Variant report

Variant	rs7040038
Chromosome Location	chr9:73786741-73786742
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 92 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:90)

rs_ID	r²[population]
rs10117928	0.85[ASN][1000 genomes]
rs10123263	0.97[ASN][1000 genomes]
rs10125889	0.85[ASN][1000 genomes]
rs1027721	0.88[ASN][1000 genomes]
rs1027722	0.88[ASN][1000 genomes]
rs10732701	0.94[ASN][1000 genomes]
rs10746861	0.88[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs10746862	0.97[ASN][1000 genomes]
rs10780991	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs10780993	0.97[AFR][1000 genomes];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs10780998	0.83[ASN][1000 genomes]
rs10868965	0.97[ASN][1000 genomes]
rs10868967	0.97[ASN][1000 genomes]
rs10868968	0.95[ASN][1000 genomes]
rs10868971	0.88[ASN][1000 genomes]
rs10868981	0.85[ASN][1000 genomes]
rs10868982	0.85[ASN][1000 genomes]
rs10868983	0.85[ASN][1000 genomes]
rs11142699	0.83[ASN][1000 genomes]
rs11142709	0.97[ASN][1000 genomes]
rs11142716	0.95[ASN][1000 genomes]
rs11142735	0.85[ASN][1000 genomes]
rs11142746	0.83[ASN][1000 genomes]
rs12337266	0.83[ASN][1000 genomes]
rs12346443	0.85[ASN][1000 genomes]
rs1329762	0.90[ASN][1000 genomes]
rs1329764	0.94[ASN][1000 genomes]
rs1329765	0.94[ASN][1000 genomes]
rs1329767	0.80[ASN][1000 genomes]
rs1329769	0.95[ASN][1000 genomes]
rs1329770	0.97[ASN][1000 genomes]
rs1360201	0.95[ASN][1000 genomes]
rs1360202	0.95[ASN][1000 genomes]
rs1360203	0.95[ASN][1000 genomes]
rs1394305	0.83[AFR][1000 genomes]
rs1411165	0.88[ASN][1000 genomes]
rs1411166	0.97[ASN][1000 genomes]
rs1411167	0.95[ASN][1000 genomes]
rs1411168	0.94[AFR][1000 genomes];0.93[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1504394	0.85[ASN][1000 genomes]
rs1504396	0.85[ASN][1000 genomes]
rs1504397	0.85[ASN][1000 genomes]
rs1504403	0.97[ASN][1000 genomes]
rs1604854	0.83[ASN][1000 genomes]
rs1831312	0.97[AFR][1000 genomes];0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1854555	0.97[ASN][1000 genomes]
rs1854556	0.95[ASN][1000 genomes]
rs1854557	0.95[ASN][1000 genomes]
rs2134862	0.97[ASN][1000 genomes]
rs2174305	0.85[ASN][1000 genomes]
rs2174306	0.85[ASN][1000 genomes]
rs2174307	0.95[ASN][1000 genomes]
rs2183017	0.89[ASN][1000 genomes]
rs2309841	0.85[ASN][1000 genomes]
rs4744623	0.95[ASN][1000 genomes]
rs4744624	0.95[ASN][1000 genomes]
rs4745062	0.97[ASN][1000 genomes]
rs4745063	0.95[ASN][1000 genomes]
rs4745064	0.94[ASN][1000 genomes]
rs4745071	0.85[ASN][1000 genomes]
rs4745073	0.85[ASN][1000 genomes]
rs4745074	0.82[ASN][1000 genomes]
rs4745075	0.83[ASN][1000 genomes]
rs6560182	0.97[ASN][1000 genomes]
rs6560183	0.95[ASN][1000 genomes]
rs6560184	0.95[ASN][1000 genomes]
rs6560185	0.88[ASN][1000 genomes]
rs6560186	0.87[ASN][1000 genomes]
rs6560191	0.83[ASN][1000 genomes]
rs7019473	0.97[ASN][1000 genomes]
rs7022632	0.94[ASN][1000 genomes]
rs7028656	0.97[ASN][1000 genomes]
rs7029914	0.88[ASN][1000 genomes]
rs7038966	0.94[ASN][1000 genomes]
rs7038986	0.94[ASN][1000 genomes]
rs7042684	0.95[ASN][1000 genomes]
rs7043845	0.97[ASN][1000 genomes]
rs7044340	0.82[AMR][1000 genomes]
rs7049121	0.85[ASN][1000 genomes]
rs7469513	0.95[ASN][1000 genomes]
rs7849553	0.83[ASN][1000 genomes]
rs7850409	0.85[ASN][1000 genomes]
rs7850909	0.88[ASN][1000 genomes]
rs7851045	0.88[ASN][1000 genomes]
rs7860967	0.88[ASN][1000 genomes]
rs7861071	0.83[ASN][1000 genomes]
rs7862622	0.95[ASN][1000 genomes]
rs7865847	0.97[AFR][1000 genomes];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7870937	0.88[ASN][1000 genomes]
rs7870970	0.87[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1035505	chr9:73709852-73934353	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	nsv893442	chr9:73778502-74115344	Bivalent Enhancer Flanking Active TSS Enhancers Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs7040038	FAM108B1	cis	parietal	SCAN

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:73786200-73787200	Enhancers	HUES48 Cell Line	embryonic stem cell
2	chr9:73786200-73787400	Enhancers	iPS-18 Cell Line	embryonic stem cell
3	chr9:73786400-73786800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr9:73786400-73786800	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
5	chr9:73786600-73787000	Enhancers	H1 Cell Line	embryonic stem cell
6	chr9:73786600-73787000	Enhancers	H9 Cell Line	embryonic stem cell
7	chr9:73786600-73788600	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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