Variant report

Variant	rs62127129
Chromosome Location	chr2:10006771-10006772
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:10006138..10008945-chr2:10011171..10013813,2	K562	blood:

Extended variants
information (count: 76 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:66)

rs_ID	r²[population]
rs1014509	0.90[AFR][1000 genomes];0.88[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs1036058	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs10495575	0.91[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs10929617	0.90[AFR][1000 genomes];0.87[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs10929618	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs12468582	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs12470216	0.90[AFR][1000 genomes];0.88[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs12476490	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs12611655	0.90[AFR][1000 genomes];0.87[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs12613533	0.90[AFR][1000 genomes];0.91[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs12613568	0.90[AFR][1000 genomes]
rs12617615	0.90[AFR][1000 genomes];0.87[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs12621415	0.90[AFR][1000 genomes];0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs12622420	0.90[AFR][1000 genomes];0.91[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs12623017	0.90[AFR][1000 genomes];0.91[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs1469543	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs1469545	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs1469546	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs1473962	0.90[AFR][1000 genomes];0.88[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs16867195	0.90[AFR][1000 genomes];0.88[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs16867196	0.90[AFR][1000 genomes];0.88[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs16867211	0.90[AFR][1000 genomes];0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs16867242	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1967518	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4143791	0.90[AFR][1000 genomes];0.88[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4143793	0.96[AFR][1000 genomes];0.90[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs452480	0.85[EUR][1000 genomes]
rs4610025	0.90[AFR][1000 genomes];0.91[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4627538	0.96[AFR][1000 genomes];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4669470	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs4669471	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4669472	0.90[AFR][1000 genomes];0.88[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4669473	0.90[AFR][1000 genomes];0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4669475	0.93[AFR][1000 genomes];0.91[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs4669476	0.90[AFR][1000 genomes];0.87[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4669477	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4669478	0.90[AFR][1000 genomes];0.87[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4669479	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs4669481	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs4669484	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs4669485	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs59288259	0.86[EUR][1000 genomes]
rs62127130	0.90[AFR][1000 genomes];0.91[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs62127131	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs62127132	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs62127136	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs62127137	0.90[AFR][1000 genomes];0.88[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs62127138	0.90[AFR][1000 genomes];0.87[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs62127143	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs62127144	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs62127146	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs62127466	0.86[EUR][1000 genomes]
rs62127564	0.90[AFR][1000 genomes];0.91[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs62127565	0.90[AFR][1000 genomes];0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6707551	0.84[AFR][1000 genomes];0.85[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs6743707	0.89[AFR][1000 genomes]
rs6743866	0.89[AFR][1000 genomes]
rs6753379	0.89[AFR][1000 genomes]
rs718255	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs718256	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs72782635	0.90[AFR][1000 genomes];0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7559653	0.86[AFR][1000 genomes]
rs7563385	0.90[AFR][1000 genomes];0.91[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7579559	0.90[AFR][1000 genomes];0.93[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7602449	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7608055	0.90[AFR][1000 genomes];0.88[AMR][1000 genomes];0.90[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1003026	chr2:9854939-10012516	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription Active TSS Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	34 gene(s)	inside rSNPs	diseases
