Variant report

Variant	rs55833904
Chromosome Location	chr16:81858864-81858865
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 38 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs13335168	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28380426	0.90[AFR][1000 genomes]
rs28546769	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28550771	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28609062	0.81[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28731296	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56134131	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57963515	1.00[ASN][1000 genomes]
rs61635216	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62046684	0.83[AMR][1000 genomes]
rs6564925	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67174651	1.00[ASN][1000 genomes]
rs67283254	1.00[ASN][1000 genomes]
rs68118517	1.00[ASN][1000 genomes]
rs7194131	1.00[ASN][1000 genomes]
rs7204645	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72832045	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72832046	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72832048	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72832051	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72832057	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72832061	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72832066	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72832068	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72832071	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72832080	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8044282	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8059316	1.00[ASN][1000 genomes]
rs8061071	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9922196	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9923151	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9932427	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9933031	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9940462	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9940492	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	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
2	nsv573365	chr16:81804972-81975892	Strong transcription Bivalent/Poised TSS Weak transcription ZNF genes & repeats Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
3	nsv1061544	chr16:81834313-81877375	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:27 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:81850800-81868200	Weak transcription	Esophagus	oesophagus
2	chr16:81855600-81865000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr16:81856000-81864800	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr16:81856800-81862400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr16:81857200-81860600	Enhancers	Primary neutrophils fromperipheralblood	blood
6	chr16:81857200-81864600	Weak transcription	Rectal Mucosa Donor 29	rectum
7	chr16:81857200-81865200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
8	chr16:81857200-81866400	Weak transcription	Right Atrium	heart
9	chr16:81857200-81867400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr16:81857400-81864400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
11	chr16:81857600-81862600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
12	chr16:81857600-81864400	Weak transcription	Duodenum Mucosa	Duodenum
13	chr16:81857800-81861600	Genic enhancers	Primary hematopoietic stem cells short term culture	blood
14	chr16:81858000-81860800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr16:81858000-81864800	Genic enhancers	Primary B cells from peripheral blood	blood
16	chr16:81858200-81860800	Genic enhancers	Primary B cells from cord blood	blood
17	chr16:81858200-81861800	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
18	chr16:81858400-81861600	Weak transcription	Primary hematopoietic stem cells	blood
19	chr16:81858400-81862200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr16:81858400-81862200	Weak transcription	Spleen	Spleen
21	chr16:81858400-81864800	Weak transcription	Thymus	Thymus
22	chr16:81858800-81859800	Weak transcription	Placenta	Placenta
23	chr16:81858800-81860200	Genic enhancers	GM12878-XiMat	blood
24	chr16:81858800-81860600	Weak transcription	Primary monocytes fromperipheralblood	blood
25	chr16:81858800-81860600	Strong transcription	Monocytes-CD14+_RO01746	blood
26	chr16:81858800-81867400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
27	chr16:81858800-81878800	Weak transcription	Fetal Intestine Small	intestine

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