Variant report

Variant	rs10756879
Chromosome Location	chr9:17397381-17397382
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 183 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:166)

rs_ID	r²[population]
rs10115784	0.85[CEU][hapmap];0.89[YRI][hapmap]
rs10117379	0.99[ASN][1000 genomes]
rs10119233	1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs10119863	0.81[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs10119902	0.81[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs10120006	1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs10120013	0.81[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs10120733	1.00[CHB][hapmap];0.93[JPT][hapmap];0.85[YRI][hapmap];0.81[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs10120761	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap];0.81[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs10125886	0.81[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs1023778	0.94[CHB][hapmap];0.88[JPT][hapmap];0.83[YRI][hapmap];0.93[ASN][1000 genomes]
rs10738475	0.87[AFR][1000 genomes]
rs10738477	0.81[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs10756864	0.82[ASN][1000 genomes]
rs10756865	0.82[ASN][1000 genomes]
rs10810753	0.82[ASN][1000 genomes]
rs10810783	1.00[CHB][hapmap];0.93[JPT][hapmap];1.00[ASN][1000 genomes]
rs10962922	0.89[CHB][hapmap];0.80[JPT][hapmap]
rs10962924	0.89[CHB][hapmap];0.81[JPT][hapmap]
rs10962939	0.88[CHB][hapmap];0.80[JPT][hapmap]
rs10962995	0.85[CEU][hapmap]
rs10963028	0.82[ASN][1000 genomes]
rs10963056	0.85[CEU][hapmap]
rs10963067	0.84[CEU][hapmap]
rs10963070	0.85[CEU][hapmap]
rs10963081	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs10963085	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10963088	0.97[ASN][1000 genomes]
rs10963103	0.87[CHB][hapmap];0.92[JPT][hapmap];0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10963105	0.85[CEU][hapmap];0.88[CHB][hapmap];1.00[JPT][hapmap];0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1113379	0.88[CHB][hapmap];0.80[JPT][hapmap];0.82[ASN][1000 genomes]
rs1113380	0.89[CHB][hapmap];0.81[JPT][hapmap];0.93[YRI][hapmap];0.82[ASN][1000 genomes]
rs1113382	0.82[ASN][1000 genomes]
rs12235811	0.92[CEU][hapmap]
rs12236896	0.93[YRI][hapmap]
rs12346397	0.93[YRI][hapmap]
rs1318162	0.83[JPT][hapmap]
rs1348279	0.82[AFR][1000 genomes]
rs1372700	0.99[ASN][1000 genomes]
rs1372704	0.85[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1413418	0.82[CHB][hapmap];0.81[JPT][hapmap]
rs1413419	0.81[JPT][hapmap]
rs1442518	0.81[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs1442520	0.99[ASN][1000 genomes]
rs1442521	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap];0.81[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs1442522	1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[YRI][hapmap];0.81[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs1442525	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap];0.81[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs1442526	1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[YRI][hapmap];0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs1576958	0.88[CHB][hapmap];0.80[JPT][hapmap]
rs1582029	0.88[CHB][hapmap];0.80[JPT][hapmap]
rs1583985	0.85[CEU][hapmap]
rs16935416	0.84[CEU][hapmap];0.92[YRI][hapmap]
rs1759452	0.82[CHB][hapmap];0.81[JPT][hapmap]
rs1759453	0.82[CHB][hapmap];0.81[JPT][hapmap]
rs1759457	0.92[YRI][hapmap]
rs1759458	0.81[CHB][hapmap];0.80[JPT][hapmap]
rs1759459	0.82[CHB][hapmap];0.81[JPT][hapmap]
rs1759460	0.82[CHB][hapmap];0.81[JPT][hapmap]
rs1759462	0.82[CHB][hapmap];0.81[JPT][hapmap]
rs1759463	0.82[CHB][hapmap];0.81[JPT][hapmap]
rs1759464	0.87[YRI][hapmap]
rs1759465	0.81[CHB][hapmap]
rs1759616	0.82[CHB][hapmap];0.81[JPT][hapmap]
rs1930639	0.89[CHB][hapmap];0.81[JPT][hapmap];0.93[YRI][hapmap]
rs1930641	0.81[CHB][hapmap];0.80[JPT][hapmap];0.92[YRI][hapmap]
rs1930647	0.81[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs1930648	0.81[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs2010086	0.88[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs2039413	0.89[CHB][hapmap]
