Variant report

Variant	rs7251924
Chromosome Location	chr19:19796620-19796621
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 40 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs10402516	0.83[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10405234	0.82[ASN][1000 genomes]
rs10423311	0.82[ASN][1000 genomes]
rs11667828	0.82[ASN][1000 genomes]
rs11670710	0.94[ASN][1000 genomes]
rs12974308	0.95[ASN][1000 genomes]
rs12976582	0.95[ASN][1000 genomes]
rs12980482	0.92[ASN][1000 genomes]
rs12981165	0.84[ASN][1000 genomes]
rs12982049	0.95[ASN][1000 genomes]
rs12982500	0.95[ASN][1000 genomes]
rs12983292	0.94[ASN][1000 genomes]
rs1433079	0.84[ASN][1000 genomes]
rs16996227	0.95[ASN][1000 genomes]
rs2288865	0.90[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs2288867	0.82[ASN][1000 genomes]
rs28472726	0.85[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs28635562	0.82[ASN][1000 genomes]
rs34558847	0.94[ASN][1000 genomes]
rs35035906	0.84[ASN][1000 genomes]
rs35445661	0.84[ASN][1000 genomes]
rs35449009	0.95[ASN][1000 genomes]
rs35792080	0.96[ASN][1000 genomes]
rs35801717	0.95[ASN][1000 genomes]
rs3752152	0.84[ASN][1000 genomes]
rs4808209	0.95[ASN][1000 genomes]
rs4808976	0.82[ASN][1000 genomes]
rs4808979	0.92[ASN][1000 genomes]
rs4808981	0.92[ASN][1000 genomes]
rs7247142	0.88[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs7249670	0.94[ASN][1000 genomes]
rs74181147	0.95[ASN][1000 genomes]
rs74181148	0.95[ASN][1000 genomes]
rs74181149	0.95[ASN][1000 genomes]
rs74181150	0.95[ASN][1000 genomes]
rs74181151	0.95[ASN][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	esv1828240	chr19:19591146-19900900	Weak transcription Enhancers Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Active TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	55 gene(s)	inside rSNPs	diseases
2	nsv1063273	chr19:19591146-20061367	ZNF genes & repeats Genic enhancers Active TSS Flanking Active TSS Weak transcription Enhancers Strong transcription 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 target site	67 gene(s)	inside rSNPs	diseases
3	esv3330851	chr19:19755507-19852881	Strong transcription Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats 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	23 gene(s)	inside rSNPs	diseases
4	nsv519533	chr19:19789528-19831544	ZNF genes & repeats Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:19782000-19798200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr19:19790800-19797000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr19:19791000-19798400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr19:19791000-19799200	Weak transcription	Fetal Kidney	kidney
5	chr19:19791000-19802000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
6	chr19:19791200-19816800	Weak transcription	Right Ventricle	heart
7	chr19:19791600-19810000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr19:19792000-19797200	Weak transcription	Brain Hippocampus Middle	brain
9	chr19:19792400-19798000	Weak transcription	Left Ventricle	heart
10	chr19:19792400-19810000	Weak transcription	Ovary	ovary
11	chr19:19792600-19798000	Weak transcription	H9 Cell Line	embryonic stem cell
12	chr19:19793800-19799000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
13	chr19:19795000-19798000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr19:19795400-19811200	Weak transcription	Dnd41	blood
15	chr19:19796000-19797200	ZNF genes & repeats	Thymus	Thymus
16	chr19:19796600-19797000	Weak transcription	Primary T helper naive cells from peripheral blood	blood

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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