Variant report

Variant	rs67863076
Chromosome Location	chr7:111665941-111665942
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr7:111662019..111663825-chr7:111665040..111667172,2	K562	blood:
2	chr7:111662127..111663825-chr7:111665482..111667172,2	K562	blood:
3	chr7:111657467..111660599-chr7:111663952..111668324,4	K562	blood:

Extended variants
information (count: 33 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs10273234	1.00[ASN][1000 genomes]
rs10273453	1.00[ASN][1000 genomes]
rs11982254	1.00[ASN][1000 genomes]
rs1468207	1.00[ASN][1000 genomes]
rs17564870	1.00[ASN][1000 genomes]
rs17565212	1.00[ASN][1000 genomes]
rs35518766	1.00[ASN][1000 genomes]
rs55963629	1.00[ASN][1000 genomes]
rs6969874	1.00[ASN][1000 genomes]
rs73210921	1.00[ASN][1000 genomes]
rs73210924	1.00[ASN][1000 genomes]
rs73210927	1.00[ASN][1000 genomes]
rs73210929	1.00[ASN][1000 genomes]
rs73210930	1.00[ASN][1000 genomes]
rs7785891	1.00[ASN][1000 genomes]
rs7805672	1.00[ASN][1000 genomes]
rs7808736	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9649349	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:15 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv608196	chr7:111073710-111794368	Enhancers Strong transcription Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
2	nsv1021527	chr7:111194596-111851619	Weak transcription Enhancers Strong transcription Bivalent Enhancer Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
3	nsv539086	chr7:111194596-111851619	Enhancers Weak transcription Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
4	nsv1028740	chr7:111227747-111679401	Weak transcription Enhancers Active TSS ZNF genes & repeats Genic enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
5	nsv1015267	chr7:111303294-111714771	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
6	nsv539087	chr7:111303294-111714771	Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
7	nsv539088	chr7:111333899-111722341	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
8	nsv531435	chr7:111333900-111926292	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
9	nsv491934	chr7:111333900-111975504	Active TSS Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
10	nsv532335	chr7:111411990-112054905	Enhancers Strong transcription Flanking Active TSS Weak transcription ZNF genes & repeats Genic enhancers 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	18 gene(s)	inside rSNPs	diseases
11	nsv533924	chr7:111529515-111784369	Enhancers Strong transcription Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	8 gene(s)	inside rSNPs	diseases
12	nsv1023261	chr7:111593889-111780337	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
13	nsv1016663	chr7:111622107-111813223	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
14	nsv1034249	chr7:111656902-111748774	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Strong transcription	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
15	nsv539089	chr7:111656902-111748774	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:27 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:111647200-111666400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr7:111649400-111673800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr7:111651400-111668200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
4	chr7:111654600-111673400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr7:111659800-111666400	Enhancers	Brain Hippocampus Middle	brain
6	chr7:111662200-111666000	Enhancers	Brain Anterior Caudate	brain
7	chr7:111662600-111671200	Weak transcription	Fetal Lung	lung
8	chr7:111663600-111668000	Weak transcription	Brain Angular Gyrus	brain
9	chr7:111664400-111666400	Enhancers	HUVEC	blood vessel
10	chr7:111664600-111669600	Weak transcription	Pancreatic Islets	Pancreatic Islet
11	chr7:111664800-111668000	Weak transcription	Brain Cingulate Gyrus	brain
12	chr7:111665200-111666400	Enhancers	H9 Cell Line	embryonic stem cell
13	chr7:111665200-111668000	Weak transcription	Brain Inferior Temporal Lobe	brain
14	chr7:111665400-111666000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
15	chr7:111665400-111666400	Enhancers	Lung	lung
16	chr7:111665400-111666400	Enhancers	Psoas Muscle	Psoas
17	chr7:111665400-111668000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
18	chr7:111665400-111669600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
19	chr7:111665600-111666000	Enhancers	Skeletal Muscle Female	skeletal muscle
20	chr7:111665600-111667800	Weak transcription	HUES48 Cell Line	embryonic stem cell
21	chr7:111665600-111667800	Weak transcription	Brain Substantia Nigra	brain
22	chr7:111665800-111666200	Enhancers	Left Ventricle	heart
23	chr7:111665800-111666200	Enhancers	Spleen	Spleen
24	chr7:111665800-111666400	Enhancers	Right Atrium	heart
25	chr7:111665800-111669400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
26	chr7:111665800-111672600	Weak transcription	HUES6 Cell Line	embryonic stem cell
27	chr7:111665800-111672800	Weak transcription	HUES64 Cell Line	embryonic stem cell

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