Variant report

Variant	rs8107638
Chromosome Location	chr19:21293527-21293528
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 172 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:154)

rs_ID	r²[population]
rs10164375	0.95[ASN][1000 genomes]
rs10401931	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];0.92[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10403266	0.81[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10405180	0.94[ASN][1000 genomes]
rs10405218	0.94[ASN][1000 genomes]
rs10405406	0.88[ASN][1000 genomes]
rs10406661	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];0.95[ASN][1000 genomes]
rs10408496	0.81[JPT][hapmap]
rs10409844	1.00[CEU][hapmap];0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10409877	0.85[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];0.94[ASN][1000 genomes]
rs10410901	1.00[CHB][hapmap];0.91[JPT][hapmap];1.00[ASN][1000 genomes]
rs10411038	1.00[ASN][1000 genomes]
rs10412267	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];0.97[ASN][1000 genomes]
rs10412509	0.94[JPT][hapmap];1.00[YRI][hapmap];0.88[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs10412688	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs10413175	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10413692	0.80[AMR][1000 genomes];0.95[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs10413983	0.97[ASN][1000 genomes]
rs10414134	0.97[ASN][1000 genomes]
rs10417165	0.82[ASN][1000 genomes]
rs10421819	0.95[ASN][1000 genomes]
rs10423541	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];0.92[ASN][1000 genomes]
rs10424283	0.97[ASN][1000 genomes]
rs10425969	0.94[ASN][1000 genomes]
rs10454116	0.82[ASN][1000 genomes]
rs11085424	0.82[ASN][1000 genomes]
rs11085429	0.83[CEU][hapmap]
rs11085431	1.00[CEU][hapmap];0.86[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11666640	0.94[ASN][1000 genomes]
rs11666869	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11667674	0.91[ASN][1000 genomes]
rs11668952	0.91[ASN][1000 genomes]
rs11668985	0.89[ASN][1000 genomes]
rs11669248	0.98[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11670162	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11671397	0.91[ASN][1000 genomes]
rs11672142	0.81[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11672727	1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs11672747	1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs11878599	0.91[ASN][1000 genomes]
rs12052091	0.83[CEU][hapmap]
rs12104220	0.97[ASN][1000 genomes]
rs12608706	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12608931	0.89[EUR][1000 genomes]
rs12609005	0.94[ASN][1000 genomes]
rs12609167	0.89[CEU][hapmap];0.86[CHB][hapmap];0.94[JPT][hapmap];0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12609427	0.98[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12609831	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12611115	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs12973640	0.83[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12973921	0.91[ASN][1000 genomes]
rs12974016	1.00[ASN][1000 genomes]
rs12975789	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12976796	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs12981855	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1470021	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs1470022	0.97[ASN][1000 genomes]
rs1609441	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs1968523	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1975056	0.83[CEU][hapmap]
rs2013048	0.97[ASN][1000 genomes]
rs2081050	0.80[ASN][1000 genomes]
rs2081055	0.85[EUR][1000 genomes]
rs2081056	0.85[EUR][1000 genomes]
rs2082003	0.91[ASN][1000 genomes]
rs2098681	0.80[ASN][1000 genomes]
rs2112803	0.89[EUR][1000 genomes]
rs2115493	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];0.91[ASN][1000 genomes]
rs2115494	1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs2115495	1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs2115496	0.94[JPT][hapmap]
rs2164988	0.89[ASN][1000 genomes]
rs2164989	0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2195453	1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs2195454	1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs2358792	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2358795	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2358803	0.91[ASN][1000 genomes]
rs2358804	0.91[ASN][1000 genomes]
rs2884554	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs34726293	0.80[EUR][1000 genomes]
rs35137761	1.00[ASN][1000 genomes]
rs4292035	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs4365405	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs4488591	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs4808275	1.00[ASN][1000 genomes]
rs4808276	0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4809119	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4809122	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs62122564	0.85[EUR][1000 genomes]
