Variant report

Variant	rs16852327
Chromosome Location	chr3:142122144-142122145
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr3:142115156..142117920-chr3:142121507..142123536,2	K562	blood:
2	chr3:142114882..142116518-chr3:142121327..142122867,2	MCF-7	breast:
3	chr3:142121474..142124130-chr3:142126023..142128529,2	MCF-7	breast:
4	chr3:142116420..142117922-chr3:142120653..142123536,2	K562	blood:

Variant related genes	Relation type
ENSG00000251804	Chromatin interaction

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs16852330	1.00[MEX][hapmap]
rs4462984	1.00[ASW][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs55712145	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs55720941	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs55810370	0.82[AFR][1000 genomes]
rs56044159	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56791995	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58286086	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58978582	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59954506	0.87[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs60153076	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61076760	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61265290	0.95[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs6440079	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6440080	1.00[ASW][hapmap];0.82[LWK][hapmap];1.00[MEX][hapmap];0.92[YRI][hapmap];0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6440081	0.96[AFR][1000 genomes]
rs6796807	1.00[ASW][hapmap];0.82[LWK][hapmap];1.00[MEX][hapmap];0.91[YRI][hapmap];0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6797767	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73864538	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73864539	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73864541	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73867022	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73867024	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73867035	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73867040	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73867041	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7618139	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949709	chr3:141295050-142178144	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers Active TSS Bivalent Enhancer 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 target site	61 gene(s)	inside rSNPs	diseases
2	esv2757892	chr3:141728870-142129836	Weak transcription Active TSS Strong transcription Genic enhancers ZNF genes & repeats Enhancers Flanking Active TSS 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	26 gene(s)	inside rSNPs	diseases
3	esv2759182	chr3:141728870-142129836	Enhancers Strong transcription Flanking Active TSS Weak transcription ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
4	nsv522549	chr3:141812759-142164735	Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
5	nsv877556	chr3:141898980-142331360	Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	51 gene(s)	inside rSNPs	diseases
6	nsv523945	chr3:141933649-142219542	Enhancers Genic enhancers Strong transcription Flanking Active TSS Weak transcription Active TSS 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	25 gene(s)	inside rSNPs	diseases
7	nsv1000083	chr3:141956718-142172666	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS Genic 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 target site	11 gene(s)	inside rSNPs	diseases
8	nsv877557	chr3:142090402-142150204	Strong transcription Weak transcription Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region miRNA target site	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:121 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:142076000-142136400	Weak transcription	H1 Cell Line	embryonic stem cell
2	chr3:142076800-142138200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr3:142083600-142158600	Weak transcription	NHEK	skin
4	chr3:142105000-142151800	Strong transcription	Primary T helper cells fromperipheralblood	blood
5	chr3:142105600-142123000	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
6	chr3:142105800-142136600	Strong transcription	Fetal Intestine Large	intestine
7	chr3:142106800-142123000	Weak transcription	Fetal Brain Male	brain
8	chr3:142106800-142150800	Weak transcription	H9 Cell Line	embryonic stem cell
9	chr3:142109200-142141800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr3:142112200-142133200	Strong transcription	Duodenum Mucosa	Duodenum
11	chr3:142112200-142145000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr3:142112200-142145400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr3:142112200-142151600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
14	chr3:142112200-142152000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
15	chr3:142112200-142152200	Strong transcription	Primary T cells fromperipheralblood	blood
16	chr3:142112200-142154600	Strong transcription	Monocytes-CD14+_RO01746	blood
17	chr3:142112400-142142400	Strong transcription	Rectal Mucosa Donor 31	rectum
18	chr3:142112400-142146600	Strong transcription	Primary neutrophils fromperipheralblood	blood
19	chr3:142112600-142141600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr3:142112600-142150600	Strong transcription	Placenta	Placenta
21	chr3:142112800-142142800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr3:142113000-142152200	Strong transcription	Primary monocytes fromperipheralblood	blood
23	chr3:142113400-142151800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr3:142113400-142151800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr3:142114600-142126600	Weak transcription	Fetal Heart	heart
26	chr3:142114800-142151800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr3:142115200-142126600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
28	chr3:142115200-142129400	Weak transcription	Small Intestine	intestine
29	chr3:142115800-142123200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
30	chr3:142115800-142123400	Weak transcription	K562	blood
31	chr3:142115800-142125200	Weak transcription	Psoas Muscle	Psoas
32	chr3:142115800-142125400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr3:142115800-142125400	Weak transcription	Aorta	Aorta
34	chr3:142115800-142125400	Weak transcription	Lung	lung
35	chr3:142115800-142125400	Weak transcription	Spleen	Spleen
36	chr3:142115800-142126600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
37	chr3:142115800-142126600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
38	chr3:142115800-142126800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
39	chr3:142115800-142126800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
40	chr3:142115800-142127000	Weak transcription	Gastric	stomach
41	chr3:142115800-142128200	Weak transcription	Hela-S3	cervix
42	chr3:142115800-142134800	Weak transcription	Right Ventricle	heart
43	chr3:142115800-142136400	Weak transcription	Pancreatic Islets	Pancreatic Islet
44	chr3:142115800-142138000	Weak transcription	Esophagus	oesophagus
45	chr3:142116000-142123600	Weak transcription	Brain Germinal Matrix	brain
46	chr3:142116000-142126800	Weak transcription	A549	lung
47	chr3:142116000-142127000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
48	chr3:142116200-142123600	Weak transcription	Brain Angular Gyrus	brain
49	chr3:142116200-142125400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr3:142116200-142126400	Weak transcription	iPS-20b Cell Line	embryonic stem cell

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