Variant report

Variant	rs9496382
Chromosome Location	chr6:142766980-142766981
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:142765212..142767183-chr6:142771549..142773633,2	K562	blood:
2	chr6:142763089..142766069-chr6:142766128..142768909,2	K562	blood:
3	chr6:142756302..142759239-chr6:142765557..142767364,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000112414	Chromatin interaction

Extended variants
information (count: 32 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs10223419	1.00[YRI][hapmap];0.90[AFR][1000 genomes]
rs13437159	1.00[AFR][1000 genomes]
rs28489749	0.90[AFR][1000 genomes]
rs9321864	0.90[AFR][1000 genomes]
rs9321868	1.00[YRI][hapmap];0.90[AFR][1000 genomes]
rs9484622	0.90[AFR][1000 genomes]
rs9484623	0.90[AFR][1000 genomes]
rs9484624	0.90[AFR][1000 genomes]
rs9484625	0.90[AFR][1000 genomes]
rs9484626	0.90[AFR][1000 genomes]
rs9484637	1.00[AFR][1000 genomes]
rs9484642	0.81[AFR][1000 genomes]
rs9484643	0.90[AFR][1000 genomes]
rs9496335	0.90[AFR][1000 genomes]
rs9496337	1.00[YRI][hapmap];0.90[AFR][1000 genomes]
rs9496339	0.90[AFR][1000 genomes]
rs9496340	0.90[AFR][1000 genomes]
rs9496342	0.90[AFR][1000 genomes]
rs9496343	1.00[YRI][hapmap]
rs9496344	1.00[YRI][hapmap];0.90[AFR][1000 genomes]
rs9496345	1.00[YRI][hapmap];0.90[AFR][1000 genomes]
rs9496347	1.00[YRI][hapmap]
rs9496348	1.00[YRI][hapmap];0.90[AFR][1000 genomes]
rs9496352	1.00[YRI][hapmap];0.90[AFR][1000 genomes]
rs9496353	1.00[YRI][hapmap];0.90[AFR][1000 genomes]
rs9496366	0.90[AFR][1000 genomes]
rs9496370	1.00[YRI][hapmap];0.90[AFR][1000 genomes]
rs9496377	1.00[AFR][1000 genomes]
rs9496380	1.00[YRI][hapmap];1.00[AFR][1000 genomes]
rs9496389	0.90[AFR][1000 genomes]
rs9496390	0.90[AFR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949088	chr6:142561402-143128849	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:43 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:142738000-142774200	Weak transcription	NHEK	skin
2	chr6:142743200-142769200	Weak transcription	HMEC	breast
3	chr6:142748000-142782600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr6:142751600-142780000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr6:142752400-142774600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr6:142753600-142774000	Strong transcription	Liver	Liver
7	chr6:142754000-142772800	Strong transcription	HepG2	liver
8	chr6:142760000-142770600	Weak transcription	Lung	lung
9	chr6:142760400-142767800	Weak transcription	Esophagus	oesophagus
10	chr6:142762200-142773000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr6:142764200-142767000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr6:142764800-142767800	Enhancers	Fetal Lung	lung
13	chr6:142765400-142767000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr6:142765400-142767000	Enhancers	Hela-S3	cervix
15	chr6:142765400-142770800	Strong transcription	Placenta	Placenta
16	chr6:142765600-142767200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr6:142765600-142768000	Strong transcription	A549	lung
18	chr6:142765800-142767200	Enhancers	HUES48 Cell Line	embryonic stem cell
19	chr6:142766000-142767000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr6:142766000-142770400	Strong transcription	HUVEC	blood vessel
21	chr6:142766000-142777600	Weak transcription	HSMM	muscle
22	chr6:142766200-142767400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr6:142766200-142767600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
24	chr6:142766200-142768600	Weak transcription	Fetal Intestine Small	intestine
25	chr6:142766200-142772400	Weak transcription	Pancreas	Pancrea
26	chr6:142766200-142773800	Weak transcription	Placenta Amnion	Placenta Amnion
27	chr6:142766200-142782800	Weak transcription	NHLF	lung
28	chr6:142766400-142767200	Weak transcription	Primary hematopoietic stem cells	blood
29	chr6:142766400-142767600	Weak transcription	H1 Cell Line	embryonic stem cell
30	chr6:142766400-142767600	Weak transcription	H9 Cell Line	embryonic stem cell
31	chr6:142766400-142767600	Weak transcription	HUES6 Cell Line	embryonic stem cell
32	chr6:142766400-142767800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
33	chr6:142766400-142767800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr6:142766400-142768800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr6:142766400-142769000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr6:142766400-142769000	Weak transcription	Fetal Intestine Large	intestine
37	chr6:142766400-142774000	Weak transcription	Duodenum Mucosa	Duodenum
38	chr6:142766400-142778000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
39	chr6:142766600-142767600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr6:142766600-142767600	Weak transcription	Primary T cells from cord blood	blood
41	chr6:142766600-142767600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr6:142766600-142770000	Weak transcription	Fetal Stomach	stomach
43	chr6:142766800-142774800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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