Variant report

Variant	rs2077407
Chromosome Location	chr19:41119829-41119830
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	chr19:41119128-41120954	GM12878	blood:	n/a	n/a
2	POLR2A	chr19:41119610-41119950	A549	lung:	n/a	n/a
3	PBX3	chr19:41119748-41120119	GM12878	blood:	n/a	chr19:41119997-41120006
4	SP1	chr19:41119543-41120167	K562	blood:	n/a	chr19:41119593-41119602 chr19:41119754-41119764 chr19:41119952-41119961 chr19:41120055-41120066 chr19:41119591-41119603 chr19:41119952-41119961 chr19:41119592-41119601 chr19:41119951-41119963 chr19:41119754-41119764 chr19:41119953-41119962 chr19:41119672-41119681 chr19:41119951-41119963 chr19:41120019-41120030 chr19:41119593-41119602 chr19:41119592-41119602 chr19:41119588-41119602 chr19:41120035-41120046 chr19:41119591-41119603 chr19:41119592-41119602
5	POLR2A	chr19:41119238-41120019	GM12891	blood:	n/a	n/a
6	MAX	chr19:41119491-41120783	MCF-7	breast:	n/a	n/a
7	POLR2A	chr19:41119016-41120123	GM12878	blood:	n/a	n/a
8	NFYA	chr19:41119771-41120054	GM12878	blood:	n/a	n/a
9	E2F6	chr19:41119204-41120106	H1-hESC	embryonic stem cell:	n/a	chr19:41119592-41119601 chr19:41119227-41119236 chr19:41119779-41119790
10	SP1	chr19:41118953-41120109	GM12878	blood:	n/a	chr19:41119593-41119602 chr19:41119754-41119764 chr19:41119952-41119961 chr19:41119228-41119237 chr19:41120055-41120066 chr19:41119591-41119603 chr19:41119223-41119237 chr19:41119952-41119961 chr19:41119592-41119601 chr19:41119228-41119237 chr19:41119951-41119963 chr19:41118956-41118965 chr19:41119754-41119764 chr19:41119226-41119238 chr19:41119953-41119962 chr19:41119173-41119187 chr19:41119672-41119681 chr19:41118954-41118966 chr19:41119951-41119963 chr19:41119227-41119236 chr19:41120019-41120030 chr19:41119226-41119238 chr19:41119593-41119602 chr19:41119592-41119602 chr19:41118955-41118965 chr19:41119588-41119602 chr19:41119227-41119237 chr19:41119227-41119237 chr19:41119246-41119258 chr19:41118955-41118969 chr19:41120035-41120046 chr19:41119591-41119603 chr19:41119592-41119602
11	MYC	chr19:41119704-41120026	MCF-7	breast:	n/a	n/a
12	YY1	chr19:41119613-41119943	K562	blood:	n/a	n/a
13	RCOR1	chr19:41119167-41120184	K562	blood:	n/a	n/a
14	HCFC1	chr19:41119182-41119913	K562	blood:	n/a	n/a
15	POLR2A	chr19:41118763-41120672	H1-hESC	embryonic stem cell:	n/a	n/a
16	BCL3	chr19:41119032-41119886	A549	lung:	n/a	chr19:41119190-41119198
17	SPI1	chr19:41119570-41119847	GM12878	blood:	n/a	n/a
18	POLR2A	chr19:41119223-41120081	GM12878	blood:	n/a	n/a
19	NFYB	chr19:41119768-41120104	K562	blood:	n/a	n/a
20	POLR2A	chr19:41119600-41119961	A549	lung:	n/a	n/a
21	MAZ	chr19:41119378-41121483	IMR90	lung:	n/a	chr19:41121193-41121202 chr19:41121098-41121108
22	E2F6	chr19:41119198-41120097	K562	blood:	n/a	chr19:41119592-41119601 chr19:41119227-41119236 chr19:41119779-41119790
23	POLR2A	chr19:41118887-41120030	A549	lung:	n/a	n/a
24	ELK1	chr19:41119287-41119959	GM12878	blood:	n/a	n/a
25	MAX	chr19:41119111-41120261	A549	lung:	n/a	chr19:41119225-41119235
26	SP1	chr19:41119166-41120109	A549	lung:	n/a	chr19:41119593-41119602 chr19:41119754-41119764 chr19:41119952-41119961 chr19:41119228-41119237 chr19:41120055-41120066 chr19:41119591-41119603 chr19:41119223-41119237 chr19:41119952-41119961 chr19:41119592-41119601 chr19:41119228-41119237 chr19:41119951-41119963 chr19:41119754-41119764 chr19:41119226-41119238 chr19:41119953-41119962 chr19:41119173-41119187 chr19:41119672-41119681 chr19:41119951-41119963 chr19:41119227-41119236 chr19:41120019-41120030 chr19:41119226-41119238 chr19:41119593-41119602 chr19:41119592-41119602 chr19:41119588-41119602 chr19:41119227-41119237 chr19:41119227-41119237 chr19:41119246-41119258 chr19:41120035-41120046 chr19:41119591-41119603 chr19:41119592-41119602
