Variant report

Variant	rs7584303
Chromosome Location	chr2:10322913-10322914
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs10205991	0.99[ASN][1000 genomes]
rs1035120	1.00[ASN][1000 genomes]
rs11891059	0.84[ASN][1000 genomes]
rs13403621	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs17379350	0.91[ASN][1000 genomes]
rs4550641	1.00[ASN][1000 genomes]
rs4630742	1.00[ASN][1000 genomes]
rs4669544	0.84[ASN][1000 genomes]
rs55642251	0.80[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs55728000	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6711940	1.00[ASN][1000 genomes]
rs6718918	1.00[ASN][1000 genomes]
rs72786692	0.91[ASN][1000 genomes]
rs72786699	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs72786701	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs72788303	0.93[ASN][1000 genomes]
rs72788304	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs72788306	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs72788307	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs72788313	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72788315	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72788320	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72788324	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72788326	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72788352	0.99[ASN][1000 genomes]
rs72788354	0.99[ASN][1000 genomes]
rs7566844	0.99[ASN][1000 genomes]
rs7593918	0.86[ASN][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	nsv873634	chr2:10275814-10337034	Enhancers Genic enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA	11 gene(s)	inside rSNPs	diseases
2	nsv873635	chr2:10286466-10344465	Weak transcription Bivalent Enhancer Enhancers Genic enhancers Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	9 gene(s)	inside rSNPs	diseases
3	nsv873636	chr2:10300390-10331919	Strong transcription Weak transcription Genic enhancers Enhancers Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Active TSS	Chromatin interactive region	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:32 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:10273800-10330400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
2	chr2:10286400-10331400	Weak transcription	Spleen	Spleen
3	chr2:10290200-10351400	Strong transcription	Dnd41	blood
4	chr2:10302400-10337600	Weak transcription	Duodenum Mucosa	Duodenum
5	chr2:10304400-10339800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr2:10308200-10324600	Weak transcription	Fetal Lung	lung
7	chr2:10311800-10331200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr2:10311800-10337000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr2:10312800-10326800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
10	chr2:10313000-10327000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
11	chr2:10313000-10344400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr2:10313200-10327400	Weak transcription	H1 Cell Line	embryonic stem cell
13	chr2:10314000-10340400	Weak transcription	HepG2	liver
14	chr2:10318600-10323600	Strong transcription	Monocytes-CD14+_RO01746	blood
15	chr2:10319200-10323200	Weak transcription	A549	lung
16	chr2:10319200-10326800	Weak transcription	Fetal Intestine Small	intestine
17	chr2:10320200-10326600	Weak transcription	Primary neutrophils fromperipheralblood	blood
18	chr2:10320400-10323200	Weak transcription	Fetal Muscle Leg	muscle
19	chr2:10320400-10326600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr2:10320600-10324400	Weak transcription	Fetal Brain Female	brain
21	chr2:10320600-10337200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
22	chr2:10320800-10324200	Weak transcription	Brain Germinal Matrix	brain
23	chr2:10320800-10324600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr2:10320800-10324600	Weak transcription	Fetal Brain Male	brain
25	chr2:10320800-10332400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
26	chr2:10320800-10336800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr2:10321600-10324600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr2:10321800-10325600	Weak transcription	Fetal Thymus	thymus
29	chr2:10321800-10333400	Weak transcription	Primary monocytes fromperipheralblood	blood
30	chr2:10321800-10338000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr2:10322400-10325000	Strong transcription	Thymus	Thymus
32	chr2:10322800-10323000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links