Variant report

Variant	rs6913353
Chromosome Location	chr6:166780481-166780482
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:166756008..166757539-chr6:166779896..166782312,2	MCF-7	breast:
2	chr6:166780289..166781935-chr6:166782190..166784893,2	K562	blood:
3	chr6:166744531..166747958-chr6:166778201..166781775,3	K562	blood:

Variant related genes	Relation type
ENSG00000198818	Chromatin interaction
ENSG00000060762	Chromatin interaction

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs4599613	1.00[MEX][hapmap]
rs55920189	1.00[AMR][1000 genomes]
rs6456080	1.00[AMR][1000 genomes]
rs6933688	0.90[AMR][1000 genomes]
rs6941755	1.00[AMR][1000 genomes]
rs73265128	1.00[AMR][1000 genomes]
rs73265154	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3490076	chr6:166727901-167306743	Strong transcription Weak transcription Flanking Active TSS Genic enhancers Enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	25 gene(s)	inside rSNPs	diseases
2	esv3490077	chr6:166727901-167306743	Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	25 gene(s)	inside rSNPs	diseases
3	esv1797072	chr6:166766142-166782143	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:106 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:166773200-166794600	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr6:166773400-166790000	Weak transcription	Fetal Brain Male	brain
3	chr6:166774400-166790600	Weak transcription	Psoas Muscle	Psoas
4	chr6:166774800-166783400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr6:166774800-166784000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
6	chr6:166774800-166787200	Weak transcription	Esophagus	oesophagus
7	chr6:166774800-166795000	Weak transcription	Placenta Amnion	Placenta Amnion
8	chr6:166775000-166793800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
9	chr6:166775200-166788400	Weak transcription	HMEC	breast
10	chr6:166775400-166785400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
11	chr6:166775400-166787000	Weak transcription	Fetal Kidney	kidney
12	chr6:166775800-166794800	Weak transcription	Primary hematopoietic stem cells	blood
13	chr6:166776000-166781200	Strong transcription	HepG2	liver
14	chr6:166776200-166780600	Genic enhancers	Liver	Liver
15	chr6:166776200-166780600	Strong transcription	Fetal Lung	lung
16	chr6:166776200-166780800	Strong transcription	Primary T cells from cord blood	blood
17	chr6:166776200-166782600	Strong transcription	Primary monocytes fromperipheralblood	blood
18	chr6:166776200-166782600	Strong transcription	Rectal Mucosa Donor 31	rectum
19	chr6:166776200-166782600	Strong transcription	Monocytes-CD14+_RO01746	blood
20	chr6:166776200-166784600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
21	chr6:166776400-166780600	Strong transcription	Duodenum Mucosa	Duodenum
22	chr6:166776400-166780600	Strong transcription	Rectal Mucosa Donor 29	rectum
23	chr6:166776400-166780600	Strong transcription	Sigmoid Colon	Sigmoid Colon
24	chr6:166776400-166780800	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
25	chr6:166776400-166781800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
26	chr6:166776600-166780600	Strong transcription	Primary T cells fromperipheralblood	blood
27	chr6:166776600-166780600	Strong transcription	Primary T helper cells fromperipheralblood	blood
28	chr6:166776600-166780600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
29	chr6:166776600-166780600	Strong transcription	GM12878-XiMat	blood
30	chr6:166776600-166782600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
31	chr6:166777400-166780800	Enhancers	Cortex derived primary cultured neurospheres	brain
32	chr6:166777400-166795400	Weak transcription	Gastric	stomach
33	chr6:166777600-166780600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr6:166777800-166788400	Weak transcription	NHEK	skin
35	chr6:166778000-166780800	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr6:166778000-166781000	Enhancers	iPS-15b Cell Line	embryonic stem cell
37	chr6:166778200-166781000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr6:166778200-166790600	Weak transcription	Right Ventricle	heart
39	chr6:166778200-166790800	Weak transcription	Fetal Brain Female	brain
40	chr6:166778200-166792800	Weak transcription	Aorta	Aorta
41	chr6:166778200-166794600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
42	chr6:166778200-166795000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr6:166778400-166784000	Weak transcription	Spleen	Spleen
44	chr6:166778400-166786600	Weak transcription	H9 Cell Line	embryonic stem cell
45	chr6:166778400-166790600	Weak transcription	Pancreas	Pancrea
46	chr6:166778400-166792600	Weak transcription	Lung	lung
47	chr6:166778400-166794600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
48	chr6:166778400-166794600	Weak transcription	Fetal Intestine Small	intestine
49	chr6:166778400-166794600	Weak transcription	Stomach Smooth Muscle	stomach
50	chr6:166778400-166794800	Weak transcription	Fetal Stomach	stomach

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links