Variant report

Variant	rs1449627
Chromosome Location	chr11:47290984-47290985
allele	G/T
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	GATA3	chr11:47290482-47291864	A549	lung:	n/a	chr11:47290536-47290546 chr11:47291058-47291068
2	REST	chr11:47290301-47291880	PFSK-1	brain:	n/a	chr11:47291210-47291223 chr11:47291653-47291663 chr11:47290941-47290954
3	REST	chr11:47290868-47291852	SK-N-SH	brain:	n/a	chr11:47291210-47291223 chr11:47291653-47291663 chr11:47290941-47290954
4	REST	chr11:47290794-47291122	A549	lung:	n/a	chr11:47290941-47290954
5	HMGN3	chr11:47290376-47291896	K562	blood:	n/a	n/a
6	POLR2A	chr11:47290276-47291902	HUVEC	blood vessel:	n/a	n/a
7	MAX	chr11:47290627-47291871	H1-hESC	embryonic stem cell:	n/a	chr11:47291637-47291647
8	EBF1	chr11:47290976-47291713	GM12878	blood:	n/a	n/a
9	ELF1	chr11:47290124-47291312	MCF-7	breast:	n/a	chr11:47290538-47290549 chr11:47291054-47291067 chr11:47290911-47290922 chr11:47291096-47291108 chr11:47290537-47290548 chr11:47291211-47291223
10	EP300	chr11:47290332-47291123	K562	blood:	n/a	chr11:47290538-47290547 chr11:47290913-47290922
11	IRF1	chr11:47290220-47291902	K562	blood:	n/a	chr11:47291060-47291069 chr11:47290893-47290906 chr11:47291308-47291322
12	PML	chr11:47290271-47291942	K562	blood:	n/a	chr11:47290674-47290682
13	REST	chr11:47289996-47291336	HL-60	blood:	n/a	chr11:47291210-47291223 chr11:47290941-47290954
14	SPI1	chr11:47290248-47291151	GM12891	blood:	n/a	chr11:47290911-47290924 chr11:47290537-47290550 chr11:47290910-47290923 chr11:47290538-47290547
15	TBP	chr11:47290448-47291836	H1-hESC	embryonic stem cell:	n/a	n/a
16	MAX	chr11:47290400-47291869	Hela-S3	cervix:	n/a	chr11:47291637-47291647
17	MBD4	chr11:47290734-47291158	HepG2	liver:	n/a	n/a
18	TAF1	chr11:47290414-47291906	ECC-1	luminal epithelium:	n/a	n/a
19	REST	chr11:47290363-47291270	PFSK-1	brain:	n/a	chr11:47291210-47291223 chr11:47290941-47290954
20	KAP1	chr11:47290398-47291098	U2OS	brain:	n/a	chr11:47290674-47290682
21	FOXM1	chr11:47290343-47291636	GM12878	blood:	n/a	chr11:47291129-47291137
22	POLR2A	chr11:47290308-47291919	U87	brain:	n/a	n/a
23	ETS1	chr11:47290782-47291174	A549	lung:	n/a	chr11:47290914-47290928 chr11:47290915-47290922 chr11:47291127-47291140
24	POLR2A	chr11:47290566-47291930	GM12878	blood:	n/a	n/a
25	POLR2A	chr11:47290665-47291221	GM12891	blood:	n/a	n/a
26	RUNX3	chr11:47290263-47291865	GM12878	blood:	n/a	n/a
27	CHD2	chr11:47290513-47291700	HepG2	liver:	n/a	n/a
28	POLR2A	chr11:47290131-47291929	K562	blood:	n/a	n/a
29	CBX3	chr11:47290189-47291670	K562	blood:	n/a	n/a
30	POLR2A	chr11:47290109-47292622	K562	blood:	n/a	n/a
31	GABPA	chr11:47290298-47291329	HL-60	blood:	n/a	n/a
32	REST	chr11:47290858-47291196	HepG2	liver:	n/a	chr11:47290941-47290954
33	SPI1	chr11:47290141-47291281	HL-60	blood:	n/a	chr11:47290911-47290924 chr11:47290537-47290550 chr11:47290910-47290923 chr11:47290538-47290547
34	EGR1	chr11:47290613-47291519	H1-hESC	embryonic stem cell:	n/a	chr11:47290914-47290923 chr11:47291216-47291230 chr11:47291508-47291518 chr11:47290857-47290870 chr11:47291219-47291232
35	POLR2A	chr11:47290731-47291307	HepG2	liver:	n/a	n/a
36	USF2	chr11:47290472-47291160	Hela-S3	cervix:	n/a	chr11:47290951-47290972
37	TCF12	chr11:47290240-47291991	A549	lung:	n/a	n/a
38	POLR2A	chr11:47290443-47291869	U87	brain:	n/a	n/a
39	ELF1	chr11:47290935-47291913	K562	blood:	n/a	chr11:47291054-47291067 chr11:47291632-47291644 chr11:47291746-47291755 chr11:47291096-47291108 chr11:47291211-47291223
40	POLR2A	chr11:47290308-47291867	PBDE	blood:	n/a	n/a
41	POLR2A	chr11:47290765-47291863	A549	lung:	n/a	n/a
42	GABPA	chr11:47290151-47291414	MCF-7	breast:	n/a	n/a
43	CHD2	chr11:47290763-47291532	H1-hESC	embryonic stem cell:	n/a	n/a
44	POLR2A	chr11:47290329-47291941	GM18526	blood:	n/a	n/a
45	ZMIZ1	chr11:47290428-47291844	K562	blood:	n/a	n/a
46	MYBL2	chr11:47290320-47291745	HepG2	liver:	n/a	n/a
47	POLR2A	chr11:47290335-47291889	HepG2	liver:	n/a	n/a
48	POLR2A	chr11:47290264-47291932	GM12891	blood:	n/a	n/a
49	POLR2A	chr11:47290093-47291914	GM12878	blood:	n/a	n/a
50	SP1	chr11:47290566-47291645	H1-hESC	embryonic stem cell:	n/a	chr11:47291097-47291108 chr11:47291308-47291320 chr11:47290695-47290704 chr11:47291099-47291108 chr11:47291309-47291318

