Variant report

Variant	rs10800151
Chromosome Location	chr1:161914283-161914284
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:161903370..161905220-chr1:161914130..161916639,2	K562	blood:
2	chr1:161896648..161898427-chr1:161911622..161914345,2	K562	blood:

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs10737521	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs10918270	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12079579	0.86[AFR][1000 genomes]
rs2341471	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3795649	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs9783050	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs9783069	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv33393	chr1:161478681-162080327	Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	59 gene(s)	inside rSNPs	diseases
2	nsv464206	chr1:161798239-162067447	Flanking Active TSS Weak transcription Enhancers Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
3	nsv470744	chr1:161798239-162067447	Strong transcription Flanking Active TSS Weak transcription Enhancers Genic enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
4	nsv548077	chr1:161798239-162067447	Enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:102 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:161824200-161928400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr1:161861600-161936000	Weak transcription	Fetal Intestine Small	intestine
3	chr1:161883200-161916000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr1:161883400-161928200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
5	chr1:161884600-161927600	Weak transcription	NHEK	skin
6	chr1:161884800-161922600	Weak transcription	Brain Anterior Caudate	brain
7	chr1:161885000-161914400	Weak transcription	Rectal Mucosa Donor 31	rectum
8	chr1:161885000-161928000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
9	chr1:161885800-161919200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr1:161887000-161918600	Weak transcription	Duodenum Smooth Muscle	Duodenum
11	chr1:161887000-161928200	Weak transcription	Rectal Mucosa Donor 29	rectum
12	chr1:161887200-161915600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr1:161887200-161929600	Weak transcription	Hela-S3	cervix
14	chr1:161891000-161915600	Weak transcription	Fetal Muscle Trunk	muscle
15	chr1:161891800-161915800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr1:161896200-161916400	Weak transcription	Fetal Stomach	stomach
17	chr1:161897800-161928400	Weak transcription	Cortex derived primary cultured neurospheres	brain
18	chr1:161897800-161940000	Weak transcription	Brain Germinal Matrix	brain
19	chr1:161899400-161914400	Weak transcription	Psoas Muscle	Psoas
20	chr1:161899800-161918400	Weak transcription	Skeletal Muscle Male	skeletal muscle
21	chr1:161900000-161916000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
22	chr1:161900200-161918600	Weak transcription	Rectal Smooth Muscle	rectum
23	chr1:161900600-161915600	Weak transcription	HSMM	muscle
24	chr1:161900600-161915600	Weak transcription	NHLF	lung
25	chr1:161901400-161935400	Weak transcription	Fetal Lung	lung
26	chr1:161902400-161923000	Weak transcription	Brain Substantia Nigra	brain
27	chr1:161902800-161943400	Weak transcription	Esophagus	oesophagus
28	chr1:161903600-161930400	Weak transcription	Fetal Brain Female	brain
29	chr1:161903800-161914400	Weak transcription	Spleen	Spleen
30	chr1:161903800-161918800	Weak transcription	Pancreatic Islets	Pancreatic Islet
31	chr1:161903800-161923800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr1:161904400-161915600	Weak transcription	HSMMtube	muscle
33	chr1:161904400-161923200	Weak transcription	Brain Cingulate Gyrus	brain
34	chr1:161904800-161956600	Weak transcription	Fetal Brain Male	brain
35	chr1:161905000-161920600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr1:161906000-161914600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
37	chr1:161906000-161923200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
38	chr1:161906000-161923200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
39	chr1:161906000-161927800	Weak transcription	Thymus	Thymus
40	chr1:161906800-161918000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
41	chr1:161906800-161923200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
42	chr1:161906800-161928000	Weak transcription	Stomach Smooth Muscle	stomach
43	chr1:161906800-161932200	Weak transcription	Stomach Mucosa	stomach
44	chr1:161907000-161919200	Weak transcription	Brain Hippocampus Middle	brain
45	chr1:161907000-161923200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
46	chr1:161908400-161915400	Strong transcription	Primary B cells from peripheral blood	blood
47	chr1:161910400-161915200	Strong transcription	Primary monocytes fromperipheralblood	blood
48	chr1:161910600-161914600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
49	chr1:161910600-161915800	Strong transcription	Primary B cells from cord blood	blood
50	chr1:161910600-161922600	Weak transcription	Brain Angular Gyrus	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links