Variant report

Variant	rs1168333
Chromosome Location	chr12:66761377-66761378
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr12:66755875..66758507-chr12:66758802..66761903,3	K562	blood:

Extended variants
information (count: 85 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:81)

rs_ID	r²[population]
rs1027399	0.93[EUR][1000 genomes]
rs1027400	0.96[EUR][1000 genomes]
rs1027401	0.97[EUR][1000 genomes]
rs1039056	0.97[EUR][1000 genomes]
rs1060724	0.95[EUR][1000 genomes]
rs10784525	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1168290	0.90[EUR][1000 genomes]
rs1168291	0.95[EUR][1000 genomes]
rs1168292	0.95[EUR][1000 genomes]
rs1168293	0.94[EUR][1000 genomes]
rs1168294	0.95[EUR][1000 genomes]
rs1168295	0.94[EUR][1000 genomes]
rs1168296	0.83[AFR][1000 genomes];0.95[EUR][1000 genomes]
rs1168297	0.94[EUR][1000 genomes]
rs1168298	0.95[EUR][1000 genomes]
rs1168299	0.94[EUR][1000 genomes]
rs1168300	0.95[EUR][1000 genomes]
rs1168301	0.83[AFR][1000 genomes];0.95[EUR][1000 genomes]
rs1168302	0.94[EUR][1000 genomes]
rs1168303	0.95[EUR][1000 genomes]
rs1168304	0.95[EUR][1000 genomes]
rs1168305	0.95[EUR][1000 genomes]
rs1168306	0.95[EUR][1000 genomes]
rs1168307	0.93[EUR][1000 genomes]
rs1168308	0.95[EUR][1000 genomes]
rs1168309	0.93[EUR][1000 genomes]
rs1168310	0.94[EUR][1000 genomes]
rs1168311	0.94[EUR][1000 genomes]
rs1168314	0.95[EUR][1000 genomes]
rs1168315	0.95[EUR][1000 genomes]
rs1168316	0.95[EUR][1000 genomes]
rs1168317	0.95[EUR][1000 genomes]
rs1168318	0.97[EUR][1000 genomes]
rs1168319	0.95[EUR][1000 genomes]
rs1168320	0.95[EUR][1000 genomes]
rs1168321	0.95[EUR][1000 genomes]
rs1168322	0.95[EUR][1000 genomes]
rs1168325	0.91[EUR][1000 genomes]
rs1168327	0.95[EUR][1000 genomes]
rs1168328	0.94[EUR][1000 genomes]
rs1168329	0.94[EUR][1000 genomes]
rs1168330	0.96[EUR][1000 genomes]
rs1168332	0.97[EUR][1000 genomes]
rs1168334	0.97[EUR][1000 genomes]
rs1168338	0.92[EUR][1000 genomes]
rs1168339	0.91[EUR][1000 genomes]
rs1168340	0.91[EUR][1000 genomes]
rs1168341	0.92[EUR][1000 genomes]
rs1168342	0.92[EUR][1000 genomes]
rs1168343	0.96[EUR][1000 genomes]
rs1168344	0.96[EUR][1000 genomes]
rs1168345	0.95[EUR][1000 genomes]
rs1168346	0.96[EUR][1000 genomes]
rs1168347	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1168348	0.93[EUR][1000 genomes]
rs1168351	0.94[EUR][1000 genomes]
rs1168352	0.93[AFR][1000 genomes];0.83[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1168353	0.94[EUR][1000 genomes]
rs1168356	0.90[AFR][1000 genomes];0.81[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1168357	0.95[EUR][1000 genomes]
rs1168358	0.90[AFR][1000 genomes];0.81[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1177555	0.94[EUR][1000 genomes]
rs1179889	0.85[EUR][1000 genomes]
rs1183272	0.94[EUR][1000 genomes]
rs1183274	0.95[EUR][1000 genomes]
rs1184551	0.92[EUR][1000 genomes]
rs1184552	0.88[EUR][1000 genomes]
rs1185244	0.94[EUR][1000 genomes]
rs1495497	0.95[EUR][1000 genomes]
rs1795527	0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1795529	0.90[EUR][1000 genomes]
rs2172881	0.90[EUR][1000 genomes]
rs2951656	0.94[EUR][1000 genomes]
rs4762091	0.95[EUR][1000 genomes]
rs61925898	0.86[EUR][1000 genomes]
rs6581677	0.95[EUR][1000 genomes]
rs6581678	0.87[EUR][1000 genomes]
rs903587	0.95[EUR][1000 genomes]
rs903589	0.89[AFR][1000 genomes];0.97[EUR][1000 genomes]
rs903590	0.89[AFR][1000 genomes];0.96[EUR][1000 genomes]
rs961049	0.96[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][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	nsv1052503	chr12:66293898-67269495	Weak transcription Flanking Active TSS Enhancers Strong transcription Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	51 gene(s)	inside rSNPs	diseases
2	nsv541515	chr12:66293898-67269495	Strong transcription Enhancers Active TSS Genic enhancers ZNF genes & repeats Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	51 gene(s)	inside rSNPs	diseases
3	nsv1051713	chr12:66745716-66889411	Strong transcription Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	nsv1040682	chr12:66750103-67328053	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Strong transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs1168333	HELB	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:26 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:66710200-66792800	Weak transcription	Fetal Kidney	kidney
2	chr12:66736000-66766400	Weak transcription	Stomach Smooth Muscle	stomach
3	chr12:66738000-66792800	Weak transcription	Rectal Smooth Muscle	rectum
4	chr12:66738200-66770400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
5	chr12:66738800-66770400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
6	chr12:66739400-66765800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
7	chr12:66739400-66766200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
8	chr12:66743000-66787600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
9	chr12:66743200-66763400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
10	chr12:66743200-66763800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr12:66743400-66761600	Weak transcription	Colon Smooth Muscle	Colon
12	chr12:66743600-66764000	Weak transcription	Duodenum Smooth Muscle	Duodenum
13	chr12:66744600-66767400	Weak transcription	Primary T cells fromperipheralblood	blood
14	chr12:66746800-66772200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
15	chr12:66747000-66763800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
16	chr12:66747400-66762000	Weak transcription	Primary T helper cells fromperipheralblood	blood
17	chr12:66747400-66772000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr12:66748200-66761400	Weak transcription	Brain Germinal Matrix	brain
19	chr12:66748200-66766600	Weak transcription	Fetal Brain Male	brain
20	chr12:66749000-66763400	Weak transcription	Fetal Brain Female	brain
21	chr12:66759800-66770400	Weak transcription	Placenta	Placenta
22	chr12:66760000-66761400	Weak transcription	Primary T cells from cord blood	blood
23	chr12:66760200-66783200	Weak transcription	Primary T helper cells PMA-I stimulated	--
24	chr12:66760400-66761400	Enhancers	Monocytes-CD14+_RO01746	blood
25	chr12:66760400-66767200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
26	chr12:66761200-66772400	Weak transcription	Primary monocytes fromperipheralblood	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links