No.	Distal block	Cell Line	Cell type
1	chr11:47290636..47291503-chr7:26239910..26240778,2	Hela-S3	cervix:
2	chr11:47267881..47272421-chr11:47288787..47294481,12	K562	blood:
3	chr11:47290254..47293439-chr11:47374246..47378968,6	MCF-7	breast:
4	chr11:46867608..46869466-chr11:47290892..47293495,3	MCF-7	breast:
5	chr11:47195816..47200318-chr11:47289518..47292814,8	K562	blood:
6	chr11:47289845..47291400-chr11:47428671..47431411,2	K562	blood:
7	chr11:47194502..47201735-chr11:47289181..47294156,14	K562	blood:
8	chr11:47290598..47291112-chr8:141467475..141468152,2	Hela-S3	cervix:
9	chr11:47289567..47294786-chr11:47310778..47315538,7	MCF-7	breast:
10	chr11:47190024..47192945-chr11:47289457..47292109,2	MCF-7	breast:
11	chr11:46401780..46403457-chr11:47290200..47292891,2	MCF-7	breast:
12	chr11:47279843..47284326-chr11:47288675..47293634,16	MCF-7	breast:
13	chr11:47263865..47272320-chr11:47288426..47294726,14	MCF-7	breast:
14	chr11:47264797..47267629-chr11:47289343..47292246,3	K562	blood:
15	chr11:47290951..47293321-chr11:47445782..47448016,2	K562	blood:
16	chr11:47277336..47279783-chr11:47290576..47292976,4	MCF-7	breast:
17	chr11:47235395..47237642-chr11:47289103..47291887,3	K562	blood:
18	chr11:47290799..47291583-chr8:120867901..120868534,2	Hela-S3	cervix:
19	chr11:47289554..47292260-chr11:47397624..47400665,3	K562	blood:
20	chr11:47235321..47238553-chr11:47290387..47292949,4	K562	blood:
21	chr11:47290532..47291465-chr12:46765987..46766807,2	Hela-S3	cervix:
22	chr11:47277979..47283267-chr11:47289057..47293509,9	K562	blood:
23	chr11:47204494..47207545-chr11:47289955..47292546,3	K562	blood:
24	chr11:47268938..47272778-chr11:47288986..47293565,7	MCF-7	breast:
25	chr11:47268303..47273264-chr11:47289525..47294481,12	K562	blood:
26	chr11:47195231..47200543-chr11:47288487..47293127,12	MCF-7	breast:
27	chr11:47290550..47292544-chr11:47348957..47351454,2	MCF-7	breast:
28	chr11:47205837..47210171-chr11:47289770..47293955,7	MCF-7	breast:
29	chr11:47235151..47238129-chr11:47286989..47291992,5	MCF-7	breast:
30	chr11:47290389..47294105-chr11:47428413..47432863,5	MCF-7	breast:
31	chr11:47290429..47293321-chr11:47445782..47448351,3	K562	blood:
32	chr11:47290760..47291689-chr16:67694026..67694999,2	Hela-S3	cervix:
33	chr11:47234552..47236757-chr11:47290593..47292750,2	MCF-7	breast:
34	chr11:47207085..47210178-chr11:47288214..47292056,4	MCF-7	breast:
35	chr11:47196068..47203526-chr11:47288943..47293025,13	MCF-7	breast:

