Variant report

Variant	rs4435368
Chromosome Location	chr19:41120377-41120378
allele	A/G
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	CHD2	chr19:41120372-41120704	K562	blood:	n/a	n/a
2	CUX1	chr19:41120326-41120520	GM12878	blood:	n/a	n/a
3	MTA3	chr19:41119128-41120954	GM12878	blood:	n/a	n/a
4	ATF2	chr19:41120309-41120893	H1-hESC	embryonic stem cell:	n/a	n/a
5	GABPA	chr19:41120361-41120839	K562	blood:	n/a	n/a
6	MAX	chr19:41119491-41120783	MCF-7	breast:	n/a	n/a
7	POLR2A	chr19:41120301-41120398	HUVEC	blood vessel:	n/a	n/a
8	SP1	chr19:41120153-41121080	GM12878	blood:	n/a	chr19:41120965-41120977 chr19:41120622-41120631 chr19:41120642-41120654 chr19:41120643-41120653 chr19:41120643-41120653 chr19:41120642-41120654 chr19:41120643-41120652 chr19:41120965-41120977 chr19:41120643-41120652 chr19:41120644-41120653 chr19:41120966-41120975 chr19:41121049-41121063 chr19:41120643-41120657
9	TEAD4	chr19:41120095-41120824	K562	blood:	n/a	n/a
10	POLR2A	chr19:41118763-41120672	H1-hESC	embryonic stem cell:	n/a	n/a
11	SP1	chr19:41120285-41121224	K562	blood:	n/a	chr19:41120965-41120977 chr19:41120622-41120631 chr19:41120642-41120654 chr19:41120643-41120653 chr19:41120643-41120653 chr19:41120642-41120654 chr19:41120643-41120652 chr19:41120965-41120977 chr19:41120643-41120652 chr19:41120644-41120653 chr19:41120966-41120975 chr19:41121049-41121063 chr19:41120643-41120657
12	MAZ	chr19:41119378-41121483	IMR90	lung:	n/a	chr19:41121193-41121202 chr19:41121098-41121108
13	SIN3A	chr19:41119010-41120846	H1-hESC	embryonic stem cell:	n/a	chr19:41119191-41119204 chr19:41120571-41120582
14	MAX	chr19:41119127-41120599	ECC-1	luminal epithelium:	n/a	chr19:41119225-41119235
15	CTCF	chr19:41120320-41120470	HRPEpiC	eye:	n/a	n/a
16	GTF2F1	chr19:41120373-41120600	K562	blood:	n/a	n/a
17	MAFK	chr19:41120357-41120666	K562	blood:	n/a	n/a
18	EBF1	chr19:41120184-41120654	GM12878	blood:	n/a	chr19:41120408-41120418 chr19:41120409-41120418 chr19:41120408-41120419
19	RUNX3	chr19:41120276-41120745	GM12878	blood:	n/a	n/a
20	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
21	RCOR1	chr19:41119096-41120611	GM12878	blood:	n/a	n/a
22	CCNT2	chr19:41120259-41120473	K562	blood:	n/a	n/a
23	POLR2A	chr19:41119122-41120991	Raji	blood:	n/a	n/a
24	ZEB1	chr19:41120292-41120773	GM12878	blood:	n/a	chr19:41120338-41120350
25	MYC	chr19:41120190-41120433	MCF-7	breast:	n/a	n/a
26	POLR2A	chr19:41118781-41120856	H1-hESC	embryonic stem cell:	n/a	n/a
27	RUNX3	chr19:41120338-41120791	GM12878	blood:	n/a	n/a
28	MAX	chr19:41120168-41121253	ECC-1	luminal epithelium:	n/a	chr19:41121193-41121202 chr19:41121098-41121108
29	IRF1	chr19:41119045-41121250	K562	blood:	n/a	chr19:41120694-41120703 chr19:41120640-41120654 chr19:41119226-41119240 chr19:41119591-41119605 chr19:41119176-41119190 chr19:41119246-41119260 chr19:41120963-41120977 chr19:41119949-41119963 chr19:41121107-41121121
30	POLR2A	chr19:41119000-41120951	MCF-7	breast:	n/a	n/a
31	TCF12	chr19:41118745-41121104	A549	lung:	n/a	chr19:41119559-41119569
32	MAX	chr19:41119061-41120751	K562	blood:	n/a	chr19:41119225-41119235
