Variant report

Variant	rs16924931
Chromosome Location	chr9:6911935-6911936
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs10114023	1.00[CEU][hapmap];0.84[EUR][1000 genomes]
rs10122648	1.00[CEU][hapmap];0.84[EUR][1000 genomes]
rs10815482	1.00[AFR][1000 genomes];0.90[EUR][1000 genomes]
rs10975897	0.86[JPT][hapmap];0.87[EUR][1000 genomes]
rs2153498	0.82[CEU][hapmap];0.84[CHB][hapmap];0.93[JPT][hapmap];1.00[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs4740862	0.82[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:15 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv870402	chr9:6565246-7016784	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	72 gene(s)	inside rSNPs	diseases
2	nsv1033539	chr9:6566610-7022554	Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Strong transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	72 gene(s)	inside rSNPs	diseases
3	nsv466111	chr9:6567841-7017391	Strong transcription Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	72 gene(s)	inside rSNPs	diseases
4	nsv613208	chr9:6567841-7017391	Flanking Active TSS Weak transcription Enhancers Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	72 gene(s)	inside rSNPs	diseases
5	nsv1024831	chr9:6573752-7018641	Enhancers Weak transcription Strong transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	70 gene(s)	inside rSNPs	diseases
6	nsv892166	chr9:6602821-7222495	Strong transcription Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	71 gene(s)	inside rSNPs	diseases
7	nsv892181	chr9:6680477-7070962	Enhancers Strong transcription Active TSS Weak transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	70 gene(s)	inside rSNPs	diseases
8	nsv1016109	chr9:6712314-6924843	Bivalent/Poised TSS Enhancers Flanking Active TSS Weak transcription Genic enhancers Strong transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
9	nsv613252	chr9:6715730-7022554	Strong transcription Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
10	nsv831499	chr9:6723287-6930933	Active TSS Strong transcription Enhancers Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
11	nsv1023906	chr9:6731786-7372132	Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
12	nsv1023461	chr9:6774993-7022554	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
13	nsv831500	chr9:6847952-6992535	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
14	nsv831501	chr9:6868099-7058526	Weak transcription Enhancers Genic enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
15	nsv892184	chr9:6906384-6985602	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:87 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:6882800-6912000	Weak transcription	Skeletal Muscle Male	skeletal muscle
2	chr9:6889600-6929000	Weak transcription	Colon Smooth Muscle	Colon
3	chr9:6890000-6912000	Weak transcription	Spleen	Spleen
4	chr9:6890000-6987200	Weak transcription	Aorta	Aorta
5	chr9:6893800-6981600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
6	chr9:6894000-6921200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
7	chr9:6894800-6912000	Weak transcription	Fetal Muscle Leg	muscle
8	chr9:6894800-6922000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
9	chr9:6894800-6931600	Weak transcription	Dnd41	blood
10	chr9:6895600-6919800	Weak transcription	Rectal Mucosa Donor 29	rectum
11	chr9:6896200-6959000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
12	chr9:6897600-6932200	Weak transcription	Small Intestine	intestine
13	chr9:6898200-6921200	Weak transcription	Rectal Mucosa Donor 31	rectum
14	chr9:6898200-6928800	Weak transcription	Ovary	ovary
15	chr9:6898200-6930800	Weak transcription	HSMMtube	muscle
16	chr9:6898400-6912000	Weak transcription	Brain Anterior Caudate	brain
17	chr9:6900000-6921200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
18	chr9:6900600-6943000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
19	chr9:6901600-6917400	Weak transcription	Thymus	Thymus
20	chr9:6901600-6944200	Weak transcription	Duodenum Mucosa	Duodenum
21	chr9:6901800-6922000	Weak transcription	Primary T helper cells PMA-I stimulated	--
22	chr9:6901800-6931600	Weak transcription	Fetal Intestine Large	intestine
23	chr9:6902000-6913400	Weak transcription	K562	blood
24	chr9:6902000-6923800	Weak transcription	Fetal Intestine Small	intestine
25	chr9:6902800-6912000	Weak transcription	Right Ventricle	heart
26	chr9:6902800-6931000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
27	chr9:6903000-6912000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr9:6903000-6916800	Weak transcription	GM12878-XiMat	blood
29	chr9:6903000-6921800	Weak transcription	NHEK	skin
30	chr9:6903000-6938600	Weak transcription	Primary monocytes fromperipheralblood	blood
31	chr9:6903200-6920000	Weak transcription	HSMM	muscle
32	chr9:6903600-6912400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr9:6906000-6912000	Weak transcription	Primary T helper cells fromperipheralblood	blood
34	chr9:6906000-6921200	Weak transcription	Monocytes-CD14+_RO01746	blood
35	chr9:6906400-6919800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr9:6906400-6933200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr9:6906600-6917000	Weak transcription	Primary B cells from peripheral blood	blood
38	chr9:6906600-6938200	Weak transcription	Adipose Nuclei	Adipose
39	chr9:6906800-6915600	Weak transcription	Primary T cells from cord blood	blood
40	chr9:6907000-6915600	Weak transcription	H1 Cell Line	embryonic stem cell
41	chr9:6908200-6912000	Weak transcription	HUES6 Cell Line	embryonic stem cell
42	chr9:6908600-6914600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
43	chr9:6908800-6915600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
44	chr9:6908800-6942600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
45	chr9:6909000-6915200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
46	chr9:6909400-6913400	Weak transcription	Primary B cells from cord blood	blood
47	chr9:6909600-6915400	Weak transcription	Fetal Heart	heart
48	chr9:6910800-6918600	Weak transcription	HepG2	liver
49	chr9:6911000-6913400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
50	chr9:6911400-6914400	Weak transcription	HUES48 Cell Line	embryonic stem cell

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