Variant related genes	Relation type
MADD	TF binding region
ENSG00000175216	Chromatin interaction
ENSG00000270060	Chromatin interaction
ENSG00000136982	Chromatin interaction
ENSG00000102977	Chromatin interaction
ENSG00000255197	Chromatin interaction
ENSG00000066336	Chromatin interaction
ENSG00000134574	Chromatin interaction
ENSG00000110492	Chromatin interaction
ENSG00000165912	Chromatin interaction
ENSG00000110514	Chromatin interaction
ENSG00000165915	Chromatin interaction
ENSG00000134571	Chromatin interaction
ENSG00000134575	Chromatin interaction
ENSG00000122566	Chromatin interaction
ENSG00000165916	Chromatin interaction
ENSG00000134294	Chromatin interaction
ENSG00000247675	Chromatin interaction
ENSG00000149182	Chromatin interaction
ENSG00000025434	Chromatin interaction
ENSG00000167632	Chromatin interaction
ENSG00000102981	Chromatin interaction

Extended variants
information (count: 75 )
Associated
traits (count: 13 )

rSNPs within LD-proxies of this variant (count:70)

rs_ID	r²[population]
rs10501321	0.82[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];0.94[JPT][hapmap];0.91[MEX][hapmap];1.00[TSI][hapmap];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1051006	0.82[MEX][hapmap]
rs1052373	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];0.96[YRI][hapmap];0.86[AFR][1000 genomes];0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1055510	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10742799	0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10742801	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10769252	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10769253	0.82[MEX][hapmap]
rs10769255	0.82[MEX][hapmap]
rs10838681	0.81[ASW][hapmap];0.95[MEX][hapmap];0.81[TSI][hapmap];0.86[YRI][hapmap];0.81[AMR][1000 genomes]
rs10838684	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs10838687	0.82[ASW][hapmap];0.83[CHB][hapmap];0.80[CHD][hapmap];0.89[LWK][hapmap];0.86[MEX][hapmap];0.94[MKK][hapmap];0.83[YRI][hapmap];0.87[AFR][1000 genomes]
rs10838689	0.82[MEX][hapmap]
rs10838690	0.87[AFR][1000 genomes];0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10838691	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10838692	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.98[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];0.96[YRI][hapmap];0.92[AFR][1000 genomes];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10838693	0.83[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11039156	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs11039166	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.87[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11039167	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12575456	0.90[AFR][1000 genomes];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1375688	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.93[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2013867	0.90[CEU][hapmap];0.98[GIH][hapmap];0.86[MEX][hapmap];0.87[TSI][hapmap];0.85[EUR][1000 genomes]
rs2167079	0.90[CEU][hapmap];0.98[GIH][hapmap];0.86[MEX][hapmap];0.87[TSI][hapmap];0.84[EUR][1000 genomes]
rs2242261	0.81[MEX][hapmap]
rs2269434	0.94[CEU][hapmap];0.95[CHB][hapmap];0.84[EUR][1000 genomes]
rs2279238	0.82[MEX][hapmap]
rs2279239	0.92[AFR][1000 genomes];0.99[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2290146	0.86[MEX][hapmap]
rs2290148	0.86[MEX][hapmap]
rs2291119	0.89[JPT][hapmap];0.86[ASN][1000 genomes]
rs2301216	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2305280	0.82[ASW][hapmap];0.80[CHD][hapmap];0.82[LWK][hapmap]
rs326214	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];1.00[TSI][hapmap];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs326217	0.86[CHD][hapmap];0.89[JPT][hapmap];0.84[ASN][1000 genomes]
