Variant report

Variant	rs7949394
Chromosome Location	chr11:67349320-67349321
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:27)
CpG islands
(count:61)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:27 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	HNF4A	chr11:67348983-67349386	HepG2	liver:	n/a	chr11:67349210-67349225
2	ESR1	chr11:67348909-67349363	ECC-1	luminal epithelium:	n/a	n/a
3	SP1	chr11:67348942-67349338	H1-hESC	embryonic stem cell:	n/a	n/a
4	RXRA	chr11:67348942-67349355	HepG2	liver:	n/a	n/a
5	ZNF217	chr11:67349049-67349326	MCF-7	breast:	n/a	n/a
6	HDAC2	chr11:67348918-67349372	HepG2	liver:	n/a	n/a
7	TEAD4	chr11:67348822-67349378	H1-hESC	embryonic stem cell:	n/a	n/a
8	NR2F2	chr11:67348907-67349392	HepG2	liver:	n/a	n/a
9	EP300	chr11:67348940-67349343	H1-hESC	embryonic stem cell:	n/a	n/a
10	GATA3	chr11:67348740-67350617	MCF-7	breast:	n/a	n/a
11	SP1	chr11:67348913-67349365	H1-hESC	embryonic stem cell:	n/a	n/a
12	ESR1	chr11:67348972-67349343	ECC-1	luminal epithelium:	n/a	n/a
13	TCF7L2	chr11:67349055-67349323	MCF-7	breast:	n/a	chr11:67349212-67349226
14	ATF2	chr11:67348900-67349371	H1-hESC	embryonic stem cell:	n/a	n/a
15	EP300	chr11:67348871-67349431	HepG2	liver:	n/a	n/a
16	NR2F2	chr11:67348924-67349518	HepG2	liver:	n/a	n/a
17	HNF4G	chr11:67349017-67349370	HepG2	liver:	n/a	n/a
18	NR2F2	chr11:67348895-67349493	MCF-7	breast:	n/a	n/a
19	ARID3A	chr11:67348839-67349354	HepG2	liver:	n/a	n/a
20	BACH1	chr11:67349004-67349371	H1-hESC	embryonic stem cell:	n/a	n/a
21	NR2F2	chr11:67348945-67349496	MCF-7	breast:	n/a	n/a
22	HNF4A	chr11:67349085-67349345	HepG2	liver:	n/a	chr11:67349210-67349225
23	TEAD4	chr11:67348877-67349448	H1-hESC	embryonic stem cell:	n/a	n/a
24	TCF7L2	chr11:67349153-67349348	Hela-S3	cervix:	n/a	chr11:67349212-67349226
25	SP1	chr11:67348940-67349463	HepG2	liver:	n/a	n/a
26	TEAD4	chr11:67348794-67349375	HepG2	liver:	n/a	n/a
27	HDAC2	chr11:67348937-67349358	H1-hESC	embryonic stem cell:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:67349309-67349359	MCF-7	breast:	n/a
2	chr11:67349309-67349359	PANC-1	pancreas:	n/a
3	chr11:67349309-67349359	SK-N-SH	brain:	n/a
4	chr11:67349309-67349359	A549	lung:	n/a
5	chr11:67349309-67349359	HCPEpiC	choroid plexus:	n/a
6	chr11:67349309-67349359	BE2_C	brain:	n/a
7	chr11:67349309-67349359	AG09309	skin:	n/a
8	chr11:67349309-67349359	NT2-D1	testis:	n/a
9	chr11:67349309-67349359	Hela-S3	cervix:	n/a
10	chr11:67349309-67349359	H1-hESC	embryonic stem cell:	embryo
11	chr11:67349309-67349359	HRCEpiC	kidney:	n/a
12	chr11:67349309-67349359	HAEpiC	amniotic membrane:	n/a
13	chr11:67349309-67349359	ProgFib	skin:	n/a
14	chr11:67349309-67349359	Hepatocyte	liver:	n/a
15	chr11:67349309-67349359	HEK293	kidney:	embryo
16	chr11:67349309-67349359	Jurkat	blood:	n/a
17	chr11:67349309-67349359	HRPEpiC	eye:	n/a
18	chr11:67349309-67349359	ECC-1	luminal epithelium:	n/a
19	chr11:67349309-67349359	HL-60	blood:	n/a
20	chr11:67349309-67349359	PFSK-1	brain:	n/a
21	chr11:67349309-67349359	Caco-2	colon:	n/a
22	chr11:67349309-67349359	GM06990	blood:	n/a
23	chr11:67349309-67349359	U87	brain:	n/a
24	chr11:67349309-67349359	AoSMC	blood vessel:	n/a
25	chr11:67349309-67349359	HEEpiC	esophagus:	n/a
26	chr11:67349309-67349359	MCF10A-Er-Src	breast:	n/a
27	chr11:67349309-67349359	HIPEpiC	eye:	n/a
28	chr11:67349309-67349359	SK-N-SH_RA	brain:	n/a
29	chr11:67349309-67349359	NH-A	brain:	n/a
30	chr11:67349309-67349359	GM19239	blood:	n/a
31	chr11:67349309-67349359	HNPCEpiC	eye:	n/a
32	chr11:67349309-67349359	HepG2	liver:	n/a
33	chr11:67349309-67349359	K562	blood:	n/a
34	chr11:67349309-67349359	BJ	skin:	n/a
35	chr11:67349309-67349359	HPAEpiC	pulmonary alveolar:	n/a
36	chr11:67349309-67349359	HCF	heart:	n/a
37	chr11:67349309-67349359	SAEC	small airway:	n/a
38	chr11:67349309-67349359	AG04449	skin:	fetal
39	chr11:67349309-67349359	HCT-116	colon:	n/a
40	chr11:67349309-67349359	AG04450	lung:	fetal
41	chr11:67349309-67349359	ovcar-3	ovarian:	n/a
42	chr11:67349309-67349359	CMK	blood:	n/a
43	chr11:67349309-67349359	AG09319	gingival:	n/a
44	chr11:67349309-67349359	HCM	heart:	n/a
45	chr11:67349309-67349359	IMR90	lung:	fetal
46	chr11:67349309-67349359	RPTEC	kidney:	n/a
47	chr11:67349309-67349359	GM12878	blood:	n/a
48	chr11:67349309-67349359	T-47D	breast:	n/a
49	chr11:67349309-67349359	LNCaP	prostate:	n/a
50	chr11:67349309-67349359	GM12891	blood:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:67349088..67352896-chr11:67377453..67387652,15	K562	blood:
2	chr11:67275111..67277928-chr11:67348479..67351408,2	MCF-7	breast:
3	chr11:67348020..67353194-chr11:67379787..67385803,14	K562	blood:
4	chr11:67347575..67355744-chr11:67372717..67376912,13	K562	blood:
5	chr11:67348370..67350367-chr11:67374395..67376609,2	MCF-7	breast:
6	chr11:67347249..67355748-chr11:67372717..67377095,16	K562	blood:
7	chr11:67344360..67352769-chr11:67395394..67400721,12	K562	blood:
8	chr11:67349032..67351635-chr11:67571367..67573562,2	K562	blood:
9	chr11:67348847..67353254-chr11:67396059..67399206,10	K562	blood:

