Variant report

Variant	rs570013746
Chromosome Location	chr1:171295162-171295163
allele	-/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 5 )
Associated
traits (count: 0)

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	nsv1001228	chr1:170885787-171452579	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	23 gene(s)	inside rSNPs	diseases
2	esv14617	chr1:171016086-171726961	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
3	esv10193	chr1:171128845-171414611	Weak transcription Active TSS Enhancers Bivalent Enhancer Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
4	nsv831882	chr1:171166224-171326083	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
5	nsv1002423	chr1:171294384-171376936	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:40 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:171283600-171297800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
2	chr1:171284000-171295200	Weak transcription	Skeletal Muscle Male	skeletal muscle
3	chr1:171284000-171295400	Weak transcription	Stomach Mucosa	stomach
4	chr1:171284000-171312200	Weak transcription	Brain Hippocampus Middle	brain
5	chr1:171284200-171295400	Weak transcription	Esophagus	oesophagus
6	chr1:171284200-171295800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
7	chr1:171284200-171307400	Weak transcription	Primary T cells fromperipheralblood	blood
8	chr1:171284200-171313600	Weak transcription	Right Ventricle	heart
9	chr1:171284200-171313800	Weak transcription	Rectal Mucosa Donor 31	rectum
10	chr1:171286800-171309200	Weak transcription	Placenta Amnion	Placenta Amnion
11	chr1:171288400-171313000	Weak transcription	Gastric	stomach
12	chr1:171288600-171299400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
13	chr1:171288600-171303000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr1:171288600-171303800	Weak transcription	Fetal Muscle Leg	muscle
15	chr1:171288600-171312400	Weak transcription	Sigmoid Colon	Sigmoid Colon
16	chr1:171289400-171299400	Weak transcription	Stomach Smooth Muscle	stomach
17	chr1:171289400-171301000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr1:171289400-171309600	Weak transcription	Primary B cells from cord blood	blood
19	chr1:171289400-171313400	Weak transcription	Fetal Lung	lung
20	chr1:171289600-171295600	Weak transcription	Lung	lung
21	chr1:171289600-171309000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
22	chr1:171289600-171309000	Weak transcription	Pancreas	Pancrea
23	chr1:171289600-171313000	Weak transcription	Adipose Nuclei	Adipose
24	chr1:171289800-171298000	Weak transcription	Primary T helper cells fromperipheralblood	blood
25	chr1:171289800-171298000	Weak transcription	Duodenum Smooth Muscle	Duodenum
26	chr1:171289800-171298200	Weak transcription	Aorta	Aorta
27	chr1:171289800-171299600	Weak transcription	Rectal Smooth Muscle	rectum
28	chr1:171289800-171300200	Weak transcription	Rectal Mucosa Donor 29	rectum
29	chr1:171289800-171300600	Weak transcription	Primary T cells from cord blood	blood
30	chr1:171289800-171309000	Weak transcription	Spleen	Spleen
31	chr1:171289800-171309200	Weak transcription	Left Ventricle	heart
32	chr1:171289800-171312600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr1:171289800-171313000	Weak transcription	Duodenum Mucosa	Duodenum
34	chr1:171290000-171308200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
35	chr1:171290000-171309200	Weak transcription	Ovary	ovary
36	chr1:171290200-171296000	Weak transcription	Fetal Intestine Large	intestine
37	chr1:171292200-171297000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
38	chr1:171294200-171296200	Weak transcription	Liver	Liver
39	chr1:171294400-171297000	Enhancers	Fetal Heart	heart
40	chr1:171295000-171296600	Enhancers	Fetal Intestine Small	intestine

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