Variant report

Variant	rs73929052
Chromosome Location	chr2:38781957-38781958
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:38781085..38783046-chr2:38956281..38958070,2	K562	blood:
2	chr2:38780413..38785333-chr2:38976910..38979938,6	K562	blood:
3	chr2:38773369..38778839-chr2:38780028..38785171,8	K562	blood:
4	chr2:38780591..38782565-chr2:38977127..38979529,2	MCF-7	breast:
5	chr2:38781681..38785973-chr2:38793517..38796311,3	K562	blood:
6	chr2:38781921..38784416-chr2:38785346..38789078,4	K562	blood:
7	chr2:38780198..38783785-chr2:38971693..38974497,3	K562	blood:
8	chr2:38778308..38782276-chr2:38966801..38969709,4	K562	blood:

No data

Variant related genes	Relation type
ENSG00000152147	Chromatin interaction
ENSG00000115875	Chromatin interaction

Extended variants
information (count: 34 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs12614876	1.00[EUR][1000 genomes]
rs12616367	0.83[EUR][1000 genomes]
rs12619629	0.83[EUR][1000 genomes]
rs12621565	0.83[EUR][1000 genomes]
rs12621788	1.00[EUR][1000 genomes]
rs1543881	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17576044	0.97[AFR][1000 genomes];0.91[AMR][1000 genomes];0.83[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs17603782	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34133986	0.83[EUR][1000 genomes]
rs36024292	0.83[EUR][1000 genomes]
rs3765001	0.83[EUR][1000 genomes]
rs55785223	0.87[AFR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs55833813	0.87[AFR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs56956410	1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs58720388	0.83[EUR][1000 genomes]
rs59065420	0.83[EUR][1000 genomes]
rs6710613	0.81[AMR][1000 genomes]
rs6748685	0.81[AMR][1000 genomes]
rs6754893	1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs72895897	1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs72905831	0.87[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs72905839	0.87[AFR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72907906	0.81[AMR][1000 genomes]
rs72907918	0.81[AMR][1000 genomes]
rs72907929	0.81[AMR][1000 genomes]
rs73929040	1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7579783	0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7580657	0.91[AMR][1000 genomes]
rs7584862	0.98[AFR][1000 genomes];0.91[AMR][1000 genomes];0.83[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7606515	0.83[EUR][1000 genomes];0.91[ASN][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	nsv916059	chr2:38332341-39119398	Weak transcription Flanking Active TSS Enhancers Genic enhancers Strong transcription Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	143 gene(s)	inside rSNPs	diseases
2	nsv9646	chr2:38358311-39082189	Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	141 gene(s)	inside rSNPs	diseases
3	nsv873881	chr2:38745624-38877636	Enhancers Flanking Active TSS Active TSS Strong transcription Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
4	esv1796304	chr2:38766721-38790750	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:97 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:38763600-38809600	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr2:38768200-38812800	Weak transcription	Psoas Muscle	Psoas
3	chr2:38768400-38787800	Weak transcription	Rectal Mucosa Donor 29	rectum
4	chr2:38768400-38788000	Weak transcription	Fetal Muscle Trunk	muscle
5	chr2:38768400-38791600	Weak transcription	Sigmoid Colon	Sigmoid Colon
6	chr2:38769000-38793200	Weak transcription	Rectal Smooth Muscle	rectum
7	chr2:38769200-38782800	Weak transcription	Stomach Smooth Muscle	stomach
8	chr2:38769200-38787800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
9	chr2:38769200-38788400	Weak transcription	Cortex derived primary cultured neurospheres	brain
10	chr2:38770000-38788600	Weak transcription	Colon Smooth Muscle	Colon
11	chr2:38770400-38786600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr2:38770400-38787200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr2:38770400-38787200	Weak transcription	Duodenum Mucosa	Duodenum
14	chr2:38770400-38787200	Weak transcription	Fetal Intestine Large	intestine
15	chr2:38770400-38787200	Weak transcription	NHLF	lung
16	chr2:38770400-38787200	Weak transcription	Osteobl	bone
17	chr2:38770400-38787400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr2:38770400-38787400	Weak transcription	Duodenum Smooth Muscle	Duodenum
19	chr2:38770400-38791000	Weak transcription	Muscle Satellite Cultured Cells	--
20	chr2:38770400-38794600	Weak transcription	H9 Cell Line	embryonic stem cell
21	chr2:38770600-38785800	Weak transcription	NH-A	brain
22	chr2:38770600-38787400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
23	chr2:38770600-38794800	Weak transcription	NHEK	skin
24	chr2:38770800-38794400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr2:38771000-38786200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
26	chr2:38771200-38787200	Weak transcription	H1 Cell Line	embryonic stem cell
27	chr2:38771200-38787400	Weak transcription	HUVEC	blood vessel
28	chr2:38772800-38787400	Weak transcription	HepG2	liver
29	chr2:38775200-38783600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr2:38775800-38821800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr2:38776400-38787400	Weak transcription	Fetal Kidney	kidney
32	chr2:38776600-38787200	Weak transcription	Brain Inferior Temporal Lobe	brain
33	chr2:38776600-38787400	Weak transcription	Placenta	Placenta
34	chr2:38776600-38788000	Weak transcription	Brain Germinal Matrix	brain
35	chr2:38776600-38791000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
36	chr2:38776800-38782000	Weak transcription	Fetal Brain Female	brain
37	chr2:38776800-38785200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
38	chr2:38776800-38787200	Weak transcription	HUES64 Cell Line	embryonic stem cell
39	chr2:38776800-38787200	Weak transcription	Fetal Lung	lung
40	chr2:38776800-38787400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
41	chr2:38776800-38788800	Weak transcription	Fetal Brain Male	brain
42	chr2:38777000-38787200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
43	chr2:38777000-38794600	Weak transcription	Brain Anterior Caudate	brain
44	chr2:38777000-38807200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
45	chr2:38777200-38787200	Weak transcription	HUES48 Cell Line	embryonic stem cell
46	chr2:38777200-38794200	Weak transcription	Ovary	ovary
47	chr2:38777400-38783000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
48	chr2:38777400-38792600	Weak transcription	Thymus	Thymus
49	chr2:38777600-38787200	Weak transcription	A549	lung
50	chr2:38777600-38787400	Weak transcription	HMEC	breast

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