Variant report

Variant	rs571339919
Chromosome Location	chr11:65405938-65405939
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	MTA3	chr11:65405158-65406719	GM12878	blood:	n/a	n/a
2	CTCF	chr11:65405880-65406030	K562	blood:	n/a	chr11:65405916-65405925 chr11:65405910-65405928
3	EBF1	chr11:65405836-65406592	GM12878	blood:	n/a	chr11:65406115-65406126
4	EBF1	chr11:65405412-65406330	GM12878	blood:	n/a	chr11:65406115-65406126
5	CTCF	chr11:65405800-65405950	AoAF	blood vessel:	n/a	chr11:65405916-65405925 chr11:65405910-65405928
6	ZNF143	chr11:65405256-65406124	H1-hESC	embryonic stem cell:	n/a	n/a
7	CTCF	chr11:65405920-65406070	NHDF-neo	bronchial:	n/a	chr11:65406055-65406065
8	CTCF	chr11:65405931-65406166	GM10266	blood:	n/a	chr11:65406055-65406065
9	POLR2A	chr11:65405137-65406416	HUVEC	blood vessel:	n/a	n/a
10	MXI1	chr11:65405363-65406495	GM12878	blood:	n/a	n/a
11	POLR2A	chr11:65405185-65406448	HUVEC	blood vessel:	n/a	n/a
12	CTCF	chr11:65405720-65406010	GM12871	blood:	n/a	chr11:65405916-65405925 chr11:65405910-65405928
13	PML	chr11:65405433-65405982	MCF-7	breast:	n/a	n/a
14	BHLHE40	chr11:65405938-65406242	K562	blood:	n/a	n/a
15	CHD2	chr11:65405326-65406392	GM12878	blood:	n/a	n/a
16	ATF2	chr11:65405265-65406275	GM12878	blood:	n/a	n/a
17	POLR2A	chr11:65405255-65406578	GM12878	blood:	n/a	n/a
18	CTCF	chr11:65405791-65406072	K562	blood:	n/a	chr11:65405916-65405925 chr11:65405910-65405928 chr11:65406055-65406065
19	CBX3	chr11:65405180-65406426	K562	blood:	n/a	n/a
20	CTCF	chr11:65405705-65406168	GM12891	blood:	n/a	chr11:65405916-65405925 chr11:65405910-65405928 chr11:65406055-65406065
21	SP1	chr11:65405159-65406160	H1-hESC	embryonic stem cell:	n/a	chr11:65405938-65405947 chr11:65406148-65406160 chr11:65406145-65406159 chr11:65406149-65406159 chr11:65406150-65406159 chr11:65405937-65405951 chr11:65405936-65405948 chr11:65406150-65406159 chr11:65406148-65406160 chr11:65405936-65405948 chr11:65406149-65406159 chr11:65406149-65406158
22	MAZ	chr11:65405375-65406510	GM12878	blood:	n/a	chr11:65406393-65406403 chr11:65406147-65406157
23	POLR2A	chr11:65404916-65406624	PFSK-1	brain:	n/a	n/a
24	POLR2A	chr11:65405192-65406035	ECC-1	luminal epithelium:	n/a	n/a
25	MYC	chr11:65405219-65406231	K562	blood:	n/a	chr11:65406147-65406157
26	NR2F2	chr11:65404983-65406269	K562	blood:	n/a	n/a
27	POLR2A	chr11:65405564-65406179	H1-hESC	embryonic stem cell:	n/a	n/a
28	ZBTB7A	chr11:65405794-65406456	ECC-1	luminal epithelium:	n/a	chr11:65406053-65406062
29	CTCF	chr11:65405900-65406050	HVMF	connective:	n/a	chr11:65405916-65405925 chr11:65405910-65405928
30	ZNF143	chr11:65405231-65406231	Hela-S3	cervix:	n/a	n/a
31	RCOR1	chr11:65405873-65406052	K562	blood:	n/a	n/a
32	ZBTB7A	chr11:65405262-65406454	K562	blood:	n/a	chr11:65406053-65406062
33	MAX	chr11:65404960-65406338	K562	blood:	n/a	chr11:65406147-65406157
34	CTCF	chr11:65405820-65405970	HFF-Myc	foreskin:	n/a	chr11:65405916-65405925 chr11:65405910-65405928
35	CTCF	chr11:65405860-65406010	BJ	skin:	n/a	chr11:65405916-65405925 chr11:65405910-65405928
36	TCF12	chr11:65405888-65406414	ECC-1	luminal epithelium:	n/a	n/a
37	CEBPD	chr11:65405937-65406297	HepG2	liver:	n/a	n/a
38	CTCF	chr11:65405860-65406010	HRPEpiC	eye:	n/a	chr11:65405916-65405925 chr11:65405910-65405928
39	POLR2A	chr11:65405394-65406536	GM12891	blood:	n/a	n/a
40	PML	chr11:65405205-65406095	K562	blood:	n/a	n/a
41	EP300	chr11:65405713-65406360	GM12878	blood:	n/a	n/a
42	PBX3	chr11:65405303-65406101	A549	lung:	n/a	n/a
43	MTA3	chr11:65405780-65406131	GM12878	blood:	n/a	n/a
44	RELA	chr11:65405279-65406307	GM19099	blood:	n/a	n/a
45	CTCF	chr11:65405920-65406070	HCT-116	colon:	n/a	chr11:65406055-65406065
46	SPI1	chr11:65405917-65406201	GM12878	blood:	n/a	chr11:65406109-65406122
47	CTCF	chr11:65405890-65406194	GM19239	blood:	n/a	chr11:65405916-65405925 chr11:65405910-65405928 chr11:65406055-65406065
48	CHD2	chr11:65405308-65406199	Hela-S3	cervix:	n/a	n/a
49	CTCF	chr11:65405920-65406070	GM12865	blood:	n/a	chr11:65406055-65406065
50	CTCF	chr11:65405920-65406070	NHEK	skin:	n/a	chr11:65406055-65406065

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:65405903-65405953	Hela-S3	cervix:	n/a