33	ZC3H11A	chr19:41120345-41120857	K562	blood:	n/a	n/a
34	MAZ	chr19:41119130-41121252	K562	blood:	n/a	chr19:41121193-41121202 chr19:41121098-41121108 chr19:41119225-41119235
35	UBTF	chr19:41120310-41121075	K562	blood:	n/a	n/a
36	STAT5A	chr19:41120226-41120903	GM12878	blood:	n/a	chr19:41120490-41120497
37	ELF1	chr19:41118849-41121125	GM12878	blood:	n/a	n/a
38	SP1	chr19:41120247-41120873	A549	lung:	n/a	chr19:41120622-41120631 chr19:41120642-41120654 chr19:41120643-41120653 chr19:41120643-41120653 chr19:41120642-41120654 chr19:41120643-41120652 chr19:41120643-41120652 chr19:41120644-41120653 chr19:41120643-41120657
39	SP1	chr19:41118947-41121158	A549	lung:	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
40	POLR2A	chr19:41119187-41121012	PBDE	blood:	n/a	n/a
41	POLR2A	chr19:41118605-41121457	PFSK-1	brain:	n/a	n/a
42	POLR2A	chr19:41119099-41120385	MCF-7	breast:	n/a	n/a
43	SP4	chr19:41120374-41121074	H1-hESC	embryonic stem cell:	n/a	chr19:41120640-41120656
44	YY1	chr19:41120278-41120733	K562	blood:	n/a	n/a
45	JUND	chr19:41120088-41120973	MCF-7	breast:	n/a	chr19:41120588-41120602
46	SP4	chr19:41120358-41120870	H1-hESC	embryonic stem cell:	n/a	chr19:41120640-41120656
47	SRF	chr19:41120367-41121267	MCF-7	breast:	n/a	n/a
48	MAZ	chr19:41119092-41121096	GM12878	blood:	n/a	chr19:41119225-41119235
49	POLR2A	chr19:41118749-41121117	SK-N-MC	brain:	n/a	n/a
50	POLR2A	chr19:41119756-41120985	IMR90	lung:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:41120329-41120379	AG04449	skin:	fetal
2	chr19:41120329-41120379	MCF-7	breast:	n/a
3	chr19:41120329-41120379	NB4	blood:	n/a
4	chr19:41120329-41120379	HepG2	liver:	n/a
5	chr19:41120329-41120379	HUVEC	blood vessel:	n/a
6	chr19:41120329-41120379	MCF10A-Er-Src	breast:	n/a
7	chr19:41120329-41120379	Hela-S3	cervix:	n/a
8	chr19:41120329-41120379	PFSK-1	brain:	n/a
9	chr19:41120329-41120379	A549	lung:	n/a
10	chr19:41120329-41120379	AG09319	gingival:	n/a
11	chr19:41120329-41120379	LNCaP	prostate:	n/a
12	chr19:41120329-41120379	NT2-D1	testis:	n/a
13	chr19:41120329-41120379	AG10803	skin:	n/a
14	chr19:41120329-41120379	Caco-2	colon:	n/a
15	chr19:41120329-41120379	HRE	kidney:	n/a
16	chr19:41120329-41120379	HEK293	kidney:	embryo
17	chr19:41120329-41120379	HIPEpiC	eye:	n/a
18	chr19:41120329-41120379	BJ	skin:	n/a
19	chr19:41120329-41120379	HRCEpiC	kidney:	n/a
20	chr19:41120329-41120379	GM19239	blood:	n/a
21	chr19:41120329-41120379	HEEpiC	esophagus:	n/a
22	chr19:41120329-41120379	ProgFib	skin:	n/a
23	chr19:41120329-41120379	T-47D	breast:	n/a
24	chr19:41120329-41120379	HRPEpiC	eye:	n/a
25	chr19:41120329-41120379	SK-N-SH_RA	brain:	n/a
26	chr19:41120329-41120379	HCT-116	colon:	n/a
27	chr19:41120329-41120379	PANC-1	pancreas:	n/a
28	chr19:41120329-41120379	HCM	heart:	n/a
29	chr19:41120329-41120379	PrEC	prostate:	n/a
30	chr19:41120329-41120379	GM12891	blood:	n/a
31	chr19:41120329-41120379	ovcar-3	ovarian:	n/a
32	chr19:41120329-41120379	Hepatocyte	liver:	n/a
33	chr19:41120329-41120379	CMK	blood:	n/a
34	chr19:41120329-41120379	HNPCEpiC	eye:	n/a
