Variant report

Variant	rs353628
Chromosome Location	chr11:35188507-35188508
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr11:35160960..35162794-chr11:35186248..35188654,2	MCF-7	breast:
2	chr11:35187046..35189640-chr11:35384110..35385949,2	MCF-7	breast:
3	chr11:35183121..35185456-chr11:35188061..35190243,2	MCF-7	breast:
4	chr11:35186608..35189447-chr11:35199235..35201624,2	MCF-7	breast:

Extended variants
information (count: 25 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs102518	1.00[CEU][hapmap];0.88[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs193276	1.00[CEU][hapmap];0.84[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs353612	0.84[CEU][hapmap]
rs353629	0.89[CEU][hapmap];0.88[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs353631	1.00[CEU][hapmap];0.88[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs353632	1.00[CEU][hapmap];0.88[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs353636	1.00[CEU][hapmap];0.89[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs353638	0.95[CEU][hapmap];0.89[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs353639	1.00[CEU][hapmap];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs353641	1.00[CEU][hapmap];0.84[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs353642	1.00[CEU][hapmap];0.83[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs353643	0.89[CEU][hapmap];0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs3794108	0.86[CHB][hapmap]
rs3794116	0.86[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	nsv1045837	chr11:34893992-35395190	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
2	esv2758263	chr11:35029933-35226784	Genic enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
3	esv2759818	chr11:35029933-35238578	Enhancers Strong transcription Weak transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
4	nsv541001	chr11:35053717-35224624	Weak transcription Enhancers Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
5	esv2757437	chr11:35067482-35238578	Weak transcription Enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
6	esv2752912	chr11:35074167-35238578	Weak transcription Flanking Active TSS Active TSS Strong transcription Enhancers Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
7	nsv508623	chr11:35094933-35203363	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
8	nsv541002	chr11:35101282-35224624	Weak transcription Flanking Active TSS Genic enhancers Enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
9	nsv541003	chr11:35122694-35261451	Genic enhancers Flanking Active TSS Enhancers Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
10	nsv541004	chr11:35122694-35297414	Strong transcription Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
11	esv3693078	chr11:35179651-35217745	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:104 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:35161200-35197400	Transcr. at gene 5' and 3'	Primary T helper cells PMA-I stimulated	--
2	chr11:35172200-35196000	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr11:35177600-35191000	Genic enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr11:35180800-35189400	Weak transcription	Fetal Intestine Small	intestine
5	chr11:35182600-35190200	Enhancers	Primary monocytes fromperipheralblood	blood
6	chr11:35184000-35190200	Enhancers	Rectal Mucosa Donor 31	rectum
7	chr11:35184200-35189600	Enhancers	Pancreas	Pancrea
8	chr11:35184400-35191000	Enhancers	Fetal Stomach	stomach
9	chr11:35185000-35188600	Enhancers	Colonic Mucosa	Colon
10	chr11:35185600-35190600	Enhancers	Small Intestine	intestine
11	chr11:35185600-35194200	Weak transcription	HUES64 Cell Line	embryonic stem cell
12	chr11:35185800-35189200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr11:35186200-35189400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr11:35186200-35189600	Enhancers	HUVEC	blood vessel
15	chr11:35186200-35191400	Weak transcription	Fetal Kidney	kidney
16	chr11:35186400-35188600	Enhancers	Stomach Mucosa	stomach
17	chr11:35186400-35188600	Flanking Active TSS	Dnd41	blood
18	chr11:35186400-35189600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
19	chr11:35186400-35189800	Enhancers	Left Ventricle	heart
20	chr11:35186400-35190400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
21	chr11:35186600-35188600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr11:35186600-35189200	Flanking Active TSS	A549	lung
23	chr11:35186600-35194600	Weak transcription	Gastric	stomach
24	chr11:35186800-35188600	Enhancers	Cortex derived primary cultured neurospheres	brain
25	chr11:35186800-35188800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr11:35186800-35193000	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
27	chr11:35187000-35188600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr11:35187000-35188800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
29	chr11:35187000-35189800	Enhancers	Placenta	Placenta
30	chr11:35187000-35190400	Enhancers	Skeletal Muscle Male	skeletal muscle
31	chr11:35187200-35188600	Flanking Active TSS	Primary B cells from cord blood	blood
32	chr11:35187200-35188800	Flanking Active TSS	Muscle Satellite Cultured Cells	--
33	chr11:35187200-35189600	Flanking Active TSS	Hela-S3	cervix
34	chr11:35187400-35188600	Flanking Active TSS	HMEC	breast
35	chr11:35187400-35189400	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr11:35187400-35190800	Enhancers	Fetal Lung	lung
37	chr11:35187400-35192800	Enhancers	Skeletal Muscle Female	skeletal muscle
38	chr11:35187600-35188600	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
39	chr11:35187600-35188800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr11:35187600-35188800	Flanking Active TSS	NH-A	brain
41	chr11:35187600-35188800	Transcr. at gene 5' and 3'	NHEK	skin
42	chr11:35187600-35188800	Flanking Active TSS	Osteobl	bone
43	chr11:35187600-35189400	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr11:35187600-35189600	Enhancers	Brain Hippocampus Middle	brain
45	chr11:35187800-35188600	Flanking Active TSS	Primary T cells fromperipheralblood	blood
46	chr11:35187800-35188600	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
47	chr11:35187800-35188600	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
48	chr11:35187800-35188600	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
49	chr11:35187800-35188600	Enhancers	Stomach Smooth Muscle	stomach
50	chr11:35187800-35188600	Flanking Active TSS	GM12878-XiMat	blood

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