Variant report

Variant	rs2054214
Chromosome Location	chr16:30971442-30971443
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:13)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:30967331..30971455-chr16:31189672..31193521,14	K562	blood:
2	chr16:30969849..30973969-chr16:31007050..31010528,3	MCF-7	breast:
3	chr16:30968063..30971621-chr16:31128915..31132343,4	K562	blood:
4	chr16:30967183..30971961-chr16:31469060..31471569,4	MCF-7	breast:
5	chr16:30967386..30971624-chr16:31189375..31193961,9	K562	blood:
6	chr16:30971023..30973428-chr16:31042651..31045607,2	MCF-7	breast:
7	chr16:30946481..30948013-chr16:30971111..30973974,2	MCF-7	breast:
8	chr16:30968251..30971465-chr16:31104162..31108928,5	MCF-7	breast:
9	chr16:30967393..30971949-chr16:31083830..31088417,7	K562	blood:
10	chr16:30661294..30664208-chr16:30968481..30971665,3	MCF-7	breast:
11	chr16:30968024..30972662-chr16:31101043..31106214,4	MCF-7	breast:
12	chr16:30967179..30972282-chr16:31082507..31088894,13	MCF-7	breast:
13	chr16:30968978..30971725-chr16:31006942..31010708,4	K562	blood:

No data

Variant related genes	Relation type
ENSG00000262766	Chromatin interaction
ENSG00000103496	Chromatin interaction
ENSG00000103510	Chromatin interaction
ENSG00000260267	Chromatin interaction
ENSG00000099365	Chromatin interaction
ENSG00000167395	Chromatin interaction
ENSG00000167397	Chromatin interaction
ENSG00000156858	Chromatin interaction
ENSG00000255439	Chromatin interaction
ENSG00000089280	Chromatin interaction
ENSG00000167394	Chromatin interaction
ENSG00000140691	Chromatin interaction

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs11644370	1.00[YRI][hapmap]
rs11645814	1.00[LWK][hapmap]
rs12929007	0.91[AFR][1000 genomes];0.84[EUR][1000 genomes]
rs17708472	1.00[ASW][hapmap];1.00[GIH][hapmap];0.90[LWK][hapmap];0.84[MEX][hapmap]
rs2359674	1.00[ASW][hapmap];1.00[GIH][hapmap]
rs28360556	0.84[EUR][1000 genomes]
rs55731737	0.91[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs55886019	0.96[EUR][1000 genomes]
rs55908605	0.91[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs56193946	1.00[AFR][1000 genomes];0.87[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs72799363	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs72799368	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs72800842	0.81[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs72800845	0.91[AFR][1000 genomes]
rs72800846	0.91[AFR][1000 genomes]
rs72800849	0.91[AFR][1000 genomes]
rs8058472	0.90[EUR][1000 genomes]
rs9788865	0.95[GIH][hapmap]
rs9927295	1.00[GIH][hapmap];0.84[MEX][hapmap]

