Variant report

Variant	rs34677748
Chromosome Location	chr2:151940684-151940685
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 44 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs12989503	1.00[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs12990096	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12997492	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13009048	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13010851	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs13013474	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13014189	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs13026983	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13035255	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs16823204	1.00[AFR][1000 genomes]
rs16829612	1.00[AFR][1000 genomes]
rs16829613	1.00[AFR][1000 genomes]
rs16829671	1.00[AFR][1000 genomes]
rs16829674	1.00[AFR][1000 genomes]
rs16829680	1.00[AFR][1000 genomes]
rs16829682	1.00[AFR][1000 genomes]
rs16829715	1.00[AFR][1000 genomes]
rs16829723	1.00[AFR][1000 genomes]
rs16829752	1.00[AFR][1000 genomes]
rs34221803	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs34238735	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34557584	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34573599	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs34873254	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35052859	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35110064	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35451836	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs35555169	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35643506	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35691151	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35758708	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35868647	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs36104725	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61637122	1.00[AFR][1000 genomes]
rs71208329	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs71415117	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs71415118	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs71415119	1.00[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs71415121	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs71415122	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.86[EUR][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:27 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:151927400-151941000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr2:151937400-151941000	Weak transcription	H1 Cell Line	embryonic stem cell
3	chr2:151937800-151940800	Weak transcription	HUES6 Cell Line	embryonic stem cell
4	chr2:151938000-151941000	Weak transcription	HUES64 Cell Line	embryonic stem cell
5	chr2:151938200-151940800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
6	chr2:151939400-151941600	Enhancers	Primary T cells from cord blood	blood
7	chr2:151939600-151941400	Enhancers	ES-I3 Cell Line	embryonic stem cell
8	chr2:151939800-151941000	Enhancers	Brain Germinal Matrix	brain
9	chr2:151939800-151941400	Enhancers	Primary T helper cells PMA-I stimulated	--
10	chr2:151939800-151941600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr2:151939800-151941600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
12	chr2:151939800-151941600	Enhancers	Fetal Brain Male	brain
13	chr2:151940000-151940800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
14	chr2:151940000-151940800	Enhancers	Dnd41	blood
15	chr2:151940000-151942400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr2:151940000-151942800	Enhancers	Fetal Stomach	stomach
17	chr2:151940200-151941800	Enhancers	Adipose Nuclei	Adipose
18	chr2:151940400-151941400	Enhancers	HUES48 Cell Line	embryonic stem cell
19	chr2:151940400-151941600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr2:151940400-151942200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
21	chr2:151940400-151942200	Enhancers	Cortex derived primary cultured neurospheres	brain
22	chr2:151940400-151942400	Enhancers	Fetal Brain Female	brain
23	chr2:151940400-151942600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr2:151940400-151942600	Enhancers	NHDF-Ad	bronchial
25	chr2:151940600-151941200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
26	chr2:151940600-151941400	Enhancers	iPS-18 Cell Line	embryonic stem cell
27	chr2:151940600-151941400	Enhancers	iPS-20b Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links