Variant report

Variant	rs6510516
Chromosome Location	chr19:36552081-36552082
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr19:36550207..36552576-chr19:36592409..36594270,2	K562	blood:
2	chr19:36550570..36553436-chr19:36705929..36708473,2	K562	blood:
3	chr19:36544812..36547842-chr19:36549137..36553614,5	MCF-7	breast:
4	chr19:36551993..36554665-chr19:36606239..36608133,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000075702	Chromatin interaction
ENSG00000105254	Chromatin interaction
ENSG00000161277	Chromatin interaction
ENSG00000167635	Chromatin interaction
ENSG00000196357	Chromatin interaction
ENSG00000105258	Chromatin interaction

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

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs10406862	0.89[YRI][hapmap]
rs10425700	0.82[LWK][hapmap];0.89[YRI][hapmap]
rs12608517	0.94[YRI][hapmap]
rs12981698	0.80[YRI][hapmap]
rs4555271	0.82[LWK][hapmap];0.89[YRI][hapmap]
rs4806249	0.89[YRI][hapmap]
rs4806254	0.89[YRI][hapmap]
rs4806276	0.82[LWK][hapmap];0.89[YRI][hapmap]
rs58159114	1.00[AMR][1000 genomes]
rs61704180	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7258807	0.89[YRI][hapmap]
rs73601695	1.00[AMR][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	esv3526489	chr19:36306483-36741945	Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	114 gene(s)	inside rSNPs	diseases
2	esv3526490	chr19:36306483-36741945	Genic enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	114 gene(s)	inside rSNPs	diseases
3	esv1831737	chr19:36324324-36690874	Weak transcription Strong transcription Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	103 gene(s)	inside rSNPs	diseases
4	nsv833815	chr19:36519803-36624936	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:90 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:36546400-36577600	Weak transcription	Esophagus	oesophagus
2	chr19:36546400-36584000	Weak transcription	Right Atrium	heart
3	chr19:36546600-36556600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
4	chr19:36546600-36556800	Weak transcription	Spleen	Spleen
5	chr19:36546600-36557800	Weak transcription	Sigmoid Colon	Sigmoid Colon
6	chr19:36546600-36572400	Weak transcription	Lung	lung
7	chr19:36546600-36602200	Weak transcription	Colonic Mucosa	Colon
8	chr19:36546600-36604800	Weak transcription	Rectal Mucosa Donor 31	rectum
9	chr19:36546800-36557800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr19:36546800-36572000	Weak transcription	Primary T cells from cord blood	blood
11	chr19:36546800-36572800	Weak transcription	Primary B cells from cord blood	blood
12	chr19:36546800-36572800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
13	chr19:36546800-36580200	Weak transcription	Fetal Kidney	kidney
14	chr19:36546800-36588000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
15	chr19:36546800-36592200	Weak transcription	Placenta Amnion	Placenta Amnion
16	chr19:36546800-36601400	Weak transcription	Rectal Mucosa Donor 29	rectum
17	chr19:36547000-36561200	Weak transcription	NH-A	brain
18	chr19:36547200-36557600	Weak transcription	Placenta	Placenta
19	chr19:36547400-36561200	Weak transcription	Duodenum Mucosa	Duodenum
20	chr19:36547400-36562000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr19:36547600-36553400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr19:36547600-36553600	Weak transcription	Fetal Lung	lung
23	chr19:36547600-36555800	Weak transcription	HMEC	breast
24	chr19:36547600-36559200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr19:36547600-36559200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
26	chr19:36547600-36584200	Weak transcription	Fetal Heart	heart
27	chr19:36547800-36552400	Weak transcription	Fetal Brain Female	brain
28	chr19:36547800-36555800	Weak transcription	NHDF-Ad	bronchial
29	chr19:36548000-36559200	Strong transcription	Fetal Thymus	thymus
30	chr19:36548200-36596400	Strong transcription	H1 Cell Line	embryonic stem cell
31	chr19:36548400-36552600	Strong transcription	Cortex derived primary cultured neurospheres	brain
32	chr19:36548400-36559200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
33	chr19:36548400-36559200	Strong transcription	A549	lung
34	chr19:36548400-36571000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
35	chr19:36548600-36559400	Strong transcription	HUES48 Cell Line	embryonic stem cell
36	chr19:36548600-36560800	Weak transcription	HUVEC	blood vessel
37	chr19:36548800-36552400	Strong transcription	K562	blood
38	chr19:36548800-36552600	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
39	chr19:36548800-36559200	Strong transcription	HUES6 Cell Line	embryonic stem cell
40	chr19:36548800-36560400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr19:36548800-36567800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
42	chr19:36549200-36552200	Enhancers	Skeletal Muscle Male	skeletal muscle
43	chr19:36549200-36559400	Strong transcription	HUES64 Cell Line	embryonic stem cell
44	chr19:36549200-36559400	Strong transcription	Fetal Stomach	stomach
45	chr19:36549400-36552200	Strong transcription	iPS DF 6.9 Cell Line	embryonic stem cell
46	chr19:36549400-36552200	Enhancers	Skeletal Muscle Female	skeletal muscle
47	chr19:36549400-36553400	Strong transcription	Hela-S3	cervix
48	chr19:36549400-36553800	Strong transcription	Primary monocytes fromperipheralblood	blood
49	chr19:36549400-36558800	Strong transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr19:36549400-36558800	Strong transcription	H9 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links