Variant report

Variant	rs10411908
Chromosome Location	chr19:42783666-42783667
allele	G/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	POLR2A	chr19:42783448-42785016	GM12892	blood:	n/a	n/a
2	POLR2A	chr19:42783644-42783859	A549	lung:	n/a	n/a
3	ETS1	chr19:42783344-42784802	A549	lung:	n/a	chr19:42784030-42784043 chr19:42784101-42784112
4	TAF1	chr19:42783600-42784796	PFSK-1	brain:	n/a	n/a
5	POLR2A	chr19:42783605-42784919	PANC-1	pancreas:	n/a	n/a
6	POLR2A	chr19:42783290-42786530	K562	blood:	n/a	n/a
7	POLR2A	chr19:42783589-42784955	GM12891	blood:	n/a	n/a
8	ATF3	chr19:42783212-42785007	A549	lung:	n/a	chr19:42784295-42784304 chr19:42784977-42784986 chr19:42784547-42784556 chr19:42784588-42784597
9	ATF3	chr19:42783631-42784898	A549	lung:	n/a	chr19:42784295-42784304 chr19:42784547-42784556 chr19:42784588-42784597
10	SIX5	chr19:42782692-42785106	A549	lung:	n/a	n/a
11	RAD21	chr19:42783252-42785037	SK-N-SH	brain:	n/a	chr19:42784058-42784072 chr19:42784086-42784099 chr19:42784087-42784097 chr19:42784555-42784569 chr19:42783408-42783421
12	POLR2A	chr19:42783506-42785027	PBDE	blood:	n/a	n/a
13	MAX	chr19:42783361-42789666	A549	lung:	n/a	chr19:42784941-42784951 chr19:42786707-42786717 chr19:42786161-42786171 chr19:42788533-42788543 chr19:42786706-42786717
14	POLR2A	chr19:42782865-42784912	HepG2	liver:	n/a	n/a
15	SP1	chr19:42783495-42785168	A549	lung:	n/a	chr19:42785069-42785078 chr19:42784624-42784645 chr19:42784918-42784927 chr19:42785023-42785032 chr19:42784913-42784922 chr19:42784654-42784675 chr19:42784574-42784584 chr19:42784308-42784322 chr19:42785068-42785078 chr19:42784914-42784928
16	SP1	chr19:42783636-42785271	HCT-116	colon:	n/a	chr19:42785069-42785078 chr19:42784624-42784645 chr19:42784918-42784927 chr19:42785023-42785032 chr19:42784913-42784922 chr19:42784654-42784675 chr19:42784574-42784584 chr19:42784308-42784322 chr19:42785068-42785078 chr19:42784914-42784928
17	ELF1	chr19:42783499-42785011	A549	lung:	n/a	chr19:42784711-42784720 chr19:42784103-42784112 chr19:42784256-42784265 chr19:42784104-42784116
18	ZBTB33	chr19:42783546-42784915	A549	lung:	n/a	chr19:42784584-42784594
19	PBX3	chr19:42783505-42785234	A549	lung:	n/a	chr19:42784664-42784673 chr19:42784634-42784643
20	POLR2A	chr19:42783661-42784968	U87	brain:	n/a	n/a
21	CTCF	chr19:42781622-42785846	A549	lung:	n/a	chr19:42784097-42784110 chr19:42783407-42783420 chr19:42783100-42783113 chr19:42784251-42784264 chr19:42782182-42782200 chr19:42784085-42784103 chr19:42784087-42784100 chr19:42782184-42782205 chr19:42783097-42783115
22	HMGN3	chr19:42783643-42785042	K562	blood:	n/a	n/a
23	EP300	chr19:42783530-42785008	A549	lung:	n/a	chr19:42784254-42784270 chr19:42784549-42784565 chr19:42784053-42784069 chr19:42784937-42784946 chr19:42784097-42784113
24	RAD21	chr19:42783660-42784547	SK-N-SH_RA	brain:	n/a	chr19:42784058-42784072 chr19:42784086-42784099 chr19:42784087-42784097
25	ZMIZ1	chr19:42783663-42784857	K562	blood:	n/a	n/a
26	SIX5	chr19:42783624-42784181	A549	lung:	n/a	n/a
27	GABPA	chr19:42783522-42784113	A549	lung:	n/a	n/a
28	CTCF	chr19:42783560-42783710	AG10803	skin:	n/a	n/a
29	POLR2A	chr19:42783624-42785066	A549	lung:	n/a	n/a
30	POLR2A	chr19:42783321-42783673	GM12891	blood:	n/a	n/a
31	POLR2A	chr19:42783386-42785011	GM12878	blood:	n/a	n/a
32	POLR2A	chr19:42781501-42785091	PFSK-1	brain:	n/a	n/a
33	MYC	chr19:42783657-42785587	K562	blood:	n/a	chr19:42784941-42784951
34	POLR2A	chr19:42782012-42786927	U87	brain:	n/a	n/a
35	MTA3	chr19:42783390-42785837	GM12878	blood:	n/a	n/a
36	PML	chr19:42783474-42785110	GM12878	blood:	n/a	n/a
37	POLR2A	chr19:42783476-42785074	GM12892	blood:	n/a	n/a
38	ETS1	chr19:42783610-42784984	A549	lung:	n/a	chr19:42784030-42784043 chr19:42784899-42784908 chr19:42784101-42784112
39	POLR2A	chr19:42783313-42786769	K562	blood:	n/a	n/a
40	SIN3AK20	chr19:42783573-42785029	A549	lung:	n/a	n/a
41	GATA3	chr19:42783381-42785267	A549	lung:	n/a	chr19:42783394-42783407 chr19:42783396-42783404 chr19:42784320-42784329 chr19:42785137-42785147
42	SIN3AK20	chr19:42783377-42784167	A549	lung:	n/a	n/a
43	TCF12	chr19:42783241-42785257	A549	lung:	n/a	chr19:42784112-42784122 chr19:42783464-42783474 chr19:42785031-42785038 chr19:42783818-42783826 chr19:42784035-42784045