27	ZNF143	chr19:41119173-41120123	GM12878	blood:	n/a	n/a
28	CHD2	chr19:41119652-41120172	H1-hESC	embryonic stem cell:	n/a	n/a
29	STAT1	chr19:41119156-41120174	GM12878	blood:	n/a	chr19:41119493-41119505
30	SP4	chr19:41118995-41119981	H1-hESC	embryonic stem cell:	n/a	chr19:41119244-41119260 chr19:41119589-41119605 chr19:41119224-41119240 chr19:41119587-41119603 chr19:41119751-41119767
31	SIN3A	chr19:41119010-41120846	H1-hESC	embryonic stem cell:	n/a	chr19:41119191-41119204 chr19:41120571-41120582
32	MAX	chr19:41119485-41120074	K562	blood:	n/a	n/a
33	MAX	chr19:41119127-41120599	ECC-1	luminal epithelium:	n/a	chr19:41119225-41119235
34	E2F6	chr19:41119113-41120112	H1-hESC	embryonic stem cell:	n/a	chr19:41119592-41119601 chr19:41119227-41119236 chr19:41119779-41119790
35	BCL3	chr19:41119067-41119897	A549	lung:	n/a	chr19:41119190-41119198
36	POLR2A	chr19:41119175-41120130	GM19099	blood:	n/a	n/a
37	MAX	chr19:41119554-41119970	GM12878	blood:	n/a	n/a
38	POLR2A	chr19:41118766-41120158	HCT-116	colon:	n/a	n/a
39	GABPA	chr19:41119054-41119846	A549	lung:	n/a	chr19:41119227-41119236 chr19:41119592-41119601
40	SIN3A	chr19:41119197-41119934	GM12878	blood:	n/a	n/a
41	TBL1XR1	chr19:41119700-41120211	K562	blood:	n/a	n/a
42	TAF1	chr19:41119643-41120142	H1-hESC	embryonic stem cell:	n/a	n/a
43	TEAD4	chr19:41119153-41119976	K562	blood:	n/a	n/a
44	EP300	chr19:41119815-41119933	GM12878	blood:	n/a	n/a
45	POLR2A	chr19:41119085-41120075	ECC-1	luminal epithelium:	n/a	n/a
46	FOXP2	chr19:41119638-41120032	PFSK-1	brain:	n/a	n/a
47	CTCF	chr19:41119634-41119866	Spleen_OC	spleen:	n/a	n/a
48	POLR2A	chr19:41119612-41120014	GM12878	blood:	n/a	n/a
49	SP1	chr19:41118911-41121215	H1-hESC	embryonic stem cell:	n/a	chr19:41119593-41119602 chr19:41120965-41120977 chr19:41119754-41119764 chr19:41119952-41119961 chr19:41119228-41119237 chr19:41120622-41120631 chr19:41120055-41120066 chr19:41120642-41120654 chr19:41120643-41120653 chr19:41119591-41119603 chr19:41119223-41119237 chr19:41119952-41119961 chr19:41119592-41119601 chr19:41119228-41119237 chr19:41119951-41119963 chr19:41118956-41118965 chr19:41119754-41119764 chr19:41119226-41119238 chr19:41120643-41120653 chr19:41119953-41119962 chr19:41119173-41119187 chr19:41119672-41119681 chr19:41118954-41118966 chr19:41120642-41120654 chr19:41119951-41119963 chr19:41120643-41120652 chr19:41119227-41119236 chr19:41120019-41120030 chr19:41119226-41119238 chr19:41119593-41119602 chr19:41119592-41119602 chr19:41120965-41120977 chr19:41118955-41118965 chr19:41120643-41120652 chr19:41119588-41119602 chr19:41120644-41120653 chr19:41120966-41120975 chr19:41119227-41119237 chr19:41119227-41119237 chr19:41119246-41119258 chr19:41118955-41118969 chr19:41120035-41120046 chr19:41121049-41121063 chr19:41119591-41119603 chr19:41119592-41119602 chr19:41120643-41120657
50	POLR2A	chr19:41119609-41120114	GM12878	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:41119829-41119879	NHBE	bronchial:	n/a
2	chr19:41119829-41119879	GM12891	blood:	n/a
3	chr19:41119829-41119879	A549	lung:	n/a
4	chr19:41119829-41119879	PFSK-1	brain:	n/a
5	chr19:41119829-41119879	PANC-1	pancreas:	n/a
6	chr19:41119829-41119879	ovcar-3	ovarian:	n/a
7	chr19:41119829-41119879	HRCEpiC	kidney:	n/a
8	chr19:41119829-41119879	BE2_C	brain:	n/a
9	chr19:41119829-41119879	HCF	heart:	n/a
10	chr19:41119829-41119879	AG04449	skin:	fetal
11	chr19:41119829-41119879	NB4	blood:	n/a
