Variant report

Variant	rs7119372
Chromosome Location	chr11:85231475-85231476
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 125 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:113)

rs_ID	r²[population]
rs10501595	0.94[CHB][hapmap]
rs1072253	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10751126	0.95[ASN][1000 genomes]
rs1118578	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11234359	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.91[CHD][hapmap];1.00[GIH][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1160187	0.88[ASN][1000 genomes]
rs1160188	0.88[ASN][1000 genomes]
rs11603984	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11605203	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11607685	0.91[ASN][1000 genomes]
rs11821005	0.81[AMR][1000 genomes]
rs1192	0.95[CHB][hapmap]
rs1213257	0.85[AMR][1000 genomes]
rs1214001	0.95[CHB][hapmap]
rs12420907	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1354397	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[CHD][hapmap];1.00[GIH][hapmap];0.83[LWK][hapmap];1.00[MEX][hapmap];0.90[MKK][hapmap];1.00[TSI][hapmap];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1425223	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1504027	0.88[ASN][1000 genomes]
rs1504029	0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs158217	0.95[ASN][1000 genomes]
rs166998	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs17208492	0.95[CHB][hapmap]
rs17208519	0.95[CHB][hapmap]
rs17810659	0.95[CHB][hapmap]
rs1806414	0.91[ASN][1000 genomes]
rs184057	0.97[ASN][1000 genomes]
rs185932	0.90[ASN][1000 genomes]
rs1863256	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs188311	0.84[CHB][hapmap]
rs1892872	0.94[CHB][hapmap]
rs1991923	0.95[CHB][hapmap]
rs207060	0.94[ASN][1000 genomes]
rs2175189	0.91[ASN][1000 genomes]
rs2290823	0.95[CHB][hapmap]
rs2467059	0.95[CHB][hapmap]
rs2512800	0.94[ASN][1000 genomes]
rs2512803	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs286494	0.92[ASN][1000 genomes]
rs286495	0.92[ASN][1000 genomes]
rs286496	0.94[ASN][1000 genomes]
rs286498	0.92[ASN][1000 genomes]
rs286499	1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs286507	0.83[AMR][1000 genomes]
rs286508	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs286509	0.97[ASN][1000 genomes]
rs286510	0.97[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs286511	0.85[AMR][1000 genomes]
rs286512	0.97[ASN][1000 genomes]
rs286513	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs286515	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.84[GIH][hapmap];1.00[JPT][hapmap];0.95[MEX][hapmap];1.00[TSI][hapmap];0.86[EUR][1000 genomes]
rs286521	0.94[ASN][1000 genomes]
rs286522	0.93[ASN][1000 genomes]
rs286523	0.94[ASN][1000 genomes]
rs286524	0.94[ASN][1000 genomes]
rs286525	0.94[ASN][1000 genomes]
rs286526	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs286527	0.91[ASN][1000 genomes]
rs286528	0.82[AMR][1000 genomes]
rs286529	0.90[ASN][1000 genomes]
rs286530	0.92[ASN][1000 genomes]
rs286531	0.95[ASN][1000 genomes]
rs286534	0.94[ASN][1000 genomes]
rs286535	0.86[AMR][1000 genomes];0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs286537	0.95[ASN][1000 genomes]
rs286538	0.97[ASN][1000 genomes]
rs286539	0.97[ASN][1000 genomes]
rs286540	0.97[ASN][1000 genomes]
rs286541	0.97[ASN][1000 genomes]
rs286542	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs290175	0.84[CHB][hapmap]
rs290177	0.95[CHB][hapmap]
rs290182	0.95[CHB][hapmap]
rs290186	0.95[CHB][hapmap]
rs290194	0.84[CHB][hapmap]
rs290196	0.84[CHB][hapmap]
rs290199	0.80[CHB][hapmap]
rs35097455	0.88[ASN][1000 genomes]
rs4280023	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4943918	1.00[CHB][hapmap];0.89[CHD][hapmap];0.95[JPT][hapmap]
rs4943923	0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4943925	0.93[CHB][hapmap]
rs4944520	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4944529	0.95[CHB][hapmap]
rs4944531	0.95[CHB][hapmap]
rs55739259	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs55933855	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs56073783	0.83[ASN][1000 genomes]
rs56238215	0.87[ASN][1000 genomes]
rs56256400	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs56273824	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs56321405	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs56579	0.95[CHB][hapmap]
rs56737296	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs57223077	0.83[ASN][1000 genomes]
rs58757261	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs58930391	0.91[ASN][1000 genomes]
rs59082411	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs60484561	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs61133973	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs61286868	0.84[ASN][1000 genomes]
rs62388	0.95[ASN][1000 genomes]
rs7108137	0.83[ASN][1000 genomes]
rs7110363	1.00[CHB][hapmap];0.95[JPT][hapmap]
rs7116340	0.80[EUR][1000 genomes]
rs7119617	0.95[CHB][hapmap]
rs73499156	0.94[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs73499163	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7943586	0.95[CHB][hapmap]
rs7948778	1.00[CEU][hapmap];0.95[CHB][hapmap];0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7949567	0.81[AMR][1000 genomes]
rs881121	0.95[CHB][hapmap]
rs947861	0.95[CHB][hapmap]
rs947863	0.95[CHB][hapmap]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1044370	chr11:84748993-85293233	Enhancers Weak transcription ZNF genes & repeats Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
2	nsv1051155	chr11:85006564-85721261	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Active TSS Genic enhancers 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	64 gene(s)	inside rSNPs	diseases
3	nsv541110	chr11:85006564-85721261	Enhancers Strong transcription Weak transcription Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	64 gene(s)	inside rSNPs	diseases
4	nsv1050363	chr11:85163437-85293233	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
5	nsv541111	chr11:85163437-85293233	Enhancers ZNF genes & repeats Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Bivalent/Poised TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
6	nsv898046	chr11:85180409-85300458	Enhancers ZNF genes & repeats Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
7	nsv898047	chr11:85180409-85377707	Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
8	esv2758279	chr11:85180480-85603988	Flanking Active TSS Active TSS Weak transcription Enhancers Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
9	esv2759845	chr11:85180480-85603988	Flanking Active TSS Weak transcription Enhancers Genic enhancers Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
10	nsv898048	chr11:85206156-85404138	Flanking Active TSS Genic enhancers Active TSS Weak transcription Strong transcription Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
11	nsv976462	chr11:85227017-85253774	Strong transcription Weak transcription ZNF genes & repeats Enhancers Active TSS Flanking Active TSS	TF binding region CpG island lncRNA	1 gene(s)	inside rSNPs	diseases
12	nsv898049	chr11:85231475-85292310	ZNF genes & repeats Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs7119372	DDAH1	trans	lymphoblastoid	seeQTL
rs7119372	TMEM126A	cis	Nerve Tibial	GTEx

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:85195200-85238200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr11:85220600-85233000	Weak transcription	Pancreas	Pancrea
3	chr11:85228000-85232400	Weak transcription	Ovary	ovary
4	chr11:85230400-85233200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr11:85230400-85236400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr11:85231000-85232600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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