Variant report

Variant	rs150463722
Chromosome Location	chr11:35179675-35179676
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:13 , 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	nsv540999	chr11:35021936-35185471	Weak transcription Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
3	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
4	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
5	nsv541000	chr11:35053717-35185471	Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
6	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
7	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
8	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
9	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
10	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
11	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
12	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
13	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:102 , 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	chr11:35163800-35183400	Genic enhancers	Primary B cells from peripheral blood	blood
3	chr11:35167200-35179800	Weak transcription	Fetal Lung	lung
4	chr11:35167400-35185800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
5	chr11:35167600-35184200	Genic enhancers	Primary T cells fromperipheralblood	blood
6	chr11:35167600-35186200	Genic enhancers	NHDF-Ad	bronchial
7	chr11:35167600-35186400	Genic enhancers	HMEC	breast
8	chr11:35167800-35185800	Genic enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr11:35172200-35196000	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr11:35173400-35180600	Genic enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
11	chr11:35174200-35180000	Weak transcription	HSMMtube	muscle
12	chr11:35174400-35179800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr11:35174400-35180400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr11:35174400-35184000	Weak transcription	GM12878-XiMat	blood
15	chr11:35175200-35180200	Enhancers	Primary T helper naive cells from peripheral blood	blood
16	chr11:35175800-35180800	Weak transcription	Primary neutrophils fromperipheralblood	blood
17	chr11:35175800-35181800	Enhancers	Duodenum Mucosa	Duodenum
18	chr11:35176600-35182000	Enhancers	Sigmoid Colon	Sigmoid Colon
19	chr11:35176600-35184000	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
20	chr11:35177600-35180400	Strong transcription	Monocytes-CD14+_RO01746	blood
21	chr11:35177600-35182200	Enhancers	Colon Smooth Muscle	Colon
22	chr11:35177600-35191000	Genic enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr11:35177800-35179800	Enhancers	Primary T killer memory cells from peripheral blood	blood
24	chr11:35177800-35182600	Genic enhancers	Primary monocytes fromperipheralblood	blood
25	chr11:35177800-35186600	Genic enhancers	Osteobl	bone
26	chr11:35178000-35180000	Enhancers	Primary T helper cells fromperipheralblood	blood
27	chr11:35178000-35180600	Transcr. at gene 5' and 3'	Primary T helper 17 cells PMA-I stimulated	--
28	chr11:35178000-35180600	Enhancers	Pancreas	Pancrea
29	chr11:35178000-35181600	Enhancers	Adipose Nuclei	Adipose
30	chr11:35178000-35183000	Genic enhancers	Fetal Muscle Leg	muscle
31	chr11:35178200-35179800	Enhancers	Thymus	Thymus
32	chr11:35178200-35180200	Enhancers	Spleen	Spleen
33	chr11:35178200-35181200	Enhancers	Skeletal Muscle Female	skeletal muscle
34	chr11:35178200-35181400	Genic enhancers	Primary T cells from cord blood	blood
35	chr11:35178400-35180600	Enhancers	Esophagus	oesophagus
36	chr11:35178400-35182000	Genic enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr11:35178600-35181600	Enhancers	Rectal Mucosa Donor 31	rectum
38	chr11:35178800-35180400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
39	chr11:35178800-35181200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr11:35179000-35180200	Enhancers	Breast Myoepithelial Primary Cells	Breast
41	chr11:35179000-35180800	Enhancers	Psoas Muscle	Psoas
42	chr11:35179000-35180800	Enhancers	HUVEC	blood vessel
43	chr11:35179000-35181200	Enhancers	Aorta	Aorta
44	chr11:35179000-35181800	Enhancers	Placenta	Placenta
45	chr11:35179000-35182000	Enhancers	Left Ventricle	heart
46	chr11:35179000-35186200	Genic enhancers	Hela-S3	cervix
47	chr11:35179000-35186400	Genic enhancers	NHLF	lung
48	chr11:35179200-35179800	Enhancers	HUES48 Cell Line	embryonic stem cell
49	chr11:35179200-35179800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr11:35179200-35180000	Transcr. at gene 5' and 3'	NHEK	skin

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