12	chr19:41119829-41119879	HCM	heart:	n/a
13	chr19:41119829-41119879	Jurkat	blood:	n/a
14	chr19:41119829-41119879	GM12878	blood:	n/a
15	chr19:41119829-41119879	ProgFib	skin:	n/a
16	chr19:41119829-41119879	H1-hESC	embryonic stem cell:	embryo
17	chr19:41119829-41119879	HL-60	blood:	n/a
18	chr19:41119829-41119879	NHDF-neo	bronchial:	n/a
19	chr19:41119829-41119879	HRE	kidney:	n/a
20	chr19:41119829-41119879	NH-A	brain:	n/a
21	chr19:41119829-41119879	HPAEpiC	pulmonary alveolar:	n/a
22	chr19:41119829-41119879	U87	brain:	n/a
23	chr19:41119829-41119879	GM12892	blood:	n/a
24	chr19:41119829-41119879	LNCaP	prostate:	n/a
25	chr19:41119829-41119879	AoSMC	blood vessel:	n/a
26	chr19:41119829-41119879	SAEC	small airway:	n/a
27	chr19:41119829-41119879	Hela-S3	cervix:	n/a
28	chr19:41119829-41119879	K562	blood:	n/a
29	chr19:41119829-41119879	HepG2	liver:	n/a
30	chr19:41119829-41119879	HIPEpiC	eye:	n/a
31	chr19:41119829-41119879	AG10803	skin:	n/a
32	chr19:41119829-41119879	HEK293	kidney:	embryo
33	chr19:41119829-41119879	NT2-D1	testis:	n/a
34	chr19:41119829-41119879	HCPEpiC	choroid plexus:	n/a
35	chr19:41119829-41119879	SK-N-SH	brain:	n/a
36	chr19:41119829-41119879	Caco-2	colon:	n/a
37	chr19:41119829-41119879	HUVEC	blood vessel:	n/a
38	chr19:41119829-41119879	AG09319	gingival:	n/a
39	chr19:41119829-41119879	SK-N-SH_RA	brain:	n/a
40	chr19:41119829-41119879	MCF10A-Er-Src	breast:	n/a
41	chr19:41119829-41119879	HAEpiC	amniotic membrane:	n/a
42	chr19:41119829-41119879	AG09309	skin:	n/a
43	chr19:41119829-41119879	GM06990	blood:	n/a
44	chr19:41119829-41119879	T-47D	breast:	n/a
45	chr19:41119829-41119879	SK-N-MC	brain:	n/a
46	chr19:41119829-41119879	HRPEpiC	eye:	n/a
47	chr19:41119829-41119879	IMR90	lung:	fetal
48	chr19:41119829-41119879	SKMC	muscle:	n/a
49	chr19:41119829-41119879	HNPCEpiC	eye:	n/a
50	chr19:41119829-41119879	AG04450	lung:	fetal

No.	Distal block	Cell Line	Cell type
1	chr19:41118984..41122545-chr19:41130944..41134653,3	MCF-7	breast:
2	chr19:40971486..40973237-chr19:41118621..41121542,2	MCF-7	breast:
3	chr19:41081421..41083065-chr19:41119695..41121280,2	MCF-7	breast:
4	chr19:40970617..40972953-chr19:41119604..41121764,2	K562	blood:
5	chr19:41119264..41121274-chr19:41121495..41123120,2	MCF-7	breast:
6	chr19:40948473..40950774-chr19:41118397..41120012,2	MCF-7	breast:
7	chr19:41076913..41079410-chr19:41119355..41120987,2	K562	blood:
8	chr19:41101978..41104325-chr19:41119218..41120800,2	MCF-7	breast:
9	chr19:41088760..41090446-chr19:41117467..41120079,2	K562	blood:
10	chr19:40789948..40791553-chr19:41119261..41121070,2	K562	blood:
11	chr19:40930456..40933734-chr19:41119113..41120830,3	K562	blood:
12	chr19:41117621..41122754-chr19:41128365..41133445,15	K562	blood:
13	chr19:40930456..40932097-chr19:41118468..41120699,2	K562	blood:

Variant related genes	Relation type
LTBP4	TF binding region
LTBP4	CpG island
ENSG00000160460	Chromatin interaction
ENSG00000105221	Chromatin interaction
ENSG00000268366	Chromatin interaction
ENSG00000090013	Chromatin interaction
ENSG00000167565	Chromatin interaction
ENSG00000090006	Chromatin interaction
ENSG00000197019	Chromatin interaction
ENSG00000160410	Chromatin interaction

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

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs11665867	1.00[ASN][1000 genomes]
rs11666504	1.00[ASN][1000 genomes]
rs11667119	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11668042	1.00[ASN][1000 genomes]
rs11672227	1.00[ASN][1000 genomes]
rs11672651	1.00[ASN][1000 genomes]
rs36012476	1.00[ASN][1000 genomes]
