Variant report

Variant	rs34789089
Chromosome Location	chr6:114272701-114272702
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:114272303..114275586-chr6:114290537..114293049,3	MCF-7	breast:
2	chr6:114270741..114273479-chr6:114282715..114285279,2	K562	blood:
3	chr6:114260434..114263162-chr6:114272567..114274765,2	MCF-7	breast:
4	chr6:114270201..114271867-chr6:114272109..114273738,2	MCF-7	breast:
5	chr6:114267467..114269651-chr6:114272687..114274488,2	K562	blood:

Variant related genes	Relation type
ENSG00000196591	Chromatin interaction
ENSG00000228624	Chromatin interaction

Extended variants
information (count: 27 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs12660414	0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12660832	0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12665655	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs13191525	0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs13191982	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs13194921	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs13201727	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13204434	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs13204445	0.88[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13206211	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs13208986	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs13209064	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs13212298	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs13213007	0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs13213042	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs13216873	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs13219947	0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1322453	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1358945	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs17075712	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2025191	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs34319597	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs35846930	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs3778216	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[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	nsv1021774	chr6:114063971-114407280	Enhancers Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	60 gene(s)	inside rSNPs	diseases
2	nsv538422	chr6:114063971-114407280	Genic enhancers Enhancers Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	60 gene(s)	inside rSNPs	diseases
3	esv3363275	chr6:114101331-114302866	Weak transcription Active TSS Flanking Active TSS Enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:121 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:114253000-114289800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr6:114253400-114290600	Weak transcription	Aorta	Aorta
3	chr6:114254600-114281800	Strong transcription	Dnd41	blood
4	chr6:114255400-114281600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr6:114255600-114276600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr6:114258400-114274200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr6:114258400-114279600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr6:114258600-114282600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr6:114258600-114291000	Weak transcription	Lung	lung
10	chr6:114258800-114279600	Strong transcription	Fetal Intestine Large	intestine
11	chr6:114258800-114281000	Strong transcription	HUES64 Cell Line	embryonic stem cell
12	chr6:114258800-114281600	Weak transcription	Gastric	stomach
13	chr6:114258800-114285600	Weak transcription	Right Ventricle	heart
14	chr6:114258800-114289800	Weak transcription	Spleen	Spleen
15	chr6:114259000-114289200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
16	chr6:114259400-114279800	Strong transcription	Primary monocytes fromperipheralblood	blood
17	chr6:114259400-114281400	Strong transcription	HUES48 Cell Line	embryonic stem cell
18	chr6:114259600-114279600	Strong transcription	Monocytes-CD14+_RO01746	blood
19	chr6:114259600-114281000	Strong transcription	iPS-18 Cell Line	embryonic stem cell
20	chr6:114259800-114274200	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr6:114259800-114274400	Strong transcription	HSMM	muscle
22	chr6:114259800-114280000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
23	chr6:114259800-114280600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
24	chr6:114259800-114280600	Strong transcription	Fetal Thymus	thymus
25	chr6:114259800-114280800	Strong transcription	HUES6 Cell Line	embryonic stem cell
26	chr6:114259800-114280800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
27	chr6:114259800-114281000	Strong transcription	Primary T helper cells fromperipheralblood	blood
28	chr6:114260000-114274400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
29	chr6:114260000-114280400	Strong transcription	Primary B cells from peripheral blood	blood
30	chr6:114260200-114274800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr6:114260200-114275400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr6:114260200-114279600	Strong transcription	H1 Cell Line	embryonic stem cell
33	chr6:114264800-114289800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
34	chr6:114265200-114280800	Weak transcription	Brain Hippocampus Middle	brain
35	chr6:114265600-114282000	Weak transcription	Brain Substantia Nigra	brain
36	chr6:114266000-114272800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
37	chr6:114266000-114283800	Weak transcription	Colonic Mucosa	Colon
38	chr6:114266000-114289600	Weak transcription	Esophagus	oesophagus
39	chr6:114266200-114277000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
40	chr6:114266200-114285600	Weak transcription	Psoas Muscle	Psoas
41	chr6:114266400-114285600	Weak transcription	Small Intestine	intestine
42	chr6:114266400-114289800	Weak transcription	Pancreas	Pancrea
43	chr6:114266600-114273600	Strong transcription	Hela-S3	cervix
44	chr6:114267200-114274000	Weak transcription	NHEK	skin
45	chr6:114267200-114274200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
46	chr6:114267200-114275000	Weak transcription	HSMMtube	muscle
47	chr6:114267400-114273200	Weak transcription	A549	lung
48	chr6:114267400-114274000	Weak transcription	HMEC	breast
49	chr6:114267400-114275200	Weak transcription	H9 Cell Line	embryonic stem cell
50	chr6:114267400-114275600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood

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