Variant report

Variant	rs56013073
Chromosome Location	chr17:38357705-38357706
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr17:38356192..38359891-chr17:38364494..38367617,3	K562	blood:
2	chr17:38356805..38359543-chr17:38443822..38445339,2	K562	blood:
3	chr17:38356687..38358293-chr17:38474492..38476337,2	MCF-7	breast:
4	chr17:38355152..38357799-chr17:38421791..38424703,2	K562	blood:

Variant related genes	Relation type
ENSG00000094804	Chromatin interaction
ENSG00000131759	Chromatin interaction

Extended variants
information (count: 49 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:47)

rs_ID	r²[population]
rs12103921	0.99[ASN][1000 genomes]
rs12944717	0.93[ASN][1000 genomes]
rs16965687	0.82[ASN][1000 genomes]
rs2280400	0.90[AMR][1000 genomes];0.88[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2314338	0.83[ASN][1000 genomes]
rs28537537	0.82[ASN][1000 genomes]
rs28663197	0.81[ASN][1000 genomes]
rs34223321	0.98[ASN][1000 genomes]
rs3744806	0.98[ASN][1000 genomes]
rs45567834	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs55772196	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs55835834	0.84[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs55991953	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs56029626	0.84[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs59018914	0.90[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs59861136	0.84[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs61024420	0.91[ASN][1000 genomes]
rs6503537	0.84[ASN][1000 genomes]
rs6503539	0.82[ASN][1000 genomes]
rs67597966	0.94[ASN][1000 genomes]
rs72836633	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs72836634	0.90[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs72836635	0.82[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs72836636	0.82[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs72836639	0.82[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs72836640	0.90[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs72836641	0.82[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs72836642	0.84[ASN][1000 genomes]
rs72836648	0.82[ASN][1000 genomes]
rs7359537	0.82[ASN][1000 genomes]
rs7405635	0.93[ASN][1000 genomes]
rs8073925	0.98[ASN][1000 genomes]
rs8082192	0.98[ASN][1000 genomes]
rs9891718	0.81[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs9892404	0.82[ASN][1000 genomes]
rs9892973	0.97[AFR][1000 genomes];0.88[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9893520	0.81[ASN][1000 genomes]
rs9895163	0.81[ASN][1000 genomes]
rs9897092	0.81[ASN][1000 genomes]
rs9904021	0.82[AMR][1000 genomes]
rs9906409	0.82[ASN][1000 genomes]
rs9907683	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9908034	0.86[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs9908354	0.98[ASN][1000 genomes]
rs9911840	0.82[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs9912082	0.82[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs9916782	0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv833444	chr17:38242823-38437280	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	62 gene(s)	inside rSNPs	diseases
2	nsv525796	chr17:38306365-38405037	Active TSS Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA miRNA target site	23 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:38348400-38358200	Weak transcription	Adipose Nuclei	Adipose
2	chr17:38348400-38358400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr17:38348600-38358200	Weak transcription	HUVEC	blood vessel
4	chr17:38348600-38358200	Weak transcription	Osteobl	bone
5	chr17:38350200-38359400	Weak transcription	Colonic Mucosa	Colon
6	chr17:38350400-38358000	Weak transcription	Liver	Liver
7	chr17:38350400-38358200	Weak transcription	Brain Hippocampus Middle	brain
8	chr17:38350400-38358200	Weak transcription	Rectal Smooth Muscle	rectum
9	chr17:38350400-38358600	Weak transcription	Rectal Mucosa Donor 29	rectum
10	chr17:38350800-38359400	Weak transcription	Rectal Mucosa Donor 31	rectum
11	chr17:38350800-38359400	Weak transcription	Sigmoid Colon	Sigmoid Colon
12	chr17:38354800-38358200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr17:38356000-38358000	Weak transcription	HepG2	liver
14	chr17:38357400-38358000	Enhancers	Placenta	Placenta
15	chr17:38357600-38358000	Weak transcription	A549	lung

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links