Variant report

Variant	rs11211299
Chromosome Location	chr1:46988613-46988614
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:18)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:46913874..46916850-chr1:46987729..46989869,4	K562	blood:
2	chr1:46985914..46991197-chr1:46993744..46997835,5	K562	blood:
3	chr1:46916965..46919039-chr1:46986661..46989583,2	K562	blood:
4	chr1:46985009..46990560-chr1:46990823..46993646,5	K562	blood:
5	chr1:46954395..46956906-chr1:46986850..46988638,2	MCF-7	breast:
6	chr1:46945138..46947370-chr1:46988064..46989764,2	K562	blood:
7	chr1:46874023..46875964-chr1:46987964..46989966,2	MCF-7	breast:
8	chr1:46971533..46973952-chr1:46986776..46988731,3	K562	blood:
9	chr1:46986798..46990832-chr1:46991693..46995331,8	K562	blood:
10	chr1:46919084..46921023-chr1:46985929..46988838,3	K562	blood:
11	chr1:46908155..46911848-chr1:46987375..46989663,3	K562	blood:
12	chr1:46943210..46943796-chr1:46988470..46989208,2	K562	blood:
13	chr1:46908155..46911848-chr1:46987375..46989961,4	K562	blood:
14	chr1:46975501..46977043-chr1:46987288..46989781,2	K562	blood:
15	chr1:46907848..46908563-chr1:46988064..46988933,2	K562	blood:
16	chr1:46945870..46948145-chr1:46988064..46989957,2	K562	blood:
17	chr1:46981951..46984222-chr1:46986722..46989512,3	MCF-7	breast:
18	chr1:46950640..46959255-chr1:46986389..46991936,15	K562	blood:

No data

Variant related genes	Relation type
ENSG00000117480	Chromatin interaction
ENSG00000197587	Chromatin interaction
ENSG00000224863	Chromatin interaction

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:4)

rs_ID	r²[population]
rs17102247	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2025382	0.89[CHB][hapmap]
rs2025384	0.89[CHB][hapmap]
rs35270239	0.89[CHB][hapmap]

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	esv2761743	chr1:46339858-47026743	Active TSS Weak transcription Bivalent Enhancer Enhancers Strong transcription Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	80 gene(s)	inside rSNPs	diseases
2	nsv1001455	chr1:46828004-47326539	Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS Weak transcription Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
3	nsv534950	chr1:46828004-47326539	Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Enhancers Flanking Active TSS Weak transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
4	nsv1000562	chr1:46832451-47027044	Enhancers Bivalent Enhancer Bivalent/Poised TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
5	nsv1015045	chr1:46910546-47067492	Bivalent Enhancer Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
6	nsv534952	chr1:46910546-47067492	Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
7	nsv1009193	chr1:46939999-47085667	Active TSS Bivalent Enhancer Flanking Active TSS Weak transcription Strong transcription Genic enhancers Enhancers 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 target site	17 gene(s)	inside rSNPs	diseases
8	nsv998422	chr1:46969626-47023671	Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Strong transcription Genic enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
9	nsv534953	chr1:46969626-47023671	Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Strong transcription Enhancers Genic enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
10	nsv1010578	chr1:46977818-47010579	Bivalent/Poised TSS Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
11	esv3403110	chr1:46988614-46988778	Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:67 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:46983200-46989800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
2	chr1:46985000-46990200	Enhancers	HMEC	breast
3	chr1:46985800-46989800	Enhancers	Adipose Nuclei	Adipose
4	chr1:46986400-46988800	Enhancers	HSMM	muscle
5	chr1:46986600-46988800	Enhancers	NH-A	brain
6	chr1:46986600-46989000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr1:46986600-46989000	Enhancers	Muscle Satellite Cultured Cells	--
8	chr1:46986600-46990000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr1:46986600-46991200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr1:46986800-46989600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr1:46987000-46988800	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
12	chr1:46987200-46988800	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
13	chr1:46987200-46989000	Enhancers	GM12878-XiMat	blood
14	chr1:46987200-46989800	Flanking Active TSS	K562	blood
15	chr1:46987200-46990600	Enhancers	Esophagus	oesophagus
16	chr1:46987400-46988800	Enhancers	NHDF-Ad	bronchial
17	chr1:46987400-46990200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr1:46987600-46988800	Enhancers	Duodenum Mucosa	Duodenum
19	chr1:46987600-46989200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
20	chr1:46987600-46990400	Enhancers	Stomach Mucosa	stomach
21	chr1:46987800-46988800	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
22	chr1:46987800-46988800	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
23	chr1:46987800-46988800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr1:46987800-46988800	Enhancers	Liver	Liver
25	chr1:46987800-46988800	Flanking Active TSS	Hela-S3	cervix
26	chr1:46987800-46989000	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
27	chr1:46987800-46989000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr1:46987800-46989000	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
29	chr1:46987800-46989000	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
30	chr1:46987800-46989000	Enhancers	Fetal Lung	lung
31	chr1:46987800-46989000	Enhancers	Gastric	stomach
32	chr1:46987800-46989000	Enhancers	Pancreas	Pancrea
33	chr1:46987800-46990000	Enhancers	Breast Myoepithelial Primary Cells	Breast
34	chr1:46987800-46990000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr1:46987800-46991000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
36	chr1:46987800-46993800	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
37	chr1:46988000-46988800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
38	chr1:46988000-46988800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
39	chr1:46988000-46988800	Enhancers	Brain Hippocampus Middle	brain
40	chr1:46988000-46988800	Enhancers	Right Ventricle	heart
41	chr1:46988000-46989000	Enhancers	Skeletal Muscle Female	skeletal muscle
42	chr1:46988000-46989400	Bivalent Enhancer	Placenta	Placenta
43	chr1:46988200-46988800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
44	chr1:46988200-46988800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr1:46988200-46988800	Enhancers	Brain Angular Gyrus	brain
46	chr1:46988200-46988800	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
47	chr1:46988200-46989000	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
48	chr1:46988200-46989000	Enhancers	Ovary	ovary
49	chr1:46988200-46989200	Genic enhancers	Right Atrium	heart
50	chr1:46988400-46988800	Enhancers	Brain Cingulate Gyrus	brain

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