Variant report

Variant	rs73506048
Chromosome Location	chr11:67272538-67272539
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	POLR2A	chr11:67272463-67273930	Hela-S3	cervix:	n/a	n/a
2	RUNX3	chr11:67272408-67273960	GM12878	blood:	n/a	n/a
3	ETS1	chr11:67272538-67272866	K562	blood:	n/a	n/a
4	YY1	chr11:67272494-67272896	K562	blood:	n/a	chr11:67272694-67272708 chr11:67272873-67272882 chr11:67272868-67272882 chr11:67272731-67272742 chr11:67272614-67272625
5	POLR2A	chr11:67272381-67272988	A549	lung:	n/a	n/a
6	SIN3AK20	chr11:67271730-67273077	PANC-1	pancreas:	n/a	n/a
7	POLR2A	chr11:67272382-67273180	HL-60	blood:	n/a	n/a
8	UBTF	chr11:67271720-67272981	K562	blood:	n/a	n/a
9	CCNT2	chr11:67271695-67273022	K562	blood:	n/a	chr11:67272733-67272742 chr11:67272873-67272882
10	POLR2A	chr11:67272497-67272936	IMR90	lung:	n/a	n/a
11	ZBTB7A	chr11:67271800-67273994	ECC-1	luminal epithelium:	n/a	chr11:67272728-67272737 chr11:67272109-67272116 chr11:67271941-67271949
12	POLR2A	chr11:67272146-67273172	K562	blood:	n/a	n/a
13	RFX5	chr11:67272376-67272898	Hela-S3	cervix:	n/a	n/a
14	MXI1	chr11:67271041-67274152	SK-N-SH	brain:	n/a	n/a
15	CHD1	chr11:67271489-67275717	IMR90	lung:	n/a	chr11:67272871-67272881
16	HMGN3	chr11:67271436-67273890	K562	blood:	n/a	n/a
17	MAZ	chr11:67271837-67273937	Hela-S3	cervix:	n/a	chr11:67272738-67272748 chr11:67271919-67271928
18	POLR2A	chr11:67272533-67273032	Gliobla	brain:	n/a	n/a
19	POLR2A	chr11:67272466-67273080	A549	lung:	n/a	n/a
20	POLR2A	chr11:67271946-67273313	SK-N-MC	brain:	n/a	n/a
21	SPI1	chr11:67272290-67272823	HL-60	blood:	n/a	chr11:67272805-67272812 chr11:67272587-67272600
22	CREB1	chr11:67272423-67273070	A549	lung:	n/a	n/a
23	MTA3	chr11:67271995-67272687	GM12878	blood:	n/a	n/a
24	ELF1	chr11:67272434-67273022	GM12878	blood:	n/a	chr11:67272739-67272751 chr11:67272757-67272769
25	YY1	chr11:67272476-67273099	K562	blood:	n/a	chr11:67272924-67272938 chr11:67272694-67272708 chr11:67272873-67272882 chr11:67272868-67272882 chr11:67272731-67272742 chr11:67272614-67272625
26	MXI1	chr11:67270977-67274595	IMR90	lung:	n/a	n/a
27	POLR2A	chr11:67271683-67273966	K562	blood:	n/a	n/a
28	GABPA	chr11:67272268-67272980	K562	blood:	n/a	chr11:67272873-67272882 chr11:67272929-67272938
29	POLR2A	chr11:67272240-67273951	HepG2	liver:	n/a	n/a
30	TCF3	chr11:67272398-67272835	GM12878	blood:	n/a	chr11:67272488-67272502
31	SIN3A	chr11:67271446-67272848	H1-hESC	embryonic stem cell:	n/a	n/a
32	MXI1	chr11:67272401-67272670	GM12878	blood:	n/a	n/a
33	MYC	chr11:67272246-67272693	K562	blood:	n/a	n/a
34	MYC	chr11:67272430-67272949	K562	blood:	n/a	chr11:67272738-67272748
35	POLR2A	chr11:67272107-67273053	GM12878	blood:	n/a	n/a
36	CTCF	chr11:67272044-67274535	SK-N-SH	brain:	n/a	chr11:67273761-67273770 chr11:67273757-67273770 chr11:67273750-67273771 chr11:67273760-67273773 chr11:67273758-67273768 chr11:67272063-67272076 chr11:67272092-67272105 chr11:67273211-67273224 chr11:67273756-67273772 chr11:67273755-67273773
37	POLR2A	chr11:67272477-67273849	GM15510	blood:	n/a	n/a
38	ZBTB7A	chr11:67272491-67273144	K562	blood:	n/a	chr11:67272728-67272737
39	TCF12	chr11:67272157-67273096	ECC-1	luminal epithelium:	n/a	n/a
40	POLR2A	chr11:67271656-67273878	Hela-S3	cervix:	n/a	n/a
41	POLR2A	chr11:67272223-67273915	GM12878	blood:	n/a	n/a
42	UBTF	chr11:67272340-67273041	K562	blood:	n/a	n/a
43	MAZ	chr11:67272342-67273961	K562	blood:	n/a	chr11:67272738-67272748
44	ELF1	chr11:67271769-67273065	K562	blood:	n/a	chr11:67272739-67272751 chr11:67272757-67272769
45	TFAP2C	chr11:67272399-67273966	Hela-S3	cervix:	n/a	n/a
46	MAX	chr11:67271523-67273957	K562	blood:	n/a	chr11:67272738-67272748 chr11:67271919-67271928
47	POLR2A	chr11:67272379-67272985	GM12892	blood:	n/a	n/a
