Variant report

Variant	rs4442529
Chromosome Location	chr11:33060544-33060545
allele	C/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	chr11:33060512-33062694	GM18505	blood:	n/a	n/a
2	POLR2A	chr11:33060540-33061878	HEK293	kidney:	n/a	n/a
3	E2F6	chr11:33060521-33062013	A549	lung:	n/a	chr11:33061310-33061321 chr11:33061634-33061644 chr11:33061273-33061283 chr11:33061633-33061643
4	YY1	chr11:33060505-33061748	GM12891	blood:	n/a	chr11:33060782-33060791 chr11:33060771-33060793 chr11:33060959-33060968 chr11:33060991-33061000 chr11:33061449-33061460 chr11:33060870-33060892 chr11:33060956-33060968 chr11:33061467-33061481 chr11:33060881-33060890
5	MYBL2	chr11:33060484-33061041	HepG2	liver:	n/a	n/a
6	SIN3AK20	chr11:33060413-33061790	MCF-7	breast:	n/a	n/a
7	MAX	chr11:33060467-33062004	ECC-1	luminal epithelium:	n/a	chr11:33061193-33061202
8	NFIC	chr11:33060431-33060891	GM12878	blood:	n/a	n/a
9	E2F6	chr11:33060489-33062038	H1-hESC	embryonic stem cell:	n/a	chr11:33061310-33061321 chr11:33061634-33061644 chr11:33061273-33061283 chr11:33061633-33061643
10	POLR2A	chr11:33060374-33061575	PFSK-1	brain:	n/a	n/a
11	YY1	chr11:33060427-33061918	HepG2	liver:	n/a	chr11:33060782-33060791 chr11:33060771-33060793 chr11:33060959-33060968 chr11:33060991-33061000 chr11:33061449-33061460 chr11:33060870-33060892 chr11:33060956-33060968 chr11:33061467-33061481 chr11:33060881-33060890
12	POLR2A	chr11:33060478-33061879	H1-hESC	embryonic stem cell:	n/a	n/a
13	YY1	chr11:33060502-33061404	GM12892	blood:	n/a	chr11:33060782-33060791 chr11:33060771-33060793 chr11:33060959-33060968 chr11:33060991-33061000 chr11:33060870-33060892 chr11:33060956-33060968 chr11:33060881-33060890
14	ETS1	chr11:33060479-33061346	A549	lung:	n/a	n/a
15	POLR2A	chr11:33060469-33061747	U87	brain:	n/a	n/a
16	HA-E2F1	chr11:33060422-33061875	MCF-7	breast:	n/a	chr11:33061634-33061644 chr11:33061273-33061283 chr11:33061633-33061643
17	BCL3	chr11:33060421-33061205	A549	lung:	n/a	chr11:33060578-33060587 chr11:33060991-33061004 chr11:33061189-33061202
18	YY1	chr11:33060500-33062036	GM12878	blood:	n/a	chr11:33060782-33060791 chr11:33060771-33060793 chr11:33060959-33060968 chr11:33060991-33061000 chr11:33061449-33061460 chr11:33060870-33060892 chr11:33060956-33060968 chr11:33061467-33061481 chr11:33060881-33060890
19	FOXM1	chr11:33060525-33061975	GM12878	blood:	n/a	n/a
20	MAX	chr11:33060516-33062075	HepG2	liver:	n/a	chr11:33061193-33061202
21	POLR2A	chr11:33060441-33061806	SK-N-MC	brain:	n/a	n/a
22	REST	chr11:33060459-33062197	A549	lung:	n/a	chr11:33061645-33061654
23	STAT5A	chr11:33060482-33060806	GM12878	blood:	n/a	n/a
24	TAF1	chr11:33060491-33061680	ECC-1	luminal epithelium:	n/a	n/a
25	POLR2A	chr11:33060529-33061572	ECC-1	luminal epithelium:	n/a	n/a
26	TBP	chr11:33060522-33061977	H1-hESC	embryonic stem cell:	n/a	n/a
27	POLR2A	chr11:33060529-33061434	GM12891	blood:	n/a	n/a
