Variant report

Variant	rs9935697
Chromosome Location	chr16:69862152-69862153
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr16:69855648..69859422-chr16:69860178..69863349,3	K562	blood:

Extended variants
information (count: 48 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs13329778	1.00[AMR][1000 genomes]
rs13329812	1.00[AMR][1000 genomes]
rs13330995	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs13332544	1.00[AMR][1000 genomes]
rs13332880	1.00[AMR][1000 genomes]
rs13336041	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs13336357	1.00[AMR][1000 genomes]
rs13338911	1.00[AMR][1000 genomes]
rs13339493	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28402794	1.00[AMR][1000 genomes]
rs28429826	1.00[AMR][1000 genomes]
rs28502677	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28514573	1.00[AMR][1000 genomes]
rs28523536	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28576892	1.00[AMR][1000 genomes]
rs28583989	1.00[AMR][1000 genomes]
rs28610117	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28628240	1.00[AMR][1000 genomes]
rs28651196	1.00[AMR][1000 genomes]
rs28673794	1.00[AMR][1000 genomes]
rs28756357	1.00[AMR][1000 genomes]
rs28803823	1.00[AMR][1000 genomes]
rs28867427	1.00[AMR][1000 genomes]
rs28882509	1.00[AMR][1000 genomes]
rs9921301	1.00[AMR][1000 genomes]
rs9923096	1.00[AMR][1000 genomes]
rs9923471	1.00[AMR][1000 genomes]
rs9924073	1.00[AMR][1000 genomes]
rs9924630	1.00[AMR][1000 genomes]
rs9926382	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9928560	1.00[AMR][1000 genomes]
rs9930692	1.00[AMR][1000 genomes]
rs9931479	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9932104	1.00[AMR][1000 genomes]
rs9933583	1.00[AMR][1000 genomes]
rs9933606	1.00[AMR][1000 genomes]
rs9933745	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9935973	1.00[AMR][1000 genomes]
rs9936451	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9937762	1.00[AMR][1000 genomes]
rs9938552	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]

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	nsv906823	chr16:69711533-69959223	Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
2	nsv1062171	chr16:69854267-70188585	Flanking Active TSS Enhancers Strong transcription Weak transcription Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
3	nsv542941	chr16:69854267-70188585	Weak transcription Active TSS Flanking Active TSS Strong transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
4	nsv1059249	chr16:69854467-70188446	Enhancers Weak transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
5	nsv542942	chr16:69854467-70188446	Weak transcription Strong transcription Active TSS Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS 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 miRNA target site	63 gene(s)	inside rSNPs	diseases
6	esv2758428	chr16:69855122-70313222	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	96 gene(s)	inside rSNPs	diseases
7	esv2758652	chr16:69855122-70313222	Weak transcription Enhancers Bivalent/Poised TSS Strong transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	96 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:106 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:69823800-69874800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
2	chr16:69830600-69864200	Weak transcription	Colon Smooth Muscle	Colon
3	chr16:69830600-69867000	Weak transcription	Right Ventricle	heart
4	chr16:69833800-69864400	Weak transcription	Rectal Smooth Muscle	rectum
5	chr16:69833800-69874600	Weak transcription	Dnd41	blood
6	chr16:69833800-69875600	Weak transcription	NHEK	skin
7	chr16:69834000-69910600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
8	chr16:69834200-69892200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
9	chr16:69836400-69867400	Weak transcription	Colonic Mucosa	Colon
10	chr16:69836800-69864200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr16:69836800-69864400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr16:69837000-69905600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
13	chr16:69837800-69864600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr16:69838600-69873000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
15	chr16:69838800-69864400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr16:69838800-69874400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr16:69844200-69863000	Weak transcription	Esophagus	oesophagus
18	chr16:69846600-69874400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr16:69846600-69875200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr16:69848800-69862800	Weak transcription	Fetal Thymus	thymus
21	chr16:69852000-69862200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr16:69852000-69864200	Strong transcription	Fetal Intestine Small	intestine
23	chr16:69852000-69893200	Weak transcription	K562	blood
24	chr16:69853000-69867600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
25	chr16:69853200-69864600	Weak transcription	Spleen	Spleen
26	chr16:69853200-69864800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr16:69853200-69867200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
28	chr16:69853200-69875000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
29	chr16:69853200-69878400	Weak transcription	H9 Cell Line	embryonic stem cell
30	chr16:69853400-69862800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr16:69853400-69867000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr16:69853400-69867200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr16:69853400-69867200	Weak transcription	HUES6 Cell Line	embryonic stem cell
34	chr16:69853400-69867400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
35	chr16:69853400-69880000	Weak transcription	Hela-S3	cervix
36	chr16:69853600-69867200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
37	chr16:69855200-69863200	Weak transcription	Rectal Mucosa Donor 29	rectum
38	chr16:69855200-69867200	Weak transcription	HSMMtube	muscle
39	chr16:69855200-69873800	Weak transcription	HMEC	breast
40	chr16:69855200-69875600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
41	chr16:69855400-69864400	Weak transcription	Aorta	Aorta
42	chr16:69855400-69867200	Weak transcription	Placenta	Placenta
43	chr16:69855400-69867600	Weak transcription	Gastric	stomach
44	chr16:69855400-69874800	Weak transcription	Brain Germinal Matrix	brain
45	chr16:69855600-69864400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr16:69855600-69864400	Weak transcription	NHLF	lung
47	chr16:69855600-69864800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
48	chr16:69855600-69865200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr16:69855600-69867000	Weak transcription	Cortex derived primary cultured neurospheres	brain
50	chr16:69855600-69867000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain

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