420200-13427600	Weak transcription	Primary neutrophils fromperipheralblood	blood
22	chr6:13420200-13430000	Enhancers	Fetal Stomach	stomach
23	chr6:13420400-13422800	Weak transcription	Primary monocytes fromperipheralblood	blood
24	chr6:13420400-13423000	Enhancers	Skeletal Muscle Male	skeletal muscle
25	chr6:13420400-13423200	Enhancers	Colon Smooth Muscle	Colon
26	chr6:13420400-13423200	Weak transcription	Pancreas	Pancrea
27	chr6:13420400-13423800	Enhancers	Duodenum Smooth Muscle	Duodenum
28	chr6:13420400-13425400	Weak transcription	NHEK	skin
29	chr6:13420400-13427400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
30	chr6:13420600-13423600	Weak transcription	Esophagus	oesophagus
31	chr6:13420600-13425400	Weak transcription	Primary T cells fromperipheralblood	blood
32	chr6:13420600-13425800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr6:13420600-13428000	Weak transcription	Thymus	Thymus
34	chr6:13420800-13425600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr6:13421000-13425400	Weak transcription	Liver	Liver
36	chr6:13421000-13425400	Weak transcription	Placenta	Placenta
37	chr6:13421000-13427200	Weak transcription	Primary B cells from cord blood	blood
38	chr6:13421200-13425200	Weak transcription	Primary B cells from peripheral blood	blood
39	chr6:13421200-13426400	Weak transcription	Primary T helper cells PMA-I stimulated	--
40	chr6:13421400-13422800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr6:13421400-13423400	Enhancers	Cortex derived primary cultured neurospheres	brain
42	chr6:13421400-13424200	Enhancers	H1 Cell Line	embryonic stem cell
43	chr6:13421400-13426600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
44	chr6:13421400-13427800	Weak transcription	Primary T cells from cord blood	blood
45	chr6:13421600-13423800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
46	chr6:13421600-13424000	Enhancers	Fetal Muscle Leg	muscle
47	chr6:13421800-13422800	Enhancers	Skeletal Muscle Female	skeletal muscle
48	chr6:13421800-13423000	Enhancers	Fetal Intestine Small	intestine
49	chr6:13421800-13423400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
50	chr6:13421800-13423400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links