Variant report

Variant	rs35899247
Chromosome Location	chr4:148802759-148802760
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 75 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:70)

rs_ID	r²[population]
rs10000278	0.92[EUR][1000 genomes]
rs10001688	0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10001756	0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10003507	0.92[EUR][1000 genomes]
rs10004138	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10004691	0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10004792	0.92[EUR][1000 genomes]
rs10014593	0.92[EUR][1000 genomes]
rs10014696	0.92[EUR][1000 genomes]
rs10015875	0.84[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10025069	0.84[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10026985	0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10030358	0.92[EUR][1000 genomes]
rs10049932	0.92[EUR][1000 genomes]
rs11099671	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11099672	0.92[EUR][1000 genomes]
rs11734553	0.89[EUR][1000 genomes]
rs11735412	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12331562	0.92[EUR][1000 genomes]
rs12509618	0.89[EUR][1000 genomes]
rs12513192	0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12643550	0.92[EUR][1000 genomes]
rs13129325	0.92[EUR][1000 genomes]
rs13151898	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1369958	0.92[EUR][1000 genomes]
rs17024037	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs17613979	0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs17614025	0.91[EUR][1000 genomes]
rs17676080	0.84[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2043643	0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2043645	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs28576385	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs28614116	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2884400	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs34970355	0.89[EUR][1000 genomes]
rs35243600	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35810358	0.90[EUR][1000 genomes]
rs3893175	0.89[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs3990920	0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4240341	0.90[EUR][1000 genomes]
rs4491995	0.92[EUR][1000 genomes]
rs4571312	0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4627844	0.89[EUR][1000 genomes]
rs4835103	0.92[EUR][1000 genomes]
rs4835109	0.92[EUR][1000 genomes]
rs4835110	0.92[EUR][1000 genomes]
rs4835469	0.85[EUR][1000 genomes]
rs55650760	0.86[EUR][1000 genomes]
rs55820558	0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs57114670	0.84[ASN][1000 genomes]
rs62330732	0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs62330735	0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs62330737	0.91[EUR][1000 genomes]
rs6535569	0.85[EUR][1000 genomes]
rs6811769	0.89[EUR][1000 genomes]
rs6818371	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6832527	0.81[EUR][1000 genomes]
rs6840771	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6843392	0.84[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6856273	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7656471	0.82[EUR][1000 genomes]
rs7660508	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7677632	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7698670	0.87[EUR][1000 genomes]
rs893033	0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9991741	0.88[EUR][1000 genomes]
rs9994650	0.84[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9995956	0.92[EUR][1000 genomes]
rs9997027	0.92[EUR][1000 genomes]
rs9999321	0.92[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv498083	chr4:148519825-148917583	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	20 gene(s)	inside rSNPs	diseases
2	nsv880243	chr4:148735644-148879583	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv880244	chr4:148764252-148920089	Strong transcription Enhancers Genic enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
4	nsv1029845	chr4:148766290-148916437	Weak transcription Flanking Active TSS Genic enhancers Enhancers Strong transcription ZNF genes & repeats Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
5	nsv1030001	chr4:148773479-148916437	Genic enhancers Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:75 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:148768400-148815600	Weak transcription	Primary T cells from cord blood	blood
2	chr4:148772000-148806000	Weak transcription	Fetal Thymus	thymus
3	chr4:148777000-148823000	Weak transcription	Small Intestine	intestine
4	chr4:148784400-148810800	Weak transcription	Fetal Heart	heart
5	chr4:148786000-148804000	Weak transcription	Psoas Muscle	Psoas
6	chr4:148786000-148861400	Weak transcription	Pancreas	Pancrea
7	chr4:148788800-148803200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr4:148789800-148805800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr4:148790400-148805200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
10	chr4:148790600-148805800	Weak transcription	NHLF	lung
11	chr4:148791600-148804400	Weak transcription	Fetal Intestine Small	intestine
12	chr4:148794800-148810200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
13	chr4:148794800-148824600	Weak transcription	A549	lung
14	chr4:148796000-148809600	Weak transcription	Primary T helper cells fromperipheralblood	blood
15	chr4:148796800-148804400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr4:148796800-148804400	Weak transcription	Aorta	Aorta
17	chr4:148796800-148805600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
18	chr4:148796800-148805800	Weak transcription	HUES6 Cell Line	embryonic stem cell
19	chr4:148796800-148808200	Weak transcription	Lung	lung
20	chr4:148796800-148812800	Weak transcription	Rectal Smooth Muscle	rectum
21	chr4:148796800-148863200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
22	chr4:148796800-148866000	Weak transcription	Thymus	Thymus
23	chr4:148797000-148806400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
24	chr4:148797000-148812000	Weak transcription	Fetal Kidney	kidney
25	chr4:148797000-148834200	Weak transcription	Placenta Amnion	Placenta Amnion
26	chr4:148797000-148835800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
27	chr4:148797200-148806400	Weak transcription	HUES64 Cell Line	embryonic stem cell
28	chr4:148797400-148803400	Weak transcription	Primary T cells fromperipheralblood	blood
29	chr4:148797400-148804000	Weak transcription	Fetal Intestine Large	intestine
30	chr4:148797400-148804400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
31	chr4:148797400-148804400	Weak transcription	Esophagus	oesophagus
32	chr4:148797400-148805600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
33	chr4:148797400-148805800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr4:148797400-148805800	Weak transcription	Left Ventricle	heart
35	chr4:148797400-148808000	Weak transcription	HUVEC	blood vessel
36	chr4:148797400-148810000	Weak transcription	Duodenum Mucosa	Duodenum
37	chr4:148797400-148812400	Weak transcription	Rectal Mucosa Donor 31	rectum
38	chr4:148797400-148814400	Weak transcription	NH-A	brain
39	chr4:148797400-148815400	Weak transcription	Monocytes-CD14+_RO01746	blood
40	chr4:148797400-148879600	Weak transcription	Gastric	stomach
41	chr4:148797600-148810000	Weak transcription	Skeletal Muscle Female	skeletal muscle
42	chr4:148797600-148815200	Weak transcription	Fetal Lung	lung
43	chr4:148797600-148820000	Weak transcription	Right Ventricle	heart
44	chr4:148797600-148820200	Weak transcription	Osteobl	bone
45	chr4:148797600-148824600	Weak transcription	Skeletal Muscle Male	skeletal muscle
46	chr4:148798000-148802800	Weak transcription	Muscle Satellite Cultured Cells	--
47	chr4:148798000-148803200	Weak transcription	HSMM	muscle
48	chr4:148798200-148804200	Weak transcription	Ovary	ovary
49	chr4:148798200-148804400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr4:148798200-148809600	Weak transcription	Sigmoid Colon	Sigmoid Colon

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links