48	ZBTB7A	chr11:67271774-67273912	ECC-1	luminal epithelium:	n/a	chr11:67272728-67272737 chr11:67272109-67272116 chr11:67271941-67271949
49	RCOR1	chr11:67272450-67273939	Hela-S3	cervix:	n/a	n/a
50	MAZ	chr11:67272494-67273933	GM12878	blood:	n/a	chr11:67272738-67272748

No.	Distal block	Cell Line	Cell type
1	chr11:67118066..67122624-chr11:67272137..67276691,11	MCF-7	breast:
2	chr11:67247191..67252288-chr11:67270350..67277699,12	MCF-7	breast:
3	chr11:67207904..67210724-chr11:67272140..67274356,2	MCF-7	breast:
4	chr11:67234460..67237754-chr11:67271882..67275850,7	MCF-7	breast:
5	chr11:67272321..67273104-chr16:67217348..67218244,2	Hela-S3	cervix:
6	chr11:67157498..67160851-chr11:67271704..67276538,6	K562	blood:
7	chr11:67230107..67238941-chr11:67268499..67277838,23	MCF-7	breast:
8	chr11:67269844..67272585-chr11:67351352..67354034,3	K562	blood:
9	chr11:67157917..67161280-chr11:67271512..67274163,3	MCF-7	breast:
10	chr11:67272431..67272982-chr17:56709064..56709697,2	Hela-S3	cervix:
11	chr11:67164456..67171429-chr11:67268926..67279263,19	K562	blood:
12	chr11:67269985..67274388-chr11:67349964..67354078,4	K562	blood:
13	chr11:67211079..67212845-chr11:67271889..67273813,2	MCF-7	breast:
14	chr11:67182567..67190511-chr11:67270739..67276166,13	MCF-7	breast:
15	chr11:67272321..67272984-chr5:1523828..1524404,2	Hela-S3	cervix:
16	chr11:67272308..67273879-chr17:62223283..62223939,4	Hela-S3	cervix:
17	chr11:67070027..67071819-chr11:67270841..67273414,2	MCF-7	breast:
18	chr1:154934182..154934932-chr11:67272472..67273064,2	Hela-S3	cervix:
19	chr11:67180570..67183103-chr11:67271029..67272927,2	K562	blood:
20	chr11:67166559..67171272-chr11:67271633..67274655,6	MCF-7	breast:
21	chr11:67208782..67211032-chr11:67270751..67273545,3	K562	blood:
22	chr11:67249454..67253550-chr11:67271231..67274487,6	MCF-7	breast:
23	chr11:67270685..67273123-chr11:67274247..67277444,3	K562	blood:
24	chr11:67272189..67272690-chr17:6544274..6544793,2	Hela-S3	cervix:
25	chr11:67272308..67272858-chr5:176943726..176944588,2	Hela-S3	cervix:
26	chr11:67272246..67273016-chr5:36240996..36241835,2	Hela-S3	cervix:
27	chr11:67249912..67253635-chr11:67270546..67273534,5	K562	blood:
28	chr11:67269882..67273775-chr11:67275933..67278364,3	MCF-7	breast:
29	chr11:67271788..67274805-chr11:67372108..67375948,3	K562	blood:
30	chr11:67209787..67211313-chr11:67271082..67272865,2	MCF-7	breast:
31	chr11:67174684..67176198-chr11:67271900..67273931,2	K562	blood:
32	chr11:67271930..67272668-chr14:102553152..102554062,2	Hela-S3	cervix:
33	chr11:67207285..67211032-chr11:67270341..67273194,4	K562	blood:
34	chr11:67159421..67161559-chr11:67272153..67274079,2	K562	blood:
35	chr1:145437932..145438797-chr11:67272453..67273015,2	Hela-S3	cervix:
36	chr11:67164491..67170697-chr11:67268115..67277759,17	MCF-7	breast:
37	chr11:67232230..67238185-chr11:67272105..67277120,9	K562	blood:
38	chr11:67156232..67161608-chr11:67271298..67276147,11	MCF-7	breast:
39	chr11:67195686..67198461-chr11:67271538..67273445,2	K562	blood:
40	chr11:67201617..67208575-chr11:67270788..67277143,13	K562	blood:
41	chr11:67168005..67170770-chr11:67269467..67273329,6	K562	blood:
42	chr11:67186666..67189529-chr11:67272076..67275550,4	K562	blood:
43	chr11:67272403..67272918-chr12:7053158..7054007,2	Hela-S3	cervix:

Variant related genes	Relation type
PITPNM1	TF binding region
ENSG00000266402	Chromatin interaction
ENSG00000199753	Chromatin interaction
ENSG00000172508	Chromatin interaction
ENSG00000153395	Chromatin interaction
ENSG00000167797	Chromatin interaction
ENSG00000196123	Chromatin interaction
ENSG00000080824	Chromatin interaction
ENSG00000175634	Chromatin interaction
ENSG00000167792	Chromatin interaction
