Variant report

Variant	rs6797745
Chromosome Location	chr3:142345203-142345204
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr3:142340189..142342403-chr3:142344376..142347027,3	K562	blood:
2	chr3:142343680..142345636-chr3:142364474..142366774,2	K562	blood:
3	chr3:142344136..142346877-chr3:142364474..142366213,2	K562	blood:

Variant related genes	Relation type
ENSG00000120756	Chromatin interaction

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs13316756	0.83[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2140433	1.00[CEU][hapmap];0.85[CHB][hapmap];1.00[EUR][1000 genomes]
rs2140434	0.92[CEU][hapmap];0.85[CHB][hapmap];0.81[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2177397	1.00[CEU][hapmap];0.85[CHB][hapmap];0.86[YRI][hapmap];0.82[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28378300	1.00[EUR][1000 genomes]
rs28647471	1.00[EUR][1000 genomes]
rs28709617	1.00[EUR][1000 genomes]
rs3821647	0.85[CEU][hapmap]
rs4259003	0.85[CEU][hapmap]
rs4398471	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs4582093	0.85[CHB][hapmap];0.84[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56383228	1.00[EUR][1000 genomes]
rs58910647	0.81[AFR][1000 genomes];0.91[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs6440095	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs6440096	1.00[CEU][hapmap];0.86[YRI][hapmap];0.80[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6440097	1.00[EUR][1000 genomes]
rs6773213	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.97[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6778383	1.00[CEU][hapmap]
rs6797237	0.85[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6800573	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];0.97[AFR][1000 genomes];0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73228788	0.81[ASN][1000 genomes]
rs7622648	0.91[CEU][hapmap];1.00[CHB][hapmap];0.89[JPT][hapmap];0.97[YRI][hapmap];0.97[AFR][1000 genomes];0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7633021	0.98[EUR][1000 genomes]
rs7638338	1.00[CEU][hapmap];0.86[YRI][hapmap];0.81[AFR][1000 genomes];0.87[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7647212	1.00[CEU][hapmap];0.98[EUR][1000 genomes]
rs7647497	1.00[CEU][hapmap];0.97[EUR][1000 genomes]
rs9813377	0.97[EUR][1000 genomes]
rs9816128	0.98[EUR][1000 genomes]
rs9816275	0.96[EUR][1000 genomes]
rs9826463	0.99[EUR][1000 genomes]
rs9847445	1.00[CEU][hapmap];0.85[CHB][hapmap];0.84[AFR][1000 genomes];0.91[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs9851381	0.85[CEU][hapmap]
rs9857567	1.00[CEU][hapmap];0.84[YRI][hapmap];0.84[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9862686	1.00[CEU][hapmap];0.85[CHB][hapmap];0.86[YRI][hapmap];0.84[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9868309	1.00[CEU][hapmap];1.00[EUR][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	nsv877560	chr3:142132749-142362179	Strong transcription ZNF genes & repeats Weak transcription Active TSS Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
2	nsv932989	chr3:142204208-142423305	Weak transcription Strong transcription Active TSS Flanking Active TSS Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:142334000-142357200	Weak transcription	Pancreas	Pancrea
2	chr3:142337800-142348400	Weak transcription	Gastric	stomach
3	chr3:142340200-142345600	Weak transcription	A549	lung
4	chr3:142341400-142346200	Enhancers	Pancreatic Islets	Pancreatic Islet
5	chr3:142342800-142345800	Active TSS	Duodenum Mucosa	Duodenum
6	chr3:142343400-142348600	Weak transcription	Sigmoid Colon	Sigmoid Colon
7	chr3:142343400-142366400	Weak transcription	Fetal Intestine Small	intestine
8	chr3:142344800-142346600	Enhancers	K562	blood
9	chr3:142345000-142346000	Enhancers	Stomach Mucosa	stomach
10	chr3:142345200-142345600	Active TSS	Rectal Mucosa Donor 31	rectum
11	chr3:142345200-142353800	Weak transcription	Rectal Mucosa Donor 29	rectum

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