Variant report

Variant	rs34720471
Chromosome Location	chr19:35694041-35694042
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr19:35690432..35694282-chr19:35737406..35740998,3	K562	blood:
2	chr19:35686366..35688378-chr19:35693649..35696328,2	K562	blood:
3	chr19:35647531..35650498-chr19:35693882..35696047,2	K562	blood:
4	chr19:35691908..35694570-chr19:35738700..35740998,2	K562	blood:

Variant related genes	Relation type
ENSG00000105699	Chromatin interaction

Extended variants
information (count: 5 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:1)

rs_ID	r²[population]
rs62111403	0.88[EUR][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	nsv432045	chr19:35556260-36520760	Flanking Active TSS Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	191 gene(s)	inside rSNPs	diseases
2	nsv2470	chr19:35655281-35702565	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Enhancers Flanking Active TSS Bivalent Enhancer Active TSS	Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv1060100	chr19:35658505-36170042	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	107 gene(s)	inside rSNPs	diseases
4	nsv543993	chr19:35658505-36170042	Enhancers Strong transcription Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	107 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:31 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:35691800-35696200	Weak transcription	Gastric	stomach
2	chr19:35691800-35697000	Enhancers	Primary T helper cells PMA-I stimulated	--
3	chr19:35692000-35696800	Enhancers	H1 Cell Line	embryonic stem cell
4	chr19:35692200-35695000	Weak transcription	Spleen	Spleen
5	chr19:35692200-35696000	Weak transcription	Stomach Mucosa	stomach
6	chr19:35692400-35695000	Weak transcription	Fetal Thymus	thymus
7	chr19:35692600-35694200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
8	chr19:35693400-35696400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr19:35693400-35697000	Enhancers	iPS-15b Cell Line	embryonic stem cell
10	chr19:35693400-35699400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
11	chr19:35693400-35707000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
12	chr19:35693600-35694400	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
13	chr19:35693600-35694800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
14	chr19:35693600-35694800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr19:35693600-35696200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
16	chr19:35693600-35696800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
17	chr19:35693600-35697000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
18	chr19:35693600-35697000	Enhancers	H9 Cell Line	embryonic stem cell
19	chr19:35693600-35698800	Enhancers	Primary T helper naive cells from peripheral blood	blood
20	chr19:35693600-35701800	Weak transcription	Right Atrium	heart
21	chr19:35693800-35694200	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
22	chr19:35693800-35694400	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
23	chr19:35693800-35694400	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
24	chr19:35693800-35696000	Enhancers	K562	blood
25	chr19:35693800-35697200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
26	chr19:35694000-35694400	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
27	chr19:35694000-35694400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
28	chr19:35694000-35695000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr19:35694000-35695200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr19:35694000-35697600	Enhancers	Primary T helper cells fromperipheralblood	blood
31	chr19:35694000-35704400	Enhancers	Primary T cells fromperipheralblood	blood

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