Variant report

Variant	rs9535765
Chromosome Location	chr13:52394269-52394270
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr13:52393921..52396482-chr13:52702108..52704380,2	K562	blood:
2	chr13:52378222..52381026-chr13:52393524..52396467,2	MCF-7	breast:
3	chr13:52377626..52380067-chr13:52391975..52395506,4	K562	blood:
4	chr13:52380223..52382865-chr13:52393568..52395438,2	K562	blood:

Variant related genes	Relation type
ENSG00000102796	Chromatin interaction
ENSG00000231856	Chromatin interaction
ENSG00000197168	Chromatin interaction

Extended variants
information (count: 16 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs1543525	0.95[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs1923875	0.85[CHB][hapmap];1.00[YRI][hapmap];0.86[ASN][1000 genomes]
rs7992588	0.94[JPT][hapmap]
rs9535762	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9535763	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.88[AFR][1000 genomes];0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9535767	0.83[CEU][hapmap];0.84[CHB][hapmap];1.00[YRI][hapmap]
rs975504	0.94[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530718	chr13:52291802-52832752	Enhancers ZNF genes & repeats Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
2	nsv933424	chr13:52293482-52507732	Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
3	nsv455884	chr13:52302630-52405251	Enhancers Flanking Active TSS Strong transcription Genic enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
4	nsv561644	chr13:52302630-52405251	Enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
5	nsv455887	chr13:52318522-52405251	Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
6	nsv561645	chr13:52318522-52405251	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
7	nsv1044310	chr13:52321564-52643924	Weak transcription Flanking Active TSS ZNF genes & repeats Enhancers Strong transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
8	nsv1050117	chr13:52325116-52643924	Enhancers Genic enhancers Flanking Active TSS Strong transcription Active TSS Weak transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
9	nsv934070	chr13:52362588-53174923	Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Active TSS Enhancers Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	59 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:54 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:52389000-52394400	Enhancers	Primary T killer memory cells from peripheral blood	blood
2	chr13:52389000-52394600	Enhancers	Fetal Heart	heart
3	chr13:52389600-52395200	Enhancers	Primary neutrophils fromperipheralblood	blood
4	chr13:52389600-52398200	Weak transcription	Brain Substantia Nigra	brain
5	chr13:52389800-52395000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
6	chr13:52389800-52395200	Enhancers	Primary T helper cells fromperipheralblood	blood
7	chr13:52389800-52396000	Weak transcription	Rectal Mucosa Donor 29	rectum
8	chr13:52389800-52397600	Weak transcription	Brain Hippocampus Middle	brain
9	chr13:52390000-52394600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr13:52390000-52394800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr13:52390200-52398200	Weak transcription	Rectal Smooth Muscle	rectum
12	chr13:52391200-52394600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
13	chr13:52391400-52394400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
14	chr13:52392000-52394800	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
15	chr13:52392000-52395400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
16	chr13:52392400-52394600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr13:52392400-52404800	Enhancers	Primary monocytes fromperipheralblood	blood
18	chr13:52392600-52394400	Enhancers	GM12878-XiMat	blood
19	chr13:52392600-52396200	Enhancers	Fetal Thymus	thymus
20	chr13:52392600-52399600	Weak transcription	Fetal Lung	lung
21	chr13:52392800-52394400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr13:52392800-52395600	Enhancers	Primary B cells from cord blood	blood
23	chr13:52392800-52401800	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
24	chr13:52393200-52394800	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
25	chr13:52393200-52397800	Enhancers	Fetal Muscle Leg	muscle
26	chr13:52393400-52394800	Flanking Active TSS	Primary T cells from cord blood	blood
27	chr13:52393400-52395200	Enhancers	Monocytes-CD14+_RO01746	blood
28	chr13:52393600-52394800	Weak transcription	HUES48 Cell Line	embryonic stem cell
29	chr13:52393600-52394800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
30	chr13:52393600-52396000	Enhancers	Thymus	Thymus
31	chr13:52393600-52396200	Enhancers	Primary hematopoietic stem cells	blood
32	chr13:52393600-52406200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
33	chr13:52393600-52418600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr13:52393800-52397800	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
35	chr13:52393800-52398600	Weak transcription	Colon Smooth Muscle	Colon
36	chr13:52393800-52399200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
37	chr13:52393800-52399200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
38	chr13:52393800-52399200	Weak transcription	Adipose Nuclei	Adipose
39	chr13:52393800-52400000	Weak transcription	Duodenum Smooth Muscle	Duodenum
40	chr13:52394000-52394800	Enhancers	Primary T cells fromperipheralblood	blood
41	chr13:52394000-52394800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
42	chr13:52394000-52395000	Weak transcription	Primary B cells from peripheral blood	blood
43	chr13:52394000-52395000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
44	chr13:52394000-52396000	Weak transcription	Skeletal Muscle Male	skeletal muscle
45	chr13:52394000-52396600	Weak transcription	Spleen	Spleen
46	chr13:52394000-52399000	Weak transcription	HUES6 Cell Line	embryonic stem cell
47	chr13:52394000-52399000	Weak transcription	Right Atrium	heart
48	chr13:52394000-52399400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
49	chr13:52394000-52399600	Weak transcription	Left Ventricle	heart
50	chr13:52394000-52399800	Weak transcription	Right Ventricle	heart

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