rs62122565	0.85[EUR][1000 genomes]
rs6511179	0.89[EUR][1000 genomes]
rs6511181	0.80[ASN][1000 genomes]
rs6511183	0.94[ASN][1000 genomes]
rs6511184	0.94[ASN][1000 genomes]
rs6511185	0.85[ASN][1000 genomes]
rs6511186	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6511187	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6511188	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6511190	0.88[ASN][1000 genomes]
rs6511191	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6511192	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];1.00[ASN][1000 genomes]
rs6511194	1.00[CHB][hapmap];0.94[JPT][hapmap];0.81[YRI][hapmap];1.00[ASN][1000 genomes]
rs6511195	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs6511196	1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[YRI][hapmap];0.94[ASN][1000 genomes]
rs6511198	0.91[ASN][1000 genomes]
rs6511199	0.91[ASN][1000 genomes]
rs6511200	0.91[ASN][1000 genomes]
rs6511201	0.91[ASN][1000 genomes]
rs7246723	0.86[CHB][hapmap];1.00[JPT][hapmap];0.87[YRI][hapmap];0.97[ASN][1000 genomes]
rs7247413	0.82[ASN][1000 genomes]
rs7248087	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs7248410	1.00[ASN][1000 genomes]
rs7249283	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7249736	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];0.94[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7250169	0.97[ASN][1000 genomes]
rs7252277	0.82[ASN][1000 genomes]
rs7253530	0.82[ASN][1000 genomes]
rs7253950	0.97[ASN][1000 genomes]
rs7254047	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs7254053	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs7254982	0.95[ASN][1000 genomes]
rs7257481	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7258195	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7258409	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7258831	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7260268	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs7260600	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7343175	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs741674	0.97[ASN][1000 genomes]
rs741676	0.97[ASN][1000 genomes]
rs8100289	0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs8100599	0.97[ASN][1000 genomes]
rs8101222	0.94[ASN][1000 genomes]
rs8101412	0.93[AFR][1000 genomes];0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs8101461	0.99[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs8103696	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs8103825	1.00[ASN][1000 genomes]
rs8106801	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs8106923	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];0.97[ASN][1000 genomes]
rs8107982	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs8109549	0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs8109577	0.81[EUR][1000 genomes]
rs8111827	1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[YRI][hapmap];0.94[ASN][1000 genomes]
rs8112054	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs8112216	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs8112500	1.00[ASN][1000 genomes]
rs8113541	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs8182465	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs9304980	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9304981	0.93[JPT][hapmap];1.00[YRI][hapmap];0.88[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs9304982	0.85[CHB][hapmap];1.00[JPT][hapmap];0.81[YRI][hapmap];0.94[ASN][1000 genomes]
rs9941463	0.82[ASN][1000 genomes]
rs9967619	0.82[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:18 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3385528	chr19:21030777-21495566	Active TSS Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
2	nsv817536	chr19:21041855-21348237	Strong transcription Enhancers Genic enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
3	esv1850387	chr19:21109758-21294264	Active TSS ZNF genes & repeats Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
4	nsv960811	chr19:21200306-21371757	Strong transcription Weak transcription Transcr. at gene 5' and 3' Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
5	esv3399352	chr19:21232738-21423323	Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
6	nsv911412	chr19:21233388-21297358	Strong transcription Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
7	nsv1065384	chr19:21249321-21350698	ZNF genes & repeats Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
8	nsv911413	chr19:21263518-21347598	Weak transcription Enhancers Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
9	esv3319019	chr19:21268262-21336383	Weak transcription ZNF genes & repeats Strong transcription Active TSS Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
10	esv3319020	chr19:21268262-21336383	Flanking Active TSS ZNF genes & repeats Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
