Variant report

Variant	rs7192882
Chromosome Location	chr16:80965775-80965776
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr16:80957146..80959233-chr16:80965352..80966876,2	MCF-7	breast:
2	chr16:80965383..80968097-chr16:81038708..81041560,2	MCF-7	breast:
3	chr16:80963937..80967554-chr16:80967751..80972204,4	K562	blood:
4	chr16:80964917..80968271-chr16:80970129..80973008,4	MCF-7	breast:
5	chr16:80950553..80953339-chr16:80965421..80967122,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000166451	Chromatin interaction
ENSG00000103121	Chromatin interaction

Extended variants
information (count: 43 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs12716902	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2042209	0.87[EUR][1000 genomes]
rs2042211	0.89[EUR][1000 genomes]
rs2161295	0.85[EUR][1000 genomes]
rs2161296	0.85[EUR][1000 genomes]
rs4467097	0.85[EUR][1000 genomes]
rs4888116	0.82[EUR][1000 genomes]
rs6564800	0.91[EUR][1000 genomes]
rs6564803	0.87[EUR][1000 genomes]
rs7184630	0.85[EUR][1000 genomes]
rs7190214	0.85[EUR][1000 genomes]
rs7195085	0.85[EUR][1000 genomes]
rs7195708	0.85[EUR][1000 genomes]
rs7197603	0.89[EUR][1000 genomes]
rs7204512	0.89[EUR][1000 genomes]
rs8044314	0.85[EUR][1000 genomes]
rs8054657	0.85[EUR][1000 genomes]
rs8054912	0.85[EUR][1000 genomes]
rs8059375	0.85[EUR][1000 genomes]
rs971078	0.86[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:23 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1060621	chr16:80532848-80980616	Weak transcription Active TSS ZNF genes & repeats Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
2	nsv542989	chr16:80532848-80980616	Enhancers Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Weak transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
3	esv3451298	chr16:80696935-80997389	Weak transcription Enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
4	esv3350075	chr16:80696955-80997359	Strong transcription Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
5	nsv948534	chr16:80867635-81160492	Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	55 gene(s)	inside rSNPs	diseases
6	nsv1065258	chr16:80887483-81081768	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
7	nsv1058045	chr16:80918138-81048242	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
8	nsv1064164	chr16:80918138-81126967	Flanking Active TSS Weak transcription Active TSS Enhancers Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
9	nsv542991	chr16:80918138-81126967	Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
10	nsv573303	chr16:80951306-80989859	Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats	Chromatin interactive region	11 gene(s)	inside rSNPs	diseases
11	nsv1055598	chr16:80954876-80993734	Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Genic enhancers	Chromatin interactive region	10 gene(s)	inside rSNPs	diseases
12	nsv1067066	chr16:80954876-80996272	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Enhancers Active TSS Weak transcription Bivalent Enhancer Genic enhancers ZNF genes & repeats	Chromatin interactive region	10 gene(s)	inside rSNPs	diseases
13	nsv1059905	chr16:80954876-80998523	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers	Chromatin interactive region	10 gene(s)	inside rSNPs	diseases
14	esv2760441	chr16:80954888-80998523	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers	Chromatin interactive region	10 gene(s)	inside rSNPs	diseases
15	nsv457561	chr16:80955393-80989859	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers	Chromatin interactive region	10 gene(s)	inside rSNPs	diseases
16	nsv457562	chr16:80955393-80989859	Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers	Chromatin interactive region	10 gene(s)	inside rSNPs	diseases
17	nsv573304	chr16:80955393-80989859	Flanking Bivalent TSS/Enh Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	Chromatin interactive region	10 gene(s)	inside rSNPs	diseases
18	nsv471101	chr16:80955393-80989860	Enhancers Weak transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Genic enhancers	Chromatin interactive region	10 gene(s)	inside rSNPs	diseases
19	nsv520122	chr16:80955393-81001915	Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS ZNF genes & repeats Genic enhancers	Chromatin interactive region	10 gene(s)	inside rSNPs	diseases
20	nsv907004	chr16:80958442-81001915	Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Genic enhancers	Chromatin interactive region	10 gene(s)	inside rSNPs	diseases