rs2083694	0.85[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.86[YRI][hapmap];0.94[AMR][1000 genomes];0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2083695	0.88[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs2099859	0.88[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs2119906	0.81[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs2119907	0.81[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs2165688	0.87[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs2210551	0.84[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs2274916	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2441991	0.85[CEU][hapmap];0.88[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2584539	0.85[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2584546	1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs2584548	0.84[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[YRI][hapmap];0.94[AMR][1000 genomes];0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2584549	0.97[ASN][1000 genomes]
rs2584550	0.93[ASN][1000 genomes]
rs2584551	0.93[ASN][1000 genomes]
rs2584552	0.80[EUR][1000 genomes]
rs2593388	1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[YRI][hapmap];0.97[ASN][1000 genomes]
rs2593389	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap];0.96[ASN][1000 genomes]
rs2593390	0.99[ASN][1000 genomes]
rs2593397	0.85[CEU][hapmap];0.82[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2593416	0.87[AMR][1000 genomes];0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2593418	0.91[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.87[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2780203	0.84[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2780204	0.81[CHB][hapmap];0.80[JPT][hapmap]
rs2780205	0.82[CHB][hapmap];0.81[JPT][hapmap]
rs2780208	0.93[ASN][1000 genomes]
rs2780210	0.94[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2780211	0.94[AMR][1000 genomes];0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2780213	0.84[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap];0.81[AFR][1000 genomes];0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2780214	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs3739488	1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[YRI][hapmap];0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs3739489	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.95[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3808781	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap];0.81[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs3808782	0.84[CEU][hapmap]
rs3808785	0.82[CHB][hapmap];0.81[JPT][hapmap]
rs3814137	0.88[CHB][hapmap];0.80[JPT][hapmap]
rs3814139	0.88[CHB][hapmap];0.80[JPT][hapmap]
rs3891457	0.94[CHB][hapmap];0.91[YRI][hapmap];0.85[AFR][1000 genomes];0.81[ASN][1000 genomes]
rs4097851	0.84[AFR][1000 genomes]
rs4147023	0.89[CHB][hapmap];0.81[JPT][hapmap]
rs4554574	0.84[CEU][hapmap];0.92[YRI][hapmap];0.87[AFR][1000 genomes]
rs4621917	0.94[CHB][hapmap];0.80[JPT][hapmap];0.82[ASN][1000 genomes]
rs4961534	0.81[CHB][hapmap];0.80[JPT][hapmap]
rs4961551	0.94[CHB][hapmap];0.82[JPT][hapmap];0.92[YRI][hapmap];0.88[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs4961554	0.94[CHB][hapmap];0.80[JPT][hapmap];0.92[YRI][hapmap];0.88[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs4961556	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap];0.81[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs5001765	0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs585682	0.80[CHB][hapmap]
rs600041	0.81[CHB][hapmap];0.80[JPT][hapmap]
rs600133	0.81[CHB][hapmap];0.80[JPT][hapmap]
rs601960	0.81[CHB][hapmap];0.92[YRI][hapmap]
rs613966	0.81[CHB][hapmap];0.80[JPT][hapmap];0.92[YRI][hapmap]
rs614412	0.82[CHB][hapmap];0.81[JPT][hapmap]
rs614471	0.81[CHB][hapmap];0.80[JPT][hapmap]
rs620280	1.00[CEU][hapmap];0.92[YRI][hapmap]
rs632176	0.82[CHB][hapmap];0.81[JPT][hapmap]
rs634383	0.82[CHB][hapmap];0.81[JPT][hapmap]
rs634446	0.82[CHB][hapmap];0.81[JPT][hapmap]
rs642582	0.82[CHB][hapmap];0.81[JPT][hapmap];0.93[YRI][hapmap]
rs646025	0.81[CHB][hapmap];0.80[JPT][hapmap];0.92[YRI][hapmap]
