Variant report

Variant	rs11231156
Chromosome Location	chr11:62366454-62366455
allele	A/G
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	chr11:62366289-62366912	GM12891	blood:	n/a	n/a
2	POLR2A	chr11:62366356-62367015	HL-60	blood:	n/a	n/a
3	POLR2A	chr11:62366438-62366835	U87	brain:	n/a	n/a
4	NFATC1	chr11:62366454-62367136	GM12878	blood:	n/a	n/a
5	NFIC	chr11:62366253-62367139	SK-N-SH	brain:	n/a	n/a
6	POLR2A	chr11:62366403-62367022	GM12891	blood:	n/a	n/a
7	MYC	chr11:62366401-62367006	H1-hESC	embryonic stem cell:	n/a	n/a
8	POLR2A	chr11:62366105-62367187	HUVEC	blood vessel:	n/a	n/a
9	NFATC1	chr11:62366437-62367039	GM12878	blood:	n/a	n/a
10	SP1	chr11:62366226-62367302	HCT-116	colon:	n/a	chr11:62366846-62366856 chr11:62366857-62366878 chr11:62367145-62367157 chr11:62366794-62366805 chr11:62367146-62367155 chr11:62366846-62366856
11	BHLHE40	chr11:62366423-62367083	GM12878	blood:	n/a	n/a
12	POLR2A	chr11:62366387-62367113	HUVEC	blood vessel:	n/a	n/a
13	POLR2A	chr11:62366082-62366933	Hela-S3	cervix:	n/a	n/a
14	POLR2A	chr11:62366282-62367004	HCT-116	colon:	n/a	n/a
15	POLR2A	chr11:62366144-62367078	GM12892	blood:	n/a	n/a
16	CHD1	chr11:62365894-62370422	IMR90	lung:	n/a	chr11:62369509-62369519 chr11:62368807-62368817 chr11:62368545-62368555
17	GATA3	chr11:62366331-62367327	A549	lung:	n/a	chr11:62367106-62367114
18	POLR2A	chr11:62365391-62367066	GM12878	blood:	n/a	n/a
19	NFIC	chr11:62366244-62367244	ECC-1	luminal epithelium:	n/a	n/a
20	STAT5A	chr11:62366378-62367075	GM12878	blood:	n/a	n/a
21	POLR2A	chr11:62366395-62366947	GM12891	blood:	n/a	n/a
22	POLR2A	chr11:62366300-62367094	H1-hESC	embryonic stem cell:	n/a	n/a
23	HCFC1	chr11:62366328-62367356	Hela-S3	cervix:	n/a	n/a
24	POLR2A	chr11:62366429-62366906	GM12891	blood:	n/a	n/a
25	CHD1	chr11:62366321-62367075	GM12878	blood:	n/a	n/a
26	POLR2A	chr11:62365868-62367108	K562	blood:	n/a	n/a
27	HEY1	chr11:62366453-62366913	K562	blood:	n/a	n/a
28	RFX5	chr11:62366290-62367038	GM12878	blood:	n/a	chr11:62366329-62366337
29	PML	chr11:62366297-62367195	GM12878	blood:	n/a	n/a
30	BCLAF1	chr11:62366229-62367053	GM12878	blood:	n/a	n/a
31	POLR2A	chr11:62366106-62367198	HUVEC	blood vessel:	n/a	n/a
32	NFIC	chr11:62366346-62367136	HepG2	liver:	n/a	n/a
33	POLR2A	chr11:62366248-62367060	SK-N-MC	brain:	n/a	n/a
34	MXI1	chr11:62366403-62367051	GM12878	blood:	n/a	n/a
35	RUNX3	chr11:62366403-62367070	GM12878	blood:	n/a	n/a
36	EBF1	chr11:62365930-62367760	GM12878	blood:	n/a	chr11:62366640-62366651
37	NFIC	chr11:62366400-62367014	HepG2	liver:	n/a	n/a
