Variant report

Variant	rs1638588
Chromosome Location	chr11:67199706-67199707
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr11:67198736-67211579	HL-60	blood:	n/a	n/a
2	POLR2A	chr11:67198696-67204329	GM12878	blood:	n/a	n/a
3	POLR2A	chr11:67199088-67207292	GM18505	blood:	n/a	n/a
4	POLR2A	chr11:67198721-67204334	GM12878	blood:	n/a	n/a
5	POLR2A	chr11:67199177-67206380	GM19099	blood:	n/a	n/a
6	POLR2A	chr11:67198947-67207334	HL-60	blood:	n/a	n/a
7	POLR2A	chr11:67199446-67204664	GM12891	blood:	n/a	n/a
8	POLR2A	chr11:67199435-67199793	K562	blood:	n/a	n/a
9	POLR2A	chr11:67198772-67200386	GM12878	blood:	n/a	n/a
10	POLR2A	chr11:67199010-67205520	GM12892	blood:	n/a	n/a
11	POLR2A	chr11:67198625-67205482	GM12891	blood:	n/a	n/a
12	POLR2A	chr11:67199678-67205474	GM18526	blood:	n/a	n/a
13	POLR2A	chr11:67198635-67206407	GM12891	blood:	n/a	n/a
14	MTA3	chr11:67198952-67207449	GM12878	blood:	n/a	n/a
15	POLR2A	chr11:67198622-67210790	GM12892	blood:	n/a	n/a
16	POLR2A	chr11:67198810-67206466	GM12878	blood:	n/a	n/a
17	POLR2A	chr11:67199064-67199728	NB4	blood:	n/a	n/a
18	POLR2A	chr11:67198820-67206485	GM19193	blood:	n/a	n/a
19	POLR2A	chr11:67198910-67207363	GM12878	blood:	n/a	n/a
20	POLR2A	chr11:67197957-67210886	GM12892	blood:	n/a	n/a
21	POLR2A	chr11:67198638-67208537	GM12892	blood:	n/a	n/a
22	POU2F2	chr11:67199684-67203080	GM12891	blood:	n/a	chr11:67200378-67200390 chr11:67200330-67200342
23	POLR2A	chr11:67198639-67205514	GM12891	blood:	n/a	n/a
24	POLR2A	chr11:67198862-67200461	K562	blood:	n/a	n/a
25	POLR2A	chr11:67199110-67207194	GM12891	blood:	n/a	n/a
26	POLR2A	chr11:67198642-67211413	K562	blood:	n/a	n/a
27	NFATC1	chr11:67199555-67203193	GM12878	blood:	n/a	n/a
28	POLR2A	chr11:67199483-67199920	K562	blood:	n/a	n/a
29	POLR2A	chr11:67197559-67209128	GM12878	blood:	n/a	n/a
30	NFATC1	chr11:67199634-67205518	GM12878	blood:	n/a	n/a
31	POLR2A	chr11:67199495-67199938	HepG2	liver:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:67198863..67199803-chr19:10513764..10514615,2	NB4	blood:
2	chr11:67194364..67200337-chr11:67272800..67277654,9	MCF-7	breast:

Variant related genes	Relation type
RPS6KB2	TF binding region
ENSG00000105401	Chromatin interaction
ENSG00000221566	Chromatin interaction
ENSG00000167797	Chromatin interaction
ENSG00000110697	Chromatin interaction

Extended variants
information (count: 64 )
Associated
traits (count: 19 )

