Variant report

Variant	rs2952521
Chromosome Location	chr7:25603695-25603696
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 6 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs2952522	0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv606426	chr7:25254125-25621579	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
2	nsv1016813	chr7:25405859-26150509	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	108 gene(s)	inside rSNPs	diseases
3	nsv538803	chr7:25405859-26150509	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	108 gene(s)	inside rSNPs	diseases
4	nsv522815	chr7:25599858-25606120	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	n/a
5	nsv523322	chr7:25601480-25606120	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:25598600-25604400	Weak transcription	Fetal Kidney	kidney
2	chr7:25599800-25603800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr7:25600800-25605200	Enhancers	Brain Germinal Matrix	brain
4	chr7:25602400-25603800	Weak transcription	Psoas Muscle	Psoas
5	chr7:25602400-25604400	Weak transcription	Stomach Smooth Muscle	stomach
6	chr7:25602600-25604000	Weak transcription	Fetal Brain Female	brain
7	chr7:25602800-25604400	Weak transcription	Fetal Muscle Leg	muscle
8	chr7:25602800-25604400	Weak transcription	Rectal Smooth Muscle	rectum
9	chr7:25602800-25604400	Weak transcription	Skeletal Muscle Male	skeletal muscle
10	chr7:25603000-25604000	Weak transcription	Colon Smooth Muscle	Colon
11	chr7:25603000-25604000	Weak transcription	Fetal Lung	lung
12	chr7:25603000-25604000	Weak transcription	Fetal Stomach	stomach
13	chr7:25603000-25604400	Weak transcription	Skeletal Muscle Female	skeletal muscle
14	chr7:25603000-25604600	Weak transcription	Fetal Muscle Trunk	muscle
15	chr7:25603600-25605200	Weak transcription	Fetal Brain Male	brain

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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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