Variant report

Variant	rs1320688
Chromosome Location	chr11:64068756-64068757
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	CTCF	chr11:64068432-64068835	T-47D	breast:	n/a	chr11:64068631-64068649 chr11:64068633-64068646 chr11:64068632-64068648
2	CTCF	chr11:64068516-64068801	GM10248	blood:	n/a	chr11:64068631-64068649 chr11:64068633-64068646 chr11:64068632-64068648
3	CREB1	chr11:64068526-64068806	A549	lung:	n/a	n/a
4	CTCF	chr11:64068197-64068852	IMR90	lung:	n/a	chr11:64068631-64068649 chr11:64068633-64068646 chr11:64068632-64068648
5	RAD21	chr11:64067835-64069007	HCT-116	colon:	n/a	chr11:64068629-64068648
6	RFX5	chr11:64068552-64068761	HepG2	liver:	n/a	n/a
7	ZNF143	chr11:64068467-64068817	K562	blood:	n/a	n/a
8	MAX	chr11:64068503-64068836	Hela-S3	cervix:	n/a	n/a
9	POLR2A	chr11:64067567-64068958	H1-neurons	neurons:	n/a	n/a
10	CTCF	chr11:64068351-64068877	MCF-7	breast:	n/a	chr11:64068631-64068649 chr11:64068633-64068646 chr11:64068632-64068648
11	CTCF	chr11:64067820-64068953	A549	lung:	n/a	chr11:64068631-64068649 chr11:64068633-64068646 chr11:64068632-64068648
12	MAX	chr11:64067917-64068872	HepG2	liver:	n/a	n/a
13	YY1	chr11:64068508-64068823	GM12892	blood:	n/a	n/a
14	CTCF	chr11:64068480-64068778	MCF-7	breast:	n/a	chr11:64068631-64068649 chr11:64068633-64068646 chr11:64068632-64068648
15	YY1	chr11:64068414-64068800	H1-hESC	embryonic stem cell:	n/a	n/a
16	MYC	chr11:64068485-64068812	MCF10A-Er-Src	breast:	n/a	n/a
17	CTCF	chr11:64067969-64068857	K562	blood:	n/a	chr11:64068631-64068649 chr11:64068633-64068646 chr11:64068632-64068648
18	UBTF	chr11:64068082-64068772	K562	blood:	n/a	n/a
19	ZNF143	chr11:64068450-64068780	Hela-S3	cervix:	n/a	n/a
20	CTCF	chr11:64068505-64068790	LNCaP	prostate:	n/a	chr11:64068631-64068649 chr11:64068633-64068646 chr11:64068632-64068648
21	CTCF	chr11:64068530-64068771	ProgFib	skin:	n/a	chr11:64068631-64068649 chr11:64068633-64068646 chr11:64068632-64068648
22	ZNF143	chr11:64068114-64068810	H1-hESC	embryonic stem cell:	n/a	n/a
23	RAD21	chr11:64068411-64068899	A549	lung:	n/a	chr11:64068629-64068648
24	FOXA1	chr11:64068535-64068773	T-47D	breast:	n/a	n/a
25	MAX	chr11:64068046-64068818	K562	blood:	n/a	n/a
26	CEBPB	chr11:64068471-64068935	ECC-1	luminal epithelium:	n/a	chr11:64068709-64068722
27	SMC3	chr11:64068451-64068844	HepG2	liver:	n/a	n/a
28	ZNF143	chr11:64068463-64068821	GM12878	blood:	n/a	n/a
29	CTCF	chr11:64068502-64068789	Gliobla	brain:	n/a	chr11:64068631-64068649 chr11:64068633-64068646 chr11:64068632-64068648
30	CTCF	chr11:64068236-64068924	HCT-116	colon:	n/a	chr11:64068631-64068649 chr11:64068633-64068646 chr11:64068632-64068648
31	TCF12	chr11:64067905-64069022	A549	lung:	n/a	n/a
32	CHD2	chr11:64068518-64068818	Hela-S3	cervix:	n/a	n/a
33	CTCF	chr11:64068535-64068764	Fibrobl	skin:	n/a	chr11:64068631-64068649 chr11:64068633-64068646 chr11:64068632-64068648
34	E2F6	chr11:64067864-64068883	A549	lung:	n/a	n/a
35	RUNX3	chr11:64068467-64068842	GM12878	blood:	n/a	n/a
36	RCOR1	chr11:64068374-64068776	Hela-S3	cervix:	n/a	n/a
37	ATF2	chr11:64068389-64068827	H1-hESC	embryonic stem cell:	n/a	n/a
38	IRF1	chr11:64068510-64068770	K562	blood:	n/a	n/a
39	CTCF	chr11:64068508-64068771	HUVEC	blood vessel:	n/a	chr11:64068631-64068649 chr11:64068633-64068646 chr11:64068632-64068648
40	POLR2A	chr11:64068206-64068864	K562	blood:	n/a	n/a
41	YY1	chr11:64068491-64068794	GM12878	blood:	n/a	n/a
42	CTCF	chr11:64068011-64068796	GM12892	blood:	n/a	chr11:64068631-64068649 chr11:64068633-64068646 chr11:64068632-64068648
43	SIN3AK20	chr11:64067959-64068841	PANC-1	pancreas:	n/a	n/a
44	TBL1XR1	chr11:64068429-64068861	K562	blood:	n/a	n/a
45	CTCF	chr11:64068013-64068809	GM19238	blood:	n/a	chr11:64068631-64068649 chr11:64068633-64068646 chr11:64068632-64068648
46	RAD21	chr11:64068428-64068826	HepG2	liver:	n/a	chr11:64068629-64068648
47	JUND	chr11:64068436-64068782	H1-hESC	embryonic stem cell:	n/a	n/a