44	POLR2A	chr19:42783262-42786908	U87	brain:	n/a	n/a
45	POLR2A	chr19:42781915-42785217	PFSK-1	brain:	n/a	n/a
46	POLR2A	chr19:42783625-42784942	SK-N-SH	brain:	n/a	n/a
47	POLR2A	chr19:42781785-42788117	SK-N-MC	brain:	n/a	n/a
48	CTCF	chr19:42783363-42785105	SK-N-SH	brain:	n/a	chr19:42784097-42784110 chr19:42783407-42783420 chr19:42784251-42784264 chr19:42784085-42784103 chr19:42784087-42784100
49	CREB1	chr19:42783655-42785056	A549	lung:	n/a	n/a
50	FOSL2	chr19:42783470-42784108	A549	lung:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr19:42744297..42761073-chr19:42776978..42802286,113	MCF-7	breast:
2	chr19:42783597..42784516-chr4:169552208..169552881,2	HCT-116	colon:
3	chr19:42719792..42722067-chr19:42782556..42784868,3	MCF-7	breast:
4	chr19:42743599..42762610-chr19:42780302..42801550,102	MCF-7	breast:
5	chr19:42783298..42787362-chr19:42802681..42808039,8	MCF-7	breast:
6	chr19:42720002..42723178-chr19:42782377..42785942,3	MCF-7	breast:

Variant related genes	Relation type
CIC	TF binding region
ENSG00000160570	Chromatin interaction
ENSG00000129116	Chromatin interaction
ENSG00000268643	Chromatin interaction
ENSG00000105723	Chromatin interaction
ENSG00000204957	Chromatin interaction
ENSG00000188368	Chromatin interaction
ENSG00000079462	Chromatin interaction
ENSG00000105722	Chromatin interaction

Extended variants
information (count: 104 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:84)

rs_ID	r²[population]
rs10401224	1.00[EUR][1000 genomes]
rs10402438	1.00[EUR][1000 genomes]
rs10404650	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10406800	1.00[AMR][1000 genomes]
rs10406972	1.00[EUR][1000 genomes]
rs10407085	1.00[EUR][1000 genomes]
rs10407155	1.00[EUR][1000 genomes]
rs10407842	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10408141	0.82[AFR][1000 genomes]
rs10408258	1.00[EUR][1000 genomes]
rs10409428	1.00[EUR][1000 genomes]
rs10409433	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10409939	1.00[EUR][1000 genomes]
rs10410129	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10410653	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10411498	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10413484	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10415759	1.00[AMR][1000 genomes]
rs10415999	1.00[EUR][1000 genomes]
rs10416535	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10418312	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10421331	1.00[AMR][1000 genomes]
rs10421409	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10421510	1.00[EUR][1000 genomes]
rs10421857	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10421902	1.00[AMR][1000 genomes]
rs10422301	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10422867	1.00[EUR][1000 genomes]
rs10423812	1.00[EUR][1000 genomes]
rs10423959	1.00[EUR][1000 genomes]
rs10423978	1.00[EUR][1000 genomes]
rs10424402	1.00[EUR][1000 genomes]
rs10425003	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10425320	1.00[EUR][1000 genomes]
rs10425783	1.00[EUR][1000 genomes]
rs10426267	1.00[EUR][1000 genomes]
rs10426284	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11878207	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11878297	1.00[EUR][1000 genomes]
rs11879073	1.00[EUR][1000 genomes]
rs11879538	1.00[EUR][1000 genomes]
rs11880214	1.00[EUR][1000 genomes]
rs11880356	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11882107	1.00[EUR][1000 genomes]
rs11882801	1.00[EUR][1000 genomes]
rs12165130	1.00[EUR][1000 genomes]
rs13343322	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13343388	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13343719	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13343761	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13343834	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13343966	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13346837	1.00[EUR][1000 genomes]
