Variant report

Variant	rs60927005
Chromosome Location	chr1:209796662-209796663
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr1:209796403-209797256	H1-neurons	neurons:	n/a	n/a
2	POLR2A	chr1:209789528-209798172	Hela-S3	cervix:	n/a	n/a
3	POLR2A	chr1:209796487-209797180	H1-neurons	neurons:	n/a	n/a

Variant related genes	Relation type
LAMB3	TF binding region

Extended variants
information (count: 35 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10489340	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12073223	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12089972	0.86[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs12090288	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12403733	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17014889	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17014906	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17014942	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17014955	0.91[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs17015006	0.82[AMR][1000 genomes]
rs2072937	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2072939	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2072942	0.95[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs2076219	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2076222	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2076232	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2076347	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2076348	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2076349	0.82[EUR][1000 genomes]
rs2076350	0.82[EUR][1000 genomes]
rs2076352	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2229465	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2229466	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2235542	0.95[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs2236889	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2236890	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2282734	0.95[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs2282736	0.95[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs2282737	0.95[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs36051870	0.86[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs58679997	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59815577	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs714971	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][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	nsv999901	chr1:209600631-210205379	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	76 gene(s)	inside rSNPs	diseases
2	nsv1014034	chr1:209759648-210501731	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	45 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:59 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:209786800-209800000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr1:209787200-209808400	Strong transcription	Placenta Amnion	Placenta Amnion
3	chr1:209787400-209816200	Strong transcription	NHEK	skin
4	chr1:209789000-209802800	Strong transcription	Hela-S3	cervix
5	chr1:209790200-209797800	Enhancers	Brain Germinal Matrix	brain
6	chr1:209791800-209801400	Enhancers	Fetal Muscle Leg	muscle
7	chr1:209792000-209797000	Genic enhancers	Fetal Intestine Large	intestine
8	chr1:209792000-209797600	Genic enhancers	Fetal Intestine Small	intestine
9	chr1:209792400-209798400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr1:209792400-209806400	Genic enhancers	Breast Myoepithelial Primary Cells	Breast
11	chr1:209793000-209801600	Enhancers	Ovary	ovary
12	chr1:209793400-209798800	Weak transcription	Brain Cingulate Gyrus	brain
13	chr1:209793600-209797400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
14	chr1:209793600-209799000	Weak transcription	Brain Hippocampus Middle	brain
15	chr1:209793600-209801600	Enhancers	Spleen	Spleen
16	chr1:209793800-209800000	Weak transcription	Lung	lung
17	chr1:209794000-209797400	Weak transcription	HSMM	muscle
18	chr1:209794000-209799000	Weak transcription	Brain Substantia Nigra	brain
19	chr1:209794200-209798600	Weak transcription	Osteobl	bone
20	chr1:209794200-209799600	Weak transcription	Stomach Mucosa	stomach
21	chr1:209794800-209803200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
22	chr1:209795000-209797400	Genic enhancers	Skeletal Muscle Male	skeletal muscle
23	chr1:209795000-209799000	Weak transcription	Fetal Lung	lung
24	chr1:209795200-209799600	Weak transcription	Brain Angular Gyrus	brain
25	chr1:209795200-209804400	Strong transcription	Sigmoid Colon	Sigmoid Colon
26	chr1:209795400-209796800	Genic enhancers	Skeletal Muscle Female	skeletal muscle
27	chr1:209795400-209797000	Enhancers	Fetal Muscle Trunk	muscle
28	chr1:209795400-209799600	Weak transcription	Liver	Liver
29	chr1:209795600-209797000	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr1:209795600-209798000	Weak transcription	HSMMtube	muscle
31	chr1:209795600-209800800	Strong transcription	Rectal Mucosa Donor 29	rectum
32	chr1:209795800-209796800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
33	chr1:209795800-209797000	Weak transcription	Fetal Heart	heart
34	chr1:209795800-209797200	Strong transcription	Gastric	stomach
35	chr1:209795800-209797800	Weak transcription	Adipose Nuclei	Adipose
36	chr1:209795800-209798000	Enhancers	Fetal Brain Male	brain
37	chr1:209795800-209799000	Weak transcription	Right Atrium	heart
38	chr1:209796000-209797000	Weak transcription	Right Ventricle	heart
39	chr1:209796000-209797400	Weak transcription	Psoas Muscle	Psoas
40	chr1:209796000-209798400	Weak transcription	Left Ventricle	heart
41	chr1:209796000-209798600	Weak transcription	Stomach Smooth Muscle	stomach
42	chr1:209796000-209800800	Strong transcription	Rectal Mucosa Donor 31	rectum
43	chr1:209796000-209801000	Weak transcription	Pancreas	Pancrea
44	chr1:209796200-209796800	Weak transcription	Esophagus	oesophagus
45	chr1:209796200-209796800	Genic enhancers	HMEC	breast
46	chr1:209796200-209797200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr1:209796200-209797600	Enhancers	Fetal Brain Female	brain
48	chr1:209796200-209798000	Genic enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
49	chr1:209796200-209799400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr1:209796200-209800800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links