Variant report

Variant	rs7521560
Chromosome Location	chr1:180573327-180573328
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs10914059	1.00[AMR][1000 genomes]
rs10914060	1.00[AMR][1000 genomes]
rs12064567	1.00[AMR][1000 genomes]
rs12072401	1.00[AMR][1000 genomes]
rs12073365	1.00[AMR][1000 genomes]
rs12079458	1.00[AMR][1000 genomes]
rs12084365	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1003359	chr1:180300936-180727561	Enhancers Strong transcription Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	48 gene(s)	inside rSNPs	diseases
2	nsv949311	chr1:180438895-180692815	ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	46 gene(s)	inside rSNPs	diseases
3	nsv872578	chr1:180510771-180842344	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:180564800-180579600	Weak transcription	Right Atrium	heart
2	chr1:180568200-180579800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr1:180569800-180575400	Weak transcription	Pancreatic Islets	Pancreatic Islet
4	chr1:180571000-180573400	Enhancers	Left Ventricle	heart
5	chr1:180572200-180573400	Enhancers	Fetal Heart	heart
6	chr1:180572400-180573400	Enhancers	Pancreas	Pancrea
7	chr1:180572400-180573400	Enhancers	Right Ventricle	heart
8	chr1:180572600-180573800	Enhancers	Breast Myoepithelial Primary Cells	Breast
9	chr1:180572800-180573400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr1:180572800-180573400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr1:180572800-180573400	Enhancers	Fetal Intestine Large	intestine
12	chr1:180572800-180573400	Enhancers	HMEC	breast
13	chr1:180573000-180573400	Enhancers	NHEK	skin
14	chr1:180573000-180573800	Enhancers	K562	blood
15	chr1:180573200-180575000	Weak transcription	Fetal Intestine Small	intestine

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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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