21	nsv1062711	chr16:80959475-80988790	Active TSS Enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers	Chromatin interactive region	10 gene(s)	inside rSNPs	diseases
22	nsv1067350	chr16:80959475-80996272	Bivalent/Poised TSS Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats	Chromatin interactive region	10 gene(s)	inside rSNPs	diseases
23	nsv1055411	chr16:80961660-80993734	Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Genic enhancers	Chromatin interactive region	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:85 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:80958800-80965800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr16:80962200-80965800	Weak transcription	Esophagus	oesophagus
3	chr16:80965000-80966800	Active TSS	Hela-S3	cervix
4	chr16:80965400-80966000	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
5	chr16:80965400-80966400	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr16:80965400-80966600	Flanking Active TSS	HUVEC	blood vessel
7	chr16:80965600-80965800	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr16:80965600-80965800	Bivalent/Poised TSS	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr16:80965600-80965800	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
10	chr16:80965600-80965800	Flanking Bivalent TSS/Enh	HUES64 Cell Line	embryonic stem cell
11	chr16:80965600-80965800	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
12	chr16:80965600-80965800	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr16:80965600-80965800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr16:80965600-80965800	Bivalent Enhancer	Primary hematopoietic stem cells short term culture	blood
15	chr16:80965600-80965800	Bivalent Enhancer	Primary T helper naive cells fromperipheralblood	blood
16	chr16:80965600-80965800	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
17	chr16:80965600-80965800	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
18	chr16:80965600-80965800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr16:80965600-80965800	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
20	chr16:80965600-80965800	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr16:80965600-80965800	Enhancers	Brain Substantia Nigra	brain
22	chr16:80965600-80965800	Active TSS	Duodenum Smooth Muscle	Duodenum
23	chr16:80965600-80965800	Active TSS	Fetal Adrenal Gland	Adrenal Gland
24	chr16:80965600-80965800	Enhancers	Fetal Heart	heart
25	chr16:80965600-80965800	Bivalent/Poised TSS	Fetal Lung	lung
26	chr16:80965600-80965800	Bivalent/Poised TSS	Fetal Muscle Leg	muscle
27	chr16:80965600-80965800	Enhancers	Placenta	Placenta
28	chr16:80965600-80965800	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
29	chr16:80965600-80965800	Enhancers	Skeletal Muscle Female	skeletal muscle
30	chr16:80965600-80965800	Flanking Active TSS	HepG2	liver
31	chr16:80965600-80965800	Enhancers	HMEC	breast
32	chr16:80965600-80966000	Enhancers	Primary hematopoietic stem cells	blood
33	chr16:80965600-80966000	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
34	chr16:80965600-80966000	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
35	chr16:80965600-80966000	Bivalent Enhancer	Primary T regulatory cells fromperipheralblood	blood
36	chr16:80965600-80966000	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
37	chr16:80965600-80966000	Flanking Active TSS	Brain Angular Gyrus	brain
38	chr16:80965600-80966000	Flanking Bivalent TSS/Enh	Brain Germinal Matrix	brain
39	chr16:80965600-80966000	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
40	chr16:80965600-80966000	Flanking Active TSS	Fetal Brain Male	brain
41	chr16:80965600-80966000	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
42	chr16:80965600-80966000	Flanking Active TSS	NH-A	brain
43	chr16:80965600-80966000	Flanking Active TSS	Osteobl	bone
44	chr16:80965600-80966400	Active TSS	H9 Cell Line	embryonic stem cell
45	chr16:80965600-80966400	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr16:80965600-80966400	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr16:80965600-80966400	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
48	chr16:80965600-80966400	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr16:80965600-80966400	Active TSS	Fetal Brain Female	brain
50	chr16:80965600-80966400	Active TSS	Fetal Intestine Large	intestine

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