Variant report

Variant	rs192208946
Chromosome Location	chr9:136820100-136820101
allele	A/G
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:12)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:136813385..136817177-chr9:136818574..136821004,3	MCF-7	breast:
2	chr9:136815263..136820961-chr9:136821414..136825553,6	MCF-7	breast:
3	chr9:136818593..136821583-chr9:136825689..136827854,2	MCF-7	breast:
4	chr9:136808878..136810435-chr9:136819072..136822048,2	K562	blood:
5	chr9:136819196..136821510-chr9:136837894..136840389,2	K562	blood:
6	chr9:136813894..136816969-chr9:136817141..136821146,4	MCF-7	breast:
7	chr9:136808221..136810435-chr9:136819072..136822048,3	K562	blood:
8	chr9:136817340..136820147-chr9:136822604..136825397,2	MCF-7	breast:
9	chr9:136819142..136821965-chr9:136822895..136826242,3	K562	blood:
10	chr9:136737400..136743457-chr9:136819359..136829756,12	MCF-7	breast:
11	chr9:136819042..136820561-chr9:136859120..136860817,2	MCF-7	breast:
12	chr9:136809714..136811790-chr9:136818542..136820175,2	MCF-7	breast:

No data

Extended variants
information (count: 16 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:16 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv894123	chr9:136682408-136852501	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
2	nsv894124	chr9:136716399-136870787	Weak transcription Enhancers Active TSS Strong transcription Genic enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
3	nsv894125	chr9:136723520-136931957	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
4	nsv894128	chr9:136753246-136906752	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Genic enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
5	nsv1046310	chr9:136762829-136872226	Enhancers Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
6	nsv894130	chr9:136767346-136906752	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Strong transcription Genic enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
7	nsv831748	chr9:136788484-136944326	Genic enhancers Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
8	nsv894131	chr9:136792765-136906752	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
9	nsv466626	chr9:136807770-136835343	Weak transcription Bivalent Enhancer Flanking Active TSS Strong transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
10	nsv615742	chr9:136807770-136835343	Enhancers Strong transcription Weak transcription Flanking Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
11	nsv831749	chr9:136809200-136915764	Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
12	nsv894132	chr9:136813341-136950691	Active TSS Genic enhancers Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
13	nsv982642	chr9:136819005-136837069	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
14	esv2761297	chr9:136819288-136825744	Enhancers Active TSS Genic enhancers Flanking Active TSS Weak transcription Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
15	esv3400405	chr9:136819556-136822104	Flanking Active TSS Enhancers Weak transcription Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	n/a	inside rSNPs	diseases
16	esv3357357	chr9:136819706-136822004	Weak transcription Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:112 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:136801200-136820200	Weak transcription	Left Ventricle	heart
2	chr9:136801400-136821200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr9:136803200-136821200	Weak transcription	Rectal Mucosa Donor 31	rectum
4	chr9:136803600-136821000	Weak transcription	HUES64 Cell Line	embryonic stem cell
5	chr9:136804200-136820200	Weak transcription	HUES48 Cell Line	embryonic stem cell
6	chr9:136804200-136821000	Weak transcription	Sigmoid Colon	Sigmoid Colon
7	chr9:136804200-136821200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
8	chr9:136809600-136821000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr9:136810400-136821200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr9:136810600-136821200	Weak transcription	Osteobl	bone
11	chr9:136811400-136820200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr9:136811400-136821000	Weak transcription	HMEC	breast
13	chr9:136811800-136821600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr9:136812200-136821800	Weak transcription	Hela-S3	cervix
15	chr9:136813800-136821000	Weak transcription	Gastric	stomach
16	chr9:136814800-136821400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
17	chr9:136815600-136821000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
18	chr9:136816200-136821000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
19	chr9:136816400-136821000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr9:136816600-136820200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr9:136816600-136821000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr9:136816600-136821000	Weak transcription	Rectal Smooth Muscle	rectum
23	chr9:136816600-136821200	Weak transcription	Colon Smooth Muscle	Colon
24	chr9:136816800-136820200	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr9:136816800-136820200	Weak transcription	Stomach Mucosa	stomach
26	chr9:136816800-136821000	Weak transcription	Ovary	ovary
27	chr9:136816800-136821000	Weak transcription	Right Atrium	heart
28	chr9:136817000-136820200	Weak transcription	Brain Germinal Matrix	brain
29	chr9:136817000-136820200	Weak transcription	Colonic Mucosa	Colon
30	chr9:136817000-136821000	Weak transcription	Fetal Lung	lung
31	chr9:136817000-136821000	Weak transcription	NHDF-Ad	bronchial
32	chr9:136817000-136821000	Weak transcription	NHLF	lung
33	chr9:136817000-136824400	Weak transcription	HepG2	liver
34	chr9:136817200-136821000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr9:136818000-136821000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr9:136818200-136821000	Enhancers	Primary B cells from peripheral blood	blood
37	chr9:136818200-136823200	Enhancers	Spleen	Spleen
38	chr9:136818600-136821000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
39	chr9:136818600-136821000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
40	chr9:136818600-136823200	Enhancers	Fetal Muscle Leg	muscle
41	chr9:136818800-136820200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
42	chr9:136819000-136820200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
43	chr9:136819000-136820200	Enhancers	Brain Cingulate Gyrus	brain
44	chr9:136819000-136820400	Enhancers	Brain Angular Gyrus	brain
45	chr9:136819000-136820400	Flanking Active TSS	GM12878-XiMat	blood
46	chr9:136819000-136821000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr9:136819000-136821000	Enhancers	HSMM	muscle
48	chr9:136819000-136822000	Enhancers	HSMMtube	muscle
49	chr9:136819000-136822600	Enhancers	Fetal Brain Male	brain
50	chr9:136819000-136822800	Enhancers	Brain Inferior Temporal Lobe	brain

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