38	MAX	chr11:62366431-62366993	GM12878	blood:	n/a	n/a
39	POLR2A	chr11:62366244-62367090	GM12892	blood:	n/a	n/a
40	POLR2A	chr11:62366446-62367088	GM12891	blood:	n/a	n/a
41	SP1	chr11:62366266-62367324	HCT-116	colon:	n/a	chr11:62366846-62366856 chr11:62366857-62366878 chr11:62367145-62367157 chr11:62366794-62366805 chr11:62367146-62367155 chr11:62366846-62366856
42	MYBL2	chr11:62366422-62367093	HepG2	liver:	n/a	n/a
43	SP1	chr11:62366415-62367228	A549	lung:	n/a	chr11:62366846-62366856 chr11:62366857-62366878 chr11:62367145-62367157 chr11:62366794-62366805 chr11:62367146-62367155 chr11:62366846-62366856
44	POLR2A	chr11:62366222-62367054	GM12892	blood:	n/a	n/a
45	WRNIP1	chr11:62366285-62367754	GM12878	blood:	n/a	n/a
46	POLR2A	chr11:62366311-62367009	HepG2	liver:	n/a	n/a
47	CBX3	chr11:62366448-62367058	K562	blood:	n/a	n/a
48	TCF12	chr11:62366347-62367262	A549	lung:	n/a	n/a
49	NFIC	chr11:62366299-62367180	ECC-1	luminal epithelium:	n/a	n/a
50	POLR2A	chr11:62365726-62367102	PFSK-1	brain:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:62366402..62370002-chr11:62419166..62421218,5	MCF-7	breast:
2	chr11:62365951..62369565-chr11:62622521..62625872,5	K562	blood:
3	chr11:62365424..62367728-chr11:62413589..62415522,2	K562	blood:
4	chr11:62365249..62367009-chr11:62521402..62523143,2	K562	blood:
5	chr11:62366079..62370074-chr11:62386678..62390504,7	MCF-7	breast:
6	chr11:62340363..62343212-chr11:62365252..62369475,4	MCF-7	breast:
7	chr11:62362631..62371847-chr11:62427548..62442313,26	MCF-7	breast:
8	chr11:62365870..62369296-chr11:62605447..62609594,6	K562	blood:
9	chr11:62366145..62371000-chr11:62493302..62496531,6	K562	blood:
10	chr11:62365873..62371127-chr11:62605447..62611263,11	K562	blood:
11	chr11:62361223..62372590-chr11:62430599..62435389,30	K562	blood:
12	chr11:62366089..62368766-chr11:62475317..62477241,2	MCF-7	breast:
13	chr11:62365667..62370630-chr11:62493549..62497299,5	MCF-7	breast:
14	chr11:62355264..62375429-chr11:62428418..62443271,77	MCF-7	breast:
15	chr11:62365983..62370724-chr11:62412063..62418373,9	K562	blood:
16	chr11:62365338..62373022-chr11:62621930..62625872,13	K562	blood:
17	chr11:62364982..62366719-chr11:62418980..62421459,2	K562	blood:
18	chr11:62363464..62373052-chr11:62429645..62434985,23	K562	blood:
19	chr11:62344267..62349689-chr11:62366431..62369887,5	MCF-7	breast:
20	chr11:62365089..62370067-chr11:62436026..62441323,7	K562	blood:
21	chr11:62364986..62367408-chr11:62393044..62395358,2	MCF-7	breast:
22	chr11:62365885..62368421-chr11:62552476..62555212,3	K562	blood:

