Variant report

Variant	rs13061767
Chromosome Location	chr3:139814626-139814627
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:4)

rs_ID	r²[population]
rs12637089	1.00[ASW][hapmap]
rs1479869	1.00[CHD][hapmap]
rs4683485	1.00[CHD][hapmap]
rs4683816	1.00[CHB][hapmap];1.00[CHD][hapmap]

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	nsv916193	chr3:139187767-139821526	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
2	nsv998423	chr3:139526446-139947336	Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv829738	chr3:139670836-139851945	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
4	nsv877545	chr3:139738645-139821310	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv829739	chr3:139797496-140002685	Enhancers Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Strong transcription Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:139812600-139819600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr3:139812600-139820400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr3:139813200-139817600	Weak transcription	Fetal Brain Male	brain
4	chr3:139813200-139817600	Weak transcription	Fetal Brain Female	brain
5	chr3:139813600-139814800	Enhancers	Brain Germinal Matrix	brain
6	chr3:139813600-139816600	Weak transcription	HSMMtube	muscle
7	chr3:139813800-139814800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr3:139813800-139814800	Weak transcription	Fetal Muscle Leg	muscle
9	chr3:139813800-139832600	Weak transcription	Ovary	ovary
10	chr3:139814400-139815800	Enhancers	Brain Angular Gyrus	brain
11	chr3:139814600-139815000	Enhancers	Psoas Muscle	Psoas
12	chr3:139814600-139815800	Enhancers	Brain Cingulate Gyrus	brain
13	chr3:139814600-139815800	Enhancers	Brain Hippocampus Middle	brain
14	chr3:139814600-139815800	Enhancers	Brain Substantia Nigra	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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