Variant report

Variant	rs16851521
Chromosome Location	chr3:105445380-105445381
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 40 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs16851398	1.00[AMR][1000 genomes]
rs16851409	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16851417	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16851429	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16851434	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16851455	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16851457	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16851530	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16851542	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16851557	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16851606	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs35835913	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs55804660	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56323302	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56405245	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60520841	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72993723	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72995636	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72995638	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72995651	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72995660	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72995662	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72995690	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72995701	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72995702	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72997617	0.92[AFR][1000 genomes]
rs72997628	1.00[AMR][1000 genomes]
rs7612706	1.00[AMR][1000 genomes]
rs7634544	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv877306	chr3:105372196-105495841	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	nsv877307	chr3:105373836-105465189	Enhancers Genic enhancers Strong transcription Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv591242	chr3:105373836-105470134	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv877308	chr3:105373836-105495841	Strong transcription Weak transcription ZNF genes & repeats Enhancers Genic enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv877309	chr3:105373836-105542435	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
6	esv2755185	chr3:105378310-105597310	Strong transcription Weak transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
7	nsv877310	chr3:105409321-105495841	ZNF genes & repeats Flanking Active TSS Weak transcription Strong transcription Genic enhancers Enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
8	nsv591243	chr3:105438320-105470134	Strong transcription Enhancers Weak transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	n/a	inside rSNPs	diseases
9	nsv591244	chr3:105438320-105495841	ZNF genes & repeats Genic enhancers Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	n/a	inside rSNPs	diseases
10	nsv591245	chr3:105438806-105469882	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	n/a	inside rSNPs	diseases
11	nsv591246	chr3:105439522-105504129	ZNF genes & repeats Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:98 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:105375800-105464600	Weak transcription	Small Intestine	intestine
2	chr3:105378000-105455400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr3:105389200-105467200	Weak transcription	Stomach Mucosa	stomach
4	chr3:105407800-105457800	Weak transcription	HepG2	liver
5	chr3:105420800-105445600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr3:105421200-105465400	Weak transcription	Colonic Mucosa	Colon
7	chr3:105432800-105463800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
8	chr3:105433600-105465600	Weak transcription	H1 Cell Line	embryonic stem cell
9	chr3:105433800-105445400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr3:105434400-105446600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
11	chr3:105434800-105463800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
12	chr3:105438800-105464000	Weak transcription	Placenta Amnion	Placenta Amnion
13	chr3:105438800-105465400	Weak transcription	Fetal Heart	heart
14	chr3:105439000-105445400	Weak transcription	Fetal Lung	lung
15	chr3:105439000-105446200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr3:105439000-105447200	Weak transcription	HSMM	muscle
17	chr3:105439000-105450600	Weak transcription	Rectal Mucosa Donor 31	rectum
18	chr3:105439000-105457800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
19	chr3:105439000-105461600	Weak transcription	Dnd41	blood
20	chr3:105439000-105464000	Weak transcription	Duodenum Mucosa	Duodenum
21	chr3:105439000-105464200	Weak transcription	HUES48 Cell Line	embryonic stem cell
22	chr3:105439000-105465400	Weak transcription	Colon Smooth Muscle	Colon
23	chr3:105439000-105465800	Weak transcription	NHLF	lung
24	chr3:105439000-105466200	Weak transcription	H9 Cell Line	embryonic stem cell
25	chr3:105439000-105466600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
26	chr3:105439000-105471200	Weak transcription	Fetal Thymus	thymus
27	chr3:105439000-105471400	Weak transcription	HUES6 Cell Line	embryonic stem cell
28	chr3:105439000-105471400	Weak transcription	HMEC	breast
29	chr3:105439000-105471600	Weak transcription	Fetal Brain Male	brain
30	chr3:105439000-105475800	Weak transcription	Esophagus	oesophagus
31	chr3:105439000-105477400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
32	chr3:105439000-105477400	Weak transcription	Lung	lung
33	chr3:105439000-105477400	Weak transcription	Skeletal Muscle Female	skeletal muscle
34	chr3:105439200-105445400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr3:105439200-105445400	Weak transcription	Gastric	stomach
36	chr3:105439200-105445600	Weak transcription	Placenta	Placenta
37	chr3:105439200-105446200	Weak transcription	HUES64 Cell Line	embryonic stem cell
38	chr3:105439200-105446200	Weak transcription	Fetal Muscle Leg	muscle
39	chr3:105439200-105447200	Weak transcription	Rectal Mucosa Donor 29	rectum
40	chr3:105439200-105447400	Weak transcription	Fetal Kidney	kidney
41	chr3:105439200-105447600	Weak transcription	Adipose Nuclei	Adipose
42	chr3:105439200-105447800	Weak transcription	Fetal Intestine Large	intestine
43	chr3:105439200-105448600	Weak transcription	Aorta	Aorta
44	chr3:105439200-105449800	Weak transcription	NHDF-Ad	bronchial
45	chr3:105439200-105450400	Weak transcription	Sigmoid Colon	Sigmoid Colon
46	chr3:105439200-105450600	Weak transcription	Duodenum Smooth Muscle	Duodenum
47	chr3:105439200-105452200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
48	chr3:105439200-105457800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
49	chr3:105439200-105457800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr3:105439200-105457800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood

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