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs10274	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.96[MEX][hapmap];1.00[TSI][hapmap];0.85[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11227793	0.92[AMR][1000 genomes];0.83[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11601325	0.89[CEU][hapmap];0.94[GIH][hapmap];0.87[MEX][hapmap];0.93[TSI][hapmap];0.87[EUR][1000 genomes]
rs12288107	0.82[CHD][hapmap]
rs12290164	0.82[CHD][hapmap]
rs12573992	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12787021	0.89[ASW][hapmap];1.00[CEU][hapmap];0.80[CHD][hapmap];1.00[GIH][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.96[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs13859	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1476792	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.86[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.85[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1626067	1.00[ASW][hapmap]
rs1628442	0.88[AFR][1000 genomes];0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1638555	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1638556	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.96[LWK][hapmap];0.96[MEX][hapmap];0.96[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1638557	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs1638565	0.89[AFR][1000 genomes];0.82[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs17501521	0.85[GIH][hapmap]
rs1790733	0.80[CHD][hapmap]
rs1790752	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.94[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1790753	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1790761	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[AFR][1000 genomes];0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1808279	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1893973	0.89[EUR][1000 genomes]
rs2109123	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2276118	0.83[CHB][hapmap];0.84[JPT][hapmap];0.91[TSI][hapmap]
rs2302264	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.94[JPT][hapmap];0.96[MEX][hapmap];1.00[TSI][hapmap];0.83[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs35787427	0.87[EUR][1000 genomes]
rs36089024	0.87[EUR][1000 genomes]
rs3741168	1.00[ASW][hapmap];1.00[CEU][hapmap];0.94[CHB][hapmap];1.00[CHD][hapmap];0.94[GIH][hapmap];0.94[JPT][hapmap];1.00[LWK][hapmap];0.96[MEX][hapmap];0.89[MKK][hapmap];0.98[TSI][hapmap];0.84[YRI][hapmap];0.95[AFR][1000 genomes];0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4084113	0.81[CEU][hapmap];0.85[GIH][hapmap];0.87[MEX][hapmap];0.89[TSI][hapmap]
rs4465371	0.81[GIH][hapmap];0.85[TSI][hapmap]
rs4930427	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs595130	0.81[AFR][1000 genomes];0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs61889868	0.85[AFR][1000 genomes];0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs630172	1.00[ASW][hapmap];1.00[CEU][hapmap];0.94[CHB][hapmap];1.00[CHD][hapmap];0.86[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];0.96[MEX][hapmap];0.98[TSI][hapmap];0.84[YRI][hapmap];0.91[AFR][1000 genomes];0.84[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7110021	0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7114510	0.89[CEU][hapmap];0.94[GIH][hapmap];0.87[MEX][hapmap];0.93[TSI][hapmap];0.87[EUR][1000 genomes]
rs7131041	0.81[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7479801	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.96[MEX][hapmap];1.00[TSI][hapmap];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs869736	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.98[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs872375	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs917570	0.81[CEU][hapmap];0.83[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:23 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv531397	chr11:66653381-67465721	Active TSS Enhancers Strong transcription Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	271 gene(s)	inside rSNPs	diseases
2	nsv897797	chr11:67023040-67293234	Flanking Active TSS Strong transcription Enhancers Active TSS Weak transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	206 gene(s)	inside rSNPs	diseases
3	nsv1043037	chr11:67027193-67357425	Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats Weak transcription Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	213 gene(s)	inside rSNPs	diseases
4	nsv897801	chr11:67033076-67432479	Bivalent Enhancer Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	236 gene(s)	inside rSNPs	diseases
5	nsv1048230	chr11:67058231-67252397	Active TSS Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	146 gene(s)	inside rSNPs	diseases
6	nsv897804	chr11:67090571-67224278	Flanking Active TSS Enhancers Weak transcription Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	103 gene(s)	inside rSNPs	diseases
7	nsv1039205	chr11:67135246-67252397	Enhancers Strong transcription Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	122 gene(s)	inside rSNPs	diseases
8	esv1818769	chr11:67138811-67300457	Flanking Active TSS Active TSS Genic enhancers Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	167 gene(s)	inside rSNPs	diseases
9	esv1798859	chr11:67139954-67272983	Active TSS Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	154 gene(s)	inside rSNPs	diseases
10	nsv897805	chr11:67155210-67283891	ZNF genes & repeats Flanking Active TSS Genic enhancers Enhancers Weak transcription Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	148 gene(s)	inside rSNPs	diseases
11	nsv897806	chr11:67155210-67294308	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	148 gene(s)	inside rSNPs	diseases
12	nsv897807	chr11:67155210-67414492	Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	176 gene(s)	inside rSNPs	diseases
13	nsv897808	chr11:67155210-67419855	Flanking Active TSS Strong transcription Enhancers Weak transcription Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	176 gene(s)	inside rSNPs	diseases
14	nsv897809	chr11:67156875-67276235	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Strong transcription Weak transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	148 gene(s)	inside rSNPs	diseases
15	nsv555254	chr11:67164495-67288594	Weak transcription Flanking Active TSS Active TSS Genic enhancers Enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	146 gene(s)	inside rSNPs	diseases
16	nsv534229	chr11:67164667-67411909	Flanking Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	175 gene(s)	inside rSNPs	diseases
17	nsv897811	chr11:67166984-67218909	Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	70 gene(s)	inside rSNPs	diseases
18	nsv897813	chr11:67175692-67283891	Bivalent Enhancer Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	132 gene(s)	inside rSNPs	diseases
19	nsv521723	chr11:67175692-67311258	Bivalent/Poised TSS Flanking Active TSS Active TSS Enhancers Weak transcription 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 miRNA target site	132 gene(s)	inside rSNPs	diseases
20	esv1847460	chr11:67182600-67219337	Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	51 gene(s)	inside rSNPs	diseases
21	nsv524096	chr11:67186000-67224988	Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Weak transcription Strong transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
22	nsv468604	chr11:67186000-67283891	Active TSS Strong transcription Bivalent/Poised TSS Weak transcription Genic enhancers Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	132 gene(s)	inside rSNPs	diseases
23	nsv555256	chr11:67186000-67283891	Enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	132 gene(s)	inside rSNPs	diseases

mRNA abundance (count:19)

