Variant report

Variant	rs1654265
Chromosome Location	chr19:20214528-20214529
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 41 )
Associated
traits (count: 3 )

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs1097511	0.83[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1230351	0.85[ASN][1000 genomes]
rs1230352	0.85[ASN][1000 genomes]
rs12459266	0.80[EUR][1000 genomes]
rs1474460	0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1474461	0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1621688	0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1654266	0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1654267	0.81[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1654268	0.81[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1654270	0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1654271	0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1654300	0.85[ASN][1000 genomes]
rs1725924	0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1725925	0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1725926	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1725927	0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1725928	0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1725929	0.81[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs836909	0.85[AFR][1000 genomes];0.89[EUR][1000 genomes]
rs865075	0.89[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:20 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv519535	chr19:19871250-20595412	Active TSS Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers Flanking Active TSS 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	56 gene(s)	inside rSNPs	diseases
2	esv3319016	chr19:19917475-20819154	Weak transcription ZNF genes & repeats Bivalent Enhancer Enhancers Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	56 gene(s)	inside rSNPs	diseases
3	esv3319017	chr19:19917475-20819154	ZNF genes & repeats Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	56 gene(s)	inside rSNPs	diseases
4	nsv1061846	chr19:19946927-20595412	Flanking Active TSS Active TSS Enhancers Weak transcription Strong transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	47 gene(s)	inside rSNPs	diseases
5	esv3390957	chr19:19965887-20819154	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	53 gene(s)	inside rSNPs	diseases
6	nsv869122	chr19:19969851-20595412	ZNF genes & repeats Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	47 gene(s)	inside rSNPs	diseases
7	nsv1059158	chr19:19973489-20576161	Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Enhancers Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	43 gene(s)	inside rSNPs	diseases
8	nsv870354	chr19:20043821-20576175	ZNF genes & repeats Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	34 gene(s)	inside rSNPs	diseases
9	nsv1066004	chr19:20053658-20592867	ZNF genes & repeats Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	35 gene(s)	inside rSNPs	diseases
10	nsv543932	chr19:20053658-20592867	Active TSS Weak transcription Strong transcription Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	35 gene(s)	inside rSNPs	diseases
11	nsv1066564	chr19:20056348-20595412	Weak transcription Active TSS ZNF genes & repeats Enhancers Strong transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	36 gene(s)	inside rSNPs	diseases
12	nsv1066375	chr19:20061084-20574512	Strong transcription ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	31 gene(s)	inside rSNPs	diseases
13	nsv543934	chr19:20061084-20574512	Strong transcription Weak transcription Flanking Active TSS ZNF genes & repeats Enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	31 gene(s)	inside rSNPs	diseases
14	nsv1057309	chr19:20072886-20595412	Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	34 gene(s)	inside rSNPs	diseases
15	nsv578801	chr19:20084681-20595412	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	33 gene(s)	inside rSNPs	diseases
16	nsv1055694	chr19:20088866-20595412	Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS Strong transcription Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	33 gene(s)	inside rSNPs	diseases
17	nsv578802	chr19:20091702-20595412	ZNF genes & repeats Flanking Active TSS Strong transcription Weak transcription Active TSS Genic enhancers Enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	33 gene(s)	inside rSNPs	diseases
18	nsv1064400	chr19:20101052-20595412	Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	33 gene(s)	inside rSNPs	diseases
19	nsv911325	chr19:20151257-21071548	ZNF genes & repeats Active TSS Weak transcription Flanking Active TSS Genic enhancers Strong transcription 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	49 gene(s)	inside rSNPs	diseases
20	nsv1066014	chr19:20165112-20595412	Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	27 gene(s)	inside rSNPs	diseases

mRNA abundance (count:3)

SNP	Gene	Cis/trans	Tissue	Source
rs1654265	ZNF682	cis	Muscle Skeletal	GTEx
rs1654265	ZNF506	Cis_1M	lymphoblastoid	RTeQTL
rs1654265	ZNF682	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:42 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:20207600-20216800	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
2	chr19:20207600-20240400	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr19:20207600-20240600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr19:20207600-20241200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr19:20207800-20216800	ZNF genes & repeats	Primary hematopoietic stem cells	blood
6	chr19:20207800-20218400	ZNF genes & repeats	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr19:20208000-20222400	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr19:20209400-20221800	Weak transcription	Rectal Smooth Muscle	rectum
9	chr19:20209400-20239000	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
10	chr19:20210000-20218000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
11	chr19:20211400-20238800	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
12	chr19:20212200-20217600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr19:20212400-20217200	Weak transcription	Fetal Stomach	stomach
14	chr19:20213200-20217600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
15	chr19:20213400-20215400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr19:20213400-20215400	Weak transcription	H9 Cell Line	embryonic stem cell
17	chr19:20213400-20215400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr19:20213400-20222000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr19:20213600-20216000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
20	chr19:20213600-20216000	Weak transcription	Fetal Kidney	kidney
21	chr19:20213600-20216200	Weak transcription	Rectal Mucosa Donor 29	rectum
22	chr19:20213600-20217800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
23	chr19:20213600-20217800	Weak transcription	Rectal Mucosa Donor 31	rectum
24	chr19:20213800-20215400	Weak transcription	H1 Cell Line	embryonic stem cell
25	chr19:20214000-20215000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr19:20214000-20216200	Weak transcription	Cortex derived primary cultured neurospheres	brain
27	chr19:20214000-20217800	Weak transcription	Placenta	Placenta
28	chr19:20214000-20227200	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr19:20214200-20215800	Weak transcription	Fetal Lung	lung
30	chr19:20214200-20217200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
31	chr19:20214200-20217400	Weak transcription	Ovary	ovary
32	chr19:20214200-20217800	Weak transcription	Fetal Heart	heart
33	chr19:20214200-20218000	Strong transcription	HUES64 Cell Line	embryonic stem cell
34	chr19:20214200-20220600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
35	chr19:20214400-20214800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr19:20214400-20215000	Weak transcription	HUES6 Cell Line	embryonic stem cell
37	chr19:20214400-20215200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
38	chr19:20214400-20216200	Strong transcription	HUES48 Cell Line	embryonic stem cell
39	chr19:20214400-20217200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr19:20214400-20217600	Weak transcription	Aorta	Aorta
41	chr19:20214400-20217800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
42	chr19:20214400-20218000	Weak transcription	Fetal Thymus	thymus

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