Variant report

Variant	rs9841753
Chromosome Location	chr3:143702978-143702979
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr3:143689459..143694662-chr3:143702114..143706390,7	K562	blood:
2	chr3:143701901..143703424-chr3:143714628..143717411,2	K562	blood:
3	chr3:143695188..143697980-chr3:143701408..143704204,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000181744	Chromatin interaction

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:5)

rs_ID	r²[population]
rs11714060	1.00[MEX][hapmap]
rs1319100	1.00[MEX][hapmap]
rs1979911	1.00[MEX][hapmap]
rs2361209	1.00[MEX][hapmap]
rs9822158	1.00[MEX][hapmap]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv877568	chr3:143621140-143992630	Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
2	esv3365190	chr3:143642195-143925886	Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
3	nsv591922	chr3:143645242-143825439	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
4	nsv518814	chr3:143666825-143703750	Flanking Active TSS Weak transcription Enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	31 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:88 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:143692600-143707800	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr3:143692800-143714200	Weak transcription	Small Intestine	intestine
3	chr3:143693400-143706800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
4	chr3:143693400-143708400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
5	chr3:143693400-143708400	Weak transcription	Psoas Muscle	Psoas
6	chr3:143693400-143713800	Weak transcription	H9 Cell Line	embryonic stem cell
7	chr3:143693600-143711600	Weak transcription	Left Ventricle	heart
8	chr3:143694000-143708000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
9	chr3:143694200-143703200	Weak transcription	Placenta	Placenta
10	chr3:143694200-143705600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr3:143694400-143708400	Weak transcription	Fetal Intestine Small	intestine
12	chr3:143694400-143718800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
13	chr3:143694400-143719400	Weak transcription	Hela-S3	cervix
14	chr3:143694800-143707200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
15	chr3:143695600-143710200	Weak transcription	Fetal Brain Male	brain
16	chr3:143695600-143716800	Weak transcription	Skeletal Muscle Female	skeletal muscle
17	chr3:143696200-143703800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
18	chr3:143696400-143711600	Weak transcription	Fetal Brain Female	brain
19	chr3:143696400-143711800	Weak transcription	Fetal Intestine Large	intestine
20	chr3:143696600-143704400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr3:143696800-143706600	Weak transcription	Ovary	ovary
22	chr3:143697000-143708000	Weak transcription	HUVEC	blood vessel
23	chr3:143697000-143708400	Weak transcription	K562	blood
24	chr3:143697000-143713400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr3:143697000-143722800	Weak transcription	Stomach Smooth Muscle	stomach
26	chr3:143697000-143729200	Weak transcription	Aorta	Aorta
27	chr3:143697200-143708400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
28	chr3:143697200-143708400	Weak transcription	HMEC	breast
29	chr3:143697200-143708400	Weak transcription	NHEK	skin
30	chr3:143697200-143710200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
31	chr3:143697200-143712000	Weak transcription	Adipose Nuclei	Adipose
32	chr3:143697200-143723000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr3:143697200-143727800	Weak transcription	Duodenum Smooth Muscle	Duodenum
34	chr3:143697400-143708400	Weak transcription	Rectal Mucosa Donor 29	rectum
35	chr3:143697800-143703200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
36	chr3:143697800-143703400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
37	chr3:143697800-143703600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
38	chr3:143697800-143704400	Weak transcription	Primary T cells from cord blood	blood
39	chr3:143697800-143707800	Weak transcription	Primary hematopoietic stem cells	blood
40	chr3:143697800-143707800	Weak transcription	Dnd41	blood
41	chr3:143697800-143708000	Weak transcription	Liver	Liver
42	chr3:143698000-143711000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
43	chr3:143698200-143708400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
44	chr3:143698400-143708400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
45	chr3:143698400-143708400	Weak transcription	Primary neutrophils fromperipheralblood	blood
46	chr3:143698400-143721200	Weak transcription	Fetal Kidney	kidney
47	chr3:143698600-143704400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr3:143698600-143707800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
49	chr3:143698800-143706200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr3:143698800-143708400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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