2	chr11:65405903-65405953	PANC-1	pancreas:	n/a
3	chr11:65405903-65405953	H1-hESC	embryonic stem cell:	embryo
4	chr11:65405903-65405953	HepG2	liver:	n/a
5	chr11:65405903-65405953	RPTEC	kidney:	n/a
6	chr11:65405903-65405953	SK-N-SH_RA	brain:	n/a
7	chr11:65405903-65405953	AoSMC	blood vessel:	n/a
8	chr11:65405903-65405953	SK-N-MC	brain:	n/a
9	chr11:65405903-65405953	HAEpiC	amniotic membrane:	n/a
10	chr11:65405903-65405953	HIPEpiC	eye:	n/a
11	chr11:65405903-65405953	AG04450	lung:	fetal
12	chr11:65405903-65405953	AG09309	skin:	n/a
13	chr11:65405903-65405953	IMR90	lung:	fetal
14	chr11:65405903-65405953	HCT-116	colon:	n/a
15	chr11:65405903-65405953	CMK	blood:	n/a
16	chr11:65405903-65405953	Caco-2	colon:	n/a
17	chr11:65405903-65405953	LNCaP	prostate:	n/a
18	chr11:65405903-65405953	A549	lung:	n/a
19	chr11:65405903-65405953	HRE	kidney:	n/a
20	chr11:65405903-65405953	NT2-D1	testis:	n/a
21	chr11:65405903-65405953	BE2_C	brain:	n/a
22	chr11:65405903-65405953	SKMC	muscle:	n/a
23	chr11:65405903-65405953	GM12878	blood:	n/a
24	chr11:65405903-65405953	SK-N-SH	brain:	n/a
25	chr11:65405903-65405953	ECC-1	luminal epithelium:	n/a
26	chr11:65405903-65405953	HCF	heart:	n/a
27	chr11:65405903-65405953	T-47D	breast:	n/a
28	chr11:65405903-65405953	PFSK-1	brain:	n/a
29	chr11:65405903-65405953	HMEC	breast:	n/a
30	chr11:65405903-65405953	SAEC	small airway:	n/a
31	chr11:65405903-65405953	NHBE	bronchial:	n/a
32	chr11:65405903-65405953	BJ	skin:	n/a
33	chr11:65405903-65405953	HCM	heart:	n/a
34	chr11:65405903-65405953	ovcar-3	ovarian:	n/a
35	chr11:65405903-65405953	K562	blood:	n/a
36	chr11:65405903-65405953	HRPEpiC	eye:	n/a
37	chr11:65405903-65405953	AG09319	gingival:	n/a
38	chr11:65405903-65405953	PrEC	prostate:	n/a
39	chr11:65405903-65405953	NH-A	brain:	n/a
40	chr11:65405903-65405953	HUVEC	blood vessel:	n/a
41	chr11:65405903-65405953	HEEpiC	esophagus:	n/a
42	chr11:65405903-65405953	NB4	blood:	n/a
43	chr11:65405903-65405953	AG10803	skin:	n/a
44	chr11:65405903-65405953	GM19239	blood:	n/a
45	chr11:65405903-65405953	MCF10A-Er-Src	breast:	n/a
46	chr11:65405903-65405953	HNPCEpiC	eye:	n/a
47	chr11:65405903-65405953	HRCEpiC	kidney:	n/a
48	chr11:65405903-65405953	HEK293	kidney:	embryo
49	chr11:65405903-65405953	Hepatocyte	liver:	n/a
50	chr11:65405903-65405953	HL-60	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:65405500..65407998-chr11:65624581..65626384,2	K562	blood:
2	chr11:65380696..65385200-chr11:65403578..65408941,10	MCF-7	breast:
3	chr11:65403669..65406096-chr11:65480097..65481780,2	MCF-7	breast:
4	chr11:65342220..65345077-chr11:65403229..65406787,3	K562	blood:
5	chr11:65401684..65407000-chr11:65623220..65627704,6	K562	blood:
6	chr11:65404733..65406830-chr11:65478478..65481431,2	K562	blood:
7	chr11:65336849..65339116-chr11:65404161..65406035,2	K562	blood:

Variant related genes	Relation type
SIPA1	TF binding region
SIPA1	CpG island
ENSG00000172977	Chromatin interaction
ENSG00000172732	Chromatin interaction
ENSG00000173442	Chromatin interaction
ENSG00000197136	Chromatin interaction
ENSG00000173327	Chromatin interaction
ENSG00000173465	Chromatin interaction
ENSG00000260233	Chromatin interaction
ENSG00000172757	Chromatin interaction

Extended variants
information (count: 28 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:28 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv897715	chr11:65083491-65427346	Enhancers Genic enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' 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	984 gene(s)	inside rSNPs	diseases
2	nsv897716	chr11:65083491-65481166	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Active TSS 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	999 gene(s)	inside rSNPs	diseases
3	nsv897718	chr11:65140209-65577516	Enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer 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	1003 gene(s)	inside rSNPs	diseases
4	nsv541071	chr11:65142779-65429352	Flanking Active TSS Enhancers Active TSS Weak transcription Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	984 gene(s)	inside rSNPs	diseases