2	nsv1013969	chr2:9888703-10023951	Enhancers Strong transcription Bivalent Enhancer Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
3	nsv948591	chr2:9922257-10141191	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
4	nsv873629	chr2:9949464-10016627	Weak transcription Strong transcription Transcr. at gene 5' and 3' Active TSS Enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	25 gene(s)	inside rSNPs	diseases
5	nsv873630	chr2:9953949-10030024	Weak transcription Active TSS Genic enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	25 gene(s)	inside rSNPs	diseases
6	nsv873631	chr2:9975557-10059770	Enhancers Genic enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	21 gene(s)	inside rSNPs	diseases
7	esv1843231	chr2:9979766-10141191	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
8	nsv580960	chr2:9993451-10066694	Weak transcription Strong transcription Enhancers ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
9	nsv1011125	chr2:9996740-10293803	Enhancers Strong transcription Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	83 gene(s)	inside rSNPs	diseases
10	nsv873632	chr2:10000978-10045014	Enhancers ZNF genes & repeats Strong transcription Weak transcription Genic enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs62127129	TAF1B	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:112 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:9987200-10038400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
2	chr2:9993600-10007400	Weak transcription	Psoas Muscle	Psoas
3	chr2:9993800-10079600	Weak transcription	Gastric	stomach
4	chr2:9995800-10038000	Weak transcription	Small Intestine	intestine
5	chr2:9996400-10016000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
6	chr2:9998200-10013800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
7	chr2:9998200-10024000	Weak transcription	Rectal Smooth Muscle	rectum
8	chr2:9998200-10035600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
9	chr2:9998400-10007400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
10	chr2:9998600-10017000	Weak transcription	K562	blood
11	chr2:9998600-10024000	Weak transcription	Pancreas	Pancrea
12	chr2:9998800-10010400	Weak transcription	Primary T helper cells PMA-I stimulated	--
13	chr2:9998800-10010400	Weak transcription	Rectal Mucosa Donor 29	rectum
14	chr2:9998800-10026000	Weak transcription	Fetal Brain Male	brain
15	chr2:9998800-10032200	Weak transcription	Fetal Heart	heart
16	chr2:9998800-10036400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
17	chr2:9999000-10008600	Weak transcription	Skeletal Muscle Female	skeletal muscle
18	chr2:9999000-10010400	Weak transcription	Duodenum Mucosa	Duodenum
19	chr2:9999000-10014200	Weak transcription	Aorta	Aorta
20	chr2:9999000-10014800	Weak transcription	Sigmoid Colon	Sigmoid Colon
21	chr2:9999000-10015200	Weak transcription	Esophagus	oesophagus
22	chr2:9999000-10015400	Weak transcription	HUVEC	blood vessel
23	chr2:9999000-10017600	Weak transcription	Brain Inferior Temporal Lobe	brain
24	chr2:9999000-10024000	Weak transcription	Colonic Mucosa	Colon
25	chr2:9999000-10024000	Weak transcription	Spleen	Spleen
26	chr2:9999000-10035800	Weak transcription	Brain Hippocampus Middle	brain
27	chr2:9999000-10035800	Weak transcription	Brain Substantia Nigra	brain
28	chr2:9999000-10037000	Weak transcription	Brain Cingulate Gyrus	brain
29	chr2:9999000-10037200	Weak transcription	Colon Smooth Muscle	Colon
30	chr2:9999200-10007400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
31	chr2:9999200-10007800	Weak transcription	Duodenum Smooth Muscle	Duodenum
32	chr2:9999200-10008000	Weak transcription	Primary T helper cells fromperipheralblood	blood
33	chr2:9999200-10013800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
34	chr2:9999200-10013800	Weak transcription	Left Ventricle	heart
35	chr2:9999200-10017000	Weak transcription	HSMMtube	muscle
36	chr2:9999200-10017600	Weak transcription	Brain Anterior Caudate	brain
37	chr2:9999200-10036200	Weak transcription	Brain Angular Gyrus	brain
38	chr2:9999200-10036400	Weak transcription	Placenta Amnion	Placenta Amnion
39	chr2:9999200-10053800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
40	chr2:9999400-10008600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr2:10000400-10007400	Weak transcription	Primary T cells from cord blood	blood
42	chr2:10000600-10010400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr2:10000600-10012600	Weak transcription	Rectal Mucosa Donor 31	rectum
44	chr2:10000800-10010600	Weak transcription	NHDF-Ad	bronchial
45	chr2:10000800-10011600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
46	chr2:10000800-10014000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
47	chr2:10000800-10014800	Weak transcription	Stomach Smooth Muscle	stomach
48	chr2:10001000-10007800	Weak transcription	A549	lung
49	chr2:10001000-10007800	Weak transcription	NHEK	skin
50	chr2:10001000-10008200	Weak transcription	Monocytes-CD14+_RO01746	blood

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