rs4435368	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4624303	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55652103	1.00[ASN][1000 genomes]
rs55658896	0.89[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs55723406	1.00[ASN][1000 genomes]
rs55856492	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56041558	1.00[ASN][1000 genomes]
rs56140728	1.00[ASN][1000 genomes]
rs7253575	0.85[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7258772	1.00[ASN][1000 genomes]
rs7259121	1.00[ASN][1000 genomes]
rs73035918	0.89[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73047051	1.00[ASN][1000 genomes]
rs73047068	1.00[ASN][1000 genomes]
rs73047073	1.00[ASN][1000 genomes]
rs73047085	1.00[ASN][1000 genomes]
rs73047100	1.00[ASN][1000 genomes]
rs73048915	1.00[ASN][1000 genomes]
rs73048925	1.00[ASN][1000 genomes]
rs73051885	0.89[AMR][1000 genomes]
rs8106578	0.89[AMR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:17 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1830682	chr19:40880127-41270055	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS Flanking Active TSS Bivalent Enhancer 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	139 gene(s)	inside rSNPs	diseases
2	nsv911714	chr19:41006426-41165252	Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
3	nsv911715	chr19:41014922-41141434	Bivalent Enhancer Flanking Active TSS Strong transcription Weak transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
4	nsv1057634	chr19:41019512-41174259	Enhancers Active TSS Strong transcription Genic enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
5	nsv911717	chr19:41023511-41141434	Enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
6	nsv911719	chr19:41033109-41147087	Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
7	nsv911720	chr19:41033109-41156940	Flanking Active TSS Enhancers Bivalent/Poised TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
8	nsv911721	chr19:41040334-41124931	Weak transcription Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Strong transcription Genic enhancers 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	33 gene(s)	inside rSNPs	diseases
9	nsv911722	chr19:41040334-41176403	Bivalent Enhancer Enhancers Weak transcription Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
10	nsv911723	chr19:41075990-41195279	Active TSS Strong transcription Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
11	nsv869561	chr19:41077513-41139834	Weak transcription Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
12	nsv1064699	chr19:41086506-41174259	Genic enhancers Bivalent Enhancer Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Strong transcription Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
13	nsv911724	chr19:41089505-41165252	Bivalent/Poised TSS Strong transcription Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
14	nsv911726	chr19:41090190-41141434	Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Enhancers Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
15	nsv911727	chr19:41111069-41200511	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
16	nsv911728	chr19:41111069-41211056	Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Strong transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
17	nsv870022	chr19:41113071-41178982	Strong transcription Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region miRNA target site	27 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:41106000-41136800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr19:41109800-41122600	Weak transcription	Aorta	Aorta
3	chr19:41116400-41120000	Enhancers	Stomach Mucosa	stomach
