Variant report

Variant	rs2369006
Chromosome Location	chr19:41120083-41120084
allele	A/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	ZMIZ1	chr19:41119989-41120142	K562	blood:	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	EGR1	chr19:41119880-41120121	K562	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	E2F6	chr19:41119204-41120106	H1-hESC	embryonic stem cell:	n/a	chr19:41119592-41119601 chr19:41119227-41119236 chr19:41119779-41119790
9	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
10	RCOR1	chr19:41119167-41120184	K562	blood:	n/a	n/a
11	POLR2A	chr19:41118763-41120672	H1-hESC	embryonic stem cell:	n/a	n/a
12	NFYB	chr19:41119768-41120104	K562	blood:	n/a	n/a
13	MAZ	chr19:41119378-41121483	IMR90	lung:	n/a	chr19:41121193-41121202 chr19:41121098-41121108
14	E2F6	chr19:41119198-41120097	K562	blood:	n/a	chr19:41119592-41119601 chr19:41119227-41119236 chr19:41119779-41119790
15	MAX	chr19:41119111-41120261	A549	lung:	n/a	chr19:41119225-41119235
16	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
17	ZNF143	chr19:41119173-41120123	GM12878	blood:	n/a	n/a
18	CHD2	chr19:41119652-41120172	H1-hESC	embryonic stem cell:	n/a	n/a
19	STAT1	chr19:41119156-41120174	GM12878	blood:	n/a	chr19:41119493-41119505
20	SIN3A	chr19:41119010-41120846	H1-hESC	embryonic stem cell:	n/a	chr19:41119191-41119204 chr19:41120571-41120582
21	MAX	chr19:41119127-41120599	ECC-1	luminal epithelium:	n/a	chr19:41119225-41119235
22	E2F6	chr19:41119113-41120112	H1-hESC	embryonic stem cell:	n/a	chr19:41119592-41119601 chr19:41119227-41119236 chr19:41119779-41119790
23	POLR2A	chr19:41119175-41120130	GM19099	blood:	n/a	n/a
24	POLR2A	chr19:41118766-41120158	HCT-116	colon:	n/a	n/a
25	TBL1XR1	chr19:41119700-41120211	K562	blood:	n/a	n/a
26	TAF1	chr19:41119643-41120142	H1-hESC	embryonic stem cell:	n/a	n/a
27	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
28	POLR2A	chr19:41119609-41120114	GM12878	blood:	n/a	n/a
29	TAF1	chr19:41119139-41120107	ECC-1	luminal epithelium:	n/a	n/a
30	POLR2A	chr19:41119199-41120129	GM12892	blood:	n/a	n/a
31	RCOR1	chr19:41119096-41120611	GM12878	blood:	n/a	n/a
32	POLR2A	chr19:41119122-41120991	Raji	blood:	n/a	n/a
33	NFYB	chr19:41119707-41120161	GM12878	blood:	n/a	n/a
34	POLR2A	chr19:41118781-41120856	H1-hESC	embryonic stem cell:	n/a	n/a
35	SP4	chr19:41118969-41120115	H1-hESC	embryonic stem cell:	n/a	chr19:41119244-41119260 chr19:41120055-41120066 chr19:41119589-41119605 chr19:41119224-41119240 chr19:41119587-41119603 chr19:41120019-41120030 chr19:41119751-41119767 chr19:41120035-41120046
36	POLR2A	chr19:41118830-41120307	HCT-116	colon:	n/a	n/a
37	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
38	CHD2	chr19:41119093-41120298	GM12878	blood:	n/a	chr19:41119593-41119603
39	POLR2A	chr19:41119000-41120951	MCF-7	breast:	n/a	n/a
40	TCF12	chr19:41118745-41121104	A549	lung:	n/a	chr19:41119559-41119569
41	MAX	chr19:41119061-41120751	K562	blood:	n/a	chr19:41119225-41119235
42	POLR2A	chr19:41119067-41120279	K562	blood:	n/a	n/a
43	MAZ	chr19:41119130-41121252	K562	blood:	n/a	chr19:41121193-41121202 chr19:41121098-41121108 chr19:41119225-41119235
44	POLR2A	chr19:41119209-41120228	GM18951	blood:	n/a	n/a
45	POLR2A	chr19:41119165-41120239	GM15510	blood:	n/a	n/a
46	POLR2A	chr19:41118948-41120131	K562	blood:	n/a	n/a
47	MAX	chr19:41119505-41120143	A549	lung:	n/a	n/a
48	SP1	chr19:41119102-41120202	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 chr19:41119754-41119764 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
49	CHD2	chr19:41119211-41120097	K562	blood:	n/a	chr19:41119593-41119603
50	ELF1	chr19:41118849-41121125	GM12878	blood:	n/a	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
ENSG00000090006	Chromatin interaction
ENSG00000105221	Chromatin interaction
ENSG00000160410	Chromatin interaction
ENSG00000160460	Chromatin interaction
ENSG00000090013	Chromatin interaction
ENSG00000197019	Chromatin interaction