No data

Variant related genes	Relation type
GSTP1	TF binding region
GSTP1	CpG island
ENSG00000160172	Chromatin interaction
ENSG00000255119	Chromatin interaction
ENSG00000231793	Chromatin interaction
ENSG00000167797	Chromatin interaction
ENSG00000184224	Chromatin interaction
ENSG00000167799	Chromatin interaction
ENSG00000167792	Chromatin interaction

Extended variants
information (count: 56 )
Associated
traits (count: 3 )

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs1079719	0.88[AFR][1000 genomes];0.85[AMR][1000 genomes];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10896181	0.91[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11603735	0.80[ASN][1000 genomes]
rs11605586	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs17593068	0.94[AFR][1000 genomes];0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1871042	0.81[ASN][1000 genomes]
rs2370141	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2370142	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2370143	0.88[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs36211089	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4930436	0.94[EUR][1000 genomes]
rs55854833	0.88[AFR][1000 genomes];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs58046082	0.87[EUR][1000 genomes]
rs597297	0.88[AFR][1000 genomes]
rs6591249	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6591251	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6591252	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6591253	0.80[ASN][1000 genomes]
rs6591254	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6591255	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6591256	0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6591258	0.81[ASN][1000 genomes]
rs7103713	0.89[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7106423	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7106675	0.89[EUR][1000 genomes]
rs7108426	0.91[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs749174	0.80[ASN][1000 genomes]
rs762803	0.92[AFR][1000 genomes];0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7927657	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7940813	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7941395	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7941648	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7945035	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7945927	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7948478	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7948823	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7948911	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7949587	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7952081	0.90[EUR][1000 genomes]
rs947895	0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:16 , 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	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
3	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
4	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
5	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
6	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
7	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
8	nsv1041988	chr11:67319916-67749246	Enhancers Weak transcription Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	84 gene(s)	inside rSNPs	diseases
9	nsv897814	chr11:67339949-67460529	Strong transcription Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
10	nsv1050463	chr11:67343421-67717338	Enhancers Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	79 gene(s)	inside rSNPs	diseases
11	nsv1038189	chr11:67345320-67749246	Transcr. at gene 5' and 3' Active TSS Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	81 gene(s)	inside rSNPs	diseases
12	nsv1047236	chr11:67345320-67764068	Bivalent Enhancer Enhancers Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	83 gene(s)	inside rSNPs	diseases
13	nsv555268	chr11:67346743-67752972	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS 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	81 gene(s)	inside rSNPs	diseases
14	nsv1036101	chr11:67346813-67828351	Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Active TSS Weak transcription Genic enhancers 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	139 gene(s)	inside rSNPs	diseases
15	nsv541079	chr11:67346813-67828351	Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	139 gene(s)	inside rSNPs	diseases
16	nsv897815	chr11:67347595-67408791	Enhancers Genic enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS 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 target site	47 gene(s)	inside rSNPs	diseases