5	nsv897720	chr11:65213434-65445950	Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' 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	665 gene(s)	inside rSNPs	diseases
6	nsv897721	chr11:65278461-65422853	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	88 gene(s)	inside rSNPs	diseases
7	nsv897722	chr11:65278461-65436888	Genic enhancers Strong transcription Active TSS Weak transcription Flanking Active TSS 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 miRNA target site	102 gene(s)	inside rSNPs	diseases
8	nsv897723	chr11:65294830-65481166	Transcr. at gene 5' and 3' Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers 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	107 gene(s)	inside rSNPs	diseases
9	nsv468599	chr11:65335705-65427346	ZNF genes & repeats Genic enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS Enhancers Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	78 gene(s)	inside rSNPs	diseases
10	nsv555213	chr11:65335705-65427346	Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Strong transcription Active TSS Genic enhancers Enhancers 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	78 gene(s)	inside rSNPs	diseases
11	nsv897732	chr11:65335705-65427346	Enhancers Genic enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Strong transcription Active 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 miRNA target site	78 gene(s)	inside rSNPs	diseases
12	nsv468600	chr11:65335705-65431360	Genic enhancers Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	92 gene(s)	inside rSNPs	diseases
13	nsv555214	chr11:65335705-65431360	Weak transcription Strong transcription Genic enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers 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	92 gene(s)	inside rSNPs	diseases
14	nsv897733	chr11:65335705-65431360	Active TSS Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' Enhancers Weak 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	92 gene(s)	inside rSNPs	diseases
15	nsv897734	chr11:65335705-65436888	Flanking Active TSS Enhancers Genic enhancers Active TSS ZNF genes & repeats Strong transcription Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	92 gene(s)	inside rSNPs	diseases
16	nsv897735	chr11:65335705-65481166	Flanking Active TSS Enhancers Strong transcription Genic enhancers Weak transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	98 gene(s)	inside rSNPs	diseases
17	nsv897736	chr11:65335705-65676516	Flanking Active TSS Active TSS Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	227 gene(s)	inside rSNPs	diseases
18	nsv897746	chr11:65349756-65427346	Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
19	nsv897747	chr11:65353906-65481166	Weak transcription Enhancers Active TSS Bivalent/Poised TSS Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	78 gene(s)	inside rSNPs	diseases
20	esv1831135	chr11:65387352-65420872	Strong transcription Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS Enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA	43 gene(s)	inside rSNPs	diseases
21	nsv897748	chr11:65392695-65466911	Active TSS Weak transcription Genic enhancers Bivalent/Poised TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
22	nsv897749	chr11:65401748-65420760	Active TSS Transcr. at gene 5' and 3' Genic enhancers Enhancers Flanking Active TSS Strong transcription Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA	39 gene(s)	inside rSNPs	diseases
23	nsv897750	chr11:65401748-65421476	Weak transcription Active TSS Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
24	nsv897751	chr11:65401748-65425167	Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region miRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
25	nsv897752	chr11:65405300-65421476	Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region miRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
26	nsv897753	chr11:65405300-65422693	Genic enhancers Active TSS Flanking Active TSS Strong transcription Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
