Variant report

Variant	rs73297566
Chromosome Location	chr14:71596715-71596716
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 52 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs11844851	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28706321	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4496061	1.00[AMR][1000 genomes]
rs56111655	1.00[AMR][1000 genomes]
rs56150143	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56195946	1.00[AMR][1000 genomes]
rs56709080	1.00[AMR][1000 genomes]
rs57509106	1.00[AMR][1000 genomes]
rs59081846	0.90[AFR][1000 genomes]
rs59122223	1.00[AMR][1000 genomes]
rs59400895	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59949441	1.00[AMR][1000 genomes]
rs60316971	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60473605	1.00[AMR][1000 genomes]
rs61989174	0.85[AFR][1000 genomes]
rs61989175	0.84[AFR][1000 genomes]
rs61992091	0.85[AFR][1000 genomes]
rs7149960	1.00[AMR][1000 genomes]
rs7155387	1.00[AMR][1000 genomes]
rs7155471	1.00[AMR][1000 genomes]
rs7161431	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73291831	1.00[AMR][1000 genomes]
rs73293803	1.00[AMR][1000 genomes]
rs73293814	1.00[AMR][1000 genomes]
rs73293816	1.00[AMR][1000 genomes]
rs73293828	1.00[AMR][1000 genomes]
rs73295506	1.00[AMR][1000 genomes]
rs73295523	1.00[AMR][1000 genomes]
rs73295548	1.00[AMR][1000 genomes]
rs73295552	1.00[AMR][1000 genomes]
rs73295570	1.00[AMR][1000 genomes]
rs73297518	1.00[AMR][1000 genomes]
rs73297526	1.00[AMR][1000 genomes]
rs73297564	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73297572	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73297577	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73297587	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73297594	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73299437	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74060582	1.00[AMR][1000 genomes]
rs74060593	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs8019019	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1041980	chr14:71196358-71767339	Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Enhancers Strong transcription Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
2	nsv542125	chr14:71196358-71767339	Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Enhancers Active TSS 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 miRNA target site	35 gene(s)	inside rSNPs	diseases
3	nsv1035416	chr14:71212882-71623271	Strong transcription Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
4	nsv542126	chr14:71212882-71623271	Weak transcription Enhancers Strong transcription Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
5	nsv1037839	chr14:71263886-71625114	Flanking Active TSS Weak transcription Genic enhancers Active TSS Strong transcription Enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
6	nsv542127	chr14:71263886-71625114	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
7	nsv1038007	chr14:71269747-71667680	Weak transcription Enhancers Genic enhancers Active TSS Strong transcription Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
8	nsv565043	chr14:71395604-71625112	Strong transcription Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
9	nsv1036929	chr14:71469148-71683412	Strong transcription Genic enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Enhancers Bivalent Enhancer Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
10	nsv1044090	chr14:71496198-71780026	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:28 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:71576800-71597000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr14:71582200-71597400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
3	chr14:71582400-71597000	Weak transcription	Primary monocytes fromperipheralblood	blood
4	chr14:71582600-71597000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr14:71582800-71597200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
6	chr14:71585800-71596800	Weak transcription	Primary neutrophils fromperipheralblood	blood
7	chr14:71586000-71596800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr14:71586200-71597000	Weak transcription	HMEC	breast
9	chr14:71586600-71596800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr14:71586600-71597200	Weak transcription	HSMM	muscle
11	chr14:71587400-71596800	Weak transcription	Osteobl	bone
12	chr14:71588400-71596800	Weak transcription	Left Ventricle	heart
13	chr14:71588800-71597400	Weak transcription	Adipose Nuclei	Adipose
14	chr14:71590800-71596800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
15	chr14:71590800-71597000	Weak transcription	Spleen	Spleen
16	chr14:71592800-71597400	Weak transcription	Duodenum Mucosa	Duodenum
17	chr14:71595600-71598400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr14:71595800-71597000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr14:71595800-71597600	Enhancers	iPS-15b Cell Line	embryonic stem cell
20	chr14:71596000-71596800	Enhancers	ES-I3 Cell Line	embryonic stem cell
21	chr14:71596400-71596800	Enhancers	K562	blood
22	chr14:71596600-71596800	Enhancers	Hela-S3	cervix
23	chr14:71596600-71597000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr14:71596600-71597400	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
25	chr14:71596600-71597400	Enhancers	iPS-20b Cell Line	embryonic stem cell
26	chr14:71596600-71597600	Enhancers	HUES64 Cell Line	embryonic stem cell
27	chr14:71596600-71597800	Enhancers	Placenta	Placenta
28	chr14:71596600-71598200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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