35	chr19:41120329-41120379	ECC-1	luminal epithelium:	n/a
36	chr19:41120329-41120379	GM12878	blood:	n/a
37	chr19:41120329-41120379	Jurkat	blood:	n/a
38	chr19:41120329-41120379	AG04450	lung:	fetal
39	chr19:41120329-41120379	SKMC	muscle:	n/a
40	chr19:41120329-41120379	GM12892	blood:	n/a
41	chr19:41120329-41120379	HCPEpiC	choroid plexus:	n/a
42	chr19:41120329-41120379	H1-hESC	embryonic stem cell:	embryo
43	chr19:41120329-41120379	NHBE	bronchial:	n/a
44	chr19:41120329-41120379	HMEC	breast:	n/a
45	chr19:41120329-41120379	AG09309	skin:	n/a
46	chr19:41120329-41120379	HPAEpiC	pulmonary alveolar:	n/a
47	chr19:41120329-41120379	U87	brain:	n/a
48	chr19:41120329-41120379	HAEpiC	amniotic membrane:	n/a
49	chr19:41120329-41120379	NHDF-neo	bronchial:	n/a
50	chr19:41120329-41120379	SAEC	small airway:	n/a

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	chr19:41119884..41122816-chr19:41127370..41130174,2	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	chr19:40789948..40791553-chr19:41119261..41121070,2	K562	blood:
10	chr19:40930456..40933734-chr19:41119113..41120830,3	K562	blood:
11	chr19:41117621..41122754-chr19:41128365..41133445,15	K562	blood:
12	chr19:40930456..40932097-chr19:41118468..41120699,2	K562	blood:

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

Extended variants
information (count: 46 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs11665867	1.00[ASN][1000 genomes]
rs11666504	1.00[ASN][1000 genomes]
rs11667119	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11668042	1.00[ASN][1000 genomes]
rs11672227	1.00[ASN][1000 genomes]
rs11672651	0.81[CEU][hapmap];1.00[ASN][1000 genomes]
rs11673027	0.81[CEU][hapmap];1.00[GIH][hapmap];0.82[MEX][hapmap];0.88[TSI][hapmap]
rs1864077	0.86[YRI][hapmap]
rs2077407	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs36012476	1.00[ASN][1000 genomes]
rs4624303	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55652103	1.00[ASN][1000 genomes]
rs55658896	1.00[ASN][1000 genomes]
rs55723406	1.00[ASN][1000 genomes]
rs55856492	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56041558	1.00[ASN][1000 genomes]
rs56140728	1.00[ASN][1000 genomes]
rs7253575	1.00[ASN][1000 genomes]
rs7258772	1.00[ASN][1000 genomes]
rs7259121	1.00[ASN][1000 genomes]
rs73035918	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]
rs8106578	0.81[CEU][hapmap];1.00[GIH][hapmap];0.82[MEX][hapmap];0.85[TSI][hapmap];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	chr19:41116600-41137000	Weak transcription	Psoas Muscle	Psoas
4	chr19:41117000-41121800	Weak transcription	Hela-S3	cervix
5	chr19:41117000-41140200	Weak transcription	Brain Angular Gyrus	brain
6	chr19:41117200-41120400	Weak transcription	Muscle Satellite Cultured Cells	--
7	chr19:41117400-41125200	Weak transcription	Brain Cingulate Gyrus	brain
8	chr19:41118400-41120400	Bivalent/Poised TSS	Rectal Smooth Muscle	rectum
9	chr19:41118800-41120600	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr19:41118800-41121200	Active TSS	H9 Cell Line	embryonic stem cell