rs2229614	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28463673	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28469564	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28474957	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28483598	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28496975	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28657829	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28663042	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28675019	1.00[EUR][1000 genomes]
rs28675764	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28699037	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28711448	1.00[EUR][1000 genomes]
rs28715574	1.00[EUR][1000 genomes]
rs33919763	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs35707383	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs36089262	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs41407146	1.00[AMR][1000 genomes]
rs59870753	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60950516	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7246232	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7248473	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7254853	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7255343	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7258727	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73552879	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73554520	1.00[EUR][1000 genomes]
rs73554531	1.00[EUR][1000 genomes]
rs73558432	1.00[AMR][1000 genomes]
rs8099885	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs8109258	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9304602	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:20 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv522854	chr19:42120283-42931004	Weak transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	104 gene(s)	inside rSNPs	diseases
2	nsv520239	chr19:42357455-42931004	Flanking Active TSS Enhancers Bivalent Enhancer Active TSS Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	92 gene(s)	inside rSNPs	diseases
3	esv1805469	chr19:42367635-42798851	Enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
4	nsv911782	chr19:42514712-42931004	Bivalent/Poised TSS Enhancers Strong transcription Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	71 gene(s)	inside rSNPs	diseases
5	esv1794508	chr19:42580026-42791462	Strong transcription Active TSS Genic enhancers Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS 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	60 gene(s)	inside rSNPs	diseases
6	nsv1055554	chr19:42619671-42821642	Bivalent Enhancer Flanking Active TSS Enhancers Strong transcription Weak transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	53 gene(s)	inside rSNPs	diseases
7	nsv526186	chr19:42676481-43203507	Enhancers Bivalent Enhancer Genic enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	62 gene(s)	inside rSNPs	diseases
8	esv2422471	chr19:42733141-43669485	Genic enhancers Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	70 gene(s)	inside rSNPs	diseases
9	nsv833834	chr19:42736444-42835027	Genic enhancers Flanking Active TSS Strong transcription Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	42 gene(s)	inside rSNPs	diseases
10	nsv911784	chr19:42741124-42787664	Flanking Active TSS Enhancers Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	36 gene(s)	inside rSNPs	diseases
11	nsv911785	chr19:42741124-42917545	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	46 gene(s)	inside rSNPs	diseases
12	nsv911786	chr19:42744234-42797959	Flanking Active TSS Enhancers Active TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	39 gene(s)	inside rSNPs	diseases
13	esv1802977	chr19:42754437-42789945	Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	31 gene(s)	inside rSNPs	diseases
14	esv1801251	chr19:42768288-42788467	Enhancers Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	21 gene(s)	inside rSNPs	diseases
15	esv1803455	chr19:42768288-42788467	Flanking Active TSS Active TSS Genic enhancers Weak transcription Strong transcription 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	21 gene(s)	inside rSNPs	diseases
16	esv1803706	chr19:42768288-42788467	Genic enhancers Enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	21 gene(s)	inside rSNPs	diseases