27	nsv897754	chr11:65405300-65436888	Transcr. at gene 5' and 3' Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Active TSS 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	59 gene(s)	inside rSNPs	diseases
28	nsv897755	chr11:65405300-65481166	Strong transcription Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	67 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	chr11:65400800-65406600	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr11:65405000-65406000	Transcr. at gene 5' and 3'	Primary T regulatory cells fromperipheralblood	blood
3	chr11:65405000-65406000	Active TSS	Gastric	stomach
4	chr11:65405000-65406400	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr11:65405000-65406400	Enhancers	Fetal Brain Male	brain
6	chr11:65405000-65406400	Flanking Active TSS	Pancreas	Pancrea
7	chr11:65405000-65406600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr11:65405000-65406600	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
9	chr11:65405000-65406600	Flanking Active TSS	Stomach Smooth Muscle	stomach
10	chr11:65405200-65406000	Transcr. at gene 5' and 3'	Primary T helper 17 cells PMA-I stimulated	--
11	chr11:65405200-65406000	Active TSS	Esophagus	oesophagus
12	chr11:65405200-65406200	Active TSS	iPS-18 Cell Line	embryonic stem cell
13	chr11:65405200-65406200	Flanking Active TSS	Colonic Mucosa	Colon
14	chr11:65405200-65406400	Transcr. at gene 5' and 3'	Primary T helper naive cells fromperipheralblood	blood
15	chr11:65405200-65406400	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr11:65405200-65406400	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr11:65405200-65406600	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
18	chr11:65405200-65406600	Flanking Active TSS	Liver	Liver
19	chr11:65405200-65406600	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
20	chr11:65405200-65406600	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
21	chr11:65405200-65406600	Active TSS	HSMMtube	muscle
22	chr11:65405200-65406600	Flanking Active TSS	NHEK	skin
23	chr11:65405200-65406800	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
24	chr11:65405200-65406800	Flanking Active TSS	Fetal Muscle Trunk	muscle
25	chr11:65405200-65409600	Flanking Active TSS	Primary B cells from cord blood	blood
26	chr11:65405200-65409600	Flanking Active TSS	Primary hematopoietic stem cells	blood
27	chr11:65405400-65406000	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr11:65405400-65406000	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr11:65405400-65406000	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
30	chr11:65405400-65406000	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr11:65405400-65406000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr11:65405400-65406000	Active TSS	Primary T helper memory cells from peripheral blood 1	blood
33	chr11:65405400-65406000	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr11:65405400-65406000	Active TSS	Brain Anterior Caudate	brain
35	chr11:65405400-65406000	Active TSS	Brain Cingulate Gyrus	brain
36	chr11:65405400-65406000	Active TSS	Fetal Brain Female	brain
37	chr11:65405400-65406000	Active TSS	Spleen	Spleen
38	chr11:65405400-65406000	Active TSS	A549	lung
39	chr11:65405400-65406200	Active TSS	ES-I3 Cell Line	embryonic stem cell
40	chr11:65405400-65406200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr11:65405400-65406200	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
42	chr11:65405400-65406200	Active TSS	HUES48 Cell Line	embryonic stem cell
43	chr11:65405400-65406200	Active TSS	HUES6 Cell Line	embryonic stem cell
44	chr11:65405400-65406200	Active TSS	HUES64 Cell Line	embryonic stem cell
45	chr11:65405400-65406200	Active TSS	iPS-15b Cell Line	embryonic stem cell
46	chr11:65405400-65406200	Active TSS	iPS-20b Cell Line	embryonic stem cell
47	chr11:65405400-65406200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr11:65405400-65406200	Active TSS	Primary T cells from cord blood	blood
49	chr11:65405400-65406200	Active TSS	Primary T helper naive cells from peripheral blood	blood
50	chr11:65405400-65406200	Active TSS	Primary T helper cells PMA-I stimulated	--

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