ENSG00000129235	Chromatin interaction
ENSG00000172663	Chromatin interaction
ENSG00000117289	Chromatin interaction
ENSG00000172531	Chromatin interaction
ENSG00000183258	Chromatin interaction
ENSG00000184224	Chromatin interaction
ENSG00000272173	Chromatin interaction
ENSG00000213402	Chromatin interaction
ENSG00000172830	Chromatin interaction
ENSG00000175482	Chromatin interaction
ENSG00000172725	Chromatin interaction
ENSG00000111678	Chromatin interaction
ENSG00000271380	Chromatin interaction
ENSG00000110711	Chromatin interaction
ENSG00000255949	Chromatin interaction
ENSG00000152620	Chromatin interaction
ENSG00000212195	Chromatin interaction
ENSG00000163348	Chromatin interaction
ENSG00000172613	Chromatin interaction
ENSG00000175463	Chromatin interaction
ENSG00000255119	Chromatin interaction
ENSG00000084207	Chromatin interaction

Extended variants
information (count: 51 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs1382089	0.85[AMR][1000 genomes]
rs1824712	0.85[AMR][1000 genomes]
rs2514013	0.85[AMR][1000 genomes]
rs2514015	0.85[AMR][1000 genomes]
rs2514018	0.85[AMR][1000 genomes]
rs2514064	0.85[AMR][1000 genomes]
rs3016861	0.85[AMR][1000 genomes]
rs56050553	1.00[AMR][1000 genomes]
rs57047868	1.00[AMR][1000 genomes]
rs57749415	1.00[AMR][1000 genomes]
rs57757103	1.00[AMR][1000 genomes]
rs58999825	0.85[AFR][1000 genomes]
rs60136955	1.00[AMR][1000 genomes]
rs61282424	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61429992	1.00[AMR][1000 genomes]
rs61610719	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7104627	0.85[AFR][1000 genomes]
rs73490545	0.85[AMR][1000 genomes]
rs73490554	0.85[AMR][1000 genomes]
rs73506015	0.85[AFR][1000 genomes]
rs73506054	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73506056	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73506069	1.00[AMR][1000 genomes]
rs73506074	1.00[AMR][1000 genomes]
rs743679	0.85[AMR][1000 genomes]
rs7947114	0.85[AMR][1000 genomes]
rs8191436	1.00[AMR][1000 genomes]
rs8191446	1.00[AMR][1000 genomes]
rs8191449	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:22 , 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	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
6	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
7	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
8	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
9	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
10	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
11	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
12	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
13	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
14	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
15	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
16	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
17	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
18	nsv527056	chr11:67207426-67294308	Genic enhancers Enhancers Flanking Active TSS Strong transcription Weak transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	115 gene(s)	inside rSNPs	diseases
19	esv2422195	chr11:67234322-67626901	Enhancers Strong transcription Bivalent Enhancer Flanking Active TSS Genic enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	146 gene(s)	inside rSNPs	diseases
20	nsv1052919	chr11:67252337-67306030	Active TSS Strong transcription Flanking Active TSS Genic enhancers Enhancers Weak transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	70 gene(s)	inside rSNPs	diseases
21	nsv541078	chr11:67252337-67306030	Weak transcription Enhancers Active TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	70 gene(s)	inside rSNPs	diseases