rs326222	0.90[CEU][hapmap];0.98[GIH][hapmap];0.86[MEX][hapmap];0.87[TSI][hapmap];0.85[EUR][1000 genomes]
rs35879051	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs3758669	0.85[EUR][1000 genomes]
rs3758672	0.87[AFR][1000 genomes];0.95[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs3758673	0.94[ASW][hapmap];0.84[CEU][hapmap];0.98[GIH][hapmap];0.86[LWK][hapmap];0.82[MEX][hapmap];0.87[MKK][hapmap];0.93[TSI][hapmap];0.89[YRI][hapmap];0.89[AFR][1000 genomes];0.99[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs3781619	0.82[MEX][hapmap]
rs3781621	0.93[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3781622	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];0.88[AFR][1000 genomes];0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs3816725	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.80[LWK][hapmap];0.95[MEX][hapmap];0.96[MKK][hapmap];1.00[TSI][hapmap];0.80[YRI][hapmap];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs3847502	0.93[AFR][1000 genomes];0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4752822	0.83[AFR][1000 genomes];0.96[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4752824	0.93[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4752825	0.93[AFR][1000 genomes];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4752973	0.82[MEX][hapmap]
rs4752977	0.86[MEX][hapmap]
rs4752979	0.82[AFR][1000 genomes]
rs4752980	0.83[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4752983	0.82[MEX][hapmap]
rs59663860	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs61896050	0.94[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6485746	0.81[AFR][1000 genomes];0.91[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7109147	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7109203	0.81[EUR][1000 genomes]
rs7118396	0.82[MEX][hapmap]
rs7120118	0.88[ASW][hapmap];0.90[CEU][hapmap];0.98[GIH][hapmap];0.91[MEX][hapmap];0.93[TSI][hapmap];0.89[YRI][hapmap];0.88[AFR][1000 genomes];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7120957	0.88[AFR][1000 genomes];0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7124955	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.94[TSI][hapmap];0.87[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7127907	0.93[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7129661	0.86[EUR][1000 genomes]
rs7395581	0.94[ASW][hapmap];0.85[CEU][hapmap];0.98[GIH][hapmap];0.86[TSI][hapmap];0.93[YRI][hapmap];0.84[EUR][1000 genomes]
rs753992	0.82[MEX][hapmap]
rs753993	0.83[CHB][hapmap]
rs7940809	0.93[AFR][1000 genomes];0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs830085	0.94[ASW][hapmap];0.90[CEU][hapmap];0.98[GIH][hapmap];0.80[LWK][hapmap];0.91[MEX][hapmap];0.87[TSI][hapmap];0.93[YRI][hapmap];0.84[EUR][1000 genomes]
rs901746	0.90[CEU][hapmap];0.98[GIH][hapmap];0.86[MEX][hapmap];0.87[TSI][hapmap];0.85[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv897323	chr11:47182926-47460306	Genic enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	96 gene(s)	inside rSNPs	diseases
2	nsv917316	chr11:47232210-47448882	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	81 gene(s)	inside rSNPs	diseases
3	esv3330173	chr11:47289256-47450681	Enhancers Flanking Active TSS Strong transcription Weak transcription Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	62 gene(s)	inside rSNPs	diseases
4	esv3416377	chr11:47289276-47450651	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	62 gene(s)	inside rSNPs	diseases
5	esv3407193	chr11:47290401-47292949	Flanking Active TSS Active TSS Enhancers Genic enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases

mRNA abundance (count:13)