4	chr19:41116600-41137000	Weak transcription	Psoas Muscle	Psoas
5	chr19:41117000-41121800	Weak transcription	Hela-S3	cervix
6	chr19:41117000-41140200	Weak transcription	Brain Angular Gyrus	brain
7	chr19:41117200-41120400	Weak transcription	Muscle Satellite Cultured Cells	--
8	chr19:41117400-41125200	Weak transcription	Brain Cingulate Gyrus	brain
9	chr19:41118400-41120400	Bivalent/Poised TSS	Rectal Smooth Muscle	rectum
10	chr19:41118800-41120600	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr19:41118800-41121200	Active TSS	H9 Cell Line	embryonic stem cell
12	chr19:41118800-41121400	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr19:41119000-41120000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
14	chr19:41119000-41120400	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr19:41119000-41120600	Active TSS	Osteobl	bone
16	chr19:41119000-41121000	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
17	chr19:41119000-41121000	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
18	chr19:41119000-41121000	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
19	chr19:41119000-41121000	Flanking Bivalent TSS/Enh	Fetal Adrenal Gland	Adrenal Gland
20	chr19:41119000-41121200	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chr19:41119000-41121200	Active TSS	HUES48 Cell Line	embryonic stem cell
22	chr19:41119000-41121200	Active TSS	iPS-15b Cell Line	embryonic stem cell
23	chr19:41119000-41121200	Active TSS	iPS-18 Cell Line	embryonic stem cell
24	chr19:41119000-41121200	Flanking Active TSS	Primary T cells fromperipheralblood	blood
25	chr19:41119000-41121400	Active TSS	HUES6 Cell Line	embryonic stem cell
26	chr19:41119000-41121400	Active TSS	HUES64 Cell Line	embryonic stem cell
27	chr19:41119000-41121400	Active TSS	iPS-20b Cell Line	embryonic stem cell
28	chr19:41119000-41121400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr19:41119000-41121400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr19:41119200-41120200	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr19:41119200-41120200	Active TSS	Breast Myoepithelial Primary Cells	Breast
32	chr19:41119200-41120200	Active TSS	Primary T cells from cord blood	blood
33	chr19:41119200-41120200	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
34	chr19:41119200-41120200	Active TSS	Primary T helper memory cells from peripheral blood 1	blood
35	chr19:41119200-41120200	Bivalent/Poised TSS	Brain Germinal Matrix	brain
36	chr19:41119200-41120200	Bivalent/Poised TSS	Duodenum Smooth Muscle	Duodenum
37	chr19:41119200-41120200	Bivalent/Poised TSS	Fetal Muscle Leg	muscle
38	chr19:41119200-41120200	Active TSS	A549	lung
39	chr19:41119200-41120200	Flanking Active TSS	HMEC	breast
40	chr19:41119200-41120200	Active TSS	NHEK	skin
41	chr19:41119200-41120400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr19:41119200-41120400	Flanking Active TSS	Pancreas	Pancrea
43	chr19:41119200-41120600	Flanking Active TSS	Esophagus	oesophagus
44	chr19:41119200-41120600	Bivalent/Poised TSS	Fetal Brain Female	brain
45	chr19:41119200-41120600	Flanking Bivalent TSS/Enh	Placenta	Placenta
46	chr19:41119200-41120600	Flanking Bivalent TSS/Enh	Stomach Smooth Muscle	stomach
47	chr19:41119200-41120800	Flanking Active TSS	Primary B cells from cord blood	blood
48	chr19:41119200-41120800	Active TSS	Brain Anterior Caudate	brain
49	chr19:41119200-41120800	Flanking Bivalent TSS/Enh	Fetal Intestine Small	intestine
50	chr19:41119200-41120800	Flanking Bivalent TSS/Enh	Fetal Stomach	stomach

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