Variant report

Variant	rs1972777
Chromosome Location	chr5:145110383-145110384
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 67 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:63)

rs_ID	r²[population]
rs10035959	0.83[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10035998	0.83[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10038598	0.90[AFR][1000 genomes];0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10041421	0.89[AFR][1000 genomes];0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1019922	0.96[AFR][1000 genomes];0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1019923	0.97[AFR][1000 genomes];0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1019925	0.90[AFR][1000 genomes];0.81[AMR][1000 genomes];0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1019926	0.88[AFR][1000 genomes];0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1025472	0.83[AFR][1000 genomes];0.83[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12518852	0.88[AFR][1000 genomes];0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs13166750	0.82[ASN][1000 genomes]
rs1347123	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1347124	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1368340	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1368341	0.87[AFR][1000 genomes];0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1368343	0.90[AFR][1000 genomes];0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1432753	0.90[AFR][1000 genomes];0.81[AMR][1000 genomes];0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1433028	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1619551	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1626062	0.82[AFR][1000 genomes];0.83[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1626734	0.85[AFR][1000 genomes];0.83[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1654134	0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1654135	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1654143	0.83[AFR][1000 genomes];0.81[AMR][1000 genomes];0.83[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1654144	0.85[AFR][1000 genomes];0.83[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1654145	0.85[AFR][1000 genomes];0.83[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1654146	0.85[AFR][1000 genomes];0.81[AMR][1000 genomes];0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1654147	0.87[AFR][1000 genomes];0.81[AMR][1000 genomes];0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1654148	0.87[AFR][1000 genomes];0.81[AMR][1000 genomes];0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1654150	0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1654230	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1654231	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1654232	0.83[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1654233	0.82[AFR][1000 genomes];0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1654234	0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1654235	0.83[AFR][1000 genomes];0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1654236	0.87[AFR][1000 genomes];0.81[AMR][1000 genomes];0.83[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1654237	0.87[AFR][1000 genomes];0.81[AMR][1000 genomes];0.83[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1654238	0.87[AFR][1000 genomes];0.81[AMR][1000 genomes];0.83[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1654239	0.87[AFR][1000 genomes];0.81[AMR][1000 genomes];0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1654240	0.86[AFR][1000 genomes];0.81[AMR][1000 genomes];0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1654242	0.84[AFR][1000 genomes];0.83[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1654243	0.85[AFR][1000 genomes];0.83[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1835931	0.83[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1897540	0.81[ASN][1000 genomes]
rs1962863	0.89[AFR][1000 genomes];0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1962864	0.90[AFR][1000 genomes];0.81[AMR][1000 genomes];0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1972778	0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2014625	0.90[AFR][1000 genomes];0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2400196	0.83[AFR][1000 genomes];0.83[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2400197	0.88[AFR][1000 genomes];0.81[AMR][1000 genomes];0.83[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2400198	0.87[AFR][1000 genomes];0.81[AMR][1000 genomes];0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2436416	0.85[AFR][1000 genomes];0.83[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs3903516	0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4521541	0.88[AFR][1000 genomes];0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6580383	0.87[AFR][1000 genomes];0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6580384	0.87[AFR][1000 genomes];0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6884968	0.90[AFR][1000 genomes];0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6896903	0.88[AFR][1000 genomes];0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7721955	0.83[AFR][1000 genomes];0.83[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs872565	0.81[ASN][1000 genomes]
rs872566	0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs987806	0.90[AFR][1000 genomes];0.83[EUR][1000 genomes];0.85[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	nsv462474	chr5:145068001-145143775	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv599934	chr5:145068001-145143775	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv969001	chr5:145097474-145111251	Weak transcription ZNF genes & repeats Enhancers Strong transcription	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	n/a
4	nsv1021851	chr5:145106686-145187560	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:22 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:145101600-145117400	Weak transcription	Gastric	stomach
2	chr5:145105200-145111200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr5:145105400-145179000	Weak transcription	Pancreas	Pancrea
4	chr5:145106000-145111400	ZNF genes & repeats	Rectal Mucosa Donor 31	rectum
5	chr5:145106200-145111400	ZNF genes & repeats	Primary hematopoietic stem cells	blood
6	chr5:145106200-145114000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr5:145106600-145110600	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
8	chr5:145107000-145114200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr5:145107000-145114800	Weak transcription	Fetal Stomach	stomach
10	chr5:145107200-145123200	Weak transcription	Aorta	Aorta
11	chr5:145107400-145111000	Weak transcription	Right Ventricle	heart
12	chr5:145107800-145111800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr5:145108000-145115000	Weak transcription	Rectal Smooth Muscle	rectum
14	chr5:145108600-145110400	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr5:145108600-145110400	ZNF genes & repeats	Duodenum Mucosa	Duodenum
16	chr5:145108800-145110800	ZNF genes & repeats	Rectal Mucosa Donor 29	rectum
17	chr5:145109400-145120600	Weak transcription	Left Ventricle	heart
18	chr5:145109400-145194400	Weak transcription	Colonic Mucosa	Colon
19	chr5:145109600-145113200	Weak transcription	Ovary	ovary
20	chr5:145109600-145116800	Weak transcription	Sigmoid Colon	Sigmoid Colon
21	chr5:145110000-145114600	Weak transcription	Duodenum Smooth Muscle	Duodenum
22	chr5:145110200-145112600	Weak transcription	Fetal Intestine Large	intestine

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