Variant report

Variant	rs17121835
Chromosome Location	chr1:61693632-61693633
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr1:61691680..61694705-chr1:61697594..61700756,3	K562	blood:
2	chr1:61684478..61689814-chr1:61689911..61696022,10	K562	blood:
3	chr1:61685407..61688554-chr1:61690743..61693664,3	K562	blood:

Extended variants
information (count: 32 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs11806791	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1336184	1.00[ASN][1000 genomes]
rs17121798	1.00[CEU][hapmap];0.84[EUR][1000 genomes]
rs17121833	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17121841	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17121845	0.82[CEU][hapmap];0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs17305204	0.82[CEU][hapmap]
rs17305218	0.80[CEU][hapmap]
rs17311684	0.82[CEU][hapmap];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17311740	0.80[CEU][hapmap]
rs17377134	1.00[CEU][hapmap];0.93[EUR][1000 genomes]
rs17377148	1.00[CEU][hapmap];0.93[EUR][1000 genomes]
rs17377218	0.80[CEU][hapmap]
rs17377267	0.82[CEU][hapmap];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17377274	0.80[CEU][hapmap];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17377281	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17377295	0.80[CEU][hapmap]
rs17377351	0.82[CEU][hapmap]
rs55878063	0.87[EUR][1000 genomes]
rs59708846	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61593957	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72911905	1.00[ASN][1000 genomes]
rs72929847	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs74086705	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs74090327	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs74090339	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs74090351	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7515011	1.00[CEU][hapmap];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs868110	1.00[CEU][hapmap];0.93[EUR][1000 genomes]
rs9970076	1.00[CEU][hapmap];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9970140	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1849929	chr1:61684084-61714142	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:55 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:61680000-61720200	Weak transcription	Fetal Muscle Trunk	muscle
2	chr1:61682000-61706800	Weak transcription	Gastric	stomach
3	chr1:61690400-61696400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr1:61690600-61696400	Weak transcription	Duodenum Mucosa	Duodenum
5	chr1:61690600-61699000	Weak transcription	Ovary	ovary
6	chr1:61691200-61694200	Enhancers	Brain Substantia Nigra	brain
7	chr1:61691800-61694200	Enhancers	Cortex derived primary cultured neurospheres	brain
8	chr1:61691800-61694200	Enhancers	Brain Hippocampus Middle	brain
9	chr1:61691800-61694200	Enhancers	Fetal Brain Male	brain
10	chr1:61691800-61694200	Enhancers	Fetal Brain Female	brain
11	chr1:61692000-61694200	Enhancers	Brain Inferior Temporal Lobe	brain
12	chr1:61692200-61696400	Weak transcription	Duodenum Smooth Muscle	Duodenum
13	chr1:61692400-61694200	Enhancers	Skeletal Muscle Male	skeletal muscle
14	chr1:61692600-61693800	Weak transcription	HMEC	breast
15	chr1:61692600-61696000	Weak transcription	A549	lung
16	chr1:61692600-61699400	Enhancers	HepG2	liver
17	chr1:61692600-61703400	Weak transcription	H9 Cell Line	embryonic stem cell
18	chr1:61692800-61693800	Weak transcription	Psoas Muscle	Psoas
19	chr1:61692800-61694000	Weak transcription	Left Ventricle	heart
20	chr1:61692800-61696000	Weak transcription	Rectal Mucosa Donor 31	rectum
21	chr1:61692800-61696000	Weak transcription	Stomach Mucosa	stomach
22	chr1:61692800-61696200	Weak transcription	Right Ventricle	heart
23	chr1:61692800-61696400	Weak transcription	Esophagus	oesophagus
24	chr1:61692800-61696400	Weak transcription	Sigmoid Colon	Sigmoid Colon
25	chr1:61692800-61706800	Weak transcription	Fetal Lung	lung
26	chr1:61692800-61707000	Weak transcription	Fetal Stomach	stomach
27	chr1:61692800-61707200	Weak transcription	Pancreas	Pancrea
28	chr1:61693000-61694000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
29	chr1:61693000-61694200	Enhancers	Adipose Nuclei	Adipose
30	chr1:61693000-61694200	Enhancers	Brain Anterior Caudate	brain
31	chr1:61693000-61694200	Enhancers	Brain Cingulate Gyrus	brain
32	chr1:61693000-61694400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr1:61693000-61696000	Weak transcription	Fetal Heart	heart
34	chr1:61693000-61696200	Weak transcription	Rectal Mucosa Donor 29	rectum
35	chr1:61693000-61704000	Weak transcription	Right Atrium	heart
36	chr1:61693000-61706800	Weak transcription	Brain Angular Gyrus	brain
37	chr1:61693000-61706800	Weak transcription	Fetal Muscle Leg	muscle
38	chr1:61693200-61693800	Enhancers	Stomach Smooth Muscle	stomach
39	chr1:61693200-61694200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr1:61693200-61694200	Enhancers	Brain Germinal Matrix	brain
41	chr1:61693200-61696000	Weak transcription	Pancreatic Islets	Pancreatic Islet
42	chr1:61693200-61696200	Weak transcription	Aorta	Aorta
43	chr1:61693200-61696200	Weak transcription	Colon Smooth Muscle	Colon
44	chr1:61693200-61696200	Weak transcription	K562	blood
45	chr1:61693400-61694000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr1:61693400-61694000	Weak transcription	Skeletal Muscle Female	skeletal muscle
47	chr1:61693400-61694200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr1:61693400-61694200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
49	chr1:61693400-61694200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr1:61693400-61694200	Enhancers	NHEK	skin

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