Variant report

Variant	rs10049439
Chromosome Location	chr3:139629108-139629109
allele	C/G
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]
rs1426052	0.92[ASN][1000 genomes]
rs1426053	0.92[ASN][1000 genomes]
rs1426054	0.92[ASN][1000 genomes]
rs727763	0.86[CHB][hapmap];0.93[JPT][hapmap];0.90[AFR][1000 genomes];0.87[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	nsv1003154	chr3:139060841-139788752	ZNF genes & repeats Flanking Active TSS Strong transcription Enhancers Weak transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
2	nsv536729	chr3:139060841-139788752	Active TSS Enhancers Strong transcription Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
3	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
4	nsv530058	chr3:139243971-139814419	Weak transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
5	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

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:139624800-139632400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr3:139625600-139632800	Weak transcription	Skeletal Muscle Female	skeletal muscle
3	chr3:139626800-139629200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr3:139628400-139629200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr3:139628400-139629600	Enhancers	HUES64 Cell Line	embryonic stem cell
6	chr3:139628400-139629800	Enhancers	iPS-20b Cell Line	embryonic stem cell
7	chr3:139628600-139629600	Enhancers	HUES6 Cell Line	embryonic stem cell
8	chr3:139628600-139629600	Enhancers	iPS-15b Cell Line	embryonic stem cell
9	chr3:139628600-139629600	Enhancers	iPS-18 Cell Line	embryonic stem cell
10	chr3:139628800-139629400	Enhancers	H9 Cell Line	embryonic stem cell
11	chr3:139628800-139629400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr3:139628800-139629600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
13	chr3:139628800-139629800	Enhancers	HUES48 Cell Line	embryonic stem cell
14	chr3:139629000-139631400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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