48	ATF3	chr11:64068338-64068837	A549	lung:	n/a	n/a
49	MAX	chr11:64068128-64068852	A549	lung:	n/a	n/a
50	CTCF	chr11:64068389-64068786	K562	blood:	n/a	chr11:64068631-64068649 chr11:64068633-64068646 chr11:64068632-64068648

No.	Distal block	Cell Line	Cell type
1	chr11:64068655..64075946-chr11:64105786..64111623,11	K562	blood:
2	chr11:64067348..64069448-chr11:64121257..64124209,2	K562	blood:
3	chr11:64033188..64045448-chr11:64059274..64075790,38	MCF-7	breast:
4	chr11:64028825..64031822-chr11:64066908..64069442,2	MCF-7	breast:
5	chr11:64066836..64070235-chr11:64070747..64073935,5	MCF-7	breast:
6	chr11:64003628..64022712-chr11:64064086..64078429,56	MCF-7	breast:
7	chr11:63990938..63995618-chr11:64068467..64075569,11	MCF-7	breast:
8	chr11:63971720..63972767-chr11:64067921..64069107,6	K562	blood:
9	chr11:64018488..64019364-chr11:64068361..64069108,3	MCF-7	breast:
10	chr11:63962905..63964449-chr11:64068026..64070756,2	MCF-7	breast:
11	chr11:64036497..64040979-chr11:64067017..64069343,5	MCF-7	breast:
12	chr11:64053956..64054808-chr11:64068204..64069163,2	MCF-7	breast:
13	chr11:63932166..63933935-chr11:64068001..64069547,2	MCF-7	breast:
14	chr11:64018424..64019424-chr11:64068141..64069014,5	K562	blood:
15	chr11:64005251..64012775-chr11:64065543..64076594,19	MCF-7	breast:

Variant related genes	Relation type
ESRRA	TF binding region
TEX40	TF binding region
ENSG00000173457	Chromatin interaction
ENSG00000219435	Chromatin interaction
ENSG00000173153	Chromatin interaction
ENSG00000168439	Chromatin interaction
ENSG00000149761	Chromatin interaction
ENSG00000168071	Chromatin interaction
ENSG00000257086	Chromatin interaction
ENSG00000173511	Chromatin interaction
ENSG00000149782	Chromatin interaction
ENSG00000133315	Chromatin interaction
ENSG00000256940	Chromatin interaction
ENSG00000173486	Chromatin interaction
ENSG00000173264	Chromatin interaction
ENSG00000149743	Chromatin interaction
ENSG00000002330	Chromatin interaction

Extended variants
information (count: 45 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs10128595	0.87[CHD][hapmap];1.00[JPT][hapmap]
rs1124660	0.87[CHD][hapmap];1.00[JPT][hapmap]
rs1207462	0.87[CHD][hapmap]
rs12575515	0.87[CHD][hapmap]
rs1468558	1.00[CHD][hapmap]
rs17159027	1.00[CHD][hapmap]
rs2079786	0.83[CHB][hapmap];0.87[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap]
rs2232410	0.94[ASW][hapmap];1.00[CHD][hapmap];0.94[LWK][hapmap];1.00[YRI][hapmap];0.84[AFR][1000 genomes]
rs2232417	0.86[AFR][1000 genomes]
rs477895	0.84[ASW][hapmap];0.94[LWK][hapmap];0.93[YRI][hapmap]
rs493052	0.94[ASW][hapmap];1.00[CHD][hapmap];0.94[LWK][hapmap];1.00[YRI][hapmap];0.82[AFR][1000 genomes]
rs605827	0.86[AFR][1000 genomes]
rs650008	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap]
rs671976	0.86[YRI][hapmap]
rs687424	0.85[AFR][1000 genomes]
rs7118199	0.84[AFR][1000 genomes]
rs7950596	0.87[CHD][hapmap]
rs7952435	0.83[CHB][hapmap];1.00[CHD][hapmap];0.94[GIH][hapmap]

Variant overlapped rSNPs/rCNVs (count:27 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv897631	chr11:63664882-64129722	Flanking Active TSS Strong transcription Enhancers Weak transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer 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	254 gene(s)	inside rSNPs	diseases
2	esv1802079	chr11:63746066-64151373	Bivalent Enhancer Flanking Active TSS Weak transcription Enhancers Genic enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	247 gene(s)	inside rSNPs	diseases
3	nsv897646	chr11:63754986-64150370	Strong transcription Weak transcription Bivalent Enhancer Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Active TSS 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	245 gene(s)	inside rSNPs	diseases
4	nsv1035875	chr11:63800238-64132030	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	234 gene(s)	inside rSNPs	diseases
