Variant report

Variant	rs11865702
Chromosome Location	chr16:70681298-70681299
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr16:70680910..70683567-chr16:70688856..70691172,2	K562	blood:
2	chr16:70681076..70682967-chr16:70686271..70687994,2	K562	blood:
3	chr16:70681046..70683051-chr16:70685956..70688661,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000157368	Chromatin interaction

Extended variants
information (count: 42 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs11075774	0.83[AFR][1000 genomes]
rs12051132	0.85[ASN][1000 genomes]
rs12596022	0.85[ASN][1000 genomes]
rs12596821	0.83[ASN][1000 genomes]
rs12596851	0.84[ASN][1000 genomes]
rs12596861	0.83[ASN][1000 genomes]
rs12596931	0.86[ASN][1000 genomes]
rs12599245	0.86[ASN][1000 genomes]
rs12708905	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12917749	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12924106	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12928124	0.86[AMR][1000 genomes];0.83[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs13330163	0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1993448	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs28393835	0.81[AFR][1000 genomes]
rs2864754	0.99[EUR][1000 genomes]
rs34538878	0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs34878593	0.80[ASN][1000 genomes]
rs3813904	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4985412	0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4985539	0.85[ASN][1000 genomes]
rs4985540	0.86[ASN][1000 genomes]
rs4985548	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4985555	0.82[AFR][1000 genomes];0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6499328	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6499329	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6499330	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7193968	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs72792838	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs8053536	0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs8061569	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8061854	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv517391	chr16:70666410-70840490	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
2	nsv457517	chr16:70666722-70840490	Strong transcription Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
3	nsv572945	chr16:70666722-70840490	Weak transcription Genic enhancers Flanking Active TSS Enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats 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	30 gene(s)	inside rSNPs	diseases
4	nsv906874	chr16:70677785-70740707	Weak transcription Flanking Active TSS Enhancers Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
5	nsv906875	chr16:70677785-70742536	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Genic enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
6	nsv906876	chr16:70677785-70757555	Active TSS Flanking Active TSS Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
7	nsv906877	chr16:70677785-70766378	Enhancers Genic enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS 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 miRNA target site	18 gene(s)	inside rSNPs	diseases
8	nsv906878	chr16:70677785-70782922	Strong transcription Enhancers Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS 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	19 gene(s)	inside rSNPs	diseases
9	nsv906879	chr16:70677785-70790831	Flanking Active TSS Weak transcription Enhancers Strong transcription Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
10	nsv906880	chr16:70677785-70796515	Flanking Active TSS Enhancers Active TSS Strong transcription Weak transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs11865702	CLEC18A	cis	Skin Sun Exposed Lower leg	GTEx

Chromatin state (count:42 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:70669600-70687800	Weak transcription	Right Atrium	heart
2	chr16:70673600-70683200	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr16:70673600-70684000	Weak transcription	Esophagus	oesophagus
4	chr16:70673800-70682800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr16:70679600-70681400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
6	chr16:70679800-70682400	Enhancers	Fetal Brain Male	brain
7	chr16:70680000-70682000	Enhancers	Fetal Muscle Leg	muscle
8	chr16:70680000-70687200	Strong transcription	Fetal Intestine Small	intestine
9	chr16:70680200-70681400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr16:70680200-70681400	Flanking Active TSS	Muscle Satellite Cultured Cells	--
11	chr16:70680200-70681800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr16:70680200-70681800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr16:70680200-70681800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
14	chr16:70680200-70681800	Enhancers	Ovary	ovary
15	chr16:70680200-70683400	Active TSS	Brain Angular Gyrus	brain
16	chr16:70680400-70681400	Active TSS	Stomach Smooth Muscle	stomach
17	chr16:70680400-70681600	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
18	chr16:70680400-70683600	Active TSS	Brain Hippocampus Middle	brain
19	chr16:70680400-70685600	Genic enhancers	Spleen	Spleen
20	chr16:70680600-70681400	Genic enhancers	Breast Myoepithelial Primary Cells	Breast
21	chr16:70680600-70681600	Flanking Active TSS	HSMMtube	muscle
22	chr16:70680600-70681800	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr16:70680600-70682000	Enhancers	Cortex derived primary cultured neurospheres	brain
24	chr16:70680600-70682200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr16:70680800-70681400	Active TSS	Brain Anterior Caudate	brain
26	chr16:70680800-70681600	Enhancers	NHLF	lung
27	chr16:70680800-70683000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr16:70680800-70687800	Weak transcription	Colonic Mucosa	Colon
29	chr16:70680800-70687800	Weak transcription	Rectal Mucosa Donor 29	rectum
30	chr16:70681000-70681400	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
31	chr16:70681000-70681400	Active TSS	Fetal Brain Female	brain
32	chr16:70681000-70681400	Enhancers	Skeletal Muscle Male	skeletal muscle
33	chr16:70681000-70681600	Enhancers	Brain Germinal Matrix	brain
34	chr16:70681000-70681800	Enhancers	HSMM	muscle
35	chr16:70681000-70682000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
36	chr16:70681200-70681400	Bivalent/Poised TSS	Brain Cingulate Gyrus	brain
37	chr16:70681200-70681400	Active TSS	Brain Inferior Temporal Lobe	brain
38	chr16:70681200-70681600	Weak transcription	Brain Substantia Nigra	brain
39	chr16:70681200-70681600	Enhancers	NH-A	brain
40	chr16:70681200-70681800	Enhancers	Osteobl	bone
41	chr16:70681200-70683000	Strong transcription	Fetal Intestine Large	intestine
42	chr16:70681200-70683200	Strong transcription	Fetal Stomach	stomach

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