Variant overlapped rSNPs/rCNVs (count:18 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1062456	chr16:30442166-31253997	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	437 gene(s)	inside rSNPs	diseases
2	nsv542898	chr16:30442166-31253997	Enhancers Active TSS Strong transcription Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	437 gene(s)	inside rSNPs	diseases
3	nsv1064134	chr16:30640293-31087327	Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Strong transcription Weak transcription Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	238 gene(s)	inside rSNPs	diseases
4	nsv905729	chr16:30642867-31247924	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	387 gene(s)	inside rSNPs	diseases
5	esv1825223	chr16:30669091-30971810	Weak transcription Enhancers Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	191 gene(s)	inside rSNPs	diseases
6	nsv431451	chr16:30682399-31340999	Transcr. at gene 5' and 3' Genic enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	350 gene(s)	inside rSNPs	diseases
7	nsv905733	chr16:30796919-31004812	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	112 gene(s)	inside rSNPs	diseases
8	nsv833190	chr16:30845051-31007863	Enhancers Genic enhancers Strong transcription Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	105 gene(s)	inside rSNPs	diseases
9	nsv833191	chr16:30864242-31048051	Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	115 gene(s)	inside rSNPs	diseases
10	nsv905734	chr16:30877544-31191482	Active TSS Strong transcription Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	271 gene(s)	inside rSNPs	diseases
11	nsv905735	chr16:30890538-31247924	Strong transcription Genic enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	264 gene(s)	inside rSNPs	diseases
12	nsv905736	chr16:30900235-30995528	Weak transcription Flanking Active TSS Active TSS Enhancers Bivalent/Poised TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	83 gene(s)	inside rSNPs	diseases
13	nsv905737	chr16:30900235-31014179	Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	95 gene(s)	inside rSNPs	diseases
14	nsv457483	chr16:30903679-31191482	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers Strong transcription Enhancers ZNF genes & repeats Weak transcription Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	253 gene(s)	inside rSNPs	diseases
15	nsv571820	chr16:30903679-31191482	Enhancers Genic enhancers Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	253 gene(s)	inside rSNPs	diseases
16	nsv905738	chr16:30906274-30973926	Strong transcription Weak transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	76 gene(s)	inside rSNPs	diseases
17	esv1797877	chr16:30948643-31188432	Flanking Active TSS Enhancers Weak transcription Strong transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	114 gene(s)	inside rSNPs	diseases
18	nsv833193	chr16:30960796-31133604	Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	109 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:30969200-30984800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr16:30970200-30980600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr16:30970400-30971600	Genic enhancers	Adipose Nuclei	Adipose
4	chr16:30970400-30971600	Genic enhancers	Duodenum Smooth Muscle	Duodenum
5	chr16:30970400-30971800	Genic enhancers	Primary mononuclear cells fromperipheralblood	Blood
6	chr16:30970400-30974600	Weak transcription	Pancreatic Islets	Pancreatic Islet
7	chr16:30970400-30985800	Strong transcription	Aorta	Aorta
8	chr16:30970400-30986200	Strong transcription	H9 Cell Line	embryonic stem cell
9	chr16:30970400-30986200	Strong transcription	HSMMtube	muscle
10	chr16:30970400-30987600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr16:30970400-30989800	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr16:30970400-30993400	Strong transcription	HUES48 Cell Line	embryonic stem cell
13	chr16:30970400-30993800	Strong transcription	Fetal Muscle Trunk	muscle
14	chr16:30970400-30994400	Strong transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr16:30970400-30996200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr16:30970400-30996400	Weak transcription	Right Atrium	heart
17	chr16:30970400-30996600	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr16:30970600-30971600	Genic enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr16:30970600-30971800	Genic enhancers	Primary T helper memory cells from peripheral blood 2	blood
20	chr16:30970600-30971800	Genic enhancers	Primary T helper cells PMA-I stimulated	--
21	chr16:30970600-30972600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr16:30970600-30976600	Strong transcription	HUVEC	blood vessel
23	chr16:30970600-30977400	Weak transcription	Stomach Mucosa	stomach
24	chr16:30970600-30983000	Weak transcription	Fetal Brain Male	brain
25	chr16:30970600-30986000	Strong transcription	Colonic Mucosa	Colon
26	chr16:30970600-30987400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr16:30970600-30987400	Strong transcription	NH-A	brain
28	chr16:30970600-30987600	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr16:30970600-30990200	Strong transcription	A549	lung
30	chr16:30970600-30993600	Strong transcription	Rectal Mucosa Donor 29	rectum
31	chr16:30970600-30994600	Strong transcription	Sigmoid Colon	Sigmoid Colon
32	chr16:30970600-30994600	Strong transcription	Thymus	Thymus
33	chr16:30970600-30995400	Strong transcription	H1 Cell Line	embryonic stem cell
34	chr16:30970600-30995400	Strong transcription	Brain Substantia Nigra	brain
35	chr16:30970600-30995400	Strong transcription	Duodenum Mucosa	Duodenum
36	chr16:30970600-30995600	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
37	chr16:30970600-30995800	Strong transcription	HUES6 Cell Line	embryonic stem cell
38	chr16:30970600-30995800	Strong transcription	Left Ventricle	heart
39	chr16:30970600-30996000	Strong transcription	iPS-15b Cell Line	embryonic stem cell
40	chr16:30970600-30996000	Strong transcription	iPS-18 Cell Line	embryonic stem cell
41	chr16:30970600-30996200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
42	chr16:30970600-30996200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
43	chr16:30970600-30996200	Strong transcription	Placenta	Placenta
44	chr16:30970600-30996400	Strong transcription	Fetal Intestine Large	intestine
45	chr16:30970600-30996400	Strong transcription	Fetal Intestine Small	intestine
46	chr16:30970800-30971600	Genic enhancers	Breast Myoepithelial Primary Cells	Breast
47	chr16:30970800-30972000	Strong transcription	Small Intestine	intestine
48	chr16:30970800-30973200	Strong transcription	Primary B cells from cord blood	blood
49	chr16:30970800-30974800	Strong transcription	Fetal Kidney	kidney
50	chr16:30970800-30975600	Strong transcription	Primary monocytes fromperipheralblood	blood

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