28	YY1	chr11:33060483-33061662	ECC-1	luminal epithelium:	n/a	chr11:33060782-33060791 chr11:33060771-33060793 chr11:33060959-33060968 chr11:33060991-33061000 chr11:33061449-33061460 chr11:33060870-33060892 chr11:33060956-33060968 chr11:33061467-33061481 chr11:33060881-33060890
29	POLR2A	chr11:33060502-33061733	HL-60	blood:	n/a	n/a
30	POLR2A	chr11:33060524-33061608	GM12892	blood:	n/a	n/a
31	YY1	chr11:33060504-33061793	SK-N-SH	brain:	n/a	chr11:33060782-33060791 chr11:33060771-33060793 chr11:33060959-33060968 chr11:33060991-33061000 chr11:33061449-33061460 chr11:33060870-33060892 chr11:33060956-33060968 chr11:33061467-33061481 chr11:33060881-33060890
32	POLR2A	chr11:33060510-33061398	GM12878	blood:	n/a	n/a
33	POLR2A	chr11:33060544-33062064	Hela-S3	cervix:	n/a	n/a
34	CBX3	chr11:33060068-33061604	K562	blood:	n/a	n/a
35	YY1	chr11:33060455-33061904	GM12892	blood:	n/a	chr11:33060782-33060791 chr11:33060771-33060793 chr11:33060959-33060968 chr11:33060991-33061000 chr11:33061449-33061460 chr11:33060870-33060892 chr11:33060956-33060968 chr11:33061467-33061481 chr11:33060881-33060890
36	YY1	chr11:33060457-33061551	H1-hESC	embryonic stem cell:	n/a	chr11:33060782-33060791 chr11:33060771-33060793 chr11:33060959-33060968 chr11:33060991-33061000 chr11:33061449-33061460 chr11:33060870-33060892 chr11:33060956-33060968 chr11:33061467-33061481 chr11:33060881-33060890
37	BCLAF1	chr11:33060479-33061508	GM12878	blood:	n/a	chr11:33061296-33061309 chr11:33061354-33061363 chr11:33061268-33061277 chr11:33060578-33060587 chr11:33060991-33061004 chr11:33061189-33061202
38	POLR2A	chr11:33060530-33062191	H1-neurons	neurons:	n/a	n/a
39	POLR2A	chr11:33060500-33062947	GM12891	blood:	n/a	n/a
40	MAX	chr11:33060507-33062016	SK-N-SH	brain:	n/a	chr11:33061193-33061202
41	POLR2A	chr11:33060533-33060792	GM12891	blood:	n/a	n/a
42	POLR2A	chr11:33060507-33062843	GM12878	blood:	n/a	n/a
43	POLR2A	chr11:33060515-33061580	HL-60	blood:	n/a	n/a
44	POLR2A	chr11:33060306-33062301	H1-hESC	embryonic stem cell:	n/a	n/a
45	ELF1	chr11:33060542-33061462	MCF-7	breast:	n/a	n/a
46	POLR2A	chr11:33060523-33061347	K562	blood:	n/a	n/a
47	POLR2A	chr11:33060453-33061747	U87	brain:	n/a	n/a
48	POLR2A	chr11:33060528-33061696	HUVEC	blood vessel:	n/a	n/a
49	KAP1	chr11:33060506-33061407	HEK293	kidney:	n/a	n/a
50	POLR2A	chr11:33060311-33061845	PFSK-1	brain:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:33057667..33060586-chr11:33062071..33064891,2	MCF-7	breast:
2	chr11:33035321..33039472-chr11:33059106..33064085,11	K562	blood:
3	chr11:33059371..33062523-chr11:33080463..33084324,4	MCF-7	breast:
4	chr11:32914351..32916676-chr11:33059902..33062238,2	K562	blood:
5	chr11:33059557..33062519-chr11:33089882..33091963,2	MCF-7	breast:
6	chr11:32912008..32915658-chr11:33059663..33062231,5	K562	blood:
7	chr11:32912801..32916780-chr11:33060030..33062962,4	MCF-7	breast:
8	chr11:33035752..33039107-chr11:33059295..33062622,5	K562	blood:

