Variant report

Variant	rs13402549
Chromosome Location	chr2:151968615-151968616
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 7 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:3)

rs_ID	r²[population]
rs10184088	1.00[AFR][1000 genomes]
rs10469704	0.85[AFR][1000 genomes]
rs13419078	1.00[AFR][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	nsv525350	chr2:151711700-152044794	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv523849	chr2:151718133-152143524	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
3	esv3693426	chr2:151725792-152295862	Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription 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 miRNA target site	27 gene(s)	inside rSNPs	diseases
4	nsv1002140	chr2:151833257-152054910	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:151967600-151969000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr2:151967600-151969000	Enhancers	NHDF-Ad	bronchial
3	chr2:151967800-151968800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr2:151967800-151970000	Enhancers	ES-I3 Cell Line	embryonic stem cell
5	chr2:151967800-151970000	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr2:151968000-151968800	Enhancers	NHEK	skin
7	chr2:151968000-151970000	Enhancers	iPS-15b Cell Line	embryonic stem cell
8	chr2:151968200-151968800	Active TSS	iPS-20b Cell Line	embryonic stem cell
9	chr2:151968200-151969000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr2:151968400-151968800	Enhancers	H9 Cell Line	embryonic stem cell
11	chr2:151968400-151968800	Enhancers	Muscle Satellite Cultured Cells	--
12	chr2:151968400-151968800	Enhancers	Osteobl	bone
13	chr2:151968400-151969600	Enhancers	HUES6 Cell Line	embryonic stem cell
14	chr2:151968600-151969000	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
15	chr2:151968600-151969000	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
16	chr2:151968600-151969000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
17	chr2:151968600-151969400	Weak transcription	H1 Cell Line	embryonic stem cell

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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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