11	chr19:41118800-41121400	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr19:41119000-41120400	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr19:41119000-41120600	Active TSS	Osteobl	bone
14	chr19:41119000-41121000	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr19:41119000-41121000	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
16	chr19:41119000-41121000	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
17	chr19:41119000-41121000	Flanking Bivalent TSS/Enh	Fetal Adrenal Gland	Adrenal Gland
18	chr19:41119000-41121200	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
19	chr19:41119000-41121200	Active TSS	HUES48 Cell Line	embryonic stem cell
20	chr19:41119000-41121200	Active TSS	iPS-15b Cell Line	embryonic stem cell
21	chr19:41119000-41121200	Active TSS	iPS-18 Cell Line	embryonic stem cell
22	chr19:41119000-41121200	Flanking Active TSS	Primary T cells fromperipheralblood	blood
23	chr19:41119000-41121400	Active TSS	HUES6 Cell Line	embryonic stem cell
24	chr19:41119000-41121400	Active TSS	HUES64 Cell Line	embryonic stem cell
25	chr19:41119000-41121400	Active TSS	iPS-20b Cell Line	embryonic stem cell
26	chr19:41119000-41121400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr19:41119000-41121400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr19:41119200-41120400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr19:41119200-41120400	Flanking Active TSS	Pancreas	Pancrea
30	chr19:41119200-41120600	Flanking Active TSS	Esophagus	oesophagus
31	chr19:41119200-41120600	Bivalent/Poised TSS	Fetal Brain Female	brain
32	chr19:41119200-41120600	Flanking Bivalent TSS/Enh	Placenta	Placenta
33	chr19:41119200-41120600	Flanking Bivalent TSS/Enh	Stomach Smooth Muscle	stomach
34	chr19:41119200-41120800	Flanking Active TSS	Primary B cells from cord blood	blood
35	chr19:41119200-41120800	Active TSS	Brain Anterior Caudate	brain
36	chr19:41119200-41120800	Flanking Bivalent TSS/Enh	Fetal Intestine Small	intestine
37	chr19:41119200-41120800	Flanking Bivalent TSS/Enh	Fetal Stomach	stomach
38	chr19:41119200-41120800	Flanking Bivalent TSS/Enh	Fetal Thymus	thymus
39	chr19:41119200-41120800	Active TSS	Small Intestine	intestine
40	chr19:41119200-41121000	Active TSS	H1 Cell Line	embryonic stem cell
41	chr19:41119200-41121000	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
42	chr19:41119200-41121000	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr19:41119200-41121000	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
44	chr19:41119200-41121000	Flanking Bivalent TSS/Enh	Primary neutrophils fromperipheralblood	blood
45	chr19:41119200-41121000	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
46	chr19:41119200-41121000	Flanking Bivalent TSS/Enh	Fetal Muscle Trunk	muscle
47	chr19:41119200-41121000	Active TSS	Left Ventricle	heart
48	chr19:41119200-41121200	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
49	chr19:41119200-41121200	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
50	chr19:41119200-41121200	Active TSS	Fetal Kidney	kidney

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