rs647013	0.82[CHB][hapmap];0.81[JPT][hapmap]
rs6475122	0.88[CHB][hapmap];0.80[JPT][hapmap]
rs6475123	0.85[CEU][hapmap]
rs6475125	0.88[CHB][hapmap];0.80[JPT][hapmap]
rs6475129	0.81[CHB][hapmap];0.80[JPT][hapmap]
rs6475140	0.85[CEU][hapmap];0.88[YRI][hapmap];0.81[AFR][1000 genomes]
rs664447	0.88[CHB][hapmap];0.80[JPT][hapmap]
rs673587	0.82[CHB][hapmap];0.81[JPT][hapmap]
rs679666	0.81[CHB][hapmap]
rs7020918	0.89[CHB][hapmap];0.81[JPT][hapmap]
rs7023305	0.99[ASN][1000 genomes]
rs7023540	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap];0.99[ASN][1000 genomes]
rs7027292	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap];0.99[ASN][1000 genomes]
rs7027539	0.94[CHB][hapmap];0.80[JPT][hapmap];0.88[YRI][hapmap];0.88[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs7028582	0.88[AFR][1000 genomes]
rs7031361	0.91[CEU][hapmap];0.85[YRI][hapmap]
rs7034768	0.88[CHB][hapmap];0.80[JPT][hapmap]
rs7035276	1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[YRI][hapmap];0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7035357	1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[YRI][hapmap];0.81[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs7035525	0.88[CHB][hapmap]
rs7037019	0.88[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs7037041	0.86[ASN][1000 genomes]
rs7042700	0.94[CHB][hapmap];0.80[JPT][hapmap];0.93[YRI][hapmap];0.88[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs7043703	0.88[CHB][hapmap]
rs7046327	0.88[CHB][hapmap];0.80[JPT][hapmap]
rs7047093	0.89[CHB][hapmap];0.81[JPT][hapmap];0.89[YRI][hapmap];0.90[ASN][1000 genomes]
rs7848118	0.82[ASN][1000 genomes]
rs7862336	0.86[AFR][1000 genomes]
rs7865807	0.94[CHB][hapmap];0.81[JPT][hapmap];0.83[ASN][1000 genomes]
rs7870334	0.84[CEU][hapmap];0.87[CHB][hapmap];0.87[JPT][hapmap];0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7870427	1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs7872910	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7874945	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs870270	0.88[CHB][hapmap];0.80[JPT][hapmap];0.92[YRI][hapmap]
rs9298777	0.99[ASN][1000 genomes]
rs9298778	0.97[ASN][1000 genomes]
rs9657595	0.92[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap];0.96[YRI][hapmap];0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:17 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1024799	chr9:16631890-17431827	Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Active TSS Strong transcription 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	20 gene(s)	inside rSNPs	diseases
2	nsv892658	chr9:17041557-17532840	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
3	nsv892661	chr9:17134245-17532840	Flanking Bivalent TSS/Enh Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
4	nsv613693	chr9:17147191-17710407	Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
5	nsv471287	chr9:17165698-17708814	Weak transcription Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
6	nsv466269	chr9:17165698-17710407	Weak transcription ZNF genes & repeats Enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Active TSS Flanking Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
7	nsv466271	chr9:17329964-17438391	Strong transcription Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
8	nsv613696	chr9:17329964-17438391	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
9	nsv1015524	chr9:17350843-17419424	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
10	nsv892668	chr9:17371690-17532840	Weak transcription Enhancers ZNF genes & repeats Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases
11	nsv892669	chr9:17378776-17438391	Strong transcription Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
12	nsv892670	chr9:17378776-17507277	Weak transcription ZNF genes & repeats Enhancers Strong transcription Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases
13	nsv892671	chr9:17378776-17610211	Bivalent Enhancer Enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Active TSS 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	4 gene(s)	inside rSNPs	diseases