22	esv3356975	chr11:67270401-67273249	Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	60 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:67270600-67276600	Enhancers	Fetal Heart	heart
2	chr11:67270800-67273000	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr11:67271000-67272600	Transcr. at gene 5' and 3'	Primary T helper 17 cells PMA-I stimulated	--
4	chr11:67271000-67273000	Active TSS	Brain Angular Gyrus	brain
5	chr11:67271000-67276800	Active TSS	Pancreatic Islets	Pancreatic Islet
6	chr11:67271200-67272600	Flanking Active TSS	Adipose Nuclei	Adipose
7	chr11:67271200-67272600	Flanking Active TSS	Brain Hippocampus Middle	brain
8	chr11:67271200-67272600	Active TSS	NHLF	lung
9	chr11:67271200-67273000	Active TSS	H9 Cell Line	embryonic stem cell
10	chr11:67271200-67273000	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr11:67271200-67273000	Active TSS	Osteobl	bone
12	chr11:67271200-67273600	Flanking Active TSS	HMEC	breast
13	chr11:67271200-67273800	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr11:67271200-67275400	Flanking Active TSS	Pancreas	Pancrea
15	chr11:67271200-67275600	Flanking Active TSS	Colonic Mucosa	Colon
16	chr11:67271400-67272800	Active TSS	ES-WA7 Cell Line	embryonic stem cell
17	chr11:67271400-67272800	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr11:67271400-67272800	Active TSS	Brain Cingulate Gyrus	brain
19	chr11:67271400-67273000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr11:67271400-67273000	Active TSS	HUES48 Cell Line	embryonic stem cell
21	chr11:67271400-67273000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr11:67271400-67273000	Active TSS	Brain Anterior Caudate	brain
23	chr11:67271400-67273000	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
24	chr11:67271400-67273000	Active TSS	A549	lung
25	chr11:67271400-67273000	Active TSS	HSMMtube	muscle
26	chr11:67271400-67273000	Active TSS	NHEK	skin
27	chr11:67271400-67273200	Flanking Active TSS	Primary hematopoietic stem cells	blood
28	chr11:67271400-67273600	Flanking Active TSS	Primary B cells from cord blood	blood
29	chr11:67271400-67273800	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
30	chr11:67271600-67272600	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr11:67271600-67272600	Bivalent/Poised TSS	Fetal Stomach	stomach
32	chr11:67271600-67272800	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr11:67271600-67272800	Active TSS	Primary B cells from peripheral blood	blood
34	chr11:67271600-67272800	Active TSS	Primary T cells fromperipheralblood	blood
35	chr11:67271600-67272800	Active TSS	Brain Inferior Temporal Lobe	brain
36	chr11:67271600-67272800	Active TSS	Gastric	stomach
37	chr11:67271600-67272800	Active TSS	Ovary	ovary
38	chr11:67271600-67272800	Active TSS	Sigmoid Colon	Sigmoid Colon
39	chr11:67271600-67272800	Active TSS	Small Intestine	intestine
40	chr11:67271600-67272800	Active TSS	NH-A	brain
41	chr11:67271600-67273000	Active TSS	H1 Cell Line	embryonic stem cell
42	chr11:67271600-67273000	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr11:67271600-67273000	Active TSS	HUES6 Cell Line	embryonic stem cell
44	chr11:67271600-67273000	Active TSS	HUES64 Cell Line	embryonic stem cell
45	chr11:67271600-67273000	Active TSS	iPS-15b Cell Line	embryonic stem cell
46	chr11:67271600-67273000	Active TSS	iPS-18 Cell Line	embryonic stem cell
47	chr11:67271600-67273000	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
48	chr11:67271600-67273000	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr11:67271600-67273000	Active TSS	Breast Myoepithelial Primary Cells	Breast
50	chr11:67271600-67273000	Active TSS	Primary monocytes fromperipheralblood	blood

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