mRNA abundance (count:3)

SNP	Gene	Cis/trans	Tissue	Source
rs7949394	PTPRCAP	cis	Artery Tibial	GTEx
rs7949394	PTPRCAP	cis	Nerve Tibial	GTEx
rs7949394	PTPRCAP	cis	Adipose Subcutaneous	GTEx

Chromatin state (count:66 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:67344400-67350600	Enhancers	Stomach Mucosa	stomach
2	chr11:67345600-67350200	Enhancers	Fetal Intestine Small	intestine
3	chr11:67346800-67350600	Enhancers	Pancreas	Pancrea
4	chr11:67346800-67351000	Enhancers	Liver	Liver
5	chr11:67347200-67350200	Weak transcription	Right Ventricle	heart
6	chr11:67347400-67349600	Weak transcription	Primary T cells from cord blood	blood
7	chr11:67347400-67349800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
8	chr11:67347400-67349800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
9	chr11:67347400-67350000	Enhancers	Fetal Kidney	kidney
10	chr11:67347400-67350000	Weak transcription	Sigmoid Colon	Sigmoid Colon
11	chr11:67347400-67350200	Weak transcription	Colonic Mucosa	Colon
12	chr11:67347400-67350400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
13	chr11:67347400-67351200	Weak transcription	Spleen	Spleen
14	chr11:67347600-67349600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
15	chr11:67347600-67349600	Weak transcription	Primary B cells from peripheral blood	blood
16	chr11:67347600-67349600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
17	chr11:67347600-67349600	Weak transcription	Primary T helper cells PMA-I stimulated	--
18	chr11:67347600-67349800	Weak transcription	Primary T helper cells fromperipheralblood	blood
19	chr11:67347600-67349800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
20	chr11:67347600-67349800	Weak transcription	Rectal Mucosa Donor 29	rectum
21	chr11:67347600-67350000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
22	chr11:67347600-67350000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
23	chr11:67347600-67350000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
24	chr11:67347600-67350000	Weak transcription	HMEC	breast
25	chr11:67347600-67350200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr11:67347600-67350200	Weak transcription	Rectal Mucosa Donor 31	rectum
27	chr11:67347600-67350400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
28	chr11:67347600-67350400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr11:67347600-67350400	Enhancers	HepG2	liver
30	chr11:67347600-67350400	Weak transcription	HSMM	muscle
31	chr11:67347800-67350000	Weak transcription	Small Intestine	intestine
32	chr11:67347800-67350800	Weak transcription	Gastric	stomach
33	chr11:67348000-67349600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
34	chr11:67348000-67350000	Weak transcription	Lung	lung
35	chr11:67348200-67350000	Enhancers	HUES48 Cell Line	embryonic stem cell
36	chr11:67348400-67350400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr11:67348400-67350800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr11:67348400-67350800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
39	chr11:67348600-67349600	Weak transcription	Duodenum Mucosa	Duodenum
40	chr11:67348600-67349800	Enhancers	iPS-15b Cell Line	embryonic stem cell
41	chr11:67348600-67350200	Enhancers	NHEK	skin
42	chr11:67348600-67350400	Enhancers	H1 Cell Line	embryonic stem cell
43	chr11:67348600-67350400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr11:67348600-67350600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
45	chr11:67348800-67349400	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
46	chr11:67348800-67349400	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
47	chr11:67348800-67349400	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
48	chr11:67348800-67349400	Flanking Active TSS	A549	lung
49	chr11:67348800-67350000	Enhancers	ES-I3 Cell Line	embryonic stem cell
50	chr11:67348800-67350000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin

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