Variant related genes	Relation type
MTA2	TF binding region
ENSG00000089597	Chromatin interaction
ENSG00000149016	Chromatin interaction
ENSG00000168003	Chromatin interaction
ENSG00000214756	Chromatin interaction
ENSG00000162194	Chromatin interaction
ENSG00000185475	Chromatin interaction
ENSG00000133316	Chromatin interaction
ENSG00000269176	Chromatin interaction
ENSG00000168000	Chromatin interaction
ENSG00000149541	Chromatin interaction
ENSG00000204922	Chromatin interaction
ENSG00000185085	Chromatin interaction
ENSG00000206597	Chromatin interaction
ENSG00000254772	Chromatin interaction
ENSG00000214753	Chromatin interaction
ENSG00000185670	Chromatin interaction
ENSG00000255508	Chromatin interaction
ENSG00000255717	Chromatin interaction
ENSG00000162222	Chromatin interaction
ENSG00000234857	Chromatin interaction
ENSG00000255432	Chromatin interaction

Extended variants
information (count: 61 )
Associated
traits (count: 12 )

rSNPs within LD-proxies of this variant (count:53)

rs_ID	r²[population]
rs1061093	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs11231138	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.87[AFR][1000 genomes];0.90[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs11231141	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.93[TSI][hapmap];0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs11231144	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.93[TSI][hapmap];0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs11231145	0.87[AFR][1000 genomes];0.97[AMR][1000 genomes];0.90[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs11231150	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11231151	0.93[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11231152	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11231154	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];1.00[MKK][hapmap];0.97[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11231155	0.96[CEU][hapmap];0.88[CHB][hapmap];0.86[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.97[TSI][hapmap];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11231161	0.96[CEU][hapmap];0.84[GIH][hapmap];0.92[MEX][hapmap];0.95[TSI][hapmap];0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11231176	1.00[JPT][hapmap]
rs11553576	0.96[CEU][hapmap];0.81[GIH][hapmap];0.92[MEX][hapmap];0.90[TSI][hapmap];0.86[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs12049914	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12223627	0.93[AFR][1000 genomes];0.87[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12225213	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12226821	0.87[AFR][1000 genomes];0.86[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs12808829	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs17773169	0.92[CEU][hapmap];1.00[CHB][hapmap];0.86[GIH][hapmap];1.00[JPT][hapmap];0.92[MEX][hapmap];0.95[TSI][hapmap];0.82[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1801144	0.92[CEU][hapmap];0.86[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2428548	0.87[CEU][hapmap];1.00[CHB][hapmap]
rs2428549	0.87[CEU][hapmap];1.00[CHB][hapmap]
rs2428551	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2509961	0.87[CEU][hapmap];1.00[CHB][hapmap];0.92[MEX][hapmap]
rs2509982	0.87[CEU][hapmap];1.00[CHB][hapmap]
rs2512562	0.87[CEU][hapmap];1.00[CHB][hapmap]
rs2512563	0.91[CEU][hapmap];1.00[CHB][hapmap]
rs2516633	0.88[CHB][hapmap];0.83[GIH][hapmap];1.00[JPT][hapmap];0.90[TSI][hapmap];0.88[ASN][1000 genomes]
rs2516634	0.83[AMR][1000 genomes];0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2849030	0.96[CEU][hapmap];0.88[CHB][hapmap];0.86[GIH][hapmap];1.00[JPT][hapmap];0.85[MEX][hapmap];0.97[TSI][hapmap];0.81[AMR][1000 genomes];0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2849031	0.96[CEU][hapmap];0.88[CHB][hapmap];0.86[GIH][hapmap];1.00[JPT][hapmap];0.95[TSI][hapmap];0.81[AMR][1000 genomes];0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs34065644	0.83[AFR][1000 genomes];0.84[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs34894392	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs35156678	0.87[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];0.96[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap]
rs35587183	1.00[ASW][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.85[LWK][hapmap];0.81[MKK][hapmap];0.85[TSI][hapmap];1.00[YRI][hapmap];0.82[AFR][1000 genomes];0.80[ASN][1000 genomes]
rs35880596	0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs3923805	0.93[ASN][1000 genomes]
rs58720921	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs60098285	0.91[AFR][1000 genomes];0.84[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs61296092	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs67308910	0.80[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs7124057	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];1.00[MKK][hapmap];0.93[TSI][hapmap];0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];0.93[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs71490390	0.87[AFR][1000 genomes];0.96[AMR][1000 genomes];0.90[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs71490392	0.87[AFR][1000 genomes];0.93[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs71490394	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72927213	0.93[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72927237	0.86[ASN][1000 genomes]
rs7928833	0.90[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs7930896	0.87[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.88[CHD][hapmap];1.00[GIH][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.96[MKK][hapmap];0.93[TSI][hapmap];1.00[YRI][hapmap];0.85[AFR][1000 genomes];0.91[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7937146	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7942154	0.91[AFR][1000 genomes];0.81[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs7942991	1.00[CHB][hapmap];0.88[CHD][hapmap];1.00[JPT][hapmap];0.84[MKK][hapmap];0.83[TSI][hapmap];0.87[AFR][1000 genomes];0.84[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs7943191	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.93[TSI][hapmap];0.96[AMR][1000 genomes];0.90[EUR][1000 genomes];0.80[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv915636	chr11:62016992-62713565	Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	1441 gene(s)	inside rSNPs	diseases
2	nsv532283	chr11:62201358-62863475	Enhancers Flanking Active TSS Genic enhancers Strong transcription Weak transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	1433 gene(s)	inside rSNPs	diseases
3	nsv532284	chr11:62220043-62630253	Weak transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Enhancers Active TSS Strong transcription 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	1401 gene(s)	inside rSNPs	diseases
4	esv3584599	chr11:62262742-62398050	Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Enhancers Weak transcription Bivalent/Poised TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	156 gene(s)	inside rSNPs	diseases
5	nsv832182	chr11:62295575-62462848	Active TSS Strong transcription Weak transcription Flanking Active TSS Enhancers Genic enhancers 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	245 gene(s)	inside rSNPs	diseases
6	nsv825939	chr11:62326083-62410577	Flanking Active TSS Genic enhancers Strong transcription Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	122 gene(s)	inside rSNPs	diseases
7	nsv497903	chr11:62330308-62608042	Weak transcription Strong transcription Active TSS Flanking Active TSS Genic enhancers Enhancers 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	489 gene(s)	inside rSNPs	diseases
8	nsv555174	chr11:62334096-62496519	Strong transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Weak transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	243 gene(s)	inside rSNPs	diseases

mRNA abundance (count:12)

