Variant report

Variant	rs7145410
Chromosome Location	chr14:56699321-56699322
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs1028972	0.82[EUR][1000 genomes]
rs1152473	0.82[EUR][1000 genomes]
rs1152474	0.82[EUR][1000 genomes]
rs1152476	0.82[EUR][1000 genomes]
rs1152481	0.82[EUR][1000 genomes]
rs1152483	0.82[EUR][1000 genomes]
rs1188692	0.82[EUR][1000 genomes]
rs1479752	0.91[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs1979420	0.91[AMR][1000 genomes];0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs242579	0.85[AMR][1000 genomes];0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs242587	0.85[AMR][1000 genomes];0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs242588	0.85[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs242592	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs242593	0.82[EUR][1000 genomes]
rs242594	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs34175054	0.82[EUR][1000 genomes]
rs375156	0.93[AMR][1000 genomes];0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs3783668	0.87[ASN][1000 genomes]
rs429676	0.93[AMR][1000 genomes];0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6573087	0.87[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs7140808	0.93[AMR][1000 genomes];0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7153057	0.93[AMR][1000 genomes];0.82[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7153858	0.96[AMR][1000 genomes];0.82[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs753109	0.87[ASN][1000 genomes]
rs754689	0.94[ASN][1000 genomes]
rs754690	0.92[ASN][1000 genomes]
rs899603	0.93[AMR][1000 genomes];0.94[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	nsv533129	chr14:56568535-56819234	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	esv1844788	chr14:56594420-56771207	Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv1044886	chr14:56689682-56834648	Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv542104	chr14:56689682-56834648	Weak transcription Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:25 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:56686800-56702000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr14:56688000-56707800	Weak transcription	Spleen	Spleen
3	chr14:56689600-56710000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr14:56689800-56715800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
5	chr14:56692400-56703000	Weak transcription	Aorta	Aorta
6	chr14:56692400-56710000	Weak transcription	Fetal Stomach	stomach
7	chr14:56692600-56701400	Weak transcription	Ovary	ovary
8	chr14:56692600-56703200	Weak transcription	Monocytes-CD14+_RO01746	blood
9	chr14:56693000-56704000	Weak transcription	Primary T cells from cord blood	blood
10	chr14:56693200-56703000	Weak transcription	Primary neutrophils fromperipheralblood	blood
11	chr14:56693200-56724400	Weak transcription	Gastric	stomach
12	chr14:56694000-56701600	Weak transcription	Pancreas	Pancrea
13	chr14:56694000-56723000	Weak transcription	Lung	lung
14	chr14:56695200-56702200	Weak transcription	Dnd41	blood
15	chr14:56696000-56703200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
16	chr14:56696000-56706400	Weak transcription	Thymus	Thymus
17	chr14:56696000-56715600	Weak transcription	Fetal Thymus	thymus
18	chr14:56696800-56703000	Weak transcription	H1 Cell Line	embryonic stem cell
19	chr14:56699200-56699400	Flanking Bivalent TSS/Enh	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr14:56699200-56699400	ZNF genes & repeats	Primary T helper memory cells from peripheral blood 2	blood
21	chr14:56699200-56699400	ZNF genes & repeats	Primary T helper naive cells from peripheral blood	blood
22	chr14:56699200-56699400	ZNF genes & repeats	Primary T helper memory cells from peripheral blood 1	blood
23	chr14:56699200-56699400	ZNF genes & repeats	Primary T helper cells fromperipheralblood	blood
24	chr14:56699200-56699400	ZNF genes & repeats	Primary T killer memory cells from peripheral blood	blood
25	chr14:56699200-56699400	ZNF genes & repeats	Stomach Mucosa	stomach

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