Variant report

Variant	rs7103529
Chromosome Location	chr11:58944683-58944684
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr11:58940155..58942428-chr11:58942468..58945192,2	MCF-7	breast:
2	chr11:58944511..58946573-chr11:58949510..58951087,2	K562	blood:
3	chr11:58942359..58944722-chr11:58959370..58962262,2	MCF-7	breast:
4	chr11:58938400..58941160-chr11:58942377..58944826,2	K562	blood:
5	chr11:58939445..58943273-chr11:58944616..58948860,5	MCF-7	breast:

Variant related genes	Relation type
ENSG00000110042	Chromatin interaction

Extended variants
information (count: 6 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:1)

rs_ID	r²[population]
rs2849735	1.00[AMR][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	nsv1050013	chr11:58394598-59221090	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer ZNF genes & repeats Genic enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
2	nsv948365	chr11:58515163-59156405	Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Strong transcription Genic enhancers Enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	59 gene(s)	inside rSNPs	diseases
3	esv2758272	chr11:58700092-59008673	Bivalent/Poised TSS Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
4	esv2759830	chr11:58700092-59008673	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
5	esv1821250	chr11:58925860-59059179	Enhancers Flanking Active TSS Weak transcription Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:80 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:58941200-58949200	Weak transcription	Aorta	Aorta
2	chr11:58941200-58949400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
3	chr11:58941600-58964000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr11:58941800-58945000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr11:58941800-58945600	Weak transcription	Pancreas	Pancrea
6	chr11:58942000-58944800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr11:58942000-58950000	Enhancers	Brain Substantia Nigra	brain
8	chr11:58942200-58946400	Enhancers	Brain Hippocampus Middle	brain
9	chr11:58942200-58949400	Weak transcription	NHLF	lung
10	chr11:58942200-58951600	Weak transcription	Colon Smooth Muscle	Colon
11	chr11:58942400-58946400	Enhancers	Fetal Lung	lung
12	chr11:58942400-58951000	Weak transcription	Muscle Satellite Cultured Cells	--
13	chr11:58942600-58947000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr11:58942600-58948000	Weak transcription	Brain Inferior Temporal Lobe	brain
15	chr11:58942600-58949000	Weak transcription	Spleen	Spleen
16	chr11:58942600-58951000	Weak transcription	Esophagus	oesophagus
17	chr11:58942800-58944800	Enhancers	Lung	lung
18	chr11:58942800-58945400	Genic enhancers	Rectal Mucosa Donor 29	rectum
19	chr11:58942800-58945800	Weak transcription	HUES64 Cell Line	embryonic stem cell
20	chr11:58942800-58946400	Genic enhancers	Fetal Intestine Small	intestine
21	chr11:58942800-58949200	Weak transcription	Brain Germinal Matrix	brain
22	chr11:58943000-58945000	Enhancers	Liver	Liver
23	chr11:58943000-58945600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
24	chr11:58943000-58946200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
25	chr11:58943000-58947800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
26	chr11:58943200-58944800	Enhancers	Adipose Nuclei	Adipose
27	chr11:58943200-58945400	Weak transcription	Primary B cells from cord blood	blood
28	chr11:58943200-58945600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr11:58943200-58946400	Strong transcription	Primary B cells from peripheral blood	blood
30	chr11:58943200-58947000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
31	chr11:58943200-58947800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr11:58943200-58949000	Weak transcription	Gastric	stomach
33	chr11:58943200-58949200	Weak transcription	Brain Angular Gyrus	brain
34	chr11:58943400-58945200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr11:58943400-58945200	Genic enhancers	Duodenum Mucosa	Duodenum
36	chr11:58943400-58945400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr11:58943400-58945400	Enhancers	Ovary	ovary
38	chr11:58943400-58947000	Genic enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr11:58943400-58949000	Weak transcription	HSMM	muscle
40	chr11:58943400-58949400	Weak transcription	Duodenum Smooth Muscle	Duodenum
41	chr11:58943400-58950200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr11:58943400-58952600	Weak transcription	Rectal Smooth Muscle	rectum
43	chr11:58943400-58954800	Weak transcription	Hela-S3	cervix
44	chr11:58943600-58945600	Weak transcription	Brain Cingulate Gyrus	brain
45	chr11:58943600-58945800	Genic enhancers	Fetal Intestine Large	intestine
46	chr11:58943600-58946000	Strong transcription	Fetal Muscle Trunk	muscle
47	chr11:58943600-58947000	Weak transcription	HMEC	breast
48	chr11:58943600-58947400	ZNF genes & repeats	GM12878-XiMat	blood
49	chr11:58943600-58949200	Weak transcription	Colonic Mucosa	Colon
50	chr11:58943600-58975400	Weak transcription	NHEK	skin

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