Variant related genes	Relation type
TCP11L1	TF binding region
ENSG00000121690	Chromatin interaction
ENSG00000176148	Chromatin interaction
ENSG00000060749	Chromatin interaction

Extended variants
information (count: 46 )
Associated
traits (count: 8 )

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs1033716	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.92[JPT][hapmap];0.95[MEX][hapmap];1.00[TSI][hapmap];0.82[YRI][hapmap];0.92[EUR][1000 genomes]
rs10430950	0.88[EUR][1000 genomes]
rs10767986	0.90[EUR][1000 genomes]
rs11032129	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.92[JPT][hapmap];0.95[MEX][hapmap];1.00[TSI][hapmap];0.82[YRI][hapmap];0.92[EUR][1000 genomes]
rs1407044	0.89[EUR][1000 genomes]
rs1964136	0.94[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[YRI][hapmap];0.91[EUR][1000 genomes]
rs2024967	1.00[CHB][hapmap];1.00[CHD][hapmap];0.92[JPT][hapmap]
rs2273539	0.90[EUR][1000 genomes]
rs2273544	0.95[CEU][hapmap];0.89[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.92[JPT][hapmap];1.00[TSI][hapmap];0.82[YRI][hapmap];0.92[EUR][1000 genomes]
rs3758743	0.92[EUR][1000 genomes]
rs4261257	0.82[AFR][1000 genomes];0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4439489	0.91[EUR][1000 genomes]
rs4561187	1.00[CHB][hapmap];0.82[CHD][hapmap];0.95[GIH][hapmap];0.86[MEX][hapmap]
rs4755486	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4755487	0.92[EUR][1000 genomes]
rs6484638	0.89[EUR][1000 genomes]
rs6484639	1.00[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap];0.82[YRI][hapmap];0.89[EUR][1000 genomes]
rs7114010	0.83[EUR][1000 genomes]
rs7125132	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7125873	0.90[EUR][1000 genomes]
rs7130318	0.92[EUR][1000 genomes]
rs7951757	0.86[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:24 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2753057	chr11:32796124-33061724	Enhancers Strong transcription Weak transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	47 gene(s)	inside rSNPs	diseases
2	esv2753743	chr11:32796124-33084924	Enhancers Strong transcription Flanking Active TSS Weak transcription Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	47 gene(s)	inside rSNPs	diseases
3	nsv1040484	chr11:32951066-33093204	Enhancers Strong transcription Weak transcription Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
4	nsv1046198	chr11:32954100-33075142	Active TSS Enhancers Genic enhancers Strong transcription Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
5	esv2762904	chr11:32969258-33586535	Flanking Active TSS Weak transcription Strong transcription Enhancers Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	65 gene(s)	inside rSNPs	diseases
6	nsv1041149	chr11:32981164-33496670	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	64 gene(s)	inside rSNPs	diseases
7	nsv1053823	chr11:32981164-33533356	Flanking Active TSS Weak transcription Active TSS Enhancers Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	64 gene(s)	inside rSNPs	diseases
8	nsv897194	chr11:32993887-33471804	Active TSS Enhancers Strong transcription Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	64 gene(s)	inside rSNPs	diseases
9	nsv1040572	chr11:33008191-33518964	Enhancers Strong transcription Weak transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	64 gene(s)	inside rSNPs	diseases
10	nsv540989	chr11:33008191-33518964	Enhancers Strong transcription Genic enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	64 gene(s)	inside rSNPs	diseases
11	nsv1042860	chr11:33008191-33562490	Active TSS Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	65 gene(s)	inside rSNPs	diseases
12	nsv540990	chr11:33008191-33562490	Enhancers Flanking Active TSS Genic enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	65 gene(s)	inside rSNPs	diseases
13	nsv533840	chr11:33008192-33595324	Bivalent Enhancer Strong transcription Genic enhancers Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	65 gene(s)	inside rSNPs	diseases
14	nsv1051521	chr11:33008435-33239765	Strong transcription Weak transcription Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
15	nsv540991	chr11:33008435-33239765	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
16	nsv1044478	chr11:33008435-33656273	Enhancers Strong transcription Flanking Active TSS Genic enhancers Weak transcription Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	65 gene(s)	inside rSNPs	diseases
17	nsv897195	chr11:33012493-33559186	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	65 gene(s)	inside rSNPs	diseases
18	nsv1053344	chr11:33028973-33499346	Bivalent Enhancer Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	64 gene(s)	inside rSNPs	diseases
19	nsv1046243	chr11:33043155-33439216	Weak transcription Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Enhancers Bivalent Enhancer Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	59 gene(s)	inside rSNPs	diseases
20	nsv540992	chr11:33043155-33439216	Genic enhancers Enhancers Weak transcription Active TSS Bivalent Enhancer Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	59 gene(s)	inside rSNPs	diseases
21	nsv1050944	chr11:33043155-33656273	Flanking Active TSS Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Weak transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
22	nsv540993	chr11:33043155-33656273	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers 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 target site	61 gene(s)	inside rSNPs	diseases
23	nsv529212	chr11:33053073-33641691	Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
24	nsv869418	chr11:33053073-33662479	Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	61 gene(s)	inside rSNPs	diseases

mRNA abundance (count:8)