17	esv1801291	chr19:42772432-42788467	Flanking Active TSS Active TSS Genic enhancers Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	21 gene(s)	inside rSNPs	diseases
18	esv1801294	chr19:42772432-42788467	Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	21 gene(s)	inside rSNPs	diseases
19	esv1801914	chr19:42772432-42788467	Active TSS Weak transcription Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	21 gene(s)	inside rSNPs	diseases
20	nsv911787	chr19:42773862-42795554	Active TSS Genic enhancers Flanking Active TSS Enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	23 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:42778400-42783800	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr19:42779400-42783800	Enhancers	Right Atrium	heart
3	chr19:42780000-42783800	Enhancers	Psoas Muscle	Psoas
4	chr19:42780600-42783800	Enhancers	Left Ventricle	heart
5	chr19:42780600-42783800	Enhancers	Placenta Amnion	Placenta Amnion
6	chr19:42781200-42783800	Enhancers	Liver	Liver
7	chr19:42781200-42783800	Enhancers	Stomach Mucosa	stomach
8	chr19:42781800-42783800	Enhancers	Rectal Mucosa Donor 31	rectum
9	chr19:42781800-42783800	Transcr. at gene 5' and 3'	NHEK	skin
10	chr19:42781800-42784000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr19:42781800-42784000	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr19:42781800-42784000	Enhancers	Lung	lung
13	chr19:42781800-42784000	Enhancers	Small Intestine	intestine
14	chr19:42781800-42784000	Flanking Active TSS	Stomach Smooth Muscle	stomach
15	chr19:42781800-42784000	Flanking Active TSS	HSMMtube	muscle
16	chr19:42781800-42784200	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
17	chr19:42782000-42783800	Enhancers	Primary T cells fromperipheralblood	blood
18	chr19:42782000-42784000	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
19	chr19:42782000-42784200	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
20	chr19:42782200-42783800	Enhancers	Primary B cells from peripheral blood	blood
21	chr19:42782400-42783800	Enhancers	Primary B cells from cord blood	blood
22	chr19:42782400-42783800	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
23	chr19:42782400-42784000	Enhancers	Sigmoid Colon	Sigmoid Colon
24	chr19:42782400-42784000	Enhancers	Spleen	Spleen
25	chr19:42782400-42784000	Flanking Active TSS	HMEC	breast
26	chr19:42782600-42783800	Enhancers	Primary T helper naive cells from peripheral blood	blood
27	chr19:42782600-42783800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
28	chr19:42782600-42784000	Flanking Active TSS	Rectal Smooth Muscle	rectum
29	chr19:42782800-42783800	Enhancers	HUVEC	blood vessel
30	chr19:42782800-42784000	Flanking Active TSS	Brain Germinal Matrix	brain
31	chr19:42782800-42784000	Flanking Active TSS	Fetal Brain Female	brain
32	chr19:42783000-42783800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr19:42783000-42783800	Enhancers	Primary monocytes fromperipheralblood	blood
34	chr19:42783000-42783800	Enhancers	Primary T cells from cord blood	blood
35	chr19:42783000-42784000	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr19:42783000-42784000	Flanking Active TSS	Dnd41	blood
37	chr19:42783000-42784000	Flanking Active TSS	GM12878-XiMat	blood
38	chr19:42783000-42784000	Flanking Active TSS	Hela-S3	cervix
39	chr19:42783000-42784200	Flanking Active TSS	Duodenum Mucosa	Duodenum
40	chr19:42783200-42783800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr19:42783200-42783800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
42	chr19:42783200-42783800	Enhancers	Placenta	Placenta
43	chr19:42783200-42784000	Flanking Active TSS	Brain Anterior Caudate	brain
44	chr19:42783200-42784200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr19:42783200-42784200	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr19:42783200-42784600	Flanking Active TSS	Adipose Nuclei	Adipose
47	chr19:42783200-42784800	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
48	chr19:42783400-42783800	Enhancers	ES-I3 Cell Line	embryonic stem cell
49	chr19:42783400-42783800	Flanking Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr19:42783400-42783800	Enhancers	iPS-15b Cell Line	embryonic stem cell

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