Variant report

Variant	rs13119696
Chromosome Location	chr4:1098797-1098798
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:1097640..1100252-chr4:1105624..1108408,2	K562	blood:
2	chr4:1098216..1100430-chr4:1120961..1123862,2	K562	blood:

Variant related genes	Relation type
ENSG00000178222	Chromatin interaction
ENSG00000251652	Chromatin interaction

Extended variants
information (count: 108 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:93)

rs_ID	r²[population]
rs10002248	1.00[CEU][hapmap]
rs10002437	1.00[CEU][hapmap]
rs10014245	1.00[CEU][hapmap]
rs10032349	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs10032470	1.00[CEU][hapmap];0.83[YRI][hapmap];0.83[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs10033163	1.00[CEU][hapmap];0.95[EUR][1000 genomes]
rs11724989	1.00[CEU][hapmap];0.83[YRI][hapmap]
rs11728360	0.83[EUR][1000 genomes]
rs11736950	0.85[EUR][1000 genomes]
rs1383660	1.00[CEU][hapmap];0.82[YRI][hapmap];0.82[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs1466214	0.83[YRI][hapmap]
rs1481167	1.00[CEU][hapmap];0.85[EUR][1000 genomes]
rs1680027	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs17164384	1.00[CEU][hapmap]
rs1825092	0.90[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs28510738	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs28514301	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs28588234	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs2924495	1.00[CEU][hapmap];0.82[YRI][hapmap];0.95[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4246683	0.82[AFR][1000 genomes];0.97[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4246684	1.00[CEU][hapmap];0.82[YRI][hapmap];0.82[AFR][1000 genomes];0.97[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4974561	1.00[CEU][hapmap];0.86[YRI][hapmap];0.83[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs4974569	1.00[CEU][hapmap];0.83[YRI][hapmap];0.82[AFR][1000 genomes];0.97[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4974571	1.00[CEU][hapmap];0.83[YRI][hapmap];0.82[AFR][1000 genomes];0.97[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4974573	1.00[CEU][hapmap]
rs4974628	1.00[CEU][hapmap];0.83[YRI][hapmap];0.83[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs4974637	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs4974639	1.00[CEU][hapmap];0.83[YRI][hapmap];0.82[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs4974642	1.00[CEU][hapmap];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs4974643	1.00[CEU][hapmap];0.83[YRI][hapmap];0.82[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs4974644	1.00[CEU][hapmap];0.82[YRI][hapmap];0.82[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs583100	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs584472	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs588824	1.00[CEU][hapmap];0.83[YRI][hapmap];0.95[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs589660	1.00[CEU][hapmap];0.83[YRI][hapmap];0.81[AFR][1000 genomes];0.95[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs59057706	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs604526	1.00[CEU][hapmap];0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs606293	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs606327	1.00[CEU][hapmap];0.83[YRI][hapmap];0.84[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs608066	1.00[CEU][hapmap];0.88[YRI][hapmap];0.84[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs614945	1.00[CEU][hapmap];0.83[YRI][hapmap];0.84[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs615381	1.00[CEU][hapmap];0.82[YRI][hapmap];0.84[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs616196	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs616569	1.00[CEU][hapmap];0.83[YRI][hapmap];0.81[AFR][1000 genomes];0.97[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs617633	0.81[EUR][1000 genomes]
rs619407	1.00[CEU][hapmap];0.83[YRI][hapmap];0.81[AFR][1000 genomes];0.95[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs620398	1.00[CEU][hapmap];0.83[YRI][hapmap];0.95[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs629638	1.00[CEU][hapmap];0.83[YRI][hapmap];0.84[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs630549	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs632319	1.00[CEU][hapmap];0.83[YRI][hapmap];0.81[AFR][1000 genomes];0.95[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs633087	1.00[CEU][hapmap];0.80[YRI][hapmap];0.81[AFR][1000 genomes];0.95[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs633141	1.00[CEU][hapmap];0.82[YRI][hapmap];0.81[AFR][1000 genomes];0.95[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs633599	1.00[CEU][hapmap];0.83[YRI][hapmap];0.95[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs633954	1.00[CEU][hapmap];0.84[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs636976	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs643043	1.00[CEU][hapmap];0.81[YRI][hapmap];0.84[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs646117	0.95[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs647828	0.95[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs648640	0.95[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs649243	1.00[CEU][hapmap];0.82[YRI][hapmap];0.84[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs649258	0.80[AFR][1000 genomes];0.95[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs649616	1.00[CEU][hapmap];0.82[YRI][hapmap];0.95[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs649950	0.83[YRI][hapmap];0.81[AMR][1000 genomes]
