Variant report

Variant	rs10265930
Chromosome Location	chr7:50627449-50627450
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:50625823..50628004-chr7:50631003..50633702,2	K562	blood:
2	chr7:50625436..50627457-chr7:50643503..50646245,2	K562	blood:

Variant related genes	Relation type
ENSG00000132437	Chromatin interaction

Extended variants
information (count: 54 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:49)

rs_ID	r²[population]
rs10239830	0.88[ASN][1000 genomes]
rs10249420	1.00[CEU][hapmap];0.85[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10250513	0.91[JPT][hapmap]
rs10267323	0.85[ASN][1000 genomes]
rs10271341	0.85[ASN][1000 genomes]
rs10276473	0.88[ASN][1000 genomes]
rs10277662	0.84[ASN][1000 genomes]
rs10899748	0.80[EUR][1000 genomes]
rs11575320	0.88[ASN][1000 genomes]
rs11976778	0.81[EUR][1000 genomes]
rs12666409	0.95[CEU][hapmap];0.92[EUR][1000 genomes]
rs12671474	0.85[ASN][1000 genomes]
rs12671598	0.82[EUR][1000 genomes]
rs12673638	0.83[EUR][1000 genomes]
rs1451373	0.95[JPT][hapmap]
rs1451374	0.95[JPT][hapmap]
rs1451375	0.95[JPT][hapmap]
rs1470747	1.00[CEU][hapmap];0.86[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1966839	1.00[JPT][hapmap]
rs2044859	0.85[ASN][1000 genomes]
rs2329340	0.95[JPT][hapmap]
rs2329342	0.95[JPT][hapmap]
rs2329346	0.82[EUR][1000 genomes]
rs2329371	0.88[ASN][1000 genomes]
rs28415418	0.86[EUR][1000 genomes]
rs3735273	0.85[ASN][1000 genomes]
rs3779074	0.85[ASN][1000 genomes]
rs3779078	0.88[ASN][1000 genomes]
rs3807552	0.88[ASN][1000 genomes]
rs3807555	0.81[CHB][hapmap];0.88[ASN][1000 genomes]
rs3807556	0.88[ASN][1000 genomes]
rs4452748	0.95[JPT][hapmap]
rs56105337	0.83[EUR][1000 genomes]
rs56661863	0.82[EUR][1000 genomes]
rs66792686	0.89[EUR][1000 genomes]
rs68011952	0.90[EUR][1000 genomes]
rs6949897	0.91[JPT][hapmap]
rs6950777	0.85[ASN][1000 genomes]
rs7779110	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7790919	0.82[EUR][1000 genomes]
rs7803440	1.00[CEU][hapmap];0.85[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7803788	1.00[CEU][hapmap];0.85[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7803903	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7807335	0.95[CEU][hapmap];0.95[EUR][1000 genomes]
rs896309	0.82[JPT][hapmap]
rs921450	0.95[JPT][hapmap]
rs921451	0.95[JPT][hapmap]
rs978784	0.82[CEU][hapmap];0.82[EUR][1000 genomes]
rs9942686	0.85[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	nsv1016665	chr7:50452552-51404524	Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
2	nsv1015758	chr7:50565404-50768153	Flanking Active TSS Genic enhancers Strong transcription Enhancers Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
3	nsv1023228	chr7:50573214-50777634	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Genic enhancers 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	6 gene(s)	inside rSNPs	diseases
4	nsv1032882	chr7:50611138-50775257	Genic enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription Enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
5	nsv538834	chr7:50611138-50775257	Enhancers Weak transcription Active TSS Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs10265930	FIGNL1	cis	lung	GTEx

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:50601600-50631400	Weak transcription	Rectal Mucosa Donor 31	rectum
2	chr7:50611000-50631800	Weak transcription	Colonic Mucosa	Colon
3	chr7:50619400-50628200	Enhancers	HepG2	liver
4	chr7:50619600-50627800	Enhancers	Fetal Intestine Large	intestine
5	chr7:50620800-50635600	Weak transcription	Lung	lung
6	chr7:50624600-50631800	Weak transcription	Rectal Mucosa Donor 29	rectum
7	chr7:50625000-50628600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr7:50625000-50628600	Weak transcription	Small Intestine	intestine
9	chr7:50625200-50628400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr7:50625400-50628400	Enhancers	Duodenum Mucosa	Duodenum
11	chr7:50625600-50628400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr7:50625600-50628600	Weak transcription	Brain Germinal Matrix	brain
13	chr7:50625800-50627600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr7:50626000-50628000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr7:50626400-50628200	Genic enhancers	Fetal Intestine Small	intestine
16	chr7:50626600-50627800	Weak transcription	Liver	Liver
17	chr7:50626600-50628200	Weak transcription	Pancreatic Islets	Pancreatic Islet
18	chr7:50626600-50628400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr7:50626600-50629600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr7:50626800-50627800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
21	chr7:50626800-50627800	Weak transcription	Ovary	ovary
22	chr7:50626800-50631800	Weak transcription	Gastric	stomach
23	chr7:50626800-50632000	Weak transcription	Stomach Mucosa	stomach
24	chr7:50627000-50628200	Weak transcription	Pancreas	Pancrea
25	chr7:50627000-50628800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links