11	esv7695	chr19:21268276-21328430	Transcr. at gene 5' and 3' Weak transcription Strong transcription Active TSS ZNF genes & repeats Genic enhancers Flanking Active TSS Enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
12	esv5909	chr19:21272333-21334753	Weak transcription Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS Enhancers Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
13	esv3420290	chr19:21272477-21336432	Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
14	esv3391713	chr19:21272485-21334631	Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
15	esv5243	chr19:21272548-21334670	Strong transcription Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
16	esv7204	chr19:21274198-21336396	Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
17	esv3518033	chr19:21278465-21747567	Strong transcription Weak transcription ZNF genes & repeats Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
18	esv3518034	chr19:21278465-21747567	ZNF genes & repeats Weak transcription Genic enhancers Active TSS Enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs8107638	ZNF714	cis	Nerve Tibial	GTEx

Chromatin state (count:94 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:21265600-21295800	Weak transcription	Small Intestine	intestine
2	chr19:21265600-21300000	Weak transcription	Brain Angular Gyrus	brain
3	chr19:21265600-21305200	Weak transcription	Psoas Muscle	Psoas
4	chr19:21265800-21297200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
5	chr19:21265800-21297200	Weak transcription	Brain Cingulate Gyrus	brain
6	chr19:21265800-21299600	Weak transcription	Brain Inferior Temporal Lobe	brain
7	chr19:21265800-21299800	Weak transcription	Skeletal Muscle Female	skeletal muscle
8	chr19:21265800-21302200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
9	chr19:21265800-21302800	Weak transcription	Fetal Muscle Trunk	muscle
10	chr19:21265800-21303000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
11	chr19:21266000-21297400	Weak transcription	HUVEC	blood vessel
12	chr19:21266200-21296600	Weak transcription	Primary T helper cells PMA-I stimulated	--
13	chr19:21266200-21301600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr19:21267200-21295800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr19:21271200-21296000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr19:21275400-21294200	Weak transcription	Duodenum Smooth Muscle	Duodenum
17	chr19:21275400-21297200	Weak transcription	Rectal Smooth Muscle	rectum
18	chr19:21275400-21301400	Weak transcription	Fetal Brain Male	brain
19	chr19:21275400-21304600	Weak transcription	Stomach Smooth Muscle	stomach
20	chr19:21275600-21299000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
21	chr19:21280000-21297400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
22	chr19:21281800-21300000	Weak transcription	HMEC	breast
23	chr19:21282800-21293600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
24	chr19:21283200-21297200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr19:21284200-21302600	Weak transcription	Brain Substantia Nigra	brain
26	chr19:21284600-21296600	Weak transcription	K562	blood
27	chr19:21284600-21306800	Weak transcription	Left Ventricle	heart
28	chr19:21285000-21297200	Weak transcription	HepG2	liver
29	chr19:21285200-21300200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
30	chr19:21285200-21302000	Weak transcription	Skeletal Muscle Male	skeletal muscle
31	chr19:21286000-21300000	Weak transcription	Hela-S3	cervix
32	chr19:21287800-21296000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr19:21288200-21296400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr19:21288400-21297000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
35	chr19:21288400-21299000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
36	chr19:21288600-21305400	Weak transcription	Fetal Heart	heart
37	chr19:21288800-21300000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
38	chr19:21288800-21303600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr19:21289000-21294400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr19:21289000-21295800	Weak transcription	Esophagus	oesophagus
41	chr19:21289000-21295800	Weak transcription	Lung	lung
42	chr19:21289000-21296600	Weak transcription	Primary T helper cells fromperipheralblood	blood
43	chr19:21289200-21296200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
44	chr19:21289800-21295800	Weak transcription	Fetal Stomach	stomach
45	chr19:21289800-21295800	Weak transcription	Thymus	Thymus
46	chr19:21289800-21296400	Weak transcription	Primary hematopoietic stem cells	blood
47	chr19:21290000-21295800	Weak transcription	Fetal Intestine Small	intestine
48	chr19:21290400-21301200	Weak transcription	Placenta	Placenta
49	chr19:21290600-21303400	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr19:21291000-21295800	Weak transcription	Fetal Thymus	thymus

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