Variant report

Variant	rs73614661
Chromosome Location	chr16:74751827-74751828
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr16:74751769..74753294-chr16:74807439..74810031,2	MCF-7	breast:
2	chr16:74732966..74736026-chr16:74749843..74752746,3	MCF-7	breast:
3	chr16:74751556..74754307-chr2:7086271..7088769,2	MCF-7	breast:
4	chr16:74751611..74753293-chr16:74754163..74756855,2	MCF-7	breast:
5	chr16:74751303..74753901-chr16:74761121..74763557,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000103089	Chromatin interaction
ENSG00000168404	Chromatin interaction

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

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs11554620	0.83[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11554621	0.90[ASN][1000 genomes]
rs34089769	0.95[ASN][1000 genomes]
rs34219496	0.95[ASN][1000 genomes]
rs56664536	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57844314	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6564160	0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7190389	0.83[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7191746	0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7192122	0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7192551	0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7193407	0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs73614642	0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs73614655	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73614659	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73614660	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8047410	0.94[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv916687	chr16:74241238-74896721	Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Strong transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	102 gene(s)	inside rSNPs	diseases
2	nsv949374	chr16:74466960-75172358	Enhancers Flanking Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	96 gene(s)	inside rSNPs	diseases
3	nsv1061095	chr16:74519718-75407020	Strong transcription Enhancers Flanking Active TSS Weak transcription Genic enhancers Active TSS 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 miRNA target site	123 gene(s)	inside rSNPs	diseases
4	nsv1061948	chr16:74660609-74882915	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	67 gene(s)	inside rSNPs	diseases
5	nsv542957	chr16:74660609-74882915	Enhancers Genic enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	67 gene(s)	inside rSNPs	diseases
6	nsv906906	chr16:74664743-74805668	Active TSS Flanking Active TSS Enhancers Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	57 gene(s)	inside rSNPs	diseases
7	nsv532560	chr16:74692406-75411912	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	111 gene(s)	inside rSNPs	diseases
8	nsv906907	chr16:74702254-74785902	Active TSS Enhancers Bivalent Enhancer Weak transcription Strong transcription Bivalent/Poised TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	53 gene(s)	inside rSNPs	diseases
9	nsv517513	chr16:74743736-74812676	Enhancers Weak transcription Bivalent/Poised TSS Genic enhancers Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	36 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:26 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:74735000-74760000	Weak transcription	Esophagus	oesophagus
2	chr16:74743800-74759000	Weak transcription	Rectal Mucosa Donor 31	rectum
3	chr16:74743800-74759400	Weak transcription	Rectal Mucosa Donor 29	rectum
4	chr16:74743800-74760800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
5	chr16:74744000-74752400	Weak transcription	Thymus	Thymus
6	chr16:74744000-74760600	Weak transcription	Hela-S3	cervix
7	chr16:74744000-74760800	Weak transcription	Stomach Mucosa	stomach
8	chr16:74744000-74760800	Weak transcription	A549	lung
9	chr16:74744200-74758200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
10	chr16:74747200-74752000	Weak transcription	Fetal Thymus	thymus
11	chr16:74747400-74753000	Strong transcription	Fetal Intestine Small	intestine
12	chr16:74748200-74758400	Weak transcription	H9 Cell Line	embryonic stem cell
13	chr16:74748400-74758200	Weak transcription	Gastric	stomach
14	chr16:74749000-74758200	Weak transcription	Colonic Mucosa	Colon
15	chr16:74750400-74752200	Strong transcription	Fetal Stomach	stomach
16	chr16:74750400-74758200	Weak transcription	Pancreas	Pancrea
17	chr16:74750600-74752800	Enhancers	Brain Substantia Nigra	brain
18	chr16:74750800-74752400	Enhancers	Brain Inferior Temporal Lobe	brain
19	chr16:74750800-74752600	Enhancers	Brain Angular Gyrus	brain
20	chr16:74751000-74752600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr16:74751400-74752800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr16:74751400-74755400	Weak transcription	Lung	lung
23	chr16:74751600-74752400	Genic enhancers	Brain Cingulate Gyrus	brain
24	chr16:74751600-74752800	Genic enhancers	Brain Hippocampus Middle	brain
25	chr16:74751600-74755400	Weak transcription	Brain Anterior Caudate	brain
26	chr16:74751800-74753400	Strong transcription	Sigmoid Colon	Sigmoid Colon

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