Variant report

Variant	rs10137272
Chromosome Location	chr14:81973302-81973303
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr14:81970292..81972362-chr14:81972711..81975217,3	K562	blood:

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs10047898	1.00[YRI][hapmap];0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10131720	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10132734	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10142746	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10145556	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10150824	1.00[ASW][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17115576	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28495615	0.95[AFR][1000 genomes]
rs28502051	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56943057	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61404288	1.00[EUR][1000 genomes]
rs73346179	1.00[EUR][1000 genomes]
rs8012824	1.00[EUR][1000 genomes]
rs9323706	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][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	nsv1047694	chr14:81831147-82534026	Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
2	nsv542145	chr14:81831147-82534026	Weak transcription Active TSS Genic enhancers Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats 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	18 gene(s)	inside rSNPs	diseases
3	nsv902120	chr14:81953242-82067555	ZNF genes & repeats Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:124 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:81938400-81973400	Strong transcription	Primary neutrophils fromperipheralblood	blood
2	chr14:81938400-81974000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr14:81938400-81977000	Strong transcription	Monocytes-CD14+_RO01746	blood
4	chr14:81938800-81977600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
5	chr14:81939600-81974600	Strong transcription	Primary monocytes fromperipheralblood	blood
6	chr14:81940600-81975000	Strong transcription	Liver	Liver
7	chr14:81941200-81973800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
8	chr14:81941200-81973800	Strong transcription	Rectal Mucosa Donor 29	rectum
9	chr14:81941400-81975600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
10	chr14:81941600-81974600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr14:81941600-81975000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
12	chr14:81941600-81975200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr14:81941800-81975000	Strong transcription	Primary B cells from peripheral blood	blood
14	chr14:81941800-81985600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
15	chr14:81942000-81975000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr14:81942000-81976600	Strong transcription	Primary T helper cells PMA-I stimulated	--
17	chr14:81942600-81975000	Strong transcription	Primary T helper cells fromperipheralblood	blood
18	chr14:81943400-81976400	Strong transcription	Dnd41	blood
19	chr14:81943600-81977000	Weak transcription	Pancreatic Islets	Pancreatic Islet
20	chr14:81947200-81974800	Strong transcription	Primary T cells fromperipheralblood	blood
21	chr14:81948400-81974400	Strong transcription	Placenta	Placenta
22	chr14:81948600-81975800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
23	chr14:81948800-81973800	Strong transcription	Fetal Thymus	thymus
24	chr14:81948800-81974000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr14:81948800-81977800	Strong transcription	Primary B cells from cord blood	blood
26	chr14:81949600-81975400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr14:81950000-81975400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
28	chr14:81950200-81974600	Strong transcription	Primary T cells from cord blood	blood
29	chr14:81950400-81974800	Strong transcription	Fetal Brain Female	brain
30	chr14:81955600-81973600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
31	chr14:81958400-81976400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr14:81958800-81974800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr14:81959000-81974200	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
34	chr14:81959400-81973400	Strong transcription	Cortex derived primary cultured neurospheres	brain
35	chr14:81960200-81983600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
36	chr14:81960400-81973800	Strong transcription	Brain Angular Gyrus	brain
37	chr14:81960400-81985800	Weak transcription	Stomach Mucosa	stomach
38	chr14:81962600-81977600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
39	chr14:81963000-81973800	Strong transcription	GM12878-XiMat	blood
40	chr14:81963200-81974200	Strong transcription	HSMM	muscle
41	chr14:81964000-81980000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
42	chr14:81964200-81985200	Weak transcription	K562	blood
43	chr14:81964400-81983000	Weak transcription	H9 Cell Line	embryonic stem cell
44	chr14:81966600-81973600	Strong transcription	Sigmoid Colon	Sigmoid Colon
45	chr14:81966800-81973600	Strong transcription	Skeletal Muscle Female	skeletal muscle
46	chr14:81966800-81974800	Strong transcription	HSMMtube	muscle
47	chr14:81966800-81976200	Weak transcription	Psoas Muscle	Psoas
48	chr14:81967000-81973400	Strong transcription	Brain Hippocampus Middle	brain
49	chr14:81967000-81973800	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr14:81967000-81974800	Strong transcription	Fetal Lung	lung

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