Variant report

Variant	rs13110070
Chromosome Location	chr4:106582280-106582281
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:106575884..106578355-chr4:106580539..106582862,2	K562	blood:

Extended variants
information (count: 51 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10019217	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs10030620	0.95[ASN][1000 genomes]
rs10049527	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10516522	0.86[CHB][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs1157775	0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11930244	0.86[CHB][hapmap];1.00[JPT][hapmap]
rs11930965	1.00[CEU][hapmap];0.86[CHB][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs11942577	0.86[CHB][hapmap]
rs12504088	0.86[CHB][hapmap];1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs12511885	0.81[ASN][1000 genomes]
rs12512339	0.95[ASN][1000 genomes]
rs13145251	0.81[AFR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs17036093	1.00[CEU][hapmap];0.82[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs17036097	0.86[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs17036102	0.86[CHB][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs17036254	0.86[CHB][hapmap];1.00[JPT][hapmap]
rs2193852	0.86[CHB][hapmap];1.00[JPT][hapmap]
rs2193854	0.86[CHB][hapmap];1.00[JPT][hapmap]
rs28370551	0.85[ASN][1000 genomes]
rs28391170	0.85[ASN][1000 genomes]
rs28450989	0.85[ASN][1000 genomes]
rs28559909	0.88[ASN][1000 genomes]
rs28698939	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3796926	0.85[ASN][1000 genomes]
rs4235415	0.88[ASN][1000 genomes]
rs4490460	0.85[ASN][1000 genomes]
rs4698950	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4698951	0.86[CHB][hapmap];1.00[JPT][hapmap]
rs4699192	1.00[ASN][1000 genomes]
rs4699193	0.82[CHB][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs4699194	0.85[CHB][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs4699195	0.85[ASN][1000 genomes]
rs4699197	0.86[CHB][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs4699198	0.86[CHB][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs4699199	0.86[CHB][hapmap];1.00[JPT][hapmap]
rs56849622	0.87[AFR][1000 genomes];0.94[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs58388061	0.81[ASN][1000 genomes]
rs58914657	0.81[AFR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs60774107	0.83[ASN][1000 genomes]
rs6817029	1.00[CEU][hapmap];0.86[CHB][hapmap];1.00[JPT][hapmap];0.81[YRI][hapmap];0.81[AFR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6820671	0.86[CHB][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs6825379	0.86[CHB][hapmap];1.00[JPT][hapmap]
rs7658055	0.86[CHB][hapmap];1.00[JPT][hapmap]
rs7659526	0.86[CHB][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs7696836	1.00[ASN][1000 genomes]
rs7697619	0.81[ASN][1000 genomes]
rs989775	0.91[AFR][1000 genomes];0.80[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[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	nsv879699	chr4:106212562-106698892	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
2	esv3467298	chr4:106577722-106583287	Weak transcription Strong transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
3	esv3467299	chr4:106577722-106583287	Weak transcription Enhancers Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
4	esv14749	chr4:106577867-106583120	Enhancers Weak transcription Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:106559400-106602800	Weak transcription	Duodenum Mucosa	Duodenum
2	chr4:106569800-106600400	Weak transcription	Rectal Mucosa Donor 29	rectum
3	chr4:106574400-106585400	Weak transcription	Rectal Smooth Muscle	rectum
4	chr4:106578200-106588200	Weak transcription	Pancreas	Pancrea
5	chr4:106578600-106607000	Weak transcription	Small Intestine	intestine
6	chr4:106580400-106603400	Weak transcription	Sigmoid Colon	Sigmoid Colon
7	chr4:106580400-106613200	Weak transcription	Fetal Intestine Small	intestine
8	chr4:106580600-106588600	Weak transcription	Rectal Mucosa Donor 31	rectum
9	chr4:106580600-106593800	Weak transcription	Gastric	stomach
10	chr4:106581400-106588200	Weak transcription	Fetal Intestine Large	intestine

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