14	nsv466273	chr9:17391531-17436662	Flanking Active TSS Enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
15	nsv613697	chr9:17391531-17436662	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
16	nsv523411	chr9:17394536-17454799	Enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
17	esv2422265	chr9:17396711-17598187	Flanking Active TSS Weak transcription Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Enhancers Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:51 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:17368400-17457800	Weak transcription	Pancreas	Pancrea
2	chr9:17368600-17411200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr9:17368600-17411400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr9:17368600-17411400	Weak transcription	Aorta	Aorta
5	chr9:17368800-17411400	Weak transcription	Duodenum Smooth Muscle	Duodenum
6	chr9:17369400-17411200	Weak transcription	Fetal Muscle Trunk	muscle
7	chr9:17377600-17403000	Weak transcription	Fetal Stomach	stomach
8	chr9:17379400-17404200	Weak transcription	Psoas Muscle	Psoas
9	chr9:17380600-17411000	Weak transcription	Left Ventricle	heart
10	chr9:17381000-17411200	Weak transcription	Fetal Muscle Leg	muscle
11	chr9:17381200-17411200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
12	chr9:17381400-17397400	Weak transcription	Ovary	ovary
13	chr9:17381400-17422800	Weak transcription	Colon Smooth Muscle	Colon
14	chr9:17385400-17411400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr9:17387000-17411200	Weak transcription	Dnd41	blood
16	chr9:17388200-17411400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr9:17389000-17404200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr9:17391400-17397400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr9:17391600-17411200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
20	chr9:17393400-17400600	Weak transcription	NH-A	brain
21	chr9:17393400-17411400	Weak transcription	Lung	lung
22	chr9:17393400-17433000	Weak transcription	Primary monocytes fromperipheralblood	blood
23	chr9:17393600-17412800	Weak transcription	Fetal Kidney	kidney
24	chr9:17393600-17413000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
25	chr9:17393800-17413000	Weak transcription	A549	lung
26	chr9:17395000-17398400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
27	chr9:17395200-17397400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
28	chr9:17395400-17397400	Weak transcription	Fetal Heart	heart
29	chr9:17395400-17413600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr9:17395400-17417800	Weak transcription	NHDF-Ad	bronchial
31	chr9:17395600-17410600	Weak transcription	Monocytes-CD14+_RO01746	blood
32	chr9:17395600-17411200	Weak transcription	Fetal Lung	lung
33	chr9:17395800-17405000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr9:17396000-17399200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
35	chr9:17396000-17410800	Weak transcription	Primary hematopoietic stem cells	blood
36	chr9:17396200-17398400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
37	chr9:17396200-17413200	Weak transcription	Stomach Smooth Muscle	stomach
38	chr9:17396200-17440000	Weak transcription	Adipose Nuclei	Adipose
39	chr9:17396400-17398400	Weak transcription	H9 Cell Line	embryonic stem cell
40	chr9:17396800-17397400	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
41	chr9:17396800-17397400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr9:17396800-17398800	Weak transcription	Liver	Liver
43	chr9:17396800-17411000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr9:17397000-17397600	Active TSS	ES-I3 Cell Line	embryonic stem cell
45	chr9:17397000-17399800	Enhancers	iPS-18 Cell Line	embryonic stem cell
46	chr9:17397200-17397400	Enhancers	HUES6 Cell Line	embryonic stem cell
47	chr9:17397200-17397800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr9:17397200-17398600	Enhancers	H1 Cell Line	embryonic stem cell
49	chr9:17397200-17399600	Enhancers	iPS-20b Cell Line	embryonic stem cell
50	chr9:17397200-17399800	Enhancers	HUES48 Cell Line	embryonic stem cell

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