Variant report

Variant	rs112532114
Chromosome Location	chr10:43891601-43891602
allele	C/T
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:11)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:43631919..43634384-chr10:43890115..43892168,2	K562	blood:
2	chr10:43868700..43874062-chr10:43890607..43893448,6	MCF-7	breast:
3	chr10:43696369..43700743-chr10:43891529..43894634,3	K562	blood:
4	chr10:43868968..43875759-chr10:43890269..43893335,11	MCF-7	breast:
5	chr10:43697420..43700683-chr10:43890424..43894292,4	K562	blood:
6	chr10:43891174..43892847-chr10:44101479..44103589,2	K562	blood:
7	chr10:43891265..43892240-chr10:43903154..43903688,2	MCF-7	breast:
8	chr10:43889891..43893674-chr10:43930869..43934431,5	MCF-7	breast:
9	chr10:43887055..43906178-chr10:43946385..43955803,85	K562	blood:
10	chr1:152940729..152943667-chr10:43889848..43892528,2	MCF-7	breast:
11	chr10:43846613..43849361-chr10:43890166..43892037,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000198298	Chromatin interaction
ENSG00000169826	Chromatin interaction
ENSG00000184148	Chromatin interaction
ENSG00000169813	Chromatin interaction
ENSG00000232004	Chromatin interaction
ENSG00000273008	Chromatin interaction
ENSG00000252532	Chromatin interaction
ENSG00000150201	Chromatin interaction
ENSG00000243660	Chromatin interaction
ENSG00000198915	Chromatin interaction

Extended variants
information (count: 7 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv430159	chr10:43291894-43946294	Flanking Active TSS Enhancers Active TSS Strong transcription Weak transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	92 gene(s)	inside rSNPs	diseases
2	nsv895087	chr10:43783339-43982390	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	73 gene(s)	inside rSNPs	diseases
3	nsv831842	chr10:43846541-43987501	Strong transcription Flanking Active TSS Active TSS Weak transcription Enhancers Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	69 gene(s)	inside rSNPs	diseases
4	nsv895088	chr10:43871999-44003101	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
5	nsv825354	chr10:43883418-43949936	Flanking Active TSS Active TSS Enhancers Genic enhancers Weak transcription Transcr. at gene 5' and 3' Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	66 gene(s)	inside rSNPs	diseases
6	nsv825355	chr10:43890579-43923802	Weak transcription Active TSS Flanking Active TSS Enhancers Genic enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	55 gene(s)	inside rSNPs	diseases
7	esv3387789	chr10:43891371-43893919	Flanking Active TSS Active TSS Enhancers Transcr. at gene 5' and 3' Genic enhancers Weak transcription Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:43889000-43892000	Transcr. at gene 5' and 3'	Primary hematopoietic stem cells short term culture	blood
2	chr10:43889000-43892200	Transcr. at gene 5' and 3'	Dnd41	blood
3	chr10:43890000-43892000	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr10:43890200-43891800	Transcr. at gene 5' and 3'	HUES64 Cell Line	embryonic stem cell
5	chr10:43890200-43891800	Flanking Active TSS	HUVEC	blood vessel
6	chr10:43890200-43892000	Transcr. at gene 5' and 3'	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr10:43890200-43892000	Transcr. at gene 5' and 3'	Fetal Intestine Small	intestine
8	chr10:43890400-43891800	Transcr. at gene 5' and 3'	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr10:43890400-43891800	Transcr. at gene 5' and 3'	Fetal Thymus	thymus
10	chr10:43890400-43892000	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
11	chr10:43890400-43892000	Transcr. at gene 5' and 3'	Primary T helper cells PMA-I stimulated	--
12	chr10:43890400-43892200	Transcr. at gene 5' and 3'	Primary T helper 17 cells PMA-I stimulated	--
13	chr10:43890400-43893600	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
14	chr10:43890600-43891800	Flanking Active TSS	Primary T cells from cord blood	blood
15	chr10:43890600-43891800	Transcr. at gene 5' and 3'	K562	blood
16	chr10:43890600-43891800	Transcr. at gene 5' and 3'	Osteobl	bone
17	chr10:43890600-43892000	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
18	chr10:43890600-43892000	Transcr. at gene 5' and 3'	Fetal Stomach	stomach
19	chr10:43890600-43892200	Transcr. at gene 5' and 3'	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr10:43890600-43893000	Active TSS	Fetal Kidney	kidney
21	chr10:43890600-43893200	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
22	chr10:43890600-43893200	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr10:43890800-43891800	Transcr. at gene 5' and 3'	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr10:43890800-43891800	Flanking Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr10:43890800-43891800	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
26	chr10:43890800-43891800	Active TSS	Brain Germinal Matrix	brain
27	chr10:43890800-43891800	Flanking Active TSS	Fetal Brain Male	brain
28	chr10:43890800-43891800	Flanking Active TSS	Fetal Muscle Leg	muscle
29	chr10:43890800-43892200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr10:43890800-43892200	Flanking Active TSS	Adipose Nuclei	Adipose
31	chr10:43890800-43892200	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
32	chr10:43890800-43892200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
33	chr10:43890800-43893200	Active TSS	HSMMtube	muscle
34	chr10:43890800-43893400	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
35	chr10:43890800-43893400	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
36	chr10:43891000-43891800	Transcr. at gene 5' and 3'	Primary mononuclear cells fromperipheralblood	Blood
37	chr10:43891000-43891800	Flanking Active TSS	Brain Substantia Nigra	brain
38	chr10:43891000-43891800	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
39	chr10:43891000-43891800	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
40	chr10:43891000-43892000	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
41	chr10:43891000-43892000	Transcr. at gene 5' and 3'	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr10:43891000-43892000	Flanking Active TSS	Brain Anterior Caudate	brain
43	chr10:43891000-43892000	Flanking Active TSS	Brain Hippocampus Middle	brain
44	chr10:43891000-43892000	Flanking Active TSS	Placenta	Placenta
45	chr10:43891000-43892000	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
46	chr10:43891000-43892000	Transcr. at gene 5' and 3'	Hela-S3	cervix
47	chr10:43891000-43892200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
48	chr10:43891000-43892200	Flanking Active TSS	Primary B cells from cord blood	blood
49	chr10:43891000-43892200	Flanking Active TSS	Primary T cells fromperipheralblood	blood
50	chr10:43891000-43892800	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived

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