Variant report

Variant	rs13428236
Chromosome Location	chr2:54629326-54629327
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr2:54569839..54572791-chr2:54629016..54630836,2	K562	blood:
2	chr2:54628611..54630630-chr2:54636433..54637977,2	K562	blood:
3	chr2:54629237..54631678-chr2:54647068..54649301,2	K562	blood:
4	chr2:54629042..54631678-chr2:54646319..54649301,2	K562	blood:

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs10084337	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11892709	0.84[EUR][1000 genomes]
rs17045857	0.80[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs17045859	0.84[EUR][1000 genomes]
rs35821147	0.80[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3936082	0.87[GIH][hapmap]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1003205	chr2:54220049-54700843	Weak transcription Active TSS Enhancers Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
2	esv2762639	chr2:54220049-54700855	Flanking Bivalent TSS/Enh Weak transcription Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
3	nsv1011790	chr2:54220049-54714553	Flanking Active TSS ZNF genes & repeats Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
4	nsv1002891	chr2:54227005-54682169	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
5	nsv535722	chr2:54227005-54682169	Strong transcription Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
6	nsv1011690	chr2:54255361-54700843	Flanking Active TSS Weak transcription Enhancers Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
7	nsv532512	chr2:54453210-54630755	Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:25 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:54615400-54643000	Weak transcription	Right Ventricle	heart
2	chr2:54618600-54647200	Weak transcription	Left Ventricle	heart
3	chr2:54621600-54629600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr2:54623600-54643000	Weak transcription	Lung	lung
5	chr2:54626000-54630600	Weak transcription	Brain Substantia Nigra	brain
6	chr2:54627800-54629400	Enhancers	Skeletal Muscle Male	skeletal muscle
7	chr2:54627800-54630800	Enhancers	Ovary	ovary
8	chr2:54628000-54630200	Enhancers	Fetal Stomach	stomach
9	chr2:54628000-54631200	Enhancers	NHLF	lung
10	chr2:54628200-54630800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
11	chr2:54628400-54629800	Enhancers	Right Atrium	heart
12	chr2:54628400-54630000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr2:54628400-54630400	Enhancers	Adipose Nuclei	Adipose
14	chr2:54628400-54630600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr2:54628400-54630600	Enhancers	Fetal Lung	lung
16	chr2:54629000-54629600	Bivalent Enhancer	HepG2	liver
17	chr2:54629000-54630000	Enhancers	HUVEC	blood vessel
18	chr2:54629000-54631200	Enhancers	NHDF-Ad	bronchial
19	chr2:54629200-54629400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr2:54629200-54629800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr2:54629200-54630000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
22	chr2:54629200-54630000	Enhancers	NH-A	brain
23	chr2:54629200-54630400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr2:54629200-54630600	Enhancers	Fetal Muscle Leg	muscle
25	chr2:54629200-54630600	Enhancers	Osteobl	bone

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