Extended variants
information (count: 58 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs10402698	0.80[ASN][1000 genomes]
rs10403467	0.98[ASN][1000 genomes]
rs10403833	0.98[ASN][1000 genomes]
rs10403963	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs10405930	1.00[CHB][hapmap];0.95[JPT][hapmap];0.97[ASN][1000 genomes]
rs10410606	1.00[CHB][hapmap];0.95[JPT][hapmap];0.97[ASN][1000 genomes]
rs1051303	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs11083561	0.92[ASN][1000 genomes]
rs1131620	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs11667706	0.97[ASN][1000 genomes]
rs11667772	0.95[ASN][1000 genomes]
rs12610819	0.83[CHB][hapmap]
rs12611045	0.87[AFR][1000 genomes];0.87[AMR][1000 genomes];0.90[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12980111	0.98[ASN][1000 genomes]
rs1318544	0.97[ASN][1000 genomes]
rs1864074	1.00[CHB][hapmap];0.84[JPT][hapmap];0.92[ASN][1000 genomes]
rs1864078	1.00[CHB][hapmap];0.90[JPT][hapmap];0.92[ASN][1000 genomes]
rs1869712	0.97[ASN][1000 genomes]
rs2278246	0.98[ASN][1000 genomes]
rs2303727	0.96[ASN][1000 genomes]
rs2303729	1.00[CHB][hapmap];0.95[JPT][hapmap];0.97[ASN][1000 genomes]
rs2604902	1.00[CHB][hapmap];0.94[JPT][hapmap];0.97[ASN][1000 genomes]
rs28649715	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs28655571	0.98[ASN][1000 genomes]
rs392726	0.94[CHB][hapmap];0.86[ASN][1000 genomes]
rs393569	0.94[CHB][hapmap];0.82[ASN][1000 genomes]
rs396118	0.85[ASN][1000 genomes]
rs404584	0.88[CHB][hapmap];0.83[ASN][1000 genomes]
rs406133	0.81[ASN][1000 genomes]
rs410101	0.83[CHB][hapmap]
rs413901	0.83[CHB][hapmap]
rs415075	0.83[ASN][1000 genomes]
rs420720	0.85[ASN][1000 genomes]
rs4803348	0.83[AFR][1000 genomes];0.94[AMR][1000 genomes];0.83[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs56353506	0.98[ASN][1000 genomes]
rs7171	0.86[ASN][1000 genomes]
rs7259067	0.94[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs7259237	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs7259554	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs8107014	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs919307	0.97[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	chr19:41119200-41120200	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr19:41119200-41120200	Active TSS	Breast Myoepithelial Primary Cells	Breast
30	chr19:41119200-41120200	Active TSS	Primary T cells from cord blood	blood
31	chr19:41119200-41120200	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
32	chr19:41119200-41120200	Active TSS	Primary T helper memory cells from peripheral blood 1	blood
33	chr19:41119200-41120200	Bivalent/Poised TSS	Brain Germinal Matrix	brain
34	chr19:41119200-41120200	Bivalent/Poised TSS	Duodenum Smooth Muscle	Duodenum
35	chr19:41119200-41120200	Bivalent/Poised TSS	Fetal Muscle Leg	muscle
36	chr19:41119200-41120200	Active TSS	A549	lung
37	chr19:41119200-41120200	Flanking Active TSS	HMEC	breast
38	chr19:41119200-41120200	Active TSS	NHEK	skin
39	chr19:41119200-41120400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr19:41119200-41120400	Flanking Active TSS	Pancreas	Pancrea
41	chr19:41119200-41120600	Flanking Active TSS	Esophagus	oesophagus
42	chr19:41119200-41120600	Bivalent/Poised TSS	Fetal Brain Female	brain
43	chr19:41119200-41120600	Flanking Bivalent TSS/Enh	Placenta	Placenta
44	chr19:41119200-41120600	Flanking Bivalent TSS/Enh	Stomach Smooth Muscle	stomach
45	chr19:41119200-41120800	Flanking Active TSS	Primary B cells from cord blood	blood
46	chr19:41119200-41120800	Active TSS	Brain Anterior Caudate	brain
47	chr19:41119200-41120800	Flanking Bivalent TSS/Enh	Fetal Intestine Small	intestine
48	chr19:41119200-41120800	Flanking Bivalent TSS/Enh	Fetal Stomach	stomach
49	chr19:41119200-41120800	Flanking Bivalent TSS/Enh	Fetal Thymus	thymus
50	chr19:41119200-41120800	Active TSS	Small Intestine	intestine

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