Variant report

Variant	rs4076068
Chromosome Location	chr6:144853588-144853589
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:144852020..144854174-chr6:144867954..144869789,2	K562	blood:

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs12661566	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12663647	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12664494	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12664819	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1918751	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1918752	0.81[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1997252	0.83[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2091486	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2293536	0.89[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs3811100	0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4896728	0.86[ASN][1000 genomes]
rs9321980	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9376823	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9376824	0.90[ASN][1000 genomes]
rs9376826	0.86[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs9376828	0.84[ASN][1000 genomes]
rs9386070	0.82[AFR][1000 genomes];0.83[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9386071	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9386072	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9386073	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9390170	0.82[AFR][1000 genomes];0.83[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9390172	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9390174	0.84[ASN][1000 genomes]
rs9390175	0.86[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs9390176	0.84[ASN][1000 genomes]
rs9390178	0.84[ASN][1000 genomes]
rs9399480	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9399481	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9403563	0.86[ASN][1000 genomes]
rs9403564	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9403567	0.84[ASN][1000 genomes]
rs9497003	0.82[AMR][1000 genomes]
rs9497009	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][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	nsv1031253	chr6:144599055-144883013	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv538461	chr6:144599055-144883013	Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Genic enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
3	nsv1015228	chr6:144780458-144989321	Strong transcription Enhancers ZNF genes & repeats Weak transcription Genic enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	nsv538462	chr6:144780458-144989321	Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 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	chr6:144803400-144869800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
2	chr6:144807400-144904000	Weak transcription	Brain Substantia Nigra	brain
3	chr6:144812400-144881000	Weak transcription	Stomach Mucosa	stomach
4	chr6:144812600-144869800	Weak transcription	Colon Smooth Muscle	Colon
5	chr6:144815000-144855400	Weak transcription	Psoas Muscle	Psoas
6	chr6:144815200-144881000	Weak transcription	NHEK	skin
7	chr6:144816600-144881400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
8	chr6:144821200-144861000	Weak transcription	Rectal Smooth Muscle	rectum
9	chr6:144827200-144857200	Strong transcription	Primary T cells fromperipheralblood	blood
10	chr6:144829800-144854200	Weak transcription	Gastric	stomach
11	chr6:144829800-144863800	Weak transcription	H9 Cell Line	embryonic stem cell
12	chr6:144831400-144879000	Strong transcription	Primary B cells from cord blood	blood
13	chr6:144831800-144857000	Strong transcription	Primary B cells from peripheral blood	blood
14	chr6:144832200-144856800	Strong transcription	Monocytes-CD14+_RO01746	blood
15	chr6:144832400-144862200	Weak transcription	Small Intestine	intestine
16	chr6:144833800-144857000	Strong transcription	Primary T helper cells fromperipheralblood	blood
17	chr6:144833800-144857200	Strong transcription	Primary T cells from cord blood	blood
18	chr6:144833800-144868200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
19	chr6:144835000-144856400	Strong transcription	Primary T helper cells PMA-I stimulated	--
20	chr6:144837200-144880800	Weak transcription	Brain Angular Gyrus	brain
21	chr6:144839600-144855400	Weak transcription	HSMMtube	muscle
22	chr6:144843000-144854800	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr6:144843200-144855800	Strong transcription	Rectal Mucosa Donor 29	rectum
24	chr6:144843600-144857200	Strong transcription	Primary hematopoietic stem cells	blood
25	chr6:144844400-144861400	Weak transcription	Muscle Satellite Cultured Cells	--
26	chr6:144844400-144870000	Weak transcription	Brain Hippocampus Middle	brain
27	chr6:144844600-144860800	Weak transcription	HUES48 Cell Line	embryonic stem cell
28	chr6:144845400-144853600	Weak transcription	Duodenum Mucosa	Duodenum
29	chr6:144847000-144855400	Strong transcription	Adipose Nuclei	Adipose
30	chr6:144847200-144854600	Strong transcription	Fetal Thymus	thymus
31	chr6:144847200-144856000	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
32	chr6:144847200-144857000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr6:144847600-144856400	Strong transcription	Liver	Liver
34	chr6:144847800-144857000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr6:144847800-144857200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
36	chr6:144848000-144856400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
37	chr6:144849000-144856000	Strong transcription	HepG2	liver
38	chr6:144849200-144853600	Strong transcription	Lung	lung
39	chr6:144849200-144854400	Strong transcription	Sigmoid Colon	Sigmoid Colon
40	chr6:144849600-144855000	Strong transcription	Fetal Intestine Large	intestine
41	chr6:144849600-144856000	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
42	chr6:144850000-144864200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
43	chr6:144850000-144864200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
44	chr6:144850200-144858600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
45	chr6:144850200-144877400	Weak transcription	HMEC	breast
46	chr6:144850400-144856200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
47	chr6:144850400-144856200	Strong transcription	Dnd41	blood
48	chr6:144850400-144857000	Strong transcription	Primary T helper memory cells from peripheral blood 1	blood
49	chr6:144850400-144864000	Weak transcription	Placenta Amnion	Placenta Amnion
50	chr6:144850400-144864200	Weak transcription	Cortex derived primary cultured neurospheres	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links