Variant report

Variant	rs4145255
Chromosome Location	chr9:99914953-99914954
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 40 )
Associated
traits (count: 3 )

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs10817170	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10817171	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10817173	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10980874	0.81[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10981209	0.81[EUR][1000 genomes]
rs10981280	0.88[CEU][hapmap];0.86[CHB][hapmap]
rs10981288	0.88[CEU][hapmap];0.87[CHB][hapmap];0.82[GIH][hapmap];0.95[MEX][hapmap]
rs10981296	0.82[CEU][hapmap]
rs10981329	0.85[CEU][hapmap];0.87[CHB][hapmap];0.84[GIH][hapmap];0.81[MEX][hapmap]
rs11562326	0.82[EUR][1000 genomes]
rs11791310	0.85[CEU][hapmap];0.87[CHB][hapmap];0.82[GIH][hapmap];0.85[MEX][hapmap]
rs12003313	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12235734	0.80[EUR][1000 genomes]
rs13298346	0.85[CEU][hapmap];0.87[CHB][hapmap];0.82[GIH][hapmap];0.85[MEX][hapmap]
rs13299627	0.85[CEU][hapmap];0.87[CHB][hapmap]
rs1544203	0.85[CEU][hapmap];0.82[CHB][hapmap];0.82[GIH][hapmap];0.85[MEX][hapmap]
rs1857083	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2219664	0.85[CEU][hapmap];0.82[CHB][hapmap]
rs2374923	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2615143	0.85[CEU][hapmap];0.82[CHB][hapmap];0.82[GIH][hapmap];0.85[MEX][hapmap]
rs2615145	0.85[CEU][hapmap];0.82[CHB][hapmap];0.82[GIH][hapmap];0.85[MEX][hapmap]
rs2795367	0.80[CEU][hapmap]
rs2818238	0.85[CEU][hapmap];0.82[CHB][hapmap];0.82[GIH][hapmap];0.85[MEX][hapmap]
rs2818243	0.85[CEU][hapmap];0.82[GIH][hapmap];0.85[MEX][hapmap]
rs3214072	0.85[CEU][hapmap];0.82[CHB][hapmap]
rs35988269	0.84[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4014783	0.81[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4014789	0.92[EUR][1000 genomes]
rs4452918	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4743072	0.82[CHB][hapmap]
rs7031789	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs713066	0.82[CHB][hapmap];0.82[GIH][hapmap];0.84[MEX][hapmap]
rs750674	0.82[CHB][hapmap]
rs7869959	0.80[EUR][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	nsv831662	chr9:99752521-99939231	Bivalent Enhancer Strong transcription Active TSS Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv972432	chr9:99874607-99958095	Enhancers Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv973382	chr9:99894731-99916071	Weak transcription Enhancers ZNF genes & repeats Genic enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3'	lncRNA	n/a	inside rSNPs	diseases
4	nsv931946	chr9:99895658-100005099	Bivalent/Poised TSS Strong transcription Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
5	nsv893607	chr9:99906545-99996548	Enhancers Bivalent/Poised TSS ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Flanking Bivalent TSS/Enh Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
6	nsv893608	chr9:99906545-100005128	Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases

mRNA abundance (count:3)

SNP	Gene	Cis/trans	Tissue	Source
rs4145255	LOC441455	cis	lymphoblastoid	seeQTL
rs4145255	LOC57653	cis	parietal	SCAN
rs4145255	ANKRD18CP	cis	Thyroid	GTEx

Chromatin state (count:19 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:99901000-99921000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr9:99909800-99920200	Weak transcription	Brain Angular Gyrus	brain
3	chr9:99911600-99957600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
4	chr9:99912200-99915200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr9:99912200-99915400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr9:99912200-99921200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr9:99912200-99922800	Weak transcription	Brain Anterior Caudate	brain
8	chr9:99912200-99923800	Strong transcription	H1 Cell Line	embryonic stem cell
9	chr9:99912800-99915000	Strong transcription	ES-I3 Cell Line	embryonic stem cell
10	chr9:99913000-99920000	Strong transcription	H9 Cell Line	embryonic stem cell
11	chr9:99913000-99924400	Strong transcription	HUES6 Cell Line	embryonic stem cell
12	chr9:99913200-99923600	Strong transcription	iPS-15b Cell Line	embryonic stem cell
13	chr9:99913200-99924200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
14	chr9:99913400-99918400	Strong transcription	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr9:99913400-99924600	Strong transcription	HUES48 Cell Line	embryonic stem cell
16	chr9:99913400-99930800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
17	chr9:99913600-99924200	Strong transcription	iPS-18 Cell Line	embryonic stem cell
18	chr9:99913600-99930800	Strong transcription	HUES64 Cell Line	embryonic stem cell
19	chr9:99914200-99917000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain

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