SNP	Gene	Cis/trans	Tissue	Source
rs1638588	AP003419.16	cis	Heart Left Ventricle	GTEx
rs1638588	CORO1B	cis	cerebellum	SCAN
rs1638588	RPS6KB2	cis	Lymphoblastoid	GTEx
rs1638588	NDUFV1	cis	parietal	SCAN
rs1638588	PTPRCAP	cis	Esophagus Muscularis	GTEx
rs1638588	PTPRCAP	cis	Heart Left Ventricle	GTEx
rs1638588	PTPRCAP	cis	Adipose Subcutaneous	GTEx
rs1638588	SYVN1	cis	parietal	SCAN
rs1638588	PTPRCAP	cis	Artery Tibial	GTEx
rs1638588	PTPRCAP	cis	Thyroid	GTEx
rs1638588	RPS6KB2	cis	multi-tissue	Pritchard
rs1638588	RPS6KB2	cis	lymphoblastoid	seeQTL
rs1638588	GSTP1	cis	cerebellum	SCAN
rs1638588	GSTP1	cis	parietal	SCAN
rs1638588	PTPRCAP	cis	Nerve Tibial	GTEx
rs1638588	CDC42EP2	cis	parietal	SCAN
rs1638588	PTPRCAP	cis	Skin Sun Exposed Lower leg	GTEx
rs1638588	ATG2A	cis	parietal	SCAN
rs1638588	PTPRCAP	cis	Muscle Skeletal	GTEx

Chromatin state (count:124 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:67196800-67210200	Weak transcription	Fetal Kidney	kidney
2	chr11:67197000-67199800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
3	chr11:67197000-67201000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
4	chr11:67197000-67201400	Genic enhancers	Primary T cells fromperipheralblood	blood
5	chr11:67197000-67202400	Genic enhancers	Fetal Thymus	thymus
6	chr11:67197000-67202800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr11:67197200-67200200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr11:67197200-67200200	Weak transcription	HUES64 Cell Line	embryonic stem cell
9	chr11:67197200-67200200	Weak transcription	HUVEC	blood vessel
10	chr11:67197200-67200400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr11:67197200-67200600	Strong transcription	Thymus	Thymus
12	chr11:67197200-67200800	Weak transcription	Primary hematopoietic stem cells	blood
13	chr11:67197200-67201000	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr11:67197200-67201200	Strong transcription	Fetal Lung	lung
15	chr11:67197200-67201400	Genic enhancers	Primary T regulatory cells fromperipheralblood	blood
16	chr11:67197200-67201800	Weak transcription	Psoas Muscle	Psoas
17	chr11:67197200-67202000	Genic enhancers	Dnd41	blood
18	chr11:67197200-67202800	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr11:67197200-67203000	Weak transcription	HSMM	muscle
20	chr11:67197200-67203400	Strong transcription	Primary monocytes fromperipheralblood	blood
21	chr11:67197200-67203400	Strong transcription	Sigmoid Colon	Sigmoid Colon
22	chr11:67197200-67203600	Strong transcription	Fetal Stomach	stomach
23	chr11:67197200-67203600	Weak transcription	Small Intestine	intestine
24	chr11:67197200-67203800	Strong transcription	Primary neutrophils fromperipheralblood	blood
25	chr11:67197200-67203800	Weak transcription	NH-A	brain
26	chr11:67197200-67206200	Strong transcription	Brain Cingulate Gyrus	brain
27	chr11:67197200-67206800	Weak transcription	Hela-S3	cervix
28	chr11:67197200-67206800	Weak transcription	NHDF-Ad	bronchial
29	chr11:67197200-67207000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr11:67197200-67207000	Weak transcription	Right Atrium	heart
31	chr11:67197200-67209400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr11:67197200-67209800	Weak transcription	Fetal Heart	heart
33	chr11:67197200-67210000	Strong transcription	Fetal Brain Female	brain
34	chr11:67197200-67210000	Weak transcription	Pancreatic Islets	Pancreatic Islet
35	chr11:67197400-67200000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
36	chr11:67197400-67200200	Weak transcription	Stomach Mucosa	stomach
37	chr11:67197400-67202200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
38	chr11:67197400-67206800	Strong transcription	Brain Hippocampus Middle	brain
39	chr11:67197400-67209400	Strong transcription	Fetal Intestine Large	intestine
40	chr11:67197600-67200800	Strong transcription	Fetal Muscle Trunk	muscle
41	chr11:67197600-67202000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr11:67197600-67202200	Strong transcription	Fetal Muscle Leg	muscle
43	chr11:67197600-67203400	Strong transcription	H9 Cell Line	embryonic stem cell
44	chr11:67197600-67203600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr11:67197600-67203600	Strong transcription	Rectal Mucosa Donor 31	rectum
46	chr11:67197600-67204400	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
47	chr11:67197600-67204800	Strong transcription	Fetal Intestine Small	intestine
48	chr11:67197600-67204800	Strong transcription	Right Ventricle	heart
49	chr11:67197600-67208200	Strong transcription	Brain Germinal Matrix	brain
50	chr11:67197600-67209400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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