rs651135	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs651509	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs658320	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs6599282	1.00[CEU][hapmap];0.83[EUR][1000 genomes]
rs6599283	1.00[CEU][hapmap];0.85[EUR][1000 genomes]
rs6599284	1.00[CEU][hapmap]
rs6599285	0.87[CEU][hapmap]
rs661364	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs671790	1.00[CEU][hapmap]
rs674347	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs6814094	0.81[AFR][1000 genomes];0.97[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6817989	1.00[CEU][hapmap]
rs681857	1.00[CEU][hapmap];0.82[YRI][hapmap];0.95[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs682243	1.00[CEU][hapmap];0.80[YRI][hapmap];0.95[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs682787	1.00[CEU][hapmap];0.83[YRI][hapmap];0.92[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6836158	1.00[CEU][hapmap]
rs6836335	0.87[CEU][hapmap]
rs6839768	1.00[CEU][hapmap];0.82[YRI][hapmap];0.82[AFR][1000 genomes];0.97[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6840162	1.00[CEU][hapmap];0.80[YRI][hapmap];0.81[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs687939	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs689216	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs73074169	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7676956	1.00[CEU][hapmap]
rs7679718	1.00[CEU][hapmap]
rs7684536	0.82[CEU][hapmap]
rs7686839	0.82[AFR][1000 genomes];0.97[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7690300	0.87[CEU][hapmap]
rs7690832	1.00[CEU][hapmap]
rs7691553	0.81[AFR][1000 genomes];0.95[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs9992322	1.00[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:15 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv822425	chr4:540105-1413799	Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	108 gene(s)	inside rSNPs	diseases
2	nsv530490	chr4:614355-1399150	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	104 gene(s)	inside rSNPs	diseases
3	nsv1003219	chr4:769894-1105464	Strong transcription Weak transcription Flanking Bivalent TSS/Enh Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
4	nsv536980	chr4:827866-1167377	Active TSS Weak transcription Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
5	nsv1009619	chr4:901897-1215657	Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
6	nsv1003876	chr4:927509-1191316	Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription Active TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
7	nsv1000381	chr4:927509-1198766	Weak transcription Enhancers Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
8	esv3339080	chr4:970630-1546223	Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	82 gene(s)	inside rSNPs	diseases
9	nsv1004727	chr4:1015652-1158207	Enhancers Strong transcription Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
10	nsv536984	chr4:1015652-1158207	Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS Bivalent/Poised TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
11	nsv1005990	chr4:1015652-1167619	Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
12	nsv1000594	chr4:1045099-1129975	Enhancers Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
13	nsv1001165	chr4:1051512-1129975	Enhancers Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
14	nsv1012892	chr4:1086871-1176630	Enhancers Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
15	nsv829835	chr4:1097586-1304239	Enhancers Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	59 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs13119696	AC092574.2	cis	lung	GTEx

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:1094000-1105800	Weak transcription	Ovary	ovary
2	chr4:1098000-1099800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr4:1098000-1099800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr4:1098000-1100200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr4:1098000-1100600	Enhancers	Pancreas	Pancrea
6	chr4:1098200-1099200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr4:1098200-1100400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr4:1098600-1100600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived

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