Variant report

Variant	rs574535336
Chromosome Location	chr9:2746930-2746931
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:20 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530929	chr9:1998911-2925112	Active TSS Weak transcription Strong transcription Flanking Active TSS Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
2	nsv916750	chr9:2430846-2826706	Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Weak transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
3	nsv1017581	chr9:2494815-3172020	Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
4	nsv539934	chr9:2494815-3172020	Strong transcription Weak transcription Enhancers Genic enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
5	nsv892079	chr9:2681430-2931341	Weak transcription Enhancers Strong transcription Bivalent Enhancer Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
6	nsv531565	chr9:2682523-2784028	Enhancers Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
7	nsv516425	chr9:2690980-2790307	ZNF genes & repeats Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
8	nsv892081	chr9:2691186-2851026	Active TSS Genic enhancers Weak transcription Strong transcription Enhancers ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
9	nsv1032667	chr9:2691667-2788242	Enhancers ZNF genes & repeats Weak transcription Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
10	nsv1019973	chr9:2691812-2790419	Strong transcription Enhancers Genic enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
11	nsv539935	chr9:2691812-2790419	Enhancers Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
12	nsv892082	chr9:2699606-2833267	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases
13	nsv1021572	chr9:2703159-2790123	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
14	nsv1024262	chr9:2703159-3067931	Strong transcription Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
15	nsv1032100	chr9:2720207-2766110	Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
16	nsv1033982	chr9:2724666-2780665	ZNF genes & repeats Strong transcription Weak transcription Flanking Active TSS Enhancers Genic enhancers Bivalent Enhancer Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
17	nsv539936	chr9:2724666-2780665	Strong transcription Enhancers ZNF genes & repeats Weak transcription Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
18	nsv1023850	chr9:2736931-2790123	Strong transcription ZNF genes & repeats Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
19	nsv466087	chr9:2746548-2790307	Strong transcription Genic enhancers Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
20	nsv613142	chr9:2746548-2790307	Strong transcription Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:85 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:2718000-2772800	Weak transcription	Aorta	Aorta
2	chr9:2719200-2768400	Weak transcription	Cortex derived primary cultured neurospheres	brain
3	chr9:2719200-2768400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr9:2723200-2758000	Weak transcription	HSMM	muscle
5	chr9:2723200-2768400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr9:2726200-2768400	Weak transcription	Sigmoid Colon	Sigmoid Colon
7	chr9:2728200-2755600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr9:2728200-2761200	Weak transcription	GM12878-XiMat	blood
9	chr9:2728200-2768400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr9:2728400-2759400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
11	chr9:2728400-2759400	Weak transcription	Skeletal Muscle Female	skeletal muscle
12	chr9:2728600-2758800	Weak transcription	Fetal Lung	lung
13	chr9:2728600-2759200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr9:2728600-2768400	Weak transcription	Primary B cells from cord blood	blood
15	chr9:2728600-2772400	Weak transcription	Brain Hippocampus Middle	brain
16	chr9:2728800-2750600	Weak transcription	HepG2	liver
17	chr9:2729200-2768400	Weak transcription	NHLF	lung
18	chr9:2729200-2768800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
19	chr9:2729600-2747000	Weak transcription	Right Ventricle	heart
20	chr9:2729600-2759200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr9:2729600-2768400	Weak transcription	HMEC	breast
22	chr9:2730000-2759000	Weak transcription	NHDF-Ad	bronchial
23	chr9:2735200-2761200	Weak transcription	H9 Cell Line	embryonic stem cell
24	chr9:2737200-2769400	Weak transcription	Fetal Brain Female	brain
25	chr9:2737200-2777000	Weak transcription	Esophagus	oesophagus
26	chr9:2737800-2768200	Weak transcription	Hela-S3	cervix
27	chr9:2740200-2764200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
28	chr9:2740600-2768400	Weak transcription	Left Ventricle	heart
29	chr9:2740800-2761200	Weak transcription	Osteobl	bone
30	chr9:2741600-2748200	Weak transcription	Primary T cells fromperipheralblood	blood
31	chr9:2742000-2750400	Weak transcription	Small Intestine	intestine
32	chr9:2742200-2758200	Weak transcription	Fetal Muscle Leg	muscle
33	chr9:2742400-2759000	Weak transcription	Colon Smooth Muscle	Colon
34	chr9:2742600-2751800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr9:2742600-2764600	Weak transcription	Brain Substantia Nigra	brain
36	chr9:2743000-2764000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
37	chr9:2743600-2763800	Weak transcription	Primary hematopoietic stem cells	blood
38	chr9:2744000-2747600	Weak transcription	Fetal Intestine Small	intestine
39	chr9:2744000-2747800	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr9:2744000-2759000	Weak transcription	Adipose Nuclei	Adipose
41	chr9:2744400-2749400	Weak transcription	K562	blood
42	chr9:2744600-2752200	Weak transcription	Primary B cells from peripheral blood	blood
43	chr9:2744800-2747200	Weak transcription	Brain Germinal Matrix	brain
44	chr9:2744800-2763600	Weak transcription	Primary T helper cells fromperipheralblood	blood
45	chr9:2745200-2764000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
46	chr9:2745400-2747000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr9:2745600-2747000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr9:2745600-2747200	Strong transcription	Fetal Stomach	stomach
49	chr9:2745600-2747800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr9:2745800-2747000	Strong transcription	Dnd41	blood

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