Variant report

Variant	rs73445456
Chromosome Location	chr7:70045668-70045669
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 26 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs1013869	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1013870	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs13237311	0.86[ASN][1000 genomes]
rs17141754	0.80[ASN][1000 genomes]
rs17569846	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs57441877	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs59969518	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs62455787	0.80[ASN][1000 genomes]
rs62455788	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs62455789	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs62455790	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs62455794	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs62455825	0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs62455829	0.84[AFR][1000 genomes];0.80[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs62455830	0.91[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs9690719	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes];0.90[ASN][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	nsv532782	chr7:69383651-70189959	Weak transcription Genic enhancers Enhancers Active TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv532783	chr7:69939570-70245396	Enhancers Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	esv3341834	chr7:69968031-70288098	Weak transcription ZNF genes & repeats Genic enhancers Enhancers Strong transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv532784	chr7:69969631-70204548	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv1025522	chr7:69971452-70173513	Weak transcription Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv1032378	chr7:70010392-70190353	Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
7	nsv538929	chr7:70010392-70190353	Bivalent/Poised TSS Enhancers Genic enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
8	nsv1024498	chr7:70016323-70190353	Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
9	nsv538930	chr7:70016323-70190353	Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Enhancers Weak transcription Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
10	nsv1024524	chr7:70031241-70138924	Weak transcription Enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:37 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:70024000-70046400	Weak transcription	Primary B cells from cord blood	blood
2	chr7:70034000-70048600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr7:70034800-70047600	Weak transcription	Fetal Lung	lung
4	chr7:70035400-70047200	Weak transcription	Ovary	ovary
5	chr7:70036600-70047600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
6	chr7:70036800-70060800	Weak transcription	Colon Smooth Muscle	Colon
7	chr7:70037400-70048200	Weak transcription	Fetal Intestine Large	intestine
8	chr7:70037800-70049200	Weak transcription	Stomach Smooth Muscle	stomach
9	chr7:70038600-70059600	Weak transcription	Primary B cells from peripheral blood	blood
10	chr7:70039800-70060600	Weak transcription	Brain Inferior Temporal Lobe	brain
11	chr7:70040800-70048400	Weak transcription	Placenta Amnion	Placenta Amnion
12	chr7:70041000-70047400	Weak transcription	Fetal Heart	heart
13	chr7:70041600-70047200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr7:70042000-70047800	Weak transcription	Fetal Brain Female	brain
15	chr7:70042000-70048200	Weak transcription	Fetal Brain Male	brain
16	chr7:70042000-70048600	Weak transcription	Brain Anterior Caudate	brain
17	chr7:70044600-70050400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr7:70045000-70045800	Enhancers	iPS-18 Cell Line	embryonic stem cell
19	chr7:70045200-70047200	Weak transcription	HUES64 Cell Line	embryonic stem cell
20	chr7:70045200-70047600	Weak transcription	Fetal Kidney	kidney
21	chr7:70045200-70051600	Weak transcription	HSMMtube	muscle
22	chr7:70045400-70046600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr7:70045400-70047000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr7:70045400-70047200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr7:70045400-70047200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
26	chr7:70045400-70047200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
27	chr7:70045400-70048400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr7:70045400-70048400	Weak transcription	NHEK	skin
29	chr7:70045400-70048600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr7:70045400-70048600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr7:70045400-70049400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr7:70045400-70049600	Weak transcription	Pancreas	Pancrea
33	chr7:70045400-70051400	Weak transcription	HSMM	muscle
34	chr7:70045400-70060800	Weak transcription	Gastric	stomach
35	chr7:70045600-70047000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
36	chr7:70045600-70047200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr7:70045600-70047400	Weak transcription	Fetal Stomach	stomach

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