Variant report

Variant	rs8090667
Chromosome Location	chr18:12974073-12974074
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:9)
CpG islands
(count:0)
Chromatin interactive
region (count:5)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:9 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	TEAD4	chr18:12973764-12974203	K562	blood:	n/a	n/a
2	SPI1	chr18:12973974-12974121	K562	blood:	n/a	n/a
3	TAL1	chr18:12973829-12974141	K562	blood:	n/a	n/a
4	TRIM28	chr18:12973758-12974248	K562	blood:	n/a	n/a
5	RCOR1	chr18:12974006-12974085	K562	blood:	n/a	n/a
6	CEBPD	chr18:12973776-12974162	K562	blood:	n/a	n/a
7	SETDB1	chr18:12973744-12974145	U2OS	brain:	n/a	n/a
8	CBX3	chr18:12973628-12974205	K562	blood:	n/a	n/a
9	MAX	chr18:12973851-12974128	K562	blood:	n/a	n/a

No data

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr18:12961017..12963035-chr18:12972346..12974165,2	K562	blood:
2	chr18:12966070..12968300-chr18:12972176..12974458,3	K562	blood:
3	chr18:12971249..12974224-chr18:12989349..12991861,2	MCF-7	breast:
4	chr18:12972698..12975600-chr18:12984314..12986199,2	MCF-7	breast:
5	chr18:12972872..12975575-chr18:12990467..12992405,2	K562	blood:

No data

Variant related genes	Relation type
SEH1L	TF binding region
ENSG00000266969	Chromatin interaction
ENSG00000101639	Chromatin interaction

Extended variants
information (count: 66 )
Associated
traits (count: 9 )

rSNPs within LD-proxies of this variant (count:60)

rs_ID	r²[population]
rs10163827	0.89[ASN][1000 genomes]
rs11080616	0.86[YRI][hapmap]
rs11080617	0.93[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.83[TSI][hapmap];0.97[ASN][1000 genomes]
rs11080618	0.84[CEU][hapmap];0.93[CHB][hapmap];0.96[CHD][hapmap];0.87[GIH][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs11661908	1.00[CEU][hapmap];0.88[CHB][hapmap];1.00[GIH][hapmap];0.94[JPT][hapmap];0.87[MEX][hapmap];0.95[TSI][hapmap];0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11662634	0.89[ASN][1000 genomes]
rs11662766	0.87[JPT][hapmap]
rs11664213	0.95[ASN][1000 genomes]
rs11664469	0.93[CHB][hapmap];0.96[CHD][hapmap];1.00[JPT][hapmap];0.83[TSI][hapmap];0.97[ASN][1000 genomes]
rs12604538	0.81[CHB][hapmap];0.89[CHD][hapmap];0.87[JPT][hapmap]
rs12605267	0.97[ASN][1000 genomes]
rs12607398	0.85[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs12607919	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.95[GIH][hapmap];0.94[JPT][hapmap];0.88[MEX][hapmap];0.98[TSI][hapmap];0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12953783	0.87[ASN][1000 genomes]
rs12957380	0.93[CHB][hapmap];0.96[CHD][hapmap];1.00[JPT][hapmap];0.81[TSI][hapmap];0.89[ASN][1000 genomes]
rs12960349	0.84[CEU][hapmap];0.93[CHB][hapmap];0.96[CHD][hapmap];0.84[GIH][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs12961596	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12963426	0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12970503	0.89[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs13381779	0.89[ASN][1000 genomes]
rs1523064	1.00[CEU][hapmap];0.88[CHB][hapmap];0.94[JPT][hapmap];0.80[YRI][hapmap];0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs17603207	0.93[CHB][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs17659689	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.83[MEX][hapmap];0.86[TSI][hapmap];0.82[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17659749	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17659896	0.93[CHB][hapmap];0.96[CHD][hapmap];1.00[JPT][hapmap];0.83[TSI][hapmap];0.95[ASN][1000 genomes]
rs2015763	0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2282540	0.85[ASN][1000 genomes]
rs2282541	1.00[CHB][hapmap];0.96[CHD][hapmap];1.00[JPT][hapmap];0.83[TSI][hapmap];0.92[ASN][1000 genomes]
rs28551661	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs28654613	0.94[ASN][1000 genomes]
rs34166083	0.99[ASN][1000 genomes]
rs34302481	0.95[ASN][1000 genomes]
rs35368962	0.83[AFR][1000 genomes];0.84[AMR][1000 genomes];0.84[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs35563947	0.95[ASN][1000 genomes]
rs3809914	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs3976787	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4499304	0.92[CEU][hapmap]
rs56263236	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6505772	0.87[CHB][hapmap];0.89[CHD][hapmap];0.81[JPT][hapmap]
rs68004799	0.99[ASN][1000 genomes]
rs7228684	0.93[CHB][hapmap];0.96[CHD][hapmap];1.00[JPT][hapmap];0.83[TSI][hapmap];0.93[ASN][1000 genomes]
rs7229406	0.87[CHB][hapmap]
rs7229869	0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7230391	0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7230435	0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7234163	0.92[CEU][hapmap]
rs7234938	0.89[ASN][1000 genomes]
rs7236710	0.83[ASN][1000 genomes]
rs7237711	0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7239486	0.92[ASN][1000 genomes]
rs8083393	0.87[JPT][hapmap]
rs8083401	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs8086882	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs8089724	0.88[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs8092888	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs8093236	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.95[GIH][hapmap];0.94[JPT][hapmap];0.88[MEX][hapmap];0.98[TSI][hapmap];0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs8093576	1.00[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8096860	1.00[CEU][hapmap];0.88[CHB][hapmap];0.94[JPT][hapmap];0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs8566	0.99[ASN][1000 genomes]
rs9950241	0.80[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1062014	chr18:12687210-13183383	Enhancers Active TSS Weak transcription Genic enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	101 gene(s)	inside rSNPs	diseases
2	nsv543655	chr18:12687210-13183383	Flanking Bivalent TSS/Enh Strong transcription Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	101 gene(s)	inside rSNPs	diseases
3	nsv1057083	chr18:12916779-13207538	Weak transcription Strong transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
4	nsv576524	chr18:12918318-13183609	Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
5	nsv1056593	chr18:12926314-13183383	Strong transcription Weak transcription Active TSS Flanking Active TSS Enhancers Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
6	nsv1064364	chr18:12926314-13207686	Strong transcription Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	46 gene(s)	inside rSNPs	diseases