5	nsv469961	chr11:63822940-64085967	Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Enhancers Active TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	224 gene(s)	inside rSNPs	diseases
6	nsv897660	chr11:63860826-64125142	Weak transcription Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription 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	231 gene(s)	inside rSNPs	diseases
7	nsv897661	chr11:63863405-64129722	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	233 gene(s)	inside rSNPs	diseases
8	nsv897662	chr11:63889749-64150370	Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	237 gene(s)	inside rSNPs	diseases
9	nsv897664	chr11:63919742-64150370	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh 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	237 gene(s)	inside rSNPs	diseases
10	nsv869944	chr11:63932152-64123062	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	227 gene(s)	inside rSNPs	diseases
11	nsv468593	chr11:63941734-64089874	Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Genic enhancers Strong transcription Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	212 gene(s)	inside rSNPs	diseases
12	nsv555185	chr11:63941734-64089874	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	212 gene(s)	inside rSNPs	diseases
13	nsv555186	chr11:63949095-64097233	Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Strong transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	212 gene(s)	inside rSNPs	diseases
14	nsv897667	chr11:63964657-64078380	Enhancers Strong transcription Flanking Active TSS Weak transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	141 gene(s)	inside rSNPs	diseases
15	nsv897668	chr11:63964657-64085298	Weak transcription Genic enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	163 gene(s)	inside rSNPs	diseases
16	nsv897669	chr11:63964657-64089874	Genic enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	164 gene(s)	inside rSNPs	diseases
17	nsv897670	chr11:63964657-64097233	Flanking Active TSS Weak transcription Active TSS Enhancers Strong transcription Genic enhancers 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	164 gene(s)	inside rSNPs	diseases
18	nsv897671	chr11:63964657-64150370	Active TSS Flanking Active TSS Genic enhancers Weak transcription Enhancers Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	179 gene(s)	inside rSNPs	diseases
19	nsv832186	chr11:63972260-64170059	Active TSS Genic enhancers Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	180 gene(s)	inside rSNPs	diseases
20	nsv897672	chr11:63979643-64082807	Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Weak transcription Strong transcription Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	140 gene(s)	inside rSNPs	diseases
21	esv1802320	chr11:63987425-64154633	Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Weak transcription Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	178 gene(s)	inside rSNPs	diseases
22	nsv897679	chr11:63994692-64150370	Enhancers Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	169 gene(s)	inside rSNPs	diseases
23	nsv897682	chr11:63999529-64170500	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	164 gene(s)	inside rSNPs	diseases
24	nsv1043277	chr11:64002997-64132030	Bivalent/Poised TSS Enhancers Active TSS Flanking Active TSS Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	157 gene(s)	inside rSNPs	diseases
25	nsv897685	chr11:64048912-64150370	Strong transcription Bivalent Enhancer Weak transcription Flanking Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	102 gene(s)	inside rSNPs	diseases
26	nsv897686	chr11:64049021-64072244	Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
27	nsv897687	chr11:64049021-64078380	Flanking Bivalent TSS/Enh Enhancers Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	59 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:100 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:64066600-64068800	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
