Variant report

Variant	rs16955120
Chromosome Location	chr16:81385887-81385888
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr16:81382053..81384349-chr16:81385028..81387799,2	MCF-7	breast:
2	chr16:81384947..81387617-chr16:81411669..81414559,2	K562	blood:
3	chr16:81347524..81349454-chr16:81385294..81387320,2	K562	blood:
4	chr16:81384234..81386036-chr16:81388157..81390233,2	MCF-7	breast:
5	chr16:81381387..81384964-chr16:81385741..81388867,5	K562	blood:

Variant related genes	Relation type
ENSG00000261609	Chromatin interaction

Extended variants
information (count: 55 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:48)

rs_ID	r²[population]
rs1075352	0.83[AMR][1000 genomes]
rs1075353	0.83[AMR][1000 genomes]
rs11861054	0.88[AMR][1000 genomes];0.80[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11861072	1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11861112	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs11861158	0.85[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.80[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11861322	1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11861886	0.85[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.80[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11862082	1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs11862778	0.83[AMR][1000 genomes]
rs11862805	0.83[AMR][1000 genomes]
rs11866294	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11866308	0.83[AMR][1000 genomes];0.80[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11866327	0.88[AMR][1000 genomes]
rs11866374	0.85[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.80[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11866407	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11866408	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11866700	0.88[AMR][1000 genomes]
rs16955014	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs16955018	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs16955027	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs16955031	0.82[CHB][hapmap];0.85[JPT][hapmap];0.88[AMR][1000 genomes];0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs16955040	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs16955059	0.82[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs16955067	0.82[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs16955071	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs16955074	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs16955083	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16955109	1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16955113	1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16955138	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs16955149	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs16955164	0.88[AMR][1000 genomes]
rs16955173	0.88[AMR][1000 genomes]
rs2317129	0.85[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.80[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs28560203	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs28561847	0.88[AMR][1000 genomes]
rs28864156	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34684636	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3803653	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs56859781	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs57928297	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs58590084	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58594614	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs59579335	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59586584	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs9925624	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs9935105	1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[YRI][hapmap];0.86[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv532569	chr16:80980356-81700149	Weak transcription Flanking Active TSS Genic enhancers Enhancers Strong transcription Active TSS Bivalent Enhancer 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 miRNA miRNA target site	71 gene(s)	inside rSNPs	diseases
2	nsv532597	chr16:81009718-81388348	Active TSS Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
3	nsv1058519	chr16:81177767-81735333	Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Enhancers Transcr. at gene 5' and 3' Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	36 gene(s)	inside rSNPs	diseases
4	nsv948448	chr16:81198147-81906766	Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS Bivalent Enhancer Genic enhancers 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	37 gene(s)	inside rSNPs	diseases
5	nsv1061359	chr16:81349826-81471867	Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Enhancers Genic enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	17 gene(s)	inside rSNPs	diseases
6	nsv542992	chr16:81349826-81471867	Weak transcription Enhancers ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	17 gene(s)	inside rSNPs	diseases
7	esv1792674	chr16:81375316-81391868	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers Active TSS	Chromatin interactive region	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:107 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:81353400-81390400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr16:81354200-81391600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr16:81379400-81410600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr16:81380600-81388000	Weak transcription	Lung	lung
5	chr16:81380600-81396200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr16:81381000-81392600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
7	chr16:81381200-81387600	Weak transcription	HepG2	liver
8	chr16:81381200-81388000	Weak transcription	H1 Cell Line	embryonic stem cell
9	chr16:81381200-81388000	Weak transcription	HMEC	breast
10	chr16:81381200-81390200	Weak transcription	Rectal Mucosa Donor 31	rectum
11	chr16:81381200-81390400	Weak transcription	Brain Substantia Nigra	brain
12	chr16:81381200-81391000	Weak transcription	Osteobl	bone
13	chr16:81381200-81396000	Weak transcription	Right Ventricle	heart
14	chr16:81381800-81387200	Weak transcription	HUES64 Cell Line	embryonic stem cell
15	chr16:81382000-81387200	Weak transcription	Primary T cells fromperipheralblood	blood
16	chr16:81382000-81388600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
17	chr16:81382200-81388000	Weak transcription	HUES48 Cell Line	embryonic stem cell
18	chr16:81382200-81390200	Weak transcription	NHEK	skin
19	chr16:81382200-81391400	Weak transcription	Fetal Heart	heart
20	chr16:81382400-81388600	Weak transcription	Aorta	Aorta
21	chr16:81382400-81390400	Weak transcription	Cortex derived primary cultured neurospheres	brain
22	chr16:81382400-81390400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr16:81382400-81391400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
24	chr16:81382400-81396200	Weak transcription	Pancreas	Pancrea
25	chr16:81382400-81418400	Weak transcription	Small Intestine	intestine
26	chr16:81382600-81387200	Weak transcription	Rectal Mucosa Donor 29	rectum
27	chr16:81382600-81388200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr16:81382600-81390200	Weak transcription	A549	lung
29	chr16:81382600-81391400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr16:81382600-81391400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
31	chr16:81382600-81391400	Weak transcription	Brain Angular Gyrus	brain
32	chr16:81382600-81396000	Weak transcription	Primary B cells from peripheral blood	blood
33	chr16:81382600-81398600	Weak transcription	Fetal Thymus	thymus
34	chr16:81382800-81388000	Weak transcription	Fetal Stomach	stomach
35	chr16:81382800-81390400	Weak transcription	Skeletal Muscle Male	skeletal muscle
36	chr16:81382800-81391400	Weak transcription	Thymus	Thymus
37	chr16:81383000-81387600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
38	chr16:81383000-81387800	Weak transcription	Placenta	Placenta
39	chr16:81383000-81391400	Weak transcription	H9 Cell Line	embryonic stem cell
40	chr16:81383000-81391400	Weak transcription	HSMM	muscle
41	chr16:81383000-81391400	Weak transcription	HUVEC	blood vessel
42	chr16:81383000-81395200	Weak transcription	Fetal Brain Female	brain
43	chr16:81383000-81395800	Weak transcription	Brain Germinal Matrix	brain
44	chr16:81383000-81396200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
45	chr16:81383200-81387200	Weak transcription	Esophagus	oesophagus
46	chr16:81383200-81387800	Weak transcription	Left Ventricle	heart
47	chr16:81383200-81390200	Weak transcription	Gastric	stomach
48	chr16:81383200-81391400	Weak transcription	Fetal Muscle Trunk	muscle
49	chr16:81383200-81396000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
50	chr16:81383400-81395800	Weak transcription	Colonic Mucosa	Colon

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