Variant report

Variant	rs35759897
Chromosome Location	chr19:39824903-39824904
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr19:39823125..39825473-chr19:39831028..39833555,3	K562	blood:

Variant related genes	Relation type
ENSG00000179134	Chromatin interaction
ENSG00000269246	Chromatin interaction
ENSG00000130755	Chromatin interaction

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

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs12975430	0.87[EUR][1000 genomes]
rs12978870	0.84[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs12979175	0.84[AMR][1000 genomes]
rs12980571	0.88[ASN][1000 genomes]
rs12980978	0.89[AFR][1000 genomes];0.88[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs35543324	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs35797139	0.84[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs39587	0.88[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv432048	chr19:39572060-39850060	Bivalent/Poised TSS Bivalent Enhancer Weak transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
2	nsv833830	chr19:39709538-39837846	Enhancers Bivalent Enhancer Genic enhancers Strong transcription Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
3	nsv911679	chr19:39735106-39924129	Active TSS Flanking Active TSS Weak transcription Enhancers Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	198 gene(s)	inside rSNPs	diseases
4	nsv1058514	chr19:39744112-39902580	Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	187 gene(s)	inside rSNPs	diseases
5	nsv911680	chr19:39792460-39924129	Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	194 gene(s)	inside rSNPs	diseases
6	nsv911681	chr19:39797716-39856246	Strong transcription Weak transcription Genic enhancers Bivalent/Poised TSS Flanking Active TSS Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
7	esv10629	chr19:39811570-39886212	Flanking Active TSS Strong transcription Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
8	nsv870133	chr19:39822160-39938468	Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	233 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:48 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:39811400-39825800	Weak transcription	Gastric	stomach
2	chr19:39812000-39825600	Weak transcription	Right Ventricle	heart
3	chr19:39814800-39826000	Weak transcription	Sigmoid Colon	Sigmoid Colon
4	chr19:39817200-39825800	Weak transcription	Placenta	Placenta
5	chr19:39818600-39831600	Weak transcription	H1 Cell Line	embryonic stem cell
6	chr19:39818800-39825800	Weak transcription	Left Ventricle	heart
7	chr19:39818800-39826800	Weak transcription	H9 Cell Line	embryonic stem cell
8	chr19:39819200-39825000	Weak transcription	Rectal Mucosa Donor 29	rectum
9	chr19:39819200-39825200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
10	chr19:39819200-39825800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
11	chr19:39819200-39825800	Weak transcription	K562	blood
12	chr19:39820200-39826000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr19:39820400-39825000	Enhancers	Primary T helper naive cells from peripheral blood	blood
14	chr19:39820400-39825000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
15	chr19:39820800-39825800	Weak transcription	Liver	Liver
16	chr19:39821000-39825000	Weak transcription	GM12878-XiMat	blood
17	chr19:39822000-39825000	Weak transcription	Duodenum Mucosa	Duodenum
18	chr19:39822000-39826000	Weak transcription	Fetal Intestine Small	intestine
19	chr19:39822200-39826000	Weak transcription	Fetal Intestine Large	intestine
20	chr19:39822400-39825000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
21	chr19:39822400-39825000	Weak transcription	Adipose Nuclei	Adipose
22	chr19:39822400-39825800	Weak transcription	Lung	lung
23	chr19:39823600-39825000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
24	chr19:39823600-39825200	Enhancers	Primary monocytes fromperipheralblood	blood
25	chr19:39823800-39825800	Weak transcription	HepG2	liver
26	chr19:39823800-39831200	Weak transcription	A549	lung
27	chr19:39824200-39825200	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
28	chr19:39824200-39825400	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
29	chr19:39824200-39826200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr19:39824400-39825000	Enhancers	Primary hematopoietic stem cells	blood
31	chr19:39824400-39825400	Enhancers	Primary B cells from peripheral blood	blood
32	chr19:39824400-39825400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
33	chr19:39824600-39825000	Enhancers	Primary B cells from cord blood	blood
34	chr19:39824600-39825000	Active TSS	Primary T cells from cord blood	blood
35	chr19:39824600-39825000	Enhancers	Primary hematopoietic stem cells short term culture	blood
36	chr19:39824600-39825000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
37	chr19:39824600-39825000	Enhancers	Primary T helper cells PMA-I stimulated	--
38	chr19:39824600-39825000	Enhancers	Primary T helper cells fromperipheralblood	blood
39	chr19:39824600-39825000	Enhancers	Primary T killer memory cells from peripheral blood	blood
40	chr19:39824600-39825000	Enhancers	Fetal Thymus	thymus
41	chr19:39824600-39825800	Weak transcription	Spleen	Spleen
42	chr19:39824600-39825800	Flanking Active TSS	Dnd41	blood
43	chr19:39824800-39825000	Enhancers	Thymus	Thymus
44	chr19:39824800-39825200	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
45	chr19:39824800-39825800	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
46	chr19:39824800-39826000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr19:39824800-39826000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
48	chr19:39824800-39826200	Flanking Active TSS	Primary T cells fromperipheralblood	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links