mRNA abundance (count:9)

SNP	Gene	Cis/trans	Tissue	Source
rs8090667	CEP192	cis	Artery Tibial	GTEx
rs8090667	CEP192	cis	lung	GTEx
rs8090667	CEP192	Cis_1M	lymphoblastoid	RTeQTL
rs8090667	CEP192	cis	Nerve Tibial	GTEx
rs8090667	CEP192	cis	Thyroid	GTEx
rs8090667	CEP192	cis	Adipose Subcutaneous	GTEx
rs8090667	CEP192	cis	Esophagus Muscularis	GTEx
rs8090667	CEP192	cis	parietal	SCAN
rs8090667	CEP192	cis	cerebellum	SCAN

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:12948800-12976600	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr18:12948800-12989000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr18:12949000-12975400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
4	chr18:12949200-12989400	Weak transcription	Psoas Muscle	Psoas
5	chr18:12950000-12990200	Weak transcription	Fetal Brain Male	brain
6	chr18:12951400-12990200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
7	chr18:12951600-12988200	Weak transcription	Primary neutrophils fromperipheralblood	blood
8	chr18:12951800-12978400	Strong transcription	HUES64 Cell Line	embryonic stem cell
9	chr18:12953200-12979000	Strong transcription	Fetal Thymus	thymus
10	chr18:12956200-12975800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr18:12957400-12978400	Strong transcription	Dnd41	blood
12	chr18:12959000-12990200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
13	chr18:12959200-12978200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr18:12961000-12978400	Strong transcription	Fetal Intestine Small	intestine
15	chr18:12961200-12975400	Weak transcription	Stomach Mucosa	stomach
16	chr18:12961400-12975600	Weak transcription	Right Atrium	heart
17	chr18:12961600-12975400	Weak transcription	Fetal Heart	heart
18	chr18:12962800-12975800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr18:12963200-12978600	Strong transcription	Fetal Intestine Large	intestine
20	chr18:12963600-12978600	Strong transcription	Fetal Stomach	stomach
21	chr18:12964000-12975400	Weak transcription	Colonic Mucosa	Colon
22	chr18:12968600-12983000	Weak transcription	HUVEC	blood vessel
23	chr18:12969400-12976000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
24	chr18:12969800-12979000	Strong transcription	Primary B cells from cord blood	blood
25	chr18:12969800-12979000	Strong transcription	Osteobl	bone
26	chr18:12970000-12979000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
27	chr18:12970000-12979000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr18:12970200-12976600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr18:12970200-12976600	Strong transcription	K562	blood
30	chr18:12970200-12976800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr18:12970200-12978200	Strong transcription	HUES6 Cell Line	embryonic stem cell
32	chr18:12970200-12978600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
33	chr18:12970200-12978800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
34	chr18:12970200-12978800	Strong transcription	Liver	Liver
35	chr18:12970200-12979000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr18:12970200-12979000	Strong transcription	Cortex derived primary cultured neurospheres	brain
37	chr18:12970400-12975800	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
38	chr18:12970400-12976400	Strong transcription	iPS-18 Cell Line	embryonic stem cell
39	chr18:12970400-12978200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
40	chr18:12970400-12978600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
41	chr18:12970400-12979000	Strong transcription	Primary T cells from cord blood	blood
42	chr18:12970400-12979000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr18:12970400-12979000	Strong transcription	Fetal Muscle Trunk	muscle
44	chr18:12970400-12979200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
45	chr18:12970400-12979200	Strong transcription	Primary T helper cells fromperipheralblood	blood
46	chr18:12970600-12974400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
47	chr18:12970600-12976400	Strong transcription	Skeletal Muscle Male	skeletal muscle
48	chr18:12970600-12978400	Strong transcription	HUES48 Cell Line	embryonic stem cell
49	chr18:12970600-12978400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
50	chr18:12970600-12978800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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