Variant report

Variant	rs6807701
Chromosome Location	chr3:69122943-69122944
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr3:69110122..69112933-chr3:69121991..69123834,2	K562	blood:
2	chr3:69120698..69123415-chr3:69132362..69134206,2	K562	blood:
3	chr3:69117327..69121246-chr3:69122493..69127551,4	K562	blood:

Variant related genes	Relation type
ENSG00000144746	Chromatin interaction

Extended variants
information (count: 43 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs11128107	0.88[EUR][1000 genomes]
rs13063094	0.81[EUR][1000 genomes]
rs13084180	0.80[EUR][1000 genomes]
rs13085120	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs13090606	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs13099820	0.81[EUR][1000 genomes]
rs2009602	0.86[EUR][1000 genomes]
rs2271118	0.94[EUR][1000 genomes]
rs2271120	0.86[AFR][1000 genomes];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2271122	0.82[EUR][1000 genomes]
rs2279936	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2292199	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs35718539	0.86[EUR][1000 genomes]
rs3755717	0.82[EUR][1000 genomes]
rs3772977	0.98[ASN][1000 genomes]
rs3772979	0.85[EUR][1000 genomes]
rs3821562	0.87[EUR][1000 genomes]
rs3853157	0.85[EUR][1000 genomes]
rs56156415	0.83[EUR][1000 genomes]
rs58950441	0.86[EUR][1000 genomes]
rs6549162	0.84[EUR][1000 genomes]
rs6549163	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs6549164	0.86[EUR][1000 genomes]
rs6549165	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs6549167	0.84[EUR][1000 genomes]
rs6549169	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs6549181	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs6775065	0.86[EUR][1000 genomes]
rs6777032	0.87[EUR][1000 genomes]
rs6804833	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs714300	0.86[EUR][1000 genomes]
rs7426798	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7430692	0.88[EUR][1000 genomes]
rs7432824	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7434153	0.88[EUR][1000 genomes]
rs7611878	0.86[EUR][1000 genomes]
rs7614090	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9813514	0.81[EUR][1000 genomes]
rs9853259	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs9857898	0.87[EUR][1000 genomes]
rs9873272	0.84[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv876933	chr3:69059023-69227379	Enhancers Strong transcription Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
2	nsv876934	chr3:69111512-69166895	Enhancers Genic enhancers Strong transcription Flanking Active TSS Active TSS Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region miRNA target site	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:69101400-69127000	Weak transcription	Small Intestine	intestine
2	chr3:69101800-69128400	Weak transcription	Aorta	Aorta
3	chr3:69102000-69128200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr3:69102000-69128400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr3:69102200-69127200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr3:69108400-69128200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr3:69110200-69127000	Weak transcription	Hela-S3	cervix
8	chr3:69110600-69127000	Weak transcription	Brain Angular Gyrus	brain
9	chr3:69110600-69127600	Weak transcription	Brain Inferior Temporal Lobe	brain
10	chr3:69110600-69128200	Weak transcription	Right Ventricle	heart
11	chr3:69110600-69128400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr3:69110600-69128400	Weak transcription	Gastric	stomach
13	chr3:69110600-69128400	Weak transcription	Psoas Muscle	Psoas
14	chr3:69110800-69127000	Weak transcription	Pancreas	Pancrea
15	chr3:69110800-69127600	Weak transcription	Brain Substantia Nigra	brain
16	chr3:69110800-69127800	Weak transcription	Rectal Smooth Muscle	rectum
17	chr3:69110800-69128600	Weak transcription	Esophagus	oesophagus
18	chr3:69110800-69128800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr3:69110800-69128800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr3:69111000-69128600	Weak transcription	Lung	lung
21	chr3:69111000-69128800	Weak transcription	Spleen	Spleen
22	chr3:69111200-69128000	Weak transcription	K562	blood
23	chr3:69111200-69128200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
24	chr3:69111200-69128200	Weak transcription	Colonic Mucosa	Colon
25	chr3:69111400-69127000	Weak transcription	Colon Smooth Muscle	Colon
26	chr3:69111400-69128400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
27	chr3:69111600-69128200	Weak transcription	H9 Cell Line	embryonic stem cell
28	chr3:69111800-69126800	Weak transcription	Skeletal Muscle Male	skeletal muscle
29	chr3:69111800-69128200	Weak transcription	A549	lung
30	chr3:69112200-69128200	Weak transcription	Fetal Kidney	kidney
31	chr3:69112600-69123000	Weak transcription	Muscle Satellite Cultured Cells	--
32	chr3:69112600-69128200	Weak transcription	Fetal Brain Female	brain
33	chr3:69112600-69128200	Weak transcription	Placenta Amnion	Placenta Amnion
34	chr3:69113000-69128200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
35	chr3:69113400-69127400	Weak transcription	Fetal Lung	lung
36	chr3:69115000-69126800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
37	chr3:69115000-69127800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
38	chr3:69115000-69128400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
39	chr3:69115400-69126400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
40	chr3:69115600-69126800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
41	chr3:69115600-69127000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
42	chr3:69115800-69128200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
43	chr3:69116000-69127000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr3:69116400-69123400	Weak transcription	NH-A	brain
45	chr3:69116400-69127200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
46	chr3:69116800-69125400	Strong transcription	Fetal Thymus	thymus
47	chr3:69117600-69125800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
48	chr3:69118200-69124800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr3:69118600-69124800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr3:69118600-69126000	Strong transcription	Primary T cells fromperipheralblood	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links