SNP	Gene	Cis/trans	Tissue	Source
rs1449627	ACP2	cis	multi-tissue	Pritchard
rs1449627	DDB2	cis	lymphoblastoid	seeQTL
rs1449627	ACP2	Cis_1M	lymphoblastoid	RTeQTL
rs1449627	MADD	cis	cerebellum	SCAN
rs1449627	MTCH2	cis	cerebellum	SCAN
rs1449627	NR1H3	cis	parietal	SCAN
rs1449627	PACSIN3	cis	Esophagus Mucosa	GTEx
rs1449627	ACP2	cis	Thyroid	GTEx
rs1449627	NR1H3	cis	lymphoblastoid	seeQTL
rs1449627	ACP2	cis	lymphoblastoid	seeQTL
rs1449627	DGKZ	cis	cerebellum	SCAN
rs1449627	MADD	cis	parietal	SCAN
rs1449627	ATG13	cis	cerebellum	SCAN

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:47289400-47291200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr11:47289600-47291200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
3	chr11:47289800-47291000	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
4	chr11:47289800-47291000	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
5	chr11:47289800-47291200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr11:47290000-47291000	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
7	chr11:47290000-47291000	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
8	chr11:47290000-47291000	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
9	chr11:47290000-47291000	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
10	chr11:47290000-47291000	Flanking Active TSS	Colon Smooth Muscle	Colon
11	chr11:47290000-47291000	Flanking Active TSS	Fetal Lung	lung
12	chr11:47290000-47291000	Flanking Active TSS	Rectal Smooth Muscle	rectum
13	chr11:47290000-47291000	Flanking Active TSS	NH-A	brain
14	chr11:47290000-47291000	Flanking Active TSS	NHDF-Ad	bronchial
15	chr11:47290000-47291000	Flanking Active TSS	Osteobl	bone
16	chr11:47290000-47291200	Flanking Active TSS	Primary T cells fromperipheralblood	blood
17	chr11:47290000-47291200	Flanking Active TSS	Primary hematopoietic stem cells	blood
18	chr11:47290000-47291200	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
19	chr11:47290000-47291200	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
20	chr11:47290200-47291000	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
21	chr11:47290200-47291000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr11:47290200-47291000	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
23	chr11:47290200-47291000	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
24	chr11:47290200-47291000	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
25	chr11:47290200-47291000	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
26	chr11:47290200-47291000	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
27	chr11:47290200-47291000	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr11:47290200-47291000	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr11:47290200-47291000	Flanking Active TSS	Adipose Nuclei	Adipose
30	chr11:47290200-47291000	Flanking Active TSS	Brain Cingulate Gyrus	brain
31	chr11:47290200-47291000	Flanking Active TSS	Brain Germinal Matrix	brain
32	chr11:47290200-47291000	Flanking Active TSS	Brain Hippocampus Middle	brain
33	chr11:47290200-47291000	Transcr. at gene 5' and 3'	Fetal Thymus	thymus
34	chr11:47290200-47291000	Flanking Active TSS	Stomach Mucosa	stomach
35	chr11:47290200-47291000	Flanking Active TSS	Stomach Smooth Muscle	stomach
36	chr11:47290200-47291000	Flanking Active TSS	A549	lung
37	chr11:47290200-47291000	Flanking Active TSS	GM12878-XiMat	blood
38	chr11:47290200-47291000	Flanking Active TSS	HMEC	breast
39	chr11:47290200-47291000	Flanking Active TSS	HSMMtube	muscle
40	chr11:47290200-47291200	Flanking Active TSS	Primary B cells from cord blood	blood
41	chr11:47290200-47291200	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
42	chr11:47290200-47291200	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
43	chr11:47290200-47291200	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
44	chr11:47290200-47291200	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
45	chr11:47290200-47291200	Flanking Active TSS	Dnd41	blood
46	chr11:47290200-47291200	Flanking Active TSS	HUVEC	blood vessel
47	chr11:47290200-47291200	Flanking Active TSS	NHEK	skin
48	chr11:47290400-47291000	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr11:47290400-47291000	Flanking Active TSS	Primary B cells from peripheral blood	blood
50	chr11:47290400-47291000	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood

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