Variant report

Variant	rs35802750
Chromosome Location	chr7:117146391-117146392
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 74 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:71)

rs_ID	r²[population]
rs10487370	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17132544	0.83[AMR][1000 genomes]
rs17132545	1.00[AMR][1000 genomes]
rs17132549	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17139750	0.83[AMR][1000 genomes]
rs17139754	0.83[AMR][1000 genomes]
rs17139756	0.83[AMR][1000 genomes]
rs17139757	0.83[AMR][1000 genomes]
rs17139762	0.83[AMR][1000 genomes]
rs17139765	0.83[AMR][1000 genomes]
rs17139783	0.83[AMR][1000 genomes]
rs17139810	1.00[AMR][1000 genomes]
rs17139813	1.00[AMR][1000 genomes]
rs17139819	1.00[AMR][1000 genomes]
rs17139824	1.00[AMR][1000 genomes]
rs17139866	1.00[AMR][1000 genomes]
rs17139874	1.00[AMR][1000 genomes]
rs17139887	1.00[AMR][1000 genomes]
rs17139929	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17139984	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17139994	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17140013	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17140095	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17140169	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs34009249	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs34034688	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs34123455	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs34239891	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs34340257	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs34427586	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs34436445	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs34463627	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs34484276	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs34530771	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs34558486	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs34599010	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs34710125	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs34717021	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs34808223	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs34870970	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs35011694	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs35026177	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs35045003	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs35113266	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs35114123	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs35197837	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs35278352	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs35314519	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs35321167	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs35376221	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs35396010	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs35435021	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs35490261	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs35493996	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs35508774	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs35666329	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs35714998	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs35753200	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs35778610	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs35821559	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs35827235	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs35855138	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs36143091	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6944750	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6953663	0.83[AMR][1000 genomes]
rs6971294	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6972328	0.83[AMR][1000 genomes]
rs6978006	0.83[AMR][1000 genomes]
rs7789582	0.83[AMR][1000 genomes]
rs7811667	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs916726	0.83[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv889076	chr7:117064625-117147547	Active TSS Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	nsv889077	chr7:117129404-117238379	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv889078	chr7:117135025-117246315	Strong transcription Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:117126800-117151200	Weak transcription	Pancreas	Pancrea
2	chr7:117142400-117147000	Weak transcription	Rectal Mucosa Donor 29	rectum
3	chr7:117143200-117147000	Weak transcription	Rectal Mucosa Donor 31	rectum
4	chr7:117143200-117152600	Weak transcription	Sigmoid Colon	Sigmoid Colon
5	chr7:117144600-117147800	Strong transcription	Duodenum Mucosa	Duodenum
6	chr7:117145200-117146400	Strong transcription	Fetal Intestine Large	intestine
7	chr7:117145600-117146600	Strong transcription	Fetal Intestine Small	intestine

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links