Variant report

Variant	rs2760409
Chromosome Location	chr9:5801675-5801676
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr9:5801176..5803220-chr9:5803404..5804983,2	K562	blood:
2	chr9:5799205..5801900-chr9:5831455..5833894,2	MCF-7	breast:
3	chr9:5793511..5796072-chr9:5800042..5802982,3	K562	blood:

Variant related genes	Relation type
ENSG00000099219	Chromatin interaction

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

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs10975340	1.00[EUR][1000 genomes]
rs1141025	1.00[EUR][1000 genomes]
rs1260128	0.95[YRI][hapmap];0.90[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs1260130	1.00[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1260132	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1260134	0.84[YRI][hapmap];0.89[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs1260135	1.00[EUR][1000 genomes]
rs1745887	0.82[AFR][1000 genomes];0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1745888	0.93[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs1776008	1.00[YRI][hapmap];0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2476262	0.82[YRI][hapmap];0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2760408	0.81[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs2760410	0.95[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2797512	1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2797514	1.00[EUR][1000 genomes]
rs2797516	0.89[YRI][hapmap];0.93[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs2797517	0.91[AFR][1000 genomes]
rs2797519	1.00[EUR][1000 genomes]
rs58370080	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6477001	1.00[EUR][1000 genomes]
rs6477002	1.00[EUR][1000 genomes]
rs7037680	0.94[YRI][hapmap];0.89[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs7038243	1.00[YRI][hapmap]
rs7042100	1.00[EUR][1000 genomes]
rs7046793	1.00[EUR][1000 genomes]
rs73377834	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1017103	chr9:5509431-5987907	Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
2	nsv539965	chr9:5509431-5987907	ZNF genes & repeats Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
3	nsv1019444	chr9:5598677-5807009	Weak transcription Flanking Active TSS Enhancers Genic enhancers Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
4	nsv892151	chr9:5602528-5841438	Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
5	nsv948847	chr9:5712626-6417677	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
6	esv3331803	chr9:5766129-5905103	Weak transcription Enhancers Bivalent/Poised TSS Genic enhancers Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:108 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:5779200-5809600	Weak transcription	NHDF-Ad	bronchial
2	chr9:5779200-5832200	Weak transcription	Fetal Brain Male	brain
3	chr9:5779600-5814000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
4	chr9:5779600-5827800	Weak transcription	Small Intestine	intestine
5	chr9:5784200-5831600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr9:5786800-5832200	Weak transcription	Placenta Amnion	Placenta Amnion
7	chr9:5787000-5830200	Weak transcription	Dnd41	blood
8	chr9:5787200-5804200	Weak transcription	HUES6 Cell Line	embryonic stem cell
9	chr9:5787200-5815000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
10	chr9:5787400-5832000	Weak transcription	Fetal Brain Female	brain
11	chr9:5787600-5806400	Weak transcription	Fetal Stomach	stomach
12	chr9:5787600-5809400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
13	chr9:5787600-5809600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
14	chr9:5787600-5809600	Weak transcription	Brain Cingulate Gyrus	brain
15	chr9:5787600-5809600	Weak transcription	Left Ventricle	heart
16	chr9:5787600-5812400	Weak transcription	Fetal Muscle Trunk	muscle
17	chr9:5787600-5812800	Weak transcription	Lung	lung
18	chr9:5787600-5817600	Weak transcription	H1 Cell Line	embryonic stem cell
19	chr9:5787600-5831600	Weak transcription	Rectal Smooth Muscle	rectum
20	chr9:5787600-5832000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
21	chr9:5787600-5832200	Weak transcription	Esophagus	oesophagus
22	chr9:5787800-5818000	Weak transcription	HSMM	muscle
23	chr9:5788000-5809600	Weak transcription	HUES64 Cell Line	embryonic stem cell
24	chr9:5788000-5817600	Weak transcription	K562	blood
25	chr9:5789800-5802400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr9:5789800-5825200	Weak transcription	Gastric	stomach
27	chr9:5790000-5824000	Weak transcription	Pancreas	Pancrea
28	chr9:5790600-5808200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
29	chr9:5791400-5809400	Weak transcription	HUES48 Cell Line	embryonic stem cell
30	chr9:5791600-5809400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr9:5791800-5809600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr9:5791800-5809600	Weak transcription	Primary B cells from peripheral blood	blood
33	chr9:5792000-5814000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr9:5792200-5809400	Weak transcription	Skeletal Muscle Female	skeletal muscle
35	chr9:5792400-5805600	Weak transcription	Fetal Muscle Leg	muscle
36	chr9:5794000-5808400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
37	chr9:5794600-5821800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
38	chr9:5794600-5825600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
39	chr9:5795000-5809800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
40	chr9:5795200-5809600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
41	chr9:5795200-5809800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
42	chr9:5797000-5805200	Weak transcription	Primary neutrophils fromperipheralblood	blood
43	chr9:5797000-5805200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
44	chr9:5797400-5831400	Weak transcription	Psoas Muscle	Psoas
45	chr9:5798000-5809200	Weak transcription	Primary T helper cells PMA-I stimulated	--
46	chr9:5798200-5809600	Weak transcription	Primary B cells from cord blood	blood
47	chr9:5798400-5831200	Weak transcription	Colon Smooth Muscle	Colon
48	chr9:5798600-5803600	Strong transcription	GM12878-XiMat	blood
49	chr9:5798600-5809600	Weak transcription	Primary monocytes fromperipheralblood	blood
50	chr9:5798800-5806000	Strong transcription	Primary T cells from cord blood	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links