SNP	Gene	Cis/trans	Tissue	Source
rs4442529	LOC283267	Cis_1M	lymphoblastoid	RTeQTL
rs4442529	TCP11L1	cis	Artery Tibial	GTEx
rs4442529	TCP11L1	Cis_1M	lymphoblastoid	RTeQTL
rs4442529	TCP11L1	cis	lymphoblastoid	seeQTL
rs4442529	PIGCP1	cis	Skin Sun Exposed Lower leg	GTEx
rs4442529	PIGCP1	cis	Artery Tibial	GTEx
rs4442529	TCP11L1	cis	parietal	SCAN
rs4442529	TCP11L1	cis	Whole Blood	GTEx

Chromatin state (count:118 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:33045200-33060600	Weak transcription	Small Intestine	intestine
2	chr11:33047000-33060600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr11:33053800-33060600	Weak transcription	NHDF-Ad	bronchial
4	chr11:33057000-33060800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr11:33060000-33062200	Active TSS	GM12878-XiMat	blood
6	chr11:33060200-33060600	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
7	chr11:33060200-33060600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr11:33060200-33060600	Enhancers	Fetal Brain Male	brain
9	chr11:33060200-33060600	Enhancers	Stomach Mucosa	stomach
10	chr11:33060200-33060600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
11	chr11:33060200-33060800	Active TSS	Primary T regulatory cells fromperipheralblood	blood
12	chr11:33060200-33060800	Active TSS	Right Atrium	heart
13	chr11:33060200-33061400	Active TSS	Primary hematopoietic stem cells	blood
14	chr11:33060200-33061400	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr11:33060200-33061600	Active TSS	Primary hematopoietic stem cells short term culture	blood
16	chr11:33060200-33061600	Active TSS	Primary T helper cells fromperipheralblood	blood
17	chr11:33060200-33061600	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
18	chr11:33060200-33061600	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr11:33060200-33061600	Active TSS	Adipose Nuclei	Adipose
20	chr11:33060200-33061600	Active TSS	Liver	Liver
21	chr11:33060200-33061800	Active TSS	iPS-18 Cell Line	embryonic stem cell
22	chr11:33060200-33061800	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr11:33060200-33061800	Active TSS	Primary T helper naive cells from peripheral blood	blood
24	chr11:33060200-33061800	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr11:33060200-33061800	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
26	chr11:33060200-33061800	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
27	chr11:33060200-33061800	Active TSS	Brain Anterior Caudate	brain
28	chr11:33060200-33061800	Active TSS	Brain Germinal Matrix	brain
29	chr11:33060200-33061800	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
30	chr11:33060200-33061800	Active TSS	Fetal Intestine Small	intestine
31	chr11:33060200-33061800	Active TSS	Rectal Mucosa Donor 29	rectum
32	chr11:33060200-33061800	Active TSS	Rectal Mucosa Donor 31	rectum
33	chr11:33060200-33061800	Active TSS	Rectal Smooth Muscle	rectum
34	chr11:33060200-33061800	Active TSS	Stomach Smooth Muscle	stomach
35	chr11:33060200-33061800	Active TSS	Osteobl	bone
36	chr11:33060200-33062000	Active TSS	iPS-15b Cell Line	embryonic stem cell
37	chr11:33060200-33062000	Active TSS	Breast Myoepithelial Primary Cells	Breast
38	chr11:33060200-33062000	Active TSS	Brain Angular Gyrus	brain
39	chr11:33060200-33062000	Active TSS	Duodenum Smooth Muscle	Duodenum
40	chr11:33060200-33062000	Active TSS	Fetal Brain Female	brain
41	chr11:33060200-33062000	Active TSS	Fetal Kidney	kidney
42	chr11:33060200-33062000	Active TSS	Skeletal Muscle Male	skeletal muscle
43	chr11:33060200-33062000	Active TSS	A549	lung
44	chr11:33060200-33062000	Active TSS	NHLF	lung
45	chr11:33060200-33062200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr11:33060200-33062200	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
47	chr11:33060200-33062200	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr11:33060200-33062200	Active TSS	Brain Cingulate Gyrus	brain
49	chr11:33060200-33062200	Active TSS	Brain Inferior Temporal Lobe	brain
50	chr11:33060200-33062200	Active TSS	Colonic Mucosa	Colon

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