Variant report

Variant	rs1148182
Chromosome Location	chr10:28616419-28616420
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr10:28616149..28619065-chr10:28621804..28623481,2	K562	blood:

Variant related genes	Relation type
ENSG00000150054	Chromatin interaction

Extended variants
information (count: 48 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:43)

rs_ID	r²[population]
rs11006935	0.82[CHB][hapmap]
rs11006941	0.82[CHB][hapmap]
rs11006942	0.82[CHB][hapmap]
rs1148177	0.88[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1148178	0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1148179	0.99[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1148180	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1148181	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1148183	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1148185	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.96[LWK][hapmap];0.99[MKK][hapmap];0.93[TSI][hapmap];0.81[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1148186	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1148187	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1148189	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12098315	0.96[ASN][1000 genomes]
rs12098714	0.83[ASN][1000 genomes]
rs12098807	0.96[ASN][1000 genomes]
rs12254745	0.82[CHB][hapmap]
rs1249340	0.86[ASN][1000 genomes]
rs1249347	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1249348	0.99[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1273097	0.99[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs16928633	0.82[CHB][hapmap]
rs1762188	0.86[ASN][1000 genomes]
rs2100614	1.00[CHB][hapmap]
rs2447629	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs34827546	0.96[ASN][1000 genomes]
rs61845947	0.93[ASN][1000 genomes]
rs703015	0.80[ASN][1000 genomes]
rs7078271	0.82[CHB][hapmap]
rs7100335	0.82[CHB][hapmap]
rs72803699	0.93[ASN][1000 genomes]
rs72805609	1.00[ASN][1000 genomes]
rs72805627	0.96[ASN][1000 genomes]
rs72805630	0.90[ASN][1000 genomes]
rs72805631	0.86[ASN][1000 genomes]
rs786392	0.80[ASN][1000 genomes]
rs786397	0.80[ASN][1000 genomes]
rs786399	0.80[ASN][1000 genomes]
rs7898888	1.00[JPT][hapmap]
rs7911615	0.82[CHB][hapmap]
rs7916525	0.82[CHB][hapmap]
rs811496	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs813081	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv917149	chr10:28018919-28688694	Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
2	nsv1041555	chr10:28419399-29304934	Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Genic enhancers Strong transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
3	nsv1037863	chr10:28419399-29378871	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
4	nsv540521	chr10:28419399-29378871	Flanking Active TSS Enhancers Weak transcription Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
5	nsv1044938	chr10:28601993-28659440	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:84 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:28596800-28618800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
2	chr10:28614000-28619000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
3	chr10:28614600-28617800	Enhancers	Fetal Stomach	stomach
4	chr10:28614800-28617000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
5	chr10:28614800-28620600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
6	chr10:28615000-28617000	Enhancers	Primary hematopoietic stem cells	blood
7	chr10:28615000-28617000	Enhancers	Primary T helper naive cells from peripheral blood	blood
8	chr10:28615000-28620000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
9	chr10:28615200-28616800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr10:28615200-28616800	Enhancers	Primary B cells from cord blood	blood
11	chr10:28615200-28616800	Enhancers	Primary T killer memory cells from peripheral blood	blood
12	chr10:28615200-28616800	Enhancers	Esophagus	oesophagus
13	chr10:28615200-28617000	Enhancers	iPS-18 Cell Line	embryonic stem cell
14	chr10:28615200-28617000	Enhancers	Primary hematopoietic stem cells short term culture	blood
15	chr10:28615200-28617000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr10:28615200-28617000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
17	chr10:28615200-28617000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr10:28615200-28617200	Enhancers	Primary T helper cells fromperipheralblood	blood
19	chr10:28615200-28617400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr10:28615200-28619200	Enhancers	Primary T helper cells PMA-I stimulated	--
21	chr10:28615200-28621000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
22	chr10:28615400-28616800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr10:28615400-28617000	Enhancers	ES-I3 Cell Line	embryonic stem cell
24	chr10:28615400-28617000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
25	chr10:28615400-28617000	Enhancers	HUES64 Cell Line	embryonic stem cell
26	chr10:28615400-28617000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr10:28615400-28617000	Enhancers	Breast Myoepithelial Primary Cells	Breast
28	chr10:28615400-28617000	Enhancers	Primary monocytes fromperipheralblood	blood
29	chr10:28615400-28617000	Enhancers	Sigmoid Colon	Sigmoid Colon
30	chr10:28615400-28617000	Enhancers	Stomach Mucosa	stomach
31	chr10:28615400-28617400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr10:28615400-28617600	Enhancers	Muscle Satellite Cultured Cells	--
33	chr10:28615600-28616600	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
34	chr10:28615600-28616800	Enhancers	H9 Cell Line	embryonic stem cell
35	chr10:28615600-28616800	Enhancers	HUES6 Cell Line	embryonic stem cell
36	chr10:28615600-28616800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
37	chr10:28615600-28616800	Enhancers	Placenta Amnion	Placenta Amnion
38	chr10:28615600-28617000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
39	chr10:28615600-28617000	Enhancers	H1 Cell Line	embryonic stem cell
40	chr10:28615600-28617000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr10:28615600-28617000	Enhancers	iPS-15b Cell Line	embryonic stem cell
42	chr10:28615600-28617000	Enhancers	iPS-20b Cell Line	embryonic stem cell
43	chr10:28615600-28617200	Enhancers	NH-A	brain
44	chr10:28615600-28617400	Enhancers	Primary T cells from cord blood	blood
45	chr10:28615600-28617400	Enhancers	HMEC	breast
46	chr10:28615800-28616800	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr10:28615800-28617000	Enhancers	Aorta	Aorta
48	chr10:28615800-28617000	Enhancers	Brain Substantia Nigra	brain
49	chr10:28615800-28617000	Enhancers	HUVEC	blood vessel
50	chr10:28615800-28617000	Enhancers	NHDF-Ad	bronchial

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