SNP	Gene	Cis/trans	Tissue	Source
rs11231156	CFL1	cis	parietal	SCAN
rs11231156	EML3	cis	Whole Blood	GTEx
rs11231156	ROM1	cis	Thyroid	GTEx
rs11231156	EML3	cis	cerebellum	SCAN
rs11231156	SLC22A25	cis	parietal	SCAN
rs11231156	EEF1G///LOC729998	N/A	lymphoblastoid	RTeQTL
rs11231156	MTA2	cis	Esophagus Mucosa	GTEx
rs11231156	EEF1G	cis	multi-tissue	Pritchard
rs11231156	C11orf48	cis	cerebellum	SCAN
rs11231156	SCYL1	cis	parietal	SCAN
rs11231156	TUT1	cis	parietal	SCAN
rs11231156	EML3	cis	Esophagus Mucosa	GTEx

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:62359800-62368200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr11:62360200-62367200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr11:62360200-62367200	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr11:62360400-62367400	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr11:62360800-62366600	Strong transcription	Esophagus	oesophagus
6	chr11:62361000-62366600	Strong transcription	Fetal Intestine Large	intestine
7	chr11:62361000-62366800	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr11:62361200-62366600	Strong transcription	Colonic Mucosa	Colon
9	chr11:62361200-62366600	Strong transcription	Lung	lung
10	chr11:62361400-62366600	Weak transcription	Right Atrium	heart
11	chr11:62361800-62366600	Strong transcription	Cortex derived primary cultured neurospheres	brain
12	chr11:62364600-62367200	Weak transcription	Pancreatic Islets	Pancreatic Islet
13	chr11:62365000-62367000	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
14	chr11:62365000-62368000	Transcr. at gene 5' and 3'	Hela-S3	cervix
15	chr11:62365200-62368200	Transcr. at gene 5' and 3'	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr11:62365400-62367200	Weak transcription	Small Intestine	intestine
17	chr11:62365400-62367400	Genic enhancers	Skeletal Muscle Female	skeletal muscle
18	chr11:62365600-62367800	Transcr. at gene 5' and 3'	GM12878-XiMat	blood
19	chr11:62365800-62366600	Genic enhancers	Fetal Brain Female	brain
20	chr11:62365800-62366600	Weak transcription	Ovary	ovary
21	chr11:62365800-62366600	Weak transcription	Pancreas	Pancrea
22	chr11:62365800-62366600	Weak transcription	Psoas Muscle	Psoas
23	chr11:62365800-62366800	Weak transcription	Placenta Amnion	Placenta Amnion
24	chr11:62365800-62367200	Genic enhancers	Fetal Muscle Trunk	muscle
25	chr11:62365800-62367400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
26	chr11:62366000-62366600	Transcr. at gene 5' and 3'	Primary T killer memory cells from peripheral blood	blood
27	chr11:62366000-62366600	Genic enhancers	Brain Germinal Matrix	brain
28	chr11:62366000-62366600	Genic enhancers	Brain Inferior Temporal Lobe	brain
29	chr11:62366000-62366600	Genic enhancers	Fetal Adrenal Gland	Adrenal Gland
30	chr11:62366000-62367200	Genic enhancers	Fetal Muscle Leg	muscle
31	chr11:62366000-62367400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr11:62366000-62367400	Weak transcription	H9 Cell Line	embryonic stem cell
33	chr11:62366000-62367400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr11:62366000-62367400	Genic enhancers	Fetal Stomach	stomach
35	chr11:62366000-62368000	Weak transcription	Gastric	stomach
36	chr11:62366000-62368200	Transcr. at gene 5' and 3'	K562	blood
37	chr11:62366200-62366600	Genic enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr11:62366200-62366600	Flanking Active TSS	Primary T cells from cord blood	blood
39	chr11:62366200-62366600	Transcr. at gene 5' and 3'	Primary T helper naive cells from peripheral blood	blood
40	chr11:62366200-62366600	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
41	chr11:62366200-62366600	Transcr. at gene 5' and 3'	Primary T regulatory cells fromperipheralblood	blood
42	chr11:62366200-62366600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr11:62366200-62366600	Weak transcription	Brain Anterior Caudate	brain
44	chr11:62366200-62366600	Enhancers	Brain Cingulate Gyrus	brain
45	chr11:62366200-62366600	Genic enhancers	Brain Dorsolateral Prefrontal Cortex	brain
46	chr11:62366200-62366600	Genic enhancers	Duodenum Mucosa	Duodenum
47	chr11:62366200-62366600	Weak transcription	Left Ventricle	heart
48	chr11:62366200-62366600	Weak transcription	Sigmoid Colon	Sigmoid Colon
49	chr11:62366200-62366600	Transcr. at gene 5' and 3'	HMEC	breast
50	chr11:62366200-62366600	Transcr. at gene 5' and 3'	HSMM	muscle

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