2	chr11:64066600-64068800	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 1	blood
3	chr11:64066600-64068800	Flanking Bivalent TSS/Enh	Skeletal Muscle Male	skeletal muscle
4	chr11:64066800-64068800	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
5	chr11:64066800-64068800	Flanking Bivalent TSS/Enh	Primary T regulatory cells fromperipheralblood	blood
6	chr11:64066800-64068800	Enhancers	Spleen	Spleen
7	chr11:64067000-64068800	Flanking Bivalent TSS/Enh	Primary T cells from cord blood	blood
8	chr11:64067000-64068800	Flanking Bivalent TSS/Enh	Primary T helper naive cells fromperipheralblood	blood
9	chr11:64067000-64069000	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
10	chr11:64067200-64068800	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
11	chr11:64067200-64068800	Flanking Active TSS	Brain Hippocampus Middle	brain
12	chr11:64067200-64068800	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
13	chr11:64067200-64069200	Bivalent Enhancer	Fetal Thymus	thymus
14	chr11:64067200-64069400	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
15	chr11:64067400-64069000	Flanking Bivalent TSS/Enh	Primary T helper cells PMA-I stimulated	--
16	chr11:64067600-64068800	Flanking Bivalent TSS/Enh	Primary T cells effector/memory enriched fromperipheralblood	blood
17	chr11:64067600-64072000	Weak transcription	Aorta	Aorta
18	chr11:64067800-64068800	Flanking Bivalent TSS/Enh	Primary T helper cells fromperipheralblood	blood
19	chr11:64068000-64068800	Flanking Bivalent TSS/Enh	Primary B cells from cord blood	blood
20	chr11:64068000-64068800	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells short term culture	blood
21	chr11:64068000-64068800	Flanking Bivalent TSS/Enh	Fetal Adrenal Gland	Adrenal Gland
22	chr11:64068000-64068800	Bivalent/Poised TSS	Fetal Kidney	kidney
23	chr11:64068000-64069000	Bivalent/Poised TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr11:64068000-64069000	Flanking Bivalent TSS/Enh	Stomach Smooth Muscle	stomach
25	chr11:64068000-64069400	Active TSS	A549	lung
26	chr11:64068200-64068800	Flanking Active TSS	Dnd41	blood
27	chr11:64068200-64068800	Flanking Bivalent TSS/Enh	NH-A	brain
28	chr11:64068200-64068800	Bivalent/Poised TSS	Osteobl	bone
29	chr11:64068200-64069200	Active TSS	Hela-S3	cervix
30	chr11:64068400-64068800	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
31	chr11:64068400-64068800	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
32	chr11:64068400-64068800	Active TSS	Right Atrium	heart
33	chr11:64068400-64068800	Active TSS	HSMM	muscle
34	chr11:64068400-64068800	Active TSS	HSMMtube	muscle
35	chr11:64068400-64069000	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
36	chr11:64068400-64069000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr11:64068400-64069000	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr11:64068400-64069000	Bivalent Enhancer	Fetal Heart	heart
39	chr11:64068400-64069000	Active TSS	NHDF-Ad	bronchial
40	chr11:64068400-64071400	Weak transcription	Gastric	stomach
41	chr11:64068400-64071600	Weak transcription	Lung	lung
42	chr11:64068600-64068800	Active TSS	ES-WA7 Cell Line	embryonic stem cell
43	chr11:64068600-64068800	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
44	chr11:64068600-64068800	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
45	chr11:64068600-64068800	Active TSS	Primary monocytes fromperipheralblood	blood
46	chr11:64068600-64068800	Bivalent Enhancer	Primary T helper 17 cells PMA-I stimulated	--
47	chr11:64068600-64068800	Active TSS	Muscle Satellite Cultured Cells	--
48	chr11:64068600-64068800	Enhancers	Cortex derived primary cultured neurospheres	brain
